[(2R,3S,4S,5R,6S)-6-[3,5-dihydroxy-2-(4-hydroxybenzoyl)phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate

Details

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Internal ID 546510b5-b9cf-45e4-9ca0-a227d8dc2b05
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name [(2R,3S,4S,5R,6S)-6-[3,5-dihydroxy-2-(4-hydroxybenzoyl)phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate
SMILES (Canonical) C1=CC(=CC=C1C(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O)O
SMILES (Isomeric) C1=CC(=CC=C1C(=O)C2=C(C=C(C=C2O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O)O
InChI InChI=1S/C26H24O14/c27-12-3-1-10(2-4-12)20(32)19-14(29)7-13(28)8-17(19)39-26-24(36)23(35)22(34)18(40-26)9-38-25(37)11-5-15(30)21(33)16(31)6-11/h1-8,18,22-24,26-31,33-36H,9H2/t18-,22-,23+,24-,26-/m1/s1
InChI Key JASLYQNADNGFOP-UUGZZFCKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H24O14
Molecular Weight 560.50 g/mol
Exact Mass 560.11660544 g/mol
Topological Polar Surface Area (TPSA) 244.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.19
H-Bond Acceptor 14
H-Bond Donor 9
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2R,3S,4S,5R,6S)-6-[3,5-dihydroxy-2-(4-hydroxybenzoyl)phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7977 79.77%
Caco-2 - 0.9167 91.67%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.6685 66.85%
OATP2B1 inhibitior - 0.5559 55.59%
OATP1B1 inhibitior + 0.7603 76.03%
OATP1B3 inhibitior - 0.2136 21.36%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.6914 69.14%
P-glycoprotein inhibitior + 0.6135 61.35%
P-glycoprotein substrate - 0.7706 77.06%
CYP3A4 substrate + 0.5899 58.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8671 86.71%
CYP3A4 inhibition - 0.8723 87.23%
CYP2C9 inhibition - 0.7955 79.55%
CYP2C19 inhibition - 0.9121 91.21%
CYP2D6 inhibition - 0.9425 94.25%
CYP1A2 inhibition - 0.9315 93.15%
CYP2C8 inhibition + 0.8275 82.75%
CYP inhibitory promiscuity - 0.8531 85.31%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.7284 72.84%
Eye corrosion - 0.9931 99.31%
Eye irritation - 0.8224 82.24%
Skin irritation - 0.8454 84.54%
Skin corrosion - 0.9617 96.17%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7474 74.74%
Micronuclear + 0.6466 64.66%
Hepatotoxicity - 0.7949 79.49%
skin sensitisation - 0.8722 87.22%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.8937 89.37%
Acute Oral Toxicity (c) III 0.7395 73.95%
Estrogen receptor binding + 0.7006 70.06%
Androgen receptor binding + 0.7325 73.25%
Thyroid receptor binding - 0.5065 50.65%
Glucocorticoid receptor binding + 0.5869 58.69%
Aromatase binding - 0.5484 54.84%
PPAR gamma + 0.6084 60.84%
Honey bee toxicity - 0.8771 87.71%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9129 91.29%

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 98.20% 91.11%
CHEMBL3194 P02766 Transthyretin 97.78% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.06% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.05% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.73% 86.33%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 91.22% 95.64%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.69% 94.00%
CHEMBL4208 P20618 Proteasome component C5 90.31% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.92% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 87.62% 94.73%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 87.05% 83.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.18% 95.89%
CHEMBL226 P30542 Adenosine A1 receptor 84.98% 95.93%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 84.67% 85.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.90% 90.71%
CHEMBL3891 P07384 Calpain 1 82.52% 93.04%
CHEMBL5255 O00206 Toll-like receptor 4 81.93% 92.50%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.30% 95.50%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.54% 95.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.04% 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.
Planchonella obovata

Cross-Links

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PubChem 46193175
LOTUS LTS0062250
wikiData Q105123994