(3E,6S,10S,14S)-2,6,10,14-tetramethylhexadeca-1,3-diene

Details

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Internal ID 3e990cbd-0b81-4774-866d-c06bf1b7f5af
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3E,6S,10S,14S)-2,6,10,14-tetramethylhexadeca-1,3-diene
SMILES (Canonical) CCC(C)CCCC(C)CCCC(C)CC=CC(=C)C
SMILES (Isomeric) CC[C@H](C)CCC[C@H](C)CCC[C@H](C)C/C=C/C(=C)C
InChI InChI=1S/C20H38/c1-7-18(4)12-9-14-20(6)16-10-15-19(5)13-8-11-17(2)3/h8,11,18-20H,2,7,9-10,12-16H2,1,3-6H3/b11-8+/t18-,19+,20-/m0/s1
InChI Key HPXTYQIQNKBSIK-UQYDPPGPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H38
Molecular Weight 278.50 g/mol
Exact Mass 278.297351212 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 9.30
Atomic LogP (AlogP) 7.17
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3E,6S,10S,14S)-2,6,10,14-tetramethylhexadeca-1,3-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9895 98.95%
Caco-2 + 0.8836 88.36%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Nucleus 0.3955 39.55%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9068 90.68%
OATP1B3 inhibitior + 0.9394 93.94%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6325 63.25%
P-glycoprotein inhibitior - 0.8303 83.03%
P-glycoprotein substrate - 0.8159 81.59%
CYP3A4 substrate - 0.6024 60.24%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7751 77.51%
CYP3A4 inhibition - 0.9476 94.76%
CYP2C9 inhibition - 0.8999 89.99%
CYP2C19 inhibition - 0.8947 89.47%
CYP2D6 inhibition - 0.9312 93.12%
CYP1A2 inhibition - 0.6082 60.82%
CYP2C8 inhibition - 0.9302 93.02%
CYP inhibitory promiscuity - 0.5751 57.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.4623 46.23%
Eye corrosion + 0.7684 76.84%
Eye irritation - 0.4809 48.09%
Skin irritation + 0.7689 76.89%
Skin corrosion - 0.9819 98.19%
Ames mutagenesis - 0.9123 91.23%
Human Ether-a-go-go-Related Gene inhibition + 0.7638 76.38%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.9039 90.39%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.6454 64.54%
Acute Oral Toxicity (c) III 0.8690 86.90%
Estrogen receptor binding + 0.6064 60.64%
Androgen receptor binding - 0.8178 81.78%
Thyroid receptor binding + 0.6856 68.56%
Glucocorticoid receptor binding - 0.5083 50.83%
Aromatase binding - 0.5335 53.35%
PPAR gamma + 0.5892 58.92%
Honey bee toxicity - 0.9580 95.80%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9968 99.68%

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
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 92.49% 97.34%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.73% 97.29%
CHEMBL2581 P07339 Cathepsin D 88.41% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.71% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 86.63% 87.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.63% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.98% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.57% 94.73%
CHEMBL1977 P11473 Vitamin D receptor 82.20% 99.43%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.05% 96.47%

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.
Lemna minor

Cross-Links

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PubChem 162845689
LOTUS LTS0107588
wikiData Q105032015