(6E,10E,12E,14E,16E,18E,20E,22E,24E,26E,28Z)-31-methoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,12,14,16,18,20,22,24,26,28-dodecaene

Details

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Internal ID d4aaec37-b0d1-4718-95ae-594f575ead6a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name (6E,10E,12E,14E,16E,18E,20E,22E,24E,26E,28Z)-31-methoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,12,14,16,18,20,22,24,26,28-dodecaene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C41H60O/c1-34(2)20-14-23-37(5)26-17-29-38(6)27-15-24-35(3)21-12-13-22-36(4)25-16-28-39(7)30-18-31-40(8)32-19-33-41(9,10)42-11/h12-13,15-16,18-22,24-28,30-32H,14,17,23,29,33H2,1-11H3/b13-12+,24-15+,25-16+,30-18+,32-19-,35-21+,36-22+,37-26+,38-27+,39-28+,40-31+
InChI Key FJOCMTHZSURUFA-GCDUZBLISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C41H60O
Molecular Weight 568.90 g/mol
Exact Mass 568.464416533 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 14.70
Atomic LogP (AlogP) 12.79
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 18

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6E,10E,12E,14E,16E,18E,20E,22E,24E,26E,28Z)-31-methoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,12,14,16,18,20,22,24,26,28-dodecaene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 - 0.7667 76.67%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.4368 43.68%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.8566 85.66%
OATP1B3 inhibitior + 0.9310 93.10%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9931 99.31%
P-glycoprotein inhibitior + 0.8294 82.94%
P-glycoprotein substrate - 0.7797 77.97%
CYP3A4 substrate + 0.6003 60.03%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7504 75.04%
CYP3A4 inhibition - 0.9449 94.49%
CYP2C9 inhibition - 0.8549 85.49%
CYP2C19 inhibition - 0.8041 80.41%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.7669 76.69%
CYP2C8 inhibition - 0.7531 75.31%
CYP inhibitory promiscuity - 0.7615 76.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.5371 53.71%
Eye corrosion - 0.7601 76.01%
Eye irritation - 0.9153 91.53%
Skin irritation + 0.7243 72.43%
Skin corrosion - 0.9949 99.49%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9502 95.02%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6774 67.74%
skin sensitisation + 0.8541 85.41%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.7282 72.82%
Acute Oral Toxicity (c) III 0.8319 83.19%
Estrogen receptor binding + 0.8429 84.29%
Androgen receptor binding + 0.6086 60.86%
Thyroid receptor binding + 0.7801 78.01%
Glucocorticoid receptor binding + 0.5526 55.26%
Aromatase binding - 0.6289 62.89%
PPAR gamma + 0.7649 76.49%
Honey bee toxicity - 0.7598 75.98%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.8591 85.91%

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 95.43% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.30% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.09% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.38% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 85.95% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.88% 85.14%
CHEMBL2581 P07339 Cathepsin D 85.84% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.06% 89.34%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.00% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.32% 96.95%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 81.98% 87.16%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 81.46% 92.68%
CHEMBL1870 P28702 Retinoid X receptor beta 80.65% 95.00%

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.
There are no matching plants.

Cross-Links

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PubChem 20055173
LOTUS LTS0192034
wikiData Q104996245