7-Hydroxyoct-2-enoic acid

Details

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Internal ID 8f440d10-e489-4e19-91ee-b04e0efb16b4
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name 7-hydroxyoct-2-enoic acid
SMILES (Canonical) CC(CCCC=CC(=O)O)O
SMILES (Isomeric) CC(CCCC=CC(=O)O)O
InChI InChI=1S/C8H14O3/c1-7(9)5-3-2-4-6-8(10)11/h4,6-7,9H,2-3,5H2,1H3,(H,10,11)
InChI Key TWDBRKLFYIPUTJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O3
Molecular Weight 158.19 g/mol
Exact Mass 158.094294304 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.18
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Hydroxyoct-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 + 0.9726 97.26%
Caco-2 + 0.6006 60.06%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7097 70.97%
OATP2B1 inhibitior - 0.8495 84.95%
OATP1B1 inhibitior + 0.9250 92.50%
OATP1B3 inhibitior + 0.9072 90.72%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9595 95.95%
P-glycoprotein inhibitior - 0.9893 98.93%
P-glycoprotein substrate - 0.9388 93.88%
CYP3A4 substrate - 0.6306 63.06%
CYP2C9 substrate - 0.5995 59.95%
CYP2D6 substrate - 0.8951 89.51%
CYP3A4 inhibition - 0.9493 94.93%
CYP2C9 inhibition - 0.9418 94.18%
CYP2C19 inhibition - 0.9499 94.99%
CYP2D6 inhibition - 0.9591 95.91%
CYP1A2 inhibition + 0.5071 50.71%
CYP2C8 inhibition - 0.9914 99.14%
CYP inhibitory promiscuity - 0.9373 93.73%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7135 71.35%
Carcinogenicity (trinary) Non-required 0.7173 71.73%
Eye corrosion + 0.7436 74.36%
Eye irritation + 0.8484 84.84%
Skin irritation + 0.7681 76.81%
Skin corrosion + 0.9466 94.66%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8174 81.74%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.7091 70.91%
skin sensitisation + 0.5000 50.00%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.8488 84.88%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6003 60.03%
Acute Oral Toxicity (c) III 0.7322 73.22%
Estrogen receptor binding - 0.9300 93.00%
Androgen receptor binding - 0.8428 84.28%
Thyroid receptor binding - 0.8246 82.46%
Glucocorticoid receptor binding - 0.6600 66.00%
Aromatase binding - 0.9166 91.66%
PPAR gamma - 0.7269 72.69%
Honey bee toxicity - 0.9727 97.27%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.6835 68.35%

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 89.45% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.10% 96.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.65% 96.47%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 86.53% 100.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.43% 97.29%
CHEMBL2581 P07339 Cathepsin D 84.62% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.84% 93.56%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 82.05% 98.75%

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 86014029
LOTUS LTS0259142
wikiData Q105265736