acetohexamide ๐Ÿถ Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
antihyperglycaemics 57 968-81-0

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • dymelor
  • acetohexamide
  • acetohexamid
A sulfonylurea hypoglycemic agent that is metabolized in the liver to 1-hydrohexamide.
  • Molecular weight: 324.40
  • Formula: C15H20N2O4S
  • CLOGP: 2.25
  • LIPINSKI: 0
  • HAC: 6
  • HDO: 2
  • TPSA: 92.34
  • ALOGS: -3.83
  • ROTB: 3

  • Status: OFM

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

Drug dosage:

DoseUnitRoute
0.50 g O

ADMET properties:

PropertyValueReference
BDDCS (Biopharmaceutical Drug Disposition Classification System) 1 Benet LZ, Broccatelli F, Oprea TI
S (Water solubility) 3.43 mg/mL Benet LZ, Broccatelli F, Oprea TI
MRTD (Maximum Recommended Therapeutic Daily Dose) 77.06 ยตM/kg/day Contrera JF, Matthews EJ, Kruhlak NL, Benz RD

Approvals:

DateAgencyCompanyOrphan
Dec. 23, 1964 FDA LILLY

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 A10BB31 ALIMENTARY TRACT AND METABOLISM
DRUGS USED IN DIABETES
BLOOD GLUCOSE LOWERING DRUGS, EXCL. INSULINS
Sulfonylureas
MeSH PA D007004 Hypoglycemic Agents
CHEBI has role CHEBI:35526 antidiabetic
CHEBI has role CHEBI:90415 insulin secretagogues

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

DiseaseRelationSNOMED_IDDOID
Diabetes mellitus type 2 indication 44054006 DOID:9352




๐Ÿถ Veterinary Drug Use

None

๐Ÿถ Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 4.63 acidic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Sulfonylurea receptor 1, Kir6.2 Ion channel BLOCKER Ki 4.64 SCIENTIFIC LITERATURE SCIENTIFIC LITERATURE

External reference:

IDSource
4017503 VUID
N0000145888 NUI
D00219 KEGG_DRUG
173 RXNORM
C0000992 UMLSCUI
CHEBI:28052 CHEBI
CHEMBL1589 ChEMBL_ID
DB00414 DRUGBANK_ID
D000092 MESH_DESCRIPTOR_UI
1989 PUBCHEM_CID
6793 IUPHAR_LIGAND_ID
1134 INN_ID
QGC8W08I6I UNII
387210001 SNOMEDCT_US
39064002 SNOMEDCT_US
4017503 VANDF
4123 MMSL
522 MMSL
873 MMSL
d00162 MMSL
000907 NDDF

Pharmaceutical products:

None