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Bisrubescensins A−C: Three New Dimeric ent-Kauranoids Isolated from Isodon rubescens

https://doi.org/10.1021/ol0531379
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-3-030-12858-6openalex-snapshot
Progress in the Chemistry of Organic Natural Products 109
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Lovastatin Nonaketide Synthase Catalyzes an Intramolecular Diels−Alder Reaction of a Substrate Analogue
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Enzymatic catalysis of the Diels–Alder reaction in the biosynthesis of natural products
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inferredcites →https://doi.org/10.1093/jnci/83.11.766openalex-snapshot
Effects of a Low-Fat Diet on Levels of Oxidative Damage to DNA in Human Peripheral Nucleated Blood Cells
inferredcites →https://doi.org/10.1360/csb1978-23-1-58openalex-snapshot
枳实升压的药理研究

What points at this work

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

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Callicarpnoids A-C, Structurally Intriguing Ent -Clerodane Diterpenoid Dimers with Cytotoxicity Against MCF-7 And HCT-116 Cell Lines From Callicarpa Arborea
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Bisrubescensins A—C: Thee New Dimeric ent‐Kauranoids Isolated from Isodon rubescens.
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ent‐Kaurane Diterpenoids from Isodon japonicus
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Simultaneous qualitative and quantitative analysis of 28 components in Isodon rubescens by HPLC‐ESI‐MS/MS
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Chemistry and Bioactivity of ent -Kaurene Diterpenoids
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A novel analysis method for diterpenoids in rat plasma by liquid chromatography–electrospray ionization mass spectrometry
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Callicarpnoids A–C, structurally intriguing ent-Clerodane diterpenoid dimers with cytotoxicity against MCF-7 and HCT-116 cell lines from Callicarpa arborea Roxb
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Design and synthesis of 6,20-epoxy A-ring modified oridonin derivatives with antitumor activity through extrinsic and mitochondrial pathways
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Structural modification and biological evaluation of spirolactone type ent-kauranoid isodonal as potential anti-melanoma agents
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Cytotoxic ent-kaurane diterpenoids from Isodon sinuolata
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Guanacastane-type diterpenoids from Coprinus radians
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Hikiokoshins A–I, diterpenes from the leaves of Isodon japonicus
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Isodonoids A–L: Ent-kauranoid diterpenoid-flavanone conjugates from Isodon rubescens
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Towards EPC-syntheses of the structural class of cochleamycins and macquarimicins. Part 1: EPC-synthesis of the hydrindene subunit of the cochleamycins
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Towards EPC-syntheses of the structural class of cochleamycins and macquarimicins. Part 2: EPC-synthesis of the hydrindene subunit of the macquarimicins
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A new rearranged and a new seco-ent-kaurane diterpenoids from Isodon parvifolius
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.10.133openalex-snapshot
Sculponins A–C, three new 6,7-seco-ent-kauranoids from Isodon sculponeatus
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.04.034openalex-snapshot
Symmetric and asymmetric ent-kaurane dimers isolated from Isodon japonicus
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.02.102openalex-snapshot
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Bisleuconins A–D: a pair of epimeric ent-kauranoid dimers and two new asymmetric analogues isolated from Isodon leucophyllus
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Asymmetric dimeric ent-kauranoids from Croton tonkinensis and their cytotoxicity
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Natural Products Chemistry Research 2006's Progress in China
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Three new ent-kaurane diterpenoids from Isodon rubescens and their cytotoxicities
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Isoxerophilusins A and B, Two Novel Polycyclic Asymmetric Diterpene Dimers from Isodon xerophilus: Structural Elucidation, Modification, and Inhibitory Activities against α-Glucosidase
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Pierisketolide A and Pierisketones B and C, Three Diterpenes with an Unusual Carbon Skeleton from the Roots of Pieris formosa
inferred← citeshttps://doi.org/10.1021/np100110uopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np200439nopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np5005196openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np9000366openalex-snapshot
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Ternifolide A, a New Diterpenoid Possessing a Rare Macrolide Motif from Isodon ternifolius
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ent-Kaurane-based regio- and stereoselective inverse electron demand hetero-Diels–Alder reactions: synthesis of dihydropyran-fused diterpenoids
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Diterpenoids from Isodon species: an update
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Cunlanceloic acids A–D: unprecedented labdane diterpenoid dimers with AChE inhibitory and cytotoxic activities from Cunninghamia lanceolata
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Biogenetic and biomimetic synthesis of natural bisditerpenoids: hypothesis and practices
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Isoxerophilins A and B, two diterpene heterodimers from Isodon xerophilus : structural elucidation and semisynthesis of isoxerophilin analogues
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Naturally Occurring Diterpenoid Dimers: Source, Biosynthesis, Chemistry and Bioactivities
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Two cytotoxic 6,7-seco-spiro-lacton-ent-kauranoids from Isodon rubescens
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QUANTITATIVE ANALYSIS OF TEN DITERPENOIDS IN RAT BILE AFTER ORAL ADMINISTRATION OF Isodon rubescens EXTRACT BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY-ELECTROSPRAY IONIZATION TANDEM MASS SPECTROMETRY
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Specific 12α-hydroxylation of grandiflorenic acid by permeabilised fungus Fusarium graminearum
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New 3,4- Seco-ent -kaurene Dimers from Croton micans
inferred← citeshttps://doi.org/10.1248/cpb.58.56openalex-snapshot
Four New ent-Kauranoids from Isodon rubescens var. lushanensis and Data Reassignment of Dayecrystal B
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Henrin A: A New Anti-HIV Ent-Kaurane Diterpene from Pteris henryi
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Antitumor and Antibacterial Derivatives of Oridonin: A Main Composition of Dong-Ling-Cao
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Therapeutic Potential of Oridonin and Its Analogs: From Anticancer and Antiinflammation to Neuroprotection
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3,4-Seco-Isopimarane Diterpenes from the Twigs and Leaves of Isodon Flavidus
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Comparative transcriptome analysis and simple sequence repeat marker development for two closely related Isodon species used as ‘Xihuangcao’ herbs
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