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Diterpenoid lanceolatins A–G from Cephalotaxus lanceolata and their anti-inflammatory and anti-tumor activities

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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/cbdv.201200105openalex-snapshot
Alkaloids from Cephalotaxus lanceolata and Their Cytotoxicities
inferredcites →https://doi.org/10.1002/jps.2600610812openalex-snapshot
Antitumor Alkaloids from Cephalotaxus harringtonia: Structure and Activity
inferredcites →https://doi.org/10.1016/0031-9422(91)85148-sopenalex-snapshot
Diterpenoid acids from the leaves of armand pine
inferredcites →https://doi.org/10.1016/0040-4020(72)88007-4openalex-snapshot
Deoxyharringtonine, a new antitumor alkaloid from Cephalotaxus: Structure and synthetic studies
inferredcites →https://doi.org/10.1016/j.bmc.2009.11.055openalex-snapshot
Isolation, structure, and bioactivities of abiesadines A–Y, 25 new diterpenes from Abies georgei Orr
inferredcites →https://doi.org/10.1016/s0031-9422(00)85230-9openalex-snapshot
The occurrence of imbricatolic acid in cupressus resins
inferredcites →https://doi.org/10.1016/s0040-4020(01)80415-4openalex-snapshot
C-16 hydroxylated abietane diterpenes from salvia mellifera. Absolute configuration and biogenetic implications.
inferredcites →https://doi.org/10.1016/s0040-4039(01)97839-6openalex-snapshot
Structures of harringtonine, isoharringtonine, and homoharringtonine
inferredcites →https://doi.org/10.1021/jo00399a047openalex-snapshot
Harringtonolide, a plant growth inhibitory tropone from Cephalotaxus harringtonia (Forbes) K. Koch
inferredcites →https://doi.org/10.1021/jo00951a040openalex-snapshot
Structures of some of the minor alkaloids of Cephalotaxus fortunei
inferredcites →https://doi.org/10.1021/jo01044a010openalex-snapshot
The Alkaloids of Cephalotaxus drupacea and Cephalotaxus fortunei
inferredcites →https://doi.org/10.1021/jo01350a510openalex-snapshot
The Isolation of Dehydroabietic Acid from Disproportionated Rosin
inferredcites →https://doi.org/10.1021/np9900270openalex-snapshot
Two New Lactones from Cephalotaxus fortunei var. alpnia
inferredcites →https://doi.org/10.1021/ol3004639openalex-snapshot
Incarvilleatone, a New Cyclohexylethanoid Dimer from Incarvillea younghusbandii and Its Inhibition against Nitric Oxide (NO) Release
inferredcites →https://doi.org/10.1021/ol8029577openalex-snapshot
Tunicyclin A, the First Plant Tricyclic Ring Cycloheptapeptide from Psammosilene tunicoides
inferredcites →https://doi.org/10.1039/c2np20037fopenalex-snapshot
Natural products from Cephalotaxus sp.: chemical diversity and synthetic aspects
inferredcites →https://doi.org/10.1055/s-0030-1270930openalex-snapshot
New Sesquiterpenoids fromAinsliaea macrocephalaand Their Nitric Oxide Inhibitory Activity
inferredcites →https://doi.org/10.1055/s-2003-39713openalex-snapshot
Antimicrobial Diterpenes from the Seeds ofCephalotaxus harringtoniavar.drupacea

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.2021.112939zenodo-depositor-declared
Progress in structure, synthesis and biological activity of natural cephalotane diterpenoids
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113187zenodo-depositor-declared
Abietane diterpenes from the twigs and leaves of Cephalotaxus oliveri Mast. with antitumor activity
inferred← citeshttps://doi.org/10.1002/9783527825578.c02-25openalex-snapshot
Cephalotaxus Species
inferred← citeshttps://doi.org/10.1002/ange.202402931openalex-snapshot
Bioinspired Total Synthesis of Cephalotaxus Diterpenoids and Their Structural Analogues
inferred← citeshttps://doi.org/10.1002/ange.202407757openalex-snapshot
Divergent Synthesis of 17‐ nor ‐Cephalotane Diterpenoids through Developed Ynol‐diene Cyclization
inferred← citeshttps://doi.org/10.1002/anie.202402931openalex-snapshot
Bioinspired Total Synthesis of Cephalotaxus Diterpenoids and Their Structural Analogues
inferred← citeshttps://doi.org/10.1002/anie.202407757openalex-snapshot
Divergent Synthesis of 17‐ nor ‐Cephalotane Diterpenoids through Developed Ynol‐diene Cyclization
inferred← citeshttps://doi.org/10.1002/cbdv.202000210openalex-snapshot
Diterpenoids and Flavonoids from the Twigs of Cephalotaxus fortunei var. alpina
inferred← citeshttps://doi.org/10.1002/cbdv.202500458openalex-snapshot
Ionones With Promoting Neurite Growth From Cephalotaxus oliveri Mast
inferred← citeshttps://doi.org/10.1002/chin.201524219openalex-snapshot
ChemInform Abstract: Diterpenoid Lanceolatins A—G from Cephalotaxus lanceolata and Their Antiinflammatory and Antitumor Activities.
