1-O,2-O,6-O-Trigalloyl-alpha-D-glucopyranose

Details

Top
Internal ID e9865ad5-49e0-4cf1-861f-cda565cd90c3
Taxonomy Phenylpropanoids and polyketides > Tannins
IUPAC Name [(2R,3S,4S,5R,6R)-3,4-dihydroxy-5,6-bis[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate
SMILES (Canonical) C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O
SMILES (Isomeric) C1=C(C=C(C(=C1O)O)O)C(=O)OC[C@@H]2[C@H]([C@@H]([C@H]([C@H](O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O
InChI InChI=1S/C27H24O18/c28-11-1-8(2-12(29)18(11)34)24(39)42-7-17-21(37)22(38)23(44-25(40)9-3-13(30)19(35)14(31)4-9)27(43-17)45-26(41)10-5-15(32)20(36)16(33)6-10/h1-6,17,21-23,27-38H,7H2/t17-,21-,22+,23-,27-/m1/s1
InChI Key LLENXGNWVNSBQG-WPNCQGPHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C27H24O18
Molecular Weight 636.50 g/mol
Exact Mass 636.09626391 g/mol
Topological Polar Surface Area (TPSA) 311.00 Ų
XlogP 0.40
Atomic LogP (AlogP) -0.28
H-Bond Acceptor 18
H-Bond Donor 11
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1-O,2-O,6-O-Trigalloyl-alpha-D-glucopyranose

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7977 79.77%
Caco-2 - 0.8783 87.83%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6685 66.85%
OATP2B1 inhibitior - 0.5661 56.61%
OATP1B1 inhibitior - 0.5644 56.44%
OATP1B3 inhibitior - 0.2136 21.36%
MATE1 inhibitior - 0.5400 54.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.5946 59.46%
P-glycoprotein inhibitior + 0.6918 69.18%
P-glycoprotein substrate - 0.9445 94.45%
CYP3A4 substrate + 0.5097 50.97%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8410 84.10%
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 - 0.6428 64.28%
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 - 0.8656 86.56%
Skin irritation - 0.8454 84.54%
Skin corrosion - 0.9617 96.17%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6932 69.32%
Micronuclear + 0.6466 64.66%
Hepatotoxicity - 0.8625 86.25%
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 - 0.9697 96.97%
Acute Oral Toxicity (c) III 0.7395 73.95%
Estrogen receptor binding + 0.7446 74.46%
Androgen receptor binding + 0.6526 65.26%
Thyroid receptor binding - 0.5052 50.52%
Glucocorticoid receptor binding + 0.5668 56.68%
Aromatase binding - 0.5192 51.92%
PPAR gamma + 0.6329 63.29%
Honey bee toxicity - 0.9007 90.07%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6550 65.50%
Fish aquatic toxicity + 0.9129 91.29%

Targets

Top

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 98.70% 91.11%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 96.90% 95.64%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 94.98% 83.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.58% 96.09%
CHEMBL3194 P02766 Transthyretin 91.76% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.63% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 89.35% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 89.23% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.93% 86.33%
CHEMBL5255 O00206 Toll-like receptor 4 86.44% 92.50%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.17% 89.34%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.99% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.89% 94.00%
CHEMBL2581 P07339 Cathepsin D 83.83% 98.95%
CHEMBL4208 P20618 Proteasome component C5 82.94% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.27% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.02% 97.21%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.71% 95.17%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.33% 80.78%

Plants that contains it

Top
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.
Bupleurum chinense
Carphephorus odoratissimus
Carya tonkinensis
Cornus officinalis
Euphorbia maculata
Heliotropium arboreum
Holocarpha obconica
Leonurus sibiricus
Monochaetum multiflorum
Plantago indica
Plectranthus fruticosus
Zanthoxylum americanum

Cross-Links

Top
PubChem 11969002
NPASS NPC54308
LOTUS LTS0197326
wikiData Q105153462