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Monoterpenoid Indole Alkaloids from Kopsia officinalis and the Immunosuppressive Activity of Rhazinilam

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What this work says

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

inferredcites →https://doi.org/10.1002/1529-0131(200011)43:11<2455::aid-anr12>3.0.co;2-kopenalex-snapshot
Increased interleukin-17 production in patients with systemic sclerosis
inferredcites →https://doi.org/10.1002/1529-0131(200109)44:9<2097::aid-art360>3.0.co;2-6openalex-snapshot
Predominance of Th1 immune response in diffuse proliferative lupus nephritis
inferredcites →https://doi.org/10.1002/cjoc.19890070211openalex-snapshot
The isolation and characterization of indole alkaloids from the fruits of Kopsia officinalis
inferredcites →https://doi.org/10.1002/cm.970280405openalex-snapshot
Rhazinilam mimics the cellular effects of taxol by different mechanisms of action
inferredcites →https://doi.org/10.1002/hlca.19680510522openalex-snapshot
Optische Rotationsdispersion von Indolinalkaloiden mit Ketogruppen
inferredcites →https://doi.org/10.1002/hlca.200690053openalex-snapshot
Three New Indole Alkaloids from the Leaves of Kopsia officinalis
inferredcites →https://doi.org/10.1007/bf00575758openalex-snapshot
The NMR investigation of alkaloids. VII.13C NMR spectra and structure of ?kopsanone? and kopsinilam
inferredcites →https://doi.org/10.1007/s11418-009-0334-8openalex-snapshot
Kopsiyunnanines F and isocondylocarpines: new tubotaiwine-type alkaloids from Yunnan Kopsia arborea
inferredcites →https://doi.org/10.1016/0378-8741(85)90004-2openalex-snapshot
Muscle relaxant activity and hypotensive activity of some tabernaemontana alkaloids
inferredcites →https://doi.org/10.1016/0378-8741(94)90030-2openalex-snapshot
A preliminary chemotaxonomic review of Kopsia (Apocynaceae)
inferredcites →https://doi.org/10.1016/j.phytochem.2014.09.014openalex-snapshot
Corynanthean, eburnan, secoleuconoxine, and pauciflorine alkaloids from Kopsia pauciflora
inferredcites →https://doi.org/10.1016/j.tet.2014.10.002openalex-snapshot
Indole alkaloids from Kopsia jasminiflora
inferredcites →https://doi.org/10.1016/s0031-9422(00)95027-1openalex-snapshot
Methyl chanofruticosinates from leaves of Kopsia arborea
inferredcites →https://doi.org/10.1016/s0031-9422(01)00119-4openalex-snapshot
Methyl chanofruticosinates from leaves of Kopsia flavida Blume
inferredcites →https://doi.org/10.1016/s0031-9422(98)00492-0openalex-snapshot
Leishmanicidal alkaloids from Kopsia griffithii
inferredcites →https://doi.org/10.1016/s0040-4020(01)85802-6openalex-snapshot
Alkaloids of leuconotis griffithii and L. Eugenifolia (Apocynaceae)
inferredcites →https://doi.org/10.1016/s1099-4831(08)00201-0openalex-snapshot
Chapter 1 Alkaloids of Kopsia
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00992openalex-snapshot
Aspidofractinine and Eburnane Alkaloids from a North Borneo Kopsia . Ring-Contracted, Additional Ring-Fused, and Paucidactine-Type Aspidofractinine Alkaloids from K. pauciflora
inferredcites →https://doi.org/10.1021/ja00966a043openalex-snapshot
Revised Structures of the Pleiocarpa Alkaloids Pleiocarpoline (Pleiocarpine Nb-Oxide), Pleiocarpolinine (Pleiocarpinine Nb-Oxide), and Kopsinoline (Kopsinine Nb-Oxide)
inferredcites →https://doi.org/10.1021/np0703747openalex-snapshot
Biologically Active Aspidofractinine, Rhazinilam, Akuammiline, and Vincorine Alkaloids from Kopsia
inferredcites →https://doi.org/10.1021/np1004938openalex-snapshot
Macrophyllionium and Macrophyllines A and B, Oxindole Alkaloids from Uncaria macrophylla
inferredcites →https://doi.org/10.1021/np200008gopenalex-snapshot
Grandilodines A−C, Biologically Active Indole Alkaloids from Kopsia grandifolia
inferredcites →https://doi.org/10.1021/np50031a016openalex-snapshot
Kopsoffine: A New Dimeric Indole Alkaloid of Pleiomutine Type from Kopsia offcinalis
inferredcites →https://doi.org/10.1021/np800489eopenalex-snapshot
Rhazinilam and Quebrachamine Derivatives from Yunnan Kopsia arborea
