PAECILOQUINONE-A, PAECILOQUINONE-B, PAECILOQUINONE-C, PAECILOQUINONE-D, PAECILOQUINONE-E AND PAECILOQUINONE-F - NEW POTENT INHIBITORS OF PROTEIN-TYROSINE KINASE PRODUCED BY PAECILOMYCES-CARNEUS .2. CHARACTERIZATION AND STRUCTURE DETERMINATION

Citation
A. Fredenhagen et al., PAECILOQUINONE-A, PAECILOQUINONE-B, PAECILOQUINONE-C, PAECILOQUINONE-D, PAECILOQUINONE-E AND PAECILOQUINONE-F - NEW POTENT INHIBITORS OF PROTEIN-TYROSINE KINASE PRODUCED BY PAECILOMYCES-CARNEUS .2. CHARACTERIZATION AND STRUCTURE DETERMINATION, Journal of antibiotics, 48(3), 1995, pp. 199-204
Citations number
10
Categorie Soggetti
Pharmacology & Pharmacy",Immunology,"Biothechnology & Applied Migrobiology
Journal title
ISSN journal
00218820
Volume
48
Issue
3
Year of publication
1995
Pages
199 - 204
Database
ISI
SICI code
0021-8820(1995)48:3<199:PPPP>2.0.ZU;2-6
Abstract
Paeciloquinones A to F and versiconol have been isolated as inhibitors of protein tyrosine kinases from the culture broth of the fungus Paec ilomyces carneus P-177. The structures of the new anthraquinones were determined by spectroscopic methods, mainly H-1 NMR and C-13 NMR. The substitution pattern was established by investigation of the respectiv e methylated derivatives.