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Meroterpenoids produced by fungi
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1522-2675(20010131)84:1<259::aid-hlca259>3.0.co;2-oopenalex-snapshot
Albaconol, A Novel Prenylated Resorcinol (=Benzene-1,3-diol) from BasidiomycetesAlbatrellus confluens
inferredcites →https://doi.org/10.1002/ardp.200390008openalex-snapshot
Activities of Prenylphenol Derivatives from Fruitbodies of Albatrellus spp. on the Human and Rat Vanilloid Receptor 1 (VR1) and Characterisation of the Novel Natural Product, Confluentin
inferredcites →https://doi.org/10.1002/cbdv.200890032openalex-snapshot
Larvicidal Effects of Fungal Meroterpenoids in the Control of Aedes aegypti L., the Main Vector of Dengue and Yellow Fever
inferredcites →https://doi.org/10.1002/cbdv.200890047openalex-snapshot
A New Meroterpenoid Pigment from the Basidiomycete Albatrellus confluens
inferredcites →https://doi.org/10.1002/cber.19751081202openalex-snapshot
Pilzpigmente, XXIII. Tridentochinon, ein [13](3,6)Benzofuranophan aus Suillus tridentinus (Boletales)
inferredcites →https://doi.org/10.1002/ejoc.200500714openalex-snapshot
Chromogenic Meroterpenoids from the Mushrooms Russula ochroleuca and R. viscida
inferredcites →https://doi.org/10.1002/ejoc.200601022openalex-snapshot
Meroterpenoid Pigments from Albatrellus flettii (Basidiomycetes)
inferredcites →https://doi.org/10.1002/ejoc.200700908openalex-snapshot
Studies on the Structure and Biosynthesis of Tridentoquinone and Related Meroterpenoids from the Mushroom Suillus tridentinus (Boletales)
inferredcites →https://doi.org/10.1002/jlac.198119811203openalex-snapshot
Antibiotika aus Basidiomyceten, XII. Cristatsäure, ein modifiziertes Farnesylphenol aus Fruchtkörpern von Albatrellus cristatus
inferredcites →https://doi.org/10.1007/3-540-69542-7_1openalex-snapshot
Application of Isotopic Methods to Secondary Metabolic Pathways
inferredcites →https://doi.org/10.1016/0031-9422(75)83041-xopenalex-snapshot
Ascochlorin: A terpenoid metabolite from Acremonium luzulae
inferredcites →https://doi.org/10.1016/0031-9422(92)80127-zopenalex-snapshot
Chromans, hericenones F, G and H from the mushroom Hericium erinaceum
inferredcites →https://doi.org/10.1016/0040-4039(91)80039-9openalex-snapshot
Hericenones C, D and E, stimulators of nerve growth factor (NGF)-synthesis, from the mushroom Hericium erinaceum
inferredcites →https://doi.org/10.1016/0040-4039(91)80828-topenalex-snapshot
The structures of citreohybridone A and B novel sesterterpenoid-type metabolites of a hybrid strain KO 0031 derived from penicillium citreo-viride B. IFO 6200 and 4692
inferredcites →https://doi.org/10.1016/0040-4039(95)02412-3openalex-snapshot
Andrastins A∼C, new protein farnesyltransferase inhibitors, produced by Penicillium sp. FO-3929
inferredcites →https://doi.org/10.1016/0041-008x(73)90057-4openalex-snapshot
Viridicatumtoxin, a new mycotoxin from Penicillium viridicatum westling
inferredcites →https://doi.org/10.1016/0045-2068(74)90031-5openalex-snapshot
Biosynthesis of an antibiotic, siccanin
inferredcites →https://doi.org/10.1016/j.bmc.2005.08.005openalex-snapshot
Grifolin derivatives from Albatrellus caeruleoporus, new inhibitors of nitric oxide production in RAW 264.7 cells
inferredcites →https://doi.org/10.1016/j.bmcl.2004.10.067openalex-snapshot
Isoterreulactone A, a novel meroterpenoid with anti-acetylcholinesterase activity produced by Aspergillus terreus
inferredcites →https://doi.org/10.1016/j.chroma.2004.07.031openalex-snapshot
Analysis of some cytokinins in coconut (Cocos nucifera L.) water by micellar electrokinetic capillary chromatography after solid-phase extraction
inferredcites →https://doi.org/10.1016/j.phytochem.2006.01.008openalex-snapshot
Tropolactones A–D, four meroterpenoids from a marine-derived fungus of the genus Aspergillus
inferredcites →https://doi.org/10.1016/j.tet.2004.06.059openalex-snapshot
Absolute stereochemistries and total synthesis of (+)-arisugacins A and B, potent, orally bioactive and selective inhibitors of acetylcholinesterase
inferredcites →https://doi.org/10.1016/j.tetlet.2005.06.145openalex-snapshot
Synthetic studies toward pondaplin: total synthesis of pondaplin analogues
inferredcites →https://doi.org/10.1016/s0007-1536(88)80119-0openalex-snapshot
Sclerotial metabolites of Aspergillus Flavus toxic to a detritivorous maize insect (Carpophilus Hemipterus, Nitidulidae)
inferredcites →https://doi.org/10.1016/s0031-9422(00)00268-5openalex-snapshot
Bicycloalternarenes produced by the phytopathogenic fungus Alternaria alternata
inferredcites →https://doi.org/10.1016/s0031-9422(00)00459-3openalex-snapshot
Biosynthesis of the bicycloalternarenes, mixed terpenoids of Alternaria alternata
inferredcites →https://doi.org/10.1016/s0031-9422(00)86077-xopenalex-snapshot
The biosynthesis of phenols—XII.
inferredcites →https://doi.org/10.1016/s0031-9422(00)88793-2openalex-snapshot
Phenolic meroterpenoids from the basidiomycete Albatrellus ovinus
inferredcites →https://doi.org/10.1016/s0031-9422(02)00050-xopenalex-snapshot
Neogrifolin derivatives possessing anti-oxidative activity from the mushroom Albatrellus ovinus
inferredcites →https://doi.org/10.1016/s0031-9422(02)00379-5openalex-snapshot
Meroterpenes from Penicillium sp found in association with Melia azedarach
inferredcites →https://doi.org/10.1016/s0031-9422(03)00275-9openalex-snapshot
Stachybotrys chartarum : a fungus for our time
inferredcites →https://doi.org/10.1016/s0031-9422(96)00528-6openalex-snapshot
Citreohybriddione C, a meroterpenoid of a hybrid strain KO 0031 derived from Penicillium citreo-viride B. IFO 6200 and 4692
inferredcites →https://doi.org/10.1016/s0031-9422(97)00124-6openalex-snapshot
Prenylated phenylpropenes from Coleonema pulchellum with antimicrobial activity
inferredcites →https://doi.org/10.1016/s0031-9422(97)00278-1openalex-snapshot
Tricycloalternarenes produced by Alternaria alternata related to ACTG-toxins
inferredcites →https://doi.org/10.1016/s0031-9422(99)00275-7openalex-snapshot
New tricycloalternarenes produced by the phytopathogenic fungus Alternaria alternata
inferredcites →https://doi.org/10.1016/s0040-4020(01)80357-4openalex-snapshot
Isolation and structure determination of pycnidione, A novel bistropolone stromelysin inhibitor from a Phoma sp.
