2,31-Dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaen-3-one

Details

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Internal ID 1c2e02af-492d-496b-92ad-41b340d6fdee
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name 2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaen-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H58O3/c1-34(22-15-24-36(3)26-17-28-38(5)30-19-33-41(7,8)44-11)20-13-14-21-35(2)23-16-25-37(4)27-18-29-39(6)31-32-40(43)42(9,10)45-12/h13-32H,33H2,1-12H3
InChI Key AUIMFBMJZYMMRO-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C42H58O3
Molecular Weight 610.90 g/mol
Exact Mass 610.43859571 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 13.10
Atomic LogP (AlogP) 11.37
H-Bond Acceptor 3
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 2,31-Dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaen-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 - 0.8144 81.44%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6538 65.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8342 83.42%
OATP1B3 inhibitior + 0.9397 93.97%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9969 99.69%
P-glycoprotein inhibitior + 0.8219 82.19%
P-glycoprotein substrate - 0.8247 82.47%
CYP3A4 substrate + 0.5673 56.73%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.8421 84.21%
CYP3A4 inhibition - 0.8919 89.19%
CYP2C9 inhibition - 0.8409 84.09%
CYP2C19 inhibition - 0.8093 80.93%
CYP2D6 inhibition - 0.9316 93.16%
CYP1A2 inhibition - 0.8702 87.02%
CYP2C8 inhibition - 0.8544 85.44%
CYP inhibitory promiscuity - 0.7543 75.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5040 50.40%
Carcinogenicity (trinary) Non-required 0.5218 52.18%
Eye corrosion - 0.7065 70.65%
Eye irritation - 0.8862 88.62%
Skin irritation + 0.5936 59.36%
Skin corrosion - 0.9910 99.10%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9225 92.25%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5327 53.27%
skin sensitisation + 0.8971 89.71%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.7425 74.25%
Acute Oral Toxicity (c) IV 0.7053 70.53%
Estrogen receptor binding + 0.8053 80.53%
Androgen receptor binding - 0.5824 58.24%
Thyroid receptor binding + 0.7364 73.64%
Glucocorticoid receptor binding + 0.7415 74.15%
Aromatase binding - 0.4859 48.59%
PPAR gamma + 0.7465 74.65%
Honey bee toxicity - 0.8046 80.46%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.7021 70.21%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 92.18% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.38% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.26% 96.95%
CHEMBL2581 P07339 Cathepsin D 88.62% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.81% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.43% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.95% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.94% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 82.86% 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 73229446
LOTUS LTS0213734
wikiData Q104918936