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References from Kaurepenoid A, a 2-nor-ent-kaurane diterpenoid with P-glycoprotein-mediated reversal of multidrug resistance activity from the fungus Bipolaris sp.. Local targets link to admitted publications; unresolved targets remain external evidence.
Unveiling the potential of ent-kaurane diterpenoids: multifaceted natural products for drug discovery
10.3390/ph17040510 · 2024 · External reference
Cytotoxic ent-kaurane diterpenoids from Isodon eriocalyx
10.1002/cbdv.200590136 · 2005 · External reference
Ent‐kaurane diterpenoids from Isodon eriocalyx var
10.1002/cjoc.201100653 · 2012 · External reference
Bioactive ent-kaurane diterpenoids from Isodon rosthornii
10.1021/np400190n · 2013 · External reference
Diterpenoids from Isodon species: an update
2017 · External reference
Recent developments in the syntheses of C-20-oxygenated ent-kaurane diterpenoids
10.1002/cplu.202300676 · 2024 · External reference
Discovery of ent-kaurane diterpenoids, characteristic metabolites of Isodon species, from an endophytic fungal strain Geopyxis sp
10.1016/j.fitote.2022.105160 · 2022 · External reference
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 · External reference
Ent-kaurene diterpenoids from Isodon phyllostachys
10.1016/j.tetlet.2016.12.034 · 2017 · External reference
Maoecrystal V, cytotoxic diterpenoid with a novel C19 skeleton from Isodon eriocalyx (Dunn
10.1021/ol0481535 · 2004 · External reference
Crokonoids A−C, a highly rearranged and dual-bridged spiro diterpenoid and two other diterpenoids from Croton kongensis
10.1021/acs.orglett.9b04484 · 2020 · External reference
Scalable synthesis enabling multilevel bio-evaluations of natural products for discovery of lead compounds
10.1038/s41467-018-03546-9 · 2018 · External reference
Ent-kaurene diterpenoids from Sideritis lycia with antiviral and cytotoxic activities
2020 · External reference
Selective cytotoxicity of ent-kaurene diterpenoids isolated from Baccharis lateralis and Baccharis retusa (Asteraceae)
10.1002/ardp.202200083 · 2022 · External reference
Synthesis, biological activity, and apoptotic properties of NO-donor/enmein-type ent-kauranoid hybrids
10.3390/ijms17060747 · 2016 · External reference
Antithrombotic activity of the steroids and ent-kaurane diterpenoids from Canna indica Rhizomes
10.1007/s43450-023-00472-w · 2024 · External reference
Anti-inflammatory ent-kaurane dterpenoids from Isodon serra
10.1021/acs.jnatprod.9b01281 · 2020 · External reference
Anti-biofilm and anti-inflammatory active diterpene isolated from the fruit of Xylopia benthamii R.E.Fr.
10.1080/14786419.2023.2208357 · 2024 · External reference
Ent-kauranes and ent-atisanes from Euphorbia wallichii and their anti-inflammatory activity
10.1016/j.phytochem.2023.113643 · 2023 · External reference
Trypanocidal and anti-inflammatory effects of three ent-kaurane diterpenoids from Gymnocoronis spilanthoides var
10.3390/pharmaceutics16030415 · 2024 · External reference
Dimeric ent-kauranoids isolated from Isodon japonica var
10.1016/j.fitote.2024.105840 · 2024 · External reference
Anti-inflammatory diterpenoids from the aerial parts of Isodon suzhouensis
10.1021/acsomega.5c00223 · 2025 · External reference
Total synthesis of the Isodon diterpene sculponeatin N
10.1002/anie.201310060 · 2014 · External reference
Asymmetric total synthesis of (−)-maoecrystal V
10.1002/asia.201500564 · 2015 · External reference
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 · External reference
Synthesis and biological evaluation of steviol derivatives with improved cytotoxic activity and selectivity
10.1021/acs.jnatprod.2c00161 · 2022 · External reference
Selective oxidations in the synthesis of complex natural ent-kauranes and ent-beyeranes
10.1021/acs.joc.2c01051 · 2022 · External reference
Synthesis and in vivo evaluation of new steviol derivatives that protect against cardiomyopathy by inhibiting ferroptosis
