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Phytosteroids and triterpenoids with potent cytotoxicities from the leaves of Chisocheton cumingianus

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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/anie.197903631openalex-snapshot

Circular Dichroism and Absolute Conformation: Application of Qualitative MO Theory to Chiroptical Phenomena

inferredcites →https://doi.org/10.1002/biof.97openalex-snapshot

Modulation of signal transduction in cancer cells by phytosterols

inferredcites →https://doi.org/10.1016/j.bbrc.2014.01.148openalex-snapshot

Recent advances in Phytosterol Oxidation Products

inferredcites →https://doi.org/10.1016/j.bmc.2011.01.007openalex-snapshot

Chisopanins A–K, 11 new protolimonoids from Chisocheton paniculatus and their anti-inflammatory activities

inferredcites →https://doi.org/10.1016/j.phytochem.2012.10.008openalex-snapshot

Tetracyclic triterpenoids and terpenylated coumarins from the bark of Ailanthus altissima (“Tree of Heaven”)

inferredcites →https://doi.org/10.1016/j.plipres.2007.10.001openalex-snapshot

Biological effects of oxidized phytosterols: A review of the current knowledge

inferredcites →https://doi.org/10.1016/j.tet.2014.07.006openalex-snapshot

Diverse prieurianin-type limonoid derivatives from the fruits of Aphanamixis grandifolia and their absolute configuration determination

inferredcites →https://doi.org/10.1016/s0040-4020(97)00303-7openalex-snapshot

First examples of dammarane triterpenes isolated from Celastraceae

inferredcites →https://doi.org/10.1021/jf204737eopenalex-snapshot

Oxidized Derivatives of Dihydrobrassicasterol: Cytotoxic and Apoptotic Potential in U937 and HepG2 Cells

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Determination of Absolute Configuration of Acyclic 1,2-Diols with Mo2(OAc)4. 1. Snatzke's Method Revisited

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Practical Method for the Absolute Configuration Assignment of tert / tert 1,2-Diols Using Their Complexes with Mo 2 (OAc) 4

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Efficient Route to 7α-(Benzoyloxy)-3-dioxolane Cholestan-24(R)-ol, a Key Intermediate in the Synthesis of Squalamine

inferredcites →https://doi.org/10.1021/jp102730popenalex-snapshot

Molecular Dynamics Simulation and Binding Studies of β-Sitosterol with Human Serum Albumin and Its Biological Relevance

inferredcites →https://doi.org/10.1021/np020577popenalex-snapshot

Sterol and Triterpenoid Constituents of Verbena littoralis with NGF-Potentiating Activity

inferredcites →https://doi.org/10.1021/np100599gopenalex-snapshot

Triterpenoids from Aglaia abbreviata and Their Cytotoxic Activities

inferredcites →https://doi.org/10.1021/np900485topenalex-snapshot

Tetranortriterpenoids from Chisocheton paniculatus

inferredcites →https://doi.org/10.1021/np9905923openalex-snapshot

Phytochemical Investigation of Aglaia rubiginosa

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Compound Representatives of a New Type of Triterpenoid from Aglaia odorata

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Synthesis of the Aglycone of the Shark Repellent Pavoninin-4 Using Remote Functionalization

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Synthesis of Primary Arylselenoamides by Reaction of Aryl Nitriles with Woollins' Reagent

inferredcites →https://doi.org/10.1039/b615897hopenalex-snapshot

Production of epoxydammaranes by the enzymatic reactions of (3R)- and (3S)-2,3-squalene diols and those of 2,3:22,23-dioxidosqualenes with recombinant squalene cyclase and the mechanistic insight into the polycyclization reactions

inferredcites →https://doi.org/10.1039/c5ra05006eopenalex-snapshot

Mexicanolide limonoids with in vitro neuroprotective activities from seeds of Khaya senegalensis

inferredcites →https://doi.org/10.1039/p19780000360openalex-snapshot

Flavone and triterpenoid constituents of Elaegia utilis

inferredcites →https://doi.org/10.1055/s-0033-1348741openalex-snapshot

Isolation and Structure Determination of New Secondary Metabolites from the Endangered Plant Rhododendron brachycarpum G.Don

