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Ganoweberianones A and B, Antimalarial Lanostane Dimers from Cultivated Fruiting Bodies of the Basidiomycete Ganoderma weberianum

https://doi.org/10.1021/acs.jnatprod.0c00879
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1097-0290(19991020)65:2<201::aid-bit10>3.0.co;2-hopenalex-snapshot
GFP-expressing mammalian cells for fast, sensitive, noninvasive cell growth assessment in a kinetic mode
inferredcites →https://doi.org/10.1016/j.fitote.2016.09.010openalex-snapshot
New lanostane-type triterpenoids from the fruiting body of Ganoderma hainanense
inferredcites →https://doi.org/10.1016/j.fitote.2017.03.007openalex-snapshot
Highly oxygenated lanostane-type triterpenoids and their bioactivity from the fruiting body of Ganoderma gibbosum
inferredcites →https://doi.org/10.1016/j.phytochem.2006.07.004openalex-snapshot
Ganoderma – A therapeutic fungal biofactory
inferredcites →https://doi.org/10.1016/j.phytochem.2012.11.022openalex-snapshot
Lanostane triterpenes from cultures of the Basidiomycete Ganoderma orbiforme BCC 22324
inferredcites →https://doi.org/10.1016/j.phytochem.2014.10.009openalex-snapshot
Lanostane triterpenoids from Ganoderma hainanense J. D. Zhao
inferredcites →https://doi.org/10.1016/j.phytochem.2015.03.010openalex-snapshot
Secondary metabolites from Ganoderma
inferredcites →https://doi.org/10.1016/j.phytochem.2019.112225openalex-snapshot
Lanostane triterpenoids from cultivated fruiting bodies of the wood-rot basidiomycete Ganoderma casuarinicola
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00973openalex-snapshot
Antitubercular Activity of Mycelium-Associated Ganoderma Lanostanoids
inferredcites →https://doi.org/10.1021/acs.jnatprod.8b00869openalex-snapshot
Highly Modified Lanostane Triterpenes from Fruiting Bodies of the Basidiomycete Tomophagus sp.
inferredcites →https://doi.org/10.1021/acs.jnatprod.9b00947openalex-snapshot
Highly Modified Lanostane Triterpenes from the Wood-Rot Basidiomycete Ganoderma colossus: Comparative Chemical Investigations of Natural and Artificially Cultivated Fruiting Bodies and Mycelial Cultures
inferredcites →https://doi.org/10.1021/jo991218aopenalex-snapshot
Phenylglycine Methyl Ester, a Useful Tool for Absolute Configuration Determination of Various Chiral Carboxylic Acids
inferredcites →https://doi.org/10.1021/np200205nopenalex-snapshot
Semisynthesis and Biological Evaluation of Ganodermanontriol and Its Stereoisomeric Triols
inferredcites →https://doi.org/10.1021/np50048a029openalex-snapshot
Two New Lanostanoids from Ganoderma lucidum
inferredcites →https://doi.org/10.1021/np50055a006openalex-snapshot
Revision of 1H- and 13C-nmr Assignments of Lanostanoids from Ganoderma lucidum by 2D-nmr Studies
inferredcites →https://doi.org/10.1021/np800687topenalex-snapshot
Triterpene-Farnesyl Hydroquinone Conjugates from Ganoderma sinense
inferredcites →https://doi.org/10.1039/c8ra05282dopenalex-snapshot
Rearranged lanostane-type triterpenoids with anti-hepatic fibrosis activities from Ganoderma applanatum
inferredcites →https://doi.org/10.1128/aac.16.6.710openalex-snapshot
Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique
inferredcites →https://doi.org/10.1128/aac.47.12.3682-3687.2003openalex-snapshot
Improved Green Fluorescent Protein Reporter Gene-BasedMicroplate Screening for Antituberculosis Compounds by Utilizing anAcetamidasePromoter
inferredcites →https://doi.org/10.3390/molecules191117478openalex-snapshot
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.

