(2S)-2-[3-[4-[[4-[4-(trifluoromethyl)phenyl]triazol-1-yl]methyl]phenyl]-1,2,4-oxadiazol-5-yl]pyrrolidine-1-carboximidamide;hydrochloride结构式
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常用名 | (2S)-2-[3-[4-[[4-[4-(trifluoromethyl)phenyl]triazol-1-yl]methyl]phenyl]-1,2,4-oxadiazol-5-yl]pyrrolidine-1-carboximidamide;hydrochloride | 英文名 | (2S)-2-[3-[4-[[4-[4-(trifluoromethyl)phenyl]triazol-1-yl]methyl]phenyl]-1,2,4-oxadiazol-5-yl]pyrrolidine-1-carboximidamide;hydrochloride |
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| CAS号 | 2927429-64-7 | 分子量 | 518.9 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C23H22ClF3N8O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | (2S)-2-[3-[4-[[4-[4-(trifluoromethyl)phenyl]triazol-1-yl]methyl]phenyl]-1,2,4-oxadiazol-5-yl]pyrrolidine-1-carboximidamide;hydrochloride |
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| 分子式 | C23H22ClF3N8O |
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| 分子量 | 518.9 |
| InChIKey | AFCPZBLOMXYPNG-FYZYNONXSA-N |
| SMILES | C1C[C@H](N(C1)C(=N)N)C2=NC(=NO2)C3=CC=C(C=C3)CN4C=C(N=N4)C5=CC=C(C=C5)C(F)(F)F.Cl |
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实验名称:Inhibition of recombinant human N-terminal His-tagged SphK2 (2 to 654 residues) expre...
来源:ChEMBL
靶标:Sphingosine kinase 2
External Id:CHEMBL4710642
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实验名称:Inhibition of recombinant human SphK1 at 125 uM using d-erythro-sphingosine as substr...
来源:ChEMBL
靶标:Sphingosine kinase 1
External Id:CHEMBL4710643
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实验名称:Inhibition of recombinant human N-terminal His-tagged SphK2 (2 to 654 residues) expre...
来源:ChEMBL
靶标:Sphingosine kinase 2
External Id:CHEMBL4710644
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实验名称:Cytotoxicity against human U-251MG cells assessed as reduction in cell viability at 1...
来源:ChEMBL
靶标:U-251
External Id:CHEMBL4710645
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