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| Stem definition | Drug id | CAS RN |
|---|---|---|
| 1689 | 25990-43-6 |
| Dose | Unit | Route |
|---|---|---|
| 0.10 | g | O |
| Property | Value | Reference |
|---|---|---|
| BDDCS (Biopharmaceutical Drug Disposition Classification System) | 1 | Bocci G, Oprea TI, Benet LZ |
| Property | Description | Value | Unit | Confidence | Similarity |
|---|---|---|---|---|---|
| azlogd74 | LogD at pH 7.4 | -0.499 | High | 1 | |
| caco2-efflux | Caco-2 efflux ratio (BA/AB) | 2.366 | High | 1 | |
| caco2-intrinsic-papp | Caco-2 intrinsic apparent permeability | 0.652 | 10^-6 cm/s | High | 1 |
| dh-clint | Dog hepatocyte intrinsic clearance | 4.519 | uL/min/10^6 cells | High | 1 |
| dppb | Dog plasma protein binding (% unbound) | 69.030 | % | High | 1 |
| fcs-ppb | Fetal calf serum protein binding (% unbound) | 61.910 | % | High | 1 |
| herg | hERG pIC50 | 4.525 | pIC50 | High | 1 |
| hh-clint | Human hepatocyte intrinsic clearance | 1.396 | uL/min/10^6 cells | High | 1 |
| hlm-clint | Human liver microsomal intrinsic clearance | 3.981 | uL/min/mg protein | High | 1 |
| hppb | Human plasma protein binding (% unbound) | 63.470 | % | High | 1 |
| kinase-safety-class | ACVR2A,ACVR2B,AXL,BRAF,BTK,CAMK2B,CAMK2D,CDK5,CDK9,DYRK1B,EIF2AK3,EPHB4,ERBB2,GRK2,ITK,MAP3K7,MAPK7,NTRK2,PDK1,PDK2,PDK4,PIK3CB,PRKDC,SIK2,SIK3,TEK,TGFBR1 | 27 | |||
| kinase-selectivity-class | AXL,GRK2,PDK4 | 3 | |||
| mdck-mdr1-efflux | MDCK-MDR1 efflux ratio | 1.500 | High | 1 | |
| mh-clint | Mouse hepatocyte intrinsic clearance | 75.683 | High | 1 | |
| mppb | Mouse plasma protein binding (% unbound) | 67.580 | High | 1 | |
| nih-mdck-mdr1-efflux | NIH MDCK-MDR1 efflux ratio | 2.249 | High | 1 | |
| pfas-class | PFAS structural alert (1 = True, 0 = False) | 0 | |||
| pppb | Pig plasma protein binding (% unbound) | 76.810 | % | High | 1 |
| rh-clint | Rat hepatocyte intrinsic clearance | 117.220 | uL/min/10^6 cells | High | 1 |
| rh-fuinc | Rat hepatocyte fraction unbound in incubation | 84.780 | % | High | 1 |
| rppb | Rat plasma protein binding (% unbound) | 58.610 | % | High | 1 |
| solubility-dd | Solubility at pH 7.4 in DMSO | 901.571 | uM | High | 1 |
| Date | Agency | Company | Orphan |
|---|---|---|---|
| Nov. 14, 1956 | FDA | SANOFI AVENTIS US |
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| Source | Code | Description |
|---|---|---|
| ATC | A03AB12 | ALIMENTARY TRACT AND METABOLISM DRUGS FOR FUNCTIONAL GASTROINTESTINAL DISORDERS DRUGS FOR FUNCTIONAL GASTROINTESTINAL DISORDERS Synthetic anticholinergics, quaternary ammonium compounds |
| FDA MoA | N0000175370 | Cholinergic Antagonists |
| FDA EPC | N0000175574 | Anticholinergic |
| Disease | Relation | SNOMED_ID | DOID |
|---|---|---|---|
| Peptic ulcer | indication | 13200003 | DOID:750 |
| Gastric ulcer | indication | 397825006 | DOID:10808 |
| Irritable bowel syndrome | off-label use | 10743008 | DOID:9778 |
| Tachyarrhythmia | contraindication | 6285003 | |
| Urinary tract obstruction | contraindication | 7163005 | DOID:5200 |
| Disorder of autonomic nervous system | contraindication | 15241006 | |
| Glaucoma | contraindication | 23986001 | DOID:1686 |
| Toxic megacolon | contraindication | 28536002 | DOID:1770 |
| Atony of colon | contraindication | 29479008 | |
| Hyperthyroidism | contraindication | 34486009 | DOID:7998 |
| Hypertensive disorder | contraindication | 38341003 | DOID:10763 |
| Conduction disorder of the heart | contraindication | 44808001 | |
| Chronic heart failure | contraindication | 48447003 | |
| Paralytic ileus | contraindication | 55525008 | DOID:8442 |
| Peptic reflux disease | contraindication | 57643001 | |
| Ulcerative colitis | contraindication | 64766004 | DOID:8577 |
| Kidney disease | contraindication | 90708001 | DOID:557 |
| Myasthenia gravis | contraindication | 91637004 | DOID:437 |
| Gastrointestinal obstruction | contraindication | 126765001 | |
| Bleeding | contraindication | 131148009 | |
| Disease of liver | contraindication | 235856003 | DOID:409 |
| Benign prostatic hyperplasia | contraindication | 266569009 | |
| Disorder of coronary artery | contraindication | 414024009 |
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| Dissociation level | Dissociation constant | Type (acidic/basic) |
|---|---|---|
| pKa1 | 13.68 | acidic |
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| Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
|---|---|---|---|---|---|---|---|---|---|
| Muscarinic acetylcholine receptor M1 | GPCR | ANTAGONIST | CHEMBL | CHEMBL | |||||
| Muscarinic acetylcholine receptor M3 | GPCR | ANTAGONIST | Ki | 8.59 | CHEMBL | CHEMBL | |||
| Muscarinic acetylcholine receptor M2 | GPCR | Ki | 9.17 | CHEMBL | |||||
| Solute carrier family 22 member 1 | Transporter | IC50 | 4.19 | CHEMBL |
| ID | Source |
|---|---|
| 4019812 | VUID |
| N0000147901 | NUI |
| D00720 | KEGG_DRUG |
| 76-90-4 | SECONDARY_CAS_RN |
| 4018609 | VANDF |
| 4019812 | VANDF |
| C0360172 | UMLSCUI |
| CHEBI:6752 | CHEBI |
| CHEMBL524004 | ChEMBL_ID |
| DB04843 | DRUGBANK_ID |
| CHEMBL1724 | ChEMBL_ID |
| C005101 | MESH_SUPPLEMENTAL_RECORD_UI |
| 4057 | PUBCHEM_CID |
| ONW3LB39P7 | UNII |
| 107770 | RXNORM |
| 5045 | MMSL |
| d00995 | MMSL |
| 001746 | NDDF |
| 004701 | NDDF |
| 372834001 | SNOMEDCT_US |
| 60289002 | SNOMEDCT_US |
| 74022005 | SNOMEDCT_US |
| 889 | INN_ID |
| ONW3LB39P7 | INXIGHT DRUGS |
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