5,7-Dimethoxy-2-propylchromen-4-one

Details

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Internal ID d23f7e3d-647c-4923-9821-5570b13bbf03
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 5,7-dimethoxy-2-propylchromen-4-one
SMILES (Canonical) CCCC1=CC(=O)C2=C(O1)C=C(C=C2OC)OC
SMILES (Isomeric) CCCC1=CC(=O)C2=C(O1)C=C(C=C2OC)OC
InChI InChI=1S/C14H16O4/c1-4-5-9-6-11(15)14-12(17-3)7-10(16-2)8-13(14)18-9/h6-8H,4-5H2,1-3H3
InChI Key OWKICUYZFSTQDO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H16O4
Molecular Weight 248.27 g/mol
Exact Mass 248.10485899 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.76
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,7-Dimethoxy-2-propylchromen-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 + 0.9894 98.94%
Caco-2 + 0.8912 89.12%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5493 54.93%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9288 92.88%
OATP1B3 inhibitior + 0.9742 97.42%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7703 77.03%
P-glycoprotein inhibitior - 0.7256 72.56%
P-glycoprotein substrate - 0.7718 77.18%
CYP3A4 substrate - 0.5380 53.80%
CYP2C9 substrate - 0.6462 64.62%
CYP2D6 substrate - 0.7880 78.80%
CYP3A4 inhibition - 0.6182 61.82%
CYP2C9 inhibition - 0.7542 75.42%
CYP2C19 inhibition - 0.5549 55.49%
CYP2D6 inhibition - 0.8642 86.42%
CYP1A2 inhibition + 0.8364 83.64%
CYP2C8 inhibition - 0.7509 75.09%
CYP inhibitory promiscuity + 0.5871 58.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6094 60.94%
Eye corrosion - 0.9539 95.39%
Eye irritation + 0.6443 64.43%
Skin irritation - 0.8446 84.46%
Skin corrosion - 0.9719 97.19%
Ames mutagenesis - 0.5264 52.64%
Human Ether-a-go-go-Related Gene inhibition + 0.6469 64.69%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.8897 88.97%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6017 60.17%
Acute Oral Toxicity (c) III 0.6965 69.65%
Estrogen receptor binding + 0.6698 66.98%
Androgen receptor binding + 0.6589 65.89%
Thyroid receptor binding - 0.5859 58.59%
Glucocorticoid receptor binding + 0.6132 61.32%
Aromatase binding + 0.7595 75.95%
PPAR gamma + 0.6239 62.39%
Honey bee toxicity - 0.8811 88.11%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8050 80.50%

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 93.36% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.91% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.77% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.78% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.93% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 84.51% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.16% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.12% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 83.94% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.68% 92.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.03% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.47% 95.50%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.39% 93.99%

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.
Baeckea frutescens

Cross-Links

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PubChem 44559643
LOTUS LTS0135532
wikiData Q105202064