(4R)-5,7-dihydroxy-4-(4-methoxyphenyl)-3,4-dihydrochromen-2-one

Details

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Internal ID 6e207bb6-4da3-458f-b3fc-8a8ff6fa890d
Taxonomy Phenylpropanoids and polyketides > Neoflavonoids > Neoflavans
IUPAC Name (4R)-5,7-dihydroxy-4-(4-methoxyphenyl)-3,4-dihydrochromen-2-one
SMILES (Canonical) COC1=CC=C(C=C1)C2CC(=O)OC3=CC(=CC(=C23)O)O
SMILES (Isomeric) COC1=CC=C(C=C1)[C@H]2CC(=O)OC3=CC(=CC(=C23)O)O
InChI InChI=1S/C16H14O5/c1-20-11-4-2-9(3-5-11)12-8-15(19)21-14-7-10(17)6-13(18)16(12)14/h2-7,12,17-18H,8H2,1H3/t12-/m1/s1
InChI Key OKBWVJGQTFYYQA-GFCCVEGCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H14O5
Molecular Weight 286.28 g/mol
Exact Mass 286.08412354 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.55
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R)-5,7-dihydroxy-4-(4-methoxyphenyl)-3,4-dihydrochromen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9175 91.75%
Caco-2 + 0.6423 64.23%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.7653 76.53%
OATP2B1 inhibitior - 0.7283 72.83%
OATP1B1 inhibitior + 0.9139 91.39%
OATP1B3 inhibitior + 0.9633 96.33%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5163 51.63%
P-glycoprotein inhibitior - 0.8759 87.59%
P-glycoprotein substrate - 0.9570 95.70%
CYP3A4 substrate + 0.5474 54.74%
CYP2C9 substrate + 0.5975 59.75%
CYP2D6 substrate - 0.6803 68.03%
CYP3A4 inhibition + 0.7145 71.45%
CYP2C9 inhibition + 0.8464 84.64%
CYP2C19 inhibition + 0.7522 75.22%
CYP2D6 inhibition - 0.5284 52.84%
CYP1A2 inhibition + 0.7825 78.25%
CYP2C8 inhibition - 0.5766 57.66%
CYP inhibitory promiscuity + 0.6696 66.96%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5459 54.59%
Eye corrosion - 0.9832 98.32%
Eye irritation + 0.7478 74.78%
Skin irritation - 0.7038 70.38%
Skin corrosion - 0.9498 94.98%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6495 64.95%
Micronuclear + 0.8159 81.59%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.9520 95.20%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6377 63.77%
Acute Oral Toxicity (c) III 0.4975 49.75%
Estrogen receptor binding + 0.6711 67.11%
Androgen receptor binding + 0.7717 77.17%
Thyroid receptor binding + 0.6494 64.94%
Glucocorticoid receptor binding + 0.8645 86.45%
Aromatase binding + 0.6802 68.02%
PPAR gamma + 0.7330 73.30%
Honey bee toxicity - 0.9141 91.41%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.7858 78.58%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.24% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.77% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.66% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.89% 97.09%
CHEMBL4208 P20618 Proteasome component C5 93.17% 90.00%
CHEMBL2581 P07339 Cathepsin D 92.55% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.49% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.26% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.36% 99.17%
CHEMBL1929 P47989 Xanthine dehydrogenase 86.87% 96.12%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.57% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.36% 95.89%
CHEMBL2535 P11166 Glucose transporter 85.29% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.99% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.98% 94.45%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.36% 93.99%
CHEMBL1907 P15144 Aminopeptidase N 83.28% 93.31%
CHEMBL4040 P28482 MAP kinase ERK2 82.83% 83.82%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.50% 92.94%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.27% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.63% 92.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.60% 85.14%

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.
Polygonum perfoliatum

Cross-Links

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PubChem 25768654
NPASS NPC216687
LOTUS LTS0079889
wikiData Q105193460