L-Moses (L-45) dihydrochloride is the first potent, selective, and cell-active p300/CBP-associated factor ( PCAF ) bromodomain ( Brd ) inhibitor with a K d of 126 nM. Appearance:Solid IC50& Target:Brd 126 nM (Kd) In Vitro:L-Moses (L-45) disrupts PCAF-Brd histone H3.3 interaction in cells using a nanoBRET assay, and a co-crystal structure of L-Moses with the homologous Brd Pf GCN5 from Plasmodium falciparum rationalizes the high selectivity for PCAF and GCN5 bromodomains. A In Vivo:L-Moses (L-45) shows no observable cytotoxicity in peripheral blood mononuclear cells (PBMC), good cell-permeability, and metabolic stability in human and mouse liver microsomes, supporting its potential for in vivo use. MCE has not independently con Biological Activity:L-Moses (L-45) dihydrochloride is the first potent, selective, and cell-active p300/CBP-associated factor ( PCAF ) bromodomain ( Brd ) inhibitor with a K d of 126 nM.
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L-Moses dihydrochloride
CAS number:unknown molecular formula:C21H26Cl2N6
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| Chinese alias | L-摩西二盐酸盐 | ||
| English alias | - | ||
| CAS number | unknown | molecular formula | C21H26Cl2N6 |
| molecular weight | 433.38 g/mol | Exact mass | - |
| PSA | - | logp | - |
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