2,6-Dimethylocta-1,5,7-trien-3-ol

Details

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Internal ID a00e1920-d894-41ef-bf82-ff50eea2515d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (5E)-2,6-dimethylocta-1,5,7-trien-3-ol
SMILES (Canonical) CC(=C)C(CC=C(C)C=C)O
SMILES (Isomeric) CC(=C)C(C/C=C(\C)/C=C)O
InChI InChI=1S/C10H16O/c1-5-9(4)6-7-10(11)8(2)3/h5-6,10-11H,1-2,7H2,3-4H3/b9-6+
InChI Key TYDDWHVJHGIJCW-RMKNXTFCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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28977-58-4
Ocimenol, (E)-
1,5,7-Octatrien-3-ol, 2,6-dimethyl-, (5E)-
(E)-2,6-Dimethylocta-1,5,7-trien-3-ol
29414-56-0
RD4TJJ74P3
1,5,7-Octatrien-3-ol, 2,6-dimethyl-, (E)-
5,7-Octadien-2-ol,2,6-dimethyl
EINECS 249-346-6
EINECS 249-613-7
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,6-Dimethylocta-1,5,7-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 + 0.9913 99.13%
Caco-2 + 0.7341 73.41%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Lysosomes 0.4509 45.09%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.9428 94.28%
OATP1B3 inhibitior + 0.9599 95.99%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9200 92.00%
P-glycoprotein inhibitior - 0.9801 98.01%
P-glycoprotein substrate - 0.9453 94.53%
CYP3A4 substrate - 0.6381 63.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7192 71.92%
CYP3A4 inhibition - 0.8359 83.59%
CYP2C9 inhibition - 0.9204 92.04%
CYP2C19 inhibition - 0.7039 70.39%
CYP2D6 inhibition - 0.9196 91.96%
CYP1A2 inhibition - 0.7759 77.59%
CYP2C8 inhibition - 0.9673 96.73%
CYP inhibitory promiscuity - 0.8277 82.77%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.6283 62.83%
Carcinogenicity (trinary) Non-required 0.7329 73.29%
Eye corrosion + 0.6715 67.15%
Eye irritation + 0.9394 93.94%
Skin irritation + 0.7290 72.90%
Skin corrosion - 0.5898 58.98%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7302 73.02%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8333 83.33%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5197 51.97%
Acute Oral Toxicity (c) III 0.5744 57.44%
Estrogen receptor binding - 0.8819 88.19%
Androgen receptor binding - 0.9253 92.53%
Thyroid receptor binding - 0.8447 84.47%
Glucocorticoid receptor binding - 0.7937 79.37%
Aromatase binding - 0.8279 82.79%
PPAR gamma - 0.5821 58.21%
Honey bee toxicity - 0.8188 81.88%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.4882 48.82%

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
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 93.18% 97.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.84% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.12% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.83% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 83.62% 83.82%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.20% 85.14%

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.
Citrus maxima

Cross-Links

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PubChem 5362854
NPASS NPC155386