2-甲基-3-(1,2,3,6-四氢-4-吡啶)-1H-吲哚结构式
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常用名 | 2-甲基-3-(1,2,3,6-四氢-4-吡啶)-1H-吲哚 | 英文名 | 4-(2-methylindolyl-3)-1,2,5,6-tetrahydropyridine |
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| CAS号 | 84461-65-4 | 分子量 | 212.29000 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C14H16N2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 中文名 | 2-甲基-3-(1,2,3,6-四氢-4-吡啶)-1H-吲哚 |
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| 英文名 | 2-methyl-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole |
| 分子式 | C14H16N2 |
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| 分子量 | 212.29000 |
| 精确质量 | 212.13100 |
| PSA | 27.82000 |
| LogP | 3.18180 |
| InChIKey | JLVLNPGKFHWCCQ-UHFFFAOYSA-N |
| SMILES | Cc1[nH]c2ccccc2c1C1=CCNCC1 |
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~%
2-甲基-3-(1,2,3,6... 84461-65-4 |
| 文献:Mattsson, Cecilia; Svensson, Peder; Boettcher, Henning; Sonesson, Clas European Journal of Medicinal Chemistry, 2013 , vol. 63, p. 578 - 588 |
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~80%
2-甲基-3-(1,2,3,6... 84461-65-4 |
| 文献:Freter; Fuchs; Barsumian; Oliver Arzneimittel-Forschung/Drug Research, 1985 , vol. 35, # 1 A p. 272 - 276 |
| 2-甲基-3-(1,2,3,6-四氢-4-吡啶)-1H-吲哚上游产品 3 | |
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| 2-甲基-3-(1,2,3,6-四氢-4-吡啶)-1H-吲哚下游产品 0 | |
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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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