6''-O-Galloylprunin

Details

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Internal ID 441d64f6-bf54-4b5b-8250-cbd5226d0b07
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name [3,4,5-trihydroxy-6-[[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate
SMILES (Canonical) C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)C5=CC=C(C=C5)O
SMILES (Isomeric) C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)C5=CC=C(C=C5)O
InChI InChI=1S/C28H26O14/c29-13-3-1-11(2-4-13)19-9-16(31)22-15(30)7-14(8-20(22)41-19)40-28-26(37)25(36)24(35)21(42-28)10-39-27(38)12-5-17(32)23(34)18(33)6-12/h1-8,19,21,24-26,28-30,32-37H,9-10H2
InChI Key UNTKZTADYPALEE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H26O14
Molecular Weight 586.50 g/mol
Exact Mass 586.13225550 g/mol
Topological Polar Surface Area (TPSA) 233.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.96
H-Bond Acceptor 14
H-Bond Donor 8
Rotatable Bonds 6

Synonyms

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6''-O-Galloylprunin

2D Structure

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2D Structure of 6''-O-Galloylprunin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6055 60.55%
Caco-2 - 0.9140 91.40%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Mitochondria 0.6349 63.49%
OATP2B1 inhibitior - 0.8392 83.92%
OATP1B1 inhibitior + 0.8397 83.97%
OATP1B3 inhibitior + 0.9474 94.74%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.6190 61.90%
P-glycoprotein inhibitior + 0.5719 57.19%
P-glycoprotein substrate - 0.7601 76.01%
CYP3A4 substrate + 0.6457 64.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8544 85.44%
CYP3A4 inhibition - 0.9135 91.35%
CYP2C9 inhibition - 0.8848 88.48%
CYP2C19 inhibition - 0.9087 90.87%
CYP2D6 inhibition - 0.9593 95.93%
CYP1A2 inhibition - 0.9330 93.30%
CYP2C8 inhibition + 0.7123 71.23%
CYP inhibitory promiscuity - 0.8642 86.42%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6994 69.94%
Eye corrosion - 0.9926 99.26%
Eye irritation - 0.8835 88.35%
Skin irritation - 0.8191 81.91%
Skin corrosion - 0.9613 96.13%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.7292 72.92%
Hepatotoxicity - 0.8750 87.50%
skin sensitisation - 0.9218 92.18%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8736 87.36%
Acute Oral Toxicity (c) III 0.4217 42.17%
Estrogen receptor binding + 0.7497 74.97%
Androgen receptor binding + 0.6276 62.76%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.5771 57.71%
Aromatase binding + 0.5355 53.55%
PPAR gamma + 0.6706 67.06%
Honey bee toxicity - 0.7817 78.17%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6050 60.50%
Fish aquatic toxicity + 0.9242 92.42%

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 99.59% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.56% 97.09%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 95.83% 95.64%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.13% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.22% 89.00%
CHEMBL4208 P20618 Proteasome component C5 90.98% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.51% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.49% 94.00%
CHEMBL3194 P02766 Transthyretin 90.20% 90.71%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 90.09% 83.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.31% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.01% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.55% 99.17%
CHEMBL5255 O00206 Toll-like receptor 4 88.41% 92.50%
CHEMBL2581 P07339 Cathepsin D 87.58% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.45% 94.80%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.98% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 86.21% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.18% 99.23%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 85.92% 85.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.61% 99.15%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 84.50% 95.78%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.70% 96.21%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.30% 95.89%
CHEMBL3437 Q16853 Amine oxidase, copper containing 80.19% 94.00%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 80.17% 80.00%

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.
Phyllanthus emblica
Vachellia farnesiana var. farnesiana

Cross-Links

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PubChem 74819365
LOTUS LTS0241035
wikiData Q105276127