Peptídeos

Glutaryl-Gly-Arg-AMC hydrochloride salt is a high quality, fine chemical reagent that is useful as a building block, scaffold or intermediate. It has been used in the synthesis of other complex compounds and has been shown to have potential for use in drug discovery research. Glutaryl-Gly-Arg-AMC hydrochloride salt is a versatile building block that can be used in reactions that require the presence of an amine group, such as peptide coupling. This reagent can also be used to modify the functional groups on small molecules, such as aldehydes and carboxylic acids. Glutaryl-Gly-Arg-AMC hydrochloride salt is also useful as a reaction component in the synthesis of speciality chemicals, such as pharmaceuticals and agrochemicals.

<p>n-Hexyltrioxyethylene is a glycol ether that belongs to the group of organic solvents. It is used in detergent compositions and as a polymerization initiator for polyester resins. This compound has been shown to have antibacterial properties and can be used as a cationic surfactant in liquid crystal compositions. n-Hexyltrioxyethylene also has functional groups that are reactive with esters and hydrocarbons, which can be used in reaction solutions to form ester linkages or hydrocarbon bonds. The average particle diameter of this substance is around 100 nm.</p>

Please enquire for more information about Mca-Tyr-Val-Ala-Asp-Ala-Pro-Lys(Dnp)-OH trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>H-Glu-Thr-OH is a molecule that belongs to the group of aminoglycosides. It is a broad spectrum antibiotic that inhibits bacterial protein synthesis by binding to the 30S ribosomal subunit. H-Glu-Thr-OH has been shown to be effective against various bacteria, including those that are resistant to other antibiotics such as penicillin and erythromycin. This drug has also been shown to be effective against cancer cells in vitro. H-Glu-Thr-OH is a potent inhibitor of inflammatory bowel disease, which may be due to its ability to inhibit the production of proinflammatory cytokines such as tumor necrosis factor alpha (TNFα). The drug also has an insulin sensitizing effect in type 2 diabetes mellitus patients, which may be due to its ability to enhance glucose uptake into skeletal muscle cells and adipocytes.</p>

The E22delta (Osaka mutation) mutation of Amyloid β promotes β-sheet transformation.

<p>Neuropeptide W-23 (human) is an antibody that recognizes the neuropeptide receptor, specifically the Neuropeptide Y receptor 1. The antibody binds to the Npy1 receptor and inhibits its activity. Neuropeptide W-23 (human) can be used as a research tool in cell biology and pharmacology studies.</p>

<p>Please enquire for more information about Prostaglandin A1 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

H-Glu[Cyclo(Arg-Gly-Asp-D-Phe-Lys)]2 is a peptide that is used as a targeting agent for tumor imaging. It has been shown to be an effective imaging agent for tumors by binding to the RGD sequence in the extracellular matrix of the tumor. This peptide can be derivatized with fluorochromes and other functional groups for use as a contrast agent or as a labeling reagent. H-Glu[Cyclo(Arg-Gly-Asp-D-Phe-Lys)]2 has also been shown to inhibit angiogenesis and induce apoptosis, which may be due to its ability to bind to integrin receptors on endothelial cells and block their proliferation.

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

Gurmarin is a polycyclic diterpene that can be found in the bark of the G. lucidum tree. It has been shown to bind to glutamate receptors, which are ion channels that allow ions such as calcium and sodium to pass through cell membranes. Gurmarin has been shown to activate these receptors in vitro, and knockout or over-expression of these receptors in cells can lead to changes in receptor activity. Gurmarin has also been shown to have specific binding affinity for a certain type of receptor cell, which are cells with cation channels that may be involved in taste perception. The receptor binding site on the gurmarin molecule is thought to correspond with the sweet taste sensation.

This resin is for use in combinatorial chemistry. TentaGel is a gelatinous resin and an important support for solid phase synthesis. TentaGel resins are constructed with a backbone of low crosslinked polystyrene grafted with polyoxyethylene (polyethylene glycol) as shown below. The typical chain length of POE (n) is approximately 68 ethylene oxide units or an average MW of 3000. This long chain creates a spacer that effectively separates the reactive site (X) from the crosslinked backbone matrix. Particle size 130 µm; capacity: 0.2-0.35 meq/g Substitution Functional Group: -O-CH2-CH2-NH2

<p>(Asp-Glu-Val-Asp)2-Rh110 is a peptide substrate for caspase 3 and 7. It has been shown to be an effective inhibitor of peptidyl prolyl cis, trans isomerase (PPIase) in vitro and in vivo, which may lead to a possible therapeutic target for the treatment of neurodegenerative disorders.</p>

AF488 DBCO is a water-soluble, green-fluorescent probe for copper-less detection of azide-tagged biomolecules.  This probe is water-soluble and its fluorescence is pH independent over a wide pH range. The brightness and photostability of blue dyes are best suited to direct imaging of low-abundance targets.

