3,3'-Dihydroxychalcone

Details

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Internal ID e6365651-2d65-4db6-a20f-db4558723e62
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > Retrochalcones
IUPAC Name (E)-1,3-bis(3-hydroxyphenyl)prop-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12O3/c16-13-5-1-3-11(9-13)7-8-15(18)12-4-2-6-14(17)10-12/h1-10,16-17H/b8-7+
InChI Key UALHWTHYPDBXSN-BQYQJAHWSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O3
Molecular Weight 240.25 g/mol
Exact Mass 240.078644241 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.99
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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142784-23-4
RefChem:90688
(E)-1,3-bis(3-hydroxyphenyl)prop-2-en-1-one
CHEMBL4088114
SCHEMBL2992884
BDBM50260211
LMPK12120189
AKOS001314412
NCGC00336529-01
AB01329770-02
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,3'-Dihydroxychalcone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.6899 68.99%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8317 83.17%
OATP2B1 inhibitior - 0.7254 72.54%
OATP1B1 inhibitior + 0.9472 94.72%
OATP1B3 inhibitior - 0.2145 21.45%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6784 67.84%
P-glycoprotein inhibitior - 0.9403 94.03%
P-glycoprotein substrate - 0.9552 95.52%
CYP3A4 substrate - 0.6365 63.65%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8075 80.75%
CYP3A4 inhibition - 0.5842 58.42%
CYP2C9 inhibition - 0.5567 55.67%
CYP2C19 inhibition + 0.6890 68.90%
CYP2D6 inhibition - 0.9506 95.06%
CYP1A2 inhibition + 0.6525 65.25%
CYP2C8 inhibition + 0.7204 72.04%
CYP inhibitory promiscuity + 0.6293 62.93%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.5927 59.27%
Carcinogenicity (trinary) Non-required 0.5343 53.43%
Eye corrosion - 0.9554 95.54%
Eye irritation + 0.9893 98.93%
Skin irritation + 0.6473 64.73%
Skin corrosion - 0.9839 98.39%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8572 85.72%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.5851 58.51%
skin sensitisation + 0.8647 86.47%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.7238 72.38%
Acute Oral Toxicity (c) IV 0.5155 51.55%
Estrogen receptor binding + 0.9084 90.84%
Androgen receptor binding + 0.7038 70.38%
Thyroid receptor binding + 0.5691 56.91%
Glucocorticoid receptor binding + 0.7176 71.76%
Aromatase binding + 0.8560 85.60%
PPAR gamma + 0.8534 85.34%
Honey bee toxicity - 0.9084 90.84%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6355 63.55%
Fish aquatic toxicity + 0.9803 98.03%

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 96.67% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.34% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.75% 95.56%
CHEMBL3194 P02766 Transthyretin 90.71% 90.71%
CHEMBL2535 P11166 Glucose transporter 90.39% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.87% 99.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 86.18% 91.71%
CHEMBL3401 O75469 Pregnane X receptor 84.43% 94.73%
CHEMBL245 P20309 Muscarinic acetylcholine receptor M3 83.83% 97.53%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.77% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.47% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.37% 89.00%
CHEMBL1907588 P02708 Acetylcholine receptor; alpha1/beta1/delta/gamma 80.28% 98.33%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.16% 100.00%

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.
Primula macrophylla

Cross-Links

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PubChem 9448219
LOTUS LTS0231159
wikiData Q76393905