7,11-Dimethyldodeca-1,6,10-trien-3-ol

Details

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Internal ID e736d216-ddc0-4d71-9c33-6def083de334
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 7,11-dimethyldodeca-1,6,10-trien-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H24O/c1-5-14(15)11-7-10-13(4)9-6-8-12(2)3/h5,8,10,14-15H,1,6-7,9,11H2,2-4H3
InChI Key WASNIKZYIWZQIP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H24O
Molecular Weight 208.34 g/mol
Exact Mass 208.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7,11-Dimethyldodeca-1,6,10-trien-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9921 99.21%
Caco-2 + 0.7514 75.14%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.3296 32.96%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.9458 94.58%
OATP1B3 inhibitior + 0.9473 94.73%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7077 70.77%
P-glycoprotein inhibitior - 0.9621 96.21%
P-glycoprotein substrate - 0.9350 93.50%
CYP3A4 substrate - 0.5885 58.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6917 69.17%
CYP3A4 inhibition - 0.8624 86.24%
CYP2C9 inhibition - 0.8822 88.22%
CYP2C19 inhibition - 0.8807 88.07%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition - 0.6713 67.13%
CYP2C8 inhibition - 0.9784 97.84%
CYP inhibitory promiscuity - 0.8452 84.52%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6926 69.26%
Eye corrosion - 0.6560 65.60%
Eye irritation + 0.8240 82.40%
Skin irritation + 0.6648 66.48%
Skin corrosion - 0.9706 97.06%
Ames mutagenesis - 0.8737 87.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5538 55.38%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5887 58.87%
skin sensitisation + 0.8856 88.56%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.9329 93.29%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.4696 46.96%
Acute Oral Toxicity (c) III 0.8538 85.38%
Estrogen receptor binding - 0.9343 93.43%
Androgen receptor binding - 0.9116 91.16%
Thyroid receptor binding - 0.8402 84.02%
Glucocorticoid receptor binding - 0.5279 52.79%
Aromatase binding - 0.7612 76.12%
PPAR gamma + 0.5308 53.08%
Honey bee toxicity - 0.7791 77.91%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9436 94.36%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.89% 92.08%
CHEMBL2581 P07339 Cathepsin D 91.55% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.72% 96.09%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 85.32% 93.10%
CHEMBL3401 O75469 Pregnane X receptor 84.59% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.19% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.98% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.25% 94.45%

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 85781187
LOTUS LTS0204656
wikiData Q105300452