6-acetyl-2-(hydroxymethyl)-2-methyl-3H-chromen-4-one

Details

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Internal ID 73b23461-be67-4370-bfcb-6909133e9533
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 6-acetyl-2-(hydroxymethyl)-2-methyl-3H-chromen-4-one
SMILES (Canonical) CC(=O)C1=CC2=C(C=C1)OC(CC2=O)(C)CO
SMILES (Isomeric) CC(=O)C1=CC2=C(C=C1)OC(CC2=O)(C)CO
InChI InChI=1S/C13H14O4/c1-8(15)9-3-4-12-10(5-9)11(16)6-13(2,7-14)17-12/h3-5,14H,6-7H2,1-2H3
InChI Key BLZODKWLXWVJLS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O4
Molecular Weight 234.25 g/mol
Exact Mass 234.08920892 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.61
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-acetyl-2-(hydroxymethyl)-2-methyl-3H-chromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9781 97.81%
Caco-2 + 0.8203 82.03%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7423 74.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9129 91.29%
OATP1B3 inhibitior + 0.9537 95.37%
MATE1 inhibitior - 0.9412 94.12%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8516 85.16%
P-glycoprotein inhibitior - 0.9698 96.98%
P-glycoprotein substrate - 0.8751 87.51%
CYP3A4 substrate - 0.5664 56.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7118 71.18%
CYP3A4 inhibition - 0.6582 65.82%
CYP2C9 inhibition - 0.6907 69.07%
CYP2C19 inhibition - 0.6563 65.63%
CYP2D6 inhibition - 0.9354 93.54%
CYP1A2 inhibition + 0.5847 58.47%
CYP2C8 inhibition - 0.8012 80.12%
CYP inhibitory promiscuity - 0.8554 85.54%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6328 63.28%
Eye corrosion - 0.9792 97.92%
Eye irritation + 0.6135 61.35%
Skin irritation - 0.7937 79.37%
Skin corrosion - 0.9458 94.58%
Ames mutagenesis - 0.7523 75.23%
Human Ether-a-go-go-Related Gene inhibition - 0.6400 64.00%
Micronuclear - 0.5041 50.41%
Hepatotoxicity + 0.5857 58.57%
skin sensitisation - 0.7723 77.23%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.7442 74.42%
Acute Oral Toxicity (c) III 0.4723 47.23%
Estrogen receptor binding - 0.7258 72.58%
Androgen receptor binding - 0.6962 69.62%
Thyroid receptor binding - 0.7845 78.45%
Glucocorticoid receptor binding - 0.5112 51.12%
Aromatase binding - 0.4889 48.89%
PPAR gamma - 0.5941 59.41%
Honey bee toxicity - 0.9570 95.70%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.6656 66.56%

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 95.75% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.91% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.67% 86.33%
CHEMBL4208 P20618 Proteasome component C5 92.22% 90.00%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 90.90% 87.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.83% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.91% 89.34%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 86.75% 81.11%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.36% 93.04%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.33% 89.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.92% 96.77%
CHEMBL340 P08684 Cytochrome P450 3A4 84.93% 91.19%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.02% 96.95%
CHEMBL1811 P34995 Prostanoid EP1 receptor 83.36% 95.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.90% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.77% 99.17%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.69% 90.24%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.56% 94.80%

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.
Gynura formosana

Cross-Links

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PubChem 102064909
LOTUS LTS0038144
wikiData Q104938292