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Cytotoxic Vobasine, Tacaman, and Corynanthe-Tryptamine Bisindole Alkaloids from Tabernaemontana and Structure Revision of Tronoharine

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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.200490056openalex-snapshot

Biologically Active Ibogan and Vallesamine Derivatives from Tabernaemontana divaricata

inferredcites →https://doi.org/10.1007/978-1-4612-2908-7openalex-snapshot

Alkaloids: Chemical and Biological Perspectives

inferredcites →https://doi.org/10.1016/0031-9422(95)00050-hopenalex-snapshot

Alkaloids from stem bark and leaves of Peschiera buchtieni

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.2009.06.010openalex-snapshot

Four tetracyclic oxindole alkaloids and a taberpsychine derivative from a Malayan Tabernaemontana

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/s0040-4020(01)91102-0openalex-snapshot

Alkaloids of Tabernaemontana eglandulosa

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(00)85724-xopenalex-snapshot

Tacamine, the first example of a new class of indole alkaloids

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/s0040-4039(99)01018-7openalex-snapshot

Tronoharine, a novel hexacyclic indole alkaloid from a Malayan 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/ar50074a003openalex-snapshot

Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. Alkaloids

inferredcites →https://doi.org/10.1021/cr60233a003openalex-snapshot

Ultraviolet Spectra of Alkaloids

inferredcites →https://doi.org/10.1021/ja027906kopenalex-snapshot

First Total Synthesis of (±)-Strychnofoline via a Highly Selective Ring-Expansion Reaction

inferredcites →https://doi.org/10.1021/jo00872a046openalex-snapshot

Studies in the indole series. VII. Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. XL. Carbon-13 nuclear magnetic resonance analysis of vobasine-like indole alkaloids

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/10.1039/b301167dopenalex-snapshot

Biologically active indole and bisindole alkaloids from Tabernaemontana divaricata

What points at this work

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

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Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities

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/chem.202000415openalex-snapshot

Towards the Sarpagine‐Ajmaline‐Macroline Family of Indole Alkaloids: Enantioselective Synthesis of an N‐Demethyl Alstolactone Diastereomer

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/10.1007/s10600-022-03685-yopenalex-snapshot

Alkaloids from the Leaves and Twigs of Bousigonia angustifolia

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/b978-0-444-63929-5.00007-3openalex-snapshot

Tabernaemontana Species: Promising Sources of New Useful Drugs

inferred← citeshttps://doi.org/10.1016/b978-0-444-63931-8.00010-2openalex-snapshot

Alkaloids From Apocynaceae

inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104136openalex-snapshot

Monoterpene indole alkaloids with acetylcholinesterase inhibitory activity from the leaves of Rauvolfia vomitoria

inferred← citeshttps://doi.org/10.1016/j.bse.2021.104239openalex-snapshot

A novel tryptophan-derived alkaloid and other constituents from Guettarda speciosa (Rubiaceae: Cinchonoideae–Guettardeae)

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.2020.104704openalex-snapshot

Peraksine derivatives with potential anti-inflammatory activities from the stems of Rauvolfia vomitoria

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.phytol.2021.03.006openalex-snapshot

New monoterpenoid indole alkaloids from Tabernaemontana bovina

inferred← citeshttps://doi.org/10.1016/j.phytol.2022.03.016openalex-snapshot

New aspidosperma-type alkaloids from Tabernaemontana bovina

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/10.1016/j.tetlet.2020.152400openalex-snapshot

Taberdivamines A and B, two new quaternary indole alkaloids from Tabernaemontana divaricata

inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154303openalex-snapshot

Novel indole alkaloids from Rauvolfia yunnanensis, inhibiting ESBL producing Escherichia coli by targeting cell membrane integrity

inferred← citeshttps://doi.org/10.1016/s1875-5364(23)60393-0openalex-snapshot

Antimicrobial indole alkaloids from Tabernaemontana corymbosa

inferred← citeshttps://doi.org/10.1016/s2707-3688(23)00044-4openalex-snapshot

Two new phenylpropanoids from the leaves of Rauvolfia vomitoria

inferred← citeshttps://doi.org/10.1021/acs.jctc.0c00339openalex-snapshot

Multistate QM/QM Extrapolation of UV/Vis Absorption Spectra with Point Charge Embedding

