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Advances in Chemistry and Bioactivity of the Genus Chisocheton Blume
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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/ejoc.200901245openalex-snapshot
Trichiliton A, a Novel Limonoid from Trichilia connaroides
inferredcites →https://doi.org/10.1002/hlca.200490129openalex-snapshot
Two New Spermidine Alkaloids from Chisocheton weinlandii
inferredcites →https://doi.org/10.1007/s11101-013-9317-1openalex-snapshot
Constituents from Aphanamixis species and their biological activities
inferredcites →https://doi.org/10.1007/s11418-011-0616-9openalex-snapshot
Ceramicines J–L, new limonoids from Chisocheton ceramicus
inferredcites →https://doi.org/10.1007/s11418-013-0755-2openalex-snapshot
Ceramicine B, a limonoid with anti-lipid droplets accumulation activity from Chisocheton ceramicus
inferredcites →https://doi.org/10.1007/s12272-008-1115-8openalex-snapshot
A new sesquiterpene and other terpenoid constituents of Chisocheton penduliflorus
inferredcites →https://doi.org/10.1007/s13659-012-0065-5openalex-snapshot
New apotirucallane-type triterpenoids from Chisocheton paniculatus
inferredcites →https://doi.org/10.1016/0031-9422(83)80251-9openalex-snapshot
Limonoid extractives from Xylocarpus moluccensis
inferredcites →https://doi.org/10.1016/0031-9422(92)90003-9openalex-snapshot
Biological activity of limonoids from the rutales
inferredcites →https://doi.org/10.1016/0031-9422(93)80054-vopenalex-snapshot
A meliacin from Chisocheton paniculatus
inferredcites →https://doi.org/10.1016/0031-9422(95)90037-3openalex-snapshot
Dictionary of Natural Products
inferredcites →https://doi.org/10.1016/j.bmc.2007.05.049openalex-snapshot
Erythrocarpines A–E, new cytotoxic limonoids from Chisocheton erythrocarpus
inferredcites →https://doi.org/10.1016/j.bmc.2008.11.048openalex-snapshot
Ceramicines B–D, new antiplasmodial limonoids from Chisocheton ceramicus
inferredcites →https://doi.org/10.1016/j.bmcl.2013.01.037openalex-snapshot
Ceramicines from Chisocheton ceramicus as lipid-droplets accumulation inhibitors
inferredcites →https://doi.org/10.1016/j.bse.2011.12.022openalex-snapshot
Chemical constituents from Aglaia odorata Lour
inferredcites →https://doi.org/10.1016/j.fitote.2011.08.006openalex-snapshot
Cytotoxic nor-dammarane triterpenoids from Dysoxylum hainanense
inferredcites →https://doi.org/10.1016/j.fitote.2012.04.018openalex-snapshot
Bioactivity-guided fractionation of the lipoxygenase and cyclooxygenase inhibiting constituents from Chisocheton polyandrus Merr
inferredcites →https://doi.org/10.1016/j.fitote.2012.10.004openalex-snapshot
Triterpenes and steroids from the leaves of Aglaia exima (Meliaceae)
inferredcites →https://doi.org/10.1016/j.phymed.2008.05.004openalex-snapshot
Antimalarial, antimycobacterial and cytotoxic limonoids from Chisocheton siamensis
inferredcites →https://doi.org/10.1016/j.phytochem.2013.09.019openalex-snapshot
Androstanes and pregnanes from Trichilia emetica ssp. suberosa J.J. de Wilde
inferredcites →https://doi.org/10.1016/j.tetlet.2008.04.145openalex-snapshot
Ceramicine A and walsogyne A, novel limonoids from two species of Meliaceae
inferredcites →https://doi.org/10.1016/j.tetlet.2012.07.067openalex-snapshot
Malayanines A and B, two novel limonoids from Chisocheton erythrocarpus Hiern
