3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole结构式
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常用名 | 3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole | 英文名 | 3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole |
|---|---|---|---|---|
| CAS号 | 7496-59-5 | 分子量 | 281.17200 | |
| 密度 | 1.68g/cm3 | 沸点 | 396.4ºC at 760mmHg | |
| 分子式 | C11H9BrN2S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 193.5ºC |
| 英文名 | 3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.68g/cm3 |
|---|---|
| 沸点 | 396.4ºC at 760mmHg |
| 分子式 | C11H9BrN2S |
| 分子量 | 281.17200 |
| 闪点 | 193.5ºC |
| 精确质量 | 279.96700 |
| PSA | 45.53000 |
| LogP | 2.32900 |
| InChIKey | PVPFCMJKVBCGES-UHFFFAOYSA-N |
| SMILES | Brc1ccc(C2=CSC3=NCCN23)cc1 |
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~46%
3-(4-bromopheny... 7496-59-5 |
| 文献:Mohan; Verma; Singh Synthetic Communications, 1992 , vol. 22, # 9 p. 1293 - 1298 |
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~%
3-(4-bromopheny... 7496-59-5 |
| 文献:Fefer,M.; King,L.C. Journal of Organic Chemistry, 1961 , vol. 26, p. 828 - 835 |
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~%
3-(4-bromopheny... 7496-59-5 |
| 文献:Sharpe,C.J. et al. Journal of Medicinal Chemistry, 1971 , vol. 14, # 10 p. 977 - 982 |
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~%
3-(4-bromopheny... 7496-59-5 |
| 文献:Prakash, Om; Rani, Neena; Goyal, Seema Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1992 , # 6 p. 707 - 710 |
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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: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: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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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
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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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