Stem definition | Drug id | CAS RN |
---|---|---|
2346 | 56-54-2 |
Dose | Unit | Route |
---|---|---|
1.20 | g | O |
Property | Value | Reference |
---|---|---|
BDDCS (Biopharmaceutical Drug Disposition Classification System) | 1 | Benet LZ, Broccatelli F, Oprea TI |
S (Water solubility) | 11.10 mg/mL | Benet LZ, Broccatelli F, Oprea TI |
EoM (Fraction excreted unchanged in urine) | 18 % | Benet LZ, Broccatelli F, Oprea TI |
MRTD (Maximum Recommended Therapeutic Daily Dose) | 30.82 ยตM/kg/day | Contrera JF, Matthews EJ, Kruhlak NL, Benz RD |
BA (Bioavailability) | 75 % | Kim MT, Sedykh A, Chakravarti SK, Saiakhov RD, Zhu H |
Vd (Volume of distribution) | 2.90 L/kg | Lombardo F, Berellini G, Obach RS |
CL (Clearance) | 4 mL/min/kg | Lombardo F, Berellini G, Obach RS |
fu (Fraction unbound in plasma) | 0.26 % | Lombardo F, Berellini G, Obach RS |
t_half (Half-life) | 6.60 hours | Lombardo F, Berellini G, Obach RS |
Date | Agency | Company | Orphan |
---|---|---|---|
July 12, 1950 | FDA | LILLY |
MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
---|---|---|---|---|---|---|
Drug hypersensitivity | 47.65 | 40.88 | 25 | 283 | 310662 | 63178052 |
MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
---|---|---|---|---|---|---|
Drug ineffective | 85.21 | 40.57 | 49 | 234 | 456702 | 34499946 |
MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
---|---|---|---|---|---|---|
Drug ineffective | 73.81 | 34.39 | 63 | 568 | 1080850 | 78662907 |
Electrocardiogram QT prolonged | 72.31 | 34.39 | 27 | 604 | 90359 | 79653398 |
Multiple-drug resistance | 34.88 | 34.39 | 9 | 622 | 8799 | 79734958 |
None
Source | Code | Description |
---|---|---|
ATC | C01BA01 | CARDIOVASCULAR SYSTEM CARDIAC THERAPY ANTIARRHYTHMICS, CLASS I AND III Antiarrhythmics, class Ia |
ATC | C01BA51 | CARDIOVASCULAR SYSTEM CARDIAC THERAPY ANTIARRHYTHMICS, CLASS I AND III Antiarrhythmics, class Ia |
ATC | C01BA71 | CARDIOVASCULAR SYSTEM CARDIAC THERAPY ANTIARRHYTHMICS, CLASS I AND III Antiarrhythmics, class Ia |
FDA EPC | N0000175426 | Antiarrhythmic |
MeSH PA | D000890 | Anti-Infective Agents |
MeSH PA | D000962 | Antimalarials |
MeSH PA | D000977 | Antiparasitic Agents |
MeSH PA | D000981 | Antiprotozoal Agents |
MeSH PA | D018663 | Adrenergic Agents |
MeSH PA | D000317 | Adrenergic alpha-Antagonists |
MeSH PA | D018674 | Adrenergic Antagonists |
MeSH PA | D000889 | Anti-Arrhythmia Agents |
MeSH PA | D002317 | Cardiovascular Agents |
MeSH PA | D018678 | Cholinergic Agents |
MeSH PA | D018680 | Cholinergic Antagonists |
MeSH PA | D065690 | Cytochrome P-450 CYP2D6 Inhibitors |
MeSH PA | D065607 | Cytochrome P-450 Enzyme Inhibitors |
MeSH PA | D004791 | Enzyme Inhibitors |
MeSH PA | D049990 | Membrane Transport Modulators |
MeSH PA | D065606 | Metabolic Side Effects of Drugs and Substances |
MeSH PA | D018727 | Muscarinic Antagonists |
MeSH PA | D018377 | Neurotransmitter Agents |
MeSH PA | D026941 | Sodium Channel Blockers |
MeSH PA | D061567 | Voltage-Gated Sodium Channel Blockers |
FDA EPC | N0000182135 | Cytochrome P450 2D6 Inhibitor |
FDA MoA | N0000182137 | Cytochrome P450 2D6 Inhibitors |
CHEBI has role | CHEBI:37890 | alpha-adrenergic receptor blockaders |
CHEBI has role | CHEBI:38068 | antimalarials |
CHEBI has role | CHEBI:38070 | antiarrhythmic agent |
CHEBI has role | CHEBI:38633 | sodium channel blockers |
CHEBI has role | CHEBI:48876 | muscarinic antagonists |
CHEBI has role | CHEBI:50183 | P450 inhibitors |
CHEBI has role | CHEBI:77748 | steroid-transporting ATPase inhibitor |
CHEBI has role | CHEBI:77781 | 13-deoxydaunorubicin,NADPH:oxygen oxidoreductase (13-hydroxylating) inhibitor |
CHEBI has role | CHEBI:88188 | allergenic drug |
Disease | Relation | SNOMED_ID | DOID |
---|---|---|---|
