前往化源商城

3-羟基芬纳西泮

更新时间:2026-08-07 04:10:47

3-羟基芬纳西泮结构式
3-羟基芬纳西泮结构式
品牌特惠专场
常用名 3-羟基芬纳西泮 英文名 3-Hydroxyphenazepam
CAS号 70030-11-4 分子量 365.61
密度 1.7±0.1 g/cm3 沸点 544.5±50.0 °C at 760 mmHg
分子式 C15H10BrClN2O2 熔点 N/A
MSDS N/A 闪点 283.1±30.1 °C

 3-羟基芬纳西泮用途


3-Hydroxyphenazepam 是 Cinazepam 的活性代谢物。Cinazepam 是一种 GABAA 受体激动剂。3-Hydroxyphenazepam 可抑制突触体转运蛋白介导的 [3H]GABA 摄取。

 3-羟基芬纳西泮名称

中文名 3-羟基芬纳西泮
英文名 7-bromo-5-(2-chlorophenyl)-3-hydroxy-1,3-dihydro-1,4-benzodiazepin-2-one
英文别名 更多

 3-羟基芬纳西泮生物活性

描述 3-Hydroxyphenazepam 是 Cinazepam 的活性代谢物。Cinazepam 是一种 GABAA 受体激动剂。3-Hydroxyphenazepam 可抑制突触体转运蛋白介导的 [3H]GABA 摄取。
相关类别
参考文献

[1]. Borisova T, et, al. GABAA receptor agonist cinazepam and its active metabolite 3-hydroxyphenazepam act differently at the presynaptic site. Eur Neuropsychopharmacol. 2021 Apr;45:39-51.  

 3-羟基芬纳西泮物理化学性质

密度 1.7±0.1 g/cm3
沸点 544.5±50.0 °C at 760 mmHg
分子式 C15H10BrClN2O2
分子量 365.61
闪点 283.1±30.1 °C
精确质量 363.961395
PSA 65.18000
LogP 2.46
InChIKey KRJKJUWAZOWXNV-UHFFFAOYSA-N
SMILES O=C1Nc2ccc(Br)cc2C(c2ccccc2Cl)=NC1O
蒸汽压 0.0±1.5 mmHg at 25°C
折射率 1.712

 3-羟基芬纳西泮合成线路

~38%

3-羟基芬纳西泮结构式

3-羟基芬纳西泮

70030-11-4

查看详情
文献:Davidenko, T. I.; Zabolotskaya, N. N.; Milienko, N. P.; Andronati, S. A.; Kuznetsov, V. D.; Bogatskii, A. V. Doklady Chemistry, 1984 , vol. 278, p. 335 - 337 Dokl. Akad. Nauk SSSR Ser. Khim., 1984 , vol. 278, # 4 p. 878 - 881

~%

详细 查看详情
文献:Golovenko, N. Ya.; Zin'kovskii, V. G.; Bogatskii, A. V.; Sharbatyan, P. A.; Andronati, S. A. Pharmaceutical Chemistry Journal, 1980 , vol. 14, # 4 p. 208 - 213 Khimiko-Farmatsevticheskii Zhurnal, 1980 , vol. 14, # 4 p. 15 - 21

 3-羟基芬纳西泮上下游产品

3-羟基芬纳西泮上游产品  1

3-羟基芬纳西泮下游产品  0

 3-羟基芬纳西泮靶点实验

查看更多实验

实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
共117条,当前第1页,共12页
1
2
3
4
5

 3-羟基芬纳西泮英文别名

3-Hydroxyfenazepam
7-bromo-5-(2-chlorophenyl)-3-hydroxy-1,2-dihydro-3H-1,4-benzodiazepin-2-one
3-Oxyfenazepam
7-bromo-5-(2-chloro-phenyl)-3-hydroxy-1,3-dihydro-benzo[e][1,4]diazepin-2-one
7-Bromo-5-(2-chlorophenyl)-3-hydroxy-1,3-dihydro-2H-1,4-benzodiazepin-2-one
3-Hydroxyphenazepam
本网页内容来自不同专业数据源,如对内容有疑义,欢迎联系service1@chemsrc.com。