sotagliflozin 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
sodium glucose co-transporter inhibitors, phlorizin derivatives 5339 1018899-04-1

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • sotagliflozin
  • zynquista
  • LP-802034
  • LX4211
  • LX-4211
  • inpefa
Sotagliflozin is a dual inhibitor of sodium glucose cotransporter type 1 (SGLT1) and SGLT2. Local intestinal inhibition of SGLT1, the major transporter for glucose absorption, delays and reduces glucose absorption in the proximal intestine, resulting in a blunting and delay of postprandial hyperglycaemia. SGLT2 is the predominant transporter responsible for reabsorption of glucose from the glomerular filtrate back into the circulation. By inhibiting SGLT2, sotagliflozin reduces renal reabsorption of filtered glucose and lowers the renal threshold for glucose, and thereby increases urinary glucose excretion
  • Molecular weight: 424.94
  • Formula: C21H25ClO5S
  • CLOGP: 3.66
  • LIPINSKI: 0
  • HAC: 5
  • HDO: 3
  • TPSA: 79.15
  • ALOGS: -4.01
  • ROTB: 6

  • Status: OFP

  • Legend:
    OFP - off patent
    OFM - off market
    ONP - on patent

Drug dosage:

None

ADMET properties:

None

Approvals:

DateAgencyCompanyOrphan
April 26, 2019 EMA SANOFI-AVENTIS GROUPE
May 26, 2023 FDA LEXICON PHARMS INC

FDA Adverse Event Reporting System (Female)

None

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

None

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
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

Drug Use | Suggest Off label Use Form| |View source of the data|

DiseaseRelationSNOMED_IDDOID
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




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 12.45 acidic
pKa2 13.37 acidic

Orange Book patent data (new drug applications)

Formulation strengthTrade nameApplicantApplication numberApproval dateTypeDose formRoutePatent numberPatent expiration datePatent 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

Orange Book exclusivity data (new drug applications)

Formulation strengthTrade nameApplicantApplication numberApproval dateTypeDose formRouteExclusivity dateDescription
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

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA 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

External reference:

IDSource
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

Pharmaceutical products:

ProductCategoryIngredientsNDCFormQuantityRouteMarketingLabel
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