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Volumn 19, Issue 11, 2009, Pages 3118-3121

Potent and selective α1A adrenoceptor partial agonists-Novel imidazole frameworks

Author keywords

1A Adrenergic receptor; Partial agonist

Indexed keywords

ALPHA 1A ADRENERGIC RECEPTOR; ALPHA 1B ADRENERGIC RECEPTOR; ALPHA 1D ADRENERGIC RECEPTOR; ALPHA 2A ADRENERGIC RECEPTOR; ALPHA ADRENERGIC RECEPTOR STIMULATING AGENT; GLYCOPROTEIN P; IMIDAZOLE; LIGAND; NITRILE; PARTIAL AGONIST; ADRENERGIC RECEPTOR ALPHA(1A); ADRENERGIC RECEPTOR ALPHA(1B); ADRENERGIC RECEPTOR ALPHA(1D); ALPHA 1 ADRENERGIC RECEPTOR; ALPHA 2 ADRENERGIC RECEPTOR; IMIDAZOLE DERIVATIVE; RECEPTOR, ADRENERGIC, ALPHA 2A; RECEPTOR, ADRENERGIC, ALPHA-2A;

EID: 65149102695     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2009.03.162     Document Type: Article
Times cited : (12)

References (12)
  • 7
    • 33846100254 scopus 로고    scopus 로고
    • 1-receptor agonists, no N-alkylated imidazolines or imidazoles were described.
    • 1-receptor agonists, no N-alkylated imidazolines or imidazoles were described. Bishop M.J. Curr. Topics Med. Chem. 7 (2007) 135
    • (2007) Curr. Topics Med. Chem. , vol.7 , pp. 135
    • Bishop, M.J.1
  • 8
    • 65149095881 scopus 로고    scopus 로고
    • note
    • 2 conditions were employed.
  • 9
    • 2342586724 scopus 로고    scopus 로고
    • In silico molecular modeling calculated a 0.8 kcal/mol energy difference between axial and equatorial conformations of 5. This energy gap is well within the typical 5 kcal/mol difference observed for bound versus low energy conformations reported in the literature, see:
    • In silico molecular modeling calculated a 0.8 kcal/mol energy difference between axial and equatorial conformations of 5. This energy gap is well within the typical 5 kcal/mol difference observed for bound versus low energy conformations reported in the literature, see:. Perola E., and Charifson P.S. J. Med. Chem. 47 (2004) 2499
    • (2004) J. Med. Chem. , vol.47 , pp. 2499
    • Perola, E.1    Charifson, P.S.2
  • 11
    • 1642538361 scopus 로고    scopus 로고
    • max of 60% in our hands, which was in line with published data, see Blue, D. R.; Daniels, D. V.; Gever, J., R.; Jett, M. F.; O'Yang, C.; Tang, H. M.; Williams, T. J.; Ford, A. P. D. W. BJU Int. 2004, 93, 162. Ro 115-1240 was reported not to cause cardiovascular effects at the dose tested in the clinic, see Ref. 2.
    • max of 60% in our hands, which was in line with published data, see Blue, D. R.; Daniels, D. V.; Gever, J., R.; Jett, M. F.; O'Yang, C.; Tang, H. M.; Williams, T. J.; Ford, A. P. D. W. BJU Int. 2004, 93, 162. Ro 115-1240 was reported not to cause cardiovascular effects at the dose tested in the clinic, see Ref. 2.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.