2-methyl-3-[(4-methylpiperazin-1-yl)(thiophen-2-yl)methyl]-1H-indole

• 常用名: 2-methyl-3-[(4-methylpiperazin-1-yl)(thiophen-2-yl)methyl]-1H-indole
• 英文名: 2-methyl-3-[(4-methylpiperazin-1-yl)(thiophen-2-yl)methyl]-1H-indole
• CAS号: 618407-11-7
• 分子量: 325.5
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₉H₂₃N₃S
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: 2-methyl-3-[(4-methylpiperazin-1-yl)(thiophen-2-yl)methyl]-1H-indole

物理化学性质

• 分子式: C₁₉H₂₃N₃S
• 分子量: 325.5
• InChIKey: ZXTDMEVOZZTVJO-UHFFFAOYSA-N
• SMILES: CC1=C(C2=CC=CC=C2N1)C(C3=CC=CS3)N4CCN(CC4)C

靶点实验

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实验名称：AntiSchistosoma mansoni activity Juveniles IC50 (uM) 来源：ChEMBL 靶标：Schistosoma mansoni External Id：CHEMBL3832810

实验名称：AntiSchistosoma mansoni activity Adults IC50 (uM) 来源：ChEMBL 靶标：Schistosoma mansoni External Id：CHEMBL3832811

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：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：AntiSchistosoma mansoni activity Newly Transformed Schistosomula: inhibition at 10 uM... 来源：ChEMBL 靶标：Schistosoma mansoni External Id：CHEMBL3832812

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：Antitrypanosomal activity against Trypanosoma brucei brucei 427 bloodstream forms ass... 来源：ChEMBL 靶标：Trypanosoma brucei brucei External Id：CHEMBL4369190

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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