1,3-苯并噻唑-2-碳酰肼

• 常用名: 1,3-苯并噻唑-2-碳酰肼
• 英文名: 2-Benzothiazolecarboxylicacid, hydrazide
• CAS号: 28891-34-1
• 分子量: 193.22600
• 密度: 1.444g/cm3
• 沸点: N/A
• 分子式: C₈H₇N₃OS
• 熔点: 177-179ºC
• 闪点: N/A

1,3-苯并噻唑-2-碳酰肼名称

• 中文名: 1,3-苯并噻唑-2-碳酰肼
• 英文名: 1,3-Benzothiazole-2-carbohydrazide

1,3-苯并噻唑-2-碳酰肼物理化学性质

• 密度: 1.444g/cm3
• 熔点: 177-179ºC
• 分子式: C₈H₇N₃OS
• 分子量: 193.22600
• 精确质量: 193.03100
• PSA: 96.25000
• LogP: 1.99100
• InChIKey: GYADLBSESMQVEF-UHFFFAOYSA-N
• SMILES: NNC(=O)c1nc2ccccc2s1
• 折射率: 1.724

1,3-苯并噻唑-2-碳酰肼安全信息

• 海关编码: 2934200090

1,3-苯并噻唑-2-碳酰肼海关

• 海关编码: 2934200090
• 中文概述: 2934200090. 其他含一个苯并噻唑环系的化合物. 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: 2934200090. other compounds containing in the structure a benzothiazole ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

1,3-苯并噻唑-2-碳酰肼靶点实验

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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

实验名称：Confirm compound inhibition to esBAF complex through repress target gene Fgf4 in qPCR... 来源：Broad Institute 靶标：N/A External Id：2141-03_Inhibitor_SinglePoint_CherryPick_Activity

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：qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in... 来源：NCGC 靶标：TDP1 protein [Homo sapiens] External Id：TDP1100

实验名称：qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in... 来源：NCGC 靶标：TDP1 protein [Homo sapiens] External Id：TDP1101

实验名称：Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas... 来源：Broad Institute 靶标：N/A External Id：2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2

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

实验名称：qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima... 来源：NCGC 靶标：apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7] External Id：AMA1100

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1,3-苯并噻唑-2-碳酰肼英文别名

• benzothiazole-2-carbohydrazide
• benzothiazolecarbohydrazide
• benzothiazole hydrazide
• benzothiazole-2-carboxylic acid hydrazide
• Benzothiazol-2-carbonsaeurehydrazid
• benzothiazole-2-carboxyhydrazide