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4-Hydroxyquinazoline, 98%, Thermo Scientific Chemicals

$73.01 - $211.44

Chemical Identifiers

CAS 491-36-1
Molecular Formula C8H6N2O
Molecular Weight (g/mol) 146.149
MDL Number MFCD00511302
InChI Key QMNUDYFKZYBWQX-UHFFFAOYSA-N
Synonym 4-hydroxyquinazoline, 4-quinazolinol, quinazolin-4-ol, quinazolin-4 3h-one, 4 3h-quinazolinone, 4-quinazolone, 4-quinazolinone, 4 1h-quinazolinone, 4-oxoquinazoline, 3,4-dihydroquinazolin-4-one
PubChem CID 63112
IUPAC Name 1H-quinazolin-4-one
SMILES C1=CC=C2C(=C1)C(=O)N=CN2
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Catalog Number Mfr. No. Quantity Price Quantity  
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AAA1712909
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Thermo Scientific Chemicals
A1712909
10 g
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AAA1712918
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Thermo Scientific Chemicals
A1712918
50 g
Each for $211.44
 
Description

Description

4-Hydroxyquinazoline is been used to inhibit PARP (poly(ADP-ribose) synthetase) which catalyzes covalent attachment of the ADP-ribose moiety of NAD+ to various proteins. This compound specifically and potently inhibits PARP-1. 4-HQN demonstrates the ability to decrease activation of transcription factor NFκB and AP-1 in lipopolysaccharide-induced shock. Mechanistic studies indicate that 4-HQN activates PI3-kinase/Akt pathway in the liver, spleen, and lung and down-regulates two elements of the MAP kinase system. Additionally, this agent has been observed to decrease ischemia-reperfusion-induced increase of protein oxidation, single-strand DNA breaks, lipid peroxidation, and mitochondrial reactive oxygen species production in the reperfusion period.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
4-Hydroxyquinazoline is been used to inhibit PARP (poly(ADP-ribose) synthetase) which catalyzes covalent attachment of the ADP-ribose moiety of NAD+ to various proteins. This compound specifically and potently inhibits PARP-1. 4-HQN demonstrates the ability to decrease activation of transcription factor NFκB and AP-1 in lipopolysaccharide-induced shock. Mechanistic studies indicate that 4-HQN activates PI3-kinase/Akt pathway in the liver, spleen, and lung and down-regulates two elements of the MAP kinase system. Additionally, this agent has been observed to decrease ischemia-reperfusion-induced increase of protein oxidation, single-strand DNA breaks, lipid peroxidation, and mitochondrial reactive oxygen species production in the reperfusion period.

Solubility
Soluble in DMSO (100 mM), ethanol, methanol, and water (10 mM).

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents.
Specifications

Chemical Identifiers

491-36-1
146.149
QMNUDYFKZYBWQX-UHFFFAOYSA-N
63112
C1=CC=C2C(=C1)C(=O)N=CN2
C8H6N2O
MFCD00511302
4-hydroxyquinazoline, 4-quinazolinol, quinazolin-4-ol, quinazolin-4 3h-one, 4 3h-quinazolinone, 4-quinazolone, 4-quinazolinone, 4 1h-quinazolinone, 4-oxoquinazoline, 3,4-dihydroquinazolin-4-one
1H-quinazolin-4-one

Specifications

491-36-1
Odorless
MFCD00511302
118473
Soluble in DMSO (100 mM),ethanol,methanol,and water (10 mM).
C1=CC=C2C(=C1)C(=O)N=CN2
146.149
146.15
4-Hydroxyquinazoline
216°C to 219°C
C8H6N2O
10 g
4-hydroxyquinazoline, 4-quinazolinol, quinazolin-4-ol, quinazolin-4 3h-one, 4 3h-quinazolinone, 4-quinazolone, 4-quinazolinone, 4 1h-quinazolinone, 4-oxoquinazoline, 3,4-dihydroquinazolin-4-one
QMNUDYFKZYBWQX-UHFFFAOYSA-N
1H-quinazolin-4-one
63112
98%
Safety and Handling

Safety and Handling

GHS H Statement
H302-H315-H319-H335
Harmful if swallowed.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c

H302-H315-H319-H335

EINECSNumber : 207-735-8

RTECSNumber : VA2300000

TSCA : No

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only