Name | 4-[4-(2-fluorophenyl)phenyl]-N-(4-hydroxyphenyl)butanamide |
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Synonyms |
CMPD1
MK2a Inhibitor Mitogen-activated protein kinase-activated protein kinase 2a Inhibitor MAPKAPK2a Inhibitor |
Description | CMPD1 is a selective and non-ATP-competitive p38 MAPK-mediated MK2 phosphorylation inhibitor with apparent Ki (Kiapp) of 330 nM[1][2]. |
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Related Catalog | |
Target |
Kiapp: 330 nM (MK2 phosphorylation)[2] |
In Vitro | CMPD1 does not inhibit p38 MAPK-mediated phosphorylation of other two substrates, MBP and ATF2[1]. |
References |
Density | 1.229g/cm3 |
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Boiling Point | 585ºC at 760 mmHg |
Molecular Formula | C22H20FNO2 |
Molecular Weight | 349.40 |
Flash Point | 307.6ºC |
Exact Mass | 349.14800 |
PSA | 49.33000 |
LogP | 5.23270 |
Index of Refraction | 1.627 |
Precursor 1 | |
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DownStream 0 |