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Gelstriamine A, a Triamino Monoterpene Indole Alkaloid with a Caged 6/5/7/6/6/5 Scaffold and Analgesic Alkaloids from Gelsemium elegans Stems

https://doi.org/10.1021/acs.jnatprod.1c00062

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What this work says

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

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Monoterpenoid Indole Alkaloids Bearing an N4‐Iridoid from Gelsemium elegans

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Chiroptical properties of binuclear rhodium complexes of lanostane alcohols

inferredcites →https://doi.org/10.1016/0031-9422(90)87125-eopenalex-snapshot

Two oxindole alkaloids from Gelsemium elegans

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Medicinal plants of the genus Gelsemium (Gelsemiaceae, Gentianales)—A review of their phytochemistry, pharmacology, toxicology and traditional use

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Rhodomicranosides A−I, analgesic diterpene glucosides with diverse carbon skeletons from Rhododendron micranthum

inferredcites →https://doi.org/10.1016/j.phytochem.2019.112113openalex-snapshot

Analgesic diterpenoids with diverse carbon skeletons from the leaves of Rhododendron auriculatum

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Grayanane diterpenoid glucosides as potent analgesics from Pieris japonica

inferredcites →https://doi.org/10.1016/j.tet.2009.03.086openalex-snapshot

Gelegamines A–E: five new oxindole alkaloids from Gelsemium elegans

inferredcites →https://doi.org/10.1016/s0031-9422(00)95223-3openalex-snapshot

Oxindole alkaloids from Gelsemium elegans

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Studies on the indole alkaloids of gelsem1um elegans (thailand): structure elucidation and proposal of biogenetic route

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[Rh2(OCOCF3)4] as an auxiliary chromophore in chiroptical studies on steroidal alcohols

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Grayanane Diterpenoid Glucosides from the Leaves of Rhododendron micranthum and Their Bioactivities Evaluation

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Grayanane Diterpenoids from the Leaves of Rhododendron auriculatum and Their Analgesic Activities

inferredcites →https://doi.org/10.1021/acs.jnatprod.9b00569openalex-snapshot

Antinociceptive Grayanane Diterpenoids from the Leaves of Pieris japonica

inferredcites →https://doi.org/10.1021/acs.joc.8b00736openalex-snapshot

Gelsecorydines A–E, Five Gelsedine–Corynanthe-Type Bisindole Alkaloids from the Fruits of Gelsemium elegans

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Alstoscholarisines H–J, Indole Alkaloids from Alstonia scholaris: Structural Evaluation and Bioinspired Synthesis of Alstoscholarisine H

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Gelsekoumidines A and B: Two Pairs of Atropisomeric Bisindole Alkaloids from the Roots of Gelsemium elegans

inferredcites →https://doi.org/10.1021/acs.orglett.8b03323openalex-snapshot

Purpurolide A, 5/5/5 Spirocyclic Sesquiterpene Lactone in Nature from the Endophytic Fungus Penicillium purpurogenum

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Combining the Power of J Coupling and DP4 Analysis on Stereochemical Assignments: The J -DP4 Methods

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Assigning Stereochemistry to Single Diastereoisomers by GIAO NMR Calculation: The DP4 Probability

inferredcites →https://doi.org/10.1021/ja901219vopenalex-snapshot

Total Synthesis of the Akuammiline Alkaloid (±)-Vincorine

inferredcites →https://doi.org/10.1021/np060016oopenalex-snapshot

Isolation of Gelsedine-Type Indole Alkaloids from Gelsemium elegans and Evaluation of the Cytotoxic Activity of Gelsemium Alkaloids for A431 Epidermoid Carcinoma Cells

inferredcites →https://doi.org/10.1021/np200706nopenalex-snapshot

Cucurbitane Glucosides from the Root of Machilus yaoshansis

inferredcites →https://doi.org/10.1021/np400202fopenalex-snapshot

Guaiane-Type Sesquiterpenes from Curcuma phaeocaulis and Their Inhibitory Effects on Nitric Oxide Production

inferredcites →https://doi.org/10.1021/np4005536openalex-snapshot

Bisindole Alkaloids with Neural Anti-inflammatory Activity from Gelsemium elegans

inferredcites →https://doi.org/10.1021/np50063a019openalex-snapshot

New Humantenine-Type Alkaloids from Gelsemium elegans

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First Direct and Detailed Stereochemical Analysis of Strictosidine

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Enantioselective Total Synthesis of (+)-Reserpine

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Zephycandidine A, the First Naturally Occurring Imidazo[1,2-f]phenanthridine Alkaloid from Zephyranthes candida, Exhibits Significant Anti-tumor and Anti-acetylcholinesterase Activities

inferredcites →https://doi.org/10.1039/b711935fopenalex-snapshot

Structural biology in plant natural product biosynthesis—architecture of enzymes from monoterpenoid indole and tropane alkaloid biosynthesis

inferredcites →https://doi.org/10.1039/c3ob40843dopenalex-snapshot

Successful combination of computationally inexpensive GIAO 13C NMR calculations and artificial neural network pattern recognition: a new strategy for simple and rapid detection of structural misassignments

inferredcites →https://doi.org/10.1039/c9qo01320bopenalex-snapshot

Modified diterpenoids from the tuber of Icacina oliviformis as protein tyrosine phosphatase 1B inhibitors

inferredcites →https://doi.org/10.1039/c9qo01538hopenalex-snapshot

Discovery of highly functionalized 5,6- seco -grayanane diterpenoids as potent competitive PTP1B inhibitors

inferredcites →https://doi.org/10.1039/d0qo00735hopenalex-snapshot

Spirodesertols A and B, two highly modified spirocyclic diterpenoids with an unprecedented 6-isopropyl-3 H -spiro[benzofuran-2,1′-cyclohexane] motif from Salvia deserta

inferredcites →https://doi.org/10.1039/j39700000791openalex-snapshot

The alkaloids of Gelsemium sempervirens. Part III. Sempervirine

inferredcites →https://doi.org/10.1039/p19910001773openalex-snapshot

Stereoselective transformation of ajmaline into three minor Gelsemium alkaloids, koumidine, (19Z)-anhydrovobasinediol [(19Z)-taberpsychine] and N-demethoxyrankinidine and their absolute configuration

inferredcites →https://doi.org/10.1080/10286020.2010.492951openalex-snapshot

Antitumor activity of two gelsemine metabolites in rat liver microsomes

inferredcites →https://doi.org/10.1080/10286020.2012.742511openalex-snapshot

Four new koumine metabolites in rat liver microsomes

inferredcites →https://doi.org/10.1126/science.aat4100openalex-snapshot

Missing enzymes in the biosynthesis of the anticancer drug vinblastine in Madagascar periwinkle

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

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inferred← citeshttps://doi.org/10.1016/j.tet.2021.132572openalex-snapshot

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