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Antileishmanial and Cytotoxic Activity of Some Highly Oxidized Abietane Diterpenoids from the Bald Cypress, Taxodium distichum

https://doi.org/10.1021/acs.jnatprod.5b01131
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Enantioselective Synthesis of (+)-Royleanone from Sulfinyl Quinones
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Electronic CD Exciton Chirality Method: Principles and Applications
inferredcites →https://doi.org/10.1002/bmc.1232openalex-snapshot
Determination of ferruginol in rat plasma via high‐performance liquid chromatography and its application in pharmacokinetics study
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Struktur von Fuerstion
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262. Magnetische Nicht‐Áquivalenz von Protonen als Folge konformativer Chiralität Kinetik einer Racemisierung
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Studies on the Extractive Constituents of the Bark of Libocedrus Formosana Florin. I. The Structure of 6α‐Hydroxy‐7‐0X0‐Ferruginol
inferredcites →https://doi.org/10.1002/mrc.1245openalex-snapshot
1H and 13C NMR spectral assignments of some natural abietane diterpenoids
inferredcites →https://doi.org/10.1002/mrc.1260321211openalex-snapshot
13C NMR Data for abieta‐8,11,13‐triene diterpenoids
inferredcites →https://doi.org/10.1016/0031-9422(83)80033-8openalex-snapshot
Abietane diterpenoids from the root of Salvia phlomoides
inferredcites →https://doi.org/10.1016/0031-9422(92)83290-fopenalex-snapshot
Microstegiol, a rearranged diterpene from Salvia microstegia
inferredcites →https://doi.org/10.1016/j.bmc.2008.11.031openalex-snapshot
Redox-active dinitrodiphenylthioethers against Leishmania: Synthesis, structure–activity relationships and mechanism of action studies
inferredcites →https://doi.org/10.1016/j.ijpddr.2014.02.002openalex-snapshot
Drug repurposing and human parasitic protozoan diseases
inferredcites →https://doi.org/10.1016/j.phytochem.2014.08.029openalex-snapshot
Terpenoids, flavonoids and caffeic acid derivatives from Salvia viridis L. cvar. Blue Jeans
inferredcites →https://doi.org/10.1016/s0944-7113(96)80067-5openalex-snapshot
Effect of tannins on screening of plant extracts for enzyme inhibitory activity and techniques for their removal
inferredcites →https://doi.org/10.1021/ja01023a061openalex-snapshot
Tumor inhibitors. XXXIV. Taxodione and taxodone, two novel diterpenoid quinone methide tumor inhibitors from Taxodium distichum
inferredcites →https://doi.org/10.1021/ja01256a054openalex-snapshot
The Structure and Configuration of Resin Acids. Podocarpic Acid and Ferruginol
inferredcites →https://doi.org/10.1021/jo00043a034openalex-snapshot
Cyclization reactions of the o-naphthoquinone diterpene aethiopinone. A revision of the structure of prionitin.
inferredcites →https://doi.org/10.1021/jo01264a036openalex-snapshot
Tumor inhibitors. XLVIII. Taxodione and taxodone, two novel diterpenoid quinone methide tumor inhibitors from Taxodium distichum
inferredcites →https://doi.org/10.1021/jo102127qopenalex-snapshot
Nicholas Reactions in the Construction of Cyclohepta[de]naphthalenes and Cyclohepta[de]naphthalenones. The Total Synthesis of Microstegiol
inferredcites →https://doi.org/10.1021/jo801032nopenalex-snapshot
Koshikamide B, a Cytotoxic Peptide Lactone from a Marine Sponge Theonella sp
inferredcites →https://doi.org/10.1021/np050125nopenalex-snapshot
Terpenoids from the Roots and Rhizomes of Nardostachys chinensis
inferredcites →https://doi.org/10.1021/np100503qopenalex-snapshot
Isolation and Characterization of Minor Analogues of Silvestrol and Other Constituents from a Large-Scale Re-collection of Aglaia foveolata
inferredcites →https://doi.org/10.1021/np50063a016openalex-snapshot
7-O-Methylhorminone and Other Cytotoxic Diterpene Quinones from Lepechinia bullata
inferredcites →https://doi.org/10.1021/np50082a006openalex-snapshot
New Abietane Diterpenoids from Salvia montbretii
inferredcites →https://doi.org/10.1021/np501028uopenalex-snapshot
Northalrugosidine Is a Bisbenzyltetrahydroisoquinoline Alkaloid from Thalictrum alpinum with in Vivo Antileishmanial Activity
inferredcites →https://doi.org/10.1038/nrmicro2608openalex-snapshot
Leishmaniasis: complexity at the host–pathogen interface
inferredcites →https://doi.org/10.1039/jr9390001031openalex-snapshot
221. Miro resin. Part I. Ferruginol
inferredcites →https://doi.org/10.1073/pnas.1409061111openalex-snapshot
Taxodione and arenarone inhibit farnesyl diphosphate synthase by binding to the isopentenyl diphosphate site
inferredcites →https://doi.org/10.1093/jac/dkp206openalex-snapshot
Transgenic Leishmania donovani clinical isolates expressing green fluorescent protein constitutively for rapid and reliable ex vivo drug screening
inferredcites →https://doi.org/10.1093/jac/dkt320openalex-snapshot
Liposomal resiquimod for the treatment of Leishmania donovani infection
inferredcites →https://doi.org/10.1111/j.1469-0691.2011.03635.xopenalex-snapshot
Leishmaniasis impact and treatment access
inferredcites →https://doi.org/10.1128/aac.02398-12openalex-snapshot
Comparison of a High-Throughput High-Content Intracellular Leishmania donovani Assay with an Axenic Amastigote Assay
inferredcites →https://doi.org/10.1128/aac.05412-11openalex-snapshot
Identification of New Antileishmanial Leads from Hits Obtained by High-Throughput Screening
inferredcites →https://doi.org/10.1139/v62-232openalex-snapshot
DITERPENOID QUINONES OF INULA ROYLEANA D. C.
