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Volumn 7, Issue 2, 1997, Pages 109-115

Carboxyl-promoted enhancement of selectivity for the β3 adrenergic receptor. Selectivity is enhanced at the level of receptor binding

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Indexed keywords


EID: 0001423561     PISSN: 10542523     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (11)

References (31)
  • 7
    • 1842806139 scopus 로고    scopus 로고
    • note
    • 3 over β2, than BRL 35135. See also reference 11.
  • 10
    • 1842806138 scopus 로고    scopus 로고
    • note
    • 1 activity was measured as elevation of rat heart rate in vivo. In these assays, all esters are believed to be rapidly converted to the corresponding carboxylic acids. Compare compounds numbered 3, 4, 6, 8, 10, 14, and 15 in reference 8a.
  • 13
    • 1842705299 scopus 로고    scopus 로고
    • note
    • 2 activity as inhibition of insulin-mediated glucose incorporation into glycogen in mouse or rat soleus muscle.
  • 15
    • 1842755668 scopus 로고    scopus 로고
    • note
    • 2.
  • 16
    • 1842755670 scopus 로고    scopus 로고
    • note
    • 3 AR binding experiments comparing acids with esters were reported.10b
  • 23
    • 1842704423 scopus 로고    scopus 로고
    • Spectral data were fully consistent with the structures depicted
    • Spectral data were fully consistent with the structures depicted.
  • 29
    • 1842805266 scopus 로고    scopus 로고
    • note
    • 3. See references 10b, 15b, and 21d.
  • 31
    • 1842704428 scopus 로고    scopus 로고
    • note
    • A carboxylic acid is smaller than an ester or amide and more polar since it is ionized, and unlike an ester it can function as a H-bond donor.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.