inferredcites →https://doi.org/10.1021/ol301400eopenalex-snapshot
Calophyline A, a New Rearranged Monoterpenoid Indole Alkaloid from Winchia calophylla
inferredcites →https://doi.org/10.1038/478334bopenalex-snapshot
Many faces of a cancer-supporting protein
inferredcites →https://doi.org/10.1038/nchembio.433openalex-snapshot
Postgenomic chemical biology
inferredcites →https://doi.org/10.1038/nri3220openalex-snapshot
Therapeutic targeting of IL-17 for psoriasis
inferredcites →https://doi.org/10.1042/cs20100163openalex-snapshot
Psoriasis: from pathogenesis to novel therapeutic approaches
inferredcites →https://doi.org/10.1055/s-2007-969934openalex-snapshot
Alcaloïdes Indoliques Monomères deKopsia officinalis
inferredcites →https://doi.org/10.1056/nejmcibr1602864openalex-snapshot
Repressing Immunity in Autoimmune Disease
inferredcites →https://doi.org/10.1139/v74-335openalex-snapshot
Quaternary Bases from Hunteria eburnea Pichon
inferredcites →https://doi.org/10.1248/cpb.37.2971openalex-snapshot
Imidazo(2,1-b)benzothiazoles. II. Synthesis and antiinflammatory activity of some imidazo(2,1-b)benzothiazoles.
inferredcites →https://doi.org/10.1248/cpb.58.961openalex-snapshot
Two New Aspidosperma Indole Alkaloids from Yunnan Kopsia arborea
inferredcites →https://doi.org/10.3987/com-08-11438openalex-snapshot
Singaporentine A: A New Indole Alkaloid from Kopsia singapurensis Ridl.
inferredcites →https://doi.org/10.3987/com-12-12511openalex-snapshot
New Indole Alkaloids from Melodinus henryi

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.2020.112450zenodo-depositor-declared
Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
inferred← citeshttps://doi.org/10.1002/ange.201803372openalex-snapshot
Asymmetric Synthesis of (R)‐1‐Alkyl‐Substituted Tetrahydro‐ß‐carbolines Catalyzed by Strictosidine Synthases
inferred← citeshttps://doi.org/10.1002/ange.201805905openalex-snapshot
Thiourea‐Catalyzed Asymmetric Michael Addition of Carbazolones to 2‐Chloroacrylonitrile: Total Synthesis of 5,22‐Dioxokopsane, Kopsinidine C, and Demethoxycarbonylkopsin
inferred← citeshttps://doi.org/10.1002/ange.202009238openalex-snapshot
Collective Total Synthesis of Aspidofractinine Alkaloids through the Development of a Bischler–Napieralski/Semipinacol Rearrangement Reaction
inferred← citeshttps://doi.org/10.1002/ange.202201712openalex-snapshot
Divergent Total Synthesis of Four Kopsane Alkaloids: N‐Carbomethoxy‐10,22‐dioxokopsane, Epikopsanol‐10‐lactam, 10,22‐Dioxokopsane, and N‐Methylkopsanone
inferred← citeshttps://doi.org/10.1002/anie.201803372openalex-snapshot
Asymmetric Synthesis of ( R )‐1‐Alkyl‐Substituted Tetrahydro‐ß‐carbolines Catalyzed by Strictosidine Synthases
inferred← citeshttps://doi.org/10.1002/anie.201805905openalex-snapshot
Thiourea‐Catalyzed Asymmetric Michael Addition of Carbazolones to 2‐Chloroacrylonitrile: Total Synthesis of 5,22‐Dioxokopsane, Kopsinidine C, and Demethoxycarbonylkopsin
inferred← citeshttps://doi.org/10.1002/anie.202009238openalex-snapshot
Collective Total Synthesis of Aspidofractinine Alkaloids through the Development of a Bischler–Napieralski/Semipinacol Rearrangement Reaction
inferred← citeshttps://doi.org/10.1002/anie.202201712openalex-snapshot
Divergent Total Synthesis of Four Kopsane Alkaloids: N‐Carbomethoxy‐10,22‐dioxokopsane, Epikopsanol‐10‐lactam, 10,22‐Dioxokopsane, and N‐Methylkopsanone
inferred← citeshttps://doi.org/10.1002/cbdv.202400721openalex-snapshot
Nervogenic Acid Derivatives and Phenanthrenes from Liparis nervosa and Their Antimicrobial and Immunosuppressive Activities
inferred← citeshttps://doi.org/10.1002/ceur.202500129openalex-snapshot
Indole Synthesis via Allenyl Ester; Enantioselective Total Synthesis of Geissoschizoline
inferred← citeshttps://doi.org/10.1002/cjoc.201800160openalex-snapshot
Bioactive Alkaloids from Indole‐3‐carbinol Exposed Culture of Daldiniaeschscholzii
inferred← citeshttps://doi.org/10.1002/med.21747openalex-snapshot
Biologically active indolizidine alkaloids
inferred← citeshttps://doi.org/10.1007/s10787-026-02244-zopenalex-snapshot
