Versicolactone D

Details

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Internal ID e5eb9374-27bc-4df5-aa3f-d81524e6d4b9
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name methyl (2R)-4-hydroxy-2-[[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]methyl]-3-(4-methoxyphenyl)-5-oxofuran-2-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H26O7/c1-15(2)5-7-18-13-16(6-12-20(18)26)14-25(24(29)31-4)21(22(27)23(28)32-25)17-8-10-19(30-3)11-9-17/h5-6,8-13,26-27H,7,14H2,1-4H3/t25-/m1/s1
InChI Key NOSZCJQZUYDKAW-RUZDIDTESA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C25H26O7
Molecular Weight 438.50 g/mol
Exact Mass 438.16785316 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 3.89
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Versicolactone D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9809 98.09%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7952 79.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9157 91.57%
OATP1B3 inhibitior - 0.3218 32.18%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9495 94.95%
P-glycoprotein inhibitior + 0.7734 77.34%
P-glycoprotein substrate - 0.7044 70.44%
CYP3A4 substrate + 0.6074 60.74%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.8542 85.42%
CYP3A4 inhibition - 0.7438 74.38%
CYP2C9 inhibition + 0.6612 66.12%
CYP2C19 inhibition + 0.6869 68.69%
CYP2D6 inhibition - 0.8753 87.53%
CYP1A2 inhibition - 0.5869 58.69%
CYP2C8 inhibition + 0.6444 64.44%
CYP inhibitory promiscuity + 0.6936 69.36%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9328 93.28%
Carcinogenicity (trinary) Non-required 0.5404 54.04%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.8399 83.99%
Skin irritation - 0.7990 79.90%
Skin corrosion - 0.9490 94.90%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6704 67.04%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.7927 79.27%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6595 65.95%
Acute Oral Toxicity (c) III 0.3107 31.07%
Estrogen receptor binding + 0.8838 88.38%
Androgen receptor binding + 0.8143 81.43%
Thyroid receptor binding + 0.7161 71.61%
Glucocorticoid receptor binding + 0.8964 89.64%
Aromatase binding + 0.6222 62.22%
PPAR gamma + 0.7540 75.40%
Honey bee toxicity - 0.8046 80.46%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5800 58.00%
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 99.79% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.11% 85.14%
CHEMBL2581 P07339 Cathepsin D 96.87% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.89% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.96% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.84% 99.15%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 93.80% 95.50%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 93.68% 95.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.60% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.46% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 92.40% 90.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.80% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.41% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 90.06% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.98% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 85.84% 91.19%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.74% 96.95%
CHEMBL2535 P11166 Glucose transporter 85.51% 98.75%
CHEMBL3922 P50579 Methionine aminopeptidase 2 84.81% 97.28%
CHEMBL4208 P20618 Proteasome component C5 84.35% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.33% 96.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.98% 81.11%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 82.25% 85.30%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 81.87% 92.29%
CHEMBL1929 P47989 Xanthine dehydrogenase 80.38% 96.12%

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 139584761
LOTUS LTS0176389
wikiData Q77375367