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Volumn 23, Issue 24, 2013, Pages 6784-6788

Synthesis of novel 7-substituted pyrido[2′,3′:4,5]furo[3,2-d] pyrimidin-4-amines and their N-aryl analogues and evaluation of their inhibitory activity against Ser/Thr kinases

Author keywords

Dimroth rearrangement; Formamide degradation; Microwave assisted chemistry; Serine threonine kinases inhibitors; Suzuki Miyaura cross coupling

Indexed keywords

AMINE; CASEIN KINASE IDELTA; CASEIN KINASE IEPSILON; CYCLIN DEPENDENT KINASE 5; FORMAMIDE; GLYCOGEN SYNTHASE KINASE 3ALPHA; GLYCOGEN SYNTHASE KINASE 3BETA; HETEROCYCLIC COMPOUND; N,N DIMETHYLFORMAMIDE; PALLADIUM; PROTEIN P25; PROTEIN SERINE THREONINE KINASE; PYRIDO[2',3':4,5]FURO[3,2 D]PYRIMIDIN 4 AMINE DERIVATIVE; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84888861819     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2013.10.019     Document Type: Article
Times cited : (21)

References (26)
  • 8
    • 0011932271 scopus 로고    scopus 로고
    • For latest advances in microwave-assisted organic synthesis (MAOS), see: 3rd ed. Wiley-VCH Weinheim
    • For latest advances in microwave-assisted organic synthesis (MAOS), see: De la Hoz Hoz, and A. Loupy Microwaves in Organic Synthesis 3rd ed. 2013 Wiley-VCH Weinheim
    • (2013) Microwaves in Organic Synthesis
    • Hoz, D.L.H.1    Loupy, A.2
  • 9
    • 0028838971 scopus 로고
    • T. Hunter Cell 80 1995 225
    • (1995) Cell , vol.80 , pp. 225
    • Hunter, T.1
  • 17
    • 0015417053 scopus 로고
    • In this Letter, proposals are presented for the stepwise selection for synthesis of analogues of an active compound. The diagrams are based on a fundamental assumption of the Hansch method that a particular substituent may modify activity relative to the parent compound by virtue of resulting changes in hydrophobic, electronic and steric effects. In the case of our study, using the Topliss scheme allowed us to choose certain reagents to check the interest of our methodology, while starting to build a list of molecules with potential biological interest
    • In this Letter, proposals are presented for the stepwise selection for synthesis of analogues of an active compound. The diagrams are based on a fundamental assumption of the Hansch method that a particular substituent may modify activity relative to the parent compound by virtue of resulting changes in hydrophobic, electronic and steric effects. In the case of our study, using the Topliss scheme allowed us to choose certain reagents to check the interest of our methodology, while starting to build a list of molecules with potential biological interest. J.G. Topliss J. Med. Chem. 15 1972 1006
    • (1972) J. Med. Chem. , vol.15 , pp. 1006
    • Topliss, J.G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.