Stem definition | Drug id | CAS RN |
---|---|---|
vasopressin analogues | 2967 | 14636-12-5 |
Dose | Unit | Route |
---|---|---|
12 | mg | P |
Property | Value | Reference |
---|---|---|
Vd (Volume of distribution) | 0.24 L/kg | Lombardo F, Berellini G, Obach RS |
CL (Clearance) | 8.20 mL/min/kg | Lombardo F, Berellini G, Obach RS |
t_half (Half-life) | 0.90 hours | Lombardo F, Berellini G, Obach RS |
Date | Agency | Company | Orphan |
---|---|---|---|
Sept. 14, 2022 | FDA | MALLINCKRODT |
None
None
None
None
Source | Code | Description |
---|---|---|
ATC | H01BA04 | SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS PITUITARY AND HYPOTHALAMIC HORMONES AND ANALOGUES POSTERIOR PITUITARY LOBE HORMONES Vasopressin and analogues |
MeSH PA | D000959 | Antihypertensive Agents |
MeSH PA | D002317 | Cardiovascular Agents |
MeSH PA | D014662 | Vasoconstrictor Agents |
FDA EPC | N0000194045 | Vasopressin Receptor Agonist |
FDA MoA | N0000194046 | Vasopressin Receptor Agonists |
Disease | Relation | SNOMED_ID | DOID |
---|---|---|---|
Hepatorenal syndrome | indication | 51292008 | DOID:11823 |
Ischemia | contraindication | 52674009 | DOID:326 |
Hypoxia | contraindication | 389086002 |
None
None
Dissociation level | Dissociation constant | Type (acidic/basic) |
---|---|---|
pKa1 | 9.65 | acidic |
pKa2 | 11.89 | acidic |
pKa3 | 12.32 | acidic |
pKa4 | 12.71 | acidic |
pKa5 | 12.98 | acidic |
pKa6 | 13.08 | acidic |
pKa7 | 13.57 | acidic |
pKa8 | 13.58 | acidic |
pKa9 | 13.67 | acidic |
pKa10 | 13.96 | acidic |
pKa11 | 10.31 | Basic |
pKa12 | 7.93 | Basic |
None
Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Exclusivity date | Description |
---|---|---|---|---|---|---|---|---|---|
EQ 0.85MG BASE/VIAL | TERLIVAZ | MALLINCKRODT IRELAND | N022231 | Sept. 14, 2022 | RX | POWDER | INTRAVENOUS | Sept. 14, 2027 | NEW CHEMICAL ENTITY |
EQ 0.85MG BASE/VIAL | TERLIVAZ | MALLINCKRODT IRELAND | N022231 | Sept. 14, 2022 | RX | POWDER | INTRAVENOUS | Sept. 14, 2029 | TO IMPROVE KIDNEY FUNCTION IN ADULTS WITH HEPATORENAL SYNDROME WITH RAPID REDUCTION IN KIDNEY FUNCTION |
Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
---|---|---|---|---|---|---|---|---|---|
Vasopressin V1a receptor | GPCR | AGONIST | Ki | 5.96 | SCIENTIFIC LITERATURE | DRUG LABEL | |||
Vasopressin V2 receptor | GPCR | AGONIST | Ki | 5.16 | SCIENTIFIC LITERATURE |
ID | Source |
---|---|
D06672 | KEGG_DRUG |
4041761 | VANDF |
C0145185 | UMLSCUI |
CHEBI:135905 | CHEBI |
CHEMBL2135460 | ChEMBL_ID |
D000077585 | MESH_DESCRIPTOR_UI |
DB02638 | DRUGBANK_ID |
11241 | IUPHAR_LIGAND_ID |
5114 | INN_ID |
7Z5X49W53P | UNII |
72081 | PUBCHEM_CID |
57048 | RXNORM |
29210 | MMSL |
d04932 | MMSL |
004053 | NDDF |
013118 | NDDF |
325927008 | SNOMEDCT_US |
395899009 | SNOMEDCT_US |
734453002 | SNOMEDCT_US |
Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
---|---|---|---|---|---|---|---|---|
Terlivaz | HUMAN PRESCRIPTION DRUG LABEL | 1 | 43825-200 | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION | 0.85 mg | INTRAVENOUS | NDA | 30 sections |
Terlivaz | HUMAN PRESCRIPTION DRUG LABEL | 1 | 43825-200 | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION | 0.85 mg | INTRAVENOUS | NDA | 30 sections |