Tartronate semialdehyde

Details

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Internal ID a9e3c39b-71e9-48c8-a75e-f23af73d873c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides
IUPAC Name 2-hydroxy-3-oxopropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C3H4O4/c4-1-2(5)3(6)7/h1-2,5H,(H,6,7)
InChI Key QWBAFPFNGRFSFB-UHFFFAOYSA-N
Popularity 29 references in papers

Physical and Chemical Properties

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Molecular Formula C3H4O4
Molecular Weight 104.06 g/mol
Exact Mass 104.01095860 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP -1.10
Atomic LogP (AlogP) -1.37
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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tartronate semialdehyde
2480-77-5
hydroxymalonaldehydic acid
tartronic semialdehyde
2-hydroxy-3-oxopropanoate
Propanoic acid, 2-hydroxy-3-oxo-
tartronate-S-ald
Tartronyl semialdehyde
Formyl(hydroxyl)acetic acid
Triadimenol metabolite P05
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Tartronate semialdehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7080 70.80%
Caco-2 - 0.9050 90.50%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7956 79.56%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9468 94.68%
OATP1B3 inhibitior + 0.9682 96.82%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9660 96.60%
P-glycoprotein inhibitior - 0.9868 98.68%
P-glycoprotein substrate - 0.9927 99.27%
CYP3A4 substrate - 0.7797 77.97%
CYP2C9 substrate + 0.5973 59.73%
CYP2D6 substrate - 0.8570 85.70%
CYP3A4 inhibition - 0.9448 94.48%
CYP2C9 inhibition - 0.9400 94.00%
CYP2C19 inhibition - 0.9758 97.58%
CYP2D6 inhibition - 0.9581 95.81%
CYP1A2 inhibition - 0.9492 94.92%
CYP2C8 inhibition - 0.9952 99.52%
CYP inhibitory promiscuity - 0.9923 99.23%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.5196 51.96%
Carcinogenicity (trinary) Non-required 0.7380 73.80%
Eye corrosion - 0.7255 72.55%
Eye irritation + 0.9480 94.80%
Skin irritation + 0.5869 58.69%
Skin corrosion - 0.8715 87.15%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9009 90.09%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8828 88.28%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.7103 71.03%
Acute Oral Toxicity (c) III 0.7124 71.24%
Estrogen receptor binding - 0.8819 88.19%
Androgen receptor binding - 0.8915 89.15%
Thyroid receptor binding - 0.7774 77.74%
Glucocorticoid receptor binding - 0.8338 83.38%
Aromatase binding - 0.8726 87.26%
PPAR gamma - 0.8088 80.88%
Honey bee toxicity - 0.8358 83.58%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.9900 99.00%
Fish aquatic toxicity - 0.5529 55.29%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.79% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.49% 99.17%
CHEMBL2581 P07339 Cathepsin D 81.73% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.64% 95.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.36% 93.00%

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.
There are no matching plants.

Cross-Links

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PubChem 1122
LOTUS LTS0238703
wikiData Q15732146