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Volumn 25, Issue 22, 2015, Pages 5258-5264

Discovery of 3,5-substituted 6-azaindazoles as potent pan-Pim inhibitors

Author keywords

Fragment based screen; Kinase inhibitor; Lead optimization; Pim kinases; Screening; Structure based drug design

Indexed keywords

1H PYRAZOLO[3,4 C]PYRIDINE(6 AZAINDAZOLE); ADENOSINE TRIPHOSPHATE; INDAZOLE DERIVATIVE; PHOSPHOTRANSFERASE INHIBITOR; PROTEIN KINASE PIM 1; PROTEIN KINASE PIM 2; PROTEIN SERINE THREONINE KINASE; UNCLASSIFIED DRUG; ANTINEOPLASTIC AGENT; PIM1 PROTEIN, HUMAN; PYRAZOLE DERIVATIVE; PYRIDINE DERIVATIVE;

EID: 84945968564     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2015.09.052     Document Type: Article
Times cited : (27)

References (31)
  • 30
    • 84945920844 scopus 로고    scopus 로고
    • Synthesis of selected compounds 11, 12, and 14 is shown in Scheme 1S in Supplemental material
    • Synthesis of selected compounds 11, 12, and 14 is shown in Scheme 1S in Supplemental material.
  • 31
    • 84945938155 scopus 로고    scopus 로고
    • Synthesis of 39 is shown in Scheme 2S in Supplemental material
    • Synthesis of 39 is shown in Scheme 2S in Supplemental material.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.