1,2-Hexadecadiene, 3,7,11,15-tetramethyl-

Details

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Internal ID af95e07c-8742-4e13-b5be-f5e6d6face76
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name
SMILES (Canonical) CC(C)CCCC(C)CCCC(C)CCCC(=C=C)C
SMILES (Isomeric) CC(C)CCCC(C)CCCC(C)CCCC(=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/h17,19-20H,1,8-16H2,2-6H3
InChI Key QSDJIYUCUBTKOY-UHFFFAOYSA-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 8.80
Atomic LogP (AlogP) 7.16
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 12

Synonyms

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1,2-Hexadecadiene, 3,7,11,15-tetramethyl-
3,7,11,15-TETRAMETHYL-1,2-HEXADECADIENE
3,7,11,15-tetramethylhexadeca-1,2-diene
DTXSID30947232

2D Structure

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2D Structure of 1,2-Hexadecadiene, 3,7,11,15-tetramethyl-

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 + 0.7330 73.30%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Nucleus 0.6326 63.26%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.9544 95.44%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6556 65.56%
P-glycoprotein inhibitior - 0.8753 87.53%
P-glycoprotein substrate - 0.7790 77.90%
CYP3A4 substrate - 0.5914 59.14%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7417 74.17%
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 - 0.9776 97.76%
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 + 0.7888 78.88%
Skin irritation + 0.8426 84.26%
Skin corrosion - 0.9833 98.33%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4341 43.41%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5231 52.31%
skin sensitisation + 0.9235 92.35%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.6463 64.63%
Acute Oral Toxicity (c) III 0.9077 90.77%
Estrogen receptor binding - 0.7862 78.62%
Androgen receptor binding - 0.8579 85.79%
Thyroid receptor binding + 0.6499 64.99%
Glucocorticoid receptor binding - 0.6349 63.49%
Aromatase binding - 0.6620 66.20%
PPAR gamma - 0.6255 62.55%
Honey bee toxicity - 0.9219 92.19%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6800 68.00%
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
CHEMBL2581 P07339 Cathepsin D 93.82% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.67% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 85.85% 93.31%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.04% 91.11%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.24% 97.21%
CHEMBL2039 P27338 Monoamine oxidase B 83.89% 92.51%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.02% 97.29%
CHEMBL2885 P07451 Carbonic anhydrase III 81.74% 87.45%

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.
Arctotheca calendula
Lemna minor
Minuria leptophylla
Osteospermum rigidum

Cross-Links

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PubChem 94234
LOTUS LTS0180654
wikiData Q82924982