7,4/'-Di-O-methylapigenin 5-O-xylosylglucoside

Details

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Internal ID 472826e2-62ff-4a67-868a-6060a4f50083
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides
IUPAC Name 7-methoxy-2-(4-methoxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one
SMILES (Canonical) COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC
SMILES (Isomeric) COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO[C@H]5[C@@H]([C@H]([C@@H](CO5)O)O)O)O)O)O)OC
InChI InChI=1S/C28H32O14/c1-36-13-5-3-12(4-6-13)17-9-15(29)21-18(40-17)7-14(37-2)8-19(21)41-28-26(35)24(33)23(32)20(42-28)11-39-27-25(34)22(31)16(30)10-38-27/h3-9,16,20,22-28,30-35H,10-11H2,1-2H3/t16-,20-,22+,23-,24+,25-,26-,27+,28-/m1/s1
InChI Key ZTYIRUZJISZADH-AQLOEVPPSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C28H32O14
Molecular Weight 592.50 g/mol
Exact Mass 592.17920569 g/mol
Topological Polar Surface Area (TPSA) 203.00 Ų
XlogP -1.10
Atomic LogP (AlogP) -0.88
H-Bond Acceptor 14
H-Bond Donor 6
Rotatable Bonds 8

Synonyms

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7,4/'-Di-O-methylapigenin 5-O-xylosylglucoside
7-methoxy-2-(4-methoxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one
CHEMBL451605
ZTYIRUZJISZADH-AQLOEVPPSA-N
AKOS026674275
Genkwanin 4-methyl ether 5-O-beta-D-primeveroside
7-Methoxy-2-(4-methoxyphenyl)-5-[(6-O--D-xylopyranosyl--D-glucopyranosyl)oxy]-4H-1-benzopyran-4-one

2D Structure

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2D Structure of 7,4/'-Di-O-methylapigenin 5-O-xylosylglucoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4745 47.45%
Caco-2 - 0.8665 86.65%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.6806 68.06%
OATP2B1 inhibitior - 0.8468 84.68%
OATP1B1 inhibitior + 0.8489 84.89%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7584 75.84%
P-glycoprotein inhibitior - 0.5330 53.30%
P-glycoprotein substrate - 0.5709 57.09%
CYP3A4 substrate + 0.6341 63.41%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8241 82.41%
CYP3A4 inhibition - 0.9264 92.64%
CYP2C9 inhibition - 0.9559 95.59%
CYP2C19 inhibition - 0.9326 93.26%
CYP2D6 inhibition - 0.9163 91.63%
CYP1A2 inhibition - 0.9381 93.81%
CYP2C8 inhibition + 0.5221 52.21%
CYP inhibitory promiscuity - 0.8786 87.86%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6719 67.19%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9308 93.08%
Skin irritation - 0.8396 83.96%
Skin corrosion - 0.9637 96.37%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7477 74.77%
Micronuclear + 0.6074 60.74%
Hepatotoxicity - 0.8750 87.50%
skin sensitisation - 0.9280 92.80%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.9373 93.73%
Acute Oral Toxicity (c) III 0.7210 72.10%
Estrogen receptor binding + 0.8350 83.50%
Androgen receptor binding + 0.7007 70.07%
Thyroid receptor binding + 0.5189 51.89%
Glucocorticoid receptor binding + 0.6072 60.72%
Aromatase binding + 0.5381 53.81%
PPAR gamma + 0.7221 72.21%
Honey bee toxicity - 0.8039 80.39%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7349 73.49%
Fish aquatic toxicity + 0.8078 80.78%

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 99.17% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.72% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.24% 94.00%
CHEMBL220 P22303 Acetylcholinesterase 96.03% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.14% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.18% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.51% 97.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 92.05% 86.92%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.04% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.99% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.70% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.92% 96.77%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.43% 95.89%
CHEMBL1907 P15144 Aminopeptidase N 87.05% 93.31%
CHEMBL4208 P20618 Proteasome component C5 86.04% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.53% 92.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.27% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 83.25% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.84% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.09% 94.45%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 81.14% 95.83%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.08% 95.89%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 81.02% 89.23%
CHEMBL226 P30542 Adenosine A1 receptor 80.45% 95.93%

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.
Aquilaria sinensis

Cross-Links

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PubChem 21582635
NPASS NPC295613