inferredcites →https://doi.org/10.1055/s-0033-1351100openalex-snapshot

Bioactive Benzofuran Neolignans from Aristolochia fordiana

inferredcites →https://doi.org/10.1079/bjn20051500openalex-snapshot

Qualitative and quantitative comparison of the cytotoxic and apoptotic potential of phytosterol oxidation products with their corresponding cholesterol oxidation products

inferredcites →https://doi.org/10.1107/s0108767399004262openalex-snapshot

Absolute structure and absolute configuration

inferredcites →https://doi.org/10.1139/v11-147openalex-snapshot

Four new triterpenoids from Chisocheton paniculatus and their anti-inflammatory activities

inferredcites →https://doi.org/10.1248/cpb.45.1435openalex-snapshot

Topsentinols A-J, New Sterols with Highly Branched Side Chains from Marine Sponge Topsentia sp.

inferredcites →https://doi.org/10.1248/cpb.47.692openalex-snapshot

Studies on the Constituents of Viburnum Species. XIX. Six New Triterpenoids from Viburnum dilatatum THUNB.

inferredcites →https://doi.org/10.1248/cpb.49.1024openalex-snapshot

Semialactone, Isofouquierone Peroxide and Fouquierone, Three New Dammarane Triterpenes from Rhus javanica.

inferredcites →https://doi.org/10.1248/cpb.c12-00012openalex-snapshot

Cytotoxic Terpenes from the Stems of Dipterocarpus obtusifolius Collected in Cambodia

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/chin.201624197openalex-snapshot

ChemInform Abstract: Phytosteroids and Triterpenoids with Potent Cytotoxicities from the Leaves of Chisocheton cumingianus.

inferred← citeshttps://doi.org/10.1007/s12247-025-10018-3openalex-snapshot

Phytochemical Composition and Bioactivities of Verbena tenuisecta (Briq.) Leaf Extracts: Antimicrobial and Antibiofilm Properties

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Phytochemical Fingerprinting, GC-MS Profiling, and Broad-Spectrum Antimicrobial Activities of Glinus Lotoides L.: Inhibition of Biofilm and Pellicle Formation

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Discovery of unusual phloroglucinol–triterpenoid adducts from Leptospermum scoparium and Xanthostemon chrysanthus by building blocks-based molecular networking

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Cytotoxic seco-cytochalasins from an endophytic Aspergillus sp. harbored in Pinellia ternata tubers

inferred← citeshttps://doi.org/10.1016/j.fitote.2019.02.024openalex-snapshot

Asperfuranones A-C, 3(2H)-furanone derivatives from the fungus Aspergillus sp. and the configuration reassignment of their eighteen analogues

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Structurally diverse dammarane-derived triterpenoids from the twigs of Aglaia perviridis Hiern and their α-glucosidase and PTP1B inhibitory 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.2023.02.005openalex-snapshot

Pentandricines F-H, cytotoxic limonoids from the stem bark of Chisocheton pentandrus (Blanco) Merr

inferred← citeshttps://doi.org/10.1039/c6ra21485aopenalex-snapshot

Stereoselective glycoconjugation of steroids with selenocarbohydrates

inferred← citeshttps://doi.org/10.1088/1755-1315/1312/1/012054openalex-snapshot

Chisocheton pentandrus (Blanco) Merr. leaf as a potential antioxidant and α-glucosidase inhibitory agent

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/10.2174/0113852728382432250527075453openalex-snapshot

The Genus Chisocheton: An Extensive Review of Phytochemistry and Pharmacology

inferred← citeshttps://doi.org/10.24198/cna.v8.n2.29563openalex-snapshot

7-hidroksi-6-metoksi Kumarin (Skopoletin) dari Ekstrak Metanol Kulit Batang Chisocheton cumingianus (Meliaceae)

inferred← citeshttps://doi.org/10.3390/molecules21081047openalex-snapshot

Plant Resources, 13C-NMR Spectral Characteristic and Pharmacological Activities of Dammarane-Type Triterpenoids

inferred← citeshttps://doi.org/10.3390/molecules24122288openalex-snapshot

Maytenus macrocarpa (Ruiz & Pav.) Briq.: Phytochemistry and Pharmacological Activity

inferred← citeshttps://doi.org/10.51966/jvas.2021.52.2.135-141openalex-snapshot

Qualitative and Quantitative Analysis (GC-MS) of Methanol Extract of Crataeva nurvala stem bark

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