(4E,6E,8E,10E,12E,14E,16E,18E,20E,22E,26E)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,26-undecaene

Details

Top
Internal ID 79ec69d1-3363-4ade-aad7-bf074bea9a78
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name (4E,6E,8E,10E,12E,14E,16E,18E,20E,22E,26E)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,26-undecaene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H64O2/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/h13-17,19,21-27,29-31H,18,20,28,32-34H2,1-12H3/b14-13+,23-15+,24-16+,27-17+,31-19+,35-21+,36-22+,37-25+,38-26+,39-29+,40-30+
InChI Key ICSVGZGOGZESCK-QETIOTSESA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C42H64O2
Molecular Weight 601.00 g/mol
Exact Mass 600.49063128 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 13.90
Atomic LogP (AlogP) 12.64
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 20

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (4E,6E,8E,10E,12E,14E,16E,18E,20E,22E,26E)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,26-undecaene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9908 99.08%
Caco-2 - 0.7994 79.94%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5370 53.70%
OATP2B1 inhibitior - 0.7138 71.38%
OATP1B1 inhibitior + 0.8227 82.27%
OATP1B3 inhibitior + 0.9229 92.29%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9972 99.72%
P-glycoprotein inhibitior + 0.8235 82.35%
P-glycoprotein substrate - 0.6522 65.22%
CYP3A4 substrate + 0.6198 61.98%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7504 75.04%
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 - 0.6428 64.28%
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 - 0.9020 90.20%
Skin irritation + 0.6961 69.61%
Skin corrosion - 0.9966 99.66%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9393 93.93%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.7202 72.02%
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 + 0.5996 59.96%
Acute Oral Toxicity (c) III 0.8040 80.40%
Estrogen receptor binding + 0.8217 82.17%
Androgen receptor binding + 0.5775 57.75%
Thyroid receptor binding + 0.7314 73.14%
Glucocorticoid receptor binding + 0.6891 68.91%
Aromatase binding - 0.5826 58.26%
PPAR gamma + 0.7505 75.05%
Honey bee toxicity - 0.8135 81.35%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6900 69.00%
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 91.34% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.81% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.25% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.68% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.78% 86.33%
CHEMBL2581 P07339 Cathepsin D 85.42% 98.95%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 84.31% 87.16%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.26% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 82.36% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.52% 89.34%

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 87443299
LOTUS LTS0183533
wikiData Q76803016