TLA

L(+)-TARTARIC ACID

Created:	2002-01-22
Last modified:	2024-09-27

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590 entries where TLA is found as a standalone ligand8 entries where TLA is covalently linked to polymer or other heterogen groups

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Chemical Details
Formal Charge	0
Atom Count	16
Chiral Atom Count	2
Bond Count	15
Aromatic Bond Count	0

2D diagram of TLA

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Chemical Component Summary
Name	L(+)-TARTARIC ACID
Systematic Name (OpenEye OEToolkits)	(2R,3R)-2,3-dihydroxybutanedioic acid
Formula	C₄ H₆ O₆
Molecular Weight	150.087
Type	NON-POLYMER

Chemical Descriptors
Type	Program	Version	Descriptor
SMILES	ACDLabs	10.04	O=C(O)C(O)C(O)C(=O)O
SMILES	CACTVS	3.341	O[CH]([CH](O)C(O)=O)C(O)=O
SMILES	OpenEye OEToolkits	1.5.0	C(C(C(=O)O)O)(C(=O)O)O
Canonical SMILES	CACTVS	3.341	O[C@H]([C@@H](O)C(O)=O)C(O)=O
Canonical SMILES	OpenEye OEToolkits	1.5.0	[C@@H]([C@H](C(=O)O)O)(C(=O)O)O
InChI	InChI	1.03	InChI=1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)/t1-,2-/m1/s1
InChIKey	InChI	1.03	FEWJPZIEWOKRBE-JCYAYHJZSA-N

Drug Info: DrugBank

DrugBank ID	DB09459
Name	L-tartaric acid
Groups	experimental
Description	Tartaric acid is a white crystalline organic acid that occurs naturally in many plants, most notably in grapes.Tartaric is an alpha-hydroxy-carboxylic acid, is diprotic and aldaric in acid characteristics, and is a dihydroxyl derivative of succinic acid.
Synonyms	L-tartaric acid (2R,3R)-2,3-Dihydroxybernsteinsäure (R,R)-(+)-tartaric acid (+)-Weinsäure (+)-Tartaric acid Tartaric acid (R,R)-Tartaric acid Rechtsweinsäure Weinsteinsäure ácido tartárico L-threaric acid (+)-(R,R)-tartaric acid (2R,3R)-Tartaric acid (2R,3R)-2,3-dihydroxysuccinic acid (+)-L-tartaric acid
Brand Names	Brioschi Effervescent Antacid Brioschi Childrens Effervescent Antacid Unik Zoru Pwr Unik Zoru Tab Urasal Granules Baros Effervescent Granules Gingera Effervescent Antacid Bicaruvas E-Z-gas 2 Granules
Indication	Tartaric Acid is primarily indicated in conditions like Antiscorbutic, Antiseptic.
Categories	Acids, Acyclic Carbohydrates Chelating Agents Dicarboxylic Acids Hydroxy Acids Sugar Acids Urinary Alkalinisers
CAS number	87-69-4

Related Resource References

Resource Name	Reference
PubChem	444305
ChEMBL	CHEMBL1236315
ChEBI	CHEBI:15671
CCDC/CSD	FINTAZ02, KIMBEQ, FINTAZ03, KILNAX, IQOMIM01, IQOMIM02, IQOMIM07, IQOMIM05, IQOMIM04, IQOMIM06, IQOMIM22, ANOLIZ, IQOMIM03, IQOMIM08, IQOMIM09, DIZSUD, IRACAH, KAYZIT, HUTRIA, ANOLUL, ACETEJ, IQOMIM, IQOMIM12, IXOVUN, IQOMIM14, IQOMIM19, IQOMIM20, IQOMIM18, IQOMIM17, IQOMIM15, IQOMIM13, ACESAE, IQOMIM16, IQOMIM11, IZAHID
COD	1520169, 7200948, 2011939, 7225610, 7225609, 7225611, 7225612, 7225613, 7225614, 7225615, 7225616, 7225617, 7225628, 7225629, 7225630, 7225631, 7225633, 7225632, 7225634, 7225635, 7225636, 7225638, 7225637, 7205663, 7205665, 2021499, 2021501, 2021500, 2021502, 2021503, 2021504, 2021505, 2311127, 2021506, 2021507, 2021508, 2200365

RCSB PDB Core Operations are funded by the U.S. National Science Foundation (DBI-2321666), the US Department of Energy (DE-SC0019749), and the National Cancer Institute, National Institute of Allergy and Infectious Diseases, and National Institute of General Medical Sciences of the National Institutes of Health under grant R01GM157729.