6-Hydroxy-3-(2-hydroxypropyl)-8-methoxychromen-2-one

Details

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Internal ID a6e00535-e997-48c6-b1e8-66bc5738dae0
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins
IUPAC Name 6-hydroxy-3-(2-hydroxypropyl)-8-methoxychromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14O5/c1-7(14)3-9-4-8-5-10(15)6-11(17-2)12(8)18-13(9)16/h4-7,14-15H,3H2,1-2H3
InChI Key JJPPIWBBVUMFEW-UHFFFAOYSA-N
Popularity 0 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) 76.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.43
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Hydroxy-3-(2-hydroxypropyl)-8-methoxychromen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9421 94.21%
Caco-2 + 0.6463 64.63%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6281 62.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9011 90.11%
OATP1B3 inhibitior + 0.8431 84.31%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7394 73.94%
P-glycoprotein inhibitior - 0.9097 90.97%
P-glycoprotein substrate - 0.8643 86.43%
CYP3A4 substrate - 0.5424 54.24%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.7735 77.35%
CYP3A4 inhibition - 0.8793 87.93%
CYP2C9 inhibition - 0.8957 89.57%
CYP2C19 inhibition - 0.8377 83.77%
CYP2D6 inhibition - 0.7120 71.20%
CYP1A2 inhibition + 0.5086 50.86%
CYP2C8 inhibition - 0.7587 75.87%
CYP inhibitory promiscuity - 0.7805 78.05%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6319 63.19%
Eye corrosion - 0.9814 98.14%
Eye irritation - 0.5628 56.28%
Skin irritation - 0.7640 76.40%
Skin corrosion - 0.9659 96.59%
Ames mutagenesis - 0.6954 69.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6458 64.58%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8963 89.63%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.4893 48.93%
Acute Oral Toxicity (c) III 0.5420 54.20%
Estrogen receptor binding - 0.5916 59.16%
Androgen receptor binding + 0.6054 60.54%
Thyroid receptor binding - 0.5056 50.56%
Glucocorticoid receptor binding - 0.5542 55.42%
Aromatase binding - 0.5391 53.91%
PPAR gamma + 0.5631 56.31%
Honey bee toxicity - 0.8710 87.10%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.8876 88.76%

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 97.00% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.98% 85.14%
CHEMBL2581 P07339 Cathepsin D 96.53% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.97% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.49% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 88.97% 90.20%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.27% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.98% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.64% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.71% 99.15%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.29% 92.62%
CHEMBL2535 P11166 Glucose transporter 84.84% 98.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.82% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.85% 94.45%
CHEMBL4208 P20618 Proteasome component C5 80.87% 90.00%

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 163064219
LOTUS LTS0048909
wikiData Q104169609