메뉴 건너뛰기




Volumn 20, Issue 21, 2010, Pages 6313-6315

Discovery of a series of potent, orally active α,α- disubstituted piperidine NK1 antagonists

Author keywords

Dibasic amine metabolite; NK1 antagonist

Indexed keywords

AMIDE; DRUG METABOLITE; NEUROKININ 1 RECEPTOR ANTAGONIST; PIPERIDINE DERIVATIVE;

EID: 77957872554     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2010.08.059     Document Type: Article
Times cited : (8)

References (16)
  • 10
    • 85177159712 scopus 로고    scopus 로고
    • note
    • i values were obtained using the Cheng and Prusoff equation. Cascieri, M. A.; Macleod, A. M.; Underwood, D.; Shiao, L. L.; Ber, E.; Sadowski, S.; Yu, H.; Merchant, K. J.; Swain, C. J.; Strader, C. D.; Fong, T. M. J. Biol. Chem. 1994, 269, 6587.
  • 11
    • 0028113481 scopus 로고    scopus 로고
    • note
    • 1 antagonists were administered orally in 0.4% methylcellulose in distilled water at the dose indicated at various pretreatment times prior to injection of GR73632. Data are expressed as a percent decrease (% inhibition) in the amount of time spent foot tapping compared to vehicle-treated controls. Rupniak, N. M. J.; Williams, A. R. Eur. J. Pharmacol. 1994, 265, 179.
  • 12
    • 0033136333 scopus 로고    scopus 로고
    • The rat PK assay was run at 10 mpk (unless otherwise specified) using oral dosing with 20% HPBCD as vehicle. AUC was determined from 0 to 6 h. For reference: Cox, K. A.; Dunn-Meynell, K.; Korfmacher, W. A.; Broske, L.; Nomeir, A. A.; Lin, C. C.; Cayen, M. N.; Barr, W. H. Drug Discovery Today 1999, 4, 232
    • The rat PK assay was run at 10 mpk (unless otherwise specified) using oral dosing with 20% HPBCD as vehicle. AUC was determined from 0 to 6 h. For reference: Cox, K. A.; Dunn-Meynell, K.; Korfmacher, W. A.; Broske, L.; Nomeir, A. A.; Lin, C. C.; Cayen, M. N.; Barr, W. H. Drug Discovery Today 1999, 4, 232.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.