4-oxonon-2-enoic Acid

Details

Top
Internal ID 67686590-a411-4ab4-9023-a628a0b66cdf
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Medium-chain keto acids and derivatives
IUPAC Name 4-oxonon-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H14O3/c1-2-3-4-5-8(10)6-7-9(11)12/h6-7H,2-5H2,1H3,(H,11,12)
InChI Key QHYBPAALYZNWPK-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H14O3
Molecular Weight 170.21 g/mol
Exact Mass 170.094294304 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.78
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

Top
4-oxonon-2-enoic Acid

2D Structure

Top
2D Structure of 4-oxonon-2-enoic Acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9848 98.48%
Caco-2 + 0.9299 92.99%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5214 52.14%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9273 92.73%
OATP1B3 inhibitior + 0.9176 91.76%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9632 96.32%
P-glycoprotein inhibitior - 0.9892 98.92%
P-glycoprotein substrate - 0.9444 94.44%
CYP3A4 substrate - 0.6801 68.01%
CYP2C9 substrate - 0.6079 60.79%
CYP2D6 substrate - 0.8849 88.49%
CYP3A4 inhibition - 0.9292 92.92%
CYP2C9 inhibition - 0.9429 94.29%
CYP2C19 inhibition - 0.9396 93.96%
CYP2D6 inhibition - 0.9448 94.48%
CYP1A2 inhibition - 0.5492 54.92%
CYP2C8 inhibition - 0.9551 95.51%
CYP inhibitory promiscuity - 0.9477 94.77%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6658 66.58%
Carcinogenicity (trinary) Non-required 0.7018 70.18%
Eye corrosion + 0.8771 87.71%
Eye irritation + 0.9592 95.92%
Skin irritation + 0.8036 80.36%
Skin corrosion - 0.5429 54.29%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7908 79.08%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5976 59.76%
skin sensitisation + 0.5250 52.50%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.9161 91.61%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.6249 62.49%
Acute Oral Toxicity (c) III 0.8869 88.69%
Estrogen receptor binding - 0.7671 76.71%
Androgen receptor binding - 0.8768 87.68%
Thyroid receptor binding - 0.8132 81.32%
Glucocorticoid receptor binding - 0.7250 72.50%
Aromatase binding - 0.6981 69.81%
PPAR gamma - 0.5098 50.98%
Honey bee toxicity - 0.9910 99.10%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.5140 51.40%
Fish aquatic toxicity + 0.9326 93.26%

Targets

Top

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
CHEMBL230 P35354 Cyclooxygenase-2 97.84% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.38% 99.17%
CHEMBL2581 P07339 Cathepsin D 89.82% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.62% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.83% 97.29%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.20% 92.08%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 81.50% 96.00%
CHEMBL221 P23219 Cyclooxygenase-1 81.43% 90.17%
CHEMBL2664 P23526 Adenosylhomocysteinase 80.81% 86.67%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.30% 96.95%

Plants that contains it

Top
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

Top
PubChem 5182942
LOTUS LTS0087974
wikiData Q104195836