Glyceric acid

Details

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Internal ID 6ea61bd8-fef1-4d72-9c4d-9cd8f65a99a8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Sugar acids and derivatives
IUPAC Name 2,3-dihydroxypropanoic acid
SMILES (Canonical) C(C(C(=O)O)O)O
SMILES (Isomeric) C(C(C(=O)O)O)O
InChI InChI=1S/C3H6O4/c4-1-2(5)3(6)7/h2,4-5H,1H2,(H,6,7)
InChI Key RBNPOMFGQQGHHO-UHFFFAOYSA-N
Popularity 843 references in papers

Physical and Chemical Properties

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Molecular Formula C3H6O4
Molecular Weight 106.08 g/mol
Exact Mass 106.02660867 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP -1.50
Atomic LogP (AlogP) -1.58
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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DL-Glyceric acid
2,3-Dihydroxypropanoic acid
473-81-4
600-19-1
Propanoic acid, 2,3-dihydroxy-
Glycerolic acid
Glyceronic acid
DL-2,3-Dihydroxypropionic Acid
C3H6O4
Glyceric acid, DL-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Glyceric acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6130 61.30%
Caco-2 - 0.9444 94.44%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7177 71.77%
OATP2B1 inhibitior - 0.8493 84.93%
OATP1B1 inhibitior + 0.9610 96.10%
OATP1B3 inhibitior + 0.9109 91.09%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9585 95.85%
P-glycoprotein inhibitior - 0.9871 98.71%
P-glycoprotein substrate - 0.9947 99.47%
CYP3A4 substrate - 0.8012 80.12%
CYP2C9 substrate - 0.6069 60.69%
CYP2D6 substrate - 0.8641 86.41%
CYP3A4 inhibition - 0.9347 93.47%
CYP2C9 inhibition - 0.9626 96.26%
CYP2C19 inhibition - 0.9659 96.59%
CYP2D6 inhibition - 0.9589 95.89%
CYP1A2 inhibition - 0.9048 90.48%
CYP2C8 inhibition - 0.9972 99.72%
CYP inhibitory promiscuity - 0.9846 98.46%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.8047 80.47%
Eye corrosion - 0.9701 97.01%
Eye irritation + 0.9629 96.29%
Skin irritation - 0.5740 57.40%
Skin corrosion - 0.8916 89.16%
Ames mutagenesis - 0.8670 86.70%
Human Ether-a-go-go-Related Gene inhibition - 0.8081 80.81%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.9432 94.32%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6185 61.85%
Acute Oral Toxicity (c) IV 0.5061 50.61%
Estrogen receptor binding - 0.9308 93.08%
Androgen receptor binding - 0.8782 87.82%
Thyroid receptor binding - 0.8469 84.69%
Glucocorticoid receptor binding - 0.9138 91.38%
Aromatase binding - 0.8771 87.71%
PPAR gamma - 0.8184 81.84%
Honey bee toxicity - 0.9185 91.85%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.9500 95.00%
Fish aquatic toxicity - 0.9316 93.16%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL4523454 Q9H255 Olfactory receptor 51E2 1.9 nM
EC50
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4040 P28482 MAP kinase ERK2 94.87% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.10% 96.09%
CHEMBL2581 P07339 Cathepsin D 84.08% 98.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.21% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.85% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Agave americana
Arabidopsis thaliana
Cannabis sativa
Lemna aequinoctialis
Lupinus angustifolius
Panax ginseng
Pogostemon cablin
Populus tremula
Solanum lycopersicum

Cross-Links

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PubChem 752
NPASS NPC3525
LOTUS LTS0103735
wikiData Q424906