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Flabellipparicine, a Flabelliformide-Apparicine-Type Bisindole Alkaloid from Tabernaemontana divaricata

Cai, Y. S., Sarotti, A. M., Zhou, T. L., Huang, R., Qiu, G., Tian, C., Miao, Z. H., Mándi, A., Kurtán, T., Cao, S., Yang, S. P.: Flabellipparicine, a Flabelliformide-Apparicine-Type Bisindole Alkaloid from Tabernaemontana divaricata.
J. Nat. Prod. 81 (9), 1976-1983, 2018.
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Q1 Pharmacology
title:
Flabellipparicine, a Flabelliformide-Apparicine-Type Bisindole Alkaloid from Tabernaemontana divaricata
authors:
  • Cai, You-Sheng
  • Sarotti, Ariel M.
  • Zhou, Ting-Lan
  • Huang, Rong
  • Qiu, Guofu
  • Tian, Congkui
  • Miao, Ze-Hong
  • Mándi Attila
  • Kurtán Tibor
  • Cao, Shugeng
  • Yang, Sheng-Ping
published:
2018
type:
article
genre:
research article/review article
journal:
Journal Of Natural Products (ISSN: 0163-3864, 1520-6025)
language:
English
HAC:
Natural Sciences, Chemical Sciences
abstract:
Four new monoterpenoid bisindole alkaloids, flabellipparicine (1), 19,20-dihydrovobparicine (2), 10·-demethoxy-19,20-dihydrovobatensine D (3), and 3·-(2-oxopropyl)ervahanine A (4), and 10 known monoterpenoid indole alkaloids were isolated from the stems of Tabernaemontana divaricata. All structures were elucidated based on spectroscopic methods, and the absolute configuration of 1 was established using conformational analysis and TDDFT-ECD calculation of selected stereoisomers. Compound 1 represents the first flabelliformide-apparicine-type bisindole alkaloid, in which the flabelliformide-like unit connects to the apparicine-like unit with a C-3?C-22· bond and an N-1-C-16· bond to form an uncommon five-membered ring between the two monomers. All alkaloids were evaluated for their cytotoxicity against two human cancer cell lines, MCF-7 and A-549. Compounds 2, 4, and 14 exhibited cytotoxicity against MCF-7 and A-549 with IC50 values in the range of 2 nM to 8 mu M.
projects:
GINOP-2.3.2-15-2016-00008
DEENK University of Debrecen
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