Stem definition | Drug id | CAS RN |
---|---|---|
sodium glucose co-transporter inhibitors, phlorizin derivatives | 5339 | 1018899-04-1 |
None
None
Date | Agency | Company | Orphan |
---|---|---|---|
April 26, 2019 | EMA | SANOFI-AVENTIS GROUPE | |
May 26, 2023 | FDA | LEXICON PHARMS INC |
None
None
None
None
Source | Code | Description |
---|---|---|
ATC | A10BK06 | ALIMENTARY TRACT AND METABOLISM DRUGS USED IN DIABETES BLOOD GLUCOSE LOWERING DRUGS, EXCL. INSULINS Sodium-glucose co-transporter 2 (SGLT2) inhibitors |
MeSH PA | D007004 | Hypoglycemic Agents |
MeSH PA | D000077203 | Sodium-Glucose Transporter 2 Inhibitors |
FDA MoA | N0000185503 | P-Glycoprotein Inhibitors |
FDA MoA | N0000187058 | Sodium-Glucose Transporter 2 Inhibitors |
FDA EPC | N0000187059 | Sodium-Glucose Cotransporter 2 Inhibitor |
Disease | Relation | SNOMED_ID | DOID |
---|---|---|---|
Diabetes mellitus type 2 at increased risk of cardiovascular disease | indication | 44054006 | DOID:9352 |
Diabetes mellitus type 1 | indication | 46635009 | DOID:9744 |
Heart failure | indication | 84114007 | DOID:6000 |
Chronic kidney disease at increased risk of cardiovascular disease | indication | 709044004 |
None
None
Dissociation level | Dissociation constant | Type (acidic/basic) |
---|---|---|
pKa1 | 12.45 | acidic |
pKa2 | 13.37 | acidic |
Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Patent number | Patent expiration date | Patent use |
---|---|---|---|---|---|---|---|---|---|---|
200MG | INPEFA | LEXICON PHARMS INC | N216203 | May 26, 2023 | RX | TABLET | ORAL | 7781577 | May 4, 2028 | REDUCTION OF RISK OF CARDIOVASCULAR DEATH, HOSPITALIZATION FOR HEART FAILURE, AND URGENT HEART FAILURE IN ADULTS WITH HEART FAILURE OR TYPE 2 DIABETES MELLITUS, CHRONIC KIDNEY DISEASE, AND OTHER CARDIOVASCULAR RISK FACTORS |
400MG | INPEFA | LEXICON PHARMS INC | N216203 | May 26, 2023 | RX | TABLET | ORAL | 7781577 | May 4, 2028 | REDUCTION OF RISK OF CARDIOVASCULAR DEATH, HOSPITALIZATION FOR HEART FAILURE, AND URGENT HEART FAILURE IN ADULTS WITH HEART FAILURE OR TYPE 2 DIABETES MELLITUS, CHRONIC KIDNEY DISEASE, AND OTHER CARDIOVASCULAR RISK FACTORS |
200MG | INPEFA | LEXICON PHARMS INC | N216203 | May 26, 2023 | RX | TABLET | ORAL | 8476413 | May 29, 2028 | REDUCTION OF RISK OF CARDIOVASCULAR DEATH, HOSPITALIZATION FOR HEART FAILURE, AND URGENT HEART FAILURE IN ADULTS WITH HEART FAILURE OR TYPE 2 DIABETES MELLITUS, CHRONIC KIDNEY DISEASE, AND OTHER CARDIOVASCULAR RISK FACTORS |
400MG | INPEFA | LEXICON PHARMS INC | N216203 | May 26, 2023 | RX | TABLET | ORAL | 8476413 | May 29, 2028 | REDUCTION OF RISK OF CARDIOVASCULAR DEATH, HOSPITALIZATION FOR HEART FAILURE, AND URGENT HEART FAILURE IN ADULTS WITH HEART FAILURE OR TYPE 2 DIABETES MELLITUS, CHRONIC KIDNEY DISEASE, AND OTHER CARDIOVASCULAR RISK FACTORS |
Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Exclusivity date | Description |
---|---|---|---|---|---|---|---|---|---|
200MG | INPEFA | LEXICON PHARMS INC | N216203 | May 26, 2023 | RX | TABLET | ORAL | May 26, 2028 | NEW CHEMICAL ENTITY |
400MG | INPEFA | LEXICON PHARMS INC | N216203 | May 26, 2023 | RX | TABLET | ORAL | May 26, 2028 | NEW CHEMICAL ENTITY |
Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
---|---|---|---|---|---|---|---|---|---|
Sodium/glucose cotransporter 2 | Transporter | INHIBITOR | IC50 | 8.75 | SCIENTIFIC LITERATURE | DRUG LABEL | |||
Sodium/glucose cotransporter 1 | Transporter | INHIBITOR | IC50 | 7.44 | SCIENTIFIC LITERATURE | DRUG LABEL |
ID | Source |
---|---|
6B4ZBS263Y | UNII |
C3502471 | UMLSCUI |
CHEMBL3039507 | ChEMBL_ID |
24831714 | PUBCHEM_CID |
DB12713 | DRUGBANK_ID |
D10669 | KEGG_DRUG |
9824 | INN_ID |
C575681 | MESH_SUPPLEMENTAL_RECORD_UI |
8312 | IUPHAR_LIGAND_ID |
019461 | NDDF |
4042306 | VANDF |
2638675 | RXNORM |
367663 | MMSL |
41581 | MMSL |
d10056 | MMSL |
Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
---|---|---|---|---|---|---|---|---|
INPEFA | HUMAN PRESCRIPTION DRUG LABEL | 1 | 70183-220 | TABLET | 200 mg | ORAL | NDA | 29 sections |
INPEFA | HUMAN PRESCRIPTION DRUG LABEL | 1 | 70183-240 | TABLET | 400 mg | ORAL | NDA | 29 sections |