(1)Benzopyrano(5,4,3-cde)(1)benzopyran-5,10-dione, 2-((6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy)-3,7,8-trihydroxy-

Details

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Internal ID 8587a70c-2000-4829-a680-c02d6068b163
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name 6,7,14-trihydroxy-13-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H26O18/c27-3-9-14(30)17(33)19(35)25(41-9)39-4-10-15(31)18(34)20(36)26(42-10)40-8-2-6-12-11-5(23(37)44-22(12)16(8)32)1-7(28)13(29)21(11)43-24(6)38/h1-2,9-10,14-15,17-20,25-36H,3-4H2/t9-,10-,14-,15-,17+,18+,19-,20-,25-,26-/m1/s1
InChI Key FHIYBTOOLROABN-YMLQNWNPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H26O18
Molecular Weight 626.50 g/mol
Exact Mass 626.11191398 g/mol
Topological Polar Surface Area (TPSA) 292.00 Ų
XlogP -2.80
Atomic LogP (AlogP) -3.39
H-Bond Acceptor 18
H-Bond Donor 10
Rotatable Bonds 6

Synonyms

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2455-85-8
RefChem:1049147
DTXCID301537112
(1)Benzopyrano(5,4,3-cde)(1)benzopyran-5,10-dione, 2-((6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy)-3,7,8-trihydroxy-
Ellagic acid di-hexoside
SCHEMBL31290780
CHEBI:167699
[1]Benzopyrano[5,4,3-cde][1]benzopyran-5,10-dione, 2-[(6-O-I(2)-D-glucopyranosyl-I(2)-D-glucopyranosyl)oxy]-3,7,8-trihydroxy-
6,7,14-trihydroxy-13-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione

2D Structure

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2D Structure of (1)Benzopyrano(5,4,3-cde)(1)benzopyran-5,10-dione, 2-((6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy)-3,7,8-trihydroxy-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7525 75.25%
Caco-2 - 0.9159 91.59%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.4625 46.25%
OATP2B1 inhibitior - 0.5672 56.72%
OATP1B1 inhibitior + 0.8841 88.41%
OATP1B3 inhibitior + 0.9697 96.97%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5896 58.96%
P-glycoprotein inhibitior - 0.5821 58.21%
P-glycoprotein substrate - 0.7965 79.65%
CYP3A4 substrate + 0.5644 56.44%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.8579 85.79%
CYP3A4 inhibition - 0.9362 93.62%
CYP2C9 inhibition - 0.9277 92.77%
CYP2C19 inhibition - 0.8827 88.27%
CYP2D6 inhibition - 0.9501 95.01%
CYP1A2 inhibition - 0.9312 93.12%
CYP2C8 inhibition - 0.5625 56.25%
CYP inhibitory promiscuity - 0.9071 90.71%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6892 68.92%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.9055 90.55%
Skin irritation - 0.8481 84.81%
Skin corrosion - 0.9658 96.58%
Ames mutagenesis - 0.5655 56.55%
Human Ether-a-go-go-Related Gene inhibition + 0.7471 74.71%
Micronuclear + 0.5933 59.33%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8938 89.38%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.8875 88.75%
Acute Oral Toxicity (c) IV 0.4657 46.57%
Estrogen receptor binding + 0.7663 76.63%
Androgen receptor binding + 0.5486 54.86%
Thyroid receptor binding - 0.4918 49.18%
Glucocorticoid receptor binding - 0.5107 51.07%
Aromatase binding + 0.6458 64.58%
PPAR gamma + 0.6996 69.96%
Honey bee toxicity - 0.7756 77.56%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6349 63.49%
Fish aquatic toxicity + 0.8134 81.34%

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 99.83% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.79% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.94% 89.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 93.06% 83.57%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 91.55% 89.34%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.26% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.03% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 87.69% 91.49%
CHEMBL3194 P02766 Transthyretin 87.66% 90.71%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 87.02% 96.21%
CHEMBL3401 O75469 Pregnane X receptor 85.69% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.91% 94.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.91% 86.92%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.72% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.85% 99.17%
CHEMBL4581 P52732 Kinesin-like protein 1 81.53% 93.18%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.02% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.55% 99.15%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 80.30% 95.83%

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.
Psidium guajava

Cross-Links

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PubChem 5318135
NPASS NPC151447