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Volumn 20, Issue 9, 2010, Pages 2876-2879

Discovery and structural optimization of pyrazole derivatives as novel inhibitors of Cdc25B

Author keywords

Cdc25B inhibitor; Pyrazole derivatives; Structural optimization

Indexed keywords

3,5 DIACYL PYRAZOLE DERIVATIVE; BN 82685; MALEIMIDE; NSC 663284; PROTEIN TYROSINE PHOSPHATASE; PYRAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77950860029     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2010.03.040     Document Type: Article
Times cited : (21)

References (31)
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    • 2 under acidic condition to give ethyl diazoacetate 2a. Through converting corresponding carboxylic acids to acyl chlorides, then acylating diazomethane, compounds 2b-e were prepared. Katritzky A.R., Meth-Cohn O., and Rees C.W. (Eds), Pergamon Press, Oxford pp 144 and 276
    • 2 under acidic condition to give ethyl diazoacetate 2a. Through converting corresponding carboxylic acids to acyl chlorides, then acylating diazomethane, compounds 2b-e were prepared. Mulzer J. In: Katritzky A.R., Meth-Cohn O., and Rees C.W. (Eds). Comprehensive Organic Functional Group Transformations (1995), Pergamon Press, Oxford pp 144 and 276
    • (1995) Comprehensive Organic Functional Group Transformations
    • Mulzer, J.1
  • 28
    • 77950866062 scopus 로고    scopus 로고
    • note
    • +) 497.33.
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    • note
    • +) 503.28.
  • 30
    • 77950858290 scopus 로고    scopus 로고
    • note
    • The reversible binding assay were carried out by preincubation 0.12 μM compound 118 with Cdc25, then dialyzed for indicated time for activity recovery.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.