Chrysogenester

Details

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Internal ID 8dcc5663-dcaf-4304-855a-eb4d80ec8f18
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylated hydroquinones
IUPAC Name methyl (4E,8E)-10-(2,5-dihydroxy-4-methylphenyl)-4,8-dimethyldeca-4,8-dienoate
SMILES (Canonical) CC1=CC(=C(C=C1O)CC=C(C)CCC=C(C)CCC(=O)OC)O
SMILES (Isomeric) CC1=CC(=C(C=C1O)C/C=C(\C)/CC/C=C(\C)/CCC(=O)OC)O
InChI InChI=1S/C20H28O4/c1-14(6-5-7-15(2)9-11-20(23)24-4)8-10-17-13-18(21)16(3)12-19(17)22/h7-8,12-13,21-22H,5-6,9-11H2,1-4H3/b14-8+,15-7+
InChI Key XONZEOKWFDBLFK-DRRSQLPWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H28O4
Molecular Weight 332.40 g/mol
Exact Mass 332.19875937 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.57
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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CHEMBL4160418

2D Structure

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2D Structure of Chrysogenester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 + 0.7508 75.08%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.9002 90.02%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9254 92.54%
OATP1B3 inhibitior + 0.8614 86.14%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7941 79.41%
P-glycoprotein inhibitior - 0.5846 58.46%
P-glycoprotein substrate - 0.8477 84.77%
CYP3A4 substrate - 0.5191 51.91%
CYP2C9 substrate - 0.6075 60.75%
CYP2D6 substrate - 0.8246 82.46%
CYP3A4 inhibition - 0.5836 58.36%
CYP2C9 inhibition - 0.7109 71.09%
CYP2C19 inhibition + 0.5611 56.11%
CYP2D6 inhibition - 0.8201 82.01%
CYP1A2 inhibition + 0.6744 67.44%
CYP2C8 inhibition - 0.7327 73.27%
CYP inhibitory promiscuity - 0.6288 62.88%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7441 74.41%
Carcinogenicity (trinary) Non-required 0.7259 72.59%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.8633 86.33%
Skin irritation - 0.7745 77.45%
Skin corrosion - 0.9748 97.48%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6683 66.83%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5531 55.31%
skin sensitisation - 0.7036 70.36%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6341 63.41%
Acute Oral Toxicity (c) III 0.4007 40.07%
Estrogen receptor binding + 0.6448 64.48%
Androgen receptor binding - 0.6041 60.41%
Thyroid receptor binding + 0.6801 68.01%
Glucocorticoid receptor binding - 0.4911 49.11%
Aromatase binding + 0.7034 70.34%
PPAR gamma + 0.7886 78.86%
Honey bee toxicity - 0.8810 88.10%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 1.0000 100.00%

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 98.71% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 94.74% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.95% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.45% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.97% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.69% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.90% 95.56%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.80% 97.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.26% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.99% 96.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.50% 94.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.36% 96.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.08% 91.07%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.79% 94.45%
CHEMBL2581 P07339 Cathepsin D 81.67% 98.95%
CHEMBL4208 P20618 Proteasome component C5 81.62% 90.00%
CHEMBL2535 P11166 Glucose transporter 81.07% 98.75%

Plants that contains it

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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.
Atropa belladonna
Erythroxylum dekindtii
Erythroxylum hypericifolium

Cross-Links

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PubChem 139589899
LOTUS LTS0065344
wikiData Q104975406