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

Details

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Internal ID 36caacbe-66de-4f79-82e3-9c51b9f9e037
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-diol
SMILES (Canonical) CC(=CCCC(=CCCC(=CC(CC(C)(C=C)O)O)C)C)C
SMILES (Isomeric) CC(=CCCC(=CCCC(=CC(CC(C)(C=C)O)O)C)C)C
InChI InChI=1S/C20H34O2/c1-7-20(6,22)15-19(21)14-18(5)13-9-12-17(4)11-8-10-16(2)3/h7,10,12,14,19,21-22H,1,8-9,11,13,15H2,2-6H3
InChI Key QKVCQXKQUOAHOH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34O2
Molecular Weight 306.50 g/mol
Exact Mass 306.255880323 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 5.30
Atomic LogP (AlogP) 5.09
H-Bond Acceptor 2
H-Bond Donor 2
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-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9621 96.21%
Caco-2 + 0.7077 70.77%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Lysosomes 0.4760 47.60%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.9283 92.83%
OATP1B3 inhibitior + 0.9467 94.67%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6322 63.22%
P-glycoprotein inhibitior - 0.7969 79.69%
P-glycoprotein substrate - 0.9049 90.49%
CYP3A4 substrate + 0.5125 51.25%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7336 73.36%
CYP3A4 inhibition - 0.8425 84.25%
CYP2C9 inhibition - 0.7594 75.94%
CYP2C19 inhibition - 0.6918 69.18%
CYP2D6 inhibition - 0.9234 92.34%
CYP1A2 inhibition - 0.6441 64.41%
CYP2C8 inhibition - 0.8733 87.33%
CYP inhibitory promiscuity - 0.7099 70.99%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6693 66.93%
Eye corrosion - 0.8753 87.53%
Eye irritation - 0.7315 73.15%
Skin irritation + 0.6445 64.45%
Skin corrosion - 0.9631 96.31%
Ames mutagenesis - 0.7354 73.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4622 46.22%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5762 57.62%
skin sensitisation + 0.6662 66.62%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.5778 57.78%
Acute Oral Toxicity (c) III 0.8024 80.24%
Estrogen receptor binding - 0.6012 60.12%
Androgen receptor binding - 0.6955 69.55%
Thyroid receptor binding + 0.5977 59.77%
Glucocorticoid receptor binding - 0.4638 46.38%
Aromatase binding - 0.5964 59.64%
PPAR gamma + 0.7196 71.96%
Honey bee toxicity - 0.7079 70.79%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8976 89.76%

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 94.62% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.16% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 91.80% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.36% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.52% 99.17%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 88.47% 90.93%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.60% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.47% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.26% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.47% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.25% 94.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.80% 97.29%

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.
Geigeria burkei
Geigeria schinzii

Cross-Links

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PubChem 74052365
LOTUS LTS0014463
wikiData Q105223360