Results 91 to 100 of about 2,271 (197)

Cytotoxic and N-Acetyltransferase Inhibitory Meroterpenoids from Ganoderma cochlear

open access: yesMolecules, 2018
Seven compounds, including two pairs of new meroterpenoids, (+)- and (−)-gancochlearol C (1), (+)- and (−)-cochlearoid Q (3), and a new meroterpenoid gancochlearol D (2), together with four known meroterpenoids were isolated from the aqueous ...
Li-Zhi Cheng   +5 more
doaj   +1 more source

Cochlioquinones 1968–2024: Chemistry, Biosynthesis, and Biological Activities with Future Perspectives

open access: yesJournal of Fungi
Cochlioquinones are a member of meroterpenoids possessing a core 6/6/6/6 tetracyclic ring system, which originate from the polyketide-terpenoid hybrid biosynthesis.
Huiqi Fang, Qi Li, Lin Chen, Gang Ding
doaj   +1 more source

Meroterpenoids and Isocoumarinoids from a Myrothecium Fungus Associated with Apocynum venetum

open access: yesMarine Drugs, 2018
Four new meroterpenoids 1–4 and four new isocoumarinoids 5–8, along with five known isocoumarinoids (9–13), were isolated from the fungus Myrothecium sp.
Yanchao Xu   +6 more
doaj   +1 more source

Correction to “Absolute Configuration and Biological Activities of Meroterpenoids from an Endophytic Fungus of Lycium barbarum”

open access: yes, 2019
Correction to “Absolute Configuration and Biological Activities of Meroterpenoids from an Endophytic Fungus of Lycium ...
Kun Gao (161056)   +9 more
core   +1 more source

Meroterpenoid Hydroquinones fromCordia globosa

open access: yesJournal of the Brazilian Chemical Society, 2015
Two new meroterpenoid hydroquinones,rel-(4bE,6Z,8E,9aS,10S)-1,4-dihydroxy-9a,10-dihydro-10,12-epoxy-5-methylbenzo[a]azulen-12-one andrel-(4bZ,6Z,8E,9aS,10S)-1-hydroxy-9a,10-dihydro-4,11:10,12-diepoxy-benzo[a]azulen-11,12-dione, along with the known peptide derivative (S)-N-benzoylphenylalanine-(S)-2-benzamide-3-phenylpropyl ester, were isolated from ...
Silva, Ana Karine O.   +6 more
openaire   +3 more sources

Biomimetic total syntheses of chromane meroterpenoids, guadials B and C, guapsidial A and psiguajadial D

open access: yes, 2018
The first biomimetic total syntheses of chromane meroterpenoids, guadials B and C, guapsidial A and psiguajadial D have been completed.
Dattatraya H. Dethe   +2 more
core   +1 more source

Meroterpenoids from Marine Sponge Hyrtios sp. and Their Anticancer Activity against Human Colorectal Cancer Cells

open access: yesMarine Drugs
Two new meroterpenoids, hyrtamide A (1) and hyrfarnediol A (2), along with two known ones, 3-farnesyl-4-hydroxybenzoic acid methyl ester (3) and dictyoceratin C (4), were isolated from a South China Sea sponge Hyrtios sp. Their structures were elucidated
Jie Wang   +6 more
doaj   +1 more source

Evolution of a Strategy for the Total Synthesis of the Ganoderma Meroterpenoid Ganoapplanin

open access: yesChemistryEurope
Herein, a detailed account of the efforts leading to the recently published synthesis of the Ganoderma meroterpenoid ganoapplanin, a natural product identified as an inhibitor of T‐type voltage‐gated calcium channels, is provided. Ganoapplanin, which was
Nicolas Müller   +9 more
doaj   +1 more source

A Short Biomimetic Synthesis of the Meroterpenoids Guajadial and Psidial A

open access: yesOrganic Letters, 2010
The biosynthesis of the meroterpenoid guajadial was previously hypothesized to occur via a hetero-Diels-Alder reaction between caryophyllene and an o-quinone methide. This hypothesis has been verified via the biomimetic synthesis of guajadial and psidial A in an aqueous three-component coupling reaction, between caryophyllene, benzaldehyde, and ...
Lawrence, A   +5 more
openaire   +3 more sources

Nitric Oxide Inhibitory Meroterpenoids from the Fungus Penicillium purpurogenum MHZ 111

open access: yes, 2016
Five new meroterpenoids, purpurogenolides A–E (1–5), and four known metabolites (6–9) were isolated from the solid substrate fermentation cultures of the fungus Penicillium purpurogenum MHz 111. The structures of the new meroterpenoids were elucidated by
Jing Sun (141206)   +10 more
core   +1 more source

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