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Volumn 12, Issue 21, 2002, Pages 3219-3222

Relating the structure, activity, and physical properties of ultrashort-acting benzodiazepine receptor agonists

Author keywords

[No Author keywords available]

Indexed keywords

BENZODIAZEPINE RECEPTOR; BENZODIAZEPINE RECEPTOR STIMULATING AGENT;

EID: 18644377334     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(02)00513-9     Document Type: Article
Times cited : (17)

References (18)
  • 13
    • 0019155525 scopus 로고
    • For a C3-alkyation/decarboxylation protocol to prepare racemic triazolo-BZDs, see: Hester, J. B., Jr.; Rudzik, A. D.; VonVoigtlander, P. F. J. Med. Chem. 1980, 23, 643. It was reported herein that substitution at this position significantly reduced activity in the LRR assessment.
    • (1980) Med. Chem. , vol.23 , pp. 643
    • Hester, J.B.1    Rudzik, A.D.2    VonVoigtlander, P.F.J.3
  • 14
    • 84992283815 scopus 로고    scopus 로고
    • note
    • Chiral HPLC purification was performed using a Daicel AD Column (5×50 cm, 20 μm packing). Elution with 20% i-PrOH/hexanes, 50 mL/min flow rate and UV (270 nM) detection gave retention times of 42 min for 18a and 72 min for 18b.
  • 15
    • 84992268600 scopus 로고    scopus 로고
    • note
    • 16 Ab initio predictions of VCD spectra for model structures were performed using Gaussian '94.
  • 17
    • 84992280039 scopus 로고    scopus 로고
    • note
    • Solubility was determined by visual inspection or UV assay of a saturated sample. In both types of determinations, solubility at pH 3 was verified using solubility at other pH and spectrophotometric pKa values.
  • 18
    • 0000239062 scopus 로고    scopus 로고
    • Docking conformationally flexible molecules into protein binding sites
    • P.S. Charifson. New York: Marcel Dekker
    • Lambert M.H. Docking conformationally flexible molecules into protein binding sites. Charifson P.S. Practical Application of Computer-Aided Drug Design. 1997;243-303 Marcel Dekker, New York.
    • (1997) Practical Application of Computer-Aided Drug Design , pp. 243-303
    • Lambert, M.H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.