Asperlactone G

Details

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Internal ID b87baf13-adf8-4bc7-9288-b78cd0b69bf2
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name methyl (2R)-2-[[4-hydroxy-2,5-bis(3-methylbut-2-enyl)phenyl]methyl]-3-(4-hydroxyphenyl)-4-methoxy-5-oxofuran-2-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H34O7/c1-18(2)7-9-21-16-25(32)22(10-8-19(3)4)15-23(21)17-30(29(34)36-6)26(27(35-5)28(33)37-30)20-11-13-24(31)14-12-20/h7-8,11-16,31-32H,9-10,17H2,1-6H3/t30-/m1/s1
InChI Key XQXSEMAYCSHZGM-SSEXGKCCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H34O7
Molecular Weight 506.60 g/mol
Exact Mass 506.23045342 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 6.60
Atomic LogP (AlogP) 5.18
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Asperlactone G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9819 98.19%
Caco-2 - 0.6205 62.05%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8250 82.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8869 88.69%
OATP1B3 inhibitior - 0.2420 24.20%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9835 98.35%
P-glycoprotein inhibitior + 0.8835 88.35%
P-glycoprotein substrate - 0.6103 61.03%
CYP3A4 substrate + 0.6124 61.24%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8484 84.84%
CYP3A4 inhibition - 0.5744 57.44%
CYP2C9 inhibition + 0.6082 60.82%
CYP2C19 inhibition + 0.6578 65.78%
CYP2D6 inhibition - 0.8880 88.80%
CYP1A2 inhibition - 0.5893 58.93%
CYP2C8 inhibition + 0.6849 68.49%
CYP inhibitory promiscuity + 0.6398 63.98%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9328 93.28%
Carcinogenicity (trinary) Non-required 0.5421 54.21%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.8318 83.18%
Skin irritation - 0.7970 79.70%
Skin corrosion - 0.9545 95.45%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4705 47.05%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.8097 80.97%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5358 53.58%
Acute Oral Toxicity (c) I 0.3079 30.79%
Estrogen receptor binding + 0.9058 90.58%
Androgen receptor binding + 0.8194 81.94%
Thyroid receptor binding + 0.6441 64.41%
Glucocorticoid receptor binding + 0.8601 86.01%
Aromatase binding + 0.7001 70.01%
PPAR gamma + 0.6689 66.89%
Honey bee toxicity - 0.8254 82.54%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5700 57.00%
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 99.72% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.48% 85.14%
CHEMBL2581 P07339 Cathepsin D 97.31% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.34% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.92% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 91.57% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.68% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.09% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.64% 94.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 88.59% 97.28%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.37% 95.56%
CHEMBL2535 P11166 Glucose transporter 86.24% 98.75%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 84.33% 95.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.80% 96.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.76% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.39% 99.15%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.06% 94.33%
CHEMBL4208 P20618 Proteasome component C5 80.18% 90.00%

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 146683303
LOTUS LTS0219000
wikiData Q105340208