5-Hydroxy-7-methoxy-2-propylchromen-4-one

Details

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Internal ID 3d5046ed-5980-4671-945e-e2f5bf02344d
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 5-hydroxy-7-methoxy-2-propylchromen-4-one
SMILES (Canonical) CCCC1=CC(=O)C2=C(C=C(C=C2O1)OC)O
SMILES (Isomeric) CCCC1=CC(=O)C2=C(C=C(C=C2O1)OC)O
InChI InChI=1S/C13H14O4/c1-3-4-8-5-10(14)13-11(15)6-9(16-2)7-12(13)17-8/h5-7,15H,3-4H2,1-2H3
InChI Key TYOICPGJEBACJB-UHFFFAOYSA-N
Popularity 1 reference 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) 55.80 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.46
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-7-methoxy-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 + 0.9837 98.37%
Caco-2 + 0.9175 91.75%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5495 54.95%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.9189 91.89%
OATP1B3 inhibitior + 0.9731 97.31%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7240 72.40%
P-glycoprotein inhibitior - 0.7940 79.40%
P-glycoprotein substrate - 0.8317 83.17%
CYP3A4 substrate - 0.5393 53.93%
CYP2C9 substrate - 0.5914 59.14%
CYP2D6 substrate - 0.8089 80.89%
CYP3A4 inhibition - 0.5069 50.69%
CYP2C9 inhibition - 0.7450 74.50%
CYP2C19 inhibition + 0.5283 52.83%
CYP2D6 inhibition - 0.8403 84.03%
CYP1A2 inhibition + 0.7929 79.29%
CYP2C8 inhibition - 0.6467 64.67%
CYP inhibitory promiscuity - 0.5657 56.57%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6285 62.85%
Eye corrosion - 0.9661 96.61%
Eye irritation + 0.8324 83.24%
Skin irritation - 0.8093 80.93%
Skin corrosion - 0.9619 96.19%
Ames mutagenesis - 0.5937 59.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5692 56.92%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.8899 88.99%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6974 69.74%
Acute Oral Toxicity (c) III 0.7583 75.83%
Estrogen receptor binding + 0.7350 73.50%
Androgen receptor binding + 0.7042 70.42%
Thyroid receptor binding - 0.6548 65.48%
Glucocorticoid receptor binding + 0.7578 75.78%
Aromatase binding + 0.6436 64.36%
PPAR gamma + 0.7319 73.19%
Honey bee toxicity - 0.9147 91.47%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5732 57.32%
Fish aquatic toxicity + 0.7405 74.05%

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 98.45% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.34% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.47% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.31% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 89.63% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.25% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.71% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.35% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.00% 85.14%
CHEMBL3194 P02766 Transthyretin 84.20% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.18% 96.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.01% 93.65%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.80% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.75% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.22% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.58% 99.15%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.01% 95.50%

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 10421528
LOTUS LTS0068393
wikiData Q105267620