[(2S,3S,4R,5R)-4-hydroxy-2,5-bis(hydroxymethyl)-2-[(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxolan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

Details

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Internal ID f8dbef2e-dae3-4935-8669-bb40a85b88d7
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Pentacarboxylic acids and derivatives
IUPAC Name [(2S,3S,4R,5R)-4-hydroxy-2,5-bis(hydroxymethyl)-2-[(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxolan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H36O18/c1-13(32)40-11-21-24(41-14(2)33)25(42-15(3)34)26(43-16(4)35)28(44-21)47-29(12-31)27(23(39)20(10-30)46-29)45-22(38)8-6-17-5-7-18(36)19(37)9-17/h5-9,20-21,23-28,30-31,36-37,39H,10-12H2,1-4H3/b8-6+/t20-,21-,23-,24-,25+,26-,27+,28-,29+/m1/s1
InChI Key BEJCHAYPPPRUFL-JMZLPTSQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C29H36O18
Molecular Weight 672.60 g/mol
Exact Mass 672.19016430 g/mol
Topological Polar Surface Area (TPSA) 260.00 Ų
XlogP -0.70
Atomic LogP (AlogP) -1.44
H-Bond Acceptor 18
H-Bond Donor 5
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2S,3S,4R,5R)-4-hydroxy-2,5-bis(hydroxymethyl)-2-[(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxolan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6572 65.72%
Caco-2 - 0.8712 87.12%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.7625 76.25%
OATP2B1 inhibitior - 0.7231 72.31%
OATP1B1 inhibitior + 0.8551 85.51%
OATP1B3 inhibitior + 0.9297 92.97%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9614 96.14%
P-glycoprotein inhibitior + 0.7276 72.76%
P-glycoprotein substrate - 0.7527 75.27%
CYP3A4 substrate + 0.6506 65.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8772 87.72%
CYP3A4 inhibition - 0.8199 81.99%
CYP2C9 inhibition - 0.8574 85.74%
CYP2C19 inhibition - 0.8624 86.24%
CYP2D6 inhibition - 0.9347 93.47%
CYP1A2 inhibition - 0.8443 84.43%
CYP2C8 inhibition + 0.6777 67.77%
CYP inhibitory promiscuity - 0.7498 74.98%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6954 69.54%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9140 91.40%
Skin irritation - 0.8256 82.56%
Skin corrosion - 0.9523 95.23%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4425 44.25%
Micronuclear - 0.6326 63.26%
Hepatotoxicity - 0.7866 78.66%
skin sensitisation - 0.8403 84.03%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6844 68.44%
Acute Oral Toxicity (c) III 0.6097 60.97%
Estrogen receptor binding + 0.8265 82.65%
Androgen receptor binding + 0.6584 65.84%
Thyroid receptor binding + 0.5198 51.98%
Glucocorticoid receptor binding + 0.6638 66.38%
Aromatase binding + 0.6496 64.96%
PPAR gamma + 0.7475 74.75%
Honey bee toxicity - 0.7312 73.12%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9642 96.42%

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 99.68% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.57% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.79% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 95.63% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.72% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.62% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.26% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 93.16% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.07% 89.00%
CHEMBL226 P30542 Adenosine A1 receptor 90.74% 95.93%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.57% 94.80%
CHEMBL2581 P07339 Cathepsin D 88.92% 98.95%
CHEMBL3194 P02766 Transthyretin 87.80% 90.71%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 86.63% 83.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.56% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 84.56% 91.19%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.29% 99.17%
CHEMBL5255 O00206 Toll-like receptor 4 83.81% 92.50%
CHEMBL4208 P20618 Proteasome component C5 83.41% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.59% 99.15%

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.
Prunus ssiori

Cross-Links

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PubChem 101678893
LOTUS LTS0140943
wikiData Q104933019