S178
(R)-SKF-82957 hydrobromide
solid
别名:
(1R)-6-Chloro-2,3,4,5-tetrahydro-3-methyl-1-phenyl-1H-3-benzazepine-7,8-diol hydrobromide, 1H-3-Benzazepine-7,8-diol,6-chloro-2,3,4,5-tetrahydro-3-methyl-1-phenyl hydrobromide hydrobromide
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所有图片(1)
About This Item
经验公式（希尔记法）:
C17H18ClNO2 · HBr
CAS号:
分子量:
384.70
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
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表单
solid
质量水平
旋光性
[α]22/D +22.46°, c = 0.76 in DMF(lit.)
颜色
white
溶解性
H2O: 7.5 mg/mL
DMSO: soluble
SMILES字符串
Br[H].CN1CCc2c(Cl)c(O)c(O)cc2[C@H](C1)c3ccccc3
InChI
1S/C17H18ClNO2.BrH/c1-19-8-7-12-13(9-15(20)17(21)16(12)18)14(10-19)11-5-3-2-4-6-11;/h2-6,9,14,20-21H,7-8,10H2,1H3;1H/t14-;/m1./s1
InChI key
BCZHWHQKKPEORG-PFEQFJNWSA-N
生化/生理作用
Selective D1 dopamine receptor agonist.
注意
hygroscopic, photosensitive
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
F R Pfeiffer et al.
Journal of medicinal chemistry, 25(4), 352-358 (1982-04-01)
6-Chloro-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines were synthesized and evaluated as agonists of central and peripheral dopamine receptors. These benzazepines were prepared by cyclization of certain amino alcohols followed by demethylation of the 7,8-dimethoxy groups of the precursors to the 7,8-catecholic moiety. Preliminary evidence of
P H Andersen et al.
European journal of pharmacology, 188(6), 335-347 (1990-06-12)
Dopamine receptor selectivity was investigated for a number of dopamine receptor agonists. In vitro, the benzazepine derivatives, e.g., SKF 38393 and SKF 75670 as well as the isoquinoline derivatives, SKF 89626 and SKF 89615, were D1 receptor-selective. All other compounds
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