7-(alpha-L-Arabinofuranosyloxy)-4',5-dihydroxy-3-(2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyloxy)flavone

Details

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Internal ID f42657ef-e2b0-4780-aa92-259e6938d73e
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 7-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one
SMILES (Canonical) C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)O
SMILES (Isomeric) C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O[C@H]4[C@@H]([C@H]([C@@H](O4)CO)O)O)O)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)O
InChI InChI=1S/C32H38O20/c33-7-15-19(38)23(42)26(45)31(49-15)52-29-24(43)20(39)16(8-34)50-32(29)51-28-22(41)18-13(37)5-12(46-30-25(44)21(40)17(9-35)48-30)6-14(18)47-27(28)10-1-3-11(36)4-2-10/h1-6,15-17,19-21,23-26,29-40,42-45H,7-9H2/t15-,16-,17+,19-,20-,21+,23+,24+,25-,26-,29-,30-,31+,32+/m1/s1
InChI Key CMTMRXGGKFFOGD-ZNKZOFPESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H38O20
Molecular Weight 742.60 g/mol
Exact Mass 742.19564360 g/mol
Topological Polar Surface Area (TPSA) 324.00 Ų
XlogP -2.10
Atomic LogP (AlogP) -4.31
H-Bond Acceptor 20
H-Bond Donor 12
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(alpha-L-Arabinofuranosyloxy)-4',5-dihydroxy-3-(2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyloxy)flavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5737 57.37%
Caco-2 - 0.9169 91.69%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.6767 67.67%
OATP2B1 inhibitior - 0.7057 70.57%
OATP1B1 inhibitior + 0.9271 92.71%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.7424 74.24%
P-glycoprotein inhibitior - 0.4455 44.55%
P-glycoprotein substrate - 0.7066 70.66%
CYP3A4 substrate + 0.6434 64.34%
CYP2C9 substrate - 0.6762 67.62%
CYP2D6 substrate - 0.8575 85.75%
CYP3A4 inhibition - 0.8613 86.13%
CYP2C9 inhibition - 0.8849 88.49%
CYP2C19 inhibition - 0.8109 81.09%
CYP2D6 inhibition - 0.9082 90.82%
CYP1A2 inhibition - 0.8791 87.91%
CYP2C8 inhibition + 0.7778 77.78%
CYP inhibitory promiscuity - 0.5669 56.69%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6086 60.86%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.8967 89.67%
Skin irritation - 0.8230 82.30%
Skin corrosion - 0.9614 96.14%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7437 74.37%
Micronuclear + 0.6733 67.33%
Hepatotoxicity - 0.7446 74.46%
skin sensitisation - 0.8881 88.81%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7921 79.21%
Acute Oral Toxicity (c) III 0.5291 52.91%
Estrogen receptor binding + 0.7974 79.74%
Androgen receptor binding + 0.6704 67.04%
Thyroid receptor binding - 0.5101 51.01%
Glucocorticoid receptor binding - 0.6786 67.86%
Aromatase binding + 0.5450 54.50%
PPAR gamma + 0.7624 76.24%
Honey bee toxicity - 0.6886 68.86%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5450 54.50%
Fish aquatic toxicity + 0.8457 84.57%

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 99.34% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.82% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.58% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 95.05% 91.49%
CHEMBL2581 P07339 Cathepsin D 95.00% 98.95%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 93.17% 95.64%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.76% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 90.15% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.94% 94.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.76% 86.92%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 88.14% 95.78%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.92% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.06% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.69% 97.09%
CHEMBL3194 P02766 Transthyretin 85.19% 90.71%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.73% 85.14%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.09% 96.21%
CHEMBL242 Q92731 Estrogen receptor beta 83.84% 98.35%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.90% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.70% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.50% 95.89%

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.
Centaurea spinosa
Pyrrosia serpens

Cross-Links

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PubChem 15730574
NPASS NPC27262
LOTUS LTS0101811
wikiData Q104965133