Abstract
No public abstract is available from the verified source records.
Contact and support
Need help, have a question, or want to contact the ResearchHub team?
© 2026 ResearchHub. Built for responsible scholarly connection.
Privacy-aware community infrastructureYong Shen, Nanjin Ding, Meijia Zheng, Tianyuan Guo, Hucheng Zhu
Abstract
Authors
Institutions
No ROR-resolved institution is linked to this work yet.
Provenance
crossref
Confidence 100%
pubmed
Confidence 98%
unpaywall
Confidence 95%
datacite
Confidence 0%
No local reference links have been materialized yet.
No local citing links have been materialized yet.
Unveiling the potential of ent-kaurane diterpenoids: multifaceted natural products for drug discovery
10.3390/ph17040510 · 2024
Cytotoxic ent-kaurane diterpenoids from Isodon eriocalyx
10.1002/cbdv.200590136 · 2005
Ent‐kaurane diterpenoids from Isodon eriocalyx var
10.1002/cjoc.201100653 · 2012
Bioactive ent-kaurane diterpenoids from Isodon rosthornii
10.1021/np400190n · 2013
Diterpenoids from Isodon species: an update
2017
Recent developments in the syntheses of C-20-oxygenated ent-kaurane diterpenoids
10.1002/cplu.202300676 · 2024
Discovery of ent-kaurane diterpenoids, characteristic metabolites of Isodon species, from an endophytic fungal strain Geopyxis sp
10.1016/j.fitote.2022.105160 · 2022
Discovery and semisynthesis of aurantiacin A: a unique ascorbylated 9-epi-ent-kaurane diterpenoid from the untapped plant Isodon aurantiacus
10.1021/acs.orglett.5c00586 · 2025
Ent-kaurene diterpenoids from Isodon phyllostachys
10.1016/j.tetlet.2016.12.034 · 2017
Maoecrystal V, cytotoxic diterpenoid with a novel C19 skeleton from Isodon eriocalyx (Dunn
10.1021/ol0481535 · 2004
Crokonoids A−C, a highly rearranged and dual-bridged spiro diterpenoid and two other diterpenoids from Croton kongensis
10.1021/acs.orglett.9b04484 · 2020
Scalable synthesis enabling multilevel bio-evaluations of natural products for discovery of lead compounds
10.1038/s41467-018-03546-9 · 2018
Ent-kaurene diterpenoids from Sideritis lycia with antiviral and cytotoxic activities
2020
Selective cytotoxicity of ent-kaurene diterpenoids isolated from Baccharis lateralis and Baccharis retusa (Asteraceae)
10.1002/ardp.202200083 · 2022
Synthesis, biological activity, and apoptotic properties of NO-donor/enmein-type ent-kauranoid hybrids
10.3390/ijms17060747 · 2016
Antithrombotic activity of the steroids and ent-kaurane diterpenoids from Canna indica Rhizomes
10.1007/s43450-023-00472-w · 2024
Anti-inflammatory ent-kaurane dterpenoids from Isodon serra
10.1021/acs.jnatprod.9b01281 · 2020
Anti-biofilm and anti-inflammatory active diterpene isolated from the fruit of Xylopia benthamii R.E.Fr.
10.1080/14786419.2023.2208357 · 2024
Ent-kauranes and ent-atisanes from Euphorbia wallichii and their anti-inflammatory activity
10.1016/j.phytochem.2023.113643 · 2023
Trypanocidal and anti-inflammatory effects of three ent-kaurane diterpenoids from Gymnocoronis spilanthoides var
10.3390/pharmaceutics16030415 · 2024
Dimeric ent-kauranoids isolated from Isodon japonica var
10.1016/j.fitote.2024.105840 · 2024
Anti-inflammatory diterpenoids from the aerial parts of Isodon suzhouensis
10.1021/acsomega.5c00223 · 2025
Total synthesis of the Isodon diterpene sculponeatin N
10.1002/anie.201310060 · 2014
Asymmetric total synthesis of (−)-maoecrystal V
10.1002/asia.201500564 · 2015
Total syntheses of highly oxidized ent-kaurenoids pharicin A, pharicinin B, 7-O-acetylpseurata C, and pseurata C: a [5 + 2] cascade approach
10.1021/jacs.7b02746 · 2017
Synthesis and biological evaluation of steviol derivatives with improved cytotoxic activity and selectivity
10.1021/acs.jnatprod.2c00161 · 2022
Selective oxidations in the synthesis of complex natural ent-kauranes and ent-beyeranes
10.1021/acs.joc.2c01051 · 2022
