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

Details

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Internal ID e15b3dfe-6a18-451d-a394-a7c9925bd9eb
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides
IUPAC Name 5-hydroxy-7-methoxy-2-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one
SMILES (Canonical) COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)OC)O
InChI InChI=1S/C23H24O11/c1-30-11-6-12(25)19-13(26)8-15(32-17(19)7-11)10-3-4-14(16(5-10)31-2)33-23-22(29)21(28)20(27)18(9-24)34-23/h3-8,18,20-25,27-29H,9H2,1-2H3/t18-,20-,21+,22-,23-/m1/s1
InChI Key AOEMDACKQKXTER-DODNOZFWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H24O11
Molecular Weight 476.40 g/mol
Exact Mass 476.13186158 g/mol
Topological Polar Surface Area (TPSA) 164.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.36
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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Flavoyadorinin B
SCHEMBL31675250
BDBM50558209

2D Structure

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2D Structure of 5-hydroxy-7-methoxy-2-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-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 - 0.8346 83.46%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6238 62.38%
OATP2B1 inhibitior - 0.7033 70.33%
OATP1B1 inhibitior + 0.8973 89.73%
OATP1B3 inhibitior + 0.9678 96.78%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.6423 64.23%
P-glycoprotein inhibitior + 0.5891 58.91%
P-glycoprotein substrate - 0.6267 62.67%
CYP3A4 substrate + 0.5758 57.58%
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 + 0.7686 76.86%
CYP inhibitory promiscuity - 0.7195 71.95%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7238 72.38%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.9381 93.81%
Skin irritation - 0.8305 83.05%
Skin corrosion - 0.9609 96.09%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5100 51.00%
Micronuclear + 0.6733 67.33%
Hepatotoxicity - 0.8500 85.00%
skin sensitisation - 0.9389 93.89%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.8301 83.01%
Acute Oral Toxicity (c) III 0.6799 67.99%
Estrogen receptor binding + 0.7906 79.06%
Androgen receptor binding + 0.6227 62.27%
Thyroid receptor binding + 0.5630 56.30%
Glucocorticoid receptor binding + 0.6703 67.03%
Aromatase binding + 0.5721 57.21%
PPAR gamma + 0.7443 74.43%
Honey bee toxicity - 0.7389 73.89%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7349 73.49%
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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.45% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.48% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.95% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.71% 98.95%
CHEMBL220 P22303 Acetylcholinesterase 94.71% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.44% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 92.98% 86.92%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.76% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.49% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.28% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.22% 86.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.59% 96.21%
CHEMBL3194 P02766 Transthyretin 88.49% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.36% 99.17%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 87.22% 95.78%
CHEMBL3401 O75469 Pregnane X receptor 86.82% 94.73%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.18% 97.36%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.03% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.37% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.77% 95.50%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.15% 90.71%

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.
Viscum coloratum

Cross-Links

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PubChem 14376376
LOTUS LTS0225923
wikiData Q104915581