4-amino-N-(4-methoxyphenyl)-2-methylsulfanyl-1,3-thiazole-5-carboxamide结构式
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常用名 | 4-amino-N-(4-methoxyphenyl)-2-methylsulfanyl-1,3-thiazole-5-carboxamide | 英文名 | 4-amino-N-(4-methoxyphenyl)-2-methylsulfanyl-1,3-thiazole-5-carboxamide |
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| CAS号 | 63237-97-8 | 分子量 | 295.38100 | |
| 密度 | 1.4g/cm3 | 沸点 | N/A | |
| 分子式 | C12H13N3O2S2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 4-amino-N-(4-methoxyphenyl)-2-methylsulfanyl-1,3-thiazole-5-carboxamide |
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| 英文别名 | 更多 |
| 密度 | 1.4g/cm3 |
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| 分子式 | C12H13N3O2S2 |
| 分子量 | 295.38100 |
| 精确质量 | 295.04500 |
| PSA | 130.78000 |
| LogP | 3.36230 |
| InChIKey | JLAJOZJWUBPJDB-UHFFFAOYSA-N |
| SMILES | COc1ccc(NC(=O)c2sc(SC)nc2N)cc1 |
| 折射率 | 1.67 |
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4-amino-N-(4-me... 63237-97-8 |
| 文献:Wobig,D. Justus Liebigs Annalen der Chemie, 1977 , p. 400 - 406 |
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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:Luminescence Cell-Free Homogeneous Counter Screen to Identify Inhibitors of ADP-glo R...
来源:Broad Institute
靶标:N/A
External Id:2046-03_INHIBITORS_DOSE-TITRATION_MLPCN-CHERRYPICK
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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: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
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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:Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Syn...
来源:Broad Institute
靶标:glycogen synthase kinase 3 beta isoform 1 [Homo sapiens]
External Id:2046-02_INHIBITORS_DOSE-TITRATION_MLPCN-CHERRYPICK
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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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