31-Methoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26-dodecaene

Details

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Internal ID 96a78957-1dc2-4d4c-bbdc-a5f4aa5d9aa5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name 31-methoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26-dodecaene
SMILES (Canonical) CC(=CCCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCCC(C)(C)OC)C)C)C)C
SMILES (Isomeric) CC(=CCCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCCC(C)(C)OC)C)C)C)C
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/h12-13,15-18,20-22,24-31H,14,19,23,32-33H2,1-11H3
InChI Key DNWNJIQHOASZFU-UHFFFAOYSA-N
Popularity 0 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 14.80
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 31-Methoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26-dodecaene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 - 0.7636 76.36%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Nucleus 0.3977 39.77%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.8509 85.09%
OATP1B3 inhibitior + 0.9232 92.32%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9955 99.55%
P-glycoprotein inhibitior + 0.8235 82.35%
P-glycoprotein substrate - 0.7639 76.39%
CYP3A4 substrate + 0.5768 57.68%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7504 75.04%
CYP3A4 inhibition - 0.9360 93.60%
CYP2C9 inhibition - 0.8865 88.65%
CYP2C19 inhibition - 0.8018 80.18%
CYP2D6 inhibition - 0.9372 93.72%
CYP1A2 inhibition - 0.7901 79.01%
CYP2C8 inhibition - 0.7841 78.41%
CYP inhibitory promiscuity - 0.7183 71.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.4808 48.08%
Eye corrosion - 0.7550 75.50%
Eye irritation - 0.9142 91.42%
Skin irritation + 0.8319 83.19%
Skin corrosion - 0.9867 98.67%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9521 95.21%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.7992 79.92%
skin sensitisation + 0.8562 85.62%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.6168 61.68%
Acute Oral Toxicity (c) III 0.8402 84.02%
Estrogen receptor binding + 0.8707 87.07%
Androgen receptor binding + 0.6242 62.42%
Thyroid receptor binding + 0.7865 78.65%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.6630 66.30%
PPAR gamma + 0.7487 74.87%
Honey bee toxicity - 0.8038 80.38%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.5053 50.53%

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 91.56% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.41% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.92% 92.08%
CHEMBL2581 P07339 Cathepsin D 88.82% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.96% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.18% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.58% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 82.43% 94.73%
CHEMBL2885 P07451 Carbonic anhydrase III 81.31% 87.45%

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 73229434
LOTUS LTS0167057
wikiData Q104985792