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APHA Compound 8_Molecular_structure_CAS_676599-90-9)
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APHA Compound 8

Catalog No. A2478 Name Sigma Aldrich
CAS Number 676599-90-9 Website http://www.sigmaaldrich.com
M. F. C16H16N2O3 Telephone 1-800-521-8956
M. W. 284.30984 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 5001

SYNONYMS

IUPAC name
N-hydroxy-3-[1-methyl-4-(2-phenylacetyl)-1H-pyrrol-2-yl]prop-2-enamide
IUPAC Traditional name
N-hydroxy-3-[1-methyl-4-(2-phenylacetyl)pyrrol-2-yl]prop-2-enamide
Synonyms
3-(1-Methyl-4-phenylacetyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamide

DATABASE IDS

CAS Number 676599-90-9

PROPERTIES

Empirical Formula (Hill Notation) C16H16N2O3
Purity ≥98% (HPLC)
Apperance solid
Solubility DMSO: >10 mg/mL
Solubility H2O: insoluble
GHS Pictograms GHS05
GHS Pictograms GHS07
GHS Signal Word Danger
GHS Hazard statements H302-H317-H318
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS Precautionary statements P280-P305 + P351 + P338
Risk Statements 22-41-43
Safety Statements 26-36/37/39
Storage Temperature 2-8°C
German water hazard class 2

DETAILS

Description (English)
Biochem/physiol Actions
One of a class of aroyl pyrrole hydroxy amide (APHA) compounds showing histone deacetylase (HDAC) inhibition, Compound 8 is the most potent and HDAC class I-selective.1
Description (简体中文)
Biochem/physiol Actions
One of a class of aroyl pyrrole hydroxy amide (APHA) compounds showing histone deacetylase (HDAC) inhibition, Compound 8 is the most potent and HDAC class I-selective.1

REFERENCES