2-Hydroxy-3,4,6-trimethoxydihydrochalcone

Details

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Internal ID 0fb00c12-795a-4634-9109-1bfed78b3351
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > Retro-dihydrochalcones
IUPAC Name 3-(2-hydroxy-3,4,6-trimethoxyphenyl)-1-phenylpropan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H20O5/c1-21-15-11-16(22-2)18(23-3)17(20)13(15)9-10-14(19)12-7-5-4-6-8-12/h4-8,11,20H,9-10H2,1-3H3
InChI Key ADHYECILSBTSIG-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C18H20O5
Molecular Weight 316.30 g/mol
Exact Mass 316.13107373 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.23
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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RefChem:87365
3-(2-hydroxy-3,4,6-trimethoxyphenyl)-1-phenylpropan-1-one
279219-89-5
LMPK12120609

2D Structure

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2D Structure of 2-Hydroxy-3,4,6-trimethoxydihydrochalcone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9719 97.19%
Caco-2 + 0.8981 89.81%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.9155 91.55%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.8252 82.52%
OATP1B3 inhibitior + 0.9112 91.12%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5452 54.52%
P-glycoprotein inhibitior + 0.6137 61.37%
P-glycoprotein substrate - 0.8643 86.43%
CYP3A4 substrate - 0.5426 54.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3530 35.30%
CYP3A4 inhibition - 0.7873 78.73%
CYP2C9 inhibition - 0.7115 71.15%
CYP2C19 inhibition + 0.8095 80.95%
CYP2D6 inhibition - 0.8506 85.06%
CYP1A2 inhibition + 0.7523 75.23%
CYP2C8 inhibition + 0.8634 86.34%
CYP inhibitory promiscuity - 0.5273 52.73%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7643 76.43%
Carcinogenicity (trinary) Non-required 0.6616 66.16%
Eye corrosion - 0.9800 98.00%
Eye irritation - 0.5806 58.06%
Skin irritation - 0.7695 76.95%
Skin corrosion - 0.9549 95.49%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5642 56.42%
Micronuclear - 0.7167 71.67%
Hepatotoxicity - 0.6466 64.66%
skin sensitisation - 0.9065 90.65%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.9187 91.87%
Acute Oral Toxicity (c) III 0.7605 76.05%
Estrogen receptor binding + 0.7975 79.75%
Androgen receptor binding - 0.5693 56.93%
Thyroid receptor binding + 0.5843 58.43%
Glucocorticoid receptor binding + 0.6553 65.53%
Aromatase binding - 0.7298 72.98%
PPAR gamma + 0.5678 56.78%
Honey bee toxicity - 0.9332 93.32%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6104 61.04%
Fish aquatic toxicity + 0.8933 89.33%

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 95.72% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.44% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.29% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.52% 99.17%
CHEMBL2535 P11166 Glucose transporter 90.83% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 90.73% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.45% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.77% 95.50%
CHEMBL4208 P20618 Proteasome component C5 87.09% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.95% 96.00%
CHEMBL2581 P07339 Cathepsin D 84.89% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.89% 93.99%

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 welwitschii

Cross-Links

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PubChem 42607736
LOTUS LTS0107450
wikiData Q104909573