9-Dodecen-1-ol

Details

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Internal ID 3c5ff9b0-eafe-46f2-b503-ad83c85066b1
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name dodec-9-en-1-ol
SMILES (Canonical) CCC=CCCCCCCCCO
SMILES (Isomeric) CCC=CCCCCCCCCO
InChI InChI=1S/C12H24O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h3-4,13H,2,5-12H2,1H3
InChI Key GJNNIRNIXNLOJP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H24O
Molecular Weight 184.32 g/mol
Exact Mass 184.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.68
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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9-Dodecen-1-ol
91856-11-0
GJNNIRNIXNLOJP-UHFFFAOYSA-N
DTXSID801317400
LMFA05000636
FT-0773912

2D Structure

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2D Structure of 9-Dodecen-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 + 0.9895 98.95%
Caco-2 + 0.9060 90.60%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.5625 56.25%
OATP2B1 inhibitior - 0.8534 85.34%
OATP1B1 inhibitior + 0.8359 83.59%
OATP1B3 inhibitior + 0.9003 90.03%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7124 71.24%
P-glycoprotein inhibitior - 0.9765 97.65%
P-glycoprotein substrate - 0.9585 95.85%
CYP3A4 substrate - 0.6838 68.38%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9303 93.03%
CYP2C9 inhibition - 0.8889 88.89%
CYP2C19 inhibition - 0.9364 93.64%
CYP2D6 inhibition - 0.9357 93.57%
CYP1A2 inhibition - 0.5751 57.51%
CYP2C8 inhibition - 0.9380 93.80%
CYP inhibitory promiscuity - 0.8204 82.04%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.6630 66.30%
Eye corrosion + 0.7207 72.07%
Eye irritation + 0.9542 95.42%
Skin irritation + 0.7501 75.01%
Skin corrosion - 0.9740 97.40%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3885 38.85%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6710 67.10%
skin sensitisation + 0.8634 86.34%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.6867 68.67%
Acute Oral Toxicity (c) III 0.8455 84.55%
Estrogen receptor binding - 0.8158 81.58%
Androgen receptor binding - 0.7855 78.55%
Thyroid receptor binding - 0.5955 59.55%
Glucocorticoid receptor binding - 0.6134 61.34%
Aromatase binding - 0.7278 72.78%
PPAR gamma - 0.6296 62.96%
Honey bee toxicity - 0.9843 98.43%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.6543 65.43%
Fish aquatic toxicity - 0.5166 51.66%

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 92.00% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 91.11% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.41% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.54% 97.29%
CHEMBL2581 P07339 Cathepsin D 84.33% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.67% 96.95%
CHEMBL1781 P11387 DNA topoisomerase I 81.31% 97.00%

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.
Etlingera elatior

Cross-Links

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PubChem 93181
LOTUS LTS0011130
wikiData Q104375763