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676599-90-9

676599-90-9 Structure

676599-90-9 Structure
IdentificationBack Directory
[Name]

3-(1-METHYL-4-PHENYLACETYL-1H-2-PYRROLYL)-N-HYDROXY-2-PROPENAMIDE
[CAS]

676599-90-9
[Synonyms]

APHA-8
MC1353
MC-1353
MC 1353
APHA COMPOUND 8
Aroyl pyrrole hydroxy amide #8
3-(1-METHYL-4-PHENYLACETYL-1H-2-PYRROLYL)-N-HYDROXY-2-PROPENAMIDE
(E)-N-hydroxy-3-(1-Methyl-4-(2-phenylacetyl)-1H-pyrrol-2-yl)acrylaMide
2-Propenamide, N-hydroxy-3-[1-methyl-4-(2-phenylacetyl)-1H-pyrrol-2-yl]-
[Molecular Formula]

C16H16N2O3
[MDL Number]

MFCD05865226
[MOL File]

676599-90-9.mol
[Molecular Weight]

284.31
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

DMSO: 10 mg/mL, soluble
[form ]

solid
[InChI]

1S/C16H16N2O3/c1-18-11-13(10-14(18)7-8-16(20)17-21)15(19)9-12-5-3-2-4-6-12/h2-8,10-11,21H,9H2,1H3,(H,17,20)/b8-7+
[InChIKey]

UFQOXIMRSMFQRI-BQYQJAHWSA-N
[SMILES]

Cn1cc(cc1\C=C\C(=O)NO)C(=O)Cc2ccccc2
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictogramsGHS hazard pictograms
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H317-H318
[Precautionary statements ]

P280-P301+P312+P330-P302+P352-P305+P351+P338+P310
[Hazard Codes ]

Xn
[Risk Statements ]

22-41-43
[Safety Statements ]

26-36/37/39
[WGK Germany ]

2
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Skin Sens. 1
Hazard InformationBack Directory
[Description]

APHA compound 8 is an inhibitor of class I histone deacetylases (HDACs; IC50s = 3.7, 7.4, 0.42, and 2.8 μM for HDAC1, -2, -3, and -8, respectively) as well as class II HDACs (IC50s = 3.1, 0.1, 3.1, and 4.2 μM for HDAC4, -6, -7, and -10, respectively). It is selective for class I and II HDACs over class III HDACs (IC50s = >30 μM for SIRT1, SIRT2, and SIRT3) and the histone acetyltransferase PCAF (IC50 = >30 μM). At 48 hours post-infection, APHA compound 8 increases replication of oncolytic herpes simplex virus (oHSV) in MDA-MB-231 and 4T1 breast cancer cells when used prior to viral infection at concentrations of 10 and 50 μM.
[Uses]

HDAC-IN-69 (Compound 2) is a derivative of an HDAC inhibitor with inhibitory activity targeting maize histone deacetylase HD2[1].
[IC 50]

HD2
[References]

[1] Ragno R, et al. 3-(4-Aroyl-1-methyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides as a new class of synthetic histone deacetylase inhibitors. 3. Discovery of novel lead compounds through structure-based drug design and docking studies. J Med Chem. 2004 Mar 11;47(6):1351-9. DOI:10.1021/jm031036f
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