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Cytotoxic Triterpenoids from the Leaves of Microtropis fokienensis

https://doi.org/10.1021/np060369n
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/0022-1759(93)90088-oopenalex-snapshot
An improved MIT assay
inferredcites →https://doi.org/10.1016/0031-9422(90)80150-fopenalex-snapshot
A triterpenoid lactone from Leucas aspera
inferredcites →https://doi.org/10.1016/0031-9422(94)00581-dopenalex-snapshot
An ursane diol from the leaves of Pristimera grahamii
inferredcites →https://doi.org/10.1016/s0031-9422(00)00199-0openalex-snapshot
Minor sulfated saikosaponins from the aerial parts of Bupleurum rigidum L.
inferredcites →https://doi.org/10.1016/s0031-9422(00)00244-2openalex-snapshot
Minor flavonoids from licorice
inferredcites →https://doi.org/10.1021/jo00312a023openalex-snapshot
A new chromone and flavone synthesis and its utilization for the synthesis of potentially antitumorigenic polycyclic chromones and flavones
inferredcites →https://doi.org/10.1021/np030069vopenalex-snapshot
Ursane- and Oleanane-Type Triterpenes from Ternstroemia gymnanthera Callus Tissues
inferredcites →https://doi.org/10.1021/np050554lopenalex-snapshot
Aegicerin, the First Oleanane Triterpene with Wide-Ranging Antimycobacterial Activity, Isolated from Clavija procera
inferredcites →https://doi.org/10.1021/np058016wopenalex-snapshot
Lupane Triterpenoids from Maytenus Species
inferredcites →https://doi.org/10.1021/np50043a021openalex-snapshot
3-Oxo-28,29-Dihydroxyolean-12-Ene from Orthosphenia mexicana
inferredcites →https://doi.org/10.1039/b000678popenalex-snapshot
Celastraceae sesquiterpenoids: biological activity and synthesis
inferredcites →https://doi.org/10.1248/cpb.51.365openalex-snapshot
Antiproliferative Constituents from Umbelliferae Plants. VI. New Ursane-Type Saikosaponin Analogs from the Fruits of Bupleurum rotundifolium.

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4191548openalex-extracted
inferred← citeshttps://doi.org/10.1002/cbdv.200890129openalex-snapshot
A New Dihydroagarofuranoid Sesquiterpene and Antituberculosis Constituents from the Root of Microtropis japonica
inferred← citeshttps://doi.org/10.1002/cbdv.201400066openalex-snapshot
Microjaponin, A New Dihydroagarofuranoid Sesquiterpene from the Stem of Microtropis japonica with Antituberculosis Activity
inferred← citeshttps://doi.org/10.1002/cbdv.201700066openalex-snapshot
Cytotoxic Triterpenoids from the Stalks of Microtropis triflora
inferred← citeshttps://doi.org/10.1007/s10600-017-2121-1openalex-snapshot
Triterpenoids from Microtropis fokienensis
inferred← citeshttps://doi.org/10.1007/s12272-017-0943-9openalex-snapshot
Triterpenoid saponins from Clinopodium chinense (Benth.) O. Kuntze and their biological activity
inferred← citeshttps://doi.org/10.1016/b978-0-12-398371-8.00002-7openalex-snapshot
Terpenes
inferred← citeshttps://doi.org/10.1016/j.bse.2013.09.002openalex-snapshot
Phytochemical and chemotaxonomic study on Microtropis triflora
inferred← citeshttps://doi.org/10.1016/j.bse.2022.104516openalex-snapshot
Chemical constituents from the leaves of Craibiodendron yunnanense and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.bse.2023.104668openalex-snapshot
Phytochemical investigation on the leaves of Ailanthus altissima (Mill.) Swingle
inferred← citeshttps://doi.org/10.1016/j.phytochem.2010.01.004openalex-snapshot
Microtropiosides A–F: ent-Labdane diterpenoid glucosides from the leaves of Microtropis japonica (Celastraceae)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2013.09.027openalex-snapshot
Lupane, friedelane, oleanane, and ursane triterpenes from the stem of Siphonodon celastrineus Griff
inferred← citeshttps://doi.org/10.1016/j.phytochem.2016.07.006openalex-snapshot
Polyoxygenated ursane and oleanane triterpenes from Siphonodon celastrineus
inferred← citeshttps://doi.org/10.1016/s0959-6380(02)80009-5openalex-snapshot
Chapter 5.3 Five-membered ring systems: Furans and benzofurans
inferred← citeshttps://doi.org/10.1016/s0959-6380(08)80009-8openalex-snapshot
Chapter 5.3 Five-membered ring systems: furans and benzofurans
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00720openalex-snapshot
Digital Database of Absorption Spectra of Diverse Flavonoids Enables Structural Comparisons and Quantitative Evaluations
inferred← citeshttps://doi.org/10.1021/np070351sopenalex-snapshot
Triterpene, Antioxidant, and Antimicrobial Compounds from Melissa officinalis
inferred← citeshttps://doi.org/10.1021/np800093aopenalex-snapshot
Lupane-Type Triterpenoids from Microtropis fokienensis and Perrottetia arisanensis and the Apoptotic Effect of 28-Hydroxy-3-oxo-lup-20(29)-en-30-al
inferred← citeshttps://doi.org/10.1021/np800097topenalex-snapshot
Dihydroagarofuranoid Sesquiterpenes, a Lignan Derivative, a Benzenoid, and Antitubercular Constituents from the Stem of Microtropis japonica
inferred← citeshttps://doi.org/10.1021/np800694bopenalex-snapshot
Cytotoxic Triterpenoids from the Stems of Microtropis japonica
inferred← citeshttps://doi.org/10.1039/b718038copenalex-snapshot
Triterpenoids
inferred← citeshttps://doi.org/10.1039/b810774mopenalex-snapshot
Plant-derived triterpenoids and analogues as antitumor and anti-HIV agents
inferred← citeshttps://doi.org/10.1080/10286020.2019.1570160openalex-snapshot
Structural characterization and biological evaluation of chemical constituents from Ilex cornuta
inferred← citeshttps://doi.org/10.1080/13880209.2016.1214742openalex-snapshot
Anti-hepatocellular carcinoma activity and mechanism of chemopreventive compounds: ursolic acid derivatives
inferred← citeshttps://doi.org/10.1139/v09-078openalex-snapshot
Triterpenes of Commiphora holtziana oleo-gum resin
inferred← citeshttps://doi.org/10.3390/molecules18088929openalex-snapshot
Cytotoxic Activity of Ursolic Acid Derivatives Obtained by Isolation and Oxidative Derivatization
inferred← citeshttps://doi.org/10.3390/molecules19044608openalex-snapshot
Anti-Inflammatory Triterpenoids from the Stems of Microtropis Fokienensis
inferred← citeshttps://doi.org/10.3390/molecules27030959openalex-snapshot
Pentacyclic Triterpenoids Isolated from Celastraceae: A Focus in the 13C-NMR Data
inferred← citeshttps://doi.org/10.6227/jfda.2012200207openalex-snapshot
Cytotoxicity, anti-platelet aggregation assay and chemical components analysis of thirty-eight kinds of essential oils
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