8,10-Dodecadienol

Details

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Internal ID 7404e860-b2cb-4e5d-a338-47e1b7e59f98
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name dodeca-8,10-dien-1-ol
SMILES (Canonical) CC=CC=CCCCCCCCO
SMILES (Isomeric) CC=CC=CCCCCCCCO
InChI InChI=1S/C12H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h2-5,13H,6-12H2,1H3
InChI Key CSWBSLXBXRFNST-UHFFFAOYSA-N
Popularity 29 references in papers

Physical and Chemical Properties

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Molecular Formula C12H22O
Molecular Weight 182.30 g/mol
Exact Mass 182.167065321 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.45
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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dodeca-8,10-dien-1-ol
57002-06-9
8,10-dodecadienyl alcohol
DTXSID30860492
CSWBSLXBXRFNST-UHFFFAOYSA-N
BCP29082
FT-0604960
(e,e)-10-dodecadien-1-ol;(8E,10E)-8,10-Dodecadien-1-ol

2D Structure

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2D Structure of 8,10-Dodecadienol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9850 98.50%
Caco-2 + 0.9404 94.04%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.4644 46.44%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior + 0.8428 84.28%
OATP1B3 inhibitior + 0.9354 93.54%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7425 74.25%
P-glycoprotein inhibitior - 0.9763 97.63%
P-glycoprotein substrate - 0.9482 94.82%
CYP3A4 substrate - 0.6445 64.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7664 76.64%
CYP3A4 inhibition - 0.9444 94.44%
CYP2C9 inhibition - 0.8913 89.13%
CYP2C19 inhibition - 0.9372 93.72%
CYP2D6 inhibition - 0.9515 95.15%
CYP1A2 inhibition - 0.7041 70.41%
CYP2C8 inhibition - 0.9370 93.70%
CYP inhibitory promiscuity - 0.8878 88.78%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6829 68.29%
Eye corrosion + 0.9068 90.68%
Eye irritation + 0.9763 97.63%
Skin irritation + 0.7764 77.64%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3860 38.60%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5114 51.14%
skin sensitisation + 0.8252 82.52%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.5063 50.63%
Acute Oral Toxicity (c) III 0.8549 85.49%
Estrogen receptor binding - 0.8202 82.02%
Androgen receptor binding - 0.5196 51.96%
Thyroid receptor binding - 0.5415 54.15%
Glucocorticoid receptor binding + 0.6111 61.11%
Aromatase binding - 0.6190 61.90%
PPAR gamma - 0.5096 50.96%
Honey bee toxicity - 0.9752 97.52%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6749 67.49%
Fish aquatic toxicity - 0.6781 67.81%

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 90.52% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.52% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.46% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.69% 97.29%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.70% 91.11%
CHEMBL2581 P07339 Cathepsin D 81.06% 98.95%

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 92622
LOTUS LTS0001336
wikiData Q104969620