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Volumn 23, Issue 4, 2013, Pages 1114-1119

Discovery and SAR of PF-4693627, a potent, selective and orally bioavailable mPGES-1 inhibitor for the potential treatment of inflammation

Author keywords

Benzoxazole; Clinical candidate; Inflammation; m PGES 1; PF 4693627

Indexed keywords

ANTIINFLAMMATORY AGENT; CARRAGEENAN; CYCLOOXYGENASE 2; NAPROXEN; PF 4693627; PROSTAGLANDIN E SYNTHASE 1; UNCLASSIFIED DRUG;

EID: 84872946941     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2012.11.109     Document Type: Article
Times cited : (43)

References (23)
  • 2
  • 14
    • 84872922237 scopus 로고    scopus 로고
    • A detailed study looking at the conformation analysis of the 1,4- and 1,3-disubstituted cyclohexane analogs is published in the adjoining paper
    • A detailed study looking at the conformation analysis of the 1,4- and 1,3-disubstituted cyclohexane analogs is published in the adjoining paper.
  • 15
    • 84872906351 scopus 로고    scopus 로고
    • 50 was generally less than 30%
    • 50 was generally less than 30%.
  • 16
  • 22
    • 84872979497 scopus 로고    scopus 로고
    • Use of the animals in these studies was reviewed and approved by the Pfizer Institutional Animal Care and Use Committee
    • 80 values for each experiment were calculated using a four-parameter sigmoid model. Naproxen was used as a reference compound at 10 mg/kg.
  • 23
    • 84872895931 scopus 로고    scopus 로고
    • 2 atmosphere in High Glucose D-MEM (Invitrogen, Grand Island, NY) containing extra 10 mM HEPES buffer (Invitrogen)
    • 2 was added to the cells 40 min after addition of the compounds (or 10 min before addition of arachidonic acid). PG levels in the supernatants were assayed by ELISA.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.