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Volumn 5, Issue 5, 2014, Pages 665-670

Aminophosphonates as novel anti-leishmanial chemotypes: Synthesis, biological evaluation, and CoMFA studies

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EID: 84899415448     PISSN: 20402503     EISSN: 20402511     Source Type: Journal    
DOI: 10.1039/c3md00388d     Document Type: Article
Times cited : (61)

References (49)
  • 40
    • 33846979813 scopus 로고    scopus 로고
    • the references cited therein The reported procedure to prepare α-aminophosphonates under catalyst- and solvent-free conditions requires heating at 75-80 °C
    • S. Bhagat A. K. Chakraborti J. Org. Chem. 2007 72 1263 1270
    • (2007) J. Org. Chem. , vol.72 , pp. 1263-1270
    • Bhagat, S.1    Chakraborti, A.K.2
  • 42
    • 0021061819 scopus 로고
    • Pyrimidine nucleoside aminophosphonate hybrids have been reported to be inactive against L. donovani
    • T. Mosmann J. Immunol. Methods 1983 65 55 63
    • (1983) J. Immunol. Methods , vol.65 , pp. 55-63
    • Mosmann, T.1
  • 48
    • 84876459358 scopus 로고    scopus 로고
    • Tripos Associate Inc., 1699, S. Hanley Rd., St. Louis, MO 631444, USA
    • SYBYL7.1, Tripos Associate Inc., 1699, S. Hanley Rd., St. Louis, MO 631444, USA
    • SYBYL7.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.