Plant-derived indole alkaloids in chronic inflammatory diseases: molecular mechanisms, therapeutic potential and translational challenges
inferred← citeshttps://doi.org/10.1007/s11101-025-10102-zopenalex-snapshot
Alkaloids from the genus Vinca L. (Apocynaceae): a comprehensive biological and structural review
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00126-8openalex-snapshot
Nine-Membered Rings
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.09.013openalex-snapshot
Cytotoxic and antibacterial aspidofractinine alkaloids from Kopsia hainanensis
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104258openalex-snapshot
Chemical constituents of Kopsia officinalis and their antagonizing high glucose-evoked podocyte injury activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104547openalex-snapshot
Monoterpenoid indole alkaloids from the stems of Kopsia officinalis
inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107164openalex-snapshot
New aspidofractinine-type alkaloids with cytotoxic activity from the roots of Kopsia officinalis
inferred← citeshttps://doi.org/10.1016/j.indcrop.2020.112922openalex-snapshot
Targeted isolation of terpenoid indole alkaloids from Melodinus cochinchinensis (Lour.) Merr. using molecular networking and their biological activities
inferred← citeshttps://doi.org/10.1016/j.jep.2021.114848openalex-snapshot
Anti-inflammatory and analgesic monoterpenoid indole alkaloids of Kopsia officinalis
inferred← citeshttps://doi.org/10.1016/j.jep.2024.117771openalex-snapshot
Monoterpenoid indole alkaloids from Melodinus axillaris W.T.Wang exhibit anti-inflammatory activities by inhibiting the NF-κB signaling pathways
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114198openalex-snapshot
Immunosuppressive alkaloids from Narcissus tazetta subsp. Chinensis and the mechanism of (+)-narciclasine in vitro and in vivo
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131802openalex-snapshot
Arbolodinines A−C, biologically-active aspidofractinine-aspidofractinine, aspidofractinine-strychnan, and kopsine-strychnan bisindole alkaloids from Kopsia arborea
inferred← citeshttps://doi.org/10.1016/s1875-5364(18)30131-6openalex-snapshot
Advanced natural products chemistry research in China between 2015 and 2017
inferred← citeshttps://doi.org/10.1016/s1875-5364(19)30121-9openalex-snapshot
Cangumycins A–F, six new angucyclinone analogues with immunosuppressive activity from Streptomyces
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.jchemed.7b00494openalex-snapshot
1-Dimensional Selective Nuclear Overhauser Effect NMR Spectroscopy To Characterize Products from a Two-Step Green Chemistry Synthesis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00558openalex-snapshot
Discovery of an Oxepine-Containing Diketopiperazine Derivative Active against Concanavalin A-Induced Hepatitis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00255openalex-snapshot
A Cytotoxic Indole Characterized by Incorporation of a Unique Carbon–Nitrogen Skeleton and Two Pentacyclic Corynanthean Alkaloids Incorporating a Substituted Tetrahydrofuranone Ring from Kopsia arborea
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00903openalex-snapshot
Benwamycins A–G, Trialkyl-Substituted Benzene Derivatives from a Soil-Derived Streptomyces
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01580openalex-snapshot
Silver-Catalyzed, Chemo- and Enantioselective Intramolecular Dearomatization of Indoles to Access Sterically Congested Azaspiro Frameworks
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00852openalex-snapshot
Synthesis of Tetrahydrocarbazol-4-ones via Rh(III)-Catalyzed C–H Activation/Annulation of Arylhydrazines with Iodonium Ylides
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02860openalex-snapshot
Bisaspochalasins A–C: Three Cytochalasan Homodimers with Highly Fused Ring System from an Endophytic Aspergillus flavipes
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01714openalex-snapshot
Cascade Radical Trifluoromethylthiolation/Cyclization of Dienes To Access SCF3-Containing Medium-Sized Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01076openalex-snapshot
