2007
DOI: 10.1039/b516351j
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Simple indole alkaloids and those with a nonrearranged monoterpenoid unit

Abstract: This review covers the literature on simple indole alkaloids and those with a nonrearranged monoterpenoid unit. Newly isolated alkaloids, structure determinations, total syntheses and biological activities are included.

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Cited by 287 publications
(59 citation statements)
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References 182 publications
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“…+ , 607 (95) 1,143.3,138.9,138.8,138.3,135.2,132.7,129.8,128.5,128.3,127.5,127.4,126.2,126.0,125.8,125.8,125.3,125.1,124.4,124.1,123.4,121.2,120.8,120.7,114.6,113.1,112.9,107.5,101.5,100.1,37.8;: m/z (relative intensity) = 598 (100) [M] + ; HR-MS: m/z = 598.0654, calcd. for C 35 H 19 IN 4 [M] + : 598.0650.…”
Section: ; Lr-ms (Ei): M/z (Relative Intensity) = 608 (100) [M]mentioning
confidence: 99%
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“…+ , 607 (95) 1,143.3,138.9,138.8,138.3,135.2,132.7,129.8,128.5,128.3,127.5,127.4,126.2,126.0,125.8,125.8,125.3,125.1,124.4,124.1,123.4,121.2,120.8,120.7,114.6,113.1,112.9,107.5,101.5,100.1,37.8;: m/z (relative intensity) = 598 (100) [M] + ; HR-MS: m/z = 598.0654, calcd. for C 35 H 19 IN 4 [M] + : 598.0650.…”
Section: ; Lr-ms (Ei): M/z (Relative Intensity) = 608 (100) [M]mentioning
confidence: 99%
“…[1] Particularly, the seven-membered ring (azulene) annulated tetracyclic indole moiety occurs in numerous biologically active natural products and pharmaceutical intermediates, which display potent antihistaminic, antimicrobial and anticancer activities. [1,2] In general, the construction of medium sized rings is unambiguously considered to be a cumbersome task due to a combination of the transannular interactions and unfavourable entropic and enthalpic factors.…”
Section: Introductionmentioning
confidence: 99%
“…They are committed to synthesizing bisindole derivatives, testing drug properties, and separating new molecules. [3,4] In this review, we discussed the bioactivities and biosynthetic pathways of bisindole compounds.…”
Section: Introductionmentioning
confidence: 99%
“…Many indole molecules have been isolated from natural substances, and most of them own significant medicinal properties. [2] A hundreds of bisindole molecules [3] were separated and characterized, but their biosynthetic mechanisms have been largely unexplored. This bisindole compounds have been isolated from the shawls, sponges, plant leaves, roots, bark, flowers, algae, fungi and mycotic fungi, [3] most commonly isolated from actinomycetes, [3] a class of bacteria known for production of secondary metabolites.…”
Section: Introductionmentioning
confidence: 99%
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