2,7-Octadien-1-ol, 2-methyl-6-methylene, (E)

Details

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Internal ID b6d40ccc-1c01-4d6f-ae97-0cd874326e06
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (2Z)-2-methyl-6-methylideneocta-2,7-dien-1-ol
SMILES (Canonical) CC(=CCCC(=C)C=C)CO
SMILES (Isomeric) C/C(=C/CCC(=C)C=C)/CO
InChI InChI=1S/C10H16O/c1-4-9(2)6-5-7-10(3)8-11/h4,7,11H,1-2,5-6,8H2,3H3/b10-7-
InChI Key IEVYLQISZQFFGA-YFHOEESVSA-N
Popularity 0 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 3.10
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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SCHEMBL10986684
IEVYLQISZQFFGA-YFHOEESVSA-N
DTXSID301263030
(2Z)-2-Methyl-6-methylene-2,7-octadien-1-ol
38228-40-9

2D Structure

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2D Structure of 2,7-Octadien-1-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 + 0.9765 97.65%
Caco-2 + 0.8048 80.48%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.6855 68.55%
OATP2B1 inhibitior - 0.8551 85.51%
OATP1B1 inhibitior + 0.9249 92.49%
OATP1B3 inhibitior + 0.9486 94.86%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8984 89.84%
P-glycoprotein inhibitior - 0.9838 98.38%
P-glycoprotein substrate - 0.9305 93.05%
CYP3A4 substrate - 0.6091 60.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7621 76.21%
CYP3A4 inhibition - 0.9134 91.34%
CYP2C9 inhibition - 0.9152 91.52%
CYP2C19 inhibition - 0.9021 90.21%
CYP2D6 inhibition - 0.9267 92.67%
CYP1A2 inhibition - 0.8010 80.10%
CYP2C8 inhibition - 0.9385 93.85%
CYP inhibitory promiscuity - 0.7849 78.49%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6422 64.22%
Eye corrosion + 0.7347 73.47%
Eye irritation + 0.9357 93.57%
Skin irritation + 0.7169 71.69%
Skin corrosion - 0.9350 93.50%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7020 70.20%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.8828 88.28%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.7807 78.07%
Acute Oral Toxicity (c) III 0.7954 79.54%
Estrogen receptor binding - 0.9420 94.20%
Androgen receptor binding - 0.8724 87.24%
Thyroid receptor binding - 0.9150 91.50%
Glucocorticoid receptor binding - 0.7689 76.89%
Aromatase binding - 0.8142 81.42%
PPAR gamma - 0.8026 80.26%
Honey bee toxicity - 0.8597 85.97%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9679 96.79%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.46% 91.11%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 85.60% 97.34%
CHEMBL2581 P07339 Cathepsin D 82.04% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.01% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.79% 99.17%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.25% 82.05%

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.
Thymus vulgaris

Cross-Links

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PubChem 5352139
LOTUS LTS0272171
wikiData Q105111995