3-(10H-吩噻嗪-10-基)丙酸结构式
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常用名 | 3-(10H-吩噻嗪-10-基)丙酸 | 英文名 | 10H-Phenothiazine-10-propanoicacid |
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| CAS号 | 362-03-8 | 分子量 | 271.33400 | |
| 密度 | 1.321g/cm3 | 沸点 | 477ºC at 760mmHg | |
| 分子式 | C15H13NO2S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 242.3ºC |
| 中文名 | 10-苯并噻嗪丙酸 |
|---|---|
| 英文名 | 3-phenothiazin-10-ylpropanoic acid |
| 英文别名 | 更多 |
| 密度 | 1.321g/cm3 |
|---|---|
| 沸点 | 477ºC at 760mmHg |
| 分子式 | C15H13NO2S |
| 分子量 | 271.33400 |
| 闪点 | 242.3ºC |
| 精确质量 | 271.06700 |
| PSA | 65.84000 |
| LogP | 3.82900 |
| InChIKey | VNTAONUWHQBAMC-UHFFFAOYSA-N |
| SMILES | O=C(O)CCN1c2ccccc2Sc2ccccc21 |
| 储存条件 | 2-8°C |
| 危害码 (欧洲) | N: Dangerous for the environment; |
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| 风险声明 (欧洲) | 51/53 |
| 安全声明 (欧洲) | 24/25-61 |
| 海关编码 | 2934999090 |
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~75%
3-(10H-吩噻嗪-10-基)丙酸 362-03-8 |
| 文献:Zhang, Yanling; Eric Ballard; Zheng, Shi-Long; Gao, Xingming; Ko, Ko-Chun; Yang, Hsiuchin; Brandt, Gary; Lou, Xinhui; Tai, Phang C.; Lu, Chung-Dar; Wang, Binghe Bioorganic and Medicinal Chemistry Letters, 2007 , vol. 17, # 3 p. 707 - 711 |
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3-(10H-吩噻嗪-10-基)丙酸 362-03-8 |
| 文献:Analytical Chemistry, , vol. 75, # 4 p. 910 - 917 |
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3-(10H-吩噻嗪-10-基)丙酸 362-03-8 |
| 文献:Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, , vol. 225, p. 578 |
| 3-(10H-吩噻嗪-10-基)丙酸上游产品 3 | |
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| 3-(10H-吩噻嗪-10-基)丙酸下游产品 4 | |
| 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% |
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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
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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
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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
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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
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实验名称:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
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实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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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.
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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
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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
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实验名称:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
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| 10H-Phenothiazine-10-propanoic acid |
| 10-phenothiazinepropionic acid |
| 3-(10H-phenothiazine-10)propanoic acid |
| Phenothiazine-10-propionic acid |
| 3-(10H-Phenothiazin-10-yl)propanoic acid |