(2E,6E)-6,11-Dimethyl-2,6,10-dodecatrien-1-ol

Details

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Internal ID e4fbec22-439b-4be3-a51b-126d54cde81b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (2E,6E)-6,11-dimethyldodeca-2,6,10-trien-1-ol
SMILES (Canonical) CC(=CCCC=C(C)CCC=CCO)C
SMILES (Isomeric) CC(=CCC/C=C(\C)/CC/C=C/CO)C
InChI InChI=1S/C14H24O/c1-13(2)9-6-7-11-14(3)10-5-4-8-12-15/h4,8-9,11,15H,5-7,10,12H2,1-3H3/b8-4+,14-11+
InChI Key BVLIMWXCOVQDNN-JPYRNUIHSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H24O
Molecular Weight 208.34 g/mol
Exact Mass 208.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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SCHEMBL23802660
BVLIMWXCOVQDNN-JPYRNUIHSA-N
(2E,6E)-6,11-Dimethyl-2,6,10-dodecatrien-1-ol
(2E,6E)-6,11-Dimethyl-2,6,10-dodecatrien-1-ol #

2D Structure

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2D Structure of (2E,6E)-6,11-Dimethyl-2,6,10-dodecatrien-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 + 0.9823 98.23%
Caco-2 + 0.8802 88.02%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.5576 55.76%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.9160 91.60%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.5698 56.98%
P-glycoprotein inhibitior - 0.9771 97.71%
P-glycoprotein substrate - 0.9570 95.70%
CYP3A4 substrate - 0.6129 61.29%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9088 90.88%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.9046 90.46%
CYP2C8 inhibition - 0.9736 97.36%
CYP inhibitory promiscuity - 0.7650 76.50%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6507 65.07%
Eye corrosion + 0.5325 53.25%
Eye irritation + 0.6451 64.51%
Skin irritation + 0.8492 84.92%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4651 46.51%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.8375 83.75%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9812 98.12%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6603 66.03%
Acute Oral Toxicity (c) III 0.8552 85.52%
Estrogen receptor binding - 0.9176 91.76%
Androgen receptor binding - 0.8771 87.71%
Thyroid receptor binding - 0.7395 73.95%
Glucocorticoid receptor binding - 0.7469 74.69%
Aromatase binding - 0.8100 81.00%
PPAR gamma + 0.6373 63.73%
Honey bee toxicity - 0.8903 89.03%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9500 95.00%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.40% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.90% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.22% 96.09%
CHEMBL2581 P07339 Cathepsin D 80.77% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 80.53% 94.73%

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.
Rhodiola crenulata

Cross-Links

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PubChem 5365863
NPASS NPC33716