5-Hydroxyhex-2-enoic acid

Details

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Internal ID eadbbdfc-cda8-4421-8663-5b97360e705f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name 5-hydroxyhex-2-enoic acid
SMILES (Canonical) CC(CC=CC(=O)O)O
SMILES (Isomeric) CC(CC=CC(=O)O)O
InChI InChI=1S/C6H10O3/c1-5(7)3-2-4-6(8)9/h2,4-5,7H,3H2,1H3,(H,8,9)
InChI Key XQOCAGXQSXUMHJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10O3
Molecular Weight 130.14 g/mol
Exact Mass 130.062994177 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.40
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxyhex-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9662 96.62%
Caco-2 + 0.5824 58.24%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7099 70.99%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9464 94.64%
OATP1B3 inhibitior + 0.9482 94.82%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9741 97.41%
P-glycoprotein inhibitior - 0.9872 98.72%
P-glycoprotein substrate - 0.9862 98.62%
CYP3A4 substrate - 0.7521 75.21%
CYP2C9 substrate - 0.5995 59.95%
CYP2D6 substrate - 0.8951 89.51%
CYP3A4 inhibition - 0.9557 95.57%
CYP2C9 inhibition - 0.9445 94.45%
CYP2C19 inhibition - 0.9404 94.04%
CYP2D6 inhibition - 0.9621 96.21%
CYP1A2 inhibition - 0.9069 90.69%
CYP2C8 inhibition - 0.9911 99.11%
CYP inhibitory promiscuity - 0.9447 94.47%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.5752 57.52%
Carcinogenicity (trinary) Non-required 0.6970 69.70%
Eye corrosion + 0.9007 90.07%
Eye irritation + 0.9660 96.60%
Skin irritation + 0.7430 74.30%
Skin corrosion + 0.9855 98.55%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8353 83.53%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.6091 60.91%
skin sensitisation + 0.4843 48.43%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.6487 64.87%
Acute Oral Toxicity (c) III 0.8534 85.34%
Estrogen receptor binding - 0.9645 96.45%
Androgen receptor binding - 0.8567 85.67%
Thyroid receptor binding - 0.9013 90.13%
Glucocorticoid receptor binding - 0.8235 82.35%
Aromatase binding - 0.9397 93.97%
PPAR gamma - 0.9436 94.36%
Honey bee toxicity - 0.9784 97.84%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity - 0.4776 47.76%

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
CHEMBL221 P23219 Cyclooxygenase-1 88.09% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.93% 96.09%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.44% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.51% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 81.12% 83.82%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.78% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.11% 95.56%

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 559394
LOTUS LTS0108160
wikiData Q105339921