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

Details

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Internal ID fb2e31d9-0818-4a12-84f9-7592fa01f5b6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name (6E,8E,10E,12E,14E,16E,18E,20E,22E,26E)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-6,8,10,12,14,16,18,20,22,26-decaene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H66O2/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/h13-17,21-27,29-30H,18-20,28,31-34H2,1-12H3/b14-13+,23-15+,24-16+,27-17+,35-21+,36-22+,37-25+,38-26+,39-29+,40-30+
InChI Key YHGMOOBZWWOWOW-MRFCJBPOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C42H66O2
Molecular Weight 603.00 g/mol
Exact Mass 602.50628134 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 14.00
Atomic LogP (AlogP) 12.86
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 21

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9908 99.08%
Caco-2 - 0.7923 79.23%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5370 53.70%
OATP2B1 inhibitior - 0.7144 71.44%
OATP1B1 inhibitior + 0.8502 85.02%
OATP1B3 inhibitior + 0.9229 92.29%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 1.0000 100.00%
P-glycoprotein inhibitior + 0.8236 82.36%
P-glycoprotein substrate - 0.7487 74.87%
CYP3A4 substrate + 0.5799 57.99%
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 - 0.7456 74.56%
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 - 0.8992 89.92%
Skin irritation + 0.6961 69.61%
Skin corrosion - 0.9966 99.66%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9014 90.14%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.7452 74.52%
skin sensitisation + 0.8232 82.32%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5678 56.78%
Acute Oral Toxicity (c) III 0.8040 80.40%
Estrogen receptor binding + 0.8361 83.61%
Androgen receptor binding + 0.5853 58.53%
Thyroid receptor binding + 0.7019 70.19%
Glucocorticoid receptor binding + 0.7195 71.95%
Aromatase binding - 0.5453 54.53%
PPAR gamma + 0.7557 75.57%
Honey bee toxicity - 0.8184 81.84%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.8317 83.17%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.18% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.22% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.50% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.17% 99.17%
CHEMBL2581 P07339 Cathepsin D 86.64% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.10% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.78% 96.95%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 82.52% 87.16%
CHEMBL3401 O75469 Pregnane X receptor 82.12% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 87443532
LOTUS LTS0010123
wikiData Q105348395