(6S)-6-hydroxyoct-7-enoic acid

Details

Top
Internal ID 2f5baade-5429-42f7-939c-db8c8f1d1ba4
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name (6S)-6-hydroxyoct-7-enoic acid
SMILES (Canonical) C=CC(CCCCC(=O)O)O
SMILES (Isomeric) C=C[C@H](CCCCC(=O)O)O
InChI InChI=1S/C8H14O3/c1-2-7(9)5-3-4-6-8(10)11/h2,7,9H,1,3-6H2,(H,10,11)/t7-/m1/s1
InChI Key OULIEBSNQYVDGJ-SSDOTTSWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C8H14O3
Molecular Weight 158.19 g/mol
Exact Mass 158.094294304 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.18
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (6S)-6-hydroxyoct-7-enoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9367 93.67%
Caco-2 + 0.5108 51.08%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7797 77.97%
OATP2B1 inhibitior - 0.8468 84.68%
OATP1B1 inhibitior + 0.9486 94.86%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9370 93.70%
P-glycoprotein inhibitior - 0.9864 98.64%
P-glycoprotein substrate - 0.9743 97.43%
CYP3A4 substrate - 0.6808 68.08%
CYP2C9 substrate + 0.5992 59.92%
CYP2D6 substrate - 0.8373 83.73%
CYP3A4 inhibition - 0.8900 89.00%
CYP2C9 inhibition - 0.9137 91.37%
CYP2C19 inhibition - 0.9244 92.44%
CYP2D6 inhibition - 0.9622 96.22%
CYP1A2 inhibition - 0.8138 81.38%
CYP2C8 inhibition - 0.9837 98.37%
CYP inhibitory promiscuity - 0.9457 94.57%
UGT catelyzed - 0.5638 56.38%
Carcinogenicity (binary) - 0.7135 71.35%
Carcinogenicity (trinary) Non-required 0.6775 67.75%
Eye corrosion + 0.8529 85.29%
Eye irritation + 0.9693 96.93%
Skin irritation + 0.5520 55.20%
Skin corrosion + 0.7545 75.45%
Ames mutagenesis - 0.9237 92.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6710 67.10%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5696 56.96%
skin sensitisation + 0.4905 49.05%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7701 77.01%
Acute Oral Toxicity (c) III 0.6841 68.41%
Estrogen receptor binding - 0.9238 92.38%
Androgen receptor binding - 0.9646 96.46%
Thyroid receptor binding - 0.8630 86.30%
Glucocorticoid receptor binding - 0.6609 66.09%
Aromatase binding - 0.7787 77.87%
PPAR gamma - 0.6893 68.93%
Honey bee toxicity - 0.9224 92.24%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity + 0.6622 66.22%

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
CHEMBL4040 P28482 MAP kinase ERK2 93.82% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.32% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.73% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.26% 98.95%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 86.49% 97.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.76% 91.11%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.55% 100.00%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 82.40% 92.26%
CHEMBL340 P08684 Cytochrome P450 3A4 81.64% 91.19%

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 163042487
LOTUS LTS0260449
wikiData Q105200235