EcoDrugPlus


Synonyms	D-(-)-lactic acid D-lactic acid Lactate Lactic acid, d-
Status
Molecule Category	UNKNOWN
UNII	3Q6M5SET7W
EPA CompTox	DTXSID0047030

Synonyms

D-(-)-lactic acid

D-lactic acid

Lactate

Lactic acid, d-

Status

Molecule Category

UNKNOWN

UNII

3Q6M5SET7W

EPA CompTox

DTXSID0047030


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70


InChI Key	JVTAAEKCZFNVCJ-UWTATZPHSA-N
Smiles	C[C@@H](O)C(=O)O
InChI	InChI=1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)/t2-/m1/s1

InChI Key

JVTAAEKCZFNVCJ-UWTATZPHSA-N

Smiles

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

InChI

InChI=1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)/t2-/m1/s1

Property Name	Value
Molecular Formula	C3H6O3
Molecular Weight	90.08
AlogP	-0.55
Hydrogen Bond Acceptor	2.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	1.0
Polar Surface Area	57.53
Molecular species	ACID
Aromatic Rings	0.0
Heavy Atoms	6.0

Property Name

Value

Molecular Formula

C3H6O3

Molecular Weight

90.08

AlogP

-0.55

Hydrogen Bond Acceptor

2.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

1.0

Polar Surface Area

57.53

Molecular species

ACID

Aromatic Rings

0.0

Heavy Atoms

6.0

Resources	Reference
ChEBI	42111
ChEMBL	CHEMBL358850
DrugBank	DB03066
FDA SRS	3Q6M5SET7W
Human Metabolome Database	HMDB0000190
Guide to Pharmacology	2934
KEGG	C00256
PDB	LAC
SureChEMBL	SCHEMBL14947
ZINC	ZINC000004658562

Resources

Reference

ChEBI

ChEMBL

DrugBank

FDA SRS

Human Metabolome Database

HMDB0000190

Guide to Pharmacology

KEGG

PDB

SureChEMBL

ZINC


PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

D-LACTIC ACID

Structure

Physicochemical Descriptors

Cross References