| Stem definition | Drug id | CAS RN |
|---|---|---|
| beta-adrenoreceptor antagonists | 2176 | 13523-86-9 |
| Dose | Unit | Route |
|---|---|---|
| 15 | mg | O |
| 15 | mg | P |
| Property | Value | Reference |
|---|---|---|
| MRTD (Maximum Recommended Therapeutic Daily Dose) | 4.03 ยตM/kg/day | Contrera JF, Matthews EJ, Kruhlak NL, Benz RD |
| BDDCS (Biopharmaceutical Drug Disposition Classification System) | 1 | Hosey CM, Chan R, Benet LZ |
| S (Water solubility) | 0.86 mg/mL | Bocci G, Oprea TI, Benet LZ |
| EoM (Fraction excreted unchanged in urine) | 54 % | Hosey CM, Chan R, Benet LZ |
| BA (Bioavailability) | 88 % | Kim MT, Sedykh A, Chakravarti SK, Saiakhov RD, Zhu H |
| Vd (Volume of distribution) | 1.20 L/kg | Lombardo F, Berellini G, Obach RS |
| CL (Clearance) | 7.70 mL/min/kg | Lombardo F, Berellini G, Obach RS |
| fu (Fraction unbound in plasma) | 0.58 % | Lombardo F, Berellini G, Obach RS |
| t_half (Half-life) | 2.20 hours | Lombardo F, Berellini G, Obach RS |
| Date | Agency | Company | Orphan |
|---|---|---|---|
| Sept. 3, 1982 | FDA |
| 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 |
|---|---|---|---|---|---|---|
| Atrioventricular block complete | 112.42 | 36.50 | 24 | 618 | 8227 | 63480153 |
| Oesophagitis | 63.59 | 36.50 | 17 | 625 | 14991 | 63473389 |
| Neutrophil count abnormal | 54.35 | 36.50 | 11 | 631 | 2881 | 63485499 |
| Rhabdomyolysis | 53.07 | 36.50 | 19 | 623 | 43932 | 63444448 |
| White blood cell count abnormal | 51.15 | 36.50 | 12 | 630 | 6230 | 63482150 |
| Urinary tract infection | 48.25 | 36.50 | 31 | 611 | 264653 | 63223727 |
| Haemoglobin abnormal | 48.16 | 36.50 | 11 | 631 | 5077 | 63483303 |
| Hypertension | 44.30 | 36.50 | 30 | 612 | 279273 | 63209107 |
| Drug interaction | 37.19 | 36.50 | 25 | 617 | 229106 | 63259274 |
None
| 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 |
|---|---|---|---|---|---|---|
| Atrioventricular block complete | 98.53 | 27.36 | 24 | 691 | 16586 | 79727087 |
| Hypertension | 40.56 | 27.36 | 29 | 686 | 330963 | 79412710 |
| Rhabdomyolysis | 39.59 | 27.36 | 19 | 696 | 103112 | 79640561 |
| Chromaturia | 31.82 | 27.36 | 11 | 704 | 25735 | 79717938 |
None
| Source | Code | Description |
|---|---|---|
| ATC | C07AA03 | CARDIOVASCULAR SYSTEM BETA BLOCKING AGENTS BETA BLOCKING AGENTS Beta blocking agents, non-selective |
| ATC | C07CA03 | CARDIOVASCULAR SYSTEM BETA BLOCKING AGENTS BETA BLOCKING AGENTS AND OTHER DIURETICS Beta blocking agents, non-selective, and other diuretics |
| FDA MoA | N0000000161 | Adrenergic beta-Antagonists |
| FDA EPC | N0000175556 | beta-Adrenergic Blocker |
| MeSH PA | D018663 | Adrenergic Agents |
| MeSH PA | D018674 | Adrenergic Antagonists |
| MeSH PA | D000319 | Adrenergic beta-Antagonists |
| MeSH PA | D000959 | Antihypertensive Agents |
| MeSH PA | D002317 | Cardiovascular Agents |
| MeSH PA | D018377 | Neurotransmitter Agents |
| MeSH PA | D018490 | Serotonin Agents |
| MeSH PA | D012702 | Serotonin Antagonists |
| MeSH PA | D014665 | Vasodilator Agents |
| CHEBI has role | CHEBI:35530 | beta-adrenergic blockers |
| CHEBI has role | CHEBI:35620 | vasodilator agents |
| CHEBI has role | CHEBI:35674 | antihypertensive drugs |
| CHEBI has role | CHEBI:39456 | antiglaucoma agent |
| CHEBI has role | CHEBI:48279 | serotonin antagonists |
| Disease | Relation | SNOMED_ID | DOID |
|---|---|---|---|
| Hypertensive disorder | indication | 38341003 | DOID:10763 |
| Angina pectoris | off-label use | 194828000 | |
| Bronchospasm | contraindication | 4386001 | |
| Complete atrioventricular block | contraindication | 27885002 | |
| Depressive disorder | contraindication | 35489007 | |
| Anaphylaxis | contraindication | 39579001 | |
| Sinus bradycardia | contraindication | 49710005 | |
| Diabetes mellitus | contraindication | 73211009 | DOID:9351 |
| Pulmonary emphysema | contraindication | 87433001 | |
| Cardiogenic shock | contraindication | 89138009 | |
| Kidney disease | contraindication | 90708001 | DOID:557 |
| Myasthenia gravis | contraindication | 91637004 | DOID:437 |
| Partial atrioventricular block | contraindication | 195039008 | |
| Decompensated cardiac failure | contraindication | 195111005 | |
| Disease of liver | contraindication | 235856003 | DOID:409 |
| Raynaud's phenomenon | contraindication | 266261006 | |
| Pregnancy, function | contraindication | 289908002 | |
| Severe chronic obstructive pulmonary disease | contraindication | 313299006 | |
| Right ventricular failure | contraindication | 367363000 |
None
None
| Dissociation level | Dissociation constant | Type (acidic/basic) |
|---|---|---|
| pKa1 | 13.41 | acidic |
| pKa2 | 9.19 | Basic |
