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Vobatensines A–F, Cytotoxic Iboga-Vobasine Bisindoles from Tabernaemontana corymbosa

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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/(sici)1522-2675(19980909)81:9<1645::aid-hlca1645>3.0.co;2-popenalex-snapshot
The Absolute Configuration at C(7) of Voacangine Hydroxyindolenine
inferredcites →https://doi.org/10.1002/1522-2675(200204)85:4<1027::aid-hlca1027>3.0.co;2-1openalex-snapshot
Vobasonidine and Vobatricine, Novel Bisindole Alkaloids from a Malayan Tabernaemontana
inferredcites →https://doi.org/10.1002/cbdv.200490056openalex-snapshot
Biologically Active Ibogan and Vallesamine Derivatives from Tabernaemontana divaricata
inferredcites →https://doi.org/10.1002/hlca.19760590719openalex-snapshot
13C‐NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids
inferredcites →https://doi.org/10.1016/0031-9422(84)83102-7openalex-snapshot
13C NMR analysis of alkaloids from peschiera fuchsiaefolia
inferredcites →https://doi.org/10.1016/0031-9422(91)80111-dopenalex-snapshot
Alkaloids from leaves and root bark ofErvatamia hirta
inferredcites →https://doi.org/10.1016/0378-8741(84)90046-1openalex-snapshot
Tabernaemontana L. (Apocynaceae): A review of its taxonomy, phytochemistry, ethnobotany and pharmacology
inferredcites →https://doi.org/10.1016/j.phytochem.2013.11.014openalex-snapshot
Macroline, akuammiline, sarpagine, and ajmaline alkaloids from Alstonia macrophylla
inferredcites →https://doi.org/10.1016/j.tetlet.2008.10.066openalex-snapshot
Conolutinine, a hexacyclic indole alkaloid with a novel ring system incorporating a diazaspiro center and fused oxadiazepine–tetrahydrofuran rings
inferredcites →https://doi.org/10.1016/s0040-4039(00)00250-1openalex-snapshot
Tronocarpine, a novel pentacyclic indole incorporating a seven-membered lactam moiety
inferredcites →https://doi.org/10.1016/s0040-4039(01)00802-4openalex-snapshot
Voastrictine, a novel pentacyclic quinolinic alkaloid from Tabernaemontana
inferredcites →https://doi.org/10.1016/s0099-9598(08)60307-7openalex-snapshot
Chapter 1 Alkaloids from Tabernaemontana
inferredcites →https://doi.org/10.1016/s0735-8210(99)80005-3openalex-snapshot
Alkaloids from Malaysian Flora
inferredcites →https://doi.org/10.1016/s1099-4831(06)63004-6openalex-snapshot
Chapter 4 Bisindole Alkaloids
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00117openalex-snapshot
Ibogan, Tacaman, and Cytotoxic Bisindole Alkaloids from Tabernaemontana. Cononusine, an Iboga Alkaloid with Unusual Incorporation of a Pyrrolidone Moiety
inferredcites →https://doi.org/10.1021/ja01075a023openalex-snapshot
Voacamine and Voacorine
inferredcites →https://doi.org/10.1021/np020326gopenalex-snapshot
New Bisindole Alkaloids from Tabernaemontana corymbosa
inferredcites →https://doi.org/10.1021/np500240bopenalex-snapshot
Iboga-Type Alkaloids from Ervatamia officinalis
inferredcites →https://doi.org/10.1021/np50039a008openalex-snapshot
Antimicrobially Active Alkaloids from Tabernaemontana chippii
inferredcites →https://doi.org/10.1021/np500589uopenalex-snapshot
Cytotoxic Vobasine, Tacaman, and Corynanthe-Tryptamine Bisindole Alkaloids from Tabernaemontana and Structure Revision of Tronoharine
inferredcites →https://doi.org/10.1021/ol4021404openalex-snapshot
Voatinggine and Tabertinggine, Pentacyclic Indole Alkaloids Derived from an Iboga Precursor via a Common Cleavamine-Type Intermediate
inferredcites →https://doi.org/10.1021/ol503072gopenalex-snapshot
Criofolinine and Vernavosine, New Pentacyclic Indole Alkaloids Incorporating Pyrroloazepine and Pyridopyrimidine Moieties Derived from a Common Yohimbine Precursor
inferredcites →https://doi.org/10.1039/b301167dopenalex-snapshot
Biologically active indole and bisindole alkaloids from Tabernaemontana divaricata
inferredcites →https://doi.org/10.1055/s-2007-969101openalex-snapshot
Indole Alkaloids fromTabernaemontana elegans1
inferredcites →https://doi.org/10.1071/ch9751813openalex-snapshot
Indole alkaloids from Ervatamia orientalis . I. Isolation of alkaloids and structural identification of two dimers
inferredcites →https://doi.org/10.1248/cpb.42.280openalex-snapshot
Two New Dimeric Indole Alkaloids from Tabernaemontana subglobosa MERR. from Taiwan.
