Divaplon: Difference between revisions
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{{Short description|Chemical compound}} |
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{{Drugbox |
{{Drugbox |
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| Verifiedfields = changed |
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| IUPAC_name = (6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-yl)-phenylmethanone |
| IUPAC_name = (6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-yl)-phenylmethanone |
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| image = Divaplon. |
| image = Divaplon Structure.svg |
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| width = 180 |
| width = 180 |
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<!--Identifiers--> |
<!--Identifiers--> |
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| CAS_number_Ref = {{cascite|correct|??}} |
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| CAS_number = 90808-12-1 |
| CAS_number = 90808-12-1 |
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| ATC_prefix = none |
| ATC_prefix = none |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| DrugBank = |
| DrugBank = |
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| UNII_Ref = {{fdacite| |
| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = 4AOV43246G |
| UNII = 4AOV43246G |
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| ChemSpiderID = 59234 |
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| ChEMBL = 281164 |
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<!--Chemical data--> |
<!--Chemical data--> |
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| C=17 | H=17 | N=3 | O=2 |
| C=17 | H=17 | N=3 | O=2 |
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| molecular_weight = 295.336 |
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| smiles = CCC1=C(N2C=C(N=C2N=C1OC)C(=O)C3=CC=CC=C3)C |
| smiles = CCC1=C(N2C=C(N=C2N=C1OC)C(=O)C3=CC=CC=C3)C |
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| StdInChI = 1S/C17H17N3O2/c1-4-13-11(2)20-10-14(18-17(20)19-16(13)22-3)15(21)12-8-6-5-7-9-12/h5-10H,4H2,1-3H3 |
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| StdInChIKey = NRJVHCSYLGLURI-UHFFFAOYSA-N |
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'''Divaplon''' ('''RU-32698''') is a [[nonbenzodiazepine]], [[anxiolytic]] and [[anticonvulsant]] drug from the [[ |
'''Divaplon''' ('''RU-32698''') is a [[nonbenzodiazepine]], [[anxiolytic]] and [[anticonvulsant]] drug from the [[imidazopyrimidine]] family of drugs. It acts as a [[partial agonist]] at the "[[benzodiazepine]] site" of the [[GABAA receptor|GABA<sub>A</sub>]] [[Receptor (biochemistry)|receptor]] in the brain.<ref>{{cite journal | vauthors = Feely M, Boyland P, Picardo A, Cox A, Gent JP | title = Lack of anticonvulsant tolerance with RU 32698 and Ro 17-1812 | journal = European Journal of Pharmacology | volume = 164 | issue = 2 | pages = 377–80 | date = May 1989 | pmid = 2759183 | doi = 10.1016/0014-2999(89)90482-2 }}</ref><ref>{{cite journal | vauthors = Sanger DJ, Joly D, Perrault G | s2cid = 32627339 | title = Benzodiazepine (omega) receptor partial agonists and the acquisition of conditioned fear in mice | journal = Psychopharmacology | volume = 121 | issue = 1 | pages = 104–8 | date = September 1995 | pmid = 8539334 | doi = 10.1007/BF02245596 }}</ref><ref>{{cite journal | vauthors = Pellón R, Ruíz A, Lamas E, Rodríguez C | title = Pharmacological analysis of the effects of benzodiazepines on punished schedule-induced polydipsia in rats | journal = Behavioural Pharmacology | volume = 18 | issue = 1 | pages = 81–7 | date = February 2007 | pmid = 17218801 | doi = 10.1097/FBP.0b013e3280143212 | s2cid = 40188048 }}</ref> |
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==References== |
== References == |
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{{reflist}} |
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<references/> |
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{{Anxiolytics}} |
{{Anxiolytics}} |
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{{GABAAR PAMs}} |
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[[Category:Anxiolytics]] |
[[Category:Anxiolytics]] |
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[[Category: |
[[Category:Aromatic ketones]] |
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[[Category:Ethers]] |
[[Category:Ethers]] |
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[[Category:Imidazopyrimidines]] |
[[Category:Imidazopyrimidines]] |
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[[Category:GABAA receptor positive allosteric modulators]] |