| Stem definition | Drug id | CAS RN |
|---|---|---|
| 2142 | 50-60-2 |
| Dose | Unit | Route |
|---|---|---|
| 10 | mg | O |
| 10 | mg | P |
| Property | Value | Reference |
|---|---|---|
| MRTD (Maximum Recommended Therapeutic Daily Dose) | 15.23 ยตM/kg/day | Contrera JF, Matthews EJ, Kruhlak NL, Benz RD |
| BDDCS (Biopharmaceutical Drug Disposition Classification System) | 1 | Hosey CM, Chan R, Benet LZ |
| CL (Clearance) | 42 mL/min/kg | Lombardo F, Berellini G, Obach RS |
| t_half (Half-life) | 2.50 hours | Lombardo F, Berellini G, Obach RS |
| S (Water solubility) | 50 mg/mL | Bocci G, Oprea TI, Benet LZ |
| Date | Agency | Company | Orphan |
|---|---|---|---|
| Jan. 30, 1952 | FDA | NOVARTIS |
None
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 |
|---|---|---|---|---|---|---|
| Neutrophil count increased | 59.34 | 52.91 | 15 | 281 | 29381 | 79714711 |
| Blood urea increased | 56.31 | 52.91 | 16 | 280 | 48774 | 79695318 |
None
| Source | Code | Description |
|---|---|---|
| ATC | C04AB01 | CARDIOVASCULAR SYSTEM PERIPHERAL VASODILATORS PERIPHERAL VASODILATORS Imidazoline derivatives |
| ATC | V03AB36 | VARIOUS ALL OTHER THERAPEUTIC PRODUCTS ALL OTHER THERAPEUTIC PRODUCTS Antidotes |
| FDA MoA | N0000000099 | Adrenergic alpha-Antagonists |
| FDA EPC | N0000175553 | alpha-Adrenergic Blocker |
| MeSH PA | D018663 | Adrenergic Agents |
| MeSH PA | D000317 | Adrenergic alpha-Antagonists |
| MeSH PA | D018674 | Adrenergic Antagonists |
| MeSH PA | D000959 | Antihypertensive Agents |
| MeSH PA | D002317 | Cardiovascular Agents |
| MeSH PA | D018377 | Neurotransmitter Agents |
| CHEBI has role | CHEBI:35620 | vasodilator agents |
| CHEBI has role | CHEBI:37890 | alpha-adrenergic receptor blockaders |
| Disease | Relation | SNOMED_ID | DOID |
|---|---|---|---|
| Paroxysmal hypertension | indication | 23130000 | |
| Cerebral ischemia | indication | 287731003 | |
| Pheochromocytoma | indication | 302835009 | |
| Peripheral vascular disease | indication | 400047006 | |
| Prevention of Hypertension in Pheochromocytoma | indication | ||
| Hypertensive Emergencies | indication | ||
| Diagnostic Test for Pheochromocytoma | indication | ||
| Dermal Necrosis | indication | ||
| Hypertension Secondary to Pheochromocytoma | indication | ||
| Extravasation injury | off-label use | 371100002 | |
| Impotence | off-label use | 397803000 | |
| Sinus tachycardia | contraindication | 11092001 | |
| Myocardial infarction | contraindication | 22298006 | DOID:5844 |
| Glaucoma | contraindication | 23986001 | DOID:1686 |
| Complete atrioventricular block | contraindication | 27885002 | |
| Conduction disorder of the heart | contraindication | 44808001 | |
| Low blood pressure | contraindication | 45007003 | |
| Angina pectoris | contraindication | 194828000 | |
| Disease of liver | contraindication | 235856003 | DOID:409 |
| Chronic myocardial ischemia | contraindication | 413844008 | DOID:3393 |
| Disorder of coronary artery | contraindication | 414024009 | |
| Cardiac Conduction Delay | contraindication |
None
None
| Dissociation level | Dissociation constant | Type (acidic/basic) |
|---|---|---|
| pKa1 | 9.33 | acidic |
| pKa2 | 7.33 | Basic |
| pKa3 | 5.88 | Basic |
| Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Patent number | Patent expiration date | Patent use |
|---|---|---|---|---|---|---|---|---|---|---|