Asymmetric Total Synthesis of Pentacyclic Indole Alkaloid Andranginine and Absolute Configuration of Natural Product Isolated from Kopsia arborea
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03098openalex-snapshot
Pleiokomenines A and B: Dimeric Aspidofractinine Alkaloids Tethered with a Methylene Group
inferred← citeshttps://doi.org/10.1021/jacs.1c00840openalex-snapshot
Enantioselective Synthesis of α-All-Carbon Quaternary Center-Containing Carbazolones via Amino-palladation/Desymmetrizing Nitrile Addition Cascade
inferred← citeshttps://doi.org/10.1038/s41570-025-00735-1openalex-snapshot
Chiral medium-sized rings beyond central chirality
inferred← citeshttps://doi.org/10.1039/d0np00088dopenalex-snapshot
The chemistry of mavacurane alkaloids: a rich source of bis-indole alkaloids
inferred← citeshttps://doi.org/10.1039/d1cc02033aopenalex-snapshot
Oxyallyl cation promoted dearomative semipinacol rearrangement: a facile stereodivergent synthesis of spiro-indolines with contiguous quaternary centers
inferred← citeshttps://doi.org/10.1039/d1qo01405fopenalex-snapshot
Access to azonanes via Pd-catalyzed decarboxylative [5 + 4] cycloaddition with exclusive regioselectivity
inferred← citeshttps://doi.org/10.1039/d2qo00234eopenalex-snapshot
Acid-promoted formal [3 + 2] cyclization/ N , O -ketalization of in situ generated ortho -alkynyl quinone methides: access to bridged 2,3-cyclopentanoindoline skeletons
inferred← citeshttps://doi.org/10.1039/d2qo01767aopenalex-snapshot
Strepyrrolins A–E, five pyrrole–sesquiterpene hybrids from Streptomyces sp. KIB 015, revealing a new formation logic of pyrroles by isotope labeling
inferred← citeshttps://doi.org/10.1039/d2ra01791aopenalex-snapshot
A comprehensive review on phytochemistry and pharmacology of genus Kopsia : monoterpene alkaloids – major secondary metabolites
inferred← citeshttps://doi.org/10.1039/d3np00008gopenalex-snapshot
Finding activity through rigidity: syntheses of natural products containing tricyclic bridgehead carbon centers
inferred← citeshttps://doi.org/10.1055/a-1729-9572openalex-snapshot
Transition-Metal-Catalyzed Enantioselective Synthesis of Indoles from 2-Alkynylanilines
inferred← citeshttps://doi.org/10.1080/10286020.2018.1521804openalex-snapshot
Survey of natural products reported by Asian research groups in 2017
inferred← citeshttps://doi.org/10.1080/10286020.2019.1621851openalex-snapshot
Cytotoxic monoterpenoid indole alkaloids from the aerial parts of Kopsia officinalis
inferred← citeshttps://doi.org/10.1080/10286020.2019.1680646openalex-snapshot
Cytotoxic monoterpenoid indole alkaloids from the aerial part of Kopsia arborea
inferred← citeshttps://doi.org/10.1080/14786419.2021.1984911openalex-snapshot
Two new monoterpenoid indole alkaloids from the kernels of Kopsia arborea
inferred← citeshttps://doi.org/10.1186/s12906-025-05047-xopenalex-snapshot
Chitosan nanocarriers loaded with Egyptian Calligonum comosum L'Hér. Extract: an eco-friendly approach for investigating triple-action biological activities
inferred← citeshttps://doi.org/10.2174/1570163820666230505120553openalex-snapshot
A Review of the Therapeutic Importance of Indole Scaffold in Drug Discovery
inferred← citeshttps://doi.org/10.3389/fphar.2020.00397openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fphar.2022.816025openalex-snapshot
Recent Advances in Traditional Chinese Medicine for Treatment of Podocyte Injury
inferred← citeshttps://doi.org/10.3390/molecules24244574openalex-snapshot
Bioactivity-Guided Isolation and Identification of New and Immunosuppressive Monoterpenoid Indole Alkaloids from Rauvolfia yunnanensis Tsiang
inferred← citeshttps://doi.org/10.3390/molecules26020488openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules26216516openalex-snapshot
Monoterpene Indole Alkaloids with Cav3.1 T-Type Calcium Channel Inhibitory Activity from Catharanthus roseus
inferred← citeshttps://doi.org/10.3390/molecules29102359openalex-snapshot
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