2',4'-Dihydroxy-6'-methoxy-5'-methylchalkon

Details

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Internal ID bbca6816-b932-4ed3-9b85-28c485d1cda7
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > 2-Hydroxychalcones
IUPAC Name 1-(4,6-dihydroxy-2-methoxy-3-methylphenyl)-3-phenylprop-2-en-1-one
SMILES (Canonical) CC1=C(C(=C(C=C1O)O)C(=O)C=CC2=CC=CC=C2)OC
SMILES (Isomeric) CC1=C(C(=C(C=C1O)O)C(=O)C=CC2=CC=CC=C2)OC
InChI InChI=1S/C17H16O4/c1-11-14(19)10-15(20)16(17(11)21-2)13(18)9-8-12-6-4-3-5-7-12/h3-10,19-20H,1-2H3
InChI Key PVTAUQXAGOXGNJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O4
Molecular Weight 284.31 g/mol
Exact Mass 284.10485899 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.31
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2',4'-Dihydroxy-6'-methoxy-5'-methylchalkon

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9857 98.57%
Caco-2 + 0.6126 61.26%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8138 81.38%
OATP2B1 inhibitior - 0.7228 72.28%
OATP1B1 inhibitior + 0.9051 90.51%
OATP1B3 inhibitior + 0.9725 97.25%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9838 98.38%
BSEP inhibitior - 0.6608 66.08%
P-glycoprotein inhibitior - 0.5214 52.14%
P-glycoprotein substrate - 0.9457 94.57%
CYP3A4 substrate - 0.5644 56.44%
CYP2C9 substrate - 0.7931 79.31%
CYP2D6 substrate - 0.8493 84.93%
CYP3A4 inhibition + 0.7770 77.70%
CYP2C9 inhibition + 0.7656 76.56%
CYP2C19 inhibition + 0.9176 91.76%
CYP2D6 inhibition - 0.8817 88.17%
CYP1A2 inhibition + 0.9475 94.75%
CYP2C8 inhibition + 0.7429 74.29%
CYP inhibitory promiscuity + 0.8786 87.86%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7627 76.27%
Carcinogenicity (trinary) Non-required 0.7034 70.34%
Eye corrosion - 0.9647 96.47%
Eye irritation + 0.8062 80.62%
Skin irritation - 0.6705 67.05%
Skin corrosion - 0.8917 89.17%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5596 55.96%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.5553 55.53%
skin sensitisation - 0.7366 73.66%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.7871 78.71%
Acute Oral Toxicity (c) III 0.7234 72.34%
Estrogen receptor binding + 0.8600 86.00%
Androgen receptor binding + 0.7902 79.02%
Thyroid receptor binding + 0.5389 53.89%
Glucocorticoid receptor binding + 0.7627 76.27%
Aromatase binding + 0.7956 79.56%
PPAR gamma + 0.7450 74.50%
Honey bee toxicity - 0.9537 95.37%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6055 60.55%
Fish aquatic toxicity + 0.9866 98.66%

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 96.06% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.03% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.87% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.52% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.92% 95.50%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 87.65% 94.08%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.85% 93.99%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.01% 94.62%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.70% 91.71%
CHEMBL2581 P07339 Cathepsin D 84.26% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 84.06% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.04% 99.17%
CHEMBL3194 P02766 Transthyretin 82.12% 90.71%
CHEMBL4208 P20618 Proteasome component C5 82.04% 90.00%
CHEMBL2535 P11166 Glucose transporter 81.72% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.51% 96.09%
CHEMBL5028 O14672 ADAM10 80.43% 97.50%

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.
Brassica juncea
Dalea scandens
Phyllolobium chinense

Cross-Links

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PubChem 85126781
NPASS NPC221822
LOTUS LTS0007856
wikiData Q105215591