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Cytotoxic Terpenoids from the Roots of Dracocephalum taliense

https://doi.org/10.3390/molecules23010057

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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/anie.201000449openalex-snapshot

Glandular Trichomes of Leucosceptrum canum Harbor Defensive Sesterterpenoids

inferredcites →https://doi.org/10.1002/cbdv.200900188openalex-snapshot

Chemical Constituents of Plants from the Genus Dracocephalum

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(89)80357-7openalex-snapshot

Diterpenoids from Rabdosia kunmingensis

inferredcites →https://doi.org/10.1016/0031-9422(91)85046-3openalex-snapshot

Complete 1H and 13C NMR assignments of totarol and its derivatives

inferredcites →https://doi.org/10.1016/j.fitote.2014.05.008openalex-snapshot

Chemical constituents from the linseed meal

inferredcites →https://doi.org/10.1016/j.phytochem.2005.04.035openalex-snapshot

Xanthomicrol is the main cytotoxic component of Dracocephalum kotschyii and a potential anti-cancer agent

inferredcites →https://doi.org/10.1016/j.phytochem.2008.01.013openalex-snapshot

Stereochemistry of flavonoidal alkaloids from Dracocephalum rupestre

inferredcites →https://doi.org/10.1016/j.phytochem.2011.07.008openalex-snapshot

Terpenoids and phenethyl glucosides from Hyssopus cuspidatus (Labiatae)

inferredcites →https://doi.org/10.1016/j.phytochem.2014.02.007openalex-snapshot

Monoterpene glycosides, phenylpropanoids, and acacetin glycosides from Dracocephalum foetidum

inferredcites →https://doi.org/10.1016/j.tetlet.2003.10.202openalex-snapshot

A trypanocidal diterpene with novel skeleton from Dracocephalum komarovi

inferredcites →https://doi.org/10.1016/s0031-9422(00)83467-6openalex-snapshot

An abietane diterpene from the labiate Coleus barbatus

inferredcites →https://doi.org/10.1016/s0031-9422(00)89808-8openalex-snapshot

Diterpenoids from Salvia coulteri

inferredcites →https://doi.org/10.1016/s0031-9422(03)00291-7openalex-snapshot

The microbiological transformation of the diterpenes dehydroabietanol and teideadiol by Mucor plumbeus

inferredcites →https://doi.org/10.1016/s0031-9422(96)00609-7openalex-snapshot

Cytotoxic abietane diterpenoids from Caryopteris incana

inferredcites →https://doi.org/10.1016/s0040-4039(00)90571-9openalex-snapshot

Sempervirol, a novel type of diterpene phenol

inferredcites →https://doi.org/10.1021/acs.chemrev.7b00287openalex-snapshot

Structural and Chemical Biology of Terpenoid Cyclases

inferredcites →https://doi.org/10.1021/cr200058fopenalex-snapshot

Constituents from Salvia Species and Their Biological Activities

inferredcites →https://doi.org/10.1021/np020308zopenalex-snapshot

New Icetexane and 20-Norabietane Diterpenes with Trypanocidal Activity from Dracocephalum komarovi

inferredcites →https://doi.org/10.1021/np0304161openalex-snapshot

Antineoplastic Agents. 529. Isolation and Structure of Nootkastatins 1 and 2 from the Alaskan Yellow CedarChamaecyparisnootkatensis

inferredcites →https://doi.org/10.1021/np300609uopenalex-snapshot

Flavone Tetraglycosides and Benzyl Alcohol Glycosides from the Mongolian Medicinal Plant Dracocephalum ruyschiana

inferredcites →https://doi.org/10.1021/ol302787copenalex-snapshot

New Antifeedant C20 Terpenoids from Leucosceptrum canum

inferredcites →https://doi.org/10.1021/ol4004756openalex-snapshot

Peltate Glandular Trichomes of Colquhounia coccinea var. mollis Harbor a New Class of Defensive Sesterterpenoids

inferredcites →https://doi.org/10.1021/ol503230sopenalex-snapshot

Unraveling the Metabolic Pathway in Leucosceptrum canum by Isolation of New Defensive Leucosceptroid Degradation Products and Biomimetic Model Synthesis

