Predurmillone

Details

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Internal ID db751a9a-07cd-4414-99c6-3d21ca1aadba
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 3-(1,3-benzodioxol-5-yl)-7-hydroxy-6-methoxy-8-(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical) CC(=CCC1=C2C(=CC(=C1O)OC)C(=O)C(=CO2)C3=CC4=C(C=C3)OCO4)C
SMILES (Isomeric) CC(=CCC1=C2C(=CC(=C1O)OC)C(=O)C(=CO2)C3=CC4=C(C=C3)OCO4)C
InChI InChI=1S/C22H20O6/c1-12(2)4-6-14-21(24)19(25-3)9-15-20(23)16(10-26-22(14)15)13-5-7-17-18(8-13)28-11-27-17/h4-5,7-10,24H,6,11H2,1-3H3
InChI Key KICUOVOMFAGNLF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H20O6
Molecular Weight 380.40 g/mol
Exact Mass 380.12598835 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.41
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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7-Hydroxy-6-methoxy-3',4'-methylenedioxy-8-prenylisoflavone
LMPK12050110

2D Structure

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2D Structure of Predurmillone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.6472 64.72%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7860 78.60%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.8945 89.45%
OATP1B3 inhibitior + 0.8921 89.21%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7711 77.11%
P-glycoprotein inhibitior + 0.8696 86.96%
P-glycoprotein substrate - 0.7428 74.28%
CYP3A4 substrate + 0.6107 61.07%
CYP2C9 substrate - 0.8149 81.49%
CYP2D6 substrate - 0.7934 79.34%
CYP3A4 inhibition + 0.7918 79.18%
CYP2C9 inhibition + 0.8272 82.72%
CYP2C19 inhibition + 0.9193 91.93%
CYP2D6 inhibition - 0.6934 69.34%
CYP1A2 inhibition - 0.5427 54.27%
CYP2C8 inhibition + 0.5618 56.18%
CYP inhibitory promiscuity + 0.8911 89.11%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6163 61.63%
Eye corrosion - 0.9875 98.75%
Eye irritation - 0.6116 61.16%
Skin irritation - 0.7750 77.50%
Skin corrosion - 0.9530 95.30%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4630 46.30%
Micronuclear + 0.5774 57.74%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.7731 77.31%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6563 65.63%
Acute Oral Toxicity (c) III 0.5273 52.73%
Estrogen receptor binding + 0.9694 96.94%
Androgen receptor binding + 0.8090 80.90%
Thyroid receptor binding + 0.6761 67.61%
Glucocorticoid receptor binding + 0.8813 88.13%
Aromatase binding + 0.7410 74.10%
PPAR gamma + 0.9044 90.44%
Honey bee toxicity - 0.7658 76.58%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9923 99.23%

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 99.48% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.63% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.46% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.38% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.77% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.39% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 93.14% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.00% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.48% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 91.08% 94.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.28% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.19% 95.56%
CHEMBL3922 P50579 Methionine aminopeptidase 2 86.19% 97.28%
CHEMBL3401 O75469 Pregnane X receptor 86.08% 94.73%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 85.89% 92.38%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.86% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.85% 95.89%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 83.28% 95.78%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.67% 100.00%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.05% 89.50%

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.
Millettia ferruginea

Cross-Links

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PubChem 14730815
LOTUS LTS0207302
wikiData Q105141450