9-Decen-1-OL

Details

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Internal ID d8accec7-fa44-43a4-9941-0c3f35284961
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name dec-9-en-1-ol
SMILES (Canonical) C=CCCCCCCCCO
SMILES (Isomeric) C=CCCCCCCCCO
InChI InChI=1S/C10H20O/c1-2-3-4-5-6-7-8-9-10-11/h2,11H,1,3-10H2
InChI Key QGFSQVPRCWJZQK-UHFFFAOYSA-N
Popularity 62 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20O
Molecular Weight 156.26 g/mol
Exact Mass 156.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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13019-22-2
dec-9-en-1-ol
Decylenic alcohol
9-Decenol
omega-Decenol
1-Decen-10-ol
.omega.-Decen-1-ol
Trepanol
.omega.-Decenol
9-Decene-1-ol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 9-Decen-1-OL

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9763 97.63%
Caco-2 + 0.7264 72.64%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.4411 44.11%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.9429 94.29%
OATP1B3 inhibitior + 0.9424 94.24%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8867 88.67%
P-glycoprotein inhibitior - 0.9816 98.16%
P-glycoprotein substrate - 0.9840 98.40%
CYP3A4 substrate - 0.7109 71.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7062 70.62%
CYP3A4 inhibition - 0.9330 93.30%
CYP2C9 inhibition - 0.8635 86.35%
CYP2C19 inhibition - 0.9172 91.72%
CYP2D6 inhibition - 0.9458 94.58%
CYP1A2 inhibition - 0.7265 72.65%
CYP2C8 inhibition - 0.9348 93.48%
CYP inhibitory promiscuity - 0.8900 89.00%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.7087 70.87%
Eye corrosion + 0.9273 92.73%
Eye irritation + 0.9905 99.05%
Skin irritation + 0.7438 74.38%
Skin corrosion - 0.8982 89.82%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4856 48.56%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5281 52.81%
skin sensitisation + 0.8187 81.87%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.5781 57.81%
Acute Oral Toxicity (c) III 0.7938 79.38%
Estrogen receptor binding - 0.9382 93.82%
Androgen receptor binding - 0.8599 85.99%
Thyroid receptor binding - 0.7896 78.96%
Glucocorticoid receptor binding - 0.7937 79.37%
Aromatase binding - 0.8705 87.05%
PPAR gamma - 0.7291 72.91%
Honey bee toxicity - 0.8959 89.59%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.7478 74.78%
Fish aquatic toxicity - 0.5000 50.00%

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
CHEMBL2885 P07451 Carbonic anhydrase III 90.22% 87.45%
CHEMBL1829 O15379 Histone deacetylase 3 88.26% 95.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.58% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.96% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.13% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.43% 96.09%
CHEMBL1977 P11473 Vitamin D receptor 81.25% 99.43%

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.
Artemisia annua
Etlingera elatior
Tordylium apulum

Cross-Links

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PubChem 25612
LOTUS LTS0161213
wikiData Q27259011