{[2-(5-Methylfuran-2-yl)-1,3-thiazol-4-yl]methyl}(propan-2-yl)[(pyridin-2-yl)methyl]amine

• 常用名: {[2-(5-Methylfuran-2-yl)-1,3-thiazol-4-yl]methyl}(propan-2-yl)[(pyridin-2-yl)methyl]amine
• 英文名: {[2-(5-Methylfuran-2-yl)-1,3-thiazol-4-yl]methyl}(propan-2-yl)[(pyridin-2-yl)methyl]amine
• CAS号: 1211713-23-3
• 分子量: 327.4
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₈H₂₁N₃OS
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: {[2-(5-Methylfuran-2-yl)-1,3-thiazol-4-yl]methyl}(propan-2-yl)[(pyridin-2-yl)methyl]amine

物理化学性质

• 分子式: C₁₈H₂₁N₃OS
• 分子量: 327.4
• InChIKey: CUYSQTKDDPCISN-UHFFFAOYSA-N
• SMILES: Cc1ccc(-c2nc(CN(Cc3ccccn3)C(C)C)cs2)o1

靶点实验

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实验名称：Antimalarial activity: Asexual Blood Stage Plasmodium falciparum 3D7 IC50 (uM) 来源：ChEMBL 靶标：Plasmodium falciparum External Id：CHEMBL3832778

实验名称：HepG2 inhibition at 10 uM (%) Cytotoxicity 来源：ChEMBL 靶标：HepG2 External Id：CHEMBL3832838

实验名称：Antibacterial activity against Staphylococcus aureus MRSA ATCC 43300 (CO-ADD:GP_020);... 来源：ChEMBL 靶标：Staphylococcus aureus External Id：CHEMBL4296184

实验名称：Antimalarial activity: Gametocytes Plasmodium falciparum NF54 Gametocytes Stage V IC5... 来源：ChEMBL 靶标：Plasmodium falciparum External Id：CHEMBL3832784

实验名称：Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ... 来源：ChEMBL 靶标：Klebsiella pneumoniae External Id：CHEMBL4296186

实验名称：Antibacterial activity against Escherichia coli ATCC 25922 (CO-ADD:GN_001); MIC in CA... 来源：ChEMBL 靶标：Escherichia coli External Id：CHEMBL4296185

实验名称：Antimalarial activity: Asexual Blood Stage Plasmodium falciparum Dd2 IC50 (uM) 来源：ChEMBL 靶标：Plasmodium falciparum External Id：CHEMBL3832779

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

实验名称：Compound was evaluated for the inhibition of human FECH at 10uM 来源：ChEMBL 靶标：Ferrochelatase, mitochondrial External Id：CHEMBL3987222

实验名称：Compound was evaluated for the inhibition of human HMBS at 100uM 来源：ChEMBL 靶标：Porphobilinogen deaminase External Id：CHEMBL3987223

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