2',4'-Dihydroxy-3'-(2,6-dihydroxybenzyl)-6'-methoxychalcone

Details

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Internal ID bb458373-76cd-4fae-abd1-323939984c95
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name 1-[3-[(2,6-dihydroxyphenyl)methyl]-2,4-dihydroxy-6-methoxyphenyl]-3-phenylprop-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H20O6/c1-29-21-13-20(27)16(12-15-17(24)8-5-9-18(15)25)23(28)22(21)19(26)11-10-14-6-3-2-4-7-14/h2-11,13,24-25,27-28H,12H2,1H3
InChI Key INZGRPLRNMWDQV-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C23H20O6
Molecular Weight 392.40 g/mol
Exact Mass 392.12598835 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.00
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2',4'-Dihydroxy-3'-(2,6-dihydroxybenzyl)-6'-methoxychalcone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9835 98.35%
Caco-2 - 0.6828 68.28%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8051 80.51%
OATP2B1 inhibitior - 0.5709 57.09%
OATP1B1 inhibitior + 0.7871 78.71%
OATP1B3 inhibitior + 0.9592 95.92%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9588 95.88%
BSEP inhibitior + 0.8439 84.39%
P-glycoprotein inhibitior + 0.7170 71.70%
P-glycoprotein substrate - 0.7154 71.54%
CYP3A4 substrate + 0.5113 51.13%
CYP2C9 substrate - 0.7990 79.90%
CYP2D6 substrate - 0.8133 81.33%
CYP3A4 inhibition + 0.5595 55.95%
CYP2C9 inhibition + 0.7841 78.41%
CYP2C19 inhibition + 0.8975 89.75%
CYP2D6 inhibition - 0.8924 89.24%
CYP1A2 inhibition + 0.9172 91.72%
CYP2C8 inhibition + 0.8939 89.39%
CYP inhibitory promiscuity + 0.8712 87.12%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7816 78.16%
Carcinogenicity (trinary) Non-required 0.7051 70.51%
Eye corrosion - 0.9692 96.92%
Eye irritation - 0.5109 51.09%
Skin irritation - 0.6725 67.25%
Skin corrosion - 0.8739 87.39%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4004 40.04%
Micronuclear + 0.6559 65.59%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.6995 69.95%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.8487 84.87%
Acute Oral Toxicity (c) III 0.7158 71.58%
Estrogen receptor binding + 0.9078 90.78%
Androgen receptor binding + 0.7582 75.82%
Thyroid receptor binding + 0.5771 57.71%
Glucocorticoid receptor binding + 0.8106 81.06%
Aromatase binding + 0.6442 64.42%
PPAR gamma + 0.8159 81.59%
Honey bee toxicity - 0.8838 88.38%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9842 98.42%

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 98.06% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.24% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.24% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.93% 93.99%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 94.79% 95.50%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.42% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.34% 96.00%
CHEMBL2581 P07339 Cathepsin D 92.01% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 90.50% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.64% 99.17%
CHEMBL3194 P02766 Transthyretin 88.45% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.41% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 86.07% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.98% 99.15%
CHEMBL2535 P11166 Glucose transporter 82.97% 98.75%
CHEMBL5028 O14672 ADAM10 82.00% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.03% 89.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.02% 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.
Desmos chinensis

Cross-Links

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PubChem 91614562
LOTUS LTS0080081
wikiData Q105116528