(8,9,9,13,14,25,26,27,30,31,32-Undecahydroxy-4,7,17,22,35-pentaoxo-3,18,21,36,38,40-hexaoxaoctacyclo[18.17.1.12,19.18,12.05,10.011,16.023,28.029,34]tetraconta-5,11,13,15,23,25,27,29,31,33-decaen-39-yl) 3,4,5-trihydroxybenzoate

Details

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Internal ID c7476ce4-09ab-458b-b2bd-4298274283e0
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name (8,9,9,13,14,25,26,27,30,31,32-undecahydroxy-4,7,17,22,35-pentaoxo-3,18,21,36,38,40-hexaoxaoctacyclo[18.17.1.12,19.18,12.05,10.011,16.023,28.029,34]tetraconta-5,11,13,15,23,25,27,29,31,33-decaen-39-yl) 3,4,5-trihydroxybenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C41H28O27/c42-13-1-8(2-14(43)24(13)48)34(54)65-32-30-18-7-62-35(55)9-3-15(44)25(49)28(52)20(9)21-10(4-16(45)26(50)29(21)53)37(57)67-39(63-18)33(32)66-36(56)11-5-17(46)27(51)31-22(11)23-12(38(58)64-30)6-19(47)41(61,68-31)40(23,59)60/h1-6,18,23,30,32-33,39,42-46,48-53,59-61H,7H2
InChI Key GZIMCIFMXMTKDS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C41H28O27
Molecular Weight 952.60 g/mol
Exact Mass 952.08179561 g/mol
Topological Polar Surface Area (TPSA) 450.00 Ų
XlogP -0.60
Atomic LogP (AlogP) -1.10
H-Bond Acceptor 27
H-Bond Donor 14
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8,9,9,13,14,25,26,27,30,31,32-Undecahydroxy-4,7,17,22,35-pentaoxo-3,18,21,36,38,40-hexaoxaoctacyclo[18.17.1.12,19.18,12.05,10.011,16.023,28.029,34]tetraconta-5,11,13,15,23,25,27,29,31,33-decaen-39-yl) 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 + 0.7612 76.12%
Caco-2 - 0.8801 88.01%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6690 66.90%
OATP2B1 inhibitior - 0.7106 71.06%
OATP1B1 inhibitior + 0.7537 75.37%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.6200 62.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9358 93.58%
P-glycoprotein inhibitior + 0.7462 74.62%
P-glycoprotein substrate + 0.6410 64.10%
CYP3A4 substrate + 0.6984 69.84%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8695 86.95%
CYP3A4 inhibition - 0.8235 82.35%
CYP2C9 inhibition - 0.5802 58.02%
CYP2C19 inhibition - 0.5313 53.13%
CYP2D6 inhibition - 0.8388 83.88%
CYP1A2 inhibition - 0.7992 79.92%
CYP2C8 inhibition + 0.7376 73.76%
CYP inhibitory promiscuity - 0.7826 78.26%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6394 63.94%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.8926 89.26%
Skin irritation - 0.7325 73.25%
Skin corrosion - 0.9394 93.94%
Ames mutagenesis + 0.6009 60.09%
Human Ether-a-go-go-Related Gene inhibition + 0.6678 66.78%
Micronuclear + 0.7733 77.33%
Hepatotoxicity - 0.7197 71.97%
skin sensitisation - 0.7419 74.19%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7804 78.04%
Acute Oral Toxicity (c) III 0.4653 46.53%
Estrogen receptor binding + 0.7862 78.62%
Androgen receptor binding + 0.7668 76.68%
Thyroid receptor binding - 0.4896 48.96%
Glucocorticoid receptor binding + 0.5743 57.43%
Aromatase binding + 0.5519 55.19%
PPAR gamma + 0.7424 74.24%
Honey bee toxicity - 0.7349 73.49%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9721 97.21%

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%
CHEMBL1951 P21397 Monoamine oxidase A 96.85% 91.49%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 91.45% 83.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.43% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.82% 86.33%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.67% 95.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.35% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.12% 95.56%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 88.77% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.80% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.21% 97.09%
CHEMBL2581 P07339 Cathepsin D 87.17% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.09% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 84.72% 91.19%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.61% 99.15%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.16% 94.42%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.91% 92.94%
CHEMBL4208 P20618 Proteasome component C5 81.49% 90.00%
CHEMBL5255 O00206 Toll-like receptor 4 80.42% 92.50%

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.
Antidesma montanum var. montanum
Carpinus laxiflora

Cross-Links

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PubChem 163038117
LOTUS LTS0105651
wikiData Q105024398