1359 Results for: "peptide synthesis"

Supplier: Chemglass

Cylindrical, jacketed, peptide synthesis reaction vessel with coarse porosity fritted resin support.

Supplier: CHEM-IMPEX INTERNATIONAL, INC

Fmoc-Ala-Ala-OH is a highly regarded compound in the field of peptide synthesis, known for its role as a versatile building block in the development of peptides and proteins. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis process. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers and professionals engaged in peptide chemistry. Fmoc-Ala-Ala-OH is particularly useful in the synthesis of dipeptides and can be employed in various applications, including drug development, bioconjugation, and the design of peptide-based therapeutics. Its stability and compatibility with standard coupling reagents enhance its utility in complex peptide assembly, providing a reliable option for achieving high yields in synthetic processes. Moreover, Fmoc-Ala-Ala-OH stands out due to its ease of use and the ability to facilitate the synthesis of peptides with specific sequences, which is crucial for the development of targeted therapies. Researchers appreciate its effectiveness in generating peptides that can be utilized in a range of applications, from basic research to advanced therapeutic solutions. With its proven track record in peptide synthesis, Fmoc-Ala-Ala-OH is an indispensable tool for professionals looking to innovate in the fields of biochemistry and pharmacology.

Supplier: CHEM-IMPEX INTERNATIONAL, INC

Boc-Gly-Gly-OH, also known as N-Boc-Glycylglycine, is a versatile dipeptide derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an ideal choice for various applications in organic synthesis. Researchers often employ Boc-Gly-Gly-OH in the development of peptide-based therapeutics, as it serves as a building block for more complex peptide structures. Its unique properties allow for selective deprotection, facilitating the synthesis of peptides with desired functionalities. In addition to its role in peptide synthesis, Boc-Gly-Gly-OH is also valuable in the study of biological processes and drug design. Its ability to mimic natural peptides makes it a useful tool in the exploration of peptide-receptor interactions. The compound's favorable characteristics, such as its ease of handling and compatibility with various coupling reagents, further enhance its appeal to researchers and industry professionals. Whether in academic research or industrial applications, Boc-Gly-Gly-OH stands out as a reliable and effective compound for advancing peptide chemistry.

Supplier: CHEM-IMPEX INTERNATIONAL, INC

Fmoc-Gly-Gly-Gly-OH, also known as Fmoc-tri-glycine, is a versatile peptide derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during solid-phase peptide synthesis. Its unique structure allows for the efficient assembly of longer peptide chains, making it an invaluable tool for researchers in the fields of biochemistry and molecular biology. The practical applications of Fmoc-Gly-Gly-Gly-OH extend to the development of peptide-based therapeutics, where it serves as a building block for creating bioactive peptides with potential therapeutic properties. Additionally, its use in the synthesis of peptide libraries enables researchers to explore a wide range of biological activities, facilitating drug discovery and development. With its high purity and stability, Fmoc-Gly-Gly-Gly-OH stands out as a reliable choice for professionals seeking to enhance their peptide synthesis workflows.

Supplier: MilliporeSigma

N-Methyl-2-pyrrolidone (NMP) for peptide synthesis, Supelco®

Supplier: CHEM-IMPEX INTERNATIONAL, INC

Fmoc-Gly-Pro-OH is a valuable building block in peptide synthesis, particularly favored for its role in solid-phase peptide synthesis (SPPS). This compound, also known as Fmoc-glycine proline hydroxyl, features a fluorenylmethoxycarbonyl (Fmoc) protecting group that allows for selective deprotection during synthesis, making it an essential tool for researchers and industry professionals in the field of biochemistry and pharmaceuticals. Its unique structure enhances stability and solubility, facilitating the formation of complex peptides and proteins. This compound is particularly useful in the development of therapeutic peptides and proteins, enabling the creation of bioactive molecules with specific functionalities. Researchers have successfully utilized Fmoc-Gly-Pro-OH in the synthesis of peptide-based drugs and in studies related to protein folding and interactions. Its ability to provide a stable backbone while allowing for functional group modifications makes it a preferred choice for those looking to innovate in peptide design and development. With its proven track record in various applications, Fmoc-Gly-Pro-OH stands out as a reliable and efficient reagent for advancing peptide chemistry.

Supplier: Bachem Americas

AKH, a peptide hormone which stimulates synthesis of 1,2-diacyl-sn-glycerols in the Manduca sexta fat body.

Supplier: Kemtech America

Solid phase peptide synthesis vessels feature 2 mm PTFE stopcocks and fritted glass supports for resin beads during operation.

Supplier: CHEM-IMPEX INTERNATIONAL, INC

It is used for the synthesis of the solid phase peptide synthesis of peptide amines utilizing Fmoc-protected amino acids.

