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Volumn 19, Issue 20, 2009, Pages 5970-5974

Structure based design of novel irreversible FAAH inhibitors

Author keywords

Endocannabinoid anandamide; FAAH; Fatty acid amide hydrolase; Inflammation; Irreversible FAAH inhibitors

Indexed keywords

AZETIDINE UREA; FATTY ACID AMIDASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 70349199021     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2009.07.101     Document Type: Article
Times cited : (12)

References (19)
  • 12
    • 70349224706 scopus 로고    scopus 로고
    • note
    • Compound 2 was prepared from 3-hydroxy methylbenzoate in four steps.
  • 13
    • 70349219107 scopus 로고    scopus 로고
    • WO 9318029 A1, 1993
    • Matassa, V. G. WO 9318029 A1, 1993.
    • Matassa, V.G.1
  • 14
    • 70349222059 scopus 로고    scopus 로고
    • note
    • Olefin separation condition: Set up AI 30×250 mm chiral column elute with 20% EtOH and 80% CO2. Sample dissolved in 20 mL EtOH, 25 mg/mL, 1 mL per inject. The olefin stereochemistry was assigned by 2D NMR.
  • 15
    • 70349221966 scopus 로고    scopus 로고
    • Compound 10 was prepared as described in WO 08047229, 2008
    • Compound 10 was prepared as described in WO 08047229, 2008.
  • 18
    • 70349221967 scopus 로고    scopus 로고
    • note
    • Compound 16 was prepared through the similar sequence as compound 9.
  • 19
    • 70349221876 scopus 로고    scopus 로고
    • note
    • The Pfizer Institutional Animal Care and Use Committee reviewed and approved the animal use in these studies. The animal care and use program is fully accredited by the Association for Assessment and Accreditation of Laboratory Animal Care, International.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.