3'-(beta-D-Xylopyranosyloxy)-7-(beta-D-glucopyranosyloxy)-4',5-dihydroxyflavone

Details

Top
Internal ID aff8af01-e5f4-452a-9ac1-723f4bccd83c
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 5-hydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
SMILES (Canonical) C1C(C(C(C(O1)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O
SMILES (Isomeric) C1[C@H]([C@@H]([C@H]([C@@H](O1)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)O)O)O)O)O
InChI InChI=1S/C26H28O15/c27-7-18-21(33)22(34)24(36)26(41-18)38-10-4-12(29)19-13(30)6-15(39-17(19)5-10)9-1-2-11(28)16(3-9)40-25-23(35)20(32)14(31)8-37-25/h1-6,14,18,20-29,31-36H,7-8H2/t14-,18-,20+,21-,22+,23-,24-,25+,26-/m1/s1
InChI Key ZSSZPKPFVYSJBE-VVLSUMKGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C26H28O15
Molecular Weight 580.50 g/mol
Exact Mass 580.14282018 g/mol
Topological Polar Surface Area (TPSA) 245.00 Ų
XlogP -1.20
Atomic LogP (AlogP) -2.13
H-Bond Acceptor 15
H-Bond Donor 9
Rotatable Bonds 6

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3'-(beta-D-Xylopyranosyloxy)-7-(beta-D-glucopyranosyloxy)-4',5-dihydroxyflavone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5110 51.10%
Caco-2 - 0.9286 92.86%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.4988 49.88%
OATP2B1 inhibitior - 0.5477 54.77%
OATP1B1 inhibitior + 0.9413 94.13%
OATP1B3 inhibitior + 0.9174 91.74%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.4540 45.40%
P-glycoprotein inhibitior - 0.5477 54.77%
P-glycoprotein substrate - 0.6410 64.10%
CYP3A4 substrate + 0.6130 61.30%
CYP2C9 substrate - 0.6762 67.62%
CYP2D6 substrate - 0.8575 85.75%
CYP3A4 inhibition - 0.9373 93.73%
CYP2C9 inhibition - 0.9644 96.44%
CYP2C19 inhibition - 0.9395 93.95%
CYP2D6 inhibition - 0.9332 93.32%
CYP1A2 inhibition - 0.9304 93.04%
CYP2C8 inhibition + 0.6555 65.55%
CYP inhibitory promiscuity - 0.8779 87.79%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6882 68.82%
Eye corrosion - 0.9940 99.40%
Eye irritation - 0.8797 87.97%
Skin irritation - 0.8205 82.05%
Skin corrosion - 0.9667 96.67%
Ames mutagenesis + 0.6308 63.08%
Human Ether-a-go-go-Related Gene inhibition + 0.7063 70.63%
Micronuclear + 0.6433 64.33%
Hepatotoxicity - 0.9321 93.21%
skin sensitisation - 0.9071 90.71%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.9357 93.57%
Acute Oral Toxicity (c) III 0.4508 45.08%
Estrogen receptor binding + 0.7863 78.63%
Androgen receptor binding + 0.5998 59.98%
Thyroid receptor binding - 0.4923 49.23%
Glucocorticoid receptor binding - 0.5903 59.03%
Aromatase binding + 0.5238 52.38%
PPAR gamma + 0.7788 77.88%
Honey bee toxicity - 0.6465 64.65%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6699 66.99%
Fish aquatic toxicity + 0.7253 72.53%

Targets

Top

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 99.55% 91.11%
CHEMBL220 P22303 Acetylcholinesterase 97.59% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.33% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 95.47% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 95.45% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.20% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.90% 97.09%
CHEMBL2581 P07339 Cathepsin D 93.05% 98.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 92.45% 86.92%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 91.50% 95.78%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 90.20% 96.21%
CHEMBL3194 P02766 Transthyretin 89.05% 90.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.84% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.57% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.66% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.75% 95.89%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 85.26% 95.83%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.11% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 83.92% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.07% 86.33%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 83.00% 80.33%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 82.75% 83.57%
CHEMBL4208 P20618 Proteasome component C5 81.33% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.12% 99.17%

Plants that contains it

Top
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.
Fissistigma oldhamii
Lycium chinense
Podocarpus nivalis

Cross-Links

Top
PubChem 101423611
NPASS NPC71191
LOTUS LTS0036824
wikiData Q105382692