3-(3,4-Dihydroxy-5-oxooxolan-2-yl)-2-hydroxypropanoic acid

Details

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Internal ID 16174a36-ffaf-48ac-b127-eaa8a22c0106
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Sugar acids and derivatives
IUPAC Name 3-(3,4-dihydroxy-5-oxooxolan-2-yl)-2-hydroxypropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H10O7/c8-2(6(11)12)1-3-4(9)5(10)7(13)14-3/h2-5,8-10H,1H2,(H,11,12)
InChI Key FHTUHRLYAPRFEZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H10O7
Molecular Weight 206.15 g/mol
Exact Mass 206.04265265 g/mol
Topological Polar Surface Area (TPSA) 124.00 Ų
XlogP -2.00
Atomic LogP (AlogP) -2.53
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(3,4-Dihydroxy-5-oxooxolan-2-yl)-2-hydroxypropanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4640 46.40%
Caco-2 - 0.9706 97.06%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6958 69.58%
OATP2B1 inhibitior - 0.8510 85.10%
OATP1B1 inhibitior + 0.9328 93.28%
OATP1B3 inhibitior + 0.9532 95.32%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9830 98.30%
P-glycoprotein inhibitior - 0.9829 98.29%
P-glycoprotein substrate - 0.9725 97.25%
CYP3A4 substrate - 0.6534 65.34%
CYP2C9 substrate - 0.5942 59.42%
CYP2D6 substrate - 0.8527 85.27%
CYP3A4 inhibition - 0.9563 95.63%
CYP2C9 inhibition - 0.9726 97.26%
CYP2C19 inhibition - 0.9546 95.46%
CYP2D6 inhibition - 0.9648 96.48%
CYP1A2 inhibition - 0.9663 96.63%
CYP2C8 inhibition - 0.9832 98.32%
CYP inhibitory promiscuity - 0.9920 99.20%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6399 63.99%
Eye corrosion - 0.8845 88.45%
Eye irritation + 0.6936 69.36%
Skin irritation - 0.6283 62.83%
Skin corrosion - 0.6953 69.53%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7802 78.02%
Micronuclear + 0.5659 56.59%
Hepatotoxicity - 0.5844 58.44%
skin sensitisation - 0.9156 91.56%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.4743 47.43%
Acute Oral Toxicity (c) III 0.4589 45.89%
Estrogen receptor binding - 0.6024 60.24%
Androgen receptor binding - 0.7712 77.12%
Thyroid receptor binding - 0.5394 53.94%
Glucocorticoid receptor binding + 0.6638 66.38%
Aromatase binding - 0.8623 86.23%
PPAR gamma - 0.8465 84.65%
Honey bee toxicity - 0.8772 87.72%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.6724 67.24%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.02% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.88% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.27% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.36% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.45% 86.92%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.11% 99.23%

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.
Cereus repandus

Cross-Links

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PubChem 130020481
LOTUS LTS0014306
wikiData Q104995460