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Volumn 38, Issue 4, 1999, Pages 448-476

Bleomycin: Synthetic and mechanistic studies

Author keywords

Antitumor agent; Bioorganic chemistry; Bleomycin; DNA cleavage; Total synthesis

Indexed keywords

BLEOMYCIN A2;

EID: 0033558171     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1521-3773(19990215)38:4<448::aid-anie448>3.0.co;2-w     Document Type: Review
Times cited : (161)

References (231)
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    • 33745121166 scopus 로고    scopus 로고
    • note
    • In retrospect, the latter observations of Mascharak are especially interesting, but on the surface curious. They do not incorporate the key C4 amino group that is implicated in the structural studies of Stubbe et al. and discussed in detail in Section 3.2.8. They do, however, maintain the bleomycin pyrimidine N3, which acts as a H-bond acceptor from the guanine C2-amine cleavage site. It is conceivable that a reduced guanine cleavage selectivity is derived from a single versus double H-bonding interaction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.