inferredcites →https://doi.org/10.3987/s-1977-02-0753openalex-snapshot
The C(2) Stereochemistry of Iboluteine

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.2022.113089zenodo-depositor-declared
Iboga-type alkaloids with Indolizidino[8,7-b]Indole scaffold and bisindole alkaloids from Tabernaemontana bufalina Lour
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113587zenodo-depositor-declared
Polyneurines A−H, iboga alkaloids from Tabernaemontana polyneura
inferred← citeshttps://doi.org/10.1002/ardp.202000092openalex-snapshot
Anticancer activity of bisindole alkaloids derived from natural sources and synthetic bisindole hybrids
inferred← citeshttps://doi.org/10.1002/cbdv.202501863openalex-snapshot
Natural Alkaloids From Tabernaemontana corymbosa and Related Network Pharmacology Prediction
inferred← citeshttps://doi.org/10.1002/cjoc.202100634openalex-snapshot
Tabernaesine J, a Novel Vincamine‐Type Indole Alkaloid with 6/5/6/6/6/5/5 Heptacyclic‐Ring System Scaffold from Tabernaemontana pachysiphon
inferred← citeshttps://doi.org/10.1002/mrc.5271openalex-snapshot
Density functional theory‐nuclear magnetic resonance‐validated full structure elucidation of theionbrunonine C, an unstable N ‐oxide theionbrunonine from Mostuea brunonis
inferred← citeshttps://doi.org/10.1002/slct.202004153openalex-snapshot
Evaluation of DNA Binding and Topoisomerase I Inhibitory Activities of 16’‐Decarbomethoxydihydrovoacamine from Tabernaemontana corymbosa
inferred← citeshttps://doi.org/10.1007/978-3-319-49712-9_2openalex-snapshot
The Iboga Alkaloids
inferred← citeshttps://doi.org/10.1007/s11101-024-09964-6openalex-snapshot
Monoterpene indole alkaloids with anticancer activity from Tabernaemontana species
inferred← citeshttps://doi.org/10.1007/s11101-024-10015-3openalex-snapshot
Exploring plant-derived bisindole alkaloids: a comprehensive review of sources, phytochemistry and cytotoxicity
inferred← citeshttps://doi.org/10.1016/b978-0-12-823944-5.00008-9openalex-snapshot
Biological activity and 13C NMR spectral data of iboga-type skeleton alkaloids
inferred← citeshttps://doi.org/10.1016/j.bse.2026.105280openalex-snapshot
Chemical constituents from the aerial parts of Rauvolfia yunnanensis Tsiang and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.chempr.2018.10.009openalex-snapshot
Biosynthetically Inspired Transformation of Iboga to Monomeric Post-iboga Alkaloids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112359openalex-snapshot
Current scenario of indole derivatives with potential anti-drug-resistant cancer activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114748openalex-snapshot
Bisindole natural products: A vital source for the development of new anticancer drugs
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106851openalex-snapshot
Ethnobotanical and alkaloid composition with their cytotoxicity of Tabernaemontana polyneura: A review with in silico ADMET analysis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113384openalex-snapshot
Vobasine, vincamine, voaphylline, tacaman, and iboga alkaloids from Tabernaemontana corymbosa
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133706openalex-snapshot
Chippiine, iboga, cleavamine, vobasine, and cytotoxic bisindole alkaloids from Tabernaemontana polyneura
