1-(4-chloro-benzoyl)-3,5-dimethyl-1H-pyrazole结构式
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常用名 | 1-(4-chloro-benzoyl)-3,5-dimethyl-1H-pyrazole | 英文名 | 1-(4-chloro-benzoyl)-3,5-dimethyl-1H-pyrazole |
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| CAS号 | 36140-78-0 | 分子量 | 234.68 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C12H11ClN2O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 1-(4-chloro-benzoyl)-3,5-dimethyl-1H-pyrazole |
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| 分子式 | C12H11ClN2O |
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| 分子量 | 234.68 |
| InChIKey | JXBJSVPXZCXBOC-UHFFFAOYSA-N |
| SMILES | CC1=CC(=NN1C(=O)C2=CC=C(C=C2)Cl)C |
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实验名称:Small-molecule inhibitors of ST2 (IL1RL1)
来源:20881
靶标:interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id:ST2_IL33_Inhibitors_Primary_Screening_77700
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实验名称:Inhibition of pig kidney aminopeptidase M at 55 uM
来源:ChEMBL
靶标:Aminopeptidase N
External Id:CHEMBL895383
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实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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实验名称:Inhibition of human spleen cathepsin D at 55 uM
来源:ChEMBL
靶标:Cathepsin D
External Id:CHEMBL895384
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实验名称:Inhibition of human urokinase at 55 uM
来源:ChEMBL
靶标:Urokinase-type plasminogen activator
External Id:CHEMBL895390
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实验名称:Inhibition of human plasma kallikrein at 55 uM
来源:ChEMBL
靶标:Plasma kallikrein
External Id:CHEMBL895388
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实验名称:Inhibition of human NPP1 expressed in COS7 cells using p-nitrophenyl-5'-thymidine mon...
来源:ChEMBL
靶标:Ectonucleotide pyrophosphatase/phosphodiesterase family member 1
External Id:CHEMBL4273106
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