IRAK-4 protein kinase inhibitor 2

• 常用名: IRAK-4 protein kinase inhibitor 2
• 英文名: IRAK-4 protein kinase inhibitor 2
• CAS号: 301675-24-1
• 分子量: 282.25400
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₄H₁₀N₄O₃
• 熔点: N/A
• 闪点: N/A

IRAK-4 protein kinase inhibitor 2名称

• 英文名: N-(1H-Benzimidazol-2-yl)-3-nitrobenzamide

IRAK-4 protein kinase inhibitor 2物理化学性质

• 分子式: C₁₄H₁₀N₄O₃
• 分子量: 282.25400
• 精确质量: 282.07500
• PSA: 107.09000
• LogP: 3.63060
• InChIKey: QPKROMNIEAEFQA-UHFFFAOYSA-N
• SMILES: O=C(Nc1nc2ccccc2[nH]1)c1cccc([N+](=O)[O-])c1

IRAK-4 protein kinase inhibitor 2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

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：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：Inhibition of IRAK4 来源：ChEMBL 靶标：Interleukin-1 receptor-associated kinase 4 External Id：CHEMBL870864

实验名称：qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen 来源：NCGC External Id：tdp43-p2-repeat

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IRAK-4 protein kinase inhibitor 2英文别名

• 1-Ethylthymin
• 1-ethyl-5-methyl-1H-pyrimidine-2,4-dione
• N-1H-benzimidazol-2-yl-3-nitrobenzamide
• 1-ethylthymine
• 1-Aethyl-5-methyl-1H-pyrimidin-2,4-dion
• 2,4(1H,3H)-Pyrimidinedione,1-ethyl-5-methyl
• 3-nitro-N-(1H-benzoimidazol-2-yl)-benzamide
• 1-ethyl-5-methyl-2,4(3H)-pyrimidindione
• N1-ethylthymine