3,7-Octadien-2-ol, 2-methyl-6-methylene-, (E)-

Details

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Internal ID 99cd94fb-b889-40a6-b0f8-4cd183ef5f3d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name (3E)-2-methyl-6-methylideneocta-3,7-dien-2-ol
SMILES (Canonical) CC(C)(C=CCC(=C)C=C)O
SMILES (Isomeric) CC(C)(/C=C/CC(=C)C=C)O
InChI InChI=1S/C10H16O/c1-5-9(2)7-6-8-10(3,4)11/h5-6,8,11H,1-2,7H2,3-4H3/b8-6+
InChI Key NOEQSPUVXRMJBW-SOFGYWHQSA-N
Popularity 7 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 2.70
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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3,7-Octadien-2-ol, 2-methyl-6-methylene-, (E)-
(E)-2-Methyl-6-methylene-3,7-octadien-2-ol
Isomyrcenol
Amitinol
(3E)-2-methyl-6-methylideneocta-3,7-dien-2-ol
SCHEMBL5070794
SCHEMBL5070795
NOEQSPUVXRMJBW-SOFGYWHQSA-N
trans-2-Methyl-6-methylen-3,7-octadien-2-ol
(3E)-2-Methyl-6-methylene-3,7-octadien-2-ol #

2D Structure

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2D Structure of 3,7-Octadien-2-ol, 2-methyl-6-methylene-, (E)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9711 97.11%
Caco-2 + 0.8494 84.94%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.4163 41.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8635 86.35%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8969 89.69%
P-glycoprotein inhibitior - 0.9762 97.62%
P-glycoprotein substrate - 0.9746 97.46%
CYP3A4 substrate - 0.6340 63.40%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.7761 77.61%
CYP3A4 inhibition - 0.7614 76.14%
CYP2C9 inhibition - 0.7737 77.37%
CYP2C19 inhibition - 0.6273 62.73%
CYP2D6 inhibition - 0.9375 93.75%
CYP1A2 inhibition - 0.8389 83.89%
CYP2C8 inhibition - 0.9270 92.70%
CYP inhibitory promiscuity - 0.6183 61.83%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) + 0.5483 54.83%
Carcinogenicity (trinary) Non-required 0.5885 58.85%
Eye corrosion + 0.6494 64.94%
Eye irritation + 0.8279 82.79%
Skin irritation + 0.7925 79.25%
Skin corrosion - 0.6079 60.79%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6391 63.91%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.8111 81.11%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.6461 64.61%
Acute Oral Toxicity (c) III 0.6193 61.93%
Estrogen receptor binding - 0.8486 84.86%
Androgen receptor binding - 0.9603 96.03%
Thyroid receptor binding - 0.8810 88.10%
Glucocorticoid receptor binding - 0.6979 69.79%
Aromatase binding - 0.8920 89.20%
PPAR gamma - 0.7988 79.88%
Honey bee toxicity - 0.8939 89.39%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.7356 73.56%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.18% 97.25%
CHEMBL5251 Q06187 Tyrosine-protein kinase BTK 89.19% 98.51%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.68% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 83.57% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.82% 91.11%
CHEMBL2885 P07451 Carbonic anhydrase III 81.34% 87.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.92% 96.95%

Plants that contains it

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Cross-Links

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PubChem 5363351
NPASS NPC275670
LOTUS LTS0253813
wikiData Q76305142