5-Decenoic acid

Details

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Internal ID 865a2208-4e0d-4a36-a457-f4b2e3b93981
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name dec-5-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O2/c1-2-3-4-5-6-7-8-9-10(11)12/h5-6H,2-4,7-9H2,1H3,(H,11,12)
InChI Key UJUXUEKQHBXUEM-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H18O2
Molecular Weight 170.25 g/mol
Exact Mass 170.130679813 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.99
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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DTXSID90167732
UJUXUEKQHBXUEM-UHFFFAOYSA-N

2D Structure

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2D Structure of 5-Decenoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.7925 79.25%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Plasma membrane 0.6181 61.81%
OATP2B1 inhibitior - 0.8487 84.87%
OATP1B1 inhibitior - 0.4163 41.63%
OATP1B3 inhibitior - 0.4408 44.08%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7992 79.92%
P-glycoprotein inhibitior - 0.9888 98.88%
P-glycoprotein substrate - 0.9699 96.99%
CYP3A4 substrate - 0.7046 70.46%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.9386 93.86%
CYP2C9 inhibition - 0.8711 87.11%
CYP2C19 inhibition - 0.9373 93.73%
CYP2D6 inhibition - 0.9519 95.19%
CYP1A2 inhibition + 0.8857 88.57%
CYP2C8 inhibition - 0.9644 96.44%
CYP inhibitory promiscuity - 0.9365 93.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6635 66.35%
Carcinogenicity (trinary) Non-required 0.7143 71.43%
Eye corrosion + 0.9709 97.09%
Eye irritation + 0.9905 99.05%
Skin irritation + 0.8485 84.85%
Skin corrosion + 0.7149 71.49%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7163 71.63%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7551 75.51%
skin sensitisation + 0.8470 84.70%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.7915 79.15%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6089 60.89%
Acute Oral Toxicity (c) IV 0.7278 72.78%
Estrogen receptor binding - 0.9470 94.70%
Androgen receptor binding - 0.9202 92.02%
Thyroid receptor binding - 0.8390 83.90%
Glucocorticoid receptor binding - 0.8111 81.11%
Aromatase binding - 0.9089 90.89%
PPAR gamma + 0.7620 76.20%
Honey bee toxicity - 0.9959 99.59%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9575 95.75%

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 95.70% 99.17%
CHEMBL2581 P07339 Cathepsin D 94.46% 98.95%
CHEMBL1781 P11387 DNA topoisomerase I 91.81% 97.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.97% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.61% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.60% 96.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.76% 93.56%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 80.57% 96.00%

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.
Thymus riatarum

Cross-Links

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PubChem 53400879
LOTUS LTS0073884
wikiData Q72461666