Results 131 to 140 of about 1,055 (166)
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Leucophyllinines A and B, bisindole alkaloids from Leuconotis eugeniifolia
Journal of Natural Medicines, 2019Two new bisindole alkaloids, leucophyllinines A (1) and B (2) consisting of eburnane and quebrachamine-type skeletons were isolated from the bark of Leuconotis eugeniifolia, and their structures were elucidated on the basis of spectroscopic data. Leucophyllinines A and B showed antiplasmodial activities against Plasmodium falciparum 3D7.
Toshihiro Horii, Takahiro Tougan
exaly +4 more sources
Alternative partial synthesis of bisindole alkaloids
Tetrahedron Letters, 1990Abstract Indoline derivatives of the pericyclivine series are oxidized at position 6 with DDQ; the corresponding alcohols are coupled with nucleophilic indolines under acid conditions to yield dimers similar to undulatine.
G. Massiot +3 more
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Development of novel telomerase inhibitors based on a Bisindole unit
Bioorganic & Medicinal Chemistry Letters, 2001Telomerase is the enzyme that elongates telomere repeat at the ends of a chromosome. As high telomerase activity is observed in most cancer cells, inhibitors of human telomerase have been expected as new chemotherapeutic agents for cancer. We describe here the discovery of novel inhibitors with IC50 values in the submicromolar range.
S, Sasaki +7 more
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2006
Publisher Summary This chapter provides an overview on bisindole alkaloids. The indole–indole and tryptamine–tryptamine type, and related alkaloids are discussed. Tryptamine–tryptamine type with an additional monoterpene unit and related alkaloids are briefly discussed.
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Publisher Summary This chapter provides an overview on bisindole alkaloids. The indole–indole and tryptamine–tryptamine type, and related alkaloids are discussed. Tryptamine–tryptamine type with an additional monoterpene unit and related alkaloids are briefly discussed.
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The bisindole alkaloid catharine
Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 1976J. Guilhem +3 more
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Synthetic strategies for the construction of C3–N1′ bisindoles
Organic & Biomolecular ChemistryNatural products having a C3–N1′ bisindole framework are unique structures with potential axial chirality. This minireview summarizes the recent progress of the methodology for constructing C3–N1′ bisindoles along with the possible mechanism.
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Synthesis of a bisindole enyne with anticancer properties
Journal of the Indian Chemical Society, 2023Ganesh Chandra Midya +3 more
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