3,7,11-Trimethyldodeca-2,4-diene

Details

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Internal ID 5f39f488-426e-4d00-8260-30a77f9fd68f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,7,11-trimethyldodeca-2,4-diene
SMILES (Canonical) CC=C(C)C=CCC(C)CCCC(C)C
SMILES (Isomeric) CC=C(C)C=CCC(C)CCCC(C)C
InChI InChI=1S/C15H28/c1-6-14(4)10-8-12-15(5)11-7-9-13(2)3/h6,8,10,13,15H,7,9,11-12H2,1-5H3
InChI Key QUFVBBANWSSNQF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28
Molecular Weight 208.38 g/mol
Exact Mass 208.219100893 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.60
Atomic LogP (AlogP) 5.36
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7,11-Trimethyldodeca-2,4-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 + 0.9724 97.24%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Nucleus 0.6684 66.84%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.9364 93.64%
OATP1B3 inhibitior + 0.9380 93.80%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5297 52.97%
P-glycoprotein inhibitior - 0.9691 96.91%
P-glycoprotein substrate - 0.8159 81.59%
CYP3A4 substrate - 0.5835 58.35%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7751 77.51%
CYP3A4 inhibition - 0.9716 97.16%
CYP2C9 inhibition - 0.9099 90.99%
CYP2C19 inhibition - 0.9168 91.68%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.7354 73.54%
CYP2C8 inhibition - 0.9714 97.14%
CYP inhibitory promiscuity - 0.6923 69.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Warning 0.4712 47.12%
Eye corrosion + 0.7181 71.81%
Eye irritation + 0.6711 67.11%
Skin irritation + 0.8835 88.35%
Skin corrosion - 0.9656 96.56%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7277 72.77%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation + 0.9505 95.05%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.7248 72.48%
Acute Oral Toxicity (c) III 0.8971 89.71%
Estrogen receptor binding - 0.9063 90.63%
Androgen receptor binding - 0.9221 92.21%
Thyroid receptor binding - 0.5805 58.05%
Glucocorticoid receptor binding - 0.6952 69.52%
Aromatase binding - 0.7269 72.69%
PPAR gamma - 0.8658 86.58%
Honey bee toxicity - 0.9724 97.24%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9916 99.16%

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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.28% 97.29%
CHEMBL2885 P07451 Carbonic anhydrase III 87.34% 87.45%
CHEMBL2581 P07339 Cathepsin D 86.76% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 84.98% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.35% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.26% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.07% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.03% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.74% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 57372502
LOTUS LTS0021943
wikiData Q105228141