3,4,7,11-Tetramethyldodeca-1,3,6,10-tetraene

Details

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Internal ID 12cc57f6-754f-401b-8ff1-6417568c6e78
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,4,7,11-tetramethyldodeca-1,3,6,10-tetraene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H26/c1-7-15(5)16(6)12-11-14(4)10-8-9-13(2)3/h7,9,11H,1,8,10,12H2,2-6H3
InChI Key UIERAIUZMIXKBZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H26
Molecular Weight 218.38 g/mol
Exact Mass 218.203450829 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.70
Atomic LogP (AlogP) 5.59
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,4,7,11-Tetramethyldodeca-1,3,6,10-tetraene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.9571 95.71%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Nucleus 0.6326 63.26%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.9105 91.05%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7236 72.36%
P-glycoprotein inhibitior - 0.9215 92.15%
P-glycoprotein substrate - 0.9570 95.70%
CYP3A4 substrate - 0.5810 58.10%
CYP2C9 substrate - 0.8209 82.09%
CYP2D6 substrate - 0.7550 75.50%
CYP3A4 inhibition - 0.9627 96.27%
CYP2C9 inhibition - 0.8903 89.03%
CYP2C19 inhibition - 0.8891 88.91%
CYP2D6 inhibition - 0.9474 94.74%
CYP1A2 inhibition - 0.7161 71.61%
CYP2C8 inhibition - 0.9274 92.74%
CYP inhibitory promiscuity - 0.7252 72.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Warning 0.4862 48.62%
Eye corrosion + 0.7167 71.67%
Eye irritation + 0.8831 88.31%
Skin irritation + 0.8426 84.26%
Skin corrosion - 0.9833 98.33%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6845 68.45%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.9235 92.35%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.7001 70.01%
Acute Oral Toxicity (c) III 0.9077 90.77%
Estrogen receptor binding - 0.8507 85.07%
Androgen receptor binding - 0.7639 76.39%
Thyroid receptor binding - 0.7009 70.09%
Glucocorticoid receptor binding - 0.7066 70.66%
Aromatase binding - 0.6682 66.82%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.8246 82.46%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9962 99.62%

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 89.46% 92.08%
CHEMBL4040 P28482 MAP kinase ERK2 85.38% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.82% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.72% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.25% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.61% 91.11%

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 57067676
LOTUS LTS0043948
wikiData Q105273320