inferredcites →https://doi.org/10.1016/s0040-4020(01)81077-2openalex-snapshot
Three new aflavinines from the sclerotia of aspergillus tubingensis
inferredcites →https://doi.org/10.1016/s0040-4020(01)83433-5openalex-snapshot
Application of stable isotope labelling methodology to the biosynthesis of the mycotoxin, terretonin, by aspergillus terreus: incorporation of 13C-labelled acetates and methionine, 2H- and 13C, 18O-labelled ethyl 3,5-dimethylorsellinate and oxygen-18 gas
inferredcites →https://doi.org/10.1016/s0040-4020(01)91771-5openalex-snapshot
The isolation and structure of siccanochromenes
inferredcites →https://doi.org/10.1016/s0040-4020(03)00739-7openalex-snapshot
Meroterpenoids from Penicillium citreo-viride B. IFO 4692 and 6200 hybrid
inferredcites →https://doi.org/10.1016/s0040-4020(97)00015-xopenalex-snapshot
Biosynthesis of polyketide-terpenoid (meroterpenoid) metabolites andibenin B and andilesin A in Aspergillus variecolor
inferredcites →https://doi.org/10.1016/s0040-4039(00)00223-9openalex-snapshot
(+)-Brevione A. The first member of a novel family of bioactive spiroditerpenoids isolated from Penicillium brevicompactum Dierckx
inferredcites →https://doi.org/10.1016/s0040-4039(00)71179-8openalex-snapshot
Aflavinine, a novel indole-mevalonate metabolite from tremorgen-producing species
inferredcites →https://doi.org/10.1016/s0040-4039(00)74810-6openalex-snapshot
Biosynthesis of citreohybridones, the metabolites of a hybrid strain KO 0031 derived from penicillium citreo-viride B. IFO 6200 and 4692
inferredcites →https://doi.org/10.1016/s0040-4039(00)84464-0openalex-snapshot
Isolation and structure of pycnophorin, a novel diterpene α-pyrone with antimicrobial activity, produced by phytopathogenic
inferredcites →https://doi.org/10.1016/s0040-4039(00)88109-5openalex-snapshot
Paraherquonin, a new meroterpenoid from penicillium paraherquei
inferredcites →https://doi.org/10.1016/s0040-4039(00)89769-5openalex-snapshot
The isolation and the structure of siccanochromenes
inferredcites →https://doi.org/10.1016/s0040-4039(00)90792-5openalex-snapshot
The structure of siccanin
inferredcites →https://doi.org/10.1016/s0040-4039(00)94558-1openalex-snapshot
Hericenone A and B as cytotoxic principles from the mushroom
inferredcites →https://doi.org/10.1016/s0040-4039(01)02345-0openalex-snapshot
Structure and absolute configuration of citreohybridones isolated from Penicillium species
inferredcites →https://doi.org/10.1016/s0040-4039(01)82021-9openalex-snapshot
Biosynthesis of highly modified meroterpenoids in aspergillus variecolor. Incorporation of 13C-labelled acetates and methionine into anditomin and andilesin C
inferredcites →https://doi.org/10.1016/s0040-4039(01)88189-2openalex-snapshot
The structure op the triprenyl phenol derivatives biosynthetically related to siccanin
inferredcites →https://doi.org/10.1016/s0040-4039(01)91018-4openalex-snapshot
Fumigatonin, a new meroterpenoid from
inferredcites →https://doi.org/10.1016/s0040-4039(01)93201-0openalex-snapshot
Stemphone: A new type of natural quinone
inferredcites →https://doi.org/10.1016/s0040-4039(02)00465-3openalex-snapshot
Terreulactone A, a novel meroterpenoid with anti-acetylcholinesterase activity from Aspergillus terreus
inferredcites →https://doi.org/10.1016/s0040-4039(97)01430-5openalex-snapshot
Isolation and Biosynthetic Pathway for Citreohybridones from the Hybrid Strain KO 0031 Derived from Penicillium Species
inferredcites →https://doi.org/10.1016/s0040-4039(98)01039-9openalex-snapshot
The biosynthesis of the fungal meroterpenoids boviquinone-3 and -4 follows two different pathways
inferredcites →https://doi.org/10.1016/s0223-5234(97)89088-5openalex-snapshot
The affinity to the brain dopamine D1 receptor in vitro of triprenyl phenols isolated from the fruit bodies of Albatrellus ovinus
inferredcites →https://doi.org/10.1016/s0378-8741(01)00309-9openalex-snapshot
Active constituents isolated from Psoralea glandulosa L. with antiinflammatory and antipyretic activities
inferredcites →https://doi.org/10.1016/s0960-894x(98)00371-0openalex-snapshot
Kampanols: novel ras farnesyl-protein transferase inhibitors from Stachybotrys kampalensis
inferredcites →https://doi.org/10.1021/ja00029a033openalex-snapshot
Aspernomine: a cytotoxic antiinsectan metabolite with a novel ring system from the sclerotia of Aspergillus nomius
inferredcites →https://doi.org/10.1021/ja00105a078openalex-snapshot
Relative and Absolute Stereochemistry of Pyripyropene A, A Potent, Bioavailable Inhibitor of Acyl-CoA:Cholesterol Acyltransferase (ACAT)
inferredcites →https://doi.org/10.1021/ja00437a081openalex-snapshot
Austin, a novel polyisoprenoid mycotoxin from Aspergillus ustus
inferredcites →https://doi.org/10.1021/jo00027a026openalex-snapshot
Radarins A-D: new antiinsectan and cytotoxic indole diterpenoids from the sclerotia of Aspergillus sulphureus
inferredcites →https://doi.org/10.1021/jo00051a006openalex-snapshot
Stachybotrins A and B: novel bioactive metabolites from a brackish water isolate of the fungus Stachybotrys sp
inferredcites →https://doi.org/10.1021/jo0011078openalex-snapshot
Novel Bioactive Breviane Spiroditerpenoids from Penicillium brevicompactum Dierckx
inferredcites →https://doi.org/10.1021/jo00258a011openalex-snapshot
Antiinsectan aflavinine derivatives from the sclerotia of Aspergillus flavus
inferredcites →https://doi.org/10.1021/jo00272a012openalex-snapshot
Nominine: a new insecticidal indole diterpene from the sclerotia of Aspergillus nomius
inferredcites →https://doi.org/10.1021/jo00281a010openalex-snapshot
Tubingensin A: an antiviral carbazole alkaloid from the sclerotia of Aspergillus tubingensis
inferredcites →https://doi.org/10.1021/jo00305a030openalex-snapshot
Aflavazole: a new antiinsectan carbazole metabolite from the sclerotia of Aspergillus flavus
inferredcites →https://doi.org/10.1021/jo00394a023openalex-snapshot
Terretonin, a toxic compound from Aspergillus terreus
inferredcites →https://doi.org/10.1021/np030192mopenalex-snapshot
Thiersindoles A−C: New Indole Diterpenoids from Penicillium thiersii
inferredcites →https://doi.org/10.1021/np0496486openalex-snapshot
Antiinsectan Decaturin and Oxalicine Analogues from Penicillium thiersii
inferredcites →https://doi.org/10.1021/np070329zopenalex-snapshot
The Berkeleyacetals, Three Meroterpenes from a Deep Water Acid Mine Waste Penicillium
inferredcites →https://doi.org/10.1021/np070513kopenalex-snapshot
Noreupenifeldin, a Tropolone from an Unidentified Ascomycete
inferredcites →https://doi.org/10.1021/np50080a020openalex-snapshot
Nmr Assignments of Territrems A, B, and C and the Structure of MB2, the Major Metabolite of Territrem B by Rat Liver Microsomal Fraction
inferredcites →https://doi.org/10.1021/np9701236openalex-snapshot
Structure and Anti-Acetylcholinesterase Activity of 4α-(Hydroxymethyl)-4α-demethylterritrem B
inferredcites →https://doi.org/10.1021/np9800506openalex-snapshot
Epolones: Novel Sesquiterpene-Tropolones from Fungus OS-F69284 That Induce Erythropoietin in Human Cells
inferredcites →https://doi.org/10.1021/np9900876openalex-snapshot
Montadial A, a Cytotoxic Metabolite from Bondarzewia montana
inferredcites →https://doi.org/10.1021/ol026424aopenalex-snapshot
Thiersinines A and B: Novel Antiinsectan Indole Diterpenoids from a New Fungicolous Penicillium Species (NRRL 28147)
inferredcites →https://doi.org/10.1021/ol0340686openalex-snapshot
Novel Antiinsectan Oxalicine Alkaloids from Two Undescribed Fungicolous Penicillium spp.
inferredcites →https://doi.org/10.1021/ol048824zopenalex-snapshot
Hesseltin A, a Novel Antiviral Metabolite from Penicillium hesseltinei
inferredcites →https://doi.org/10.1021/ol049852kopenalex-snapshot
Berkeleydione and Berkeleytrione, New Bioactive Metabolites from an Acid Mine Organism
inferredcites →https://doi.org/10.1021/ol7026834openalex-snapshot
Novofumigatonin, a New Orthoester Meroterpenoid from Aspergillus novofumigatus
inferredcites →https://doi.org/10.1021/ol7029867openalex-snapshot
Three New Polyketide−Terpenoid Hybrids from Penicillium sp.