inferred← citeshttps://doi.org/10.1002/ptr.6657openalex-snapshot
A comprehensive review on ethnomedicine, phytochemistry, pharmacology, and toxicity of Tephrosia purpurea (L.) Pers.
inferred← citeshttps://doi.org/10.1007/s13659-016-0093-7openalex-snapshot
Five New Alkaloids from Cephalotaxus lanceolata and C. fortunei var. alpina
inferred← citeshttps://doi.org/10.1016/j.arabjc.2016.01.008openalex-snapshot
Modular total syntheses of thymifodioic/incanic acids
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104226openalex-snapshot
Diterpenoids from Cephalotaxus fortunei var. alpina and their cytotoxic activity
inferred← citeshttps://doi.org/10.1016/j.jep.2019.112159openalex-snapshot
A selection of eleven plants used as traditional Polynesian cosmetics and their development potential as anti-aging ingredients, hair growth promoters and whitening products
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.04.007openalex-snapshot
Bioactive norditerpenoids from Cephalotaxus fortunei var. alpina and C. lanceolata
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113457openalex-snapshot
Abietane diterpenoids from Phlegmariurus carinatus and their biological activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114356openalex-snapshot
Phlecarinatones H–N: Abietane-type diterpenoids from Phlegmariurus carinatus with proliferative inhibitory effect on U251 glioblastoma cells
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134114openalex-snapshot
Unified chemical synthesis of cephalotaxus diterpenoids: A biosynthetic reversed strategy
inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.10.017openalex-snapshot
Four new norlignan glycoside isomers from the twigs of Cephalotaxus oliveri Mast.
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00412openalex-snapshot
Cephanolides A–J, Cephalotane-Type Diterpenoids from Cephalotaxus sinensis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00059openalex-snapshot
17-nor-Cephalotane-Type Diterpenoids from Cephalotaxus fortunei
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01076openalex-snapshot
Total Synthesis of the Alleged Structure of (+)-Fimbricalyxoid A
inferred← citeshttps://doi.org/10.1021/acsmedchemlett.1c00625openalex-snapshot
Photoaffinity Probe Reveals the Potential Target of Harringtonolide for Cancer Cell Migration Inhibition
inferred← citeshttps://doi.org/10.1021/jacs.3c05455openalex-snapshot
Asymmetric Total Synthesis of Cephalotaxus Diterpenoids: Cephinoid P, Cephafortoid A, 14-epi-Cephafortoid A and Fortalpinoids M-N, P
inferred← citeshttps://doi.org/10.1021/jacsau.4c01067openalex-snapshot
Unified Total Synthesis of Benzenoid and Troponoid Cephalotaxus Diterpenoids Enabled by Regiocontrolled Phenol-to-Tropone Ring Expansion
inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-snapshot
Diterpenoids of terrestrial origin
inferred← citeshttps://doi.org/10.1039/d0qo01195aopenalex-snapshot
Asymmetric total synthesis of cephanolide B
inferred← citeshttps://doi.org/10.1039/d2qo00493copenalex-snapshot
A nickel( ii )-catalyzed enantioselective all-carbon-based inverse-electron-demand Diels–Alder reaction of 2-pyrones with indenes
inferred← citeshttps://doi.org/10.1039/d3np00067bopenalex-snapshot
Cephalotane diterpenoids: structural diversity, biological activity, biosynthetic proposal, and chemical synthesis
inferred← citeshttps://doi.org/10.1080/14786419.2017.1314280openalex-snapshot
Abietane diterpenoids from Cephalotaxus lanceolata
inferred← citeshttps://doi.org/10.1080/14786419.2020.1861616openalex-snapshot
A new diterpernoid glycoside from the fruit of Forsythia suspensa
inferred← citeshttps://doi.org/10.22159/ajpcr.2026v19i1.57157openalex-snapshot
ETHNOMEDICINAL, PHYTOCHEMICAL, AND PHARMACOLOGICAL INSIGHTS INTO TEPHROSIA PURPUREA (FABACEAE): A COMPREHENSIVE UPDATE
inferred← citeshttps://doi.org/10.26434/chemrxiv-2024-rp8s5openalex-snapshot
Total Synthesis of Cephanolide A and Harringtonolide: A Unified Strategy Connecting Benzenoid and Troponoid Cephalotaxus Diterpenoids
inferred← citeshttps://doi.org/10.3390/molecules26051380openalex-snapshot
Semi-Synthesis of Harringtonolide Derivatives and Their Antiproliferative Activity
inferred← citeshttps://doi.org/10.5772/intechopen.73215openalex-snapshot
Terpenes from Natural Products with Potential Anti-Inflammatory Activity
inferred← citeshttps://doi.org/10.6023/cjoc202408007openalex-snapshot
Progress in the Total Synthesis of Cephalotane Diterpenoid Natural Products
inferred← citeshttps://doi.org/10.6023/cjoc202408028openalex-snapshot
Research on the Biomimetic Construction of Propeller-Shaped Dual Lactone Ring System in Cephalotanin B
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