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Vedaclidine (INN,: 180 codenamed LY-297,802, NNC 11-1053) is an experimental analgesic drug which acts as a mixed agonist–antagonist at muscarinic acetylcholine receptors, being a potent and selective agonist for the M1 and M4 subtypes, yet an antagonist at the M2, M3 and M5 subtypes. It is orally active and an effective analgesic over 3× the potency of…
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analgesic m1 inn drug agonist antagonist m4 m2 m3 m5 morphine salivation tremor codenamed ly-297 802 nnc 11-1053 experimental acts
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Vedaclidine | 3D model (JSmol) | Interactive image | 1.00 | infobox |
| Vedaclidine | ATC code | None | 1.00 | infobox |
| Vedaclidine | CAS Number | 141575-50-0 | 1.00 | infobox |
| Vedaclidine | ChEMBL | ChEMBL136807 | 1.00 | infobox |
| Vedaclidine | ChemSpider | 8064764 | 1.00 | infobox |
| Vedaclidine | CompTox Dashboard (EPA) | DTXSID30275663 | 1.00 | infobox |
| Vedaclidine | Formula | C13H21N3S2 | 1.00 | infobox |
| Vedaclidine | Molar mass | 283.45 g·mol−1 | 1.00 | infobox |
| Vedaclidine | Other names | (S)-3-[4-(butylthio)-1,2,5-thiadiazol-3-yl]quinuclidine | 1.00 | infobox |
| Vedaclidine | PubChem CID | 9889093 | 1.00 | infobox |
| Vedaclidine | Routes of administration | oral | 1.00 | infobox |
| Vedaclidine | UNII | 98IW5HAV1N | 1.00 | infobox |
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