7,11,15-Trimethyl-3-methylene-1,6,10,14-hexadecatetraene

Details

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Internal ID b690e2e9-d354-4395-ae34-baaca87888c5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 7,11,15-trimethyl-3-methylidenehexadeca-1,6,10,14-tetraene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32/c1-7-18(4)12-9-14-20(6)16-10-15-19(5)13-8-11-17(2)3/h7,11,14-15H,1,4,8-10,12-13,16H2,2-3,5-6H3
InChI Key XSIVJVJUIXOEPW-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32
Molecular Weight 272.50 g/mol
Exact Mass 272.250401021 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 8.00
Atomic LogP (AlogP) 6.93
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7,11,15-Trimethyl-3-methylene-1,6,10,14-hexadecatetraene

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 + 0.8086 80.86%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Nucleus 0.6326 63.26%
OATP2B1 inhibitior - 0.8533 85.33%
OATP1B1 inhibitior + 0.9330 93.30%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5232 52.32%
P-glycoprotein inhibitior - 0.7965 79.65%
P-glycoprotein substrate - 0.9484 94.84%
CYP3A4 substrate - 0.6041 60.41%
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 - 0.9426 94.26%
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 + 0.8212 82.12%
Skin irritation + 0.8426 84.26%
Skin corrosion - 0.9833 98.33%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3955 39.55%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation + 0.9235 92.35%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.8004 80.04%
Acute Oral Toxicity (c) III 0.9077 90.77%
Estrogen receptor binding - 0.8086 80.86%
Androgen receptor binding - 0.8337 83.37%
Thyroid receptor binding - 0.5533 55.33%
Glucocorticoid receptor binding - 0.5672 56.72%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.8010 80.10%
Honey bee toxicity - 0.8406 84.06%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5300 53.00%
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 91.83% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.16% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.49% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.99% 94.45%
CHEMBL2581 P07339 Cathepsin D 81.30% 98.95%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.32% 82.05%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.01% 99.17%

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.
Nicotiana tabacum

Cross-Links

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PubChem 549681
LOTUS LTS0105998
wikiData Q105341048