Synthesis and Anticancer Activity Evaluation of Azepinobisindoles; the Isomeric Iheyamine A Derivatives
作者:Weerachai Phutdhawong、Sopita Rattanopas、Jitnapa Sirirak、Thongchai Taechowisan、Waya S. Phutdhawong
DOI:10.13005/ojc/350231
日期:2019.4.25
Azepinobisindole derivatives, the isomeric Iheyamine skeleton, were prepared and their anticancer activity evaluation were investigated against two human cancer cell lines, Hepatocellular carcinoma (HepG2) and human cervical cancer line (HeLa) as well as the normal cell line (Vero cell line) using MTT assay. The anticancer activity results indicated that 2-methoxy-5-methyl5H-azepino[2,3-b:4,5-b]diindole
A Compact Approach to an Isomeric Iheyamine A System and X-ray Crystal Structure of 5-Methyl-5<i>H</i>-azepino[2,3-<b> <i>b</i> </b>:4,5-<b> <i>b</i> </b>′]diindole
作者:John B. Bremner、Waya Sengpracha、Brian W. Skelton
DOI:10.1080/00397910801997603
日期:2008.5.23
A compact three-step synthesis of a new fused bisindole system isomeric with the heterocyclic skeleton present in the marine natural product iheyamine A has been achieved. The structure of the synthetic product was confirmed by a single-crystal X-ray structure.
SPIRO-INDOLE DERIVATIVES FOR THE TREATMENT OF PARASITIC DISEASES