| Compound Information | SONAR Target prediction |
| Name: | LOPERAMIDE HYDROCHLORIDE |
| Unique Identifier: | SPE02300241 |
| MolClass: | Checkout models in ver1.5 and ver1.0 |
| Molecular Formula: | |
| Molecular Weight: | 479.228 g/mol |
| X log p: | 28.186 (online calculus) |
| Lipinksi Failures | 1 |
| TPSA | 23.55 |
| Hydrogen Bond Donor Count: | 0 |
| Hydrogen Bond Acceptors Count: | 4 |
| Rotatable Bond Count: | 8 |
| Canonical Smiles: | Cl.CN(C)C(=O)C(CCN1CCC(O)(CC1)c1ccc(Cl)cc1)(c1ccccc1)c1ccccc1 |
| Source: | synthetic |
| Therapeutics: | Ca channel blocker |
| Generic_name: | Loperamide |
| Chemical_iupac_name: | 4-[4-(4-chlorophenyl)-4-hydroxy-1-piperidyl]-N,N-dimethyl-2,2-diphenyl-butanamide |
| Drug_type: | Approved Drug |
| Pharmgkb_id: | PA450262 |
| Kegg_compound_id: | C07080 |
| Drugbank_id: | APRD00275 |
| Melting_point: | 228 oC |
| H2o_solubility: | Slight |
| Logp: | 6.249 |
| Cas_registry_number: | 53179-11-6 |
| Drug_category: | Antidiarrheals; ATC:A07DA03; ATC:A07DA05 |
| Indication: | For the control and symptomatic relief of acute nonspecific diarrhea and of chronic diarrhea associated with inflammatory bowel disease or gastroenteritis. Also used for reducing the volume of discharge from ileostomies. |
| Pharmacology: | Loperamide is a synthetic anti-diarrheal indicated for the control and symptomatic relief of acute nonspecific diarrhea and of chronic diarrhea associated with inflammatory bowel disease. Loperamide is also indicated for reducing the volume of discharge from ileostomies. In man, Loperamide prolongs the transit time of the intestinal contents. It reduces the daily fecal volume, increases the viscosity and bulk density, and diminishes the loss of fluid and electrolytes. Tolerance to the antidiarrheal effect has not been observed. Loperamide is an opioid receptor agonist and acts on the mu opioid receptors in the myenteric plexus large intestines; it does not affect the central nervous system like other opioids. It works specifically by decreasing the activity of the myenteric plexus which decreases the motility of the circular and longitudinal smooth muscles of the intestinal wall. This increases the amount of time substances stay in the intestine, allowing for more water to be absorbed out of the fecal matter. Loperamide also decreases colonic mass movements and suppresses the gastrocolic reflex. |
| Mechanism_of_action: | In vitro and animal studies show that Loperamide acts by slowing intestinal motility and by affecting water and electrolyte movement through the bowel. Loperamide inhibits peristaltic activity by a direct effect on the circular and longitudinal muscles of the intestinal wall. It is a non-selective calcium channel blocker and binds to opioid mu-receptors. Evidence also suggests that at higher concentrations it binds to NMDA receptors and to calmodulin. |
| Organisms_affected: | Humans and other mammals |
| Found: 205 nonactive | as graph: single | with analogs | [1] << Back 81 82 83 84 85 86 87 88 89 90 Next >> [205] |
| Species: | 4932 |
| Condition: | VAM3 |
| Replicates: | 2 |
| Raw OD Value: r im | 0.6037±0.00219203 |
| Normalized OD Score: sc h | 1.0006±0.00345847 |
| Z-Score: | 0.0173±0.105791 |
| p-Value: | 0.940378 |
| Z-Factor: | -35.8986 |
| Fitness Defect: | 0.0615 |
| Bioactivity Statement: | Nonactive |
| ps |
| DBLink | Rows returned: 3 |
| 3954 | 4-[4-(4-chlorophenyl)-4-hydroxy-2,3,5,6-tetrahydropyridin-1-yl]-N,N-dimethyl-2,2-diphenyl-butanamide |
| 3955 | 4-[4-(4-chlorophenyl)-4-hydroxy-1-piperidyl]-N,N-dimethyl-2,2-diphenyl-butanamide |
| 71420 | 4-[4-(4-chlorophenyl)-4-hydroxy-1-piperidyl]-N,N-dimethyl-2,2-diphenyl-butanamide hydrochloride |
| internal high similarity DBLink | Rows returned: 1 |
| LOPAC 00444 | 1.0000 |
| active | Cluster 16161 | Additional Members: 10 | Rows returned: 4 |
| SPE01505691 | 0.512820512820513 |
| LOPAC 00317 | 0.279411764705882 |
| LOPAC 00287 | 0 |
| SPE01500325 | 0 |
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