inferredcites →https://doi.org/10.1177/1934578x1000500605openalex-snapshot
Antimicrobial and Antiparasitic Abietane Diterpenoids from the Roots of Clerodendrum eriophyllum
inferredcites →https://doi.org/10.1211/jpp.60.2.0014openalex-snapshot
Gastroprotective activity of ferruginol in mice and rats: effects on gastric secretion, endogenous prostaglandins and non-protein sulfhydryls
inferredcites →https://doi.org/10.1248/bpb.b12-00419openalex-snapshot
Leishmanicidal Activity of Two Naphthoquinones against Leishmania donovani
inferredcites →https://doi.org/10.1248/yakushi1881.59.2_124openalex-snapshot
inferredcites →https://doi.org/10.1371/journal.pone.0035671openalex-snapshot
Leishmaniasis Worldwide and Global Estimates of Its Incidence
inferredcites →https://doi.org/10.1371/journal.ppat.1003053openalex-snapshot
Determinants for the Development of Visceral Leishmaniasis Disease
inferredcites →https://doi.org/10.1656/1528-7092(2002)001[0131:pgsobt]2.0.co;2openalex-snapshot
POPULATION GENETIC STRUCTURE OF BALDCYPRESS (TAXODIUM DISTICHUM [L.] RICH. VAR. DISTICHUM) AND PONDCYPRESS (T. DISTICHUM VAR. IMBRICARIUM [NUTTALL] CROOM): BIOGEOGRAPHIC AND TAXONOMIC IMPLICATIONS
inferredcites →https://doi.org/10.2147/rrmc.s29902openalex-snapshot
Antimicrobial and antiparasitic abietane diterpenoids from Cupressus sempervirens
inferredcites →https://doi.org/10.2174/2210290601304010001openalex-snapshot
Ethnobotany, Phytochemistry, and Biological Activities of Taxodium Rich.
inferredcites →https://doi.org/10.2307/1221225openalex-snapshot
THE NOMENCLATURE OF PONDCYPRESS AND BALDCYPRESS (TAXODIACEAE)
inferredcites →https://doi.org/10.4067/s0034-98872007000800018openalex-snapshot
Peregrinaciones a las fuentes de la medicina clásica
inferredcites →https://doi.org/10.4067/s0034-98872007000800019openalex-snapshot
Cobertura de patologías en Plan AUGE de Chile
inferredcites →https://doi.org/10.5281/zenodo.16214077openalex-snapshot
Taxodium (Cupressaceae): one, two or three species? Evidence from DNA sequences and terpenoids

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Two seco-norabietane diterpenoids with unprecedented skeletons from the roots of Salvia abrotanoides (Kar.) Sytsma
inferred← citeshttps://doi.org/10.1002/cbdv.202400648openalex-snapshot
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ECD exciton chirality method today: a modern tool for determining absolute configurations
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inferred← citeshttps://doi.org/10.1007/s13659-021-00311-2openalex-snapshot
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Salcastaniols A-G, seven undescribed diterpenoids with cholinesterase inhibitory activities from Salvia castanea Diels f. tomentosa Stib
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Three new abietane-type diterpenes from the bark of Cryptomeria japonica
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Natural products in neglected tropical disease research: A two-decade scientometric and text-mining analysis
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Taxodinoids A-D, four heptacyclic C40 diterpene dimers from the seeds of Taxodium distichum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00651openalex-snapshot
In Vivo Biological Evaluation of a Synthetic Royleanone Derivative as a Promising Fast-Acting Trypanocidal Agent by Inducing Mitochondrial-Dependent Necrosis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00482openalex-snapshot
A Pair of Enantiomeric Bis-seco-abietane Diterpenoids fromCryptomeria fortunei
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02541openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.7b00892openalex-snapshot
Extraction Optimization and Structural and Thermal Characterization of the Antimicrobial Abietane 7α-Acetoxy-6β-hydroxyroyleanone
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00033openalex-snapshot
Bioinspired Synthesis of Microstegiol and Biosynthetically Related Skeleton-Rearranged Abietanes
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