(3R)-5-hydroxy-3-[4-hydroxy-2-methoxy-5-(3-methylbut-2-enyl)phenyl]-7-methoxy-2,3-dihydrochromen-4-one

Details

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Internal ID d201ff1a-2748-4e02-8b0b-209e85599995
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavans > Isoflavanones > 3-prenylated isoflavanones
IUPAC Name (3R)-5-hydroxy-3-[4-hydroxy-2-methoxy-5-(3-methylbut-2-enyl)phenyl]-7-methoxy-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H24O6/c1-12(2)5-6-13-7-15(19(27-4)10-17(13)23)16-11-28-20-9-14(26-3)8-18(24)21(20)22(16)25/h5,7-10,16,23-24H,6,11H2,1-4H3/t16-/m0/s1
InChI Key RGXQEROHDTYEQG-INIZCTEOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H24O6
Molecular Weight 384.40 g/mol
Exact Mass 384.15728848 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 4.80
Atomic LogP (AlogP) 3.98
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R)-5-hydroxy-3-[4-hydroxy-2-methoxy-5-(3-methylbut-2-enyl)phenyl]-7-methoxy-2,3-dihydrochromen-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 + 0.9939 99.39%
Caco-2 + 0.8302 83.02%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8651 86.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9073 90.73%
OATP1B3 inhibitior + 0.8177 81.77%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7891 78.91%
P-glycoprotein inhibitior + 0.7097 70.97%
P-glycoprotein substrate - 0.7171 71.71%
CYP3A4 substrate + 0.5810 58.10%
CYP2C9 substrate + 0.5973 59.73%
CYP2D6 substrate - 0.7963 79.63%
CYP3A4 inhibition - 0.8092 80.92%
CYP2C9 inhibition + 0.8655 86.55%
CYP2C19 inhibition + 0.9542 95.42%
CYP2D6 inhibition - 0.6765 67.65%
CYP1A2 inhibition + 0.9290 92.90%
CYP2C8 inhibition - 0.5853 58.53%
CYP inhibitory promiscuity + 0.9067 90.67%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.7653 76.53%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.6522 65.22%
Skin irritation - 0.8158 81.58%
Skin corrosion - 0.9652 96.52%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7055 70.55%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8425 84.25%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.6102 61.02%
Acute Oral Toxicity (c) III 0.7271 72.71%
Estrogen receptor binding + 0.8816 88.16%
Androgen receptor binding + 0.7522 75.22%
Thyroid receptor binding + 0.6493 64.93%
Glucocorticoid receptor binding + 0.8182 81.82%
Aromatase binding - 0.5358 53.58%
PPAR gamma + 0.7836 78.36%
Honey bee toxicity - 0.7716 77.16%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9909 99.09%

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 99.71% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.29% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.57% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.12% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.96% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.70% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.83% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.19% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.09% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.26% 97.09%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 88.98% 92.68%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.49% 99.15%
CHEMBL4208 P20618 Proteasome component C5 87.59% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.34% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.76% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.53% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.74% 94.00%
CHEMBL2535 P11166 Glucose transporter 84.87% 98.75%
CHEMBL340 P08684 Cytochrome P450 3A4 84.25% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.46% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.75% 91.07%
CHEMBL3401 O75469 Pregnane X receptor 82.61% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.00% 100.00%
CHEMBL240 Q12809 HERG 81.51% 89.76%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.07% 94.80%

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.
Erythrina poeppigiana

Cross-Links

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PubChem 76764360
LOTUS LTS0149430
wikiData Q105236145