6-[(2R,3S,4R,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

Details

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Internal ID f569c0fd-4e9a-493e-8d54-ee4cd90ca85c
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid C-glycosides
IUPAC Name 6-[(2R,3S,4R,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H30O14/c1-9-19(32)22(35)23(36)27(38-9)41-26-20(33)16(8-28)40-25(24(26)37)18-13(31)7-15-17(21(18)34)12(30)6-14(39-15)10-2-4-11(29)5-3-10/h2-7,9,16,19-20,22-29,31-37H,8H2,1H3/t9-,16+,19-,20+,22+,23+,24-,25+,26-,27+/m0/s1
InChI Key ZEPMWGWBBATJGD-KBVHLOSJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H30O14
Molecular Weight 578.50 g/mol
Exact Mass 578.16355563 g/mol
Topological Polar Surface Area (TPSA) 236.00 Ų
XlogP -0.90
Atomic LogP (AlogP) -1.06
H-Bond Acceptor 14
H-Bond Donor 9
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-[(2R,3S,4R,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)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 + 0.7280 72.80%
Caco-2 - 0.9215 92.15%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.6994 69.94%
OATP2B1 inhibitior - 0.5591 55.91%
OATP1B1 inhibitior + 0.8527 85.27%
OATP1B3 inhibitior + 0.8790 87.90%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7030 70.30%
P-glycoprotein inhibitior - 0.6865 68.65%
P-glycoprotein substrate - 0.5796 57.96%
CYP3A4 substrate + 0.6492 64.92%
CYP2C9 substrate - 0.6795 67.95%
CYP2D6 substrate - 0.8609 86.09%
CYP3A4 inhibition - 0.9318 93.18%
CYP2C9 inhibition - 0.9336 93.36%
CYP2C19 inhibition - 0.9282 92.82%
CYP2D6 inhibition - 0.9765 97.65%
CYP1A2 inhibition - 0.8799 87.99%
CYP2C8 inhibition + 0.7622 76.22%
CYP inhibitory promiscuity - 0.7359 73.59%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7206 72.06%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9141 91.41%
Skin irritation - 0.8137 81.37%
Skin corrosion - 0.9622 96.22%
Ames mutagenesis - 0.5037 50.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5215 52.15%
Micronuclear + 0.6633 66.33%
Hepatotoxicity - 0.8500 85.00%
skin sensitisation - 0.9085 90.85%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.8941 89.41%
Acute Oral Toxicity (c) III 0.5898 58.98%
Estrogen receptor binding + 0.7577 75.77%
Androgen receptor binding + 0.7193 71.93%
Thyroid receptor binding + 0.5590 55.90%
Glucocorticoid receptor binding + 0.5969 59.69%
Aromatase binding + 0.6058 60.58%
PPAR gamma + 0.7686 76.86%
Honey bee toxicity - 0.6804 68.04%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8193 81.93%

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 99.68% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.49% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.08% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.41% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.82% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 93.95% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.60% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 90.22% 94.73%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 89.19% 83.57%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.66% 86.92%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.18% 99.15%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 86.89% 96.21%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.43% 91.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.34% 90.71%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.48% 97.36%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.14% 99.17%
CHEMBL3038469 P24941 CDK2/Cyclin A 80.54% 91.38%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 80.50% 95.78%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.13% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.10% 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.
Crataegus monogyna

Cross-Links

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PubChem 162943042
LOTUS LTS0202155
wikiData Q105373489