Versicolactone C

Details

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Internal ID 628eac6c-1dc3-4659-9291-61b15ae1ce88
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name methyl (2R)-4-hydroxy-2-[[4-methoxy-3-(3-methylbut-2-enyl)phenyl]methyl]-5-oxo-3-phenylfuran-2-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H26O6/c1-16(2)10-12-19-14-17(11-13-20(19)29-3)15-25(24(28)30-4)21(22(26)23(27)31-25)18-8-6-5-7-9-18/h5-11,13-14,26H,12,15H2,1-4H3/t25-/m1/s1
InChI Key VAUVWTVBYIPBIM-RUZDIDTESA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C25H26O6
Molecular Weight 422.50 g/mol
Exact Mass 422.17293854 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.18
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Versicolactone C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9831 98.31%
Caco-2 + 0.5670 56.70%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8346 83.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8976 89.76%
OATP1B3 inhibitior - 0.2644 26.44%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9701 97.01%
P-glycoprotein inhibitior + 0.7802 78.02%
P-glycoprotein substrate - 0.5974 59.74%
CYP3A4 substrate + 0.5928 59.28%
CYP2C9 substrate - 0.6043 60.43%
CYP2D6 substrate - 0.8617 86.17%
CYP3A4 inhibition - 0.6457 64.57%
CYP2C9 inhibition + 0.6227 62.27%
CYP2C19 inhibition + 0.7527 75.27%
CYP2D6 inhibition - 0.8972 89.72%
CYP1A2 inhibition - 0.6195 61.95%
CYP2C8 inhibition + 0.7500 75.00%
CYP inhibitory promiscuity + 0.7341 73.41%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9039 90.39%
Carcinogenicity (trinary) Non-required 0.5149 51.49%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.8508 85.08%
Skin irritation - 0.7883 78.83%
Skin corrosion - 0.9553 95.53%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6380 63.80%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.5712 57.12%
skin sensitisation - 0.7872 78.72%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.6055 60.55%
Acute Oral Toxicity (c) III 0.3992 39.92%
Estrogen receptor binding + 0.8577 85.77%
Androgen receptor binding + 0.7154 71.54%
Thyroid receptor binding + 0.6557 65.57%
Glucocorticoid receptor binding + 0.8409 84.09%
Aromatase binding + 0.5373 53.73%
PPAR gamma + 0.8108 81.08%
Honey bee toxicity - 0.7865 78.65%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5900 59.00%
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 99.05% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.05% 85.14%
CHEMBL2581 P07339 Cathepsin D 97.95% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 96.27% 90.20%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 95.66% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.47% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.79% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.23% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 92.59% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.86% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.54% 95.56%
CHEMBL2535 P11166 Glucose transporter 84.97% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.77% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.71% 94.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.58% 91.19%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.52% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 82.77% 94.73%
CHEMBL5028 O14672 ADAM10 82.73% 97.50%

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 139588274
LOTUS LTS0142714
wikiData Q105283000