[3,4,5-Triacetyloxy-6-[1,3-diacetyloxy-1-(4-acetyloxyphenyl)propan-2-yl]oxyoxan-2-yl]methyl 4-acetyloxybenzoate

Details

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Internal ID 8972017a-f138-4774-a265-b4dd21c64d61
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name [3,4,5-triacetyloxy-6-[1,3-diacetyloxy-1-(4-acetyloxyphenyl)propan-2-yl]oxyoxan-2-yl]methyl 4-acetyloxybenzoate
SMILES (Canonical) CC(=O)OCC(C(C1=CC=C(C=C1)OC(=O)C)OC(=O)C)OC2C(C(C(C(O2)COC(=O)C3=CC=C(C=C3)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C
SMILES (Isomeric) CC(=O)OCC(C(C1=CC=C(C=C1)OC(=O)C)OC(=O)C)OC2C(C(C(C(O2)COC(=O)C3=CC=C(C=C3)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C
InChI InChI=1S/C36H40O18/c1-18(37)45-16-29(31(49-21(4)40)25-8-12-27(13-9-25)47-19(2)38)53-36-34(52-24(7)43)33(51-23(6)42)32(50-22(5)41)30(54-36)17-46-35(44)26-10-14-28(15-11-26)48-20(3)39/h8-15,29-34,36H,16-17H2,1-7H3
InChI Key HVFAYQFSPOIJJU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C36H40O18
Molecular Weight 760.70 g/mol
Exact Mass 760.22146442 g/mol
Topological Polar Surface Area (TPSA) 229.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.47
H-Bond Acceptor 18
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [3,4,5-Triacetyloxy-6-[1,3-diacetyloxy-1-(4-acetyloxyphenyl)propan-2-yl]oxyoxan-2-yl]methyl 4-acetyloxybenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9452 94.52%
Caco-2 - 0.8403 84.03%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8050 80.50%
OATP2B1 inhibitior - 0.5643 56.43%
OATP1B1 inhibitior + 0.8496 84.96%
OATP1B3 inhibitior + 0.8091 80.91%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9847 98.47%
P-glycoprotein inhibitior + 0.8814 88.14%
P-glycoprotein substrate - 0.6574 65.74%
CYP3A4 substrate + 0.6382 63.82%
CYP2C9 substrate - 0.5878 58.78%
CYP2D6 substrate - 0.8936 89.36%
CYP3A4 inhibition - 0.8942 89.42%
CYP2C9 inhibition - 0.8593 85.93%
CYP2C19 inhibition - 0.7834 78.34%
CYP2D6 inhibition - 0.9408 94.08%
CYP1A2 inhibition - 0.5785 57.85%
CYP2C8 inhibition + 0.4629 46.29%
CYP inhibitory promiscuity + 0.5072 50.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5958 59.58%
Eye corrosion - 0.9782 97.82%
Eye irritation - 0.9068 90.68%
Skin irritation - 0.8830 88.30%
Skin corrosion - 0.9803 98.03%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8266 82.66%
Micronuclear - 0.5734 57.34%
Hepatotoxicity - 0.6215 62.15%
skin sensitisation - 0.8913 89.13%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7429 74.29%
Estrogen receptor binding + 0.8057 80.57%
Androgen receptor binding + 0.7307 73.07%
Thyroid receptor binding + 0.5776 57.76%
Glucocorticoid receptor binding + 0.8026 80.26%
Aromatase binding + 0.5728 57.28%
PPAR gamma + 0.7381 73.81%
Honey bee toxicity - 0.7054 70.54%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9544 95.44%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.04% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.71% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 92.86% 94.73%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 92.69% 83.00%
CHEMBL2581 P07339 Cathepsin D 92.63% 98.95%
CHEMBL4208 P20618 Proteasome component C5 91.59% 90.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 91.32% 94.80%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.11% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.64% 86.33%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.84% 81.11%
CHEMBL226 P30542 Adenosine A1 receptor 87.35% 95.93%
CHEMBL3437 Q16853 Amine oxidase, copper containing 84.87% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.82% 96.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.50% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.86% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 82.55% 91.19%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.53% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.65% 94.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.55% 95.17%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 80.34% 91.43%

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.
Taxus mairei

Cross-Links

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PubChem 162894300
LOTUS LTS0176383
wikiData Q105034209