Tartaric Acid

drug
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Also known as E 334E-334FEMA NO. 3044INS NO.334INS-334L-tartaric acidNSC-62778Tartaric acid component of barosTartrateSID57264380SID144210475TARTARIC_acidTARTARIC-ACIDL-(+)-Tartaric acid

Summary

Tartaric Acid (CHEMBL1236315) is an approved small molecule.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • Clinical trials: 4
  • Chemistry: 150.09 Da · C4H6O6

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1236315
NameTartaric Acid
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID444305
ChEBICHEBI:15671
Molecular formulaC4H6O6
Molecular weight150.09
InChIKeyFEWJPZIEWOKRBE-JCYAYHJZSA-N

SMILES: [C@@H]([C@H](C(=O)O)O)(C(=O)O)O

IUPAC name: (2R,3R)-2,3-dihydroxybutanedioic acid

ChEBI definition: The L-enantiomer of tartaric acid.

Also known as: E 334, E-334, FEMA NO. 3044, INS NO.334, INS-334, L-tartaric acid, NSC-62778, Tartaric acid, Tartaric acid component of baros, Tartrate, SID57264380, SID144210475

Patent coverage: 24,606 distinct patent families (56,091 SureChEMBL compound mentions), from 1 matched compound structure(s). 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: 1 (assay-derived). Sample: Beta-lactamase.

Bioactivity

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

TargetpChemblTypeValueUnitActivity ID
P008116.2Potency631nMCHEMBL_ACT_4639133

Target pathways

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

Indications & clinical

Indications

0 indications (0 at ChEMBL trial phase 4).

Clinical trials

Total trials: 4.

Phase distribution

PhaseTrials
PHASE41
PHASE21
PHASE11
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00822172PHASE4COMPLETEDEvaluation of Cilostazol in Combination With L-Carnitine
NCT07108777PHASE2RECRUITINGL-Carnitine Protective Effect in Nephrotoxicity
NCT01072812PHASE1TERMINATEDStudy of the Pharmacokinetics and Pharmacodynamics of POSIPHEN® in Subjects With Amnestic Mild Cognitive Impairment
NCT03439917Not specifiedCOMPLETEDEffects of Carnitine Supplementation on Liver and Muscle

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).

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.