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Volumn 21, Issue 18, 2011, Pages 5475-5479

Discovery, synthesis and SAR of azinyl- and azolylbenzamides antagonists of the P2X 7 receptor

Author keywords

Oral bioavailability; P2X 7 antagonists; Parallel medicinal chemistry; Rheumatoid arthritis; Volume of distribution

Indexed keywords

AMINE; AZAURACIL; AZINYLBENZAMIDE DERIVATIVE; AZOLYLBENZAMIDE DERIVATIVE; PURINERGIC P2X7 RECEPTOR; PURINERGIC P2Y RECEPTOR ANTAGONIST; PYRAZOLE; UNCLASSIFIED DRUG;

EID: 80051948910     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2011.06.117     Document Type: Article
Times cited : (20)

References (18)
  • 10
    • 80051934258 scopus 로고    scopus 로고
    • WO 2,003,042,191
    • In general these compounds were 3-5× more potent in the Yo-Pro assay than in the monocyte assay. For assay protocols, see: Duplantier, A. J.; Subramanyam, C. WO 2,003,042,191, 2003.
    • (2003)
    • Duplantier, A.J.1    Subramanyam, C.2
  • 18
    • 77952106771 scopus 로고    scopus 로고
    • A recent publication from Pfizer describing work completed after the work described herein disclosed a series of orally and brain available P2X7 antagonists which began with compound 27. See: X. Chen, B. Pierce, W. Naing, M.L. Grapperhaus, and D.P. Phillion Bioorg. Med. Chem. Lett. 20 2010 3107
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 3107
    • Chen, X.1    Pierce, B.2    Naing, W.3    Grapperhaus, M.L.4    Phillion, D.P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.