8-Decenoic acid, 10-hydroxy-, (E)-

Details

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Internal ID 13c6aa56-d81b-4d46-9886-e7564bd65ba7
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name (E)-10-hydroxydec-8-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O3/c11-9-7-5-3-1-2-4-6-8-10(12)13/h5,7,11H,1-4,6,8-9H2,(H,12,13)/b7-5+
InChI Key RCXJFGCVOBRFEH-FNORWQNLSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O3
Molecular Weight 186.25 g/mol
Exact Mass 186.125594432 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.96
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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DTXSID901295794
8-Decenoic acid, 10-hydroxy-, (E)-
RefChem:1074691
DTXCID501726317
(E)-10-Hydroxy-8-decenoic acid
10-Hydroxy-8-decenoic acid
79728-54-4
(E)-10-hydroxydec-8-enoic acid
10-hydroxy-8E-decenoic acid
(8E)-10-HYDROXYDEC-8-ENOIC ACID
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 8-Decenoic acid, 10-hydroxy-, (E)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9580 95.80%
Caco-2 + 0.7430 74.30%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8064 80.64%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.8579 85.79%
OATP1B3 inhibitior + 0.9325 93.25%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8152 81.52%
P-glycoprotein inhibitior - 0.9809 98.09%
P-glycoprotein substrate - 0.9827 98.27%
CYP3A4 substrate - 0.6886 68.86%
CYP2C9 substrate + 0.5995 59.95%
CYP2D6 substrate - 0.8503 85.03%
CYP3A4 inhibition - 0.9228 92.28%
CYP2C9 inhibition - 0.9109 91.09%
CYP2C19 inhibition - 0.9524 95.24%
CYP2D6 inhibition - 0.9623 96.23%
CYP1A2 inhibition - 0.8724 87.24%
CYP2C8 inhibition - 0.9646 96.46%
CYP inhibitory promiscuity - 0.9608 96.08%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.7168 71.68%
Eye corrosion + 0.7220 72.20%
Eye irritation + 0.9619 96.19%
Skin irritation - 0.7031 70.31%
Skin corrosion - 0.9077 90.77%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5741 57.41%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.8375 83.75%
skin sensitisation - 0.8665 86.65%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.7440 74.40%
Acute Oral Toxicity (c) III 0.7474 74.74%
Estrogen receptor binding - 0.8431 84.31%
Androgen receptor binding - 0.9148 91.48%
Thyroid receptor binding - 0.8026 80.26%
Glucocorticoid receptor binding - 0.6833 68.33%
Aromatase binding - 0.7510 75.10%
PPAR gamma - 0.4853 48.53%
Honey bee toxicity - 0.9773 97.73%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.5669 56.69%
Fish aquatic toxicity - 0.3957 39.57%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 96.70% 99.17%
CHEMBL1781 P11387 DNA topoisomerase I 89.72% 97.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.35% 96.09%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 88.89% 92.26%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.62% 91.11%
CHEMBL2581 P07339 Cathepsin D 84.28% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.84% 96.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 5312741
LOTUS LTS0053487
wikiData Q76303310