MUTAGENICITY OF 4 HOMO-AZA-STEROIDAL ESTERS OF M-N, N-BIS(2-CHLOROETHYL)AMINOCINNAMIC ACID IN THE AMES TEST

Citation
G. Voutsinas et al., MUTAGENICITY OF 4 HOMO-AZA-STEROIDAL ESTERS OF M-N, N-BIS(2-CHLOROETHYL)AMINOCINNAMIC ACID IN THE AMES TEST, MUTATION RESEARCH, 319(4), 1993, pp. 325-329
Citations number
11
Categorie Soggetti
Genetics & Heredity",Toxicology
Journal title
ISSN journal
00275107
Volume
319
Issue
4
Year of publication
1993
Pages
325 - 329
Database
ISI
SICI code
0027-5107(1993)319:4<325:MO4HEO>2.0.ZU;2-B
Abstract
Four new chemicals, the homo-aza-steroidal esters of m-N,N-bis(2-chlor oethyl)aminocinnamic acid, originaly synthesized to be used as antineo plastic agents, were tested for their mutagenic activity in the Ames t est. 3 beta-Hydroxy-13 a-amino-13,17-seco-5-androsten-17-oic-13,17-lac tam ester (ACALE3) and 3 alpha-hydroxy-13 alpha-amino-13,17-seco-5 alp ha-androstan-17-oic-13,17-lactam ester of m-N,N-bis(2-chloro-ethyl)ami nocinnamic acid (ACALE4) were found to induce base-pair substitutions, causing dose-dependent increases in his(+) revertants in strains TA10 0 and TA1535, while no dose-dependent relations were established when 3 beta-hydroxy-13 alpha-amino-13,17-seco-5 alpha-androstan-17-oic-13,1 7-lactam ester (ACALE1) and 17 beta-hydroxy-3-aza-A-homo-4 alpha-andro sten-4-one ester of m-N,N-bis(2-chroroethyl)aminocinnamic acid (ACALE2 ) were tested. The presence of metabolic activation enzymes in the tes t system had no effect in his(+) revertants in strains TA100 and TA153 5. The chemicals tested although having the same alkylating moiety and a similar chemical structure exhibited different mutagenic activities .