[(1S,2S,3S,4R,5R,6R)-2,3,4,5-tetrahydroxy-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxycyclohexyl] tetradecanoate

Details

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Internal ID ffcd9e52-2058-4e44-9292-da515f48f7a1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name [(1S,2S,3S,4R,5R,6R)-2,3,4,5-tetrahydroxy-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxycyclohexyl] tetradecanoate
SMILES (Canonical) CCCCCCCCCCCCCC(=O)OC1C(C(C(C(C1OC2C(C(C(CO2)O)O)O)O)O)O)O
SMILES (Isomeric) CCCCCCCCCCCCCC(=O)O[C@H]1[C@H]([C@H]([C@H]([C@H]([C@H]1O[C@H]2[C@@H]([C@H]([C@@H](CO2)O)O)O)O)O)O)O
InChI InChI=1S/C25H46O11/c1-2-3-4-5-6-7-8-9-10-11-12-13-16(27)35-23-20(31)18(29)19(30)21(32)24(23)36-25-22(33)17(28)15(26)14-34-25/h15,17-26,28-33H,2-14H2,1H3/t15-,17+,18+,19-,20+,21-,22-,23+,24-,25+/m1/s1
InChI Key QJIXADDKHNEDBB-JVHRSCIMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H46O11
Molecular Weight 522.60 g/mol
Exact Mass 522.30401228 g/mol
Topological Polar Surface Area (TPSA) 186.00 Ų
XlogP 1.60

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2S,3S,4R,5R,6R)-2,3,4,5-tetrahydroxy-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxycyclohexyl] tetradecanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

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 97.84% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.45% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.91% 91.11%
CHEMBL5255 O00206 Toll-like receptor 4 94.31% 92.50%
CHEMBL2581 P07339 Cathepsin D 93.88% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 92.61% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.39% 97.25%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 91.49% 85.94%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.39% 92.08%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.74% 96.77%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.97% 94.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.59% 100.00%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.88% 92.86%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.66% 95.17%
CHEMBL4040 P28482 MAP kinase ERK2 83.59% 83.82%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 83.58% 82.50%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.53% 91.24%
CHEMBL299 P17252 Protein kinase C alpha 83.12% 98.03%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.53% 97.29%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 82.50% 80.33%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.56% 91.81%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.27% 95.50%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.74% 90.71%

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.
Solanum lanceolatum

Cross-Links

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PubChem 163105664
LOTUS LTS0229854
wikiData Q105222697