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Volumn 60, Issue 9, 2007, Pages 565-571

Antibacterial evaluations of thiazomycin - A potent thiazolyl peptide antibiotic from Amycolatopsis fastidiosa

Author keywords

Antibiotics; Natural products; Protein synthesis inhibitors; Thiazolyl peptide

Indexed keywords

AMINOSUGAR; BETA LACTAM; GENOMIC DNA; OXAZOLIDINONE DERIVATIVE; POLYPEPTIDE ANTIBIOTIC AGENT; QUINOLONE DERIVATIVE; RNA 23S; THIAZOMYCIN; UNCLASSIFIED DRUG; VANCOMYCIN; ANTIINFECTIVE AGENT; CYCLOPEPTIDE; PEPTIDE; PROTEIN SYNTHESIS INHIBITOR; RIBOSOME RNA; THIAZOLE DERIVATIVE;

EID: 38449116767     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.1038/ja.2007.71     Document Type: Article
Times cited : (44)

References (21)
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  • 11
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    • Synthesis of novel nocathiacin-class antibiotics. Condensation of glycolaldehyde with primary amides and tandem reductive amination of amadori-rearranged 2-oxoethyl intermediates
    • Hrnciar P, Ueda Y, Huang S, Leet JE, Bronson JJ. Synthesis of novel nocathiacin-class antibiotics. Condensation of glycolaldehyde with primary amides and tandem reductive amination of amadori-rearranged 2-oxoethyl intermediates. J Org Chem 67: 8789-8793 (2002)
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    • Li W, Leet JE, Ax HA, Gustavson DR, Brown DM, Turner L, Brown K, Clark J, Yang H, Fung-Tomc J, Lam KS. Nocathiacins, new thiazolyl peptide antibiotics from Nocardia sp. I. Taxonomy, fermentation and biological activities. J Antibiot 56: 226-231 (2003)
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    • Mild method for cleavage of dehydroalanine units: Highly efficient conversion of nocathiacin I to nocathiacin IV
    • Regueiro-Ren A, Ueda Y. Mild method for cleavage of dehydroalanine units: highly efficient conversion of nocathiacin I to nocathiacin IV. J Org Chem 67: 8699-8702 (2002)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.