(2E,6E)-2,6-dimethyl-10-methylidenedodeca-2,6,11-trien-1-ol

Details

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Internal ID 631dd7d4-90e6-4520-8d44-1d5c0500257b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2E,6E)-2,6-dimethyl-10-methylidenedodeca-2,6,11-trien-1-ol
SMILES (Canonical) CC(=CCCC(=C)C=C)CCC=C(C)CO
SMILES (Isomeric) C/C(=C\CCC(=C)C=C)/CC/C=C(\C)/CO
InChI InChI=1S/C15H24O/c1-5-13(2)8-6-9-14(3)10-7-11-15(4)12-16/h5,9,11,16H,1-2,6-8,10,12H2,3-4H3/b14-9+,15-11+
InChI Key HEOUOQSFBDQSMB-YFVJMOTDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.17
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,6E)-2,6-dimethyl-10-methylidenedodeca-2,6,11-trien-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9767 97.67%
Caco-2 + 0.8414 84.14%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.6989 69.89%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.9256 92.56%
OATP1B3 inhibitior + 0.9516 95.16%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7297 72.97%
P-glycoprotein inhibitior - 0.9464 94.64%
P-glycoprotein substrate - 0.9211 92.11%
CYP3A4 substrate - 0.5854 58.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7621 76.21%
CYP3A4 inhibition - 0.8698 86.98%
CYP2C9 inhibition - 0.9117 91.17%
CYP2C19 inhibition - 0.8995 89.95%
CYP2D6 inhibition - 0.9199 91.99%
CYP1A2 inhibition - 0.8269 82.69%
CYP2C8 inhibition - 0.9179 91.79%
CYP inhibitory promiscuity - 0.8062 80.62%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6720 67.20%
Eye corrosion + 0.6449 64.49%
Eye irritation + 0.7360 73.60%
Skin irritation + 0.6207 62.07%
Skin corrosion - 0.9573 95.73%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.9072 90.72%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.7940 79.40%
Acute Oral Toxicity (c) III 0.8058 80.58%
Estrogen receptor binding - 0.9047 90.47%
Androgen receptor binding - 0.8279 82.79%
Thyroid receptor binding - 0.8291 82.91%
Glucocorticoid receptor binding - 0.4850 48.50%
Aromatase binding - 0.6384 63.84%
PPAR gamma + 0.6220 62.20%
Honey bee toxicity - 0.8738 87.38%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9714 97.14%

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 85.95% 91.11%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 85.36% 82.05%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.56% 96.09%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 82.83% 97.34%
CHEMBL2581 P07339 Cathepsin D 82.44% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.79% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.11% 92.08%

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.
Astrantia major

Cross-Links

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PubChem 15276469
LOTUS LTS0255499
wikiData Q105026963