N-(4-氟苯基)苯并噻唑-2-胺

• 常用名: N-(4-氟苯基)苯并噻唑-2-胺
• 英文名: BENZOTHIAZOL-2-YL-(4-FLUORO-PHENYL)-AMINE
• CAS号: 348-45-8
• 分子量: 244.29
• 密度: 1.384g/cm3
• 沸点: 372.2ºC at 760mmHg
• 分子式: C₁₃H₉FN₂S
• 熔点: N/A
• 闪点: 178.9ºC

N-(4-氟苯基)苯并噻唑-2-胺用途

Protein kinase inhibitor 6 是一种蛋白激酶抑制剂。

N-(4-氟苯基)苯并噻唑-2-胺名称

• 中文名: N-(4-氟苯基)苯并噻唑-2-胺
• 英文名: N-(4-fluorophenyl)-1,3-benzothiazol-2-amine

N-(4-氟苯基)苯并噻唑-2-胺生物活性

• 描述: Protein kinase inhibitor 6 是一种蛋白激酶抑制剂。
• 相关类别:
  研究领域 >> 其他
  信号通路 >> 其他 >> 其他

N-(4-氟苯基)苯并噻唑-2-胺物理化学性质

• 密度: 1.384g/cm3
• 沸点: 372.2ºC at 760mmHg
• 分子式: C₁₃H₉FN₂S
• 分子量: 244.29
• 闪点: 178.9ºC
• 精确质量: 244.04700
• PSA: 53.16000
• LogP: 4.25200
• InChIKey: KQKQLYWDIYNFJP-UHFFFAOYSA-N
• SMILES: Fc1ccc(Nc2nc3ccccc3s2)cc1
• 外观性状: 固体
• 折射率: 1.723
• 储存条件: 室温， 惰性气体

N-(4-氟苯基)苯并噻唑-2-胺安全信息

• 危害码 (欧洲): Xn
• 海关编码: 2934999090

N-(4-氟苯基)苯并噻唑-2-胺海关

• 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%

N-(4-氟苯基)苯并噻唑-2-胺靶点实验

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：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

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：Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste... 来源：Broad Institute 靶标：N/A External Id：7124-01_Inhibitor_SinglePoint_HTS_Activity

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N-(4-氟苯基)苯并噻唑-2-胺英文别名

• N-(4-fluorophenyl)benzo[d]thiazol-2-amine
• 2-(4'-fluorophenyl)aminobenzothiazole
• Benzothiazol-2-yl-(4-fluoro-phenyl)-amine
• Benzothiazol-2-yl-(4-fluor-phenyl)-amin