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00674openalex-snapshot
A Hexacyclic, Iboga-Derived Monoterpenoid Indole with a Contracted Tetrahydroazepine C-Ring and Incorporation of an Isoxazolidine Moiety, a Seco-Corynanthean, an Aspidosperma-Aspidosperma Bisindole with Anticancer Properties, and the Absolute Configuration of the Pyridopyrimidine Indole Alkaloid,…
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00949openalex-snapshot
Taburnaemines A–I, Cytotoxic Vobasinyl-Iboga-Type Bisindole Alkaloids from Tabernaemontana corymbosa
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00191openalex-snapshot
Flabellipparicine, a Flabelliformide-Apparicine-Type Bisindole Alkaloid from Tabernaemontana divaricata
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00919openalex-snapshot
Conolodinines A–D, Aspidosperma–Aspidosperma Bisindole Alkaloids with Antiproliferative Activity from Tabernaemontana corymbosa
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00768openalex-snapshot
Tabernaesines A–I, Cytotoxic Aspidosperma–Aspidosperma-Type Bisindole Alkaloids from Tabernaemontana pachysiphon
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00856openalex-snapshot
Cytotoxic Monoterpenoid Indole Alkaloids from Tabernaemontana corymbosa as Potent Autophagy Inhibitors by the Attenuation of Lysosomal Acidification
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02648openalex-snapshot
Construction of the Azacyclic Core of Tabernaemontanine-Related Alkaloids via Tandem Reformatsky–Aza-Claisen Rearrangement
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00004openalex-snapshot
One-Pot Synthesis of Indoles by a Sequential Ugi-3CR/Wittig Reaction Starting from Odorless Isocyanide-Substituted Phosphonium Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02445openalex-snapshot
Tabercorymines A and B, Two Vobasinyl–Ibogan-Type Bisindole Alkaloids from Tabernaemontana corymbosa
inferred← citeshttps://doi.org/10.1055/a-1755-5605openalex-snapshot
Antiproliferative and Microtubule-stabilizing Activities of Two Iboga-vobasine Bisindoles Alkaloids from Tabernaemontana corymbosa in Colorectal Adenocarcinoma HT-29 Cells
inferred← citeshttps://doi.org/10.1080/14786419.2026.2718756openalex-snapshot
Monoterpenoid indole alkaloids from the aerial parts of Tabernaemontana divaricata (L.) R. Br. ex Roem. & Schult. and their anti-inflammatory activity and cytotoxicity on acute leukaemia cells
inferred← citeshttps://doi.org/10.2139/ssrn.5075214openalex-snapshot
Structurally Diverse Monoterpenoid Indole Alkaloids from Tabernaemontana Pandacaqui Lam
inferred← citeshttps://doi.org/10.2174/1568026620666200622150325openalex-snapshot
Indole Alkaloids with Potential Anticancer Activity
inferred← citeshttps://doi.org/10.3390/molecules26010070openalex-snapshot
Alkaloids with Anti-Onchocercal Activity from Voacanga africana Stapf (Apocynaceae): Identification and Molecular Modeling
inferred← citeshttps://doi.org/10.3390/molecules28186664openalex-snapshot
Two Novel Iboga-Type and an Oxindole Glucuronide Alkaloid from Tabernaemontana peduncularis Disclose Related Biosynthetic Pathways to Tabernaemontana divaricata
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