5-Acetonyl-7-hydroxy-2-hydroxymethylchromone

Details

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Internal ID 09c84f5b-ab39-4e0a-b398-27144bc9cde9
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 7-hydroxy-2-(hydroxymethyl)-5-(2-oxopropyl)chromen-4-one
SMILES (Canonical) CC(=O)CC1=C2C(=CC(=C1)O)OC(=CC2=O)CO
SMILES (Isomeric) CC(=O)CC1=C2C(=CC(=C1)O)OC(=CC2=O)CO
InChI InChI=1S/C13H12O5/c1-7(15)2-8-3-9(16)4-12-13(8)11(17)5-10(6-14)18-12/h3-5,14,16H,2,6H2,1H3
InChI Key IJAJRHZKYVCLQY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O5
Molecular Weight 248.23 g/mol
Exact Mass 248.06847348 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP -0.10
Atomic LogP (AlogP) 1.12
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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5-acetonyl-7-hydroxy-2-hydroxymethylchromone
DTXSID701167935
BDBM50259665
263368-90-7
5-acetonyl-7-hydroxy-2-hydroxymethyl-chromone
7-Hydroxy-2-(hydroxymethyl)-5-(2-oxopropyl)-4H-1-benzopyran-4-one

2D Structure

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2D Structure of 5-Acetonyl-7-hydroxy-2-hydroxymethylchromone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8873 88.73%
Caco-2 + 0.5599 55.99%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6855 68.55%
OATP2B1 inhibitior - 0.7151 71.51%
OATP1B1 inhibitior + 0.8827 88.27%
OATP1B3 inhibitior + 0.9671 96.71%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8671 86.71%
P-glycoprotein inhibitior - 0.9410 94.10%
P-glycoprotein substrate - 0.8466 84.66%
CYP3A4 substrate - 0.5518 55.18%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.8281 82.81%
CYP3A4 inhibition - 0.7758 77.58%
CYP2C9 inhibition - 0.5442 54.42%
CYP2C19 inhibition - 0.7179 71.79%
CYP2D6 inhibition - 0.8948 89.48%
CYP1A2 inhibition - 0.5233 52.33%
CYP2C8 inhibition - 0.8052 80.52%
CYP inhibitory promiscuity - 0.7573 75.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5771 57.71%
Eye corrosion - 0.9849 98.49%
Eye irritation + 0.7521 75.21%
Skin irritation - 0.7942 79.42%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis + 0.6363 63.63%
Human Ether-a-go-go-Related Gene inhibition - 0.6997 69.97%
Micronuclear + 0.5300 53.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.9085 90.85%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.4610 46.10%
Acute Oral Toxicity (c) III 0.5031 50.31%
Estrogen receptor binding - 0.7097 70.97%
Androgen receptor binding + 0.6865 68.65%
Thyroid receptor binding - 0.8340 83.40%
Glucocorticoid receptor binding + 0.8260 82.60%
Aromatase binding - 0.5584 55.84%
PPAR gamma + 0.6916 69.16%
Honey bee toxicity - 0.9026 90.26%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.7426 74.26%

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 98.74% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.61% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.11% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 90.22% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.96% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.85% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.40% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.36% 90.71%

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.
Brachylaena perrieri
Pseudostifftia kingii
Senna siamea

Cross-Links

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PubChem 10824421
LOTUS LTS0036025
wikiData Q105338395