Non-3-enoic acid

Details

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Internal ID 579978ea-9436-4775-9b6f-c22bd512ddde
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name non-3-enoic acid
SMILES (Canonical) CCCCCC=CCC(=O)O
SMILES (Isomeric) CCCCCC=CCC(=O)O
InChI InChI=1S/C9H16O2/c1-2-3-4-5-6-7-8-9(10)11/h6-7H,2-5,8H2,1H3,(H,10,11)
InChI Key ZBPYTVBKHKUNHG-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16O2
Molecular Weight 156.22 g/mol
Exact Mass 156.115029749 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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4124-88-3
DTXSID5063314
4YKK4UBI0X
RefChem:504530
DTXCID2039883
223-932-1
3-Nonenoic acid
SCHEMBL288355
orb2943978
NS00022162

2D Structure

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2D Structure of Non-3-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 + 0.9958 99.58%
Caco-2 + 0.8738 87.38%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Plasma membrane 0.7206 72.06%
OATP2B1 inhibitior - 0.8528 85.28%
OATP1B1 inhibitior + 0.7009 70.09%
OATP1B3 inhibitior - 0.3385 33.85%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9159 91.59%
P-glycoprotein inhibitior - 0.9872 98.72%
P-glycoprotein substrate - 0.9692 96.92%
CYP3A4 substrate - 0.6927 69.27%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.9424 94.24%
CYP2C9 inhibition - 0.9445 94.45%
CYP2C19 inhibition - 0.9621 96.21%
CYP2D6 inhibition - 0.9567 95.67%
CYP1A2 inhibition + 0.7956 79.56%
CYP2C8 inhibition - 0.9477 94.77%
CYP inhibitory promiscuity - 0.9581 95.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6435 64.35%
Carcinogenicity (trinary) Non-required 0.7545 75.45%
Eye corrosion + 0.9799 97.99%
Eye irritation + 0.9760 97.60%
Skin irritation + 0.9126 91.26%
Skin corrosion + 0.5196 51.96%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7877 78.77%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6926 69.26%
skin sensitisation + 0.8240 82.40%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.8396 83.96%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.6136 61.36%
Acute Oral Toxicity (c) IV 0.5527 55.27%
Estrogen receptor binding - 0.9395 93.95%
Androgen receptor binding - 0.8028 80.28%
Thyroid receptor binding - 0.8093 80.93%
Glucocorticoid receptor binding - 0.8134 81.34%
Aromatase binding - 0.8338 83.38%
PPAR gamma + 0.5225 52.25%
Honey bee toxicity - 0.9961 99.61%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity + 0.6860 68.60%
Fish aquatic toxicity + 0.9446 94.46%

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 94.92% 99.17%
CHEMBL2581 P07339 Cathepsin D 94.42% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.77% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 89.23% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.97% 92.08%
CHEMBL1781 P11387 DNA topoisomerase I 88.76% 97.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.71% 96.95%
CHEMBL221 P23219 Cyclooxygenase-1 86.05% 90.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.20% 97.29%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.87% 93.56%

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.
Petasites japonicus

Cross-Links

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PubChem 107507
NPASS NPC80053
LOTUS LTS0007799
wikiData Q81990654