3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraene-1,13-diol

Details

Top
Internal ID cf67e02f-04be-44ef-a55e-3bf37cc3e7d3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraene-1,13-diol
SMILES (Canonical) CC(=CC(CC(=CCCC(=CCCC(=CCO)C)C)C)O)C
SMILES (Isomeric) CC(=CC(CC(=CCCC(=CCCC(=CCO)C)C)C)O)C
InChI InChI=1S/C20H34O2/c1-16(2)14-20(22)15-19(5)11-7-9-17(3)8-6-10-18(4)12-13-21/h8,11-12,14,20-22H,6-7,9-10,13,15H2,1-5H3
InChI Key QYNPSRWEKFVLRS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H34O2
Molecular Weight 306.50 g/mol
Exact Mass 306.255880323 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 5.50
Atomic LogP (AlogP) 5.10
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraene-1,13-diol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9840 98.40%
Caco-2 + 0.8024 80.24%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.4472 44.72%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.9332 93.32%
OATP1B3 inhibitior + 0.9590 95.90%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8227 82.27%
P-glycoprotein inhibitior - 0.6554 65.54%
P-glycoprotein substrate - 0.9148 91.48%
CYP3A4 substrate - 0.5600 56.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7295 72.95%
CYP3A4 inhibition - 0.7838 78.38%
CYP2C9 inhibition - 0.8998 89.98%
CYP2C19 inhibition - 0.8771 87.71%
CYP2D6 inhibition - 0.8969 89.69%
CYP1A2 inhibition - 0.7880 78.80%
CYP2C8 inhibition - 0.9330 93.30%
CYP inhibitory promiscuity - 0.7609 76.09%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.7371 73.71%
Eye corrosion - 0.7414 74.14%
Eye irritation - 0.5360 53.60%
Skin irritation + 0.5592 55.92%
Skin corrosion - 0.9730 97.30%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7219 72.19%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.8375 83.75%
skin sensitisation + 0.7943 79.43%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.6010 60.10%
Acute Oral Toxicity (c) III 0.8431 84.31%
Estrogen receptor binding - 0.6336 63.36%
Androgen receptor binding - 0.7192 71.92%
Thyroid receptor binding + 0.6244 62.44%
Glucocorticoid receptor binding - 0.5760 57.60%
Aromatase binding - 0.5250 52.50%
PPAR gamma + 0.8222 82.22%
Honey bee toxicity - 0.8971 89.71%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.6999 69.99%

Targets

Top

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.76% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.08% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.11% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.15% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.29% 91.11%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.86% 93.10%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 73838000
LOTUS LTS0115464
wikiData Q105230270