inferredcites →https://doi.org/10.1016/s0031-9422(00)89645-4openalex-snapshot
Two limonoids from Chisocheton microcarpus
inferredcites →https://doi.org/10.1016/s0031-9422(99)00053-9openalex-snapshot
Dammarane triterpenes and pregnane steroids from Aglaia lawii and A. tomentosa
inferredcites →https://doi.org/10.1016/s0040-4039(98)02657-4openalex-snapshot
A triterpenoid with a novel abeo-dammarane skeleton from Dysoxylum cauliflorum
inferredcites →https://doi.org/10.1016/s1099-4831(06)63009-5openalex-snapshot
The Alkaloids Chemistry and Biology
inferredcites →https://doi.org/10.1021/cr9004023openalex-snapshot
Meliaceous Limonoids: Chemistry and Biological Activities
inferredcites →https://doi.org/10.1021/np100428uopenalex-snapshot
Phragmalin- and Mexicanolide-Type Limonoids from the Leaves of Trichilia connaroides
inferredcites →https://doi.org/10.1021/np200013gopenalex-snapshot
Chisomicines A−C, Limonoids from Chisocheton ceramicus
inferredcites →https://doi.org/10.1021/np300089xopenalex-snapshot
Correction to Tetranortriterpenoids from Chisocheton paniculatus
inferredcites →https://doi.org/10.1021/np3007588openalex-snapshot
Bioactive Flavaglines and Other Constituents Isolated from Aglaia perviridis
inferredcites →https://doi.org/10.1021/np800669copenalex-snapshot
Protolimonoids from Melia toosendan
inferredcites →https://doi.org/10.1021/np900485topenalex-snapshot
Tetranortriterpenoids from Chisocheton paniculatus
inferredcites →https://doi.org/10.1038/137255c0openalex-snapshot
A Dictionary of the Economic Products of the Malay Peninsula
inferredcites →https://doi.org/10.1039/p19790002959openalex-snapshot
Tetranortriterpenoids and related compounds. Part 22. New apotirucailol derivatives and tetranortriterpenoids from the wood and seeds of chisocheton paniculatus(meliaceae)
inferredcites →https://doi.org/10.1046/j.1095-8339.2002.00050.xopenalex-snapshot
Indeterminate leaves of Chisocheton (Meliaceae): survey of structure and development
inferredcites →https://doi.org/10.1080/13880200500383439openalex-snapshot
Muscarinic Receptor Activity of Some Malaysian Plant Species
inferredcites →https://doi.org/10.1107/s1600536808033163openalex-snapshot
17-(5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,7-diol fromChisocheton tomentosus(Meliaceae)
inferredcites →https://doi.org/10.1107/s160053681002564xopenalex-snapshot
14-Deoxyxyloccensin K fromChisocheton ceramicus(Meliaceae)
inferredcites →https://doi.org/10.1111/j.1756-1051.1994.tb00585.xopenalex-snapshot
Flora Malesiana Series I — Spermatophyta
inferredcites →https://doi.org/10.1139/v07-155openalex-snapshot
A novel limonoid from the seeds of Chisocheton siamensis
inferredcites →https://doi.org/10.1139/v11-147openalex-snapshot
Four new triterpenoids from Chisocheton paniculatus and their anti-inflammatory activities
inferredcites →https://doi.org/10.1155/2012/765316openalex-snapshot
7 α -Hydroxy- β -Sitosterol from Chisocheton tomentosus Induces Apoptosis via Dysregulation of Cellular Bax/Bcl-2 Ratio and Cell Cycle Arrest by Downregulating ERK1/2 Activation
inferredcites →https://doi.org/10.1201/9781420006803-22openalex-snapshot
Medicinal Plants Classified in the Family Melastomataceae
inferredcites →https://doi.org/10.1248/cpb.41.617openalex-snapshot
Phytochemical Studies on Meliaceous Plants. VIII. Structures and Inhibitory Effects on Epstein-Barr Virus Activation of Triterpenoids from Leaves of Chisocheton macrophyllus King.
