Nα-Fmoc-Nγ-trityl-L-asparagine-2-chlorotrityl resin
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Nα-Fmoc-Nγ-trityl-L-asparagine-2-chlorotrityl resin

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Pre-loaded resins for solid phase peptide and organic synthesis

Category
2-Chlorotrityl-Chloride-Resin with Amino Acids
Catalog number
BAT-000183
Synonyms
Fmoc-L-Asn(Trt)-2-chlorotrityl resin
DVB Crosslinking
1% DVB
Mesh Size
200-400 mesh
Substitution
0.3-0.9 meq/g
Storage
Store at 2-8°C

Nα-Fmoc-Nγ-trityl-L-asparagine-2-chlorotrityl resin, a specialized resin utilized in peptide synthesis, particularly excels in the precise preparation of asparagine-containing peptides. Here are the key applications of this resin:

Solid-Phase Peptide Synthesis (SPPS): Integral to SPPS, this resin plays a pivotal role in incorporating asparagine residues while safeguarding against undesirable side reactions. Asparagine, vulnerable to forming aspartimide and succinimide during synthesis, finds protection through the shielding groups (Fmoc and trityl), thus enhancing the purity and yield of the final peptide product.

Functional Peptide Development: Researchers harness this resin's capabilities to craft functional peptides with asparagine residues that display specific biological properties, like serving as enzyme inhibitors or signaling molecules. The resin's precise protective measures safeguard the structural integrity of these peptides, facilitating accurate biological assessments and potentially opening doors to therapeutic advancements.

Peptide-Based Drug Discovery: Within the realm of drug discovery, peptides synthesized using this resin undergo screening for activity against diverse disease targets. The high-fidelity synthesis process leads to the creation of peptide libraries with minimal by-products, expediting the exploration of novel peptide-based drugs with enhanced efficacy and safety profiles.

Glycopeptide Synthesis: This resin proves invaluable in the synthesis of glycopeptides, which entail peptides featuring carbohydrate moieties linked to asparagine residues. The strategic deployment of protecting groups ensures the availability of the asparagine side chain for glycosylation post-peptide assembly, a critical step in delving into protein glycosylation mechanisms and advancing the development of glycopeptide-oriented therapeutics.

1. The 2-chlorotrityl resin: a worthy addition to the medicinal chemist's toolbox
W J Hoekstra Curr Med Chem. 2001 May;8(6):715-9. doi: 10.2174/0929867013373192.
The polystyrene-based 2-chlorotrityl resin was originally used in the synthesis of peptides using an Fmoc-amino acid/carboxyl-linked protocol. While traditionally employed to prepare a number of biologically active peptides, the resin has received increasing attention as a support for the synthesis of pseudopeptide and non-peptide molecules recently. This review focuses on 2-chlorotrityl resin-supported synthesis of small molecules that collectively display a broad range of biological activities.
2. Biological Properties and Therapeutic Applications of Propolis
José M Sforcin Phytother Res. 2016 Jun;30(6):894-905. doi: 10.1002/ptr.5605. Epub 2016 Mar 14.
Propolis is a resinous material collected by bees from bud and exudates of the plants, mixed with bee enzymes, pollen and wax. In this review, the biological properties of propolis and some therapeutic applications are discussed. The same biological activities have been investigated until today, using samples from different geographic regions. Thus, the study of the biological properties of a given sample should always be associated with its chemical composition and botanical source, representing a particular sample of a given geographic area, exploring its biological potential and the role of its constituents. Efforts have been carried out to explain propolis' mechanisms of action in vivo and in vitro, but the majority of propolis' targets and actions are still unclear. The number of formulations containing propolis and patents have increased, although propolis extracts have been used deliberately with different recommendations, not always mentioning the chemical composition, vegetal source and the methods of extraction. Clinical studies will help to obtain criterious recommendations in view of the expected outcomes. Further investigation should explore the effects of common compounds found in the samples from all over the world in an attempt to standardize the research on propolis and to obtain new drugs.
3. Resin Glycosides from Convolvulaceae Family: An Update
Rani Maharani, Mohamad Fajar, Unang Supratman Molecules. 2022 Nov 23;27(23):8161. doi: 10.3390/molecules27238161.
Resin glycoside is a type of secondary metabolite isolated commonly from the Convolvulaceae family. It consists of oligosaccharides conjugated to organic acids with a larger percentage having a macrocyclic structure. The resin glycosides reported in this review is classified mostly based on the number of sugar units constructing the structure, which is correlated to the biological properties of the compounds. According to preliminary reviews, the protocols to isolate the compounds are not straightforward and require a special technique. Additionally, the structural determination of the isolated compounds needs to minimize the structure for the elucidation to become easier. Even though resin glycosides have a complicated structural skeleton, several total syntheses of the compounds have been reported in articles published from 2010 to date. This review is an update on the prior studies of the resin glycosides reported in 2010 and 2017. The review includes the classification, isolation techniques, structural determination, biological properties, and total synthesis of the resin glycosides.
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