[(3S,4S,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(4-hydroxyphenoxy)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl (E)-hex-2-enoate

Details

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Internal ID b55ced29-4844-4482-bac7-0f1055d8a0b0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name [(3S,4S,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(4-hydroxyphenoxy)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl (E)-hex-2-enoate
SMILES (Canonical) CCCC=CC(=O)OCC1(COC(C1O)OC2C(C(C(OC2OC3=CC=C(C=C3)O)CO)O)O)O
SMILES (Isomeric) CCC/C=C/C(=O)OC[C@]1(CO[C@H]([C@H]1O)O[C@@H]2[C@H]([C@@H]([C@H](O[C@H]2OC3=CC=C(C=C3)O)CO)O)O)O
InChI InChI=1S/C23H32O12/c1-2-3-4-5-16(26)31-11-23(30)12-32-22(20(23)29)35-19-18(28)17(27)15(10-24)34-21(19)33-14-8-6-13(25)7-9-14/h4-9,15,17-22,24-25,27-30H,2-3,10-12H2,1H3/b5-4+/t15-,17-,18+,19-,20-,21-,22+,23-/m1/s1
InChI Key LFLLAUFDKMXSRX-GCBQJQRVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H32O12
Molecular Weight 500.50 g/mol
Exact Mass 500.18937645 g/mol
Topological Polar Surface Area (TPSA) 185.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -1.06
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(3S,4S,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(4-hydroxyphenoxy)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl (E)-hex-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 + 0.6086 60.86%
Caco-2 - 0.8550 85.50%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.9000 90.00%
Subcellular localzation Mitochondria 0.7918 79.18%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.8626 86.26%
OATP1B3 inhibitior + 0.9428 94.28%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5653 56.53%
P-glycoprotein inhibitior - 0.6030 60.30%
P-glycoprotein substrate - 0.6489 64.89%
CYP3A4 substrate + 0.6817 68.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8813 88.13%
CYP3A4 inhibition - 0.7615 76.15%
CYP2C9 inhibition - 0.8170 81.70%
CYP2C19 inhibition - 0.8174 81.74%
CYP2D6 inhibition - 0.8950 89.50%
CYP1A2 inhibition - 0.8515 85.15%
CYP2C8 inhibition + 0.6121 61.21%
CYP inhibitory promiscuity - 0.6969 69.69%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5387 53.87%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.9352 93.52%
Skin irritation - 0.7608 76.08%
Skin corrosion - 0.9393 93.93%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4124 41.24%
Micronuclear - 0.7726 77.26%
Hepatotoxicity - 0.7339 73.39%
skin sensitisation - 0.8445 84.45%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7030 70.30%
Acute Oral Toxicity (c) III 0.6814 68.14%
Estrogen receptor binding + 0.7813 78.13%
Androgen receptor binding + 0.5831 58.31%
Thyroid receptor binding - 0.5629 56.29%
Glucocorticoid receptor binding - 0.5393 53.93%
Aromatase binding + 0.7226 72.26%
PPAR gamma + 0.5661 56.61%
Honey bee toxicity - 0.7987 79.87%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.7987 79.87%

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 98.62% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 95.44% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.43% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.03% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.83% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.74% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.66% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.99% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.60% 95.56%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.75% 94.33%
CHEMBL4208 P20618 Proteasome component C5 84.13% 90.00%
CHEMBL2581 P07339 Cathepsin D 83.93% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.41% 95.89%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.40% 97.36%
CHEMBL3401 O75469 Pregnane X receptor 82.80% 94.73%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 82.33% 94.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.88% 96.00%
CHEMBL5255 O00206 Toll-like receptor 4 81.57% 92.50%
CHEMBL221 P23219 Cyclooxygenase-1 80.76% 90.17%

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.
Myrsine seguinii

Cross-Links

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PubChem 163189816
LOTUS LTS0156446
wikiData Q105151064