inferredcites →https://doi.org/10.1248/cpb.55.812openalex-snapshot
New Dammarane Triterpenes from Maytenus macrocarpa
inferredcites →https://doi.org/10.1248/cpb.59.407openalex-snapshot
Ceramicines E-I, New Limonoids from Chisocheton ceramicus
inferredcites →https://doi.org/10.1371/journal.pone.0023661openalex-snapshot
Regulation of Apoptotic Effects by Erythrocarpine E, a Cytotoxic Limonoid from Chisocheton erythrocarpus in HSC-4 Human Oral Cancer Cells
inferredcites →https://doi.org/10.1663/0013-0001(2002)056[0296:prosea]2.0.co;2openalex-snapshot
Plant Resources of South East Asia. No. 14. Vegetable Oils and Fats
inferredcites →https://doi.org/10.2174/1385272003375941openalex-snapshot
The Chemistry of the Meliaceae and Ptaeroxylaceae of Southern and Eastern Africa and Madagascar
inferredcites →https://doi.org/10.2174/138527211795378254openalex-snapshot
The Advances in the Limonoid Chemistry of the Meliaceae Family
inferredcites →https://doi.org/10.22452/mjs.vol30no2.9openalex-snapshot
STEROIDS FROM Chisocheton tomentosus
inferredcites →https://doi.org/10.2307/4107807openalex-snapshot
The Reinstatement of Galearia Zoll. & Mor. and Microdesmis Hook.f. in the Pandaceae
inferredcites →https://doi.org/10.3109/13880200903008724openalex-snapshot
Lipoxygenase inhibiting activity of some Malaysian plants
inferredcites →https://doi.org/10.3987/com-11-s(p)31openalex-snapshot
Chisomicines D and E, Two New Limonoids from Chisocheton ceramicus
inferredcites →https://doi.org/10.5281/zenodo.16078260openalex-snapshot
New species of, and other notes on, Chisocheton and Walsura (Meliaceae)
inferredcites →https://doi.org/10.5962/bhl.title.10879openalex-snapshot
A dictionary of the plant names of the Philippine Islands / by Elmer D. Merrill.
inferredcites →https://doi.org/10.5962/bhl.title.17545openalex-snapshot
A manual of Indian timbers: an account of the structure, growth, distribution, and qualities of Indian woods
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.2021.112759zenodo-depositor-declared
Cytotoxic triterpenoids from Chisocheton pentandrus
inferred← citeshttps://doi.org/10.1002/ardp.202400160openalex-snapshot
Limonoids isolated from Chisocheton ceramicus Miq. and the antiadipogenic mechanism of action of ceramicine B
inferred← citeshttps://doi.org/10.1002/ceur.202500025openalex-snapshot
Acetylation‐Deacetylation‐Driven Natural Product Biosynthesis
inferred← citeshttps://doi.org/10.1002/chin.201629281openalex-snapshot
ChemInform Abstract: Advances in Chemistry and Bioactivity of the Genus Chisocheton Blume
inferred← citeshttps://doi.org/10.1007/s10600-023-03922-yopenalex-snapshot
A New Oleanane-Type Triterpenoid from the Fruits of Chisocheton macrophyllus
inferred← citeshttps://doi.org/10.1007/s13659-026-00631-1openalex-snapshot
Distribution and bioactivities of tirucallane-type triterpenoids from Meliaceae family
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104873openalex-snapshot
Chisosiamens A–E, five new ring-intact limonoids with isomerized furan ring from the fruit of Chisocheton siamensis
inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105765openalex-snapshot
Erythrocarpines IN, new limonoids from the barks of Chisocheton erythrocarpus and their neuroprotective effects against hydrogen peroxide in NG108–15 cells
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114092openalex-snapshot
Limonoids from the fruits of Chisocheton erythrocarpus and their mosquito larvicidal activities
inferred← citeshttps://doi.org/10.1016/j.phytol.2019.01.034openalex-snapshot
