Dalpatein

Details

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Internal ID e2f6dde7-3763-4ac7-8a81-445737fd08fb
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 7-hydroxy-6-methoxy-3-(6-methoxy-1,3-benzodioxol-5-yl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H14O7/c1-21-13-6-17-16(24-8-25-17)3-9(13)11-7-23-14-5-12(19)15(22-2)4-10(14)18(11)20/h3-7,19H,8H2,1-2H3
InChI Key GYUPEJCNVAKZSU-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C18H14O7
Molecular Weight 342.30 g/mol
Exact Mass 342.07395278 g/mol
Topological Polar Surface Area (TPSA) 83.50 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.91
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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CHEBI:55549
DTXSID901142115
LMPK12050124
40009-88-9
6,2'-dimethoxy-4',5'-methylenedioxyisoflavone
Q27124364
7-Hydroxy-6,2'-dimethoxy-4',5'-methylenedioxyisoflavone
7-hydroxy-6-methoxy-3-(6-methoxy-1,3-benzodioxol-5-yl)-4H-chromen-4-one
7-hydroxy-6-methoxy-3-(6-methoxy-1,3-benzodioxol-5-yl)chromen-4-one
7-Hydroxy-6-methoxy-3-(6-methoxy-1,3-benzodioxol-5-yl)-4H-1-benzopyran-4-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Dalpatein

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9794 97.94%
Caco-2 + 0.8458 84.58%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8101 81.01%
OATP2B1 inhibitior - 0.8676 86.76%
OATP1B1 inhibitior + 0.9481 94.81%
OATP1B3 inhibitior + 0.9172 91.72%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6195 61.95%
P-glycoprotein inhibitior + 0.7013 70.13%
P-glycoprotein substrate - 0.8816 88.16%
CYP3A4 substrate + 0.5634 56.34%
CYP2C9 substrate - 0.8253 82.53%
CYP2D6 substrate - 0.8058 80.58%
CYP3A4 inhibition + 0.8906 89.06%
CYP2C9 inhibition + 0.8811 88.11%
CYP2C19 inhibition + 0.8944 89.44%
CYP2D6 inhibition + 0.6487 64.87%
CYP1A2 inhibition - 0.7054 70.54%
CYP2C8 inhibition - 0.7569 75.69%
CYP inhibitory promiscuity + 0.8415 84.15%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4819 48.19%
Eye corrosion - 0.9842 98.42%
Eye irritation + 0.5619 56.19%
Skin irritation - 0.7505 75.05%
Skin corrosion - 0.9683 96.83%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6651 66.51%
Micronuclear + 0.8674 86.74%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8088 80.88%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.4891 48.91%
Acute Oral Toxicity (c) III 0.5795 57.95%
Estrogen receptor binding + 0.9543 95.43%
Androgen receptor binding + 0.7033 70.33%
Thyroid receptor binding + 0.6367 63.67%
Glucocorticoid receptor binding + 0.8831 88.31%
Aromatase binding + 0.7969 79.69%
PPAR gamma + 0.7802 78.02%
Honey bee toxicity - 0.8518 85.18%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5649 56.49%
Fish aquatic toxicity + 0.9243 92.43%

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 99.47% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.49% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.87% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.68% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.21% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.73% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.66% 85.14%
CHEMBL2535 P11166 Glucose transporter 89.11% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.95% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.80% 99.23%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 87.57% 82.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.11% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.67% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.37% 89.62%

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.
Dalbergia lanceolaria subsp. paniculata
Piscidia piscipula

Cross-Links

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PubChem 25203443
LOTUS LTS0251816
wikiData Q27124364