Supplier: CHEM-IMPEX INTERNATIONAL, INC

Boc-Ala-Ala-OH, also known as N-Boc-L-alanyl-L-alanine, is a valuable dipeptide derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers engaged in the development of peptide-based therapeutics. Its unique structure allows for selective reactions, facilitating the synthesis of more complex peptides and proteins. In the pharmaceutical industry, Boc-Ala-Ala-OH serves as a crucial intermediate in the preparation of bioactive peptides, which are essential for drug development and therapeutic applications. Its ability to protect amino groups during synthesis while maintaining reactivity makes it a preferred choice for chemists aiming to streamline their workflows. Additionally, its applications extend to the fields of biochemistry and molecular biology, where it is used in the study of protein interactions and enzyme activity. The compound's versatility and efficiency in peptide synthesis underscore its significance in advancing research and development in various scientific domains.

Supplier: CHEM-IMPEX INTERNATIONAL, INC

Boc-Gly-Gly-Gly-OH, also known as N-Boc-Glycylglycylglycine, is a versatile peptide derivative that plays a significant role in peptide synthesis and drug development. This compound is particularly valued in the pharmaceutical and biochemistry sectors for its ability to serve as a building block in the synthesis of more complex peptides. Its unique structure, featuring three glycine residues, enhances its solubility and stability, making it an ideal candidate for various applications, including the development of peptide-based therapeutics and research into protein interactions. Researchers utilize Boc-Gly-Gly-Gly-OH in the preparation of peptide libraries, enabling the exploration of new drug candidates and therapeutic agents. Its protective Boc (tert-butyloxycarbonyl) group allows for selective deprotection, facilitating the stepwise assembly of peptides. This compound's compatibility with solid-phase peptide synthesis (SPPS) further underscores its importance in the field, as it streamlines the process of creating complex peptide structures. With its robust applications and ease of use, Boc-Gly-Gly-Gly-OH is an essential tool for professionals engaged in peptide research and development.

Supplier: Thermo Scientific Chemicals

Applications: Nucleic acid and peptide synthesis

Supplier: Bachem Americas

By-product formed during the synthesis of the dipeptide Ala-Gln, glutamine source in parenteral nutrition.

Supplier: Supra Sciences

Common reagent utilized for peptide synthesis on solid support.

Supplier: Bachem Americas

Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.

Supplier: Prosci

Ribose-Phosphate Pyrophosphokinase 2 (PRPS2) is a phosphoribosyl pyrophosphate synthetase that belongs to the ribose-phosphate pyrophosphokinase family. PRPS2 is a homodimer. The active form is probably an hexamer composed of three homodimers. PRPS2 catalyzes the synthesis of phosphoribosylpyrophosphate (PRPP) that is essential for nucleotide synthesis. PRPS2 catalyzes the synthesis of 5-phosphoribosyl 1-pyrophosphate from ATP and D-ribose 5-phosphate. In addition, PRPS2 plays a central role in the synthesis of purines and pyrimidines.

Supplier: New England Biolabs (NEB)

NEBExpress GamS nuclease inhibitor is a recombinant protein that inhibits Exonuclease V (RecBCD) activity and stabilizes linear DNA templates in E. coli based in vitro protein synthesis reactions.

Supplier: Bachem Americas

Mating pheromone of mating type α cells of S. cerevisiae. This factor inhibits DNA synthesis, thereby preventing cell division of mating type a cells. The hydrophobic peptide binds to a class D G-protein-coupled receptor Ste2p.

Supplier: MilliporeSigma

N-Methyl-2-pyrrolidone (NMP) for peptide synthesis, Supelco®

Supplier: Bachem Americas

Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.

Supplier: ALADDIN SCIENTIFIC

Acetyl Coenzyme A Trilithium Salt Trihydrate is an essential cofactor and carrier of acyl groups in enzymatic acetyl transfer reactions. It is also the precursor for lipid biosynthesis and the neurotransmitter acetylcholine.Carrier of acyl groups for enzymatic reactions involving fatty acid synthesis and oxidation and in biological acetylations.Carrier of acyl groups in enzymatic reactions in fatty acid synthesis and oxidation and in biological acetylations.

Supplier: Bachem Americas

Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.

Supplier: Bachem Americas

A pheromone biosynthesis activating neuropeptide hormone which in the picomolar range induced sex pheromone synthesis in various moth species.

Supplier: MilliporeSigma

Supplier: Bachem Americas

Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.

Supplier: Thermo Scientific Chemicals

N,N-Dimethylformamide 99.8% for peptide synthesis

Supplier: CHEM-IMPEX INTERNATIONAL, INC

One of the most convenient coupling reagents for peptide synthesis without carcinogenic by-products. It replaces BOP reagent. This is especially suitable for solid-phase peptide synthesis, avoids racemization.

Supplier: Bachem Americas

For Fmoc solid phase synthesis of N-alkyl peptide amides by reductive amination.

Supplier: Bachem Americas

Educt for the synthesis of proteasome inhibitors.

Supplier: Bachem Americas

Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.