inferredcites →https://doi.org/10.1038/ja.2005.95openalex-snapshot
Stemphones, Novel Potentiators of Imipenem Activity against Methicillin-resistant Staphylococcus aureus, Produced by Aspergillus sp. FKI-2136
inferredcites →https://doi.org/10.1039/a704864eopenalex-snapshot
Biosynthesis of Xenovulene A®: formation of a cyclopentenone via a unique ring expansion–ring contraction mechanism
inferredcites →https://doi.org/10.1039/a909079gopenalex-snapshot
Polyketide biosynthesis: a millennium review
inferredcites →https://doi.org/10.1039/b704420hopenalex-snapshot
Polyketides, proteins and genes in fungi: programmed nano-machines begin to reveal their secrets
inferredcites →https://doi.org/10.1039/b708614hopenalex-snapshot
Characterisation of 3-methylorcinaldehyde synthase (MOS) in Acremonium strictum: first observation of a reductive release mechanism during polyketide biosynthesis
inferredcites →https://doi.org/10.1039/c3976000270aopenalex-snapshot
Isolation of C25 polyisoprenoids from Aspergillus sp: crystal structure of andibenin
inferredcites →https://doi.org/10.1039/c39780000533openalex-snapshot
Andilesin, a C25 polyisoprenoid from Aspergillus sp. X-Ray crystallographic and spectroscopic determination of the structure
inferredcites →https://doi.org/10.1039/c39780000626openalex-snapshot
Biosynthesis of andibenin, a novel polyketide-terpenoid metabolite of Aspergillus variecolor
inferredcites →https://doi.org/10.1039/c39790000726openalex-snapshot
Structure of K-76, a complement inhibitor produced by Stachybotrys complementi nov. Sp. K-76
inferredcites →https://doi.org/10.1039/c39790001021openalex-snapshot
(E,E)-10-(1,3-Dihydro-4,6-dihydroxy-7-methyl-3-oxoisobenzofuran-5-yl)4,8-dimethyldeca-4,8-dienoic acid: total synthesis and role in mycophenolic acid biosynthesis
inferredcites →https://doi.org/10.1039/c39810000914openalex-snapshot
Anditomin, a new C25 metabolite from Aspergillus variecolor
inferredcites →https://doi.org/10.1039/c39810001043openalex-snapshot
Biosynthesis of terretonin, a polyketide-terpenoid metabolite of Aspergillus terreus
inferredcites →https://doi.org/10.1039/c39810001265openalex-snapshot
Structures of the austalides A–E, five noval toxic metabolites from Aspergillus ustus
inferredcites →https://doi.org/10.1039/c39820000902openalex-snapshot
Biosynthesis of viridicatumtoxin, a mycotoxin from Penicilium expansum
inferredcites →https://doi.org/10.1039/c39830000716openalex-snapshot
Biosynthesis of austalide D, a meroterpenoid mycotoxin from Aspergillus ustus
inferredcites →https://doi.org/10.1039/c39860000214openalex-snapshot
Biosynthesis of the meroterpenoid austin, by Aspergillus ustus: synthesis and incorporation of 13C,18O-labelled ethyl 3,5-dimethylorsellinate
inferredcites →https://doi.org/10.1039/c39860000501openalex-snapshot
Biosynthesis of the meroterpenoid metabolite, andilesin A, by Aspergillus variecolor: origins of the oxygen atoms
inferredcites →https://doi.org/10.1039/c39880001562openalex-snapshot
Stereochemical studies on the biosynthesis of viridicatumtoxin: evidence for a 1,3-hydride shift in the formation of the spirobicyclic ring system
inferredcites →https://doi.org/10.1039/c39890000393openalex-snapshot
Absolute configuration and biosynthesis of the austalides, meroterpenoid metabolites of Aspergillus ustus: mode of cyclisation of the farnesyl moiety
inferredcites →https://doi.org/10.1039/c39890001618openalex-snapshot
X-Ray crystal structure of oxalicine A, a novel alkaloid from Penicillium oxalicum
inferredcites →https://doi.org/10.1039/cs9871600123openalex-snapshot
Applications of multinuclear NMR to structural and biosynthetic studies of polyketide microbial metabolites
inferredcites →https://doi.org/10.1039/jr9650004672openalex-snapshot
869. The biosynthesis of phenols. Part IX. Asperugin, a metabolic product of Aspergillus rugulosus
inferredcites →https://doi.org/10.1039/np9931000593openalex-snapshot
Biosynthesis of fatty acid and polyketide metabolites
inferredcites →https://doi.org/10.1039/np9951200001openalex-snapshot
Biosynthesis of fatty acid and polyketide metabolites
inferredcites →https://doi.org/10.1039/p19720002639openalex-snapshot
Biosynthesis of mycophenolic acid
inferredcites →https://doi.org/10.1039/p19720002837openalex-snapshot
The structures of alboleersin and luteoleersin; the identity of luteoleer-sin with cochlioquinone A
inferredcites →https://doi.org/10.1039/p19790002118openalex-snapshot
Studies on fungal metabolites. Part 1. The structures of andibenins-A and -C, and andilesins-A, -B, and -C, meroterpenoids from Aspergillus variecolor
inferredcites →https://doi.org/10.1039/p19820000365openalex-snapshot
6-Farnesyl-5,7-dihydroxy-4-methylphthalide oxidation mechanism in mycophenolic acid biosynthesis
inferredcites →https://doi.org/10.1039/p19820002687openalex-snapshot
Studies on fungal metabolites. Part 3. 13C N.m.r. spectral and structural studies on austin and new related meroterpenoids from Aspergillus ustus, Aspergillus variecolor, and Penicillium diversum
inferredcites →https://doi.org/10.1039/p19850000345openalex-snapshot
Metabolites of Aspergillus ustus. Part 1. Application of the heteronuclear selective population inversion (SPI) n.m.r. technique to the structure elucidation of the austalides A–F, novel ortho ester meroterpenoids
inferredcites →https://doi.org/10.1039/p19850000363openalex-snapshot
Metabolites of Aspergillus ustus. Part 3. Structure elucidation of austalides G–L
inferredcites →https://doi.org/10.1039/p19890000807openalex-snapshot
Studies on the biosynthesis of the mycotoxin austin, a meroterpenoid metabolite of Aspergillus ustus
inferredcites →https://doi.org/10.1039/p19940000135openalex-snapshot
Biosynthetic studies on citreohybridones, metabolites of a hybrid strain KO 0031 derived from Penicillium citreo-viride B. IFO 6200 and 4692
inferredcites →https://doi.org/10.1042/bj0261441openalex-snapshot
Studies in the biochemistry of micro-organisms
inferredcites →https://doi.org/10.1126/science.156.3772.202openalex-snapshot
Biosynthesis of Polyketides and Related Compounds
inferredcites →https://doi.org/10.1128/aac.8.3.321openalex-snapshot
Biosynthesis of Mycophenolic Acid: Purification and Characterization of S -Adenosyl- l -Methionine:Demethylmycophenolic Acid O -Methyltransferase
inferredcites →https://doi.org/10.1128/aem.37.3.355-357.1979openalex-snapshot
Territrems, tremorgenic mycotoxins of Aspergillus terreus
inferredcites →https://doi.org/10.1128/aem.47.1.98-100.1984openalex-snapshot
Isolation, chemical structure, acute toxicity, and some physicochemical properties of territrem C from Aspergillus terreus
inferredcites →https://doi.org/10.1139/m68-170openalex-snapshot
Stemphone, a biologically active yellow pigment produced by Stemphylium sarcinaeforme (Cav.) Wiltshire
inferredcites →https://doi.org/10.1139/v93-069openalex-snapshot
Secondary metabolites of the aspen fungus Stachybotrys cylindrospora
inferredcites →https://doi.org/10.1192/bjp.178.2.101openalex-snapshot
Pharmacology and effects of cannabis: A brief review
inferredcites →https://doi.org/10.1246/cl.1991.1811openalex-snapshot
Citreohybriddiones A and B and Related Terpenoids, New Metabolites of a Hybrid Strain KO 0031 Derived from Penicillium citreo-viride B. IFO 6200 and 4692
inferredcites →https://doi.org/10.1248/cpb.36.2918openalex-snapshot
Studies on the constituents of Polyporus dispansus and P. confluens.
inferredcites →https://doi.org/10.1248/cpb.37.1424openalex-snapshot
Bloegrevilol, a new lipid peroxidation inhibitor from the edible mushroom Suillus grevillei.
inferredcites →https://doi.org/10.1248/cpb.53.1114openalex-snapshot
Two New Meroterpenoids, Penisimplicin A and B, Isolated from Penicillium simplicissimum
inferredcites →https://doi.org/10.1248/cpb.53.1202openalex-snapshot
Two New Aromatic Compounds from Hericium erinaceum (BULL.: FR.) PERS.
inferredcites →https://doi.org/10.1271/bbb.56.1660openalex-snapshot
Tyrosinase Inhibitors fromAlbatrellus confluens
inferredcites →https://doi.org/10.1271/bbb.58.334openalex-snapshot
Acetoxydehydroaustin, a New Bioactive Compound, and Related Compound Neoaustin fromPenicilliumsp. MG–11
inferredcites →https://doi.org/10.1271/bbb.62.2260openalex-snapshot
Isolation and Identification of New Antifungal Macrophorins E, F and G as Malonyl Meroterpenes fromBotryosphaeria berengeriana
inferredcites →https://doi.org/10.1271/bbb1961.47.187openalex-snapshot
New terpene-linked cyclohexenone epoxides, macrophorin A, B and C, produced by the fungus caused Macrophoma fruit rot of apple.
inferredcites →https://doi.org/10.1271/bbb1961.48.1923openalex-snapshot
Macrophorin D, a new self-growth inhibitor of the causal fungus of Macrophoma fruit rot of apple.