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b01035openalex-snapshot

Indole Alkaloids from Hunteria zeylanica

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b01117openalex-snapshot

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

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00129openalex-snapshot

Ibogan, Aspidosperman, Vincamine, and Bisindole Alkaloids from a Malayan Tabernaemontana corymbosa: Iboga Alkaloids with C-20α Substitution

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.7b00387openalex-snapshot

Antiproliferative Dimeric Aporphinoid Alkaloids from the Roots of Thalictrum cultratum

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.joc.5b00619openalex-snapshot

Minimalist Relativistic Force Field: Prediction of Proton–Proton Coupling Constants in 1H NMR Spectra Is Perfected with NBO Hybridization Parameters

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.6c01478openalex-snapshot

Synthetic Exploration and Divergent Total Synthesis of Tacaman Monoterpenoid Indole Alkaloids

inferred← citeshttps://doi.org/10.1021/ol503734xopenalex-snapshot

Synthetic Study toward the Misassigned (±)-Tronoharine

inferred← citeshttps://doi.org/10.1039/d5np00046gopenalex-snapshot

Discovery, bioactivities and biosynthesis of spirooxindole alkaloids

inferred← citeshttps://doi.org/10.1063/1.4972000openalex-snapshot

Point charge embedding for ONIOM excited states calculations

inferred← citeshttps://doi.org/10.1080/10286020.2019.1608957openalex-snapshot

Three new isoquinoline alkaloids from the whole plants of Thalictrum tenue with cytotoxic activities

inferred← citeshttps://doi.org/10.1080/10286020.2022.2090345openalex-snapshot

Two new aspidosperma-type monoterpenoid indole alkaloids from Ervatamia officinalis

inferred← citeshttps://doi.org/10.1080/14786419.2018.1488707openalex-snapshot

Two new monoterpenoid indole alkaloids from Tabernaemontana divaricata

inferred← citeshttps://doi.org/10.1080/14786419.2023.2180503openalex-snapshot

New monoterpenoid indole alkaloids from the stems of Tabernaemontana bovina Lour (Apocynaceae)

inferred← citeshttps://doi.org/10.1111/jphp.12523openalex-snapshot

A review on ethnobotany, pharmacology and phytochemistry of Tabernaemontana corymbosa

inferred← citeshttps://doi.org/10.18632/oncotarget.7190openalex-snapshot

Bisleuconothine A, a bisindole alkaloid, inhibits colorectal cancer cell in vitro and in vivo targeting Wnt signaling

inferred← citeshttps://doi.org/10.31635/ccschem.019.20180006openalex-snapshot

Highly Diastereo- and Enantioselective Synthesis of Quinuclidine Derivatives by an Iridium-Catalyzed Intramolecular Allylic Dearomatization Reaction

inferred← citeshttps://doi.org/10.3390/molecules24071316openalex-snapshot

Preparative Separation of Monoterpenoid Indole Alkaloid Epimers from Ervatamia yunnanensis Tsiang by pH-Zone-Refining Counter-Current Chromatography Combined with Preparative High-Performance Liquid Chromatography

inferred← citeshttps://doi.org/10.3390/molecules26020488openalex-snapshot

Chemical Diversity and Bioactivities of Monoterpene Indole Alkaloids (MIAs) from Six Apocynaceae Genera

inferred← citeshttps://doi.org/10.3390/plants10020313openalex-snapshot

Major Bioactive Alkaloids and Biological Activities of Tabernaemontana Species (Apocynaceae)

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