2-Thiazolamine,4-(4-bromophenyl)-N-[4-(4-bromophenyl)-2-thiazolyl]

• 常用名: 2-Thiazolamine,4-(4-bromophenyl)-N-[4-(4-bromophenyl)-2-thiazolyl]
• 英文名: 2-Thiazolamine,4-(4-bromophenyl)-N-[4-(4-bromophenyl)-2-thiazolyl]
• CAS号: 7713-86-2
• 分子量: 493.23800
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₈H₁₁Br₂N₃S₂
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: Thiazole, 2,2'-iminobis[4-(4-bromophenyl)

物理化学性质

• 分子式: C₁₈H₁₁Br₂N₃S₂
• 分子量: 493.23800
• 精确质量: 490.87600
• PSA: 97.52000
• LogP: 6.62410
• InChIKey: HTTGIQDIXOZYHY-UHFFFAOYSA-N
• SMILES: Brc1ccc(-c2csc(Nc3nc(-c4ccc(Br)cc4)cs3)n2)cc1

靶点实验

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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：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：Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ... 来源：ChEMBL 靶标：Klebsiella pneumoniae External Id：CHEMBL4296186

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：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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英文别名

• Bis-<4-(4-brom-phenyl)-thiazol-2-yl>-amin
• 4-(4-bromophenyl)-N-[4-(4-bromophenyl)-1,3-thiazol-2-yl]-1,3-thiazol-2-amine
• bis-[4-(4-bromo-phenyl)-thiazol-2-yl]-amine