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Volumn 23, Issue 17, 2013, Pages 4761-4769

Selective orexin receptor antagonists

Author keywords

Hcrt 1; Hcrt 2; Hypocretin; Hypothalamus; Orexin

Indexed keywords

1 (2 METHYL 6 BENZOXAZOLYL) 3 (1,5 NAPHTHYRIDIN 4 YL)UREA; 1 (6,8 DIFLUORO 2 METHYL 4 QUINOLINYL) 3 (4 DIMETHYLAMINOPHENYL)UREA; ALMOREXANT; FILOREXANT; GSK 1059865; OREXIN 1 RECEPTOR; OREXIN 2 RECEPTOR; SB 410220; SB 649868; SB 674042; SUVOREXANT; UNCLASSIFIED DRUG;

EID: 84881368759     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2013.06.057     Document Type: Review
Times cited : (71)

References (92)
  • 6
    • 84871860395 scopus 로고    scopus 로고
    • For an in-depth review of orexin system cell physiology see
    • For an in-depth review of orexin system cell physiology see: J.P. Kukkonen Am. J. Physiol. Cell Physiol. 304 2013 C2
    • (2013) Am. J. Physiol. Cell Physiol. , vol.304 , pp. 2
    • Kukkonen, J.P.1
  • 31
    • 84881368816 scopus 로고    scopus 로고
    • Clinicaltrials.gov trial identifiers as of the writing of this review: NCT01021852, NCT01513291 and NCT01554176
    • Clinicaltrials.gov trial identifiers as of the writing of this review: NCT01021852, NCT01513291 and NCT01554176.
  • 60
  • 79
    • 84881367361 scopus 로고    scopus 로고
    • During the peer review of this manuscript, a patent application from published containing additional selective OX2 receptor antagonists related to 63 Patent WO 2013/059222
    • During the peer review of this manuscript, a patent application from published containing additional selective OX2 receptor antagonists related to 63: Kuduk, S. D.; Skudlarek, J. W. Patent WO 2013/059222.
    • Kuduk, S.D.1    Skudlarek, J.W.2
  • 92
    • 84881373333 scopus 로고    scopus 로고
    • Following a FDA advisory panel recomendation to approve the 15 and 30 mg doses of Suvorexant, the FDA has recently provided Merck with a Complete Response Letter indicating that the 10 mg dose should be the starting dose for most patients and must be available before approval
    • Following a FDA advisory panel recomendation to approve the 15 and 30 mg doses of Suvorexant, the FDA has recently provided Merck with a Complete Response Letter indicating that the 10 mg dose should be the starting dose for most patients and must be available before approval. (http://www.mercknewsroom. com/press-release/research-and-development-news/merck-receives-complete- response-letter-suvorexant-merck).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.