| Identification | Back Directory | [Name]
2-Fluoro-N-(3-fluoro-5-pyridin-2-yl-benzoyl)-benzenesulfonhydrazine | [CAS]
2055397-28-7 | [Synonyms]
WM-1119
WM-1110
CS-2848
WM-1119;WM 1119;WM1119;KAT6A INHIBITOR; KAT6B INHIBITOR
2-Fluoro-N-(3-fluoro-5-pyridin-2-yl-benzoyl)-benzenesulfonhydrazine
（WM-1119） 2-Fluoro-N-(3-fluoro-5-pyridin-2-yl-benzoyl)-benzenesulfonhydrazine
Benzoic acid, 3-fluoro-5-(2-pyridinyl)-, 2-[(3-fluorophenyl)sulfonyl]hydrazide
Benzoic acid, 3-fluoro-5-(2-pyridinyl)-, 2-[(2-fluorophenyl)sulfonyl]hydrazide | [EINECS(EC#)]
823-299-7 | [Molecular Formula]
C18H13F2N3O3S | [MDL Number]
MFCD31690337 | [MOL File]
2055397-28-7.mol | [Molecular Weight]
389.38 |
| Chemical Properties | Back Directory | [density ]
1.414±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
DMSO:30.0(Max Conc. mg/mL);76.97(Max Conc. mM) | [form ]
A crystalline solid | [pka]
6.79±0.25(Predicted) | [color ]
Off-white to light yellow |
| Hazard Information | Back Directory | [Uses]
WM 1119 is a highly potent and selective inhibitor of lysine acetyltransferases, KAT6A and KAT6B. | [Biological Activity]
WM-1119 is a potent and selectiveacetyl coenzyme A (Acetyl-CoA)-competitive inhibitor against MYST family histone acetyltransferases KAT6A and KAT6B (KAT6B Kd = 2.1 nM by SPRIC50 = 37 nM by activity assay; KAT7/5 Kd = 0.53/2.2 μM; no affinity toward 159 diverse biological targets). WM-1119 induces MEF G1 cell cycle arrest (1-10 μM)inhibits EMRK1184 lymphoma growth in cultures (IC50 = 250 nM) and in mice in vivo (50 mg/kg 3x or 4x i.p. per day). | [storage]
Store at +4°C |
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BOC Sciences
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16314854226 |
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www.bocsci.com |
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