Benfotiamine

drug
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Also known as 8088 C.B8088 C.B.8088CBBenfothiamineBenfotiaminaBenphothiamineBenzoylthiamine monophosphateBenzoylthiamine o-monophosphateBenzoylthiaminmonophosphatBiotaminNSC-758241S-benzoylthiamine monophosphateS-benzoylthiamine o-monophosphateSID11112674SID26749224SID144204148SID170465987BenfotiamineÊBenfotiamineÂ

Summary

Benfotiamine (CHEMBL4303665) is a phase-3 clinical-stage small molecule (ATC A11DA03); indicated across 4 conditions including diabetic neuropathy and alzheimer disease.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • ATC class: A11DA03
  • Indications: 4 conditions
  • Clinical trials: 10
  • Chemistry: 466.4 Da · C19H23N4O6PS

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4303665
NameBenfotiamine
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID3032771
ATCA11DA03
Molecular formulaC19H23N4O6PS
Molecular weight466.4
InChIKeyBTNNPSLJPBRMLZ-LGMDPLHJSA-N

SMILES: CC1=NC=C(C(=N1)N)CN(C=O)/C(=C(/CCOP(=O)(O)O)\SC(=O)C2=CC=CC=C2)/C

IUPAC name: S-[(Z)-2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-phosphonooxypent-2-en-3-yl] benzenecarbothioate

Also known as: 8088 C.B, 8088 C.B., 8088CB, Benfothiamine, Benfotiamina, Benfotiamine, Benphothiamine, Benzoylthiamine monophosphate, Benzoylthiamine o-monophosphate, Benzoylthiaminmonophosphat, Biotamin, NSC-758241

Patent coverage: 801 distinct patent families (2,501 SureChEMBL compound mentions), from 3 matched compound structure(s). One matched structure accounts for 2,357 (94%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 5 (assay-derived). Sample: Tyrosyl-DNA phosphodiesterase 1, Prelamin-A/C, 3’,5’-cyclic-AMP phosphodiesterase 4D, Cytochrome P450 3A4, Cytochrome P450 2C19.

Bioactivity

ChEMBL activities: 2 potent at pChembl ≥ 5 of 6 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
CYP2C195.5Potency3162nMCHEMBL_ACT_4014614
PDE4D5.31AC504900nMCHEMBL_ACT_25185075

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

4 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
diabetic neuropathy3MONDO:0006626EFO:1000783
Alzheimer disease2MONDO:0004975MONDO:0004975
type 2 diabetes mellitus2MONDO:0005148MONDO:0005148
type 1 diabetes mellitus1MONDO:0005147MONDO:0005147

Clinical trials

Total trials: 10.

Phase distribution

PhaseTrials
PHASE44
PHASE32
Not specified2
PHASE1/PHASE21
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00437008PHASE4COMPLETEDEffects of Benfotiamine and AGE on Endothelial Function in People With Diabetes
NCT00446810PHASE4UNKNOWNChronic Treatment With Benfotiamine Restores Endothelial Function in People With Type 2 Diabetes Mellitus
NCT00565318PHASE4COMPLETEDBenfotiamine in Diabetic Nephropathy
NCT00680121PHASE4COMPLETEDHigh Dose Vitamin B1 to Reduce Abusive Alcohol Use
NCT00785460PHASE3COMPLETEDBenfotiamine Prevents Vascular Dysfunction in Healthy Smokers
NCT01868191PHASE3UNKNOWNEffects of Benfotiamine on Intraepidermal Nerve Fiber Density (IENFD)
NCT00117026PHASE1/PHASE2COMPLETEDEffects of Vitamin B1 in Type 1 Diabetic Patients
NCT02292238PHASE2COMPLETEDBenfotiamine in Alzheimer’s Disease: A Pilot Study
NCT00703989Not specifiedCOMPLETEDReactive Oxygen Species in the Pathogenesis of Diabetic Complications
NCT02772926Not specifiedCOMPLETEDBenfotiamine Effect on Advanced Glycation End Products(AGEs) and Soluble Receptor for AGEs(sRAGE) in Diabetes Mellitus.

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).