Weight | 132.162 g/mol |
---|---|
Formula | C9H8O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2-INDANONE (615-13-4)
Score:
#2331 in Physics
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#7167 in Chemistry
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- Biphenyl-indanone A, a positive allosteric modulator of the metabotropic glutamate receptor subtype 2, has antipsychotic- and anxiolytic-like effects in mice (Journal of Pharmacology and Experimental Therapeutics, 2006)
- Efficient catalytic asymmetric alkylations. 3. A kinetic and mechanistic study of the enantioselective phase-transfer methylation of 6,7-dichloro-5-methoxy-2-phenyl-1-indanone (Journal of Organic Chemistry, 1987)
- Effects of the novel anti-inflammatory compounds, N-[2-(cyclohexyloxy)-4-nitrophenyl] methanesulphonamide (NS-398) and 5-methanesulphonamido-6-(2,4-difluorothiophenyl)-1-indanone (L-745,337), on the cyclo-oxygenase activity of human blood prostaglandin endoperoxide synthases (British Journal of Pharmacology, 1995)
- Allosteric potentiators of the metabotropic glutamate receptor 2 (mGlu2). Part 3: Identification and biological activity of indanone containing mGlu2 receptor potentiators. (Bioorganic & Medicinal Chemistry Letters, 2005)
- Cyclooxygenase-2 inhibitors. Synthesis and pharmacological activities of 5-methanesulfonamido-1-indanone derivatives (Journal of Medicinal Chemistry, 1995)
- Regiospecific and stereoselective hydroxylation of 1-indanone and 2-indanone by naphthalene dioxygenase and toluene dioxygenase. (Applied and Environmental Microbiology, 1994)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C(=O)CC2=CC=CC=C21
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InChIKeyUMJJFEIKYGFCAT-UHFFFAOYSA-N
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