Mesitene lactone

Details

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Internal ID c1b3c93e-8d3f-4b4e-8da8-97ea640c5d5e
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 4,6-dimethylpyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H8O2/c1-5-3-6(2)9-7(8)4-5/h3-4H,1-2H3
InChI Key IXYLIUKQQQXXON-UHFFFAOYSA-N
Popularity 25 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8O2
Molecular Weight 124.14 g/mol
Exact Mass 124.052429494 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.26
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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675-09-2
4,6-Dimethyl-2-pyrone
Mesitene lactone
4,6-dimethylpyran-2-one
4,6-Dimethylcoumalin
2H-PYRAN-2-ONE, 4,6-DIMETHYL-
4,6-Dimethyl-alpha-pyrone
2,4-Dimethyl-alpha-pyrone
2,4-Dimethyl-.alpha.-pyrone
4,6-Dimethyl-.alpha.-pyrone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Mesitene lactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.8888 88.88%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.7825 78.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9682 96.82%
OATP1B3 inhibitior + 0.9769 97.69%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9196 91.96%
P-glycoprotein inhibitior - 0.9795 97.95%
P-glycoprotein substrate - 0.9915 99.15%
CYP3A4 substrate - 0.7290 72.90%
CYP2C9 substrate - 0.6498 64.98%
CYP2D6 substrate - 0.8907 89.07%
CYP3A4 inhibition - 0.9040 90.40%
CYP2C9 inhibition - 0.9365 93.65%
CYP2C19 inhibition - 0.8901 89.01%
CYP2D6 inhibition - 0.9603 96.03%
CYP1A2 inhibition + 0.5159 51.59%
CYP2C8 inhibition - 0.9926 99.26%
CYP inhibitory promiscuity - 0.9179 91.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7948 79.48%
Carcinogenicity (trinary) Non-required 0.5653 56.53%
Eye corrosion + 0.8495 84.95%
Eye irritation + 0.9886 98.86%
Skin irritation + 0.8804 88.04%
Skin corrosion - 0.8213 82.13%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8089 80.89%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.5303 53.03%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.6021 60.21%
Acute Oral Toxicity (c) III 0.7929 79.29%
Estrogen receptor binding - 0.9342 93.42%
Androgen receptor binding - 0.6390 63.90%
Thyroid receptor binding - 0.8390 83.90%
Glucocorticoid receptor binding - 0.7555 75.55%
Aromatase binding - 0.8354 83.54%
PPAR gamma - 0.8131 81.31%
Honey bee toxicity - 0.9295 92.95%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity - 0.5488 54.88%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL261 P00915 Carbonic anhydrase I 19100 nM
Ki
PMID: 22137345
CHEMBL3594 Q16790 Carbonic anhydrase IX 2470 nM
Ki
PMID: 22137345

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.33% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 89.95% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.87% 93.65%
CHEMBL2581 P07339 Cathepsin D 88.12% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.12% 94.80%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.04% 94.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.37% 90.71%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 80.15% 81.11%

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.
Ficus carica

Cross-Links

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PubChem 12662
NPASS NPC234084
ChEMBL CHEMBL372284