inferredcites →https://doi.org/10.1515/znb-1971-0414openalex-snapshot
Pilzpigmente, VI / Pigments of Fungi, VI
inferredcites →https://doi.org/10.1515/znb-2007-0806openalex-snapshot
Four Additional Meroterpenes Produced by Penicillium sp Found in Association with Melia azedarach. Possible Biosynthetic Intermediates to Austin
inferredcites →https://doi.org/10.1515/znc-2003-9-1012openalex-snapshot
Further Meroterpenes Produced by Penicillium sp., an Endophyte Obtained from Melia azedarach
inferredcites →https://doi.org/10.1590/s0103-50532003000500004openalex-snapshot
Structures of meroterpenes produced by Penicillium sp, an endophytic fungus found associated with Melia azedarach
inferredcites →https://doi.org/10.3987/com-05-10501openalex-snapshot
Isolation, Synthesis and Biological Activity of Grifolic Acid Derivatives from the Inedible Mushroom Albatrellus dispansus
inferredcites →https://doi.org/10.7164/antibiotics.46.1082openalex-snapshot
Eupenifeldin, a novel cytotoxic bistropolone from Eupenicillium brefeldianum.
inferredcites →https://doi.org/10.7164/antibiotics.46.1168openalex-snapshot
Pyripyropenes, highly potent inhibitiors of ACYL-CoA: cholesterol acyltransferase produced by Aspergillus fumigatus.
inferredcites →https://doi.org/10.7164/antibiotics.47.148openalex-snapshot
Pyripyropenes, novel inhibitors of acyl-CoA: cholesterol acyltransferase produced by Aspergillus fumigatus. I. Production, isolation, and biological properties.
inferredcites →https://doi.org/10.7164/antibiotics.47.154openalex-snapshot
Pyripyropenes, novel inhibitors of acyl-CoA: cholesterol acyltransferase produced by Aspergillus fumigatus. II. Structure elucidation of pyripyropenes A, B, C and D.
inferredcites →https://doi.org/10.7164/antibiotics.47.727openalex-snapshot
Mer-NF5003B, E and F, novel sesquiterpenoids as avian myeloblastosis virus protease inhibitors produced by Stachybotrys sp.
inferredcites →https://doi.org/10.7164/antibiotics.48.447openalex-snapshot
Isolation, Characterization and Biological Activities of Novel Triprenyl Phenols as Pancreatic Cholesterol Esterase Inhibitors Produced by Stachybotrys sp. F-1839.
inferredcites →https://doi.org/10.7164/antibiotics.48.495openalex-snapshot
Pyripyropenes, Novel ACAT Inhibitors Produced by Aspergillus fumigatus. III. Structure Elucidation of Pyripyropenes E to L.
inferredcites →https://doi.org/10.7164/antibiotics.48.568openalex-snapshot
Xenovulene A, a Novel GABA-Benzodiazepine Receptor Binding Compound Produced by Acremonium strictum.
inferredcites →https://doi.org/10.7164/antibiotics.48.745openalex-snapshot
Arisugacin, a Novel and Selective Inhibitor of Acetylcholinesterase from Penicillium sp. FO-4259.
inferredcites →https://doi.org/10.7164/antibiotics.49.1278openalex-snapshot
Andrastin D, Novel Protein Farnesyltransferase Inhibitor Produced by Penicillium sp. FO-3929.
inferredcites →https://doi.org/10.7164/antibiotics.49.292openalex-snapshot
Pyripyropenes, Novel ACAT Inhibitors Produced by Aspergillus fumigatus. IV. Structure Elucidation of Pyripyropenes M to R.
inferredcites →https://doi.org/10.7164/antibiotics.49.374openalex-snapshot
Novel Spirodihydrobenzofuranlactams as Antagonists of Endothelin and as Inhibitors of HIV-1 Protease Produced by Stachybotrys sp. II. Structure Determination.
inferredcites →https://doi.org/10.7164/antibiotics.49.409openalex-snapshot
Epi-cochlioquinone A, a Novel Acyl-CoA: Cholesterol Acyltransferase Inhibitor Produced by Stachybotrys bisbyi.
inferredcites →https://doi.org/10.7164/antibiotics.49.418openalex-snapshot
Andrastins A-C, New Protein Farnesyltransferase Inbibitors Produced by Penicillium sp. FO-3929. II. Structure Elucidation and Biosynthesis.
inferredcites →https://doi.org/10.7164/antibiotics.49.611openalex-snapshot
Inhibitors of myo-Inositol Monophosphatase, ATCC 20928 Factors A and C. Isolation, Physico-chemical Characterization and Biological Properties.
inferredcites →https://doi.org/10.7164/antibiotics.49.742openalex-snapshot
Arisugacins A and B, Novel and Selective Acetylcholinesterase Inhibitors from Penicillium sp. FO-4259. I. Screening, Taxonomy, Fermentation, Isolation and Biological Activity.
inferredcites →https://doi.org/10.7164/antibiotics.49.748openalex-snapshot
Arisugacins A and B, Novel and Selective Acetylcholinesterase Inhibitors from Penicillium sp. F0-4259. II. Structure Elucidation.
inferredcites →https://doi.org/10.7164/antibiotics.49.961openalex-snapshot
Staplabin, a Novel Fungal Triprenyl Phenol which Stimulates the Binding of Plasminogen to Fibrin and U937 Cell.
inferredcites →https://doi.org/10.7164/antibiotics.50.641openalex-snapshot
Stachybotrin C and Parvisporin, Novel Neuritogenic Compounds. II. Structure Determination.
inferredcites →https://doi.org/10.7164/antibiotics.51.1059openalex-snapshot
Isolation of SMTP-3, 4, 5 and -6, Novel Analogs of Staplabin, and Their Effects on Plasminogen Activation and Fibrinolysis.
inferredcites →https://doi.org/10.7164/antibiotics.51.635openalex-snapshot
Hongoquercins A and B, New Sesquiterpenoid Antibiotics: Isolation, Structure Elucidation, and Antibacterial Activity.
inferredcites →https://doi.org/10.7164/antibiotics.52.988openalex-snapshot
Memnobotrins and Memnoconols. Novel Metabolites from Memnoniella echinata.
inferredcites →https://doi.org/10.7164/antibiotics.53.241openalex-snapshot
Activation of Fibrinolysis by SMTP-7 and -8, Novel Staplabin Analogs with a Pseudosymmetric Structure.
inferredcites →https://doi.org/10.7164/antibiotics.53.50openalex-snapshot
Arisugacins C and D, Novel Acetylcholinesterase Inhibitors and Their Related Novel Metabolites Produced by Penicillium sp. FO-4259-11.
inferredcites →https://doi.org/10.7164/antibiotics.54.386openalex-snapshot
Determination of Absolute Stereochemistries of Arisugacin F and Territrem B, Novel Acetylcholinesterase Inhibitors.
inferredcites →https://doi.org/10.7164/antibiotics.55.155openalex-snapshot
Stachyflin and Acetylstachyflin, Novel Anti-influenza A Virus Substances, Produced by Stachybotrys sp. RF-7260. I. Isolation, Structure Elucidation and Biological Activities.
inferredcites →https://doi.org/10.7164/antibiotics.55.239openalex-snapshot
Novel Stachyflin Derivatives from Stachybotrys sp. RF-7260
inferredcites →https://doi.org/10.7164/antibiotics.56.344openalex-snapshot
Terreulactones A, B, C, and D: Novel Acetylcholinesterase Inhibitors Produced by Aspergillus terreus I. Taxonomy, Fermentation, Isolation and Biological Activities
inferredcites →https://doi.org/10.7164/antibiotics.56.351openalex-snapshot
Terreulactones A, B, C, and D: Novel Acetylcholinesterase Inhibitors Produced by Aspergillus terreus II. Physico-chemical Properties and Structure Determination
inferredcites →https://doi.org/10.7164/antibiotics.56.832openalex-snapshot
SMTP-4D, -5D, -6D, -7D and -8D, a New Series of the Non-lysine-analog Plasminogen Modulators with a D-Amino Acid Moiety
inferredcites →https://doi.org/10.7164/antibiotics.57.10openalex-snapshot
A Novel Ascochlorin Glycoside from the Insect Pathogenic Fungus Verticillium hemipterigenum BCC 2370.
