3,7,11,15-Tetramethylhexadeca-1,6,10,14-tetraene-3,5,9-triol

Details

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Internal ID 7dd762da-7053-40c4-a3e6-55a8bf2f7d96
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraene-3,5,9-triol
SMILES (Canonical) CC(=CCCC(=CC(CC(=CC(CC(C)(C=C)O)O)C)O)C)C
SMILES (Isomeric) CC(=CCCC(=CC(CC(=CC(CC(C)(C=C)O)O)C)O)C)C
InChI InChI=1S/C20H34O3/c1-7-20(6,23)14-19(22)13-17(5)12-18(21)11-16(4)10-8-9-15(2)3/h7,9,11,13,18-19,21-23H,1,8,10,12,14H2,2-6H3
InChI Key ORFNMFQBYRQSRP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34O3
Molecular Weight 322.50 g/mol
Exact Mass 322.25079494 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.06
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7,11,15-Tetramethylhexadeca-1,6,10,14-tetraene-3,5,9-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9516 95.16%
Caco-2 + 0.6141 61.41%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Lysosomes 0.4469 44.69%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9205 92.05%
OATP1B3 inhibitior + 0.9458 94.58%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.5567 55.67%
P-glycoprotein inhibitior - 0.8044 80.44%
P-glycoprotein substrate - 0.8504 85.04%
CYP3A4 substrate + 0.5272 52.72%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7336 73.36%
CYP3A4 inhibition - 0.7825 78.25%
CYP2C9 inhibition - 0.7530 75.30%
CYP2C19 inhibition - 0.7143 71.43%
CYP2D6 inhibition - 0.9254 92.54%
CYP1A2 inhibition - 0.7599 75.99%
CYP2C8 inhibition - 0.8639 86.39%
CYP inhibitory promiscuity - 0.7225 72.25%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6637 66.37%
Eye corrosion - 0.9085 90.85%
Eye irritation - 0.6943 69.43%
Skin irritation + 0.6450 64.50%
Skin corrosion - 0.9327 93.27%
Ames mutagenesis - 0.7354 73.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4554 45.54%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5363 53.63%
skin sensitisation + 0.6453 64.53%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.5621 56.21%
Acute Oral Toxicity (c) III 0.7217 72.17%
Estrogen receptor binding - 0.5886 58.86%
Androgen receptor binding - 0.6092 60.92%
Thyroid receptor binding + 0.5463 54.63%
Glucocorticoid receptor binding - 0.4909 49.09%
Aromatase binding - 0.5384 53.84%
PPAR gamma + 0.6061 60.61%
Honey bee toxicity - 0.6868 68.68%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.8353 83.53%

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 95.33% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 91.57% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 90.72% 94.73%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 90.33% 90.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.09% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.04% 85.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.56% 96.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.69% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.83% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.49% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.63% 91.11%

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.
Lycopus europaeus

Cross-Links

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PubChem 74490791
LOTUS LTS0116705
wikiData Q105197534