Synthesis, antimicrobial, antimycobacterial and structure-activity relationship of substituted pyrazolo-, isoxazolo-, pyrimido- and mercaptopyrimidocyclohepta[b]indoles.

Yamuna, E and Kumar , RA and Zeller, M and Rajendra Prasad , K J (2012) Synthesis, antimicrobial, antimycobacterial and structure-activity relationship of substituted pyrazolo-, isoxazolo-, pyrimido- and mercaptopyrimidocyclohepta[b]indoles. European journal of medicinal chemistry, 47. 228-238. ISSN 1768-3254

Preview

Text
synthesis antimicrobial (eur jou of med chem).pdf
Download (877Kb) | Preview

Official URL: https://www.ncbi.nlm.nih.gov/pubmed/22119150

Abstract

A new class of heterocycles, specifically substituted pyrazolo-, isoxazolo- and pyrimidocyclohepta[b]indoles, has been prepared by condensation of substituted 7-(hydroxymethylene)-7,8,9,10-tetrahydrocyclohepta[b]indol-6(5H)-ones with hydrazine hydrate, hydroxylamine hydrochloride, phenylhydrazine, urea and thiourea, respectively. The structures of the compounds were established by IR, (1)H NMR, (13)C NMR, mass spectral analysis, X-ray diffraction, and the compounds have been screened for in vitro antimicrobial and antimycobacterial against Mycobacterium tuberculosis H37Rv (MTB). Among the compounds screened, five substances were found to have an MIC of 3.12 μg/ml or greater against MTB. Structure-activity relationship (SAR) analyses and in silico drug relevant properties (HBD, HBA, PSA, c Log P, M.wt) confirmed that the compounds are potential lead compounds for future drug discovery studies.

Item Type:	Article
Uncontrolled Keywords:	Cyclohepta[b]indoles; Antimicrobial; Antimycobacterial; Structure–activity relationship; In silico drug relevant properties
Subjects:	Parasite Biology
Depositing User:	Central Library RGCB
Date Deposited:	22 Dec 2016 06:55
Last Modified:	04 Jul 2019 07:06
URI:	http://rgcb.sciencecentral.in/id/eprint/51

Actions (login required)

View Item