1-Phenyl-3-(2,3,4,5-tetrahydroxy-6-methoxyphenyl)prop-2-en-1-one

Details

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Internal ID 27ff273c-6756-4efa-9194-c389c7f83b91
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > Retrochalcones
IUPAC Name 1-phenyl-3-(2,3,4,5-tetrahydroxy-6-methoxyphenyl)prop-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H14O6/c1-22-16-10(12(18)13(19)14(20)15(16)21)7-8-11(17)9-5-3-2-4-6-9/h2-8,18-21H,1H3
InChI Key QAESYSIYDUWHIG-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O6
Molecular Weight 302.28 g/mol
Exact Mass 302.07903816 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.41
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Phenyl-3-(2,3,4,5-tetrahydroxy-6-methoxyphenyl)prop-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9644 96.44%
Caco-2 - 0.6646 66.46%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6564 65.64%
OATP2B1 inhibitior - 0.5699 56.99%
OATP1B1 inhibitior + 0.9059 90.59%
OATP1B3 inhibitior + 0.9856 98.56%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9588 95.88%
BSEP inhibitior - 0.5734 57.34%
P-glycoprotein inhibitior - 0.7594 75.94%
P-glycoprotein substrate - 0.9394 93.94%
CYP3A4 substrate - 0.6024 60.24%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7946 79.46%
CYP3A4 inhibition + 0.5318 53.18%
CYP2C9 inhibition + 0.5451 54.51%
CYP2C19 inhibition - 0.6326 63.26%
CYP2D6 inhibition - 0.9296 92.96%
CYP1A2 inhibition + 0.9098 90.98%
CYP2C8 inhibition + 0.6546 65.46%
CYP inhibitory promiscuity + 0.7013 70.13%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8177 81.77%
Carcinogenicity (trinary) Non-required 0.6239 62.39%
Eye corrosion - 0.9634 96.34%
Eye irritation + 0.9042 90.42%
Skin irritation - 0.5521 55.21%
Skin corrosion - 0.7647 76.47%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6944 69.44%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation + 0.4823 48.23%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.6773 67.73%
Acute Oral Toxicity (c) III 0.6700 67.00%
Estrogen receptor binding + 0.8707 87.07%
Androgen receptor binding + 0.5838 58.38%
Thyroid receptor binding + 0.6202 62.02%
Glucocorticoid receptor binding + 0.8222 82.22%
Aromatase binding + 0.5347 53.47%
PPAR gamma + 0.7481 74.81%
Honey bee toxicity - 0.9558 95.58%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6555 65.55%
Fish aquatic toxicity + 0.9795 97.95%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.99% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.07% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.15% 91.11%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 89.77% 94.08%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.74% 96.00%
CHEMBL2581 P07339 Cathepsin D 86.55% 98.95%
CHEMBL2535 P11166 Glucose transporter 84.46% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.75% 95.50%
CHEMBL211 P08172 Muscarinic acetylcholine receptor M2 81.13% 94.97%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.76% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.55% 99.23%

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.
Glycyrrhiza uralensis

Cross-Links

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PubChem 140621070
LOTUS LTS0088087
wikiData Q105217358