| Weight | 195.221 g/mol |
|---|---|
| Formula | C13H9NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 0 |
acridone (578-95-0)
9-azaanthracen-10-one · 9(10H)-acridone
Score:
#1935 in Physics
,
#6057 in Chemistry
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LabBot
- Quinoline, quinazoline, and acridone alkaloids. (Natural Product Reports, 1995)
- ACRIDINE AND ACRIDONE DERIVATIVES, ANTICANCER PROPERTIES AND SYNTHETIC METHODS: WHERE ARE WE NOW? (Anti-cancer Agents in Medicinal Chemistry, 2007)
- Quinoline, quinazoline and acridone alkaloids (July 1999 to June 2000) (Natural Product Reports, 2001)
- In vitro activities of furoquinoline and acridone alkaloids against Plasmodium falciparum. (Antimicrobial Agents and Chemotherapy, 1994)
- Synthesis and evaluation of acridine- and acridone-based anti-herpes agents with topoisomerase activity. (Bioorganic & Medicinal Chemistry, 2006)
- ER-27319, an acridone-related compound, inhibits release of antigen-induced allergic mediators from mast cells by selective inhibition of Fc receptor I-mediated activation of Syk (Proceedings of the National Academy of Sciences of the United States of America, 1997)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 9-azaanthracen-10-one
- 9(10H)-acridone
-
SMILESC1=CC=C2C(=C1)C(=O)C3=CC=CC=C3N2
-
InChIKeyFZEYVTFCMJSGMP-UHFFFAOYSA-N
- Pubchem - acridone
- Wikipedia - acridone
Acridone is an organic compound based on the acridine skeleton, with a carbonyl group at the 9 position. It may be synthesized by the self-condensation of N-phenylanthranilic acid.
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acridone
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