(5,6,7,8,11,12,13,14,22,23-Decahydroxy-3,16-dioxo-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4(9),5,7,10(15),11,13-hexaen-21-yl) 3,4,5-trihydroxybenzoate

Details

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Internal ID 12bb8cbe-1db8-413a-90dc-04a8f92de50f
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name (5,6,7,8,11,12,13,14,22,23-decahydroxy-3,16-dioxo-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4(9),5,7,10(15),11,13-hexaen-21-yl) 3,4,5-trihydroxybenzoate
SMILES (Canonical) C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=C(C5=C(C(=C(C(=C5O)O)O)O)C(=O)O1)C(=C(C(=C4O)O)O)O)O
SMILES (Isomeric) C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=C(C5=C(C(=C(C(=C5O)O)O)O)C(=O)O1)C(=C(C(=C4O)O)O)O)O
InChI InChI=1S/C27H22O20/c28-5-1-4(2-6(29)12(5)30)24(41)47-27-22(40)23-13(31)7(45-27)3-44-25(42)10-8(14(32)18(36)20(38)16(10)34)9-11(26(43)46-23)17(35)21(39)19(37)15(9)33/h1-2,7,13,22-23,27-40H,3H2
InChI Key CPWYQGWOJMNXGJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H22O20
Molecular Weight 666.40 g/mol
Exact Mass 666.07044309 g/mol
Topological Polar Surface Area (TPSA) 351.00 Ų
XlogP 0.50
Atomic LogP (AlogP) -0.89
H-Bond Acceptor 20
H-Bond Donor 13
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5,6,7,8,11,12,13,14,22,23-Decahydroxy-3,16-dioxo-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4(9),5,7,10(15),11,13-hexaen-21-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 + 0.6364 63.64%
Caco-2 - 0.8960 89.60%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5868 58.68%
OATP2B1 inhibitior - 0.5629 56.29%
OATP1B1 inhibitior + 0.7685 76.85%
OATP1B3 inhibitior + 0.9166 91.66%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.5983 59.83%
P-glycoprotein inhibitior + 0.6000 60.00%
P-glycoprotein substrate - 0.7054 70.54%
CYP3A4 substrate + 0.5999 59.99%
CYP2C9 substrate - 0.7973 79.73%
CYP2D6 substrate - 0.8548 85.48%
CYP3A4 inhibition - 0.9116 91.16%
CYP2C9 inhibition - 0.9083 90.83%
CYP2C19 inhibition - 0.8377 83.77%
CYP2D6 inhibition - 0.9575 95.75%
CYP1A2 inhibition - 0.8596 85.96%
CYP2C8 inhibition + 0.5578 55.78%
CYP inhibitory promiscuity - 0.9485 94.85%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7032 70.32%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.8306 83.06%
Skin irritation - 0.7789 77.89%
Skin corrosion - 0.9548 95.48%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7658 76.58%
Micronuclear + 0.7833 78.33%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8461 84.61%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8464 84.64%
Acute Oral Toxicity (c) III 0.4887 48.87%
Estrogen receptor binding + 0.7360 73.60%
Androgen receptor binding + 0.6559 65.59%
Thyroid receptor binding - 0.5690 56.90%
Glucocorticoid receptor binding - 0.4694 46.94%
Aromatase binding - 0.6032 60.32%
PPAR gamma + 0.6607 66.07%
Honey bee toxicity - 0.7711 77.11%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8983 89.83%

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 99.44% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.43% 89.00%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 92.50% 83.00%
CHEMBL1951 P21397 Monoamine oxidase A 92.40% 91.49%
CHEMBL2581 P07339 Cathepsin D 89.13% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.03% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.99% 94.00%
CHEMBL3194 P02766 Transthyretin 87.67% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.18% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.09% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.75% 99.17%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 84.84% 96.00%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 84.37% 95.64%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.26% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 83.85% 94.73%
CHEMBL4208 P20618 Proteasome component C5 83.18% 90.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.78% 100.00%
CHEMBL2535 P11166 Glucose transporter 81.35% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.79% 97.09%

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.
Punica granatum

Cross-Links

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PubChem 162971987
LOTUS LTS0269299
wikiData Q104967818