Cytotoxic Triterpenoids from the Bark of Chisocheton patens Blume (Meliaceae)
inferred← citeshttps://doi.org/10.1016/j.phytol.2019.11.002openalex-snapshot
New cytotoxic limonoids from the stem bark of Chisocheton pentandrus (Blanco) Merr
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.02.005openalex-snapshot
Pentandricines F-H, cytotoxic limonoids from the stem bark of Chisocheton pentandrus (Blanco) Merr
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.06.015openalex-snapshot
Three new inositol derivatives from Chisocheton paniculatus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01239openalex-snapshot
chiro -Inositol Derivatives from Chisocheton paniculatus Showing Inhibition of Nitric Oxide Production
inferred← citeshttps://doi.org/10.1039/c7ra04715kopenalex-snapshot
Recent progress in the chemistry and biology of limonoids
inferred← citeshttps://doi.org/10.1080/10286020.2022.2032678openalex-snapshot
Limonoids from the fruits of Chisocheton lasiocarpus (Meliaceae)
inferred← citeshttps://doi.org/10.1080/10286020.2022.2143353openalex-snapshot
Tirucallane-type triterpenoid from the stem bark of Chisocheton lasiocarpus and its cytotoxic activity against MCF-7 breast cancer cells
inferred← citeshttps://doi.org/10.1080/10286020.2025.2501020openalex-snapshot
Cytotoxic limonoids from the barks of Chisocheton siamensis
inferred← citeshttps://doi.org/10.1080/10286020.2025.2525316openalex-snapshot
Cytotoxic limonoids from the twigs of Chisocheton paniculatus
inferred← citeshttps://doi.org/10.1080/10286020.2025.2525332openalex-snapshot
11 α -hydroxydysobinin: a new limonoid from Chisocheton macrophyllus seeds (Meliaceae)
inferred← citeshttps://doi.org/10.1093/jpp/rgac057openalex-snapshot
Phytochemistry and biological activity of Lansium domesticum Corr. species: a review
inferred← citeshttps://doi.org/10.1177/1934578x1801301005openalex-snapshot
A New Limonoid from Chisocheton paniculatus Fruit Collected in Vietnam and Its NO Production Inhibitory Activity
inferred← citeshttps://doi.org/10.1186/s12864-023-09150-6openalex-snapshot
Sequencing and analysis of the complete mitochondrial genomes of Toona sinensis and Toona ciliata reveal evolutionary features of Toona
inferred← citeshttps://doi.org/10.1186/s13765-021-00606-5openalex-snapshot
A new havanensin-type limonoid from Chisocheton macrophyllus
inferred← citeshttps://doi.org/10.1360/ssc-2025-0149openalex-snapshot
Progress in the study of non-limonoid natural products of the Meliaceae family
inferred← citeshttps://doi.org/10.15408/jkv.v8i2.27782openalex-snapshot
Nimonol from Chisocheton macrophyllus (Meliaceae) Seeds and Their Cytotoxic Activity against P-388 Leukaemia Cells
inferred← citeshttps://doi.org/10.20884/1.jm.2021.16.1.642openalex-snapshot
Four Flavan-3-ol Compounds From The Stembark of Chisocheton balansae C.DC. (MELIACEAE)
inferred← citeshttps://doi.org/10.20884/1.jm.2021.16.2.708openalex-snapshot
Two Limonoids from The Seeds of Chisocheton Macrophyllus and Their Cytotoxic Activity Against Mcf-7 Breast Cancer Cells
inferred← citeshttps://doi.org/10.20884/1.jm.2022.17.3.6425openalex-snapshot
Sesquiterpenoids from Stem Bark of Chisocheton lasiocarpus and Their Cytotoxic Activity against MCF-7 Breast Cancer Cell
inferred← citeshttps://doi.org/10.20884/1.jm.2023.18.2.6845openalex-snapshot
Morelloflavone and Molecular Docking from Stembark of Chisocheton lasiocarpus and Its Cytotoxic Activity Against Breast Cancer Mcf-7 Cell Lines
inferred← citeshttps://doi.org/10.20961/alchemy.17.2.44782.219-226openalex-snapshot
A New Limonoid from the Seeds of Chisocheton lasiocarpus (Meliaceae)
