(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-methoxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

Details

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Internal ID 4c9b9a35-9393-4bf8-84f9-8dbc96f535b4
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 8-prenylated flavans > 8-prenylated flavanones
IUPAC Name (2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-methoxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H24O6/c1-12(2)5-7-14-20(27-4)11-17(25)21-16(24)10-19(28-22(14)21)13-6-8-18(26-3)15(23)9-13/h5-6,8-9,11,19,23,25H,7,10H2,1-4H3/t19-/m0/s1
InChI Key JXAZZATUCPCXKO-IBGZPJMESA-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 4.60
Atomic LogP (AlogP) 4.33
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 (2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-methoxy-8-(3-methylbut-2-enyl)-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 + 0.9808 98.08%
Caco-2 + 0.8587 85.87%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7180 71.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8992 89.92%
OATP1B3 inhibitior + 0.9222 92.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8040 80.40%
P-glycoprotein inhibitior + 0.7387 73.87%
P-glycoprotein substrate - 0.7838 78.38%
CYP3A4 substrate + 0.5797 57.97%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7912 79.12%
CYP3A4 inhibition - 0.7872 78.72%
CYP2C9 inhibition + 0.8649 86.49%
CYP2C19 inhibition + 0.9192 91.92%
CYP2D6 inhibition + 0.5690 56.90%
CYP1A2 inhibition + 0.7470 74.70%
CYP2C8 inhibition - 0.6035 60.35%
CYP inhibitory promiscuity + 0.8959 89.59%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6590 65.90%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.7389 73.89%
Skin irritation - 0.7752 77.52%
Skin corrosion - 0.9579 95.79%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4119 41.19%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8313 83.13%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.5818 58.18%
Acute Oral Toxicity (c) III 0.5743 57.43%
Estrogen receptor binding + 0.8720 87.20%
Androgen receptor binding + 0.6290 62.90%
Thyroid receptor binding + 0.5580 55.80%
Glucocorticoid receptor binding + 0.8044 80.44%
Aromatase binding - 0.5589 55.89%
PPAR gamma + 0.8295 82.95%
Honey bee toxicity - 0.7476 74.76%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9787 97.87%

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 98.40% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.10% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.05% 94.45%
CHEMBL2581 P07339 Cathepsin D 92.49% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.21% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.85% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.31% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 89.37% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.77% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.81% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.61% 94.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 87.37% 96.12%
CHEMBL3401 O75469 Pregnane X receptor 86.72% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.68% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.64% 89.00%
CHEMBL4208 P20618 Proteasome component C5 83.58% 90.00%
CHEMBL2535 P11166 Glucose transporter 82.27% 98.75%
CHEMBL3194 P02766 Transthyretin 80.33% 90.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.23% 92.62%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.20% 96.95%

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.
Glycosmis craibii

Cross-Links

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PubChem 101480800
LOTUS LTS0255864
wikiData Q105136492