Synthesis and in vivo evaluation of new steviol derivatives that protect against cardiomyopathy by inhibiting ferroptosis
10.1016/j.bioorg.2022.106142 · 2022
Total synthesis of (+)-pierisketone B
10.1021/jacs.5c08617 · 2025
Enantioselective synthesis of (−)-maoecrystal V by enantiodetermining C–H functionalization
10.1021/ja510573v · 2014
A tandem decarboxylative cyclization/alkenylation strategy for the total syntheses of (+)-longirabdiol, (−)-longirabdolactone, and (−)-lffusin
10.1021/jacs.9b03978 · 2019
Total syntheses of (–)-macrocalyxoformins A and B and (–)-ludongnin C
10.1038/s41467-024-50374-1 · 2024
Bipoladisins A–G, uncommon sesterterpenoids with three types of carbon skeletons from Bipolaris maydis and their reversal activity on paclitaxel resistance
10.1021/acs.jnatprod.5c00024 · 2025
Oridonin and its derivatives for cancer treatment and overcoming therapeutic resistance
10.1016/j.gendis.2020.06.010 · 2021
Oridonin induces apoptosis and reverses drug resistance in cisplatin resistant human gastric cancer cells
10.3892/ol.2017.6421 · 2017
Bioactive sativene sesquiterpenoids from cultures of the endophytic fungus Bipolaris eleusines
10.1016/j.phytol.2018.07.007 · 2018
Sativene sesquiterpenoids from the plant endophytic fungus Bipolaris victoriae S27 and their potential as plant-growth regulators
10.1021/acs.jafc.3c05815 · 2024
Bipodonines A–J, a new class of natural sesquiterpenes with a 2-(tetrahydro-2H-pyran-2-yl)propan-2-ol system from the fungus Bipolaris cynodontis DJWT-01
10.1039/d3qo00235g · 2023
Coicenals A–D, four new diterpenoids with new chemical skeletons from the plant pathogenic fungus Bipolaris coicis
10.1021/ol401736z · 2013
Bipolaricins A–I, ophiobolin-type tetracyclic sesterterpenes from a phytopathogenic Bipolaris sp
10.1021/acs.jnatprod.9b00744 · 2019
Total syntheses of diepoxy-ent-kaurane diterpenoids enabled by a bridgehead-enone-initiated intramolecular cycloaddition
10.1021/jacs.4c15004 · doi-reference
Cinnabaramides A–G: analogues of lactacystin and salinosporamide from a Terrestrial streptomycete
10.1021/np060162u · doi-reference
Three new diterpenoids, tricalysiolide H and tricalysiones A and B, from Tricalysia dubia
10.1016/j.tet.2007.02.113 · doi-reference
Characterization and phytotoxicity of ophiobolins produced by Bipolaris setariae
10.47371/mycosci.2020.11.002 · doi-reference
New sesquiterpenoids with anti-inflammatory effects from phytopathogenic fungus Bipolaris sorokiniana 11134
10.1007/s13659-025-00508-9 · doi-reference
New secondary metabolites with immunosuppressive activity from the phytopathogenic fungus Bipolaris maydis
10.1016/j.bioorg.2020.103816 · doi-reference
Bipolaquinones A–J, immunosuppressive meroterpenoids from a soil-derived Bipolaris zeicola
10.1021/acs.jnatprod.1c00327 · doi-reference
Meroterpenoids with potent immunosuppressive activity from fungus Bipolaris zeicola
10.1002/cjoc.202100233 · doi-reference
Chromones from the endophytic fungus Bipolaris eleusines
10.1016/j.phytochem.2024.114046 · doi-reference
Maydisone, a novel oxime polyketide from the cultures of Bipolaris maydis
10.1080/14786419.2020.1765339 · doi-reference
The antifungal properties of terpenoids from the endophytic fungus Bipolaris eleusines
10.1007/s13659-023-00407-x · doi-reference
Genome-based mining of new antimicrobial meroterpenoids from the phytopathogenic fungus Bipolaris sorokiniana strain 11134
10.1007/s00253-020-10522-1 · doi-reference
Bioactive polyketide-terpenoid hybrids from a soil-derived fungus Bipolaris zeicola
10.1021/acs.joc.0c02237 · doi-reference
Maydisens, sesterterpenoids with anti-MDR activity from Bipolaris maydis
10.1021/acs.jnatprod.4c00658 · doi-reference
Bipoladien A, a sesterterpenoid containing an undescribed 5/8/5/7 carbon skeleton from Bipolaris maydis
10.1021/acs.jafc.3c08134 · doi-reference