None
None
| Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
|---|---|---|---|---|---|---|---|---|---|
| Beta-1 adrenergic receptor | GPCR | PARTIAL AGONIST | Ki | 9.40 | WOMBAT-PK | CHEMBL | |||
| Beta-2 adrenergic receptor | GPCR | PARTIAL AGONIST | Ki | 9 | WOMBAT-PK | CHEMBL | |||
| 5-hydroxytryptamine receptor 1A | GPCR | Ki | 8.10 | WOMBAT-PK | |||||
| 5-hydroxytryptamine receptor 2A | GPCR | AGONIST | Ki | 5 | IUPHAR | ||||
| 5-hydroxytryptamine receptor 2B | GPCR | AGONIST | Ki | 5.70 | IUPHAR | ||||
| 5-hydroxytryptamine receptor 2C | GPCR | Ki | 4.27 | CHEMBL | |||||
| Beta-3 adrenergic receptor | GPCR | Kd | 6.78 | CHEMBL | |||||
| 5-hydroxytryptamine receptor 1B | GPCR | Ki | 7.10 | WOMBAT-PK | |||||
| 5-hydroxytryptamine receptor 1D | GPCR | Ki | 5.21 | PDSP | |||||
| 5-hydroxytryptamine receptor 1B | GPCR | Ki | 7.10 | CHEMBL | |||||
| 5-hydroxytryptamine receptor 1A | GPCR | Ki | 7.70 | CHEMBL | |||||
| Serotonin 1 (5-HT1) receptor | GPCR | Ki | 7 | CHEMBL | |||||
| Serotonin 2 (5-HT2) receptor | GPCR | Ki | 4.53 | CHEMBL |
| ID | Source |
|---|---|
| 4018760 | VUID |
| N0000147063 | NUI |
| D00513 | KEGG_DRUG |
| 4018760 | VANDF |
| C0031937 | UMLSCUI |
| CHEBI:8214 | CHEBI |
| CHEMBL500 | ChEMBL_ID |
| DB00960 | DRUGBANK_ID |
| D010869 | MESH_DESCRIPTOR_UI |
| 4828 | PUBCHEM_CID |
| 91 | IUPHAR_LIGAND_ID |
| 2698 | INN_ID |
| BJ4HF6IU1D | UNII |
| 8332 | RXNORM |
| 1482 | MMSL |
| 5302 | MMSL |
| d00137 | MMSL |
| 001857 | NDDF |
| 18381001 | SNOMEDCT_US |
| 387102009 | SNOMEDCT_US |
| Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
|---|---|---|---|---|---|---|---|---|
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0378-0052 | TABLET | 5 mg | ORAL | ANDA | 21 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0378-0052 | TABLET | 5 mg | ORAL | ANDA | 21 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0378-0127 | TABLET | 10 mg | ORAL | ANDA | 21 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0378-0127 | TABLET | 10 mg | ORAL | ANDA | 21 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 10135-743 | TABLET | 5 mg | ORAL | ANDA | 19 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 10135-743 | TABLET | 5 mg | ORAL | ANDA | 19 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 10135-744 | TABLET | 10 mg | ORAL | ANDA | 19 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 10135-744 | TABLET | 10 mg | ORAL | ANDA | 19 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 29033-028 | TABLET | 5 mg | ORAL | ANDA | 14 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 29033-029 | TABLET | 10 mg | ORAL | ANDA | 14 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 57664-655 | TABLET | 5 mg | ORAL | ANDA | 21 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 57664-656 | TABLET | 10 mg | ORAL | ANDA | 21 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 62559-560 | TABLET | 5 mg | ORAL | ANDA | 19 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 62559-560 | TABLET | 5 mg | ORAL | ANDA | 19 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 62559-561 | TABLET | 10 mg | ORAL | ANDA | 19 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 62559-561 | TABLET | 10 mg | ORAL | ANDA | 19 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 68151-1320 | TABLET | 5 mg | ORAL | ANDA | 21 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 68151-3005 | TABLET | 10 mg | ORAL | ANDA | 21 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 70710-1063 | TABLET | 5 mg | ORAL | ANDA | 17 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 70710-1063 | TABLET | 5 mg | ORAL | ANDA | 17 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 70710-1064 | TABLET | 10 mg | ORAL | ANDA | 17 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 70710-1064 | TABLET | 10 mg | ORAL | ANDA | 17 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 70771-1134 | TABLET | 5 mg | ORAL | ANDA | 1 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 70771-1134 | TABLET | 5 mg | ORAL | ANDA | 1 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 70771-1135 | TABLET | 10 mg | ORAL | ANDA | 1 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 70771-1135 | TABLET | 10 mg | ORAL | ANDA | 1 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 72789-099 | TABLET | 10 mg | ORAL | ANDA | 21 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 72789-099 | TABLET | 10 mg | ORAL | ANDA | 21 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 72789-100 | TABLET | 5 mg | ORAL | ANDA | 21 sections |
| Pindolol | HUMAN PRESCRIPTION DRUG LABEL | 1 | 72789-100 | TABLET | 5 mg | ORAL | ANDA | 21 sections |