Stem definition | Drug id | CAS RN |
---|---|---|
oxytocin derivatives | 495 | 37025-55-1 |
Dose | Unit | Route |
---|---|---|
0.10 | mg | P |
None
Date | Agency | Company | Orphan |
---|---|---|---|
Nov. 5, 2007 | UK Medicines and Healthcare Products Regulatory Agency (MHRA) | Ferring Pharmaceuticals Ltd |
None
None
None
None
Source | Code | Description |
---|---|---|
ATC | H01BB03 | SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS PITUITARY AND HYPOTHALAMIC HORMONES AND ANALOGUES POSTERIOR PITUITARY LOBE HORMONES Oxytocin and analogues |
MeSH PA | D003692 | Delayed-Action Preparations |
MeSH PA | D010120 | Oxytocics |
MeSH PA | D012102 | Reproductive Control Agents |
CHEBI has role | CHEBI:36063 | oxytocic agents |
Disease | Relation | SNOMED_ID | DOID |
---|---|---|---|
Atony of uterus | indication | 9293002 | |
Prader-Willi syndrome | indication | 89392001 | DOID:11983 |
None
None
Dissociation level | Dissociation constant | Type (acidic/basic) |
---|---|---|
pKa1 | 12.59 | acidic |
pKa2 | 13.2 | acidic |
pKa3 | 13.33 | acidic |
pKa4 | 13.57 | acidic |
pKa5 | 13.94 | acidic |
pKa6 | 13.98 | acidic |
None
None
Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
---|---|---|---|---|---|---|---|---|---|
Oxytocin receptor | GPCR | AGONIST | Ki | 8.15 | SCIENTIFIC LITERATURE | DRUG LABEL | |||
Vasopressin V1a receptor | GPCR | EC50 | 7.39 | CHEMBL | |||||
Vasopressin V2 receptor | GPCR | Ki | 5.23 | SCIENTIFIC LITERATURE | |||||
Oxytocin receptor | GPCR | AGONIST | EC50 | 7.21 | IUPHAR |
ID | Source |
---|---|
D07229 | KEGG_DRUG |
C0054670 | UMLSCUI |
CHEBI:59204 | CHEBI |
CHEMBL3301668 | ChEMBL_ID |
DB01282 | DRUGBANK_ID |
C020731 | MESH_SUPPLEMENTAL_RECORD_UI |
11169 | IUPHAR_LIGAND_ID |
5014 | INN_ID |
88TWF8015Y | UNII |
16681432 | PUBCHEM_CID |
423594000 | SNOMEDCT_US |
425003007 | SNOMEDCT_US |
006738 | NDDF |
None