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苯他西泮

更新时间:2025-09-18 10:22:20

苯他西泮结构式
苯他西泮结构式
品牌特惠专场
常用名 苯他西泮 英文名 Bentazepam
CAS号 29462-18-8 分子量 296.38700
密度 1.38g/cm3 沸点 532.6ºC at 760 mmHg
分子式 C17H16N2OS 熔点 N/A
MSDS N/A 闪点 275.9ºC

 苯他西泮用途


苯他西泮(噻吩)是一种具有短效抗焦虑作用的化合物。苯他西泮具有抗惊厥和镇静作用。苯他西泮可用于抑郁症和焦虑症的研究[1]。

 苯他西泮名称

中文名 苯他西泮
英文名 5-phenyl-3,4,6,7,8,9-hexahydro-[1]benzothiolo[2,3-e][1,4]diazepin-2-one
英文别名 更多

 苯他西泮生物活性

描述 苯他西泮(噻吩)是一种具有短效抗焦虑作用的化合物。苯他西泮具有抗惊厥和镇静作用。苯他西泮可用于抑郁症和焦虑症的研究[1]。
相关类别
体内研究 苯他西泮增加氯硝西泮的抗惊厥活性[1]。

 苯他西泮物理化学性质

密度 1.38g/cm3
沸点 532.6ºC at 760 mmHg
分子式 C17H16N2OS
分子量 296.38700
闪点 275.9ºC
精确质量 296.09800
PSA 69.70000
LogP 2.99000
InChIKey AIZFEOPQVZBNGH-UHFFFAOYSA-N
SMILES O=C1CN=C(c2ccccc2)c2c(sc3c2CCCC3)N1
蒸汽压 2E-11mmHg at 25°C
折射率 1.733
储存条件 通风低温干燥

 苯他西泮毒性和生态

 苯他西泮合成线路

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苯他西泮结构式

苯他西泮

29462-18-8

文献:Tinney; Sanchez; Nogas Journal of Medicinal Chemistry, 1974 , vol. 17, # 6 p. 624 - 630

~%

苯他西泮结构式

苯他西泮

29462-18-8

文献:Nakanishi,M. et al. Journal of Medicinal Chemistry, 1973 , vol. 16, p. 214 - 219

~%

苯他西泮结构式

苯他西泮

29462-18-8

文献:Heckendorn; Gagneux Tetrahedron Letters, 1973 , vol. 25, p. 2279 - 2282

 苯他西泮上下游产品

苯他西泮上游产品  3

苯他西泮下游产品  0

 苯他西泮靶点实验

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:Binding affinity towards human GABRA1 in an in vitro assay with cellular components m...
来源:ChEMBL
靶标:Gamma-aminobutyric acid receptor subunit gamma-2
External Id:CHEMBL5291799
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:Luminescence Cell-Free Homogeneous Counter Screen to Identify Inhibitors of ADP-glo R...
来源:Broad Institute
靶标:N/A
External Id:2046-03_INHIBITORS_DOSE-TITRATION_MLPCN-CHERRYPICK
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:Binding affinity towards human ESR1 in an in vitro cell free assay (CRO assay) measur...
来源:ChEMBL
靶标:Estrogen receptor
External Id:CHEMBL5291792
实验名称:Compound was evaluated for inhibition of human F2 in an in vitro cell free assay meas...
来源:ChEMBL
靶标:Prothrombin
External Id:CHEMBL5291794
实验名称:Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Syn...
来源:Broad Institute
靶标:glycogen synthase kinase 3 beta isoform 1 [Homo sapiens]
External Id:2046-02_INHIBITORS_DOSE-TITRATION_MLPCN-CHERRYPICK
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 苯他西泮英文别名

Bentazepam
CI-718
Tiadipone
Thiadipone
1,3,6,7,8,9-Hexahydro-5-phenyl-2H-(1)benzothieno(2,3-e)-1,4-diazepin-2-one
QM-6008
5-phenyl-1,3,6,7,8,9-hexahydro-benzo[4,5]thieno[2,3-e][1,4]diazepin-2-one
Bentazepamum [INN-Latin]
2H-(1)BENZOTHIENO(2,3-e)-1,4-DIAZEPIN-2-ONE,1,3,6,7,8,9-HEXAHYDRO-5-PHENYL
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