(2R)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside

Details

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Internal ID 76c6ff0c-b7a7-44a1-b9ba-e9c0baf949d0
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name (2R)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one
SMILES (Canonical) CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@@H]([C@H](O[C@H]2OC3=CC(=C4C(=O)C[C@@H](OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O
InChI InChI=1S/C27H32O14/c1-10-20(32)22(34)24(36)26(37-10)41-25-23(35)21(33)18(9-28)40-27(25)38-13-6-14(30)19-15(31)8-16(39-17(19)7-13)11-2-4-12(29)5-3-11/h2-7,10,16,18,20-30,32-36H,8-9H2,1H3/t10-,16+,18+,20-,21+,22+,23-,24+,25+,26-,27+/m0/s1
InChI Key DFPMSGMNTNDNHN-VVEPWVCASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H32O14
Molecular Weight 580.50 g/mol
Exact Mass 580.17920569 g/mol
Topological Polar Surface Area (TPSA) 225.00 Ų
XlogP -0.50
Atomic LogP (AlogP) -1.17
H-Bond Acceptor 14
H-Bond Donor 8
Rotatable Bonds 6

Synonyms

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Naringoside
(2R)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside
MFCD00148888
2R-Naringin
58001-41-5
(2R)-Naringin
BBL010483
MFCD01461988
STK801618
AKOS005614245
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (2R)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4777 47.77%
Caco-2 - 0.9102 91.02%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.9857 98.57%
Subcellular localzation Mitochondria 0.6881 68.81%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9413 94.13%
OATP1B3 inhibitior + 0.9552 95.52%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.4758 47.58%
P-glycoprotein inhibitior - 0.9165 91.65%
P-glycoprotein substrate - 0.6697 66.97%
CYP3A4 substrate + 0.6479 64.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8479 84.79%
CYP3A4 inhibition - 0.9358 93.58%
CYP2C9 inhibition - 0.9271 92.71%
CYP2C19 inhibition - 0.9330 93.30%
CYP2D6 inhibition - 0.9643 96.43%
CYP1A2 inhibition - 0.8830 88.30%
CYP2C8 inhibition + 0.4936 49.36%
CYP inhibitory promiscuity - 0.7188 71.88%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7023 70.23%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.9292 92.92%
Skin irritation - 0.8192 81.92%
Skin corrosion - 0.9626 96.26%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7001 70.01%
Micronuclear + 0.6433 64.33%
Hepatotoxicity - 0.8750 87.50%
skin sensitisation - 0.9312 93.12%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6977 69.77%
Acute Oral Toxicity (c) III 0.5734 57.34%
Estrogen receptor binding + 0.7739 77.39%
Androgen receptor binding - 0.5890 58.90%
Thyroid receptor binding + 0.5258 52.58%
Glucocorticoid receptor binding - 0.4849 48.49%
Aromatase binding + 0.5263 52.63%
PPAR gamma + 0.7120 71.20%
Honey bee toxicity - 0.6888 68.88%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5150 51.50%
Fish aquatic toxicity + 0.8289 82.89%

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 99.58% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.15% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.06% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.95% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.15% 89.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 92.44% 96.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.51% 86.33%
CHEMBL4208 P20618 Proteasome component C5 90.78% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.23% 94.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 89.62% 97.36%
CHEMBL3401 O75469 Pregnane X receptor 89.33% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.00% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.63% 95.89%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.97% 94.80%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.87% 86.92%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.20% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.27% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.12% 99.17%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 82.21% 85.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.07% 99.23%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.86% 93.10%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.66% 90.71%
CHEMBL226 P30542 Adenosine A1 receptor 80.56% 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.
Ailanthus integrifolia

Cross-Links

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PubChem 3000627
NPASS NPC243959
LOTUS LTS0147088
wikiData Q104978212