Your browser doesn't support javascript.
loading
Porothramycin, a new antibiotic of the anthramycin group: production, isolation, structure and biological activity.
Tsunakawa, M; Kamei, H; Konishi, M; Miyaki, T; Oki, T; Kawaguchi, H.
Affiliation
  • Tsunakawa M; Bristol-Myers Research Institute, Tokyo Research Center, Japan.
J Antibiot (Tokyo) ; 41(10): 1366-73, 1988 Oct.
Article in En | MEDLINE | ID: mdl-3192492
A new antitumor antibiotic porothramycin was produced by a new strain of Streptomyces albus. The antibiotic was isolated in two active forms, the natural free hydroxyl form (porothramycin A) or the crystalline methyl ether form (porothramycin B) depending upon the isolation process used. Structural studies established that porothramycin is a new member of the pyrrolo[1,4]benzodiazepine group antibiotics having only one substituent on the benzene ring. The antibiotic exhibited antimicrobial activity against Gram-positive bacteria and anaerobes and significantly prolonged the survival times of mice implanted with experimental tumors.
Subject(s)
Search on Google
Database: MEDLINE Main subject: Benzodiazepinones / Anthramycin / Antibiotics, Antineoplastic Limits: Animals Language: En Journal: J Antibiot (Tokyo) Year: 1988 Type: Article Affiliation country: Japan
Search on Google
Database: MEDLINE Main subject: Benzodiazepinones / Anthramycin / Antibiotics, Antineoplastic Limits: Animals Language: En Journal: J Antibiot (Tokyo) Year: 1988 Type: Article Affiliation country: Japan