5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

Details

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Internal ID 99cb3db0-9734-4e9a-84e6-ad6823871310
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
SMILES (Canonical) COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)OC(=C(C2=O)O[C@H]3[C@@H]([C@@H]([C@@H]([C@H](O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O
InChI InChI=1S/C23H24O12/c1-31-10-6-12(26)16-14(7-10)33-21(9-3-4-11(25)13(5-9)32-2)22(18(16)28)35-23-20(30)19(29)17(27)15(8-24)34-23/h3-7,15,17,19-20,23-27,29-30H,8H2,1-2H3/t15-,17-,19-,20-,23+/m1/s1
InChI Key NULDUMWEBSEHPR-PRMNUAKVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O12
Molecular Weight 492.40 g/mol
Exact Mass 492.12677620 g/mol
Topological Polar Surface Area (TPSA) 185.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.07
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-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 - 0.5074 50.74%
Caco-2 - 0.8482 84.82%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6238 62.38%
OATP2B1 inhibitior - 0.5559 55.59%
OATP1B1 inhibitior + 0.9237 92.37%
OATP1B3 inhibitior + 0.9678 96.78%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.4918 49.18%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.7214 72.14%
CYP3A4 substrate + 0.6191 61.91%
CYP2C9 substrate - 0.8485 84.85%
CYP2D6 substrate - 0.8501 85.01%
CYP3A4 inhibition - 0.8862 88.62%
CYP2C9 inhibition - 0.9258 92.58%
CYP2C19 inhibition - 0.9329 93.29%
CYP2D6 inhibition - 0.9457 94.57%
CYP1A2 inhibition - 0.9089 90.89%
CYP2C8 inhibition + 0.8184 81.84%
CYP inhibitory promiscuity - 0.7195 71.95%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7238 72.38%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.8433 84.33%
Skin irritation - 0.8305 83.05%
Skin corrosion - 0.9609 96.09%
Ames mutagenesis + 0.5272 52.72%
Human Ether-a-go-go-Related Gene inhibition - 0.4916 49.16%
Micronuclear + 0.6733 67.33%
Hepatotoxicity - 0.6823 68.23%
skin sensitisation - 0.9389 93.89%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.8131 81.31%
Acute Oral Toxicity (c) III 0.6799 67.99%
Estrogen receptor binding + 0.8299 82.99%
Androgen receptor binding + 0.6857 68.57%
Thyroid receptor binding - 0.5266 52.66%
Glucocorticoid receptor binding + 0.7823 78.23%
Aromatase binding + 0.5605 56.05%
PPAR gamma + 0.6558 65.58%
Honey bee toxicity - 0.8038 80.38%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6449 64.49%
Fish aquatic toxicity + 0.7522 75.22%

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 98.95% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.23% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.95% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 95.82% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.21% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.01% 89.00%
CHEMBL2581 P07339 Cathepsin D 94.19% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.34% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.53% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.06% 86.33%
CHEMBL220 P22303 Acetylcholinesterase 88.75% 94.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.47% 86.92%
CHEMBL3401 O75469 Pregnane X receptor 87.84% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.40% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.42% 97.09%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 83.94% 95.78%
CHEMBL4208 P20618 Proteasome component C5 83.56% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.06% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.68% 95.50%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.41% 96.21%

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.
Salix alba

Cross-Links

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PubChem 163042195
LOTUS LTS0231442
wikiData Q105185926