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Volumn 66, Issue 13, 2010, Pages 2520-2528

Synthesis of new mono and bis amides projected as potential histone deacetylase (HDAC) inhibitors

Author keywords

Anticancer drugs; Docking studies; Histone deacetylase; Ring closing metathesis reaction

Indexed keywords

AMIDE; ANTINEOPLASTIC AGENT; DOCKING PROTEIN; HETEROCYCLIC COMPOUND; HISTONE DEACETYLASE; HISTONE DEACETYLASE INHIBITOR; ZINC;

EID: 77349125579     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.01.061     Document Type: Article
Times cited : (9)

References (42)
  • 12
    • 77349090732 scopus 로고    scopus 로고
    • note
    • In the calculation, the amine functionality of structures 2, 4, and 6 was considered protonated at physiological pH.
  • 14
    • 33644853300 scopus 로고    scopus 로고
    • Schrödinger LLC, New York, NY
    • MacroModel, Version 8.5 (2003), Schrödinger LLC, New York, NY
    • (2003) MacroModel, Version 8.5
  • 23
    • 77349094299 scopus 로고    scopus 로고
    • note
    • The partial charges of the zinc ion, and of the amino acids involved in the catalytic center (A169, H170, D168, D258) have been calculated at DFT B3LYP level and 6-31G(d) basis set using the Chelpg method for population analysis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.