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.2021.113075zenodo-depositor-declared
Lanostane triterpenoids from cultivated fruiting bodies of basidiomycete Ganoderma mbrekobenum
inferred← citeshttps://doi.org/10.1016/b978-0-443-18611-0.00013-9openalex-snapshot
Triterpenoids and saponins in drug discovery
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104950openalex-snapshot
(±)-Gancochlearols J − N, renoprotective meroterpenoids from Ganoderma cochlear
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106025openalex-snapshot
Antidiabetic lanostane triterpenoids from the fruiting bodies of Ganoderma weberianum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112963openalex-snapshot
Lanostane triterpenoids from cultivated fruiting bodies of Ganoderma sichuanense: Determination of the C-25 absolute configuration of ganoderic acid A and its derivatives using the phenylglycine methyl ester (PGME) method
inferred← citeshttps://doi.org/10.1016/j.phytol.2022.01.002openalex-snapshot
Ergostane triterpenoids from the cultures of basidiomycete Favolaschia calocera BCC 36684 and stereochemical elucidation of favolon
inferred← citeshttps://doi.org/10.1016/j.phytol.2022.03.001openalex-snapshot
Ganoellipsic acids A–C, lanostane triterpenoids from artificially cultivated fruiting bodies of Ganoderma ellipsoideum
inferred← citeshttps://doi.org/10.1016/j.phytol.2022.06.009openalex-snapshot
Lanostane triterpenoids from mycelial cultures of the basidiomycete Ganoderma weberianum
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.10.004openalex-snapshot
Lanostane triterpenoids from artificially cultivated fruiting bodies of Ganoderma wiiroense
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00457openalex-snapshot
Antimalarial Lanostane Dimers from Artificially Cultivated Fruiting Bodies of Ganoderma weberianum
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02042openalex-snapshot
Toward the Asymmetric de Novo Synthesis of Lanostanes: Construction of 7,11-Dideoxy-Δ5-lucidadone H
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01299openalex-snapshot
Progress toward the De Novo Asymmetric Synthesis of Euphanes
inferred← citeshttps://doi.org/10.1021/acsomega.5c06826openalex-snapshot
Lanostane–Meroterpene Conjugates with Unusual Aryl Ether Linkage and a Lanostane Dimer from Artificially Cultivated Fruiting Bodies of Ganoderma cf. hochiminhense
inferred← citeshttps://doi.org/10.1039/d5cp00817dopenalex-snapshot
Molecular dynamics simulations reveal a strong binding capacity of colossolactone H to the EGFR inactive conformation
inferred← citeshttps://doi.org/10.1080/10286020.2025.2549892openalex-snapshot
Drimane sesquiterpenoids from cultures of the basidiomycete Panellus pusillus
inferred← citeshttps://doi.org/10.1080/10286020.2025.2564414openalex-snapshot
Norlanostane triterpenoids from artificially cultivated fruiting bodies of basidiomycete Ganoderma casuarinicola
inferred← citeshttps://doi.org/10.1080/14786419.2022.2050911openalex-snapshot
Two lanostane triterpenoids with α-glucosidase inhibitory activity from the fruiting bodies of Ganoderma weberianum
inferred← citeshttps://doi.org/10.1080/14786419.2022.2124987openalex-snapshot
Colossolactone J, a highly modified lanostane triterpenoid from a natural fruiting body of Ganoderma colossus
inferred← citeshttps://doi.org/10.1080/14786419.2023.2196723openalex-snapshot
Lanostane triterpenoids from artificially cultivated fruiting bodies of Ganoderma cf. mastoporum
inferred← citeshttps://doi.org/10.12982/cmjs.2022.052openalex-snapshot
History of Thai Mycology and Resolution of Taxonomy for Thai Macrofungi Confused with Europe and American Names
inferred← citeshttps://doi.org/10.3389/fcimb.2025.1545135openalex-snapshot
Ganodermataceae—current status, research, and development in Lower Mekong Basin
inferred← citeshttps://doi.org/10.3390/jof10020144openalex-snapshot
Biological Activities of Secondary Metabolites from the Edible-Medicinal Macrofungi
inferred← citeshttps://doi.org/10.53365/nrfhh/143570openalex-snapshot
Mushrooms (Basidiomycetes) as a significant source of biologically active compounds for malaria control
inferred← citeshttps://doi.org/10.5772/intechopen.98261openalex-snapshot
Introductory Chapter: Terpenes and Terpenoids
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