| Weight | 295.426 g/mol |
|---|---|
| Formula | C20H25NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
Glemanserin (107703-78-6, 132553-86-7)
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SMILESC1CN(CCC1C(C2=CC=CC=C2)O)CCC3=CC=CC=C3
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InChIKeyAXNGJCOYCMDPQG-UHFFFAOYSA-N
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- Wikipedia - glemanserin
Glemanserin (INN) (developmental code name MDL-11,939) is a drug which acts as a potent and selective 5-HT2A receptor antagonist. The first truly selective 5-HT2A ligand to be discovered, glemanserin resulted in the development of the widely used and even more potent and selective 5-HT2A receptor antagonist volinanserin (MDL-100,907), which is a fluorinated analogue. Though it was largely superseded in scientific research by volinanserin, glemanserin was investigated clinically for the treatment of generalized anxiety disorder.
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