(6E,8E,10E,12E,14R,16E,18E,22E,26E)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-6,8,10,12,16,18,22,26-octaene

Details

Top
Internal ID b46542de-713a-466d-b55c-c236ec5b88a1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name (6E,8E,10E,12E,14R,16E,18E,22E,26E)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-6,8,10,12,16,18,22,26-octaene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H70O2/c1-35(23-15-25-37(3)27-17-29-39(5)31-19-33-41(7,8)43-11)21-13-14-22-36(2)24-16-26-38(4)28-18-30-40(6)32-20-34-42(9,10)44-12/h13-15,17,22-23,25-27,29-30,35H,16,18-21,24,28,31-34H2,1-12H3/b14-13+,23-15+,27-17+,36-22+,37-25+,38-26+,39-29+,40-30+/t35-/m1/s1
InChI Key WIFKQHKEFLOISF-YFRXQOOISA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C42H70O2
Molecular Weight 607.00 g/mol
Exact Mass 606.53758147 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 13.50
Atomic LogP (AlogP) 13.16
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 23

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (6E,8E,10E,12E,14R,16E,18E,22E,26E)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-6,8,10,12,16,18,22,26-octaene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9908 99.08%
Caco-2 - 0.7793 77.93%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5370 53.70%
OATP2B1 inhibitior - 0.7122 71.22%
OATP1B1 inhibitior + 0.7994 79.94%
OATP1B3 inhibitior + 0.9229 92.29%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 1.0000 100.00%
P-glycoprotein inhibitior + 0.8201 82.01%
P-glycoprotein substrate - 0.5984 59.84%
CYP3A4 substrate + 0.6276 62.76%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.7676 76.76%
CYP3A4 inhibition - 0.9169 91.69%
CYP2C9 inhibition - 0.8607 86.07%
CYP2C19 inhibition - 0.7700 77.00%
CYP2D6 inhibition - 0.9460 94.60%
CYP1A2 inhibition - 0.7816 78.16%
CYP2C8 inhibition - 0.6509 65.09%
CYP inhibitory promiscuity - 0.7594 75.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.5642 56.42%
Eye corrosion - 0.7330 73.30%
Eye irritation - 0.9157 91.57%
Skin irritation + 0.6961 69.61%
Skin corrosion - 0.9966 99.66%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8938 89.38%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6649 66.49%
skin sensitisation + 0.8232 82.32%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.5572 55.72%
Acute Oral Toxicity (c) III 0.8040 80.40%
Estrogen receptor binding + 0.8010 80.10%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.6431 64.31%
Glucocorticoid receptor binding + 0.6847 68.47%
Aromatase binding - 0.4883 48.83%
PPAR gamma + 0.6988 69.88%
Honey bee toxicity - 0.7725 77.25%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.8317 83.17%

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 92.84% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 92.36% 97.21%
CHEMBL2581 P07339 Cathepsin D 91.62% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.45% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.19% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.15% 96.95%
CHEMBL2885 P07451 Carbonic anhydrase III 89.48% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.83% 97.29%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 85.90% 87.16%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.63% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 84.65% 94.73%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 84.05% 96.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.30% 86.33%
CHEMBL2996 Q05655 Protein kinase C delta 81.80% 97.79%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.87% 97.25%
CHEMBL2061 P19793 Retinoid X receptor alpha 80.73% 91.67%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.72% 96.47%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 80.16% 92.88%

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 162993288
LOTUS LTS0262997
wikiData Q105306199