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BW 723C86盐酸盐

更新时间:2025-08-25 18:07:47

BW 723C86盐酸盐结构式
BW 723C86盐酸盐结构式
品牌特惠专场
常用名 BW 723C86盐酸盐 英文名 BW-723C86
CAS号 160521-72-2 分子量 322.853
密度 N/A 沸点 488.4ºC at 760 mmHg
分子式 C16H19ClN2OS 熔点 203 - 205 °C
MSDS 美版 闪点 249.2ºC

 BW 723C86盐酸盐用途


BW-723C86是一种有效且选择性的5-HT2B受体激动剂。BW-723C86具有抗焦虑作用。BW-723C86还会导致大鼠贪食和梳洗减少[1][2][3]。

 BW 723C86盐酸盐名称

中文名 BW 723C86盐酸盐
英文名 α-Methyl-5-(2-thienylmethoxy)-1H-indole-3-ethanamine Monohydrochloride
英文别名 更多

 BW 723C86盐酸盐物理化学性质

沸点 488.4ºC at 760 mmHg
熔点 203 - 205 °C
分子式 C16H19ClN2OS
分子量 322.853
闪点 249.2ºC
精确质量 322.090668
PSA 79.28000
LogP 5.20040
InChIKey PYJBJMIBANAOFJ-UHFFFAOYSA-N
SMILES CC(N)Cc1c[nH]c2ccc(OCc3cccs3)cc12.Cl
外观性状 米色, 白色粉末
蒸汽压 1.09E-09mmHg at 25°C
储存条件 室温
计算化学

1、 疏水参数计算参考值(XlogP):3

2、 氢键供体数量:2

3、 氢键受体数量:1

4、 可旋转化学键数量:5

5、 互变异构体数量:

6、 拓扑分子极性表面积(TPSA):52.7

7、 重原子数量:20

8、 表面电荷:1

9、 复杂度:315

10、同位素原子数量:0

11、确定原子立构中心数量:1

12、不确定原子立构中心数量:0

13、确定化学键立构中心数量:0

14、不确定化学键立构中心数量:0

15、共价键单元数量:1

更多

1. 性状:白色固体

2. 密度(g/mL, 20 ℃ ):未确定

3. 相对蒸汽密度(g/mL,空气=1):未确定

4. 熔点(ºC):未确定

5. 沸点(ºC,常压):未确定

6. 沸点(ºC 0.1mmHg):未确定

7. 折射率:未确定

8. 闪点(ºF):未确定

9. 比旋光度(º):未确定

10. 自燃点或引燃温度(ºC):未确定

11. 蒸气压(kPa,25ºC):未确定

12. 饱和蒸气压(kPa,60ºC):未确定

13. 燃烧热(KJ/mol):未确定

14. 临界温度(ºC):未确定

15. 临界压力(KPa):未确定

16. 油水(辛醇/水)分配系数的对数值:未确定

17. 爆炸上限(%,V/V):未确定

18. 爆炸下限(%,V/V):未确定

19. 溶解性:溶解于DMSO:>10mg/ml

 BW 723C86盐酸盐安全信息

个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
危险品运输编码 NONH for all modes of transport
WGK德国 3
RTECS号 NL8504715
海关编码 2934999090

 BW 723C86盐酸盐海关

海关编码 2934999090
中文概述 2934999090. 其他杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
申报要素 品名, 成分含量, 用途
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 BW 723C86盐酸盐文献5

更多文献
Pronociceptive and Antinociceptive Effects of Buprenorphine in the Spinal Cord Dorsal Horn Cover a Dose Range of Four Orders of Magnitude.

J. Neurosci. 35 , 9580-94, (2015)

Due to its distinct pharmacological profile and lower incidence of adverse events compared with other opioids, buprenorphine is considered a safe option for pain and substitution therapy. However, des...

BW 723C86, a 5-HT2B receptor agonist, causes hyperphagia and reduced grooming in rats.

Neuropharmacology 36 , 233-239, (1997)

The 5-HT2B receptor agonist, BW 723C86 (10 and 20 mg/kg s.c.), increased the time spent in feeding behaviour of freely-fed rats in observation cages over 15 min. BW 723C86 (20 and 50 mg/kg s.c. 30 min...

Effects of the 5-HT2B receptor agonist, BW 723C86, on three rat models of anxiety.

Br. J. Pharmacol. 117 , 1443-1448, (1996)

1. BW 723C86 (3 and 10 mg kg-1, s.c. 30 min pretest), a 5-HT2B receptor agonist, increased total interaction, but not locomotion in a rat social interaction test, a profile consistent with anxiolysis....

 BW 723C86盐酸盐靶点实验

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: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:Tocris HTS for Inhibitors of Aerobactin Synthetase lucA
来源:23265
External Id:IucA Pilot Assay Tocris Library
实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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
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 BW 723C86盐酸盐英文别名

1-[5-(2-Thienylmethoxy)-1H-indol-3-yl]propan-2-amine hydrochloride (1:1)
1-[5-(thiophen-2-ylmethoxy)-1H-indol-3-yl]propan-2-amine,hydrochloride
1-[5-(2-Thienylmethoxy)-1H-indol-3-yl]-2-propanamine hydrochloride (1:1)
1H-Indole-3-ethanamine, α-methyl-5-(2-thienylmethoxy)-, hydrochloride (1:1)
MFCD01321066
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