cis-5-Octenoic acid

Details

Top
Internal ID 52d64a1a-03ce-4137-93c1-99cced99b179
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name (Z)-oct-5-enoic acid
SMILES (Canonical) CCC=CCCCC(=O)O
SMILES (Isomeric) CC/C=C\CCCC(=O)O
InChI InChI=1S/C8H14O2/c1-2-3-4-5-6-7-8(9)10/h3-4H,2,5-7H2,1H3,(H,9,10)/b4-3-
InChI Key RRGOKSYVAZDNKR-ARJAWSKDSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C8H14O2
Molecular Weight 142.20 g/mol
Exact Mass 142.099379685 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

Top
Octenoic acid
(Z)-5-Octenoic acid
5Z-octenoic acid
(5Z)-5-octenoic acid
(Z)-oct-5-enoic acid
5-Octenoic acid, (5Z)-
UNII-6OL5TNF5WG
6OL5TNF5WG
41653-97-8
cis-delta-octenoic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of cis-5-Octenoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.8838 88.38%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Plasma membrane 0.5044 50.44%
OATP2B1 inhibitior - 0.8386 83.86%
OATP1B1 inhibitior - 0.3228 32.28%
OATP1B3 inhibitior - 0.3406 34.06%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9121 91.21%
P-glycoprotein inhibitior - 0.9916 99.16%
P-glycoprotein substrate - 0.9741 97.41%
CYP3A4 substrate - 0.6958 69.58%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.9465 94.65%
CYP2C9 inhibition - 0.8798 87.98%
CYP2C19 inhibition - 0.9638 96.38%
CYP2D6 inhibition - 0.9631 96.31%
CYP1A2 inhibition + 0.6915 69.15%
CYP2C8 inhibition - 0.9710 97.10%
CYP inhibitory promiscuity - 0.9426 94.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6935 69.35%
Carcinogenicity (trinary) Non-required 0.6373 63.73%
Eye corrosion + 0.9371 93.71%
Eye irritation + 0.9883 98.83%
Skin irritation + 0.7676 76.76%
Skin corrosion - 0.6260 62.60%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6804 68.04%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.8750 87.50%
skin sensitisation + 0.8470 84.70%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity - 0.6531 65.31%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.8050 80.50%
Acute Oral Toxicity (c) IV 0.6387 63.87%
Estrogen receptor binding - 0.9542 95.42%
Androgen receptor binding - 0.9563 95.63%
Thyroid receptor binding - 0.8942 89.42%
Glucocorticoid receptor binding - 0.8140 81.40%
Aromatase binding - 0.8765 87.65%
PPAR gamma - 0.6107 61.07%
Honey bee toxicity - 0.9905 99.05%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.8175 81.75%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 94.49% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.71% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 90.14% 97.00%
CHEMBL2581 P07339 Cathepsin D 89.99% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.51% 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.
Eucalyptus brassiana
Thymus longicaulis

Cross-Links

Top
PubChem 5282718
LOTUS LTS0123989
wikiData Q27265237