2-(3,7-Dimethylocta-2,6-dienyl)-3,7-dimethyloct-6-ene-1,3-diol

Details

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Internal ID 48afb2d4-61c1-4aad-af8d-cfdde077112d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-(3,7-dimethylocta-2,6-dienyl)-3,7-dimethyloct-6-ene-1,3-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H36O2/c1-16(2)9-7-11-18(5)12-13-19(15-21)20(6,22)14-8-10-17(3)4/h9-10,12,19,21-22H,7-8,11,13-15H2,1-6H3
InChI Key OAKVKJQFXGOQPH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H36O2
Molecular Weight 308.50 g/mol
Exact Mass 308.271530387 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 5.50
Atomic LogP (AlogP) 5.18
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(3,7-Dimethylocta-2,6-dienyl)-3,7-dimethyloct-6-ene-1,3-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9680 96.80%
Caco-2 + 0.6479 64.79%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4882 48.82%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.9312 93.12%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7067 70.67%
BSEP inhibitior + 0.8336 83.36%
P-glycoprotein inhibitior - 0.7362 73.62%
P-glycoprotein substrate - 0.9093 90.93%
CYP3A4 substrate - 0.5357 53.57%
CYP2C9 substrate - 0.7836 78.36%
CYP2D6 substrate - 0.7868 78.68%
CYP3A4 inhibition - 0.8959 89.59%
CYP2C9 inhibition - 0.7717 77.17%
CYP2C19 inhibition - 0.8000 80.00%
CYP2D6 inhibition - 0.8913 89.13%
CYP1A2 inhibition - 0.7264 72.64%
CYP2C8 inhibition - 0.9270 92.70%
CYP inhibitory promiscuity - 0.7389 73.89%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.6521 65.21%
Eye corrosion - 0.9133 91.33%
Eye irritation - 0.7665 76.65%
Skin irritation - 0.5398 53.98%
Skin corrosion - 0.9751 97.51%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7385 73.85%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7174 71.74%
skin sensitisation + 0.5302 53.02%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5350 53.50%
Acute Oral Toxicity (c) III 0.7375 73.75%
Estrogen receptor binding - 0.5984 59.84%
Androgen receptor binding - 0.8108 81.08%
Thyroid receptor binding + 0.6017 60.17%
Glucocorticoid receptor binding - 0.5273 52.73%
Aromatase binding - 0.5909 59.09%
PPAR gamma + 0.7048 70.48%
Honey bee toxicity - 0.8489 84.89%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.6941 69.41%

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
CHEMBL2581 P07339 Cathepsin D 91.67% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.07% 94.73%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.40% 97.29%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 85.57% 92.68%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.47% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.60% 97.25%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.74% 89.34%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.68% 92.88%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.16% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.08% 91.11%

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.
Peucedanum oreoselinum

Cross-Links

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PubChem 550543
LOTUS LTS0220888
wikiData Q105188720