inferredcites →https://doi.org/10.7164/antibiotics.57.59openalex-snapshot
Cochlioquinones and Epi-Cochlioquinones: Antagonists of the Human Chemokine Receptor CCR5 from Bipolaris brizae and Stachybotrys chartarum.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.02.011zenodo-depositor-declared
4-Hydroxybenzoic acid serves as an endogenous ring precursor for antroquinonol biosynthesis in Antrodia cinnamomea
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112860zenodo-depositor-declared
Terpene−Shikimate conjugated meroterpenoids from the endophytic fungus Guignardia mangiferae
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113289zenodo-depositor-declared
Proposal for structural revision of several disubstituted tricycloalternarenes
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113307zenodo-depositor-declared
Meroterpenoids from the fungus Penicillium sclerotiorum GZU-XW03-2 and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1002/9781118794623.ch10openalex-snapshot
Analyzing Fungal Secondary Metabolite Genes and Gene Clusters
inferred← citeshttps://doi.org/10.1002/9781119295266.ch4openalex-snapshot
Protecting‐Group‐Free Synthesis of Natural Products and Analogs, Part III
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc2735openalex-snapshot
αKG‐Dependent Enzyme AndA Involved in Anditomin Biosynthesis
inferred← citeshttps://doi.org/10.1002/advs.202508826openalex-snapshot
Enhancing the β ‐Oxidation‐Like Pathway for the Optimal Production of the Immunosuppressant Mycophenolic Acid
inferred← citeshttps://doi.org/10.1002/ange.201206299openalex-snapshot
Total Synthesis of the Tremorgenic Indole Diterpene Paspalinine
inferred← citeshttps://doi.org/10.1002/ange.201705654openalex-snapshot
Traversing Biosynthetic Carbocation Landscapes in the Total Synthesis of Andrastin and Terretonin Meroterpenes
inferred← citeshttps://doi.org/10.1002/ange.202011171openalex-snapshot
Exploiting the Potential of Meroterpenoid Cyclases to Expand the Chemical Space of Fungal Meroterpenoids
inferred← citeshttps://doi.org/10.1002/ange.202100541openalex-snapshot
Total Synthesis of Anti‐Cancer Meroterpenoids Dysideanone B and Dysiherbol A and Structural Reassignment of Dysiherbol A
inferred← citeshttps://doi.org/10.1002/ange.202104014openalex-snapshot
Enantioselective Total Synthesis of Berkeleyone A and Preaustinoids
inferred← citeshttps://doi.org/10.1002/ange.202210938openalex-snapshot
Biosynthetic Elucidation and Structural Revision of Brevione E: Characterization of the Key Dioxygenase for Pathway Branching from Setosusin Biosynthesis
inferred← citeshttps://doi.org/10.1002/ange.202403365openalex-snapshot
An Enzymatic Carbon‐Carbon Bond Cleavage and Aldol Reaction Cascade Converts an Angular Scaffold into the Linear Tetracyclic Core of Ochraceopones
inferred← citeshttps://doi.org/10.1002/ange.202415279openalex-snapshot
Modifications of Prenyl Side Chains in Natural Product Biosynthesis
inferred← citeshttps://doi.org/10.1002/ange.202416211openalex-snapshot
Total Synthesis of Berkeleyone A and Preaustinoid A through Epoxypolyene Cyclization
inferred← citeshttps://doi.org/10.1002/ange.202524461openalex-snapshot
Enantioselective Total Synthesis of (−)‐Bisabosqual F via N‐Heterocyclic Carbene Catalyzed (4+2) Annulation
inferred← citeshttps://doi.org/10.1002/anie.201206299openalex-snapshot
Total Synthesis of the Tremorgenic Indole Diterpene Paspalinine
inferred← citeshttps://doi.org/10.1002/anie.201705654openalex-snapshot
Traversing Biosynthetic Carbocation Landscapes in the Total Synthesis of Andrastin and Terretonin Meroterpenes
inferred← citeshttps://doi.org/10.1002/anie.202011171openalex-snapshot
Exploiting the Potential of Meroterpenoid Cyclases to Expand the Chemical Space of Fungal Meroterpenoids
inferred← citeshttps://doi.org/10.1002/anie.202100541openalex-snapshot
Total Synthesis of Anti‐Cancer Meroterpenoids Dysideanone B and Dysiherbol A and Structural Reassignment of Dysiherbol A
inferred← citeshttps://doi.org/10.1002/anie.202104014openalex-snapshot
Enantioselective Total Synthesis of Berkeleyone A and Preaustinoids
inferred← citeshttps://doi.org/10.1002/anie.202210938openalex-snapshot
Biosynthetic Elucidation and Structural Revision of Brevione E: Characterization of the Key Dioxygenase for Pathway Branching from Setosusin Biosynthesis
inferred← citeshttps://doi.org/10.1002/anie.202403365openalex-snapshot
An Enzymatic Carbon‐Carbon Bond Cleavage and Aldol Reaction Cascade Converts an Angular Scaffold into the Linear Tetracyclic Core of Ochraceopones
inferred← citeshttps://doi.org/10.1002/anie.202415279openalex-snapshot
Modifications of Prenyl Side Chains in Natural Product Biosynthesis
inferred← citeshttps://doi.org/10.1002/anie.202416211openalex-snapshot
Total Synthesis of Berkeleyone A and Preaustinoid A through Epoxypolyene Cyclization
inferred← citeshttps://doi.org/10.1002/anie.202524461openalex-snapshot
Enantioselective Total Synthesis of (−)‐Bisabosqual F via N‐Heterocyclic Carbene Catalyzed (4+2) Annulation
inferred← citeshttps://doi.org/10.1002/cbdv.202000489openalex-snapshot
Polymethylated Phloroglucinol Meroterpenoids from Rhodomyrtus tomentosa and Their Antibacterial and Acetylcholinesterase Inhibitory Effects
inferred← citeshttps://doi.org/10.1002/cbdv.202500123openalex-snapshot
Bioaspermeroterpenes A–D: Four New Meroterpenoids From the Biotransformation Extract by the Fungus Penicillium herquei GZU‐31‐6
inferred← citeshttps://doi.org/10.1002/cbic.201200124openalex-snapshot
Identification of a Key Prenyltransferase Involved in Biosynthesis of the Most Abundant Fungal Meroterpenoids Derived from 3,5‐Dimethylorsellinic Acid.
inferred← citeshttps://doi.org/10.1002/cbic.201200369openalex-snapshot
Terretonin Biosynthesis Requires Methylation as Essential Step for Cyclization
inferred← citeshttps://doi.org/10.1002/cbic.201600087openalex-snapshot
Biosynthesis of LL‐Z1272β: Discovery of a New Member of NRPS‐like Enzymes for Aryl‐Aldehyde Formation
inferred← citeshttps://doi.org/10.1002/cbic.202300008openalex-snapshot
Advances in Synthetic Biology of Fungi and Contributions to the Discovery of New Molecules
inferred← citeshttps://doi.org/10.1002/cbic.202400387openalex-snapshot
Biosynthesis and Assembly Logic of Fungal Hybrid Terpenoid Natural Products
inferred← citeshttps://doi.org/10.1002/cbic.202500377openalex-snapshot
Functional Characterization of a Diazo‐Forming Enzyme in Meroterpenoid Biosynthesis
inferred← citeshttps://doi.org/10.1002/chem.201103278openalex-snapshot
Marilines A–C: Novel Phthalimidines from the Sponge‐Derived Fungus Stachylidium sp.
