2,6-Dimethylocta-2,6-diene-1,8-diol

Details

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Internal ID 093e99d2-c388-4487-86df-0371b5491327
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 2,6-dimethylocta-2,6-diene-1,8-diol
SMILES (Canonical) CC(=CCO)CCC=C(C)CO
SMILES (Isomeric) CC(=CCO)CCC=C(C)CO
InChI InChI=1S/C10H18O2/c1-9(6-7-11)4-3-5-10(2)8-12/h5-6,11-12H,3-4,7-8H2,1-2H3
InChI Key PREUOUJFXMCMSJ-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O2
Molecular Weight 170.25 g/mol
Exact Mass 170.130679813 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.64
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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DTXSID50949359
3,7-dimethyl-2,6-octadien-1,8-diol

2D Structure

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2D Structure of 2,6-Dimethylocta-2,6-diene-1,8-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9635 96.35%
Caco-2 + 0.9155 91.55%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.5834 58.34%
OATP2B1 inhibitior - 0.8508 85.08%
OATP1B1 inhibitior + 0.9417 94.17%
OATP1B3 inhibitior + 0.9419 94.19%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8527 85.27%
P-glycoprotein inhibitior - 0.9840 98.40%
P-glycoprotein substrate - 0.9578 95.78%
CYP3A4 substrate - 0.6277 62.77%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.8744 87.44%
CYP2C9 inhibition - 0.9070 90.70%
CYP2C19 inhibition - 0.9004 90.04%
CYP2D6 inhibition - 0.9038 90.38%
CYP1A2 inhibition - 0.8272 82.72%
CYP2C8 inhibition - 0.9615 96.15%
CYP inhibitory promiscuity - 0.8025 80.25%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6171 61.71%
Eye corrosion + 0.6963 69.63%
Eye irritation + 0.8842 88.42%
Skin irritation - 0.5957 59.57%
Skin corrosion - 0.9555 95.55%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6147 61.47%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation + 0.7768 77.68%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.9145 91.45%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6028 60.28%
Acute Oral Toxicity (c) III 0.7649 76.49%
Estrogen receptor binding - 0.9387 93.87%
Androgen receptor binding - 0.8416 84.16%
Thyroid receptor binding - 0.9112 91.12%
Glucocorticoid receptor binding - 0.8440 84.40%
Aromatase binding - 0.8546 85.46%
PPAR gamma - 0.7976 79.76%
Honey bee toxicity - 0.9537 95.37%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.8999 89.99%

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 86.24% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.93% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.56% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.97% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.87% 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.
Euterpe oleracea
Isodon enanderianus
Isodon xerophilus

Cross-Links

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PubChem 537558
LOTUS LTS0116952
wikiData Q105107310