inferred← citeshttps://doi.org/10.2174/0113852728382432250527075453openalex-snapshot
The Genus Chisocheton: An Extensive Review of Phytochemistry and Pharmacology
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-2bpb9-v2openalex-snapshot
Chemistry and Biology of Novel Meliaceae Limonoids
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-2bpb9-v3openalex-snapshot
Chemistry and Biology of Novel Meliaceae Limonoids
inferred← citeshttps://doi.org/10.3390/ijms222413262openalex-snapshot
Insecticidal Triterpenes in Meliaceae: Plant Species, Molecules and Activities: Part Ⅰ (Aphanamixis-Chukrasia)
inferred← citeshttps://doi.org/10.34071/jmp.2019.1.10openalex-snapshot
DAMMARANE TRITERPENE, FLAVONE GLYCOSIDES FROM THE STEMS AND LEAVES OF CHISOCHETON PANICULATUS HIERN (MELIACEAE)
inferred← citeshttps://doi.org/10.5650/jos.ess24118openalex-snapshot
Larvicidal Activity of Chisocheton erythrocarpus Nano-emulsion Formulation against Aedes aegypti
inferred← citeshttps://doi.org/10.6084/m9.figshare.26565522openalex-snapshot
Additional file 1 of Sequencing and analysis of the complete mitochondrial genomes of Toona sinensis and Toona ciliata reveal evolutionary features of Toona
inferred← citeshttps://doi.org/10.6084/m9.figshare.26565525openalex-snapshot
Additional file 2 of Sequencing and analysis of the complete mitochondrial genomes of Toona sinensis and Toona ciliata reveal evolutionary features of Toona
inferred← citeshttps://doi.org/10.6084/m9.figshare.26565528openalex-snapshot
Additional file 3 of Sequencing and analysis of the complete mitochondrial genomes of Toona sinensis and Toona ciliata reveal evolutionary features of Toona
inferred← citeshttps://doi.org/10.6084/m9.figshare.26565531openalex-snapshot
Additional file 4 of Sequencing and analysis of the complete mitochondrial genomes of Toona sinensis and Toona ciliata reveal evolutionary features of Toona
inferred← citeshttps://doi.org/10.6084/m9.figshare.26565534openalex-snapshot
Additional file 5 of Sequencing and analysis of the complete mitochondrial genomes of Toona sinensis and Toona ciliata reveal evolutionary features of Toona
inferred← citeshttps://doi.org/10.6084/m9.figshare.26565537openalex-snapshot
Additional file 6 of Sequencing and analysis of the complete mitochondrial genomes of Toona sinensis and Toona ciliata reveal evolutionary features of Toona
inferred← citeshttps://doi.org/10.6084/m9.figshare.26565540openalex-snapshot
Additional file 7 of Sequencing and analysis of the complete mitochondrial genomes of Toona sinensis and Toona ciliata reveal evolutionary features of Toona
inferred← citeshttps://doi.org/10.6084/m9.figshare.26565543openalex-snapshot
Additional file 8 of Sequencing and analysis of the complete mitochondrial genomes of Toona sinensis and Toona ciliata reveal evolutionary features of Toona
inferred← citeshttps://doi.org/10.6084/m9.figshare.26565546openalex-snapshot
Additional file 9 of Sequencing and analysis of the complete mitochondrial genomes of Toona sinensis and Toona ciliata reveal evolutionary features of Toona
inferred← citeshttps://doi.org/10.6084/m9.figshare.26565549openalex-snapshot
Additional file 10 of Sequencing and analysis of the complete mitochondrial genomes of Toona sinensis and Toona ciliata reveal evolutionary features of Toona
inferred← citeshttps://doi.org/10.7454/mss.v28i2.2202openalex-snapshot
Limonoids Isolated from Chisocheton pentandrus (Meliaceae) Stembarks and its Cytotoxicity Towards MCF-7 Breast Cancer Cell Line
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