inferred← citeshttps://doi.org/10.1002/chem.201503969openalex-snapshot
Construction of Bridged Polycyclic Systems by Polyene Cyclization
inferred← citeshttps://doi.org/10.1002/chem.201703094openalex-snapshot
Regiodivergent Remote Arylation of Cycloalkanols to Dysideanone′s Fused Carbotetracycles and Its Bridged Isomers
inferred← citeshttps://doi.org/10.1002/chem.201805417openalex-snapshot
Construction of a Meroterpenoid‐Like Compounds Library Based on Diversity‐Enhanced Extracts
inferred← citeshttps://doi.org/10.1002/chin.200945267openalex-snapshot
ChemInform Abstract: Meroterpenoids Produced by Fungi
inferred← citeshttps://doi.org/10.1002/cjoc.202100233openalex-snapshot
Meroterpenoids with Potent Immunosuppressive Activity from Fungus Bipolaris zeicola
inferred← citeshttps://doi.org/10.1002/cjoc.202100700openalex-snapshot
(±)‐Atrachinenins A—C, Three Pairs of Caged C 27 Meroterpenoids from the Rhizomes of Atractylodes chinensis
inferred← citeshttps://doi.org/10.1002/cjoc.202400697openalex-snapshot
Recent Advances of Terpenoids with Intriguing Chemical Skeletons and Biological Activities
inferred← citeshttps://doi.org/10.1002/ejoc.201601503openalex-snapshot
Enantiospecific Syntheses of Hongoquercins A and B and Chromazonarol
inferred← citeshttps://doi.org/10.1002/ejoc.201800026openalex-snapshot
Divergent Synthesis of Bioactive Marine Meroterpenoids by Palladium‐Catalyzed Tandem Carbene Migratory Insertion
inferred← citeshttps://doi.org/10.1002/ejoc.202100301openalex-snapshot
Biomimetic Total Syntheses of Amorfrutins A, B, (S)‐D and (R)‐D and Formal Synthesis of Amorfrutin C
inferred← citeshttps://doi.org/10.1002/mrc.4049openalex-snapshot
Meroterpenes from an algicolous strain of Penicillium echinulatum
inferred← citeshttps://doi.org/10.1007/10_2014_283openalex-snapshot
Biosynthesis of Terpenoid Natural Products in Fungi
inferred← citeshttps://doi.org/10.1007/10_2014_288openalex-snapshot
Isoprenoid Drugs, Biofuels, and Chemicals—Artemisinin, Farnesene, and Beyond
inferred← citeshttps://doi.org/10.1007/978-3-030-67561-5_7openalex-snapshot
Exploring Fungal Biodiversity of Genus Epicoccum and Their Biotechnological Potential
inferred← citeshttps://doi.org/10.1007/978-3-319-07145-9_16openalex-snapshot
Meroterpenoids from Marine Microorganisms: Potential Scaffolds for New Chemotherapy Leads
inferred← citeshttps://doi.org/10.1007/978-3-642-39339-6_10openalex-snapshot
Penicillium chrysogenum: Genomics of an Antibiotics Producer
inferred← citeshttps://doi.org/10.1007/978-981-10-3421-3_8openalex-snapshot
Radical-Based Late Stage C–H Functionalization of Heteroaromatics in Drug Discovery
inferred← citeshttps://doi.org/10.1007/978-981-10-5978-0_9openalex-snapshot
Recent Advance on Bioactive Compounds from the Edible and Medicinal Fungi in China
inferred← citeshttps://doi.org/10.1007/978-981-13-0393-7_33openalex-snapshot
Co-cultivation Strategies to Induce De Novo Synthesis of Novel Chemical Scaffolds from Cryptic Secondary Metabolite Gene Clusters
inferred← citeshttps://doi.org/10.1007/978-981-97-7312-1_10openalex-snapshot
Endophytic Fungal Terpenoids: Biosynthesis and Biological Activity
inferred← citeshttps://doi.org/10.1007/s00216-012-6498-1openalex-snapshot
Negative ion tandem mass spectrometry of prenylated fungal metabolites and their derivatives
inferred← citeshttps://doi.org/10.1007/s00253-020-10522-1openalex-snapshot
Genome-based mining of new antimicrobial meroterpenoids from the phytopathogenic fungus Bipolaris sorokiniana strain 11134
inferred← citeshttps://doi.org/10.1007/s00253-021-11312-zopenalex-snapshot
Peculiarities of meroterpenoids and their bioproduction
inferred← citeshttps://doi.org/10.1007/s11101-014-9365-1openalex-snapshot
Chemical and bioactive diversities of the genera Stachybotrys and Memnoniella secondary metabolites
inferred← citeshttps://doi.org/10.1007/s11101-020-09701-9openalex-snapshot
Fungal metabolites as anti-diabetic agents: emphasis on PTP1B inhibitors
inferred← citeshttps://doi.org/10.1007/s11101-024-09923-1openalex-snapshot
Fungal phthalimidines-chemodiversity, bioactivity and biosynthesis of a unique class of natural products
inferred← citeshttps://doi.org/10.1007/s11172-010-0173-5openalex-snapshot
A new meroterpenoid from the marine fungus Aspergillus versicolor (Vuill.) Tirab.
inferred← citeshttps://doi.org/10.1007/s11356-024-35479-wopenalex-snapshot
Larvicidal activity of terpenes and their derivatives against Aedes aegypti: a systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1007/s11418-025-01880-zopenalex-snapshot
Biosynthesis of unique natural product scaffolds by Fe(II)/αKG-dependent oxygenases
inferred← citeshttps://doi.org/10.1007/s11557-023-01941-1openalex-snapshot
New isoindolinone derivatives isolated from the fruiting bodies of the basidiomycete Hericium coralloides
inferred← citeshttps://doi.org/10.1007/s12550-018-0312-7openalex-snapshot
Stachybotrychromenes A–C: novel cytotoxic meroterpenoids from Stachybotrys sp.
inferred← citeshttps://doi.org/10.1007/s13659-016-0096-4openalex-snapshot
Identification and Characterization of a δ-Cadinol Synthase Potentially Involved in the Formation of Boreovibrins in Boreostereum vibrans of Basidiomycota
inferred← citeshttps://doi.org/10.1007/s13659-023-00414-yopenalex-snapshot
Quinones from Cordia species from 1972 to 2023: isolation, structural diversity and pharmacological activities
inferred← citeshttps://doi.org/10.1007/s13659-026-00590-7openalex-snapshot
Nematode-trapping fungus Arthrobotrys oligospora is hungry for iron-chelating agent COQ7 of nematodes
inferred← citeshttps://doi.org/10.1007/s42995-026-00371-8openalex-snapshot
From discovery to mechanism: novel anti-ulcerative colitis meroterpenoids act through the PI3K/IκB-α/MAPK pathway
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14663-3openalex-snapshot
Fungal Meroterpenoids
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14780-8openalex-snapshot
Fungal Non-Reducing Polyketide Synthases
inferred← citeshttps://doi.org/10.1016/b978-0-12-816455-6.00014-7openalex-snapshot
Analysis of meroterpenoids
inferred← citeshttps://doi.org/10.1016/b978-0-12-817903-1.00006-1openalex-snapshot
Progress in studies on meroterpenoids
inferred← citeshttps://doi.org/10.1016/b978-0-323-91294-5.00003-8openalex-snapshot
Bioactive hybrid compounds from Myrtaceae: Chemical classification and biological activities
inferred← citeshttps://doi.org/10.1016/b978-0-323-95047-3.00005-8openalex-snapshot
Terpenes, meroterpenoids, and artemisinin and SARS-CoV-2
inferred← citeshttps://doi.org/10.1016/b978-0-444-59514-0.00010-9openalex-snapshot
Bioactive Natural Products as Potential Candidates to Control Aedes aegypti, the Vector of Dengue
inferred← citeshttps://doi.org/10.1016/b978-0-444-62615-8.00001-1openalex-snapshot
Bioprospecting in the Berkeley Pit
inferred← citeshttps://doi.org/10.1016/b978-0-444-63460-3.00001-8openalex-snapshot
Terpenoids and Sterols from Mushrooms
inferred← citeshttps://doi.org/10.1016/b978-0-444-63473-3.00006-xopenalex-snapshot
Drimane-Related Merosesquiterpenoids, a Promising Library of Metabolites for Drug Development
inferred← citeshttps://doi.org/10.1016/b978-0-444-63504-4.00018-9openalex-snapshot
Secondary Metabolites From Endophytic Fungi and Their Biological Activities
inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00017-4openalex-snapshot
Fungal Type I Polyketides
inferred← citeshttps://doi.org/10.1016/bs.adgen.2016.01.005openalex-snapshot
Molecular Genetics of Secondary Chemistry in Metarhizium Fungi
inferred← citeshttps://doi.org/10.1016/bs.mie.2023.09.003openalex-snapshot
Functional analysis of a fungal P450 enzyme
inferred← citeshttps://doi.org/10.1016/j.apsb.2017.12.005openalex-snapshot
Activation of an unconventional meroterpenoid gene cluster in Neosartorya glabra leads to the production of new berkeleyacetals
inferred← citeshttps://doi.org/10.1016/j.apsb.2019.06.009openalex-snapshot
Immunosuppressant mycophenolic acid biosynthesis employs a new globin-like enzyme for prenyl side chain cleavage
inferred← citeshttps://doi.org/10.1016/j.apsb.2022.09.008openalex-snapshot
Late-stage cascade of oxidation reactions during the biosynthesis of oxalicine B in Penicillium oxalicum
inferred← citeshttps://doi.org/10.1016/j.apsb.2023.03.017openalex-snapshot
Aureane-type sesquiterpene tetraketides as a novel class of immunomodulators with interleukin-17A inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.apsb.2025.09.015openalex-snapshot
Complete biosynthesis of phenylspirodrimanes with unclustered genes in Stachybotrys chartarum
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105012openalex-snapshot
Anti-inflammatory spiroditerpenoids from Penicillium bialowiezense
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105111openalex-snapshot
Furanaspermeroterpenes A and B, two unusual meroterpenoids with a unique 6/6/6/5/5 pentacyclic skeleton from the Marine-derived fungus Aspergillus terreus GZU-31-1
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105468openalex-snapshot
Clavipyrrine A, a unique polycyclic nitrogenous meroterpenoid with promising anti-glioma effects isolated from the fungus Clitocybe clavipes
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106715openalex-snapshot
Anti-inflammatory acetylenic meroterpenoids from the ascidian-derived fungus Amphichorda felina SYSU-MS7908
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106745openalex-snapshot
Peniandrastins A–H: Andrastin-type meroterpenoids with immunosuppressive activity from a Penicillium sp.