10.1016/j.bioorg.2022.106142 · 2022 · External reference
Total synthesis of (+)-pierisketone B
10.1021/jacs.5c08617 · 2025 · External reference
Enantioselective synthesis of (−)-maoecrystal V by enantiodetermining C–H functionalization
10.1021/ja510573v · 2014 · External reference
A tandem decarboxylative cyclization/alkenylation strategy for the total syntheses of (+)-longirabdiol, (−)-longirabdolactone, and (−)-lffusin
10.1021/jacs.9b03978 · 2019 · External reference
Total syntheses of (–)-macrocalyxoformins A and B and (–)-ludongnin C
10.1038/s41467-024-50374-1 · 2024 · External reference
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 · External reference
Oridonin and its derivatives for cancer treatment and overcoming therapeutic resistance
10.1016/j.gendis.2020.06.010 · 2021 · External reference
Oridonin induces apoptosis and reverses drug resistance in cisplatin resistant human gastric cancer cells
10.3892/ol.2017.6421 · 2017 · External reference
Bioactive sativene sesquiterpenoids from cultures of the endophytic fungus Bipolaris eleusines
10.1016/j.phytol.2018.07.007 · 2018 · External reference
Sativene sesquiterpenoids from the plant endophytic fungus Bipolaris victoriae S27 and their potential as plant-growth regulators
10.1021/acs.jafc.3c05815 · 2024 · External reference
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 · External reference
Coicenals A–D, four new diterpenoids with new chemical skeletons from the plant pathogenic fungus Bipolaris coicis
10.1021/ol401736z · 2013 · External reference
Bipolaricins A–I, ophiobolin-type tetracyclic sesterterpenes from a phytopathogenic Bipolaris sp
10.1021/acs.jnatprod.9b00744 · 2019 · External reference
Bipoladien A, a sesterterpenoid containing an undescribed 5/8/5/7 carbon skeleton from Bipolaris maydis
10.1021/acs.jafc.3c08134 · 2024 · External reference
Maydisens, sesterterpenoids with anti-MDR activity from Bipolaris maydis
10.1021/acs.jnatprod.4c00658 · 2024 · External reference
Bioactive polyketide-terpenoid hybrids from a soil-derived fungus Bipolaris zeicola
10.1021/acs.joc.0c02237 · 2021 · External reference
Genome-based mining of new antimicrobial meroterpenoids from the phytopathogenic fungus Bipolaris sorokiniana strain 11134
10.1007/s00253-020-10522-1 · 2020 · External reference
The antifungal properties of terpenoids from the endophytic fungus Bipolaris eleusines
10.1007/s13659-023-00407-x · 2023 · External reference
Maydisone, a novel oxime polyketide from the cultures of Bipolaris maydis
10.1080/14786419.2020.1765339 · 2020 · External reference
Chromones from the endophytic fungus Bipolaris eleusines
10.1016/j.phytochem.2024.114046 · 2024 · External reference
Meroterpenoids with potent immunosuppressive activity from fungus Bipolaris zeicola
10.1002/cjoc.202100233 · 2021 · External reference
Bipolaquinones A–J, immunosuppressive meroterpenoids from a soil-derived Bipolaris zeicola
10.1021/acs.jnatprod.1c00327 · 2021 · External reference
New secondary metabolites with immunosuppressive activity from the phytopathogenic fungus Bipolaris maydis
10.1016/j.bioorg.2020.103816 · 2020 · External reference
New sesquiterpenoids with anti-inflammatory effects from phytopathogenic fungus Bipolaris sorokiniana 11134
10.1007/s13659-025-00508-9 · 2025 · External reference
Characterization and phytotoxicity of ophiobolins produced by Bipolaris setariae
10.47371/mycosci.2020.11.002 · 2021 · External reference
Three new diterpenoids, tricalysiolide H and tricalysiones A and B, from Tricalysia dubia
10.1016/j.tet.2007.02.113 · 2007 · External reference
Cinnabaramides A–G: analogues of lactacystin and salinosporamide from a Terrestrial streptomycete
10.1021/np060162u · 2007 · External reference
Total syntheses of diepoxy-ent-kaurane diterpenoids enabled by a bridgehead-enone-initiated intramolecular cycloaddition
10.1021/jacs.4c15004 · 2025 · External reference