Results 81 to 90 of about 48,569 (170)

Strychnobaillonine, an Unsymmetrical Bisindole Alkaloid with an Unprecedented Skeleton from Strychnos icaja Roots

open access: yes, 2016
A reinvestigation of the roots of Strychnos icaja resulted in the isolation of a new bisindole alkaloid named strychnobaillonine (1) with original C-17–N-1′ and C-23–C-17′ junctions, in addition to sungucine, bisnordihydrotoxiferine, and strychnohexamine
Georges Dive (1816540)   +6 more
core   +1 more source

Biscarpamontamines A and B, an Aspidosperma−Iboga Bisindole Alkaloid and an Aspidosperma−Aspidosperma Bisindole Alkaloid, from Tabernaemontana sphaerocarpa

open access: yes, 2016
Two new bisindole alkaloids, biscarpamontamine A (1), possessing an aspidosperma−iboga-type skeleton, and biscarpamontamine B (2), having an aspidosperma−aspidosperma-type skeleton, were isolated from stems of Tabernaemontana sphaerocarpa, and their ...
Motoo Shiro (1670407)   +9 more
core   +2 more sources

Synthesis and Assignment of the Absolute Configuration of Indenotryptoline Bisindole Alkaloid BE-54017

open access: yes, 2016
Synthesis of the indenotryptoline bisindole alkaloid, BE-54017, was accomplished using osmium-promoted cis-dihydroxylation of maleimide as a key step. After optical resolution, the absolute configuration of this molecule was determined by comparing its ...
Tomoyuki Kimura (1896370)   +5 more
core   +1 more source

Synthesis of Topsentin‐A, A Bisindole Alkaloid of the Marine Sponge Topsentia genitrix

open access: yesBulletin des Sociétés Chimiques Belges, 1987
AbstractThe synthesis of topsentin‐A, a bisindole alkaloid isolated from the maring sponge Topsentia genitrix, has been achieved starting from 3‐acetylindole.
Braekman, Jean Claude   +2 more
openaire   +3 more sources

Cytotoxic Bisindole Alkaloids from a Marine Sponge Spongosorites sp.

open access: yes, 2016
Three new bisindole alkaloids of the hamacanthin class (1−3) and one new bisindole alkaloid of the topsentin class (6) were isolated along with known bisindole alkaloids (4, 5, 7−11) from the MeOH extract of a marine sponge Spongosorites sp.
Qishi Sun (2681866)   +7 more
core   +1 more source

Effect and Structure-Activity Relationship Between Isatin and its Dimer Indirubin on Neural Development of Transgenic Zebrafish

open access: yesNatural Product Communications
Objective Isatin (2,3-indolinedione, ISA), as an indole oxide, is widely distributed in mammalian tissues and fluids, with concentrations varying from less than 0.1 to greater than 10 μM. Indirubin (2-(2-oxo-1h-indol-3-ylidene)-1h-indol-3-one, IND), as a
Yonghua Liu   +7 more
doaj   +1 more source

Bisindole alkaloids

open access: yes, 2006
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 ...
Choo, Yeun Mun, Kam, Toh Seok
core   +1 more source

Cathagines A–D, new bisindole alkaloids from Catharanthus roseus

open access: yesJournal of Natural Medicines
Four new bisindole alkaloids, cathagines A (1)-D (4) consisting of an aspidosperma and the fused tetracyclic 3-spirooxindole derived from an iboga type skeleton were isolated from the whole plant of Catharanthus roseus. The structures including absolute stereochemistry were elucidated on the basis of 2D NMR data and CD spectra.
Yusuke, Hirasawa   +8 more
openaire   +2 more sources

Angustifonines A and B, Cytotoxic Bisindole Alkaloids from Bousigonia angustifolia

open access: yes, 2016
Two new bisindole alkaloids, angustifonines A (1) and B (2), comprising the union of a rearranged monoterpenoid quinoline and an aspidospermine alkaloid, as well as 27 known indole alkaloids were isolated from the twigs and leaves of Bousigonia ...
Yu Zhang (12946)   +5 more
core   +1 more source

Ajmaline, Oxindole, and Cytotoxic Macroline–Akuammiline Bisindole Alkaloids from Alstonia penangiana

open access: yes, 2018
Examination of the EtOH extract of the Malayan Alstonia penangiana resulted in the isolation of 10 new alkaloids, comprising two ajmaline (1, 2), four macroline oxindole (3–6), and four macroline–akuammiline bisindole alkaloids (7–10).
Suerialoasan Navanesan (785142)   +7 more
core   +1 more source

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