inferredcites →https://doi.org/10.1038/nchembio.2007.5openalex-snapshot

The function of terpene natural products in the natural world

inferredcites →https://doi.org/10.1039/c7np00027hopenalex-snapshot

Diterpenoids from Isodon species: an update

inferredcites →https://doi.org/10.1080/10286020.2013.837458openalex-snapshot

Three new ursane-type triterpenoids from the aerial parts ofIsodon excisoides

inferredcites →https://doi.org/10.1080/10286020108040370openalex-snapshot

Constituents fromLimonia Crenulata

inferredcites →https://doi.org/10.1177/1934578x1501001206openalex-snapshot

Macrocyclic Diterpenoids from the Latex of Euphorbia helioscopia

inferredcites →https://doi.org/10.1248/cpb.52.1249openalex-snapshot

Two New Monoterpene Glycosides and Trypanocidal Terpenoids from Dracocephalum kotschyi

inferredcites →https://doi.org/10.1515/znc-2005-1-204openalex-snapshot

Bioactive Constituents from Dracocephalum subcapitatum (O. Kuntze) Lipsky

inferredcites →https://doi.org/10.3390/molecules181114105openalex-snapshot

Chemical Composition and Antioxidant Activity of Tánara Ótó (Dracocephalum palmatum Stephan), a Medicinal Plant Used by the North-Yakutian Nomads

inferredcites →https://doi.org/10.3390/molecules200917544openalex-snapshot

Three New Cytotoxic ent-Kaurane Diterpenes from Isodon excisoides

inferredcites →https://doi.org/10.3390/molecules22020309openalex-snapshot

Ent-Abietanoids Isolated from Isodon serra

inferredcites →https://doi.org/10.3390/molecules22071168openalex-snapshot

Isolation and Characterization of Aphidicolin Derivatives from Tolypocladium inflatum

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.2021.112685zenodo-depositor-declared

Diterpenoids from Zhumeria majdae roots as potential heat shock protein 90 (HSP90) modulators

inferred← citeshttps://doi.org/10.1002/cbdv.202300913openalex-snapshot

Anthemis tricolor Containing Unusual Totarol with Cytotoxic and Acetylcholinesterase‐Inhibitory Activity

inferred← citeshttps://doi.org/10.1002/cbdv.202400808openalex-snapshot

Abietane‐Type Diterpenoids: Insights into Structural Diversity and Therapeutic Potential

inferred← citeshttps://doi.org/10.1007/s10600-022-03681-2openalex-snapshot

Isolation and Identification of Bioactive Constituents of the Stems of Illicium cambodianum

inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108892openalex-snapshot

Structurally diverse diterpenoids from cones of Taxodium ascendens inhibit colorectal cancer proliferation via regulating mitophagy

inferred← citeshttps://doi.org/10.1016/j.ejmech.2026.119218openalex-snapshot

Multi-target mechanisms underlying the antiviral and anti-inflammatory activities of tobacco-derived natural small molecules

inferred← citeshttps://doi.org/10.1016/j.exppara.2024.108807openalex-snapshot

The activities of suaveolol and other compounds from Hyptis suaveolens and Momordica charantia against the aetiological agents of African trypanosomiasis, leishmaniasis and malaria

inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107328openalex-snapshot

Chemical diversity of abietane diterpenoids from Nepeta stewartiana Diels and their anti-bacterial and antifeedant effects

inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113835openalex-snapshot

Succipenoids A-C: A dimeric abietane and nor-abietane diterpenoids from fossil Chinese medicinal succinum and their anti-inflammatory potential

inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114257openalex-snapshot

Recent progress on triterpenoid derivatives and their anticancer potential

inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114854openalex-snapshot

Diterpene-phenylpropanoid conjugates and seco-abietane diterpenoids from dried branches of Illicium cambodianum with inhibitory activity against PCSK9 secretion

inferred← citeshttps://doi.org/10.1021/acs.jafc.3c02779openalex-snapshot

Caterpillars Detoxify Diterpenoid from Nepeta stewartiana by the Molting Hormone Gene CYP306A1

inferred← citeshttps://doi.org/10.1039/d5ob00715aopenalex-snapshot

Comprehensive review of plant-derived triterpenoid types, structures and cytotoxicity: an update from 2015 to 2024

inferred← citeshttps://doi.org/10.2174/1871520620666200317110010openalex-snapshot

Cytotoxic Dehydroabietylamine Derived Compounds

inferred← citeshttps://doi.org/10.3389/fphar.2024.1449426openalex-snapshot

Pharmacophylogenetic relationships of genus Dracocephalum and its related genera based on multifaceted analysis

inferred← citeshttps://doi.org/10.3390/molecules26227013openalex-snapshot

New Polyesterified Ursane Derivatives from Leaves of Maesa membranacea and Their Cytotoxic Activity

inferred← citeshttps://doi.org/10.3390/plants12213752openalex-snapshot

Ethnobotanical, Phytochemical, and Pharmacological Properties of the Subfamily Nepetoideae (Lamiaceae) in Inflammatory Diseases

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