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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Fenobam hydrate is a selective and orally active mGluR5 antagonist ( IC 50 =84 nM) that can penetrate the blood-brain barrier. Fenobam hydrate shows the K d values of 54 nM and 31 nM on rat and human recombinant mGlu5 receptors, respectively. Fenobam hydrate has anxiolytic activity, inhibits self-administration behavior in rat, and induces apoptosis in cancer cells. Fenobam hydrate can be used for research on neurological diseases, cancer and drug addiction.
| Canonical Smiles | CN1CC(=O)NC1=NC(=O)NC2=CC(=CC=C2)Cl.O |
|---|---|
| IUPAC Name | (3E)-1-(3-chlorophenyl)-3-(1-methyl-4-oxoimidazolidin-2-ylidene)urea;hydrate |
| InChIKey | UNFQKKSADLVQJE-UHFFFAOYSA-N |
| INCHI | 1S/C11H11ClN4O2.H2O/c1-16-6-9(17)14-10(16)15-11(18)13-8-4-2-3-7(12)5-8;/h2-5H,6H2,1H3,(H2,13,14,15,17,18);1H2 |
| Isomeric SMILES | CN\1CC(=O)N/C1=N\C(=O)NC2=CC(=CC=C2)Cl.O |
| Alternate CAS | 63540-28-3 |
| PubChem CID | 135416855 |
| MeSH Entry Terms | fenobam;fenobam anhydrous;fenobam monohydrate |
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