Atrial fibrillation | indication | 49436004 | DOID:0060224 |
Malaria | indication | 61462000 | DOID:12365 |
Pseudobulbar affect | indication | 432776007 | |
Life-Threatening Ventricular Tachycardia | indication | ||
Cardioversion of Atrial Fibrillation | indication | ||
Psoriasis | contraindication | 9014002 | DOID:8893 |
Poisoning by digitalis glycoside | contraindication | 12876009 | |
Complete atrioventricular block | contraindication | 27885002 | |
Torsades de pointes | contraindication | 31722008 | |
Hypokalemia | contraindication | 43339004 | |
Low blood pressure | contraindication | 45007003 | |
Chronic heart failure | contraindication | 48447003 | |
Bradycardia | contraindication | 48867003 | |
Left ventricular hypertrophy | contraindication | 55827005 | |
Poisoning by quinidine | contraindication | 59826007 | |
Left bundle branch block | contraindication | 63467002 | |
Left heart failure | contraindication | 85232009 | |
Pulmonary emphysema | contraindication | 87433001 | |
Kidney disease | contraindication | 90708001 | DOID:557 |
Myasthenia gravis | contraindication | 91637004 | DOID:437 |
Anemia due to enzyme deficiency | contraindication | 111577008 | |
Prolonged QT interval | contraindication | 111975006 | |
Hypomagnesemia | contraindication | 190855004 | |
Partial atrioventricular block | contraindication | 195039008 | |
Disease of liver | contraindication | 235856003 | DOID:409 |
Esophageal dysmotility | contraindication | 266434009 | DOID:9192 |
Thrombocytopenic disorder | contraindication | 302215000 | DOID:1588 |
Congenital long QT syndrome | contraindication | 442917000 | |
Non-specific intraventricular conduction delay | contraindication | 698252002 | |
Digitalis Toxicity with AV Conduction Defects | contraindication |
None
None
Dissociation level | Dissociation constant | Type (acidic/basic) |
---|---|---|
pKa1 | 12.44 | acidic |
pKa2 | 8.02 | Basic |
pKa3 | 4.1 | Basic |
Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Patent number | Patent expiration date | Patent use |
---|---|---|---|---|---|---|---|---|---|---|
20MG;10MG | NUEDEXTA | AVANIR PHARMS | N021879 | Oct. 29, 2010 | RX | CAPSULE | ORAL | 8227484 | July 17, 2023 | TREATMENT OF PSEUDOBULBAR AFFECT |
20MG;10MG | NUEDEXTA | AVANIR PHARMS | N021879 | Oct. 29, 2010 | RX | CAPSULE | ORAL | 7659282 | Aug. 13, 2026 | TREATMENT OF PSEUDOBULBAR AFFECT |
None
Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
---|---|---|---|---|---|---|---|---|---|
Sodium channel protein type 5 subunit alpha | Ion channel | BLOCKER | IC50 | 5.16 | CHEMBL | CHEMBL | |||
Sodium channel alpha subunits; brain (Types I, II, III) | Ion channel | BLOCKER | IC50 | 5.49 | CHEMBL | CHEMBL | |||
Cytochrome P450 2D6 | Enzyme | INHIBITOR | Ki | 7.92 | SCIENTIFIC LITERATURE | DRUG LABEL | |||
Sodium channel subunit beta-3 | Ion channel | WOMBAT-PK | |||||||
Sodium channel subunit beta-4 | Ion channel | WOMBAT-PK | |||||||
Potassium voltage-gated channel subfamily H member 2 | Ion channel | IC50 | 6.49 | CHEMBL | |||||
Multidrug resistance protein 1 | Transporter | Ki | 5.59 | CHEMBL | |||||
Muscarinic acetylcholine receptor M2 | GPCR | Ki | 8.13 | PDSP | |||||
Cholinesterase | Enzyme | IC50 | 5.91 | CHEMBL | |||||
Potassium voltage-gated channel subfamily A member 5 | Ion channel | BLOCKER | Kd | 5.20 | IUPHAR | ||||
Potassium voltage-gated channel subfamily H member 1 | Ion channel | BLOCKER | IC50 | 5.80 | IUPHAR | ||||
Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4 | Ion channel | IC50 | 4.11 | WOMBAT-PK | |||||
Potassium voltage-gated channel subfamily A member 7 | Ion channel | BLOCKER | Kd | 4.80 | IUPHAR | ||||
Solute carrier family 22 member 2 | Transporter | IC50 | 4.06 | WOMBAT-PK | |||||