Please enquire for more information about AF488 NHS Ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

H-Asn(Trt)-2-ClTrt-Resin (100-200 mesh) 1% DVB is an alcohol resin that can be used for the synthesis of peptides. The resin has a thiol group on each side, which allows for the attachment of amines or thiols. H-Asn(Trt)-2-ClTrt-Resin (100-200 mesh) 1% DVB is available in different sizes and can be ordered as either powder or pellets.

<p>H-LCL-OH is a custom research peptide; min purity 95%, TFA salt. For different specs please use the Peptide Quote Tool</p>

Serum Amyloid A protein is a custom research peptide; min purity 95%, TFA salt. For different specs please use the Peptide Quote Tool

Ac-Asp-pNA is a carboxy, serine protease that is used as an antigen in bactericidal and antibacterial assays. It also has been shown to be effective against neutral ph organisms such as E. coli and Pseudomonas aeruginosa. Ac-Asp-pNA elutes from the column when it is inactivated under neutral ph conditions, which can be seen by the presence of reactive peaks. The protonation of Ac-Asp-pNA at high pH results in a loss of reactivity, which can be detected by the diminazene peak at low pH. This protein is activated by potassium ions and cellular proteins, which can be seen by the presence of peaks at m/z 816 and 806 respectively.

The peptide is a synthetic peptide that has been shown to have a binding affinity for the Protease-Activated Receptor 2 (PAR2). It is a PAR2 antagonist, and has been shown to reduce blood pressure in hypertensive rats. The peptide also inhibits the activity of thrombin, which may be due to its ability to inhibit the activation of PAR1.

This synthetic peptide is a hydrophobic RGD Fibronectin Peptide which enhances cell attachment and adhesion. This is due to it containing the Arg-Gly-Asp (RGD) sequence, is a highly conserved integrin recognition sequence within fibronectin. As a result it can promote the adhesion of cells to fibronectin, a protein found in the extracellular matrix and also promotes adhesin of cells to collagen and laminin. One-Letter Formula: Ac-GrGDSPASSKGGGGSrLLLLLLr-Amide

H-Phe-Ile-Arg-Val-Val-Met-Tyr-Glu-Gly-Lys-Lys is a biologically active peptide that has been shown to have angiogenic and cardiovascular properties. It has also been demonstrated to inhibit thrombospondin, which is a protein that promotes the formation of blood clots. This peptide is a member of the group of peptides and biochemicals, which are molecules that regulate the processes in living organisms.

<p>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.</p>

Fmoc8-Lys4-Lys2-Lys-ß-Ala-Wang resin is an inhibitor of protein interactions. It is a peptide that contains a sequence of amino acids that binds to other proteins and prevents them from forming. Fmoc8-Lys4-Lys2-Lys-ß-Ala-Wang resin can be used in the study of protein interactions and receptor binding, as well as for the production of antibodies.

Angiotensin I is a protein encoded by the AGTR1 gene. It is a precursor to angiotensin II, which causes vasoconstriction and has other effects on blood vessels, kidneys, and the heart. Angiotensin I is produced by proteolytic cleavage of pro-angiotensinogen in the liver. The mouse monoclonal antibody to human angiotensin I (mAb-HAI) recognizes both human and bovine angiotensin I. This antibody can be used for immunohistochemistry or Western blot analysis of cells from mice that have been injected with mAb-HAI. It has also been shown to reduce kidney fibrosis in mice when it is administered as a subcutaneous injection three times per week.

Ac-Tyr-Val-Nle-Gly-His-D-Phe-Arg-Trp-Asp-Arg-Phe-Gly-NH2 is a peptide that is a melanocortin receptor agonist. It has been shown to have biochemically active properties and can be used as a research tool in the study of peptides and their receptors.