| 0.4MG/1.7ML | ORAVERSE | SEPTODONT HOLDING | N022159 | May 9, 2008 | RX | INJECTABLE | INJECTION | 7569230 | Oct. 17, 2023 | A METHOD OF REVERSING SOFT-TISSUE ANESTHESIA I.E. ANESTHESIA OF THE LIP AND TONGUE, AND THE ASSOCIATED FUNCTIONAL DEFICITS RESULTING FROM AN INTRAORAL SUBMUCOSAL INJECTION OF A LOCAL ANESTHETIC |
None
| Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
|---|---|---|---|---|---|---|---|---|---|
| Alpha-2A adrenergic receptor | GPCR | ANTAGONIST | Ki | 8.77 | CHEMBL | CHEMBL | |||
| Alpha-1A adrenergic receptor | GPCR | ANTAGONIST | Ki | 8.39 | CHEMBL | CHEMBL | |||
| Alpha-2B adrenergic receptor | GPCR | ANTAGONIST | Ki | 8.12 | CHEMBL | CHEMBL | |||
| Alpha-2C adrenergic receptor | GPCR | ANTAGONIST | Ki | 8.08 | CHEMBL | CHEMBL | |||
| Alpha-1D adrenergic receptor | GPCR | ANTAGONIST | Ki | 7.71 | CHEMBL | CHEMBL | |||
| Alpha-1B adrenergic receptor | GPCR | ANTAGONIST | Ki | 7.32 | CHEMBL | CHEMBL | |||
| 5-hydroxytryptamine receptor 2C | GPCR | Ki | 6.68 | DRUG MATRIX | |||||
| Histamine H1 receptor | GPCR | Ki | 5.40 | PDSP | |||||
| Cytochrome P450 2D6 | Enzyme | IC50 | 5 | DRUG MATRIX | |||||
| Sodium channel alpha subunits; brain (Types I, II, III) | Ion channel | IC50 | 5.08 | CHEMBL | |||||
| Nischarin | Membrane receptor | Ki | 7.94 | CHEMBL | |||||
| Sigma non-opioid intracellular receptor 1 | Membrane receptor | IC50 | 6.26 | CHEMBL | |||||
| Potassium voltage-gated channel subfamily H member 2 | Ion channel | Ki | 4.78 | DRUG MATRIX | |||||
| 5-hydroxytryptamine receptor 1A | GPCR | Ki | 5.67 | PDSP | |||||
| 5-hydroxytryptamine receptor 2A | GPCR | Ki | 5.61 | PDSP | |||||
| 5-hydroxytryptamine receptor 2B | GPCR | Ki | 5.62 | DRUG MATRIX | |||||
| Histamine H1 receptor | GPCR | IC50 | 4.90 | CHEMBL | |||||
| Alpha-2A adrenergic receptor | GPCR | Ki | 9.03 | CHEMBL | |||||
| Alpha-1B adrenergic receptor | GPCR | Ki | 6.66 | CHEMBL | |||||
| Adrenergic receptor alpha-2 | GPCR | Ki | 8.85 | CHEMBL | |||||
| Alpha-1B adrenergic receptor | GPCR | Ki | 7.35 | DRUG MATRIX | |||||
| Alpha-1A adrenergic receptor | GPCR | IC50 | 7.96 | CHEMBL | |||||
| Alpha-1D adrenergic receptor | GPCR | Ki | 7.35 | CHEMBL | |||||
| Alpha-2A adrenergic receptor | GPCR | Ki | 8.33 | CHEMBL | |||||
| Alpha-1A adrenergic receptor | GPCR | Ki | 8.17 | CHEMBL |
| ID | Source |
|---|---|
| 4019892 | VUID |
| N0000147977 | NUI |
| D00509 | KEGG_DRUG |
| 65-28-1 | SECONDARY_CAS_RN |
| 4018791 | VANDF |
| 4019892 | VANDF |
| C0031448 | UMLSCUI |
| CHEBI:8081 | CHEBI |
| CHEMBL597 | ChEMBL_ID |
| DB00692 | DRUGBANK_ID |
| CHEMBL1200873 | ChEMBL_ID |
| D010646 | MESH_DESCRIPTOR_UI |
| 5775 | PUBCHEM_CID |
| 502 | IUPHAR_LIGAND_ID |
| 22 | INN_ID |
| 73-05-2 | SECONDARY_CAS_RN |
| Z468598HBV | UNII |
| 227240 | RXNORM |
| 11705 | MMSL |
| 5280 | MMSL |
| d00733 | MMSL |
| 001845 | NDDF |
| 001846 | NDDF |
| 001847 | NDDF |
| 32436002 | SNOMEDCT_US |
| 372863003 | SNOMEDCT_US |
| 82165003 | SNOMEDCT_US |
| CHEMBL1204146 | ChEMBL_ID |
| Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
|---|---|---|---|---|---|---|---|---|
| Phentolamine Mesylate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0143-9564 | INJECTION, POWDER, FOR SOLUTION | 5 mg | INTRAMUSCULAR | ANDA | 18 sections |
| Oraverse | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0362-0101 | INJECTION, SOLUTION | 0.24 mg | SUBMUCOSAL | NDA | 25 sections |
| Phentolamine Mesylate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 51224-012 | INJECTION | 5 mg | INTRAMUSCULAR | ANDA | 19 sections |
| PHENTOLAMINE MESYLATE | HUMAN PRESCRIPTION DRUG LABEL | 1 | 68094-101 | INJECTION | 5 mg | INTRAVENOUS | ANDA | 16 sections |