[5-Acetyloxy-3-ethoxy-3-hydroxy-2-methyl-4-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxycyclopentyl] 4-acetyloxy-3-methoxybenzoate

Details

Top
Internal ID 1081c4ba-d635-4672-85b6-b31b1fb7f2c5
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name [5-acetyloxy-3-ethoxy-3-hydroxy-2-methyl-4-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxycyclopentyl] 4-acetyloxy-3-methoxybenzoate
SMILES (Canonical) CCOC1(C(C(C(C1OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C3=CC(=C(C=C3)OC(=O)C)OC)C)O
SMILES (Isomeric) CCOC1(C(C(C(C1OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C3=CC(=C(C=C3)OC(=O)C)OC)C)O
InChI InChI=1S/C34H44O19/c1-10-45-34(42)15(2)26(52-32(41)22-11-12-23(46-17(4)36)24(13-22)43-9)29(49-20(7)39)31(34)53-33-30(50-21(8)40)28(48-19(6)38)27(47-18(5)37)25(51-33)14-44-16(3)35/h11-13,15,25-31,33,42H,10,14H2,1-9H3
InChI Key HPIFNAXCJDAOTL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C34H44O19
Molecular Weight 756.70 g/mol
Exact Mass 756.24767917 g/mol
Topological Polar Surface Area (TPSA) 241.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.92
H-Bond Acceptor 19
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [5-Acetyloxy-3-ethoxy-3-hydroxy-2-methyl-4-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxycyclopentyl] 4-acetyloxy-3-methoxybenzoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9160 91.60%
Caco-2 - 0.8403 84.03%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7935 79.35%
OATP2B1 inhibitior - 0.5637 56.37%
OATP1B1 inhibitior + 0.8092 80.92%
OATP1B3 inhibitior + 0.9175 91.75%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9697 96.97%
P-glycoprotein inhibitior + 0.8560 85.60%
P-glycoprotein substrate + 0.5238 52.38%
CYP3A4 substrate + 0.6813 68.13%
CYP2C9 substrate + 0.6035 60.35%
CYP2D6 substrate - 0.8782 87.82%
CYP3A4 inhibition - 0.8747 87.47%
CYP2C9 inhibition - 0.5805 58.05%
CYP2C19 inhibition - 0.5805 58.05%
CYP2D6 inhibition - 0.9657 96.57%
CYP1A2 inhibition - 0.6795 67.95%
CYP2C8 inhibition + 0.7409 74.09%
CYP inhibitory promiscuity - 0.7149 71.49%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6531 65.31%
Eye corrosion - 0.9869 98.69%
Eye irritation - 0.9113 91.13%
Skin irritation - 0.8464 84.64%
Skin corrosion - 0.9647 96.47%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4667 46.67%
Micronuclear - 0.6167 61.67%
Hepatotoxicity - 0.6017 60.17%
skin sensitisation - 0.8641 86.41%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.6519 65.19%
Acute Oral Toxicity (c) III 0.6310 63.10%
Estrogen receptor binding + 0.8179 81.79%
Androgen receptor binding + 0.6148 61.48%
Thyroid receptor binding + 0.5342 53.42%
Glucocorticoid receptor binding + 0.7831 78.31%
Aromatase binding + 0.6882 68.82%
PPAR gamma + 0.7533 75.33%
Honey bee toxicity - 0.7223 72.23%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6118 61.18%
Fish aquatic toxicity + 0.8915 89.15%

Targets

Top

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.24% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.37% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.45% 94.00%
CHEMBL4208 P20618 Proteasome component C5 92.11% 90.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.68% 94.80%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.64% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.79% 99.17%
CHEMBL2581 P07339 Cathepsin D 88.66% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.60% 97.21%
CHEMBL2535 P11166 Glucose transporter 85.58% 98.75%
CHEMBL5255 O00206 Toll-like receptor 4 85.34% 92.50%
CHEMBL340 P08684 Cytochrome P450 3A4 85.30% 91.19%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.98% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.91% 89.00%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 83.81% 96.90%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.63% 92.94%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.86% 94.42%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.60% 95.89%
CHEMBL3891 P07384 Calpain 1 80.43% 93.04%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.07% 82.38%

Plants that contains it

Top
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.
Angostura trifoliata

Cross-Links

Top
PubChem 162898650
LOTUS LTS0159899
wikiData Q105109931