Thiothece-474

Details

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Internal ID 9e0ffd90-4002-482c-9a66-01a789b9710f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name (6E,8E,10E,12E,14E,16E,18E,20E,22E,24E)-2-methoxy-2,6,10,14,19,23-hexamethyl-25-(2,6,6-trimethylcyclohexen-1-yl)pentacosa-6,8,10,12,14,16,18,20,22,24-decaen-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C41H58O2/c1-32(20-14-22-34(3)24-16-25-37(6)39(42)29-31-41(9,10)43-11)18-12-13-19-33(2)21-15-23-35(4)27-28-38-36(5)26-17-30-40(38,7)8/h12-16,18-25,27-28H,17,26,29-31H2,1-11H3/b13-12+,20-14+,21-15+,24-16+,28-27+,32-18+,33-19+,34-22+,35-23+,37-25+
InChI Key VOXGPKABGLVWPB-XBIRMVLJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C41H58O2
Molecular Weight 582.90 g/mol
Exact Mass 582.44368109 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 12.30
Atomic LogP (AlogP) 11.80
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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SCHEMBL2832499
CHEBI:80416
Q27149455
(6E,8E,10E,12E,14E,16E,18E,20E,22E,24E)-2-methoxy-2,6,10,14,19,23-hexamethyl-25-(2,6,6-trimethylcyclohexen-1-yl)pentacosa-6,8,10,12,14,16,18,20,22,24-decaen-5-one

2D Structure

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2D Structure of Thiothece-474

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 - 0.7856 78.56%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7176 71.76%
OATP2B1 inhibitior - 0.7147 71.47%
OATP1B1 inhibitior - 0.4794 47.94%
OATP1B3 inhibitior - 0.2354 23.54%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 1.0000 100.00%
P-glycoprotein inhibitior + 0.8558 85.58%
P-glycoprotein substrate - 0.7723 77.23%
CYP3A4 substrate + 0.6773 67.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8734 87.34%
CYP3A4 inhibition - 0.8860 88.60%
CYP2C9 inhibition - 0.8860 88.60%
CYP2C19 inhibition - 0.7875 78.75%
CYP2D6 inhibition - 0.9374 93.74%
CYP1A2 inhibition - 0.8217 82.17%
CYP2C8 inhibition + 0.5123 51.23%
CYP inhibitory promiscuity - 0.6657 66.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6348 63.48%
Carcinogenicity (trinary) Non-required 0.5243 52.43%
Eye corrosion - 0.9536 95.36%
Eye irritation - 0.9140 91.40%
Skin irritation + 0.6452 64.52%
Skin corrosion - 0.9941 99.41%
Ames mutagenesis - 0.6908 69.08%
Human Ether-a-go-go-Related Gene inhibition + 0.8783 87.83%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5561 55.61%
skin sensitisation + 0.8644 86.44%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.7132 71.32%
Acute Oral Toxicity (c) III 0.8248 82.48%
Estrogen receptor binding + 0.8617 86.17%
Androgen receptor binding + 0.7008 70.08%
Thyroid receptor binding + 0.7534 75.34%
Glucocorticoid receptor binding + 0.7828 78.28%
Aromatase binding - 0.5975 59.75%
PPAR gamma + 0.7478 74.78%
Honey bee toxicity - 0.7625 76.25%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9258 92.58%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.96% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.14% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 95.11% 89.63%
CHEMBL1870 P28702 Retinoid X receptor beta 93.84% 95.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.72% 86.33%
CHEMBL2061 P19793 Retinoid X receptor alpha 92.29% 91.67%
CHEMBL2581 P07339 Cathepsin D 90.74% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.56% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.84% 95.50%
CHEMBL2004 P48443 Retinoid X receptor gamma 89.60% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.93% 94.45%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 87.02% 98.75%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.25% 97.25%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.64% 91.71%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.65% 91.07%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.51% 95.89%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 80.39% 91.24%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.24% 96.95%

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 23724693
LOTUS LTS0193772
wikiData Q27149455