4'-Hydroxy-2'-methoxychalcone

Details

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Internal ID eace9126-fe3a-4eb3-bb8b-c996f4c8721e
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Cinnamylphenols
IUPAC Name (E)-1-(4-hydroxy-2-methoxyphenyl)-3-phenylprop-2-en-1-one
SMILES (Canonical) COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=CC=C2
SMILES (Isomeric) COC1=C(C=CC(=C1)O)C(=O)/C=C/C2=CC=CC=C2
InChI InChI=1S/C16H14O3/c1-19-16-11-13(17)8-9-14(16)15(18)10-7-12-5-3-2-4-6-12/h2-11,17H,1H3/b10-7+
InChI Key VLEOOBKBMSIDKF-JXMROGBWSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O3
Molecular Weight 254.28 g/mol
Exact Mass 254.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.30
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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2-Methoxyisoliquiritigenin
CHEMBL445232
LMPK12120017

2D Structure

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2D Structure of 4'-Hydroxy-2'-methoxychalcone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6950 69.50%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.9036 90.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9165 91.65%
OATP1B3 inhibitior + 0.9916 99.16%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5832 58.32%
P-glycoprotein inhibitior - 0.7214 72.14%
P-glycoprotein substrate - 0.9019 90.19%
CYP3A4 substrate - 0.5885 58.85%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7972 79.72%
CYP3A4 inhibition - 0.8273 82.73%
CYP2C9 inhibition - 0.8209 82.09%
CYP2C19 inhibition + 0.9257 92.57%
CYP2D6 inhibition - 0.9289 92.89%
CYP1A2 inhibition + 0.9224 92.24%
CYP2C8 inhibition + 0.8611 86.11%
CYP inhibitory promiscuity + 0.7265 72.65%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.6760 67.60%
Carcinogenicity (trinary) Non-required 0.5567 55.67%
Eye corrosion - 0.9084 90.84%
Eye irritation + 0.9642 96.42%
Skin irritation + 0.5811 58.11%
Skin corrosion - 0.9737 97.37%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5398 53.98%
Micronuclear + 0.5882 58.82%
Hepatotoxicity - 0.6342 63.42%
skin sensitisation - 0.8478 84.78%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.4517 45.17%
Acute Oral Toxicity (c) IV 0.5839 58.39%
Estrogen receptor binding + 0.9251 92.51%
Androgen receptor binding + 0.9096 90.96%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7603 76.03%
Aromatase binding + 0.8512 85.12%
PPAR gamma + 0.6791 67.91%
Honey bee toxicity - 0.9172 91.72%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6155 61.55%
Fish aquatic toxicity + 0.9818 98.18%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.00% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.72% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.92% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.59% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.22% 95.50%
CHEMBL2535 P11166 Glucose transporter 90.92% 98.75%
CHEMBL2581 P07339 Cathepsin D 88.23% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.21% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.94% 99.17%
CHEMBL3194 P02766 Transthyretin 87.08% 90.71%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.37% 91.71%
CHEMBL4208 P20618 Proteasome component C5 82.95% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 81.51% 90.20%

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.
Amorpha fruticosa
Dalbergia cochinchinensis
Oxytropis falcata

Cross-Links

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PubChem 13842401
NPASS NPC308037
ChEMBL CHEMBL445232
LOTUS LTS0122950
wikiData Q76423387