2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone

Details

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Internal ID c513aa26-b0fe-4507-9d23-4e1f159d4b1d
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > 2-Hydroxy-dihydrochalcones
IUPAC Name 1-(2,3-dihydroxy-4,6-dimethoxyphenyl)-3-phenylpropan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H18O5/c1-21-13-10-14(22-2)16(19)17(20)15(13)12(18)9-8-11-6-4-3-5-7-11/h3-7,10,19-20H,8-9H2,1-2H3
InChI Key RZFPYTZZSXAWPH-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O5
Molecular Weight 302.32 g/mol
Exact Mass 302.11542367 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.93
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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LMPK12120557

2D Structure

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2D Structure of 2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9138 91.38%
Caco-2 + 0.6860 68.60%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.9210 92.10%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.8386 83.86%
OATP1B3 inhibitior + 0.9619 96.19%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.4801 48.01%
P-glycoprotein inhibitior - 0.4783 47.83%
P-glycoprotein substrate - 0.6410 64.10%
CYP3A4 substrate - 0.5458 54.58%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7729 77.29%
CYP3A4 inhibition - 0.7647 76.47%
CYP2C9 inhibition - 0.5362 53.62%
CYP2C19 inhibition + 0.8231 82.31%
CYP2D6 inhibition - 0.7225 72.25%
CYP1A2 inhibition + 0.9097 90.97%
CYP2C8 inhibition + 0.8523 85.23%
CYP inhibitory promiscuity - 0.5957 59.57%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7854 78.54%
Carcinogenicity (trinary) Non-required 0.6815 68.15%
Eye corrosion - 0.9747 97.47%
Eye irritation + 0.7621 76.21%
Skin irritation - 0.7368 73.68%
Skin corrosion - 0.9108 91.08%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6362 63.62%
Micronuclear - 0.5582 55.82%
Hepatotoxicity - 0.5339 53.39%
skin sensitisation - 0.8552 85.52%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.8111 81.11%
Acute Oral Toxicity (c) III 0.7721 77.21%
Estrogen receptor binding + 0.8562 85.62%
Androgen receptor binding + 0.5310 53.10%
Thyroid receptor binding - 0.5528 55.28%
Glucocorticoid receptor binding + 0.7474 74.74%
Aromatase binding - 0.5270 52.70%
PPAR gamma + 0.6974 69.74%
Honey bee toxicity - 0.9392 93.92%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5704 57.04%
Fish aquatic toxicity + 0.8965 89.65%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.79% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.15% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.62% 91.11%
CHEMBL1255126 O15151 Protein Mdm4 93.12% 90.20%
CHEMBL2581 P07339 Cathepsin D 93.08% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.99% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.94% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.68% 95.50%
CHEMBL4208 P20618 Proteasome component C5 85.97% 90.00%
CHEMBL2535 P11166 Glucose transporter 85.36% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 85.21% 94.73%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 84.83% 92.67%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.55% 96.00%

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.
Uvaria dulcis

Cross-Links

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PubChem 42607714
LOTUS LTS0158161
wikiData Q105248360