Peptides

Peptide H-IL^DTAGKEEY-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.

Peptide H-VLFGLGFAI^-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.

Peptide H-LLTSFLPAQLLR^-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.

Peptide H-NTVISVNPSTK^-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.

Peptide H-VTSIQDWV^Q^K^-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.

Peptide H-NIDALSGMEGR^-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.

Peptide H-A^DQDNPWR^AYLDL^L^FPTDTLLLDLL^WCG-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.

H-Met-Asp-OH is a synthetic formyl peptide that was designed to be hydrolyzed by proteolytic enzymes. It has been shown to be able to inhibit the formation of β-amyloid, which is associated with Alzheimer's disease. H-Met-Asp-OH also has been shown to have physicochemical properties similar to aspirin, and can be used as an antiplatelet agent. In addition, it has been shown to act as a catalase inhibitor in vitro and may have some therapeutic potential for the treatment of diabetes mellitus type 2.

Suc-Ala-Glu-Pro-Phe-pNA is a peptide that is a specific interaction with neutrophils. It is an endogenous factor that has been shown to activate neutrophil functions, such as chemotaxis and phagocytosis. The substrate proteins of this peptide are involved in the regulation of neutrophil functions. Suc-Ala-Glu-Pro-Phe-pNA has also been shown to inhibit the activity of phosphatases, which may lead to inhibition of cell proliferation. The structure activity relationship studies for this peptide show that it can be used as an inhibitor for cells in early stages of development.

H-Val-Trp-OH is a noncompetitive inhibitor of the enzyme tyrosinase, which plays a role in melanin production. It also has radical scavenging activities and can inhibit the activity of other enzymes such as glucose 6-phosphate dehydrogenase and acetylcholinesterase. The compound is stable in aqueous solution and can be used to study the effects of H-Val-Trp-OH on wheat germ cells. It is composed of an amino acid sequence that resembles tyrosine, with a carboxylate group attached to the hydroxyl group at position 3. H-Val-Trp-OH is most active against tyrosinase when it is in its activated form, but it can also act as an inhibitor when it is not activated. The compound inhibits the activity of tyrosinase by binding to its active site and blocking the binding or catalysis of substrate molecules. This inhibition occurs through competitive interactions with

Boc-Asp(OBzl)-Pro-Arg-AMC·HCl is a high quality, reagent, complex compound and useful intermediate. It is a fine chemical with the CAS Number 201849-39-0 that is used in research and development. Boc-Asp(OBzl)-Pro-Arg-AMC·HCl is also a versatile building block that can be used in reactions for the synthesis of other compounds.

Fmoc-Cys(Dpm)-OH is a chemical that belongs to the group of reaction components. It is a high quality reagent for research and development and can be used as a building block in the synthesis of other fine chemicals. Fmoc-Cys(Dpm)-OH is also an intermediate for the synthesis of complex compounds such as peptides, proteins, and antibiotics. This compound has a broad range of applications in biomedicine, organic chemistry, and pharmaceuticals.

H-gamma-carboxy-Glu-OH is a synthetic peptide with the amino acid sequence H-gamma-Carboxy-Glu. It is a glp-1 analogue and its function is to regulate glucose homeostasis. The protein has been shown to have antiapoptotic effects in human osteosarcoma cells. H-gamma-carboxy-Glu-OH has also been shown to regulate mitochondrial membrane potential, which is required for cell signaling pathways and calcium binding. H-gamma-carboxy-Glu-OH's receptor molecule is known as the GPCR, which plays an important role in the regulation of cell signaling pathways and calcium binding. H gamma carboxy Glu OH is a cyclic peptide that contains disulfide bonds. This compound has the basic structure of an alpha helix, which consists of many turns of amino acids bonded together by hydrogen bonds between individual amino acids

Lys-Arg-OH acetate salt (LRA) is a protein transport peptide that is found in the neurosecretory system and has been used as a growth factor for the production of human insulin. LRA stimulates the release of pepsinogen, which breaks down food proteins into polypeptides and amino acids. It also has proteolytic activity, which helps break down proteins into peptides. LRA shares structural similarities with other peptide hormones such as vasopressin and oxytocin, but it differs by having an amide instead of an ester linkage between the lysine and arginine residues.

