| Weight | 146.149 g/mol |
|---|---|
| Formula | C8H6N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
4-Hydroxyquinazoline (491-36-1)
4(3H)-quinazolinone · quinazolin-4-one
Score:
#31 in Medicinal chemistry
,
#2372 in Biochemistry
,
#5953 in Chemistry
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- Synthesis and in vitro antitumor activity of 4(3H)-quinazolinone derivatives with dithiocarbamate side chains (Bioorganic & Medicinal Chemistry Letters, 2005)
- Gallium(III) triflate-catalyzed one-pot selective synthesis of 2,3-dihydroquinazolin-4(1H)-ones and quinazolin-4(3H)-ones (Tetrahedron Letters, 2008)
- Synthesis, antibacterial, antifungal and anti-HIV evaluation of Schiff and Mannich bases of isatin derivatives with 3-amino-2-methylmercapto quinazolin-4(3H)-one (Pharmaceutica Acta Helvetiae, 1999)
- Synthesis and pharmacological evaluation of some 3-phenyl-2-substituted-3H-quinazolin-4-one as analgesic, anti-inflammatory agents (Bioorganic & Medicinal Chemistry, 2007)
- Substituted quinazolines, part 3. Synthesis, in vitro antitumor activity and molecular modeling study of certain 2-thieno-4(3H)-quinazolinone analogs (European Journal of Medicinal Chemistry, 2009)
- Microwave-Assisted One-Pot Synthesis of 2,3-Disubstituted 3H-Quinazolin-4-ones. (Tetrahedron Letters, 2005)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4(3H)-quinazolinone
- quinazolin-4-one
-
SMILESC1=CC=C2C(=C1)C(=O)N=CN2
-
InChIKeyQMNUDYFKZYBWQX-UHFFFAOYSA-N
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