Msfocqwgxbbmov-uhfffaoysa-

Details

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Internal ID f72d0a17-dc75-417a-8800-9c02c8683808
Taxonomy Organoheterocyclic compounds > Benzofurans > Benzofuranones
IUPAC Name 3-acetyl-7-hydroxy-5-methoxy-3,4-dimethyl-2-benzofuran-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14O5/c1-6-9(17-4)5-8(15)10-11(6)13(3,7(2)14)18-12(10)16/h5,15H,1-4H3
InChI Key MSFOCQWGXBBMOV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O5
Molecular Weight 250.25 g/mol
Exact Mass 250.08412354 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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3-acetyl-7-hydroxy-5-methoxy-3,4-dimethyl-3h-isobenzofuran-1-one
InChI=1/C13H14O5/c1-6-9(17-4)5-8(15)10-11(6)13(3,7(2)14)18-12(10)16/h5,15H,1-4H3

2D Structure

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2D Structure of Msfocqwgxbbmov-uhfffaoysa-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9767 97.67%
Caco-2 + 0.5181 51.81%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6843 68.43%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior + 0.9090 90.90%
OATP1B3 inhibitior + 0.9213 92.13%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9071 90.71%
P-glycoprotein inhibitior - 0.8880 88.80%
P-glycoprotein substrate - 0.8928 89.28%
CYP3A4 substrate + 0.5724 57.24%
CYP2C9 substrate + 0.7993 79.93%
CYP2D6 substrate - 0.8590 85.90%
CYP3A4 inhibition - 0.7720 77.20%
CYP2C9 inhibition - 0.9299 92.99%
CYP2C19 inhibition - 0.9578 95.78%
CYP2D6 inhibition - 0.9636 96.36%
CYP1A2 inhibition - 0.7071 70.71%
CYP2C8 inhibition - 0.6294 62.94%
CYP inhibitory promiscuity - 0.8868 88.68%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9143 91.43%
Carcinogenicity (trinary) Non-required 0.4288 42.88%
Eye corrosion - 0.9468 94.68%
Eye irritation + 0.8194 81.94%
Skin irritation - 0.7242 72.42%
Skin corrosion - 0.9390 93.90%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7840 78.40%
Micronuclear + 0.6559 65.59%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8468 84.68%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.6248 62.48%
Acute Oral Toxicity (c) II 0.5604 56.04%
Estrogen receptor binding - 0.6285 62.85%
Androgen receptor binding - 0.5860 58.60%
Thyroid receptor binding - 0.7419 74.19%
Glucocorticoid receptor binding - 0.6354 63.54%
Aromatase binding - 0.6092 60.92%
PPAR gamma - 0.6444 64.44%
Honey bee toxicity - 0.8873 88.73%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9105 91.05%

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 98.11% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.39% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.36% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.58% 85.14%
CHEMBL2581 P07339 Cathepsin D 91.16% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.10% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.71% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.38% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.31% 99.23%
CHEMBL2535 P11166 Glucose transporter 88.11% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.09% 95.50%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.43% 91.07%
CHEMBL4208 P20618 Proteasome component C5 85.35% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 84.81% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.79% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.04% 99.15%
CHEMBL340 P08684 Cytochrome P450 3A4 83.42% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 82.28% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.52% 99.17%

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 10377405
LOTUS LTS0100065
wikiData Q105171131