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Volumn 16, Issue 21, 2008, Pages 9519-9523

Axial chirality and affinity at the GABAA receptor of pyrimido[1,2-a][1,4]benzodiazepines and related compounds

Author keywords

Atropisomer; Estazolam; GABAA receptor; Pyrimido 1,2 a 1,4 benzodiazepine; Triazolam; X ray analysis

Indexed keywords

10 CHLORO 5,6 DIHYDRO 1 METHYL 8 PHENYL 3H PYRIMIDO[1,2 A][1,5]BENZODIAZOCIN 3 ONE; 10 CHLORO 5,6 DIHYDRO 3 METHYL 8 PHENYL 1H PYRIMIDO[1,2A][1,5]BENZODIAZOCIN 1 ONE; 4 AMINOBUTYRIC ACID A RECEPTOR; 9 CHLORO 1 METHYL 7 PHENYLPYRIMIDO[1,2 A][1,4]BENZODIAZEPIN 3(5H) ONE; 9 CHLORO 3 METHYL 7 PHENYLPYRIMIDO[1,2 A][1,4]BENZODIAZEPIN 1(5H) ONE; 9 CHLORO 7 (2 CHLOROPHENYL) 1 METHYLPYRIMIDO[1,2 A][1,4]BENZODIAZEPIN 3(5H) ONE; BENZODIAZEPINE DERIVATIVE; PYRIMIDINE DERIVATIVE; PYRIMIDO[1,2 A][1,4]BENZODIAZEPINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 53749105016     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2008.09.037     Document Type: Article
Times cited : (35)

References (17)
  • 15
    • 53749085219 scopus 로고    scopus 로고
    • note
    • TM: Wavefunction Inc.), and the (aR*, aR*)-isomer, which exists in the crystal of 1c, was shown to be more stable by 2.23 kcal/mol than the other (aR*, aS*)-isomer.
  • 17
    • 0025282772 scopus 로고
    • 2 axis of the benzene-amide bond. The separated isomers showed different receptor-binding activity to reveal the eutomer with an aR-form; see:
    • 2 axis of the benzene-amide bond. The separated isomers showed different receptor-binding activity to reveal the eutomer with an aR-form; see:. Gilman N.W., Rosen P., Earley J.V., Cook C., and Todaro L.J. J. Am. Chem. Soc 112 (1990) 3969-3978
    • (1990) J. Am. Chem. Soc , vol.112 , pp. 3969-3978
    • Gilman, N.W.1    Rosen, P.2    Earley, J.V.3    Cook, C.4    Todaro, L.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.