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107315openalex-snapshot
New meroterpenoids and polyketides from the endophytic fungus Paraphaeosphaeria sp. C-XB-J-1 and their anti-inflammatory and SARS-CoV-2 Mpro inhibitory activities
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107871openalex-snapshot
Facile constructed meroterpenoids with novel hexadecahydroacephenanthrylene carbon skeleton using the biotransformation and chemical synthesis method
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107897openalex-snapshot
Penisimplinoids A-K, highly oxygenated andrastin-type meroterpenoids with diverse activities from the marine-derived fungus Penicillium simplicissimum
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2014.03.001openalex-snapshot
Metabolite induction via microorganism co-culture: A potential way to enhance chemical diversity for drug discovery
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2018.02.001openalex-snapshot
Recent advances in reconstructing microbial secondary metabolites biosynthesis in Aspergillus spp.
inferred← citeshttps://doi.org/10.1016/j.bjp.2015.09.006openalex-snapshot
Intraspecific variation of meroditerpenoids in the brown alga Stypopodium zonale guiding the isolation of new compounds
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.05.045openalex-snapshot
Novel terpenoids of the fungus Aspergillus insuetus isolated from the Mediterranean sponge Psammocinia sp. collected along the coast of Israel
inferred← citeshttps://doi.org/10.1016/j.bmcl.2019.126708openalex-snapshot
Austalides V and W, new meroterpenoids from the fungus Aspergillus ustus and their antitumor activities
inferred← citeshttps://doi.org/10.1016/j.cbi.2015.06.017openalex-snapshot
Antioxidant and antitumor effects of polysaccharides from the fungus Pleurotus abalonus
inferred← citeshttps://doi.org/10.1016/j.cbpa.2013.01.016openalex-snapshot
Squalene hopene cyclases: highly promiscuous and evolvable catalysts for stereoselective C C and C X bond formation
inferred← citeshttps://doi.org/10.1016/j.cbpa.2015.11.001openalex-snapshot
Unusual chemistries in fungal meroterpenoid biosynthesis
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.07.031openalex-snapshot
Periconones B–E, new meroterpenoids from endophytic fungus Periconia sp.
inferred← citeshttps://doi.org/10.1016/j.cclet.2018.05.019openalex-snapshot
Dimericbiscognienynes B and C: New diisoprenyl-cyclohexene-type meroterpenoid dimers from Biscogniauxia sp.
inferred← citeshttps://doi.org/10.1016/j.cclet.2019.07.068openalex-snapshot
Euphoractone, a cytotoxic meroterpenoid with an unusual ent-abietane-phloroglucinol skeleton, from Euphorbia fischeriana Steud.
inferred← citeshttps://doi.org/10.1016/j.cclet.2021.01.027openalex-snapshot
Amphichoterpenoids A–C, unprecedented picoline-derived meroterpenoids from the ascidian-derived fungus Amphichorda felina SYSU-MS7908
inferred← citeshttps://doi.org/10.1016/j.cclet.2023.108363openalex-snapshot
Structural diversification of phenylspirodrimane lactams by employing a biosynthetic intermediate
inferred← citeshttps://doi.org/10.1016/j.cclet.2023.109030openalex-snapshot
Rapid discovery of two unprecedented meroterpenoids from Daphne altaica Pall. using molecular networking integrated with MolNetEnhancer and Network Annotation Propagation
inferred← citeshttps://doi.org/10.1016/j.copbio.2020.11.016openalex-snapshot
Enzymology and biosynthesis of the orsellinic acid derived medicinal meroterpenoids
inferred← citeshttps://doi.org/10.1016/j.copbio.2022.102763openalex-snapshot
Harnessing Fe(II)/α-ketoglutarate-dependent oxygenases for structural diversification of fungal meroterpenoids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112860openalex-snapshot
Meroterpenoids produced by fungi: Occurrence, structural diversity, biological activities, and their molecular targets
inferred← citeshttps://doi.org/10.1016/j.engmic.2022.100062openalex-snapshot
Oxidative modification of free-standing amino acids by Fe(II)/αKG-dependent oxygenases
inferred← citeshttps://doi.org/10.1016/j.engmic.2023.100137openalex-snapshot
Heterologous expression facilitates the discovery and characterization of marine microbial natural products
inferred← citeshttps://doi.org/10.1016/j.engmic.2025.100259openalex-snapshot
Pathway reprogramming and catalytic network engineering for the production of bioactive aspertetranones from deep-sea Aspergillus versicolor ADS-F20
inferred← citeshttps://doi.org/10.1016/j.fgb.2016.07.004openalex-snapshot
Putative methyltransferase LaeA and transcription factor CreA are necessary for proper asexual development and controlling secondary metabolic gene cluster expression
inferred← citeshttps://doi.org/10.1016/j.fgb.2019.04.004openalex-snapshot
Identification of the gene cluster for bistropolone-humulene meroterpenoid biosynthesis in Phoma sp.
inferred← citeshttps://doi.org/10.1016/j.fitote.2014.09.021openalex-snapshot
Hawaiinolides E–G, cytotoxic cassane and cleistanthane diterpenoids from the entomogenous fungus Paraconiothyrium hawaiiense
inferred← citeshttps://doi.org/10.1016/j.fitote.2017.08.002openalex-snapshot
Chrodrimanins O–S from the fungus Penicillium sp. SCS-KFD09 isolated from a marine worm, Sipunculusnudus
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.11.005openalex-snapshot
Meroterpenoids isolated from Arnebia euchroma (Royle) Johnst. and their cytotoxic activity in human hepatocellular carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104970openalex-snapshot
Secondary metabolites of endophytic fungi isolated from Huperzia serrata
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105251openalex-snapshot
Novel geranylhydroquinone derived meroterpenoids from the fungus Clitocybe clavipes and their cytotoxic activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105390openalex-snapshot
COX-2 and iNOS inhibitory epimeric meroterpenoids from Ganoderma cochlear and structure revision of cochlearol Q
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106110openalex-snapshot
Penicianstinoids F-K, six undescribed meroterpenoids from the marine algicolous fungus Penicillium sp. RR-DL-1-7
inferred← citeshttps://doi.org/10.1016/j.fochx.2025.103242openalex-snapshot
Seaweed phenolic compounds: Relationship with antioxidant activity and application in different food products
inferred← citeshttps://doi.org/10.1016/j.foodchem.2019.125715openalex-snapshot
Rhodomyrtus tomentosa (Aiton.): A review of phytochemistry, pharmacology and industrial applications research progress
inferred← citeshttps://doi.org/10.1016/j.pestbp.2017.12.005openalex-snapshot
Natural meroterpenoids isolated from the plant pathogenic fungus Verticillium albo-atrum with noteworthy modification action against voltage-gated sodium channels of central neurons of Helicoverpa armigera
inferred← citeshttps://doi.org/10.1016/j.phytochem.2012.03.002openalex-snapshot
Guanacastane-type diterpenoids from Coprinus radians
inferred← citeshttps://doi.org/10.1016/j.phytochem.2016.03.013openalex-snapshot
Talarolutins A–D: Meroterpenoids from an endophytic fungal isolate of Talaromyces minioluteus
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.06.019openalex-snapshot
Antimicrobial polyketide furanoterpenoids from seaweed-associated heterotrophic bacterium Bacillus subtilis MTCC 10403
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.11.011openalex-snapshot
Anti-inflammatory meroterpenoids from the mangrove endophytic fungus Talaromyces amestolkiae YX1
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113180openalex-snapshot
Identification of meroterpenoids from Bipolaris victoriae S27 and their potential activity against tumor metastasis and inhibition of the NF-κB signaling pathway
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113918openalex-snapshot
Meroterpenoids with divers' rings systems from Phyllosticta capitalensis and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113955openalex-snapshot
Diisoprenyl-cyclohexene-type meroterpenoids from a mangrove endophytic fungus Aspergillus sp. GXNU-Y65 and their anti-nonalcoholic steatohepatitis activity in AML12 cells
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.113983openalex-snapshot
Meroterpenoids from the marine-derived fungus Aspergillus terreus GZU-31-1 exerts anti-liver fibrosis effects by targeting the Nrf2 signaling in vitro
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114344openalex-snapshot
Congested heptacyclic meroterpenoids with anti-SARS-CoV-2 and anti-inflammatory activities from mangrove endophytic fungus Talaromyces amestolkiae SCNU–F0041
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114461openalex-snapshot
Arnebinfuranoids A–G, seven unique heterodimers of meroterpenoids from Arnebia euchroma
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114493openalex-snapshot
A series of meroterpenoids with highly oxygenated skeletons from the endophytic fungus Penicillium sp. and their anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114680openalex-snapshot
Peniterretonins A-D, terretonin-type meroterpenoids from the marine-derived fungus Penicillium simplicissimum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114983openalex-snapshot
Anti-inflammatory compounds from Penicillium fungi: A review
inferred← citeshttps://doi.org/10.1016/j.phytol.2016.10.013openalex-snapshot
Antimicrobial meroterpenoids from the endophytic fungus Penicillium sp. T2-8 associated with Gastrodia elata
inferred← citeshttps://doi.org/10.1016/j.phytol.2017.05.008openalex-snapshot