<p>Boc-Leu-Gly-Arg-AMC acetate salt is a potential drug target for leishmaniasis. It inhibits the growth of Leishmania by binding to the 17β-estradiol receptor and inhibiting protein synthesis. This drug also has a hydrolytic activity against proteins, which is activated by an acidic environment. It has been shown to inhibit the growth of bacteria including Staphylococcus aureus and Chlamydia pneumoniae by inhibiting urokinase-type plasminogen activator (uPA) and serine protease activities. Boc-Leu-Gly-Arg-AMC acetate salt has also been shown to inhibit cellular proliferation in cancer cells.</p>

<p>Suc-Gly-Pro-Leu-Gly-Pro-AMC (SGLP) is a synthetic substrate that is hydrolyzed by proteases and has been used as a model substrate in protease studies. It has been shown to be cleaved by a number of enzymes, including chymotrypsin, trypsin, elastase, and cathepsin D. The hydrolysis products are sucrose glycolate, glycerol phosphate, leucine amino acid ester, and proline amino acid ester. SGLP has been shown to have low bioavailability in human liver cells and heart tissue. Studies have also shown that SGLP can stimulate the production of myelocytic cells in vitro. This activity may be due to its ability to act as an immunomodulator or by targeting tissue enzyme activities.</p>

IsoDTB (Isotopically labeled Desthoibiotin Azide) probes take advantage of the mass shift of stable heavy isotope labels (SHLs) to enable mass-independent chemical proteomics platform that helps to address unique challenges of the proteome characterization. In this approach a unique isotopic signature is embedded exclusively into the peptides and it serves as a computationally recognizable full-scan MS reporter. By using desthiobiotin, these probes circumvented the need to use cleavable linkers for peptide elution and thus simplifies the chemoproteomic protocol, while allowing quantification of the proteome. IsoTDB pack contains 2 mg of light (IsoDTB-L) and heave (IsoDTB) probe.

H-Pro-Arg-OH acetate salt is a synthetic, antioxidative molecule that has been shown to lower blood pressure in animals. It is also an effective inhibitor of the oxidation of diploid cells and has been shown to be safe for long-term use. H-Pro-Arg-OH acetate salt is used as a structural probe for studies on the binding of fibrinogen to plasminogen. This compound has also been shown to reduce protamine's ability to inhibit fibrinolysis, which may lead to improved blood clotting times.

H-Tyr-Val-Met-Gly-His-Phe-Arg-D-Trp-Asp-Arg-Phe-Gly-OH is a peptide that has been shown to bind to the melanocortin receptor. It is a selective agonist that binds to the melanocortin 2 receptor, but not the melanocortin 1 receptor. This peptide has no effect on body weight in mice, but it does cause an increase in food intake and fat mass. H-Tyr-Val-Met gly His Phe Arg D Trp Asp Arg Phe Gly OH also has been shown to be an effective analgesic for chronic pain in rats.

Please enquire for more information about Cyclin-D2 Human Recombinant including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Cyclin-B1 Human Recombinant including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Z-Tyr-Ser-OH is a fine chemical that is used as a versatile building block in the synthesis of complex compounds. It is also a useful intermediate for the production of many other chemicals, including pharmaceuticals, agrochemicals and research chemicals. The CAS number for Z-Tyr-Ser-OH is 20448-71-9. This compound has been shown to be a high quality reagent with many applications in research and commercial manufacturing.</p>

<p>Please enquire for more information about rec IL-10 (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Cyclo(-Leu-Trp) is a sweetener that has been used in the food industry for many years. Cyclo(-Leu-Trp) is able to bind with quinine and form a complex that can be detected using analytical methods. Cyclo(-Leu-Trp) has been investigated as a ligand that may be able to bind to receptors on cancer cells, which could lead to new treatments for cancer. Cyclo(-Leu-Trp) also has amphipathic properties and can form liposomes at high concentrations. This molecule has also been studied for its ability to induce transduction of DNA into bacterial cells and cellular thermogenesis.

<p>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.</p>

<p>AC-SDKP TRIFLUOROACETATE is a synthetic peptide, which is a derivative of the naturally occurring tetrapeptide L-seryl-L-aspartyl-L-lysyl-L-proline. This product is typically sourced through chemical synthesis, enabling precise structural and functional consistency.The mode of action of AC-SDKP involves its role as an endogenous antifibrotic agent. It functions by inhibiting the proliferation and differentiation of fibroblasts, thereby reducing collagen deposition. This action largely contributes to its ability to prevent fibrosis in various tissues. Additionally, AC-SDKP is known for its cardiovascular protective effects, partially through its interaction with the renin-angiotensin system and its ability to reduce inflammation.AC-SDKP TRIFLUOROACETATE is primarily used in scientific research focused on fibrotic diseases and cardiovascular disorders. It is a valuable tool for studying pathological mechanisms underlying fibrosis and developing potential therapeutic strategies. Its applications extend to investigating myocardial fibrosis, renal fibrosis, and idiopathic pulmonary fibrosis, among others, providing insights into treatment approaches that aim to mitigate disease progression.</p>

Ubiquitin carboxyl-terminal esterase L3 is a type of enzyme that activates ubiquitin by removing a carboxyl-terminal residue. It is an activator of the receptor for epidermal growth factor (EGF). Ubiquitin carboxyl-terminal esterase L3 interacts with EGF receptors, which are involved in cell proliferation, differentiation and apoptosis. This protein also has been shown to inhibit ion channels and bind to antibodies.

