Name | C 21 |
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Synonyms |
N-Acetyl-L-serylglycyl-N5-(2-chloroethanimidoyl)-L-ornithylglycyl-L-lysylglycylglycyl-L-lysylglycyl-L-leucylglycyl-L-lysylglycylglycyl-L-alanyl-L-lysyl-L-arginyl-L-histidyl-L-arginyl-L-lysyl-L-valin e
L-Valine, N-acetyl-L-serylglycyl-N5-(2-chloro-1-iminoethyl)-L-ornithylglycyl-L-lysylglycylglycyl-L-lysylglycyl-L-leucylglycyl-L-lysylglycylglycyl-L-alanyl-L-lysyl-L-arginyl-L-histidyl-L-arginyl-L-ly 
syl- |
Description | C21 is a potent, irreversible, and selective PRMT1 inhibitor with an IC50 of 1.8 μM. C21 inhibits PRMT6 with an IC50 of 8.8 μM[1]. |
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Related Catalog | |
Target |
IC50: 1.8 μM (PRMT1); 8.8 μM (PRMT6)[1] |
References |
Density | 1.5±0.1 g/cm3 |
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Molecular Formula | C90H161ClN36O24 |
Molecular Weight | 2166.92 |
Exact Mass | 2165.217285 |
LogP | -11.97 |
Index of Refraction | 1.653 |