2-(Methylsulfanyl)-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4-ylamine结构式
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常用名 | 2-(Methylsulfanyl)-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4-ylamine | 英文名 | 2-(Methylsulfanyl)-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4-ylamine |
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| CAS号 | 121746-14-3 | 分子量 | 251.4 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C11H13N3S2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 2-(Methylsulfanyl)-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4-ylamine |
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| 分子式 | C11H13N3S2 |
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| 分子量 | 251.4 |
| InChIKey | NJKBQFTUKUHCGH-UHFFFAOYSA-N |
| SMILES | CSC1=NC(=C2C3=C(CCCC3)SC2=N1)N |
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实验名称:qHTS screening for TAG (triacylglycerol) accumulators in algae
来源:11812
靶标:N/A
External Id:FATTTLab-Algae-Lipid
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实验名称:NOVARTIS: Inhibition of Plasmodium falciparum 3D7 (drug-susceptible) proliferation in...
来源:ChEMBL
靶标:Plasmodium falciparum
External Id:CHEMBL1040691
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实验名称:NOVARTIS: Inhibition Frequency Index (IFI) - the number of HTS assays where a compoun...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1040694
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实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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实验名称:NOVARTIS: Inhibition of Plasmodium falciparum W2 (drug-resistant) proliferation in er...
来源:ChEMBL
靶标:Plasmodium falciparum
External Id:CHEMBL1040692
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实验名称:NOVARTIS: Antimalarial liver stage activity measured as a greater than 50% reduction ...
来源:ChEMBL
靶标:Plasmodium yoelii
External Id:CHEMBL1789905
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实验名称:NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
来源:ChEMBL
靶标:Huh-7
External Id:CHEMBL1040693
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实验名称:Modulation of P-gp overexpressed in human A2780 cells assessed as daunorubicin accumu...
来源:ChEMBL
靶标:ATP-dependent translocase ABCB1
External Id:CHEMBL1048477
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实验名称:Alphascreen assay for small molecules abrogating mHTT-CaM Interaction
来源:24983
靶标:Huntingtin
External Id:KUHTS-Muma KU-CaM-Htt INH-01
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实验名称:Inhibition of LIMK1 using cofilin-2 as substrate after 60 mins by Kinase-Glo assay
来源:ChEMBL
靶标:LIM domain kinase 1
External Id:CHEMBL1839797
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