<p>Ac-Phe-Arg-AMC hydrochloride is a versatile building block that is used in the synthesis of complex compounds and research chemicals.<br>It is a fine chemical with CAS No. 177028-04-5. Ac-Phe-Arg-AMC hydrochloride is soluble in water, ethanol, and acetone, and insoluble in ether. This compound can be used as an intermediate for the synthesis of research chemicals with high quality or as a reagent. Ac-Phe-Arg-AMC hydrochloride can be used to produce a variety of useful scaffolds for medicinal chemistry or organic chemistry applications.</p>

1-Myristoyl-rac-glycerol is a fatty acid with a hydroxyl group and an antimicrobial effect. It has been shown to have clinical properties and is used in pharmaceutical preparations as an antimicrobial agent. 1-Myristoyl-rac-glycerol has been found to be active against gram negative bacteria such as E. coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae, while being inactive against gram positive bacteria such as Staphylococcus aureus or Bacillus subtilis. The antimicrobial activity of this compound is due to its ability to disrupt the integrity of bacterial cell membranes by acting on lipid synthesis. 1-Myristoyl-rac-glycerol also has hemolytic activity and can cause death in fungi and yeast cells. 1-Myristoyl-rac-glycerol is not metabolized by humans but may be metabolized by microbes such as Candida

<p>H-Ala-Phe-Lys-AMC trifluoroacetate salt is a chemical compound that can be used as an intermediate in the synthesis of peptides, peptidomimetics, and other organic compounds. This reagent is a high quality, versatile building block that can be used in the synthesis of complex compounds. H-Ala-Phe-Lys-AMC trifluoroacetate salt is a fine chemical that has been assigned CAS No. 120928-02-1. It is a useful scaffold for the synthesis of novel compounds with potential pharmaceutical value.</p>

Mca-Ala-Pro-Lys(Dnp)-OH trifluoroacetate salt is a high quality, versatile, and speciality chemical that is used as an intermediate in the synthesis of complex compounds. Mca-Ala-Pro-Lys(Dnp)-OH trifluoroacetate salt is also a useful scaffold for building block molecules and a versatile building block for peptide synthesis. This compound can be utilized in the manufacture of research chemicals and speciality chemicals.

H-D-Glu(Gly-OH)-OH is a peptide that is used to study the mechanism of glutamate receptors. It has been shown to have an excitatory effect on mouse hippocampal and cerebellar purkinje neurons, with affinity values for membrane channels. It also has been shown to reduce gamma-aminobutyric acid (GABA) levels in the hippocampus and striatum, which may be due to its ability to inhibit glutamic acid decarboxylase. H-D-Glu(Gly-OH)-OH is a potent antagonist of glutamate, binding competitively at the glutamate site on ionotropic receptors. It also inhibits acidic pH and calcium ion concentrations, which are necessary for ionotropic receptor activation.

Fmoc-Glu(OtBu)-Rink-Amide MBHA Resin is a high purity, ion channel ligand that is used in research as a pharmacological tool. It is an activator of Kv1.3 channels and inhibits the function of Kv1.2 channels. This product can be used for the study of protein interactions and receptor pharmacology. Fmoc-Glu(OtBu)-Rink-Amide MBHA Resin also has been found to inhibit the binding of antibodies to cells and can be used for immunoprecipitation experiments. This product has CAS number 188476-46-4 and is available in 1 g and 5 g sizes.

Fmoc-Tyr(tBu)-Rink-Amide MBHA Resin is a solid phase peptide synthesis resin that is used for the production of small scale peptides. This resin has high purity and can be used in the synthesis of proteins, antibodies, and other bioactive molecules. Fmoc-Tyr(tBu)-Rink-Amide MBHA Resin is an ion-exchange resin that can be used to purify peptides by binding to their charged side chains. It is also useful as a research tool for cell biology, receptor pharmacology, and as an inhibitor.

Potent agonist of proteinase-activated receptor-2 (PAR2)

<p>Peptide H-SCDKTHTCPPCPAPELLGGPSVFLFPPKPK-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.</p>

<p>Peptide H-DLDLEMLAPYIPMDDDFQLR-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.</p>

<p>Peptide H-HLMSFPQSA-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.</p>

Peptide H-TGWLGPFDYWGQGTLVTVSSASTK-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.