(4R)-5-hydroxy-4-(4-hydroxyphenyl)-7-methoxy-3,4-dihydrochromen-2-one

Details

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Internal ID d4d21898-31ff-4ccc-ae53-a49e7ee8dfdd
Taxonomy Phenylpropanoids and polyketides > Neoflavonoids > Neoflavans
IUPAC Name (4R)-5-hydroxy-4-(4-hydroxyphenyl)-7-methoxy-3,4-dihydrochromen-2-one
SMILES (Canonical) COC1=CC(=C2C(CC(=O)OC2=C1)C3=CC=C(C=C3)O)O
SMILES (Isomeric) COC1=CC(=C2[C@H](CC(=O)OC2=C1)C3=CC=C(C=C3)O)O
InChI InChI=1S/C16H14O5/c1-20-11-6-13(18)16-12(8-15(19)21-14(16)7-11)9-2-4-10(17)5-3-9/h2-7,12,17-18H,8H2,1H3/t12-/m1/s1
InChI Key FWKRAEMBDHKHAF-GFCCVEGCSA-N
Popularity 0 references 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-hydroxy-4-(4-hydroxyphenyl)-7-methoxy-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 + 0.9619 96.19%
Caco-2 + 0.5106 51.06%
Blood Brain Barrier - 0.9500 95.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8341 83.41%
OATP2B1 inhibitior - 0.7263 72.63%
OATP1B1 inhibitior + 0.8781 87.81%
OATP1B3 inhibitior + 0.9841 98.41%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.8125 81.25%
P-glycoprotein substrate - 0.9446 94.46%
CYP3A4 substrate + 0.5195 51.95%
CYP2C9 substrate + 0.5975 59.75%
CYP2D6 substrate - 0.6803 68.03%
CYP3A4 inhibition - 0.6888 68.88%
CYP2C9 inhibition + 0.9088 90.88%
CYP2C19 inhibition + 0.7527 75.27%
CYP2D6 inhibition - 0.6595 65.95%
CYP1A2 inhibition + 0.7849 78.49%
CYP2C8 inhibition - 0.5572 55.72%
CYP inhibitory promiscuity + 0.5636 56.36%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.4976 49.76%
Eye corrosion - 0.9816 98.16%
Eye irritation + 0.7803 78.03%
Skin irritation - 0.7051 70.51%
Skin corrosion - 0.9674 96.74%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7955 79.55%
Micronuclear + 0.8359 83.59%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.9641 96.41%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6325 63.25%
Acute Oral Toxicity (c) III 0.4189 41.89%
Estrogen receptor binding + 0.5491 54.91%
Androgen receptor binding + 0.7996 79.96%
Thyroid receptor binding + 0.5964 59.64%
Glucocorticoid receptor binding + 0.8112 81.12%
Aromatase binding - 0.5281 52.81%
PPAR gamma + 0.7305 73.05%
Honey bee toxicity - 0.9039 90.39%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8230 82.30%

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 98.88% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.44% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.65% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.41% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.91% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 92.68% 83.82%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.17% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.31% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.85% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.39% 94.45%
CHEMBL4208 P20618 Proteasome component C5 88.18% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.68% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.43% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.72% 99.23%
CHEMBL2535 P11166 Glucose transporter 84.22% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.67% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.52% 89.00%

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 71533321
NPASS NPC61079
LOTUS LTS0079342
wikiData Q105003338