4-Chloro-5-{[5-(methylamino)-1,3,4-thiadiazol-2-yl]sulfanyl}-2-phenyl-2,3-dihydropyridazin-3-one

• 常用名: 4-Chloro-5-{[5-(methylamino)-1,3,4-thiadiazol-2-yl]sulfanyl}-2-phenyl-2,3-dihydropyridazin-3-one
• 英文名: 4-Chloro-5-{[5-(methylamino)-1,3,4-thiadiazol-2-yl]sulfanyl}-2-phenyl-2,3-dihydropyridazin-3-one
• CAS号: 938920-79-7
• 分子量: 351.8
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₃H₁₀ClN₅OS₂
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: 4-Chloro-5-{[5-(methylamino)-1,3,4-thiadiazol-2-yl]sulfanyl}-2-phenyl-2,3-dihydropyridazin-3-one

物理化学性质

• 分子式: C₁₃H₁₀ClN₅OS₂
• 分子量: 351.8
• InChIKey: ONJKDQWJZQEXIR-UHFFFAOYSA-N
• SMILES: CNc1nnc(Sc2cnn(-c3ccccc3)c(=O)c2Cl)s1

靶点实验

查看更多实验

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

实验名称：Antischistosomal activity against Schistosoma mansoni incubated for 72 hrs by inverte... 来源：ChEMBL 靶标：Schistosoma mansoni External Id：CHEMBL4811351

实验名称：Antischistosomal activity against Schistosoma haematobium at 10 uM measured after 72 ... 来源：ChEMBL 靶标：Schistosoma haematobium External Id：CHEMBL4811352

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：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

共18条，当前第1页，共2页

1

2