CID 182171

Details

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Internal ID 68dc768b-b7e1-4d38-b644-37bb983450dc
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > Retrochalcones
IUPAC Name 3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one
SMILES (Canonical) COC1=C(C=CC(=C1)O)C=CC(=O)C2=CC=C(C=C2)O
SMILES (Isomeric) COC1=C(C=CC(=C1)O)C=CC(=O)C2=CC=C(C=C2)O
InChI InChI=1S/C16H14O4/c1-20-16-10-14(18)8-4-12(16)5-9-15(19)11-2-6-13(17)7-3-11/h2-10,17-18H,1H3
InChI Key QJKMIJNRNRLQSS-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O4
Molecular Weight 270.28 g/mol
Exact Mass 270.08920892 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.00
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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FT-0688296
B0005-464424

2D Structure

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2D Structure of CID 182171

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.9025 90.25%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8857 88.57%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.8307 83.07%
OATP1B3 inhibitior + 0.9877 98.77%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7369 73.69%
P-glycoprotein inhibitior - 0.8664 86.64%
P-glycoprotein substrate - 0.8042 80.42%
CYP3A4 substrate - 0.5325 53.25%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7829 78.29%
CYP3A4 inhibition - 0.6334 63.34%
CYP2C9 inhibition + 0.7291 72.91%
CYP2C19 inhibition + 0.9421 94.21%
CYP2D6 inhibition - 0.9234 92.34%
CYP1A2 inhibition + 0.9609 96.09%
CYP2C8 inhibition + 0.9001 90.01%
CYP inhibitory promiscuity + 0.8213 82.13%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6760 67.60%
Carcinogenicity (trinary) Non-required 0.5968 59.68%
Eye corrosion - 0.9611 96.11%
Eye irritation + 0.9742 97.42%
Skin irritation - 0.5760 57.60%
Skin corrosion - 0.9479 94.79%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6327 63.27%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.5915 59.15%
skin sensitisation - 0.8499 84.99%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.4683 46.83%
Acute Oral Toxicity (c) III 0.5305 53.05%
Estrogen receptor binding + 0.8891 88.91%
Androgen receptor binding + 0.7746 77.46%
Thyroid receptor binding + 0.5569 55.69%
Glucocorticoid receptor binding + 0.7278 72.78%
Aromatase binding + 0.8521 85.21%
PPAR gamma + 0.7398 73.98%
Honey bee toxicity - 0.9326 93.26%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9869 98.69%

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 95.97% 86.33%
CHEMBL3194 P02766 Transthyretin 94.93% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.20% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.69% 99.17%
CHEMBL4208 P20618 Proteasome component C5 91.11% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.28% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.55% 96.09%
CHEMBL2535 P11166 Glucose transporter 88.98% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 86.67% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.97% 96.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.10% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.91% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.56% 89.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.52% 97.21%
CHEMBL2581 P07339 Cathepsin D 81.12% 98.95%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.64% 91.71%

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.
Dracaena draco
Glycyrrhiza echinata
Glycyrrhiza glabra
Glycyrrhiza inflata
Glycyrrhiza pallidiflora
Glycyrrhiza uralensis

Cross-Links

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PubChem 182171
LOTUS LTS0005405
wikiData Q105222727