5,6-Dimethoxy-3-(6-methoxy-1,3-benzodioxol-5-yl)-8,8-dimethylpyrano[2,3-h]chromen-4-one

Details

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Internal ID 756fda46-5a3b-4a8c-bae5-3da7b678e851
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Pyranoisoflavonoids
IUPAC Name 5,6-dimethoxy-3-(6-methoxy-1,3-benzodioxol-5-yl)-8,8-dimethylpyrano[2,3-h]chromen-4-one
SMILES (Canonical) CC1(C=CC2=C3C(=C(C(=C2O1)OC)OC)C(=O)C(=CO3)C4=CC5=C(C=C4OC)OCO5)C
SMILES (Isomeric) CC1(C=CC2=C3C(=C(C(=C2O1)OC)OC)C(=O)C(=CO3)C4=CC5=C(C=C4OC)OCO5)C
InChI InChI=1S/C24H22O8/c1-24(2)7-6-12-20-18(22(27-4)23(28-5)21(12)32-24)19(25)14(10-29-20)13-8-16-17(31-11-30-16)9-15(13)26-3/h6-10H,11H2,1-5H3
InChI Key URZMTISBMITCOL-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H22O8
Molecular Weight 438.40 g/mol
Exact Mass 438.13146766 g/mol
Topological Polar Surface Area (TPSA) 81.70 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.40
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,6-Dimethoxy-3-(6-methoxy-1,3-benzodioxol-5-yl)-8,8-dimethylpyrano[2,3-h]chromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9897 98.97%
Caco-2 + 0.7510 75.10%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7730 77.30%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9248 92.48%
OATP1B3 inhibitior + 0.9564 95.64%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9632 96.32%
P-glycoprotein inhibitior + 0.9324 93.24%
P-glycoprotein substrate - 0.6982 69.82%
CYP3A4 substrate + 0.6428 64.28%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8223 82.23%
CYP3A4 inhibition + 0.9676 96.76%
CYP2C9 inhibition + 0.6848 68.48%
CYP2C19 inhibition + 0.9288 92.88%
CYP2D6 inhibition + 0.5597 55.97%
CYP1A2 inhibition - 0.6490 64.90%
CYP2C8 inhibition + 0.4599 45.99%
CYP inhibitory promiscuity + 0.9229 92.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Danger 0.4045 40.45%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.6823 68.23%
Skin irritation - 0.8041 80.41%
Skin corrosion - 0.9558 95.58%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8194 81.94%
Micronuclear + 0.6774 67.74%
Hepatotoxicity + 0.5426 54.26%
skin sensitisation - 0.7215 72.15%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.6106 61.06%
Acute Oral Toxicity (c) III 0.5168 51.68%
Estrogen receptor binding + 0.9195 91.95%
Androgen receptor binding + 0.6277 62.77%
Thyroid receptor binding + 0.8193 81.93%
Glucocorticoid receptor binding + 0.8767 87.67%
Aromatase binding + 0.6666 66.66%
PPAR gamma + 0.8436 84.36%
Honey bee toxicity - 0.7010 70.10%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9858 98.58%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 99.14% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.57% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.08% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.13% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.90% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.56% 94.00%
CHEMBL2535 P11166 Glucose transporter 91.53% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.40% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.10% 92.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.77% 97.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.51% 94.45%
CHEMBL4302 P08183 P-glycoprotein 1 87.17% 92.98%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 87.15% 80.96%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.08% 94.80%
CHEMBL4208 P20618 Proteasome component C5 86.85% 90.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.23% 93.99%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.45% 95.71%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 82.51% 82.67%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.83% 95.89%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.47% 96.67%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.02% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 80.92% 94.75%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 80.89% 96.09%

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 conraui

Cross-Links

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PubChem 10789149
LOTUS LTS0066763
wikiData Q105278087