149707-76-6

Upstream product

• 627466-84-6 2,3,4,6-tetra-O-benzoyl-D-galactose 
• 545-06-2 trichloroacetonitrile 
• 2592-58-7 1,2,3,4,6-Penta-O-benzoyl-α-D-galactopyranose 
• 2592-58-7 1,2,3,4,6-penta-O-benzoyl-α-D-galactopyranoside 
• 113544-55-1 2,3,4,6-tetra-O-benzoyl-α-D-galactopyranose 
• 627466-64-2 2,3,4,6-tetra-O-benzoyl-D-glucopyranose 
• 14218-11-2 2,3,4,6-tetra-O-benzoylglucosyl bromide 
• 98-88-4 benzoyl chloride 
• 165877-99-6 2,3,4,6-tetra-O-Bz-β-D-glucopyranosyl bromide 
• 2592-58-7 1,2,3,4,6-penta-O-benzoyl-β-D-glucopyranose 
• 64768-20-3 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranose 
• 492-61-5 β-D-glucose 
• 2280-44-6 D-Glucose 
• 2592-58-7 1,2,3,4,6-penta-O-benzoyl-D-glucopyranoside 

Downstream Products

• 192126-03-7 C₄₉H₅₈O₁₄SSi 
• 207284-73-9 C₄₄H₄₈O₁₂Si 
• 217298-86-7 n-propyl 2-acetamido-3-azido-6-O-benzyl-2,3-dideoxy-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 233674-88-9 2,3,4,6-Tetra-O-benzoyl-β-D-galactopyranosyl-(1->4)-1,2,3,6-tetra-O-benzoyl-α-D-mannopyranose 
• 228106-24-9 C₆₃H₆₇N₃O₁₇Si 
• 350243-33-3 1-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-3,4-O-isopropylidene-5,6-di-O-tetradecyl-D-mannitol 
• 350243-30-0 1-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-3-O-benzyl-5,6-di-O-tetradecyl-D-glucitol 
• 402923-09-5 (2R)-2-azidohexadecyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranoside 
• 402923-13-1 (2S)-2-azidohexadecyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranoside 
• 401593-00-8 isopropyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->6)-2,4-di-O-benzoyl-3-O-tert-butyldimethylsilyl-1-thio-β-D-galactopyranoside 
• 403511-57-9 C₆₁H₅₂N₂O₂₂ 
• 403511-56-8 C₆₁H₅₂N₂O₂₂ 
• 70751-57-4 C₄₆H₄₆O₁₅ 
• 492454-33-8 C₆₉H₆₂O₂₂ 

Relevant academic research and scientific papers

VACCINE COMPOSITIONS AND ANTIBODIES FOR LYME DISEASE

The present invention relates to vaccine compositions comprising lipid antigens, antibodies targeting lipid antigens, pharmaceutical compositions comprising such and their use in diagnosing, monitoring, treating, and preventing infectious disease, such as Lyme disease. In one aspect, administered is a therapeutically effective amount of a vaccine composition comprising a lipid antigen, an antibody or fragment thereof binding a lipid antigen, and/or a pharmaceutical composition comprising an antibody or fragment thereof binding a lipid antigen. Other aspects are described.

Experimental and theoretical study of the O3/O4 regioselectivity of glycosylation reactions of glucopyranosyl acceptors

The knowledge of the regioselectivity between different hydroxyl groups of glycosyl acceptors is valuable in planning simple strategies for the synthesis of oligosaccharides, minimizing the use of protecting groups. With the aim of obtaining deeper knowle

ENDOSOMAL CLEAVABLE LINKERS

The present disclosure relates generally to cleavable linkers and uses thereof.

The dehydroepiandrosterone and dehydroepiandrosterone alkone glycosylation derivative and its preparation method and application

The invention discloses epiandrosterone glycosylation derivatives and dehydrogenated epiandrosterone glycosylation derivatives, and a preparation method thereof. The preparation method comprises the following steps: respectively carrying out coupling reac

3 - monosaccharide acid oxygen glucoside oleanolic alkane type and wusu alkane triterpene saponin derivative and its preparation method and application

The invention discloses a 3-monouronic acid o-glycoside oleanane type and ursane type triterpenoid saponin derivative. The derivative has a structural formula as shown in the specification, wherein R4 is one of H atom, alkyl containing 1-10 carbons, alkyl

Cross metathesis assisted solid-phase synthesis of glycopeptoids

A solid-phase synthesis of glycopeptoids was explored through olefin cross metathesis (CM). Peptoids and sugar derivatives with appropriate olefin moieties were coupled in the presence of an olefin metathesis catalyst to afford glycopeptoids in good yield

Mitochondrial affinity of guanidine-rich molecular transporters built on monosaccharide scaffolds: Stereochemistry and lipophilicity

We synthesized eight G8 molecular transporters (MTs) based on 4 different monosaccharide scaffolds, and studied their biological properties with a special focus on possible mitochondrial targeting and tissue selectivity. The mitochondrial affinity of these MTs was found to be clearly related to the scaffold stereochemistry and also tenuously with the lipophilicity. It may be suggested that in the practical delivery strategy of drugs for the brain and mitochondrial diseases the BBB permeability and mitochondrial affinity should be considered as key parameters, and that an enhanced mitochondrial affinity appears possible by further research on the structure-property relationship of guanidine-rich molecular transporters.

Synthesis of some phenylpropanoid glycosides (PPGs) and their acetylcholinesterase/xanthine oxidase inhibitory activities

In this research, three categories of phenylpropanoid glycosides (PPGs) were designed and synthesized with PPGs isolated from Rhodiola rosea L. as lead compounds. Their inhibitory abilities toward acetylcholinesterase (AChE) and xanthine oxidase (XOD) were also tested. Some of the synthetic PPGs exhibited excellent enzyme inhibitory abilities.

Antifungal activity of 2α,3β-functionalized steroids stereoselectively increases with the addition of oligosaccharides

Invasive fungal infections pose a significant problem to the immune-compromised. Moreover, increased resistance to common antifungals requires development of novel compounds that can be used to treat invasive fungal infections. Naturally occurring steroid

Synthesis and properties of a photoactivatable analogue of psychosine (β-galactosylsphingosine)

(Chemical Equation Presented) Photoaffinity probes: The first synthesis of a photoaffinity probe of psychosine (blue) is reported, where benzophenone (red) is tethered as a crosslinking moiety. This photo-psychosine probe (shown) displayed a similar potency as psychosine in stimulating Ca2+ flux in U937 cells, suggesting that it may be useful for labeling and identifying the still unidentified psychosine receptor(s) by mass spectrometry.