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Marine Natural Products as Potent Anticancer Agents (2020-2024): Structural Diversity, SARs and Target Prediction. [PDF]
Huang Z +7 more
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Advances in microbial biosynthesis of indirubin. [PDF]
Li K +8 more
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l-Proline catalysed synthesis and in silico studies of novel α-cyano bis(indolyl)chalcones as potential anti-cancer agents. [PDF]
Malik M +5 more
europepmc +1 more source
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Crooksiine, a bisindole alkaloid from Haplophyton crooksii
Phytochemistry, 1991Abstract Crooksiine, a new bisindole alkaloid with antiacetylcholinesterase activity was isolated from Haplophyton crooksii . Its structure was established utilizing spectrometric methods.
Mohamad Mroue, Maktoob Alam
exaly +2 more sources
Ceridimine: a novel type of bisindole monoterpene alkaloid
Journal of the Chemical Society Chemical Communications, 1986The structure determination and synthesis of ceridimine (1), a novel type of bisindole monoterpene alkaloid isolated from Pagiantha cerifera(Apocynaceae), are reported.
Michel Koch
exaly +2 more sources
Bisindole alkaloid artifacts from Gonioma malagasy
Tetrahedron Letters, 2013Abstract Three new bisindole alkaloids ( 1 – 3 ), possessing a rare carbon skeleton formed by two indole moieties fused via a dihydropyran unit, were isolated from the alkaloid extract of the stem bark of Gonioma malagasy . Their structure and absolute configuration were assigned thanks to a combination of one and two dimensional NMR spectroscopy ...
Marc Litaudon +2 more
exaly +3 more sources
Vincazalidine A, a unique bisindole alkaloid from Catharanthus roseus
Journal of Natural MedicinesA new dimeric indole alkaloid, vincazalidine A consisting of an aspidosperma type and a modified iboga type with 1-azatricyclo ring system consisting of one azepane and two piperidine rings coupled with an oxazolidine ring was isolated from Catharanthus roseus, and the structure including absolute stereochemistry was elucidated on the basis of ...
, Yusuke Hirasawa, Nahoko Uchiyama
exaly +3 more sources
Partial synthesis of the antiamoebic bisindole alkaloid (−)-macrocarpamine
Tetrahedron Letters, 1996Abstract The partial synthesis of the antiamoebic bisindole alkaloid (−)-macrocarpamine 1 has been completed by coupling (−)-anhydromacrosalhine-methine 2 with plant-derived (+)-pleiocarpamine 3 in anhydrous 0.2 N HCl in THF in 75% yield.
James Cook, Tong Gan
exaly +2 more sources
Biomimetic synthesis and structure of the bisindole alkaloid alstonisidine
Journal of the Chemical Society Chemical Communications, 1972Alstonisidine, a bisindole alkaloid from Alstonia muelleriana, is assigned the revised structure (II) on the basis of its biomimetic synthesis from quebrachidine (III) and macroline (IV).
James Cook
exaly +2 more sources

