Glc(b1-4)[coumaroyl(3-OMe)(-6)]2-deoxy-D-araHex(b1-2b)Fruf

Details

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Internal ID e3c09a5d-08d8-4db0-94eb-18147baf1110
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides
IUPAC Name [(2R,3S,4R,6S)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H40O18/c1-40-15-6-12(2-4-13(15)32)3-5-19(34)41-10-18-25(44-27-24(38)23(37)21(35)16(8-29)43-27)14(33)7-20(42-18)46-28(11-31)26(39)22(36)17(9-30)45-28/h2-6,14,16-18,20-27,29-33,35-39H,7-11H2,1H3/b5-3+/t14-,16-,17-,18-,20+,21-,22-,23+,24-,25+,26+,27+,28+/m1/s1
InChI Key UBJZMZSYAYPPPD-OEYWCBMQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H40O18
Molecular Weight 664.60 g/mol
Exact Mass 664.22146442 g/mol
Topological Polar Surface Area (TPSA) 284.00 Ų
XlogP -2.80
Atomic LogP (AlogP) -4.56
H-Bond Acceptor 18
H-Bond Donor 10
Rotatable Bonds 12

Synonyms

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GlyTouCan:G18730WV
G18730WV

2D Structure

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2D Structure of Glc(b1-4)[coumaroyl(3-OMe)(-6)]2-deoxy-D-araHex(b1-2b)Fruf

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6826 68.26%
Caco-2 - 0.9093 90.93%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.9143 91.43%
Subcellular localzation Mitochondria 0.7060 70.60%
OATP2B1 inhibitior - 0.8634 86.34%
OATP1B1 inhibitior + 0.8555 85.55%
OATP1B3 inhibitior + 0.9648 96.48%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8169 81.69%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.5211 52.11%
CYP3A4 substrate + 0.6805 68.05%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.8518 85.18%
CYP3A4 inhibition - 0.8354 83.54%
CYP2C9 inhibition - 0.8908 89.08%
CYP2C19 inhibition - 0.8399 83.99%
CYP2D6 inhibition - 0.8834 88.34%
CYP1A2 inhibition - 0.8989 89.89%
CYP2C8 inhibition + 0.6967 69.67%
CYP inhibitory promiscuity - 0.7740 77.40%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6296 62.96%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9330 93.30%
Skin irritation - 0.8202 82.02%
Skin corrosion - 0.9523 95.23%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7755 77.55%
Micronuclear - 0.6226 62.26%
Hepatotoxicity - 0.8591 85.91%
skin sensitisation - 0.8078 80.78%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.9205 92.05%
Acute Oral Toxicity (c) III 0.7161 71.61%
Estrogen receptor binding + 0.7874 78.74%
Androgen receptor binding + 0.6047 60.47%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.4800 48.00%
Aromatase binding + 0.5803 58.03%
PPAR gamma + 0.7017 70.17%
Honey bee toxicity - 0.7101 71.01%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.7235 72.35%

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 99.61% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 97.93% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.78% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.37% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.81% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.81% 95.56%
CHEMBL4208 P20618 Proteasome component C5 90.50% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.76% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.35% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.23% 97.09%
CHEMBL3194 P02766 Transthyretin 86.98% 90.71%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.26% 86.92%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 85.76% 95.83%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.67% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.38% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.13% 92.94%
CHEMBL3401 O75469 Pregnane X receptor 83.56% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.59% 92.62%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.86% 96.61%
CHEMBL226 P30542 Adenosine A1 receptor 81.35% 95.93%
CHEMBL1951 P21397 Monoamine oxidase A 80.66% 91.49%
CHEMBL5028 O14672 ADAM10 80.64% 97.50%
CHEMBL5255 O00206 Toll-like receptor 4 80.22% 92.50%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.16% 96.90%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.01% 100.00%

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.
Polygala arillata

Cross-Links

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PubChem 6325725
NPASS NPC82478