Structure of the peptide antibiotic stendomycin
…, J Izdebski, I Muramatsu
Index: Bodanszky; Izdebski; Muramatsu Journal of the American Chemical Society, 1969 , vol. 91, # 9 p. 2351 - 2358
Full Text: HTML
Citation Number: 44
Abstract
Abstract: Stendomycin, an antifungal peptide antibiotic, is a mixture of closely related compounds. Their amino acid sequence was elucidated mainly through the study of peptides from partial acid hydrolysates. In all members of the stendomycin family the N- terminal amino acid, proline, is acylated by a branched-chain fatty acid; the C-terminal amino acid, a cyclic derivative of arginine, forms a lactone bond with the hydroxyl group of ...
Related Articles:
Direct asymmetric intermolecular aldol reactions catalyzed by amino acids and small peptides
[Cordova, Armando; Zou, Weibiao; Dziedzic, Pawel; Ibrahem, Ismail; Reyes, Efraim; Xu, Yongmei Chemistry - A European Journal, 2006 , vol. 12, # 20 p. 5383 - 5397]
Direct asymmetric intermolecular aldol reactions catalyzed by amino acids and small peptides
[Cordova, Armando; Zou, Weibiao; Dziedzic, Pawel; Ibrahem, Ismail; Reyes, Efraim; Xu, Yongmei Chemistry - A European Journal, 2006 , vol. 12, # 20 p. 5383 - 5397]
[Lyons, Anthony Q.; Pettit, Leslie D. Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1984 , p. 2305 - 2308]
A mild Boc deprotection and the importance of a free carboxylate
[Thaqi, Ali; McCluskey, Adam; Scott, Janet L. Tetrahedron Letters, 2008 , vol. 49, # 49 p. 6962 - 6964]
Amino group protection in peptide synthesis. 4, 5-Diphenyl-4-oxazolin-2-one group
[Sheehan,J.C.; Guziec,F.S. Journal of Organic Chemistry, 1973 , vol. 38, p. 3034 - 3040]