Yangonin

Details

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Internal ID 26889db9-0a62-45f0-8dba-962525bab7eb
Taxonomy Phenylpropanoids and polyketides > Kavalactones
IUPAC Name 4-methoxy-6-[(E)-2-(4-methoxyphenyl)ethenyl]pyran-2-one
SMILES (Canonical) COC1=CC=C(C=C1)C=CC2=CC(=CC(=O)O2)OC
SMILES (Isomeric) COC1=CC=C(C=C1)/C=C/C2=CC(=CC(=O)O2)OC
InChI InChI=1S/C15H14O4/c1-17-12-6-3-11(4-7-12)5-8-13-9-14(18-2)10-15(16)19-13/h3-10H,1-2H3/b8-5+
InChI Key XLHIYUYCSMZCCC-VMPITWQZSA-N
Popularity 145 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O4
Molecular Weight 258.27 g/mol
Exact Mass 258.08920892 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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500-62-9
4-Methoxy-6-(p-methoxystyryl)-2H-pyran-2-one
4-Methoxy-6-(beta-(p-anisyl)vinyl)-alpha-pyrone
4-methoxy-6-[(E)-2-(4-methoxyphenyl)ethenyl]pyran-2-one
NSC 212502
UNII-R970U49V3C
CCRIS 9372
DTXSID4034102
R970U49V3C
2H-PYRAN-2-ONE, 4-METHOXY-6-(p-METHOXYSTYRYL)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Yangonin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9851 98.51%
Caco-2 + 0.9169 91.69%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7627 76.27%
OATP2B1 inhibitior - 0.8625 86.25%
OATP1B1 inhibitior + 0.9458 94.58%
OATP1B3 inhibitior + 0.9686 96.86%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.5962 59.62%
P-glycoprotein inhibitior - 0.4897 48.97%
P-glycoprotein substrate - 0.9718 97.18%
CYP3A4 substrate - 0.5983 59.83%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8582 85.82%
CYP3A4 inhibition + 0.6181 61.81%
CYP2C9 inhibition - 0.7542 75.42%
CYP2C19 inhibition + 0.8060 80.60%
CYP2D6 inhibition - 0.8898 88.98%
CYP1A2 inhibition + 0.8067 80.67%
CYP2C8 inhibition - 0.8093 80.93%
CYP inhibitory promiscuity + 0.8306 83.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8441 84.41%
Carcinogenicity (trinary) Non-required 0.4861 48.61%
Eye corrosion - 0.8887 88.87%
Eye irritation + 0.7532 75.32%
Skin irritation - 0.6947 69.47%
Skin corrosion - 0.9890 98.90%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5953 59.53%
Micronuclear + 0.7000 70.00%
Hepatotoxicity - 0.5092 50.92%
skin sensitisation - 0.8943 89.43%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6071 60.71%
Acute Oral Toxicity (c) III 0.5724 57.24%
Estrogen receptor binding + 0.9370 93.70%
Androgen receptor binding + 0.8696 86.96%
Thyroid receptor binding - 0.7177 71.77%
Glucocorticoid receptor binding + 0.7058 70.58%
Aromatase binding + 0.9018 90.18%
PPAR gamma + 0.5702 57.02%
Honey bee toxicity - 0.9399 93.99%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9501 95.01%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 35481.3 nM
Potency
via CMAUP
CHEMBL3577 P00352 Aldehyde dehydrogenase 1A1 39810.7 nM
39810.7 nM
Potency
Potency
via CMAUP
via CMAUP
CHEMBL4801 P29466 Caspase-1 39810.7 nM
Potency
via CMAUP
CHEMBL3468 P55210 Caspase-7 31622.8 nM
Potency
via CMAUP
CHEMBL4096 P04637 Cellular tumor antigen p53 12589.3 nM
Potency
via CMAUP
CHEMBL4159 Q99714 Endoplasmic reticulum-associated amyloid beta-peptide-binding protein 39810.7 nM
Potency
via CMAUP
CHEMBL1293224 P10636 Microtubule-associated protein tau 11220.2 nM
Potency
via CMAUP
CHEMBL1293232 Q16637 Survival motor neuron protein 14125.4 nM
Potency
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.05% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.74% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.16% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.38% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 87.57% 93.31%
CHEMBL4208 P20618 Proteasome component C5 87.45% 90.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.19% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 83.22% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.37% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.85% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.80% 94.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.73% 91.07%

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.
Piper methysticum
Ranunculus silerifolius

Cross-Links

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PubChem 5281575
NPASS NPC109637
ChEMBL CHEMBL1098658
LOTUS LTS0110435
wikiData Q8048635