3,4-Methylenedioxy-2',4'-dimethoxychalcone

Details

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Internal ID c2296148-32d7-4c01-9bcf-91e574456520
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives
IUPAC Name (E)-3-(1,3-benzodioxol-5-yl)-1-(2,4-dimethoxyphenyl)prop-2-en-1-one
SMILES (Canonical) COC1=CC(=C(C=C1)C(=O)C=CC2=CC3=C(C=C2)OCO3)OC
SMILES (Isomeric) COC1=CC(=C(C=C1)C(=O)/C=C/C2=CC3=C(C=C2)OCO3)OC
InChI InChI=1S/C18H16O5/c1-20-13-5-6-14(17(10-13)21-2)15(19)7-3-12-4-8-16-18(9-12)23-11-22-16/h3-10H,11H2,1-2H3/b7-3+
InChI Key XMQLRMQKCIIQEY-XVNBXDOJSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O5
Molecular Weight 312.30 g/mol
Exact Mass 312.09977361 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.33
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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151703-89-8
CHEMBL1945702
(E)-3-(1,3-benzodioxol-5-yl)-1-(2,4-dimethoxyphenyl)prop-2-en-1-one
3-(1,3-benzodioxol-5-yl)-1-(2,4-dimethoxyphenyl)prop-2-en-1-one
(2E)-3-(2H-1,3-benzodioxol-5-yl)-1-(2,4-dimethoxyphenyl)prop-2-en-1-one
SCHEMBL3191606
SCHEMBL3191621
XMQLRMQKCIIQEY-XVNBXDOJSA-N
BDBM50363137
LMPK12120117
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,4-Methylenedioxy-2',4'-dimethoxychalcone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.9474 94.74%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6990 69.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9503 95.03%
OATP1B3 inhibitior + 0.9648 96.48%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.7845 78.45%
P-glycoprotein inhibitior + 0.7406 74.06%
P-glycoprotein substrate - 0.9341 93.41%
CYP3A4 substrate - 0.5342 53.42%
CYP2C9 substrate - 0.5915 59.15%
CYP2D6 substrate - 0.8174 81.74%
CYP3A4 inhibition + 0.9504 95.04%
CYP2C9 inhibition + 0.9116 91.16%
CYP2C19 inhibition + 0.9682 96.82%
CYP2D6 inhibition + 0.9027 90.27%
CYP1A2 inhibition - 0.5739 57.39%
CYP2C8 inhibition - 0.5922 59.22%
CYP inhibitory promiscuity + 0.9594 95.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.3693 36.93%
Eye corrosion - 0.9753 97.53%
Eye irritation - 0.5774 57.74%
Skin irritation - 0.7261 72.61%
Skin corrosion - 0.9682 96.82%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3872 38.72%
Micronuclear + 0.7774 77.74%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.5910 59.10%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.5651 56.51%
Acute Oral Toxicity (c) III 0.4779 47.79%
Estrogen receptor binding + 0.8838 88.38%
Androgen receptor binding + 0.8762 87.62%
Thyroid receptor binding + 0.6359 63.59%
Glucocorticoid receptor binding + 0.7459 74.59%
Aromatase binding + 0.5677 56.77%
PPAR gamma + 0.6617 66.17%
Honey bee toxicity - 0.9040 90.40%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9857 98.57%

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 98.15% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.15% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.77% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.65% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.48% 96.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 93.73% 94.80%
CHEMBL4208 P20618 Proteasome component C5 93.48% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.32% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.98% 94.45%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.83% 92.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.68% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.32% 99.17%
CHEMBL2535 P11166 Glucose transporter 85.71% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.86% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.02% 97.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.12% 97.36%

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.
Millettia erythrocalyx

Cross-Links

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PubChem 5319619
NPASS NPC296575
LOTUS LTS0171301
wikiData Q76303565