H-Arg-Gly-Asp-Cys-OH is a biomimetic amino acid that possesses the same three-dimensional structure as the amino acid sequence found in the human epidermal growth factor receptor 2 (HER2). This compound has been shown to inhibit the activity of enzymes, such as kinases, which are involved in cancer cell division. It also can be used to target and destroy cancer cells using gene therapy. H-Arg-Gly-Asp-Cys-OH binds to messenger RNA and inhibits its translation into protein, which may lead to cell death. H-Arg-Gly-Asp-Cys -OH has been shown to bind specifically with HER2 receptors on breast cancer cells and promote their destruction by inducing apoptosis.

Custom research peptide; min purity 95%. For different specs please use the Peptide Quote Tool

Nesfatin-1 (30-59) is a peptide that is isolated from the brain and has been shown to have the ability to regulate feeding behavior. It is thought to be involved in the regulation of appetite and body weight. Nesfatin-1 (30-59) has been shown to inhibit ghrelin secretion, which is a hormone involved in hunger and satiety. This peptide also appears to stimulate insulin secretion by pancreatic beta cells, which may contribute to its anti-diabetic effects.

H-Phe-Ile-Arg-Gly-Gly-Met-Tyr-Glu-Gly-Lys-Lys is a peptide that has biological activity. It is a member of the class of Biologically Active Peptides, which are biochemicals that have been shown to have cardioprotective effects. This peptide was found to reduce cardiac injury and dysfunction in animal models of myocardial infarction.

H-Arg(Me)-OH acetate salt is a chemically synthesized amino acid derivative, specifically designed for research purposes in the field of biochemistry and molecular biology. This compound is a methylated form of the naturally occurring amino acid arginine, often used as a reagent in peptide synthesis and enzymatic studies.

Z-Gly-Ala-Met-AMC is a protease inhibitor that has been shown to inhibit the amyloidogenic processing of β-amyloid and reduce the formation of amyloid plaques in vivo. It also inhibits the degradation of normal proteins by proteases, which leads to cell death. Z-Gly-Ala-Met-AMC is used as a marker for identifying and quantifying proteolytic activity in cells with high levels of proteolytic activity. The drug has been shown to be effective in assays using cell populations and homogenous assays.

Ac-Nle-Pro-Nle-Asp-AMC is a reactive molecule that has been shown to be neuroprotective and to inhibit insulin resistance in mammalian cells. Ac-Nle-Pro-Nle-Asp-AMC is able to stop neuronal death by binding to the proteolytic enzymes, such as ubiquitin ligases, and inhibiting their activity. This drug also inhibits the activity of c2c12 myotubes, which are muscle cells that have been used in research studies. Ac-Nle-Pro-Nle-Asp AMC binds to ubiquitin and prevents it from being degraded by the proteasome system, which is a cellular protein degradation pathway. Ac-Nle-Pro-Nle -Asp AMC also inhibits the release of inflammatory factors from c2c12 myotubes, which may be due to its ability to block ubiquitin ligases.

Abz-Phe-Arg-Lys(Dnp)-Pro-OH trifluoroacetate (ABA) is a low potency activator of the endogenous angiotensin system, with no known clinical use. ABA has been shown to activate the endogenous angiotensin system in vivo in rats and humans. It has also been shown to increase blood pressure in rats by activating the renal sympathetic nervous system. The activation of this system may be due to its ability to release neutrophil chemotactic factor from adipose tissue, increasing the number of neutrophils that contribute to inflammation through their release of reactive oxygen species. The mechanism underlying this activation is unknown, but may involve an interaction with enalaprilat, a potent inhibitor of angiotensin converting enzyme (ACE), or adipose tissue lipolysis.