2',4'-Dihydroxy-3',6'-dimethoxy-5'-isovaleryloxychalcone

Details

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Internal ID 40784292-7dd8-480b-be0e-1fe012411fe3
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > 2-Hydroxychalcones
IUPAC Name [2,4-dihydroxy-3,6-dimethoxy-5-(3-phenylprop-2-enoyl)phenyl] 3-methylbutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H24O7/c1-13(2)12-16(24)29-22-19(26)21(28-4)18(25)17(20(22)27-3)15(23)11-10-14-8-6-5-7-9-14/h5-11,13,25-26H,12H2,1-4H3
InChI Key YABVHCBUBNHULG-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H24O7
Molecular Weight 400.40 g/mol
Exact Mass 400.15220310 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.96
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2',4'-Dihydroxy-3',6'-dimethoxy-5'-isovaleryloxychalcone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9525 95.25%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7369 73.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8572 85.72%
OATP1B3 inhibitior - 0.2705 27.05%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9051 90.51%
P-glycoprotein inhibitior + 0.8489 84.89%
P-glycoprotein substrate - 0.7417 74.17%
CYP3A4 substrate - 0.5225 52.25%
CYP2C9 substrate - 0.7816 78.16%
CYP2D6 substrate - 0.8753 87.53%
CYP3A4 inhibition - 0.5259 52.59%
CYP2C9 inhibition + 0.6219 62.19%
CYP2C19 inhibition - 0.5514 55.14%
CYP2D6 inhibition - 0.6733 67.33%
CYP1A2 inhibition + 0.5557 55.57%
CYP2C8 inhibition + 0.5399 53.99%
CYP inhibitory promiscuity - 0.6966 69.66%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7779 77.79%
Carcinogenicity (trinary) Non-required 0.6806 68.06%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.6999 69.99%
Skin irritation - 0.8997 89.97%
Skin corrosion - 0.9572 95.72%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3768 37.68%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.7791 77.91%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.8868 88.68%
Acute Oral Toxicity (c) III 0.6052 60.52%
Estrogen receptor binding + 0.7964 79.64%
Androgen receptor binding + 0.6495 64.95%
Thyroid receptor binding + 0.5600 56.00%
Glucocorticoid receptor binding + 0.6419 64.19%
Aromatase binding - 0.5521 55.21%
PPAR gamma + 0.7694 76.94%
Honey bee toxicity - 0.8864 88.64%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5345 53.45%
Fish aquatic toxicity + 0.9949 99.49%

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 96.46% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.87% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.41% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.35% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.78% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.12% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.91% 95.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.31% 93.56%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 87.05% 94.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.89% 99.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.08% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 80.42% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 72733693
LOTUS LTS0180347
wikiData Q105345294