Multidrug and toxin extrusion protein 1 | Transporter | IC50 | 4.95 | CHEMBL | |||||
Equilibrative nucleoside transporter 4 | Transporter | INHIBITOR | Ki | 4.60 | IUPHAR | ||||
Sodium channel subunit beta-1 | Ion channel | WOMBAT-PK | |||||||
Sodium channel subunit beta-2 | Ion channel | WOMBAT-PK | |||||||
Cholinesterase | Enzyme | IC50 | 5.13 | CHEMBL | |||||
Sodium channel protein type 5 subunit alpha | Ion channel | BLOCKER | IC50 | 5 | IUPHAR | ||||
Potassium voltage-gated channel subfamily D member 2 | Ion channel | IC50 | 5.66 | CHEMBL | |||||
Potassium channel subfamily T member 1 | Ion channel | BLOCKER | IC50 | 4 | IUPHAR |
ID | Source |
---|---|
4017419 | VUID |
N0000179295 | NUI |
D00642 | KEGG_DRUG |
27555-34-6 | SECONDARY_CAS_RN |
6591-63-5 | SECONDARY_CAS_RN |
7054-25-3 | SECONDARY_CAS_RN |
4017417 | VANDF |
4017418 | VANDF |
4017419 | VANDF |
4019925 | VANDF |
C0034414 | UMLSCUI |
CHEBI:28593 | CHEBI |
QDN | PDB_CHEM_ID |
CHEMBL1294 | ChEMBL_ID |
CHEMBL21578 | ChEMBL_ID |
CHEMBL1201486 | ChEMBL_ID |
CHEMBL3707183 | ChEMBL_ID |
DB00908 | DRUGBANK_ID |
CHEMBL1200437 | ChEMBL_ID |
D011802 | MESH_DESCRIPTOR_UI |
C047144 | MESH_SUPPLEMENTAL_RECORD_UI |
C016713 | MESH_SUPPLEMENTAL_RECORD_UI |
441074 | PUBCHEM_CID |
2342 | IUPHAR_LIGAND_ID |
6151-40-2 | SECONDARY_CAS_RN |
1668-99-1 | SECONDARY_CAS_RN |
ITX08688JL | UNII |
35220 | RXNORM |
2389 | MMSL |
2395 | MMSL |
5402 | MMSL |
5403 | MMSL |
5404 | MMSL |
72295 | MMSL |
d00020 | MMSL |
000618 | NDDF |
000619 | NDDF |
000620 | NDDF |
000621 | NDDF |
004377 | NDDF |
1217203007 | SNOMEDCT_US |
31306009 | SNOMEDCT_US |
372697008 | SNOMEDCT_US |
5907009 | SNOMEDCT_US |
77632008 | SNOMEDCT_US |
82230005 | SNOMEDCT_US |
CHEMBL2165709 | ChEMBL_ID |
Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
---|---|---|---|---|---|---|---|---|
Quinidine Sulfate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0185-1047 | TABLET | 300 mg | ORAL | ANDA | 18 sections |
Quinidine Sulfate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0185-1047 | TABLET | 300 mg | ORAL | ANDA | 18 sections |
Quinidine Sulfate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0185-4346 | TABLET | 200 mg | ORAL | ANDA | 18 sections |
Quinidine Sulfate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0185-4346 | TABLET | 200 mg | ORAL | ANDA | 18 sections |
QUINIDINE SULFATE | HUMAN PRESCRIPTION DRUG LABEL | 1 | 42806-512 | TABLET | 300 mg | ORAL | ANDA | 20 sections |
QUINIDINE SULFATE | HUMAN PRESCRIPTION DRUG LABEL | 1 | 42806-513 | TABLET | 200 mg | ORAL | ANDA | 20 sections |
Quinidine Gluconate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 51407-288 | TABLET, EXTENDED RELEASE | 324 mg | ORAL | ANDA | 26 sections |
Quinidine Gluconate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 53489-141 | TABLET, EXTENDED RELEASE | 324 mg | ORAL | ANDA | 26 sections |
Quinidine Gluconate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 54738-901 | TABLET, EXTENDED RELEASE | 324 mg | ORAL | ANDA | 25 sections |
Nuedexta | HUMAN PRESCRIPTION DRUG LABEL | 2 | 59148-053 | CAPSULE, GELATIN COATED | 10 mg | ORAL | NDA | 27 sections |
NUEDEXTA | HUMAN PRESCRIPTION DRUG LABEL | 2 | 64597-301 | CAPSULE, GELATIN COATED | 10 mg | ORAL | NDA | 27 sections |
NUEDEXTA | HUMAN PRESCRIPTION DRUG LABEL | 2 | 64597-301 | CAPSULE, GELATIN COATED | 10 mg | ORAL | NDA | 27 sections |
Quinidine Sulfate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 68151-1991 | TABLET | 200 mg | ORAL | ANDA | 13 sections |
Quinidine Gluconate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 68151-2701 | TABLET, EXTENDED RELEASE | 324 mg | ORAL | ANDA | 25 sections |
Quinidine gluconate | Human Prescription Drug Label | 1 | 71930-016 | TABLET, EXTENDED RELEASE | 324 mg | ORAL | ANDA | 13 sections |