(2S,3S,5S)-2,3,5-trihydroxyhexanedioic acid

Details

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Internal ID 339fa34f-0e36-4788-90ba-9c9d7d743621
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name (2S,3S,5S)-2,3,5-trihydroxyhexanedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H10O7/c7-2(4(9)6(12)13)1-3(8)5(10)11/h2-4,7-9H,1H2,(H,10,11)(H,12,13)/t2-,3-,4-/m0/s1
InChI Key WZLURCXZSPTANB-HZLVTQRSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10O7
Molecular Weight 194.14 g/mol
Exact Mass 194.04265265 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP -2.10
Atomic LogP (AlogP) -2.37
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,3S,5S)-2,3,5-trihydroxyhexanedioic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7424 74.24%
Caco-2 - 0.9826 98.26%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6836 68.36%
OATP2B1 inhibitior - 0.8498 84.98%
OATP1B1 inhibitior + 0.9328 93.28%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9892 98.92%
P-glycoprotein inhibitior - 0.9894 98.94%
P-glycoprotein substrate - 0.9721 97.21%
CYP3A4 substrate - 0.7006 70.06%
CYP2C9 substrate + 0.5994 59.94%
CYP2D6 substrate - 0.8403 84.03%
CYP3A4 inhibition - 0.8948 89.48%
CYP2C9 inhibition - 0.9610 96.10%
CYP2C19 inhibition - 0.9639 96.39%
CYP2D6 inhibition - 0.9488 94.88%
CYP1A2 inhibition - 0.9467 94.67%
CYP2C8 inhibition - 0.9866 98.66%
CYP inhibitory promiscuity - 0.9910 99.10%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8230 82.30%
Carcinogenicity (trinary) Non-required 0.7434 74.34%
Eye corrosion - 0.8721 87.21%
Eye irritation + 0.7150 71.50%
Skin irritation + 0.5094 50.94%
Skin corrosion - 0.8592 85.92%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7870 78.70%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5050 50.50%
skin sensitisation - 0.9352 93.52%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.8667 86.67%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.5852 58.52%
Acute Oral Toxicity (c) III 0.7630 76.30%
Estrogen receptor binding - 0.7733 77.33%
Androgen receptor binding - 0.6619 66.19%
Thyroid receptor binding - 0.6459 64.59%
Glucocorticoid receptor binding + 0.5786 57.86%
Aromatase binding - 0.8552 85.52%
PPAR gamma - 0.8222 82.22%
Honey bee toxicity - 0.9330 93.30%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity - 0.7744 77.44%

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
CHEMBL4040 P28482 MAP kinase ERK2 91.60% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.36% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.64% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 83.85% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.94% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.08% 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.
Pycnandra acuminata

Cross-Links

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PubChem 92209640
LOTUS LTS0017208
wikiData Q105323317