Spiroarthrinols a and B, two novel meroterpenoids isolated from the sponge- derived fungus Arthrinium sp
inferred← citeshttps://doi.org/10.1016/j.rechem.2025.102828openalex-snapshot
Development of FTase inhibitors inspired by the structures of andrastins
inferred← citeshttps://doi.org/10.1016/j.sajb.2024.06.031openalex-snapshot
Croton's therapeutic promise: A review of its phytochemistry and critical computational ADME/Tox analysis
inferred← citeshttps://doi.org/10.1016/j.smaim.2024.11.001openalex-snapshot
Bioactive matters based on natural product for cardiovascular diseases
inferred← citeshttps://doi.org/10.1016/j.steroids.2015.12.012openalex-snapshot
Anthraquinone–steroids, evanthrasterol A and B, and a meroterpenoid, emericellic acid, from endophytic fungus, Emericella variecolor
inferred← citeshttps://doi.org/10.1016/j.tet.2011.05.066openalex-snapshot
Bioactive meroterpenoids and alkaloids from the fungus Eurotium chevalieri
inferred← citeshttps://doi.org/10.1016/j.tet.2013.07.029openalex-snapshot
Reconstituted biosynthesis of fungal meroterpenoid andrastin A
inferred← citeshttps://doi.org/10.1016/j.tet.2015.02.061openalex-snapshot
Recent advances and perspectives in the synthesis of heterocycles via carbenes
inferred← citeshttps://doi.org/10.1016/j.tet.2017.09.048openalex-snapshot
Enantiospecific synthesis of antifungal dasyscyphin E from cupressic acid
inferred← citeshttps://doi.org/10.1016/j.tet.2018.02.048openalex-snapshot
A Negishi cross-coupling reaction enables the total synthesis of (+)-stachyflin
inferred← citeshttps://doi.org/10.1016/j.tet.2019.02.037openalex-snapshot
DMOA-based meroterpenoids with diverse scaffolds from the sponge-associated fungus Penicillium brasilianum
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131326openalex-snapshot
Diverse benzyl phloroglucinol-based meroterpenoids from the fruits of Melaleuca leucadendron
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131349openalex-snapshot
Polycyclic meroterpenoids, talaromyolides E − K for antiviral activity against pseudorabies virus from the endophytic fungus Talaromyces purpureogenus
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.04.045openalex-snapshot
Recent developments in sulfur- and selenium-catalyzed oxidative and isohypsic functionalization reactions of alkenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.11.029openalex-snapshot
Stachybotrin G, a sulfate meroterpenoid from a sponge derived fungus Stachybotrys chartarum MXH-X73
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.05.096openalex-snapshot
Meroterpenoid total synthesis: Conversion of geraniol and farnesol into amorphastilbol, grifolin and grifolic acid by dioxinone- β -keto-acylation, palladium catalyzed decarboxylative allylic rearrangement and aromatization
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152172openalex-snapshot
Total syntheses of (+)-arisugacins F, G
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153855openalex-snapshot
Talarophilone, a ring-opened azaphilone from the endophytic fungus Talaromyces sp. YUD18002
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154426openalex-snapshot
Three new phenylspirodrimanes from a conch-derived fungus Stachybotrys sp. NF02434
inferred← citeshttps://doi.org/10.1021/acs.accounts.0c00781openalex-snapshot
Annulative Methods in the Synthesis of Complex Meroterpene Natural Products
inferred← citeshttps://doi.org/10.1021/acs.biochem.3c00556openalex-snapshot
QM/MM Study of the Catalytic Mechanism and Substrate Specificity of the Aromatic Substrate C-Methyltransferase Fur6
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00478openalex-snapshot
Oxidative Cyclization in Natural Product Biosynthesis
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00571openalex-snapshot
Enzymatic Halogenation and Dehalogenation Reactions: Pervasive and Mechanistically Diverse
inferred← citeshttps://doi.org/10.1021/acs.jafc.6b04346openalex-snapshot
Biosynthesis of Antroquinonol and 4-Acetylantroquinonol B via a Polyketide Pathway Using Orsellinic Acid as a Ring Precursor in Antrodia cinnamomea
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00050openalex-snapshot
Austins-Type Meroterpenoids from a Mangrove-Derived Penicillium sp.
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00327openalex-snapshot
Bipolaquinones A–J, Immunosuppressive Meroterpenoids from a Soil-Derived Bipolaris zeicola
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c01025openalex-snapshot
Seco and Nor-seco Isodhilarane-Type Meroterpenoids from Penicillium purpurogenum and the Configuration Revisions of Related Compounds
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00766openalex-snapshot
Peniandranoids A–E: Meroterpenoids with Antiviral and Immunosuppressive Activity from a Penicillium sp.
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00986openalex-snapshot
Diaporaustalides A–L, Austalide Meroterpenoids from a Plant Endophytic Diaporthe sp.
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c01121openalex-snapshot
HPPO-Derived Meroterpenoids from the Marine-Derived Fungus Penicillium sp. SCSIO 41691
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00539openalex-snapshot
Antiviral Chlorinated Drimane Meroterpenoids from the Fungus Talaromyces pinophilus LD-7 and Their Biosynthetic Pathway
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00487openalex-snapshot
Aspertetranones A–D, Putative Meroterpenoids from the Marine Algal-Associated Fungus Aspergillus sp. ZL0-1b14
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00650openalex-snapshot
Antiviral Merosesquiterpenoids Produced by the Antarctic Fungus Aspergillus ochraceopetaliformis SCSIO 05702
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00926openalex-snapshot
Dryinones: Structure Elucidation of Red Colorants from Submerged Cultures of Pleurotus dryinus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00013openalex-snapshot
Asnovolins A–G, Spiromeroterpenoids Isolated from the Fungus Aspergillus novofumigatus, and Suppression of Fibronectin Expression by Asnovolin E
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00641openalex-snapshot
Stachybotrysin, an Osteoclast Differentiation Inhibitor from the Marine-Derived Fungus Stachybotrys sp. KCB13F013
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00829openalex-snapshot
Griseofulvin Derivative and Indole Alkaloids from Penicillium griseofulvum CPCC 400528
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b01061openalex-snapshot
Chrodrimanins K–N and Related Meroterpenoids from the Fungus Penicillium sp. SCS-KFD09 Isolated from a Marine Worm, Sipunculus nudus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00030openalex-snapshot
KI/NaBr-Induced Variable Halogenated DMOA-Derived Isodhilarane-Type Meroterpenoids with Anti-inflammatory Activities from Mangrove Endophytic Fungus Talaromyces sp. SCNU-F0041
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00032openalex-snapshot
Bioactive Azaphilone Derivatives from the Fungus Talaromyces aculeatus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00042openalex-snapshot
Anti-inflammatory Meroterpenoids from Baeckea frutescens
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00438openalex-snapshot
3,5-Dimethylorsellinic Acid Derived Meroterpenoids from Penicillium chrysogenum MT-12, an Endophytic Fungus Isolated from Huperzia serrata
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00281openalex-snapshot
Phomanolides C–F from a Phoma sp.: Meroterpenoids Generated via Hetero-Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00878openalex-snapshot
Structurally Diverse Meroterpenoids from a Marine-Derived Aspergillus sp. Fungus
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02237openalex-snapshot
Bioactive Polyketide-Terpenoid Hybrids from a Soil-Derived Fungus Bipolaris zeicola
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02609openalex-snapshot
Computational Investigation of Multifaceted Cationic Rearrangement and Stereo- and Regioselectivity in the Formation of Dysideanone’s Analogues
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00369openalex-snapshot
Diisoprenyl-cyclohexene/ane-Type Meroterpenoids from Biscogniauxia sp. and Their Anti-inflammatory Activities
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01106openalex-snapshot
Total Synthesis of Enantiopure Chabrolonaphthoquinone B Via a Stereoselective Julia-Kocienski Olefination
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02800openalex-snapshot
Five Pairs of Meroterpenoid Enantiomers from Rhododendron capitatum
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01205openalex-snapshot
Enantioselective Total Synthesis of (+)-Bisabosqual A and Studies on Late-Stage C(sp3)–H Functionalization Approaches to Bisabosquals
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00746openalex-snapshot
Alternarin A, a Drimane Meroterpenoid, Suppresses Neuronal Excitability from the Coral-Associated Fungi Alternaria sp. ZH-15
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00786openalex-snapshot
Hyperprins A and B, Two Complex Meroterpenoids from Hypericum przewalskii
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02160openalex-snapshot
Penicimeroterpenoids A–C, Meroterpenoids with Rearrangement Skeletons from the Marine-Derived Fungus Penicillium sp. SCSIO 41512
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02641openalex-snapshot
Terreuspyridine: An Unexpected Pyridine-Fused Meroterpenoid Alkaloid with a Tetracyclic 6/6/6/6 Skeleton from Aspergillus terreus
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