Catechin 5,3'-di-O-gallate

Details

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Internal ID 9206784f-de04-425e-ae04-46d78992bcb5
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > Catechins > Catechin gallates
IUPAC Name [(2R,3S)-3,7-dihydroxy-2-[4-hydroxy-3-(3,4,5-trihydroxybenzoyl)oxyphenyl]-3,4-dihydro-2H-chromen-5-yl] 3,4,5-trihydroxybenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H22O14/c30-14-8-22-15(23(9-14)42-28(39)12-3-17(32)25(37)18(33)4-12)10-21(36)27(41-22)11-1-2-16(31)24(7-11)43-29(40)13-5-19(34)26(38)20(35)6-13/h1-9,21,27,30-38H,10H2/t21-,27+/m0/s1
InChI Key OVHMMCMRYOPGQY-KDYSTLNUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C29H22O14
Molecular Weight 594.50 g/mol
Exact Mass 594.10095537 g/mol
Topological Polar Surface Area (TPSA) 244.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.81
H-Bond Acceptor 14
H-Bond Donor 9
Rotatable Bonds 5

Synonyms

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LMPK12020102

2D Structure

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2D Structure of Catechin 5,3'-di-O-gallate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7918 79.18%
Caco-2 - 0.9030 90.30%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.5401 54.01%
OATP2B1 inhibitior - 0.5638 56.38%
OATP1B1 inhibitior + 0.8615 86.15%
OATP1B3 inhibitior + 0.9259 92.59%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.4816 48.16%
P-glycoprotein inhibitior + 0.7408 74.08%
P-glycoprotein substrate - 0.8251 82.51%
CYP3A4 substrate + 0.5588 55.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7048 70.48%
CYP3A4 inhibition - 0.8100 81.00%
CYP2C9 inhibition - 0.9065 90.65%
CYP2C19 inhibition - 0.9466 94.66%
CYP2D6 inhibition - 0.9386 93.86%
CYP1A2 inhibition - 0.9197 91.97%
CYP2C8 inhibition + 0.7269 72.69%
CYP inhibitory promiscuity - 0.9210 92.10%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6519 65.19%
Eye corrosion - 0.9923 99.23%
Eye irritation - 0.7970 79.70%
Skin irritation - 0.6825 68.25%
Skin corrosion - 0.9427 94.27%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6436 64.36%
Micronuclear + 0.8959 89.59%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.8716 87.16%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.8034 80.34%
Acute Oral Toxicity (c) III 0.3566 35.66%
Estrogen receptor binding + 0.7327 73.27%
Androgen receptor binding + 0.7594 75.94%
Thyroid receptor binding + 0.5458 54.58%
Glucocorticoid receptor binding + 0.7005 70.05%
Aromatase binding + 0.5363 53.63%
PPAR gamma + 0.6470 64.70%
Honey bee toxicity - 0.8142 81.42%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5850 58.50%
Fish aquatic toxicity + 0.9127 91.27%

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 99.57% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.71% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.99% 96.09%
CHEMBL3194 P02766 Transthyretin 94.05% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.67% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.22% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.00% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.10% 99.17%
CHEMBL2535 P11166 Glucose transporter 88.51% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.80% 95.56%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 85.37% 83.00%
CHEMBL2581 P07339 Cathepsin D 85.05% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.22% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.01% 94.00%
CHEMBL4208 P20618 Proteasome component C5 83.31% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.73% 99.15%

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.
Vachellia nilotica

Cross-Links

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PubChem 15689619
LOTUS LTS0031654
wikiData Q76506826