4-(4-((2,6-Bis-O-(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranosyl)oxy)phenyl)-2-butanone

Details

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Internal ID c9ceeffc-d555-4706-a44a-ffbeb6c4d5f8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name [(2R,3S,4S,5R,6S)-3,4-dihydroxy-6-[4-(3-oxobutyl)phenoxy]-5-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate
SMILES (Canonical) CC(=O)CCC1=CC=C(C=C1)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O
SMILES (Isomeric) CC(=O)CCC1=CC=C(C=C1)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O
InChI InChI=1S/C30H30O15/c1-13(31)2-3-14-4-6-17(7-5-14)43-30-27(45-29(41)16-10-20(34)24(37)21(35)11-16)26(39)25(38)22(44-30)12-42-28(40)15-8-18(32)23(36)19(33)9-15/h4-11,22,25-27,30,32-39H,2-3,12H2,1H3/t22-,25-,26+,27-,30-/m1/s1
InChI Key GLAXWGBAKGLFEU-FRLFRUAOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H30O15
Molecular Weight 630.50 g/mol
Exact Mass 630.15847025 g/mol
Topological Polar Surface Area (TPSA) 250.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.35
H-Bond Acceptor 15
H-Bond Donor 8
Rotatable Bonds 10

Synonyms

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4-(3-Oxobutyl)phenyl 2-O,6-O-digalloyl-beta-D-glucopyranoside
4-[4-[[2,6-Bis-O-(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranosyl]oxy]phenyl]-2-butanone
105274-14-4

2D Structure

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2D Structure of 4-(4-((2,6-Bis-O-(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranosyl)oxy)phenyl)-2-butanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6483 64.83%
Caco-2 - 0.8808 88.08%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8240 82.40%
OATP2B1 inhibitior - 0.7090 70.90%
OATP1B1 inhibitior - 0.3211 32.11%
OATP1B3 inhibitior + 0.8731 87.31%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.8093 80.93%
P-glycoprotein inhibitior + 0.7131 71.31%
P-glycoprotein substrate - 0.6898 68.98%
CYP3A4 substrate + 0.6339 63.39%
CYP2C9 substrate - 0.8084 80.84%
CYP2D6 substrate - 0.8680 86.80%
CYP3A4 inhibition - 0.8480 84.80%
CYP2C9 inhibition - 0.6220 62.20%
CYP2C19 inhibition - 0.8009 80.09%
CYP2D6 inhibition - 0.9149 91.49%
CYP1A2 inhibition - 0.6258 62.58%
CYP2C8 inhibition + 0.6923 69.23%
CYP inhibitory promiscuity - 0.8690 86.90%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.7337 73.37%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9089 90.89%
Skin irritation - 0.7995 79.95%
Skin corrosion - 0.9354 93.54%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3613 36.13%
Micronuclear - 0.7326 73.26%
Hepatotoxicity - 0.8738 87.38%
skin sensitisation - 0.8869 88.69%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.9851 98.51%
Acute Oral Toxicity (c) III 0.7827 78.27%
Estrogen receptor binding + 0.7534 75.34%
Androgen receptor binding + 0.6888 68.88%
Thyroid receptor binding - 0.4873 48.73%
Glucocorticoid receptor binding + 0.6234 62.34%
Aromatase binding + 0.5538 55.38%
PPAR gamma + 0.6614 66.14%
Honey bee toxicity - 0.7826 78.26%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5750 57.50%
Fish aquatic toxicity + 0.9672 96.72%

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 99.25% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.00% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 96.48% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.14% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.04% 98.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 94.04% 95.17%
CHEMBL3437 Q16853 Amine oxidase, copper containing 93.83% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.81% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.11% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 92.63% 94.73%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 91.60% 95.64%
CHEMBL4208 P20618 Proteasome component C5 90.32% 90.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 90.26% 97.21%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 90.24% 83.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.95% 96.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.55% 95.89%
CHEMBL5255 O00206 Toll-like receptor 4 85.14% 92.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.00% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.81% 97.09%
CHEMBL3194 P02766 Transthyretin 83.81% 90.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.91% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.67% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.73% 92.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.12% 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.
Glycyrrhiza uralensis
Mitracarpus hirtus

Cross-Links

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PubChem 21636074
NPASS NPC281403