(3R)-2-methyl-6-methylideneocta-1,7-dien-3-ol

Details

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Internal ID 5407962f-51b0-404e-9198-903c4725ed9a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (3R)-2-methyl-6-methylideneocta-1,7-dien-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O/c1-5-9(4)6-7-10(11)8(2)3/h5,10-11H,1-2,4,6-7H2,3H3/t10-/m1/s1
InChI Key SQRIUUSIOSHZFA-SNVBAGLBSA-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 3.30
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R)-2-methyl-6-methylideneocta-1,7-dien-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 + 0.9900 99.00%
Caco-2 + 0.5421 54.21%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Lysosomes 0.4023 40.23%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9459 94.59%
OATP1B3 inhibitior + 0.9441 94.41%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9282 92.82%
P-glycoprotein inhibitior - 0.9818 98.18%
P-glycoprotein substrate - 0.9388 93.88%
CYP3A4 substrate - 0.6366 63.66%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7192 71.92%
CYP3A4 inhibition - 0.9225 92.25%
CYP2C9 inhibition - 0.9269 92.69%
CYP2C19 inhibition - 0.8697 86.97%
CYP2D6 inhibition - 0.9375 93.75%
CYP1A2 inhibition - 0.6933 69.33%
CYP2C8 inhibition - 0.9755 97.55%
CYP inhibitory promiscuity - 0.8041 80.41%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6632 66.32%
Eye corrosion + 0.6560 65.60%
Eye irritation + 0.8845 88.45%
Skin irritation + 0.7970 79.70%
Skin corrosion - 0.5419 54.19%
Ames mutagenesis - 0.7770 77.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6714 67.14%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6872 68.72%
skin sensitisation + 0.8486 84.86%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.9523 95.23%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.7165 71.65%
Acute Oral Toxicity (c) III 0.4572 45.72%
Estrogen receptor binding - 0.8494 84.94%
Androgen receptor binding - 0.9156 91.56%
Thyroid receptor binding - 0.8125 81.25%
Glucocorticoid receptor binding - 0.6219 62.19%
Aromatase binding - 0.8174 81.74%
PPAR gamma - 0.6014 60.14%
Honey bee toxicity - 0.8115 81.15%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.5692 56.92%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.51% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.24% 96.09%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 90.96% 97.34%
CHEMBL2581 P07339 Cathepsin D 86.15% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.95% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.42% 85.14%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.06% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.01% 99.17%
CHEMBL5251 Q06187 Tyrosine-protein kinase BTK 80.95% 98.51%

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.
Artemisia salsoloides
Tanacetum annuum

Cross-Links

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PubChem 162868343
LOTUS LTS0163711
wikiData Q105258433