Aminoácidos (AA)

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

<p>Bz-Ile-Glu-Gly-Arg-pNA acetate salt is an anticoagulant that binds to heparin. It has been shown to inhibit protease activity in soybean trypsin by binding to the active site of the enzyme. Bz-Ile-Glu-Gly-Arg-pNA acetate salt has also been shown to have a molecular weight of heparin and a protein synthesis inhibition rate of fibrinogen, which is responsible for coagulation.</p>

<p>Please enquire for more information about Hippuryl-Cys(2-aminoethyl)-OH hydrochloride salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Bz-Val-Gly-Arg-AMC is a growth factor that activates the extracellular signal-regulated protein kinase (ERK) pathway. The activation of this pathway results in an increase in cellular proliferation and inhibition of tumor growth. Bz-Val-Gly-Arg-AMC has been shown to activate ERK by interacting with VSMCs, which are cells that act as a structural component of blood vessels and play a role in regulating blood flow. This compound also induces phosphorylation of glycogen synthase kinase 3β and inhibits its activity, leading to increased protein synthesis through glycolysis. Bz-Val-Gly-Arg-AMC can be used as an inhibitor to bortezomib, a proteolytic enzyme that is used to treat cancer.</p>

<p>Please enquire for more information about ([13C6]Leu6)-Endothelin-1 (human, bovine, dog, mouse, porcine, rat) acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Boc-Glu(OBzl)-Ala-Arg-AMC·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-KCDICTDEY-OH peptide, corresponding to amino acids 243-251 of human Tyrosinase. The peptide is supplied as an acetate salt.</p>

<p>H-Leu-Met-NH2 is a catecholamine that is found in the central nervous system and functions as a neurotransmitter. It has been shown to induce contractile response when injected into the carotid artery, with a maximal effect at doses of 0.5-5 mg/kg. The effect of H-Leu-Met-NH2 on cardiovascular function has not been studied. Catecholamines are also involved in other physiological processes, including regulation of blood pressure and respiration. This compound was originally isolated from adrenal glands and is found in plants such as beans and peas. The structure of this compound can be described as an h-leu-[met]-amide with a hydrochloride salt at the c-terminus.</p>

<p>Trans-4-hydroxy-L-proline methyl ester hydrochloride is a matrix metalloproteinase inhibitor. It inhibits the activity of matrix metalloproteinases, which are enzymes that break down collagen and other proteins in the extracellular matrix. The inhibition of these enzymes leads to a decrease in restenosis, which is the recurrence of artery narrowing after angioplasty or stent placement. Trans-4-hydroxy-L-proline methyl ester hydrochloride has been shown to be effective against chemokine receptors, including CCR5 receptor and chemokines such as TNFα. It also inhibits cytokine production by inhibiting signaling pathways that lead to inflammation and cell proliferation.</p>

<p>Please enquire for more information about H-Glu-Tyr-Glu-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Val-Ala-Ala-Phe-OH is a polypeptide that has been synthesized to study the effects of metal surface on mass spectrometry. The peptide has been found to be labile and nonvolatile, which means it can easily evaporate and desorb from the metal surface. The research also shows that this polypeptide is more efficient in mass spectrometers with higher resolution.</p>

<p>Please enquire for more information about Osteoblast Activating Peptide (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about H-Thr-Asp-OH TFA salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about H-Val-2-chlorotrityl resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (Nle 10)-Neurokinin A (4-10) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Suc-Leu-Leu-Val-Tyr-pNA including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>SN50 is a nuclear factor NF-KB inhibitor that blocks the activity of transcription factors that are involved in inflammation and cancer. SN50 inhibits protease activity, which may be due to its ability to bind to response elements on DNA, leading to cytosolic calcium release and activation of signal pathways. It also binds to endothelin-a receptor and induces apoptosis. SN50 has been shown to have anti-tumour effects in resistant breast cancer cells as well as reducing serum aminotransferase levels in rats. This drug also activates transcriptional regulation by binding toll-like receptors and inducing colony stimulating factors. SN50 also has cardioprotective properties, which may be due to its ability to inhibit fatty acid synthase in cardiomyocytes.</p>

<p>Intermediate in the synthesis of idelalisib (CAL 101)</p>

<p>Please enquire for more information about Z-Gly-Gly-Phe-bNA including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Neurotensin is a peptide that regulates the activity of the hypothalamus and pituitary gland. Neurotensin is synthesized from prepro-neurotensin, which is cleaved to produce neurotensin (8-13) H-Arg-Arg-Pro-Tyr-Ile-Leu-OH. It is a member of the tachykinins family of neuropeptides, which are characterized by a conserved disulfide bond. Neurotensin has been shown to increase locomotor activity in mice and rats and may be involved in pain perception. Neurotensin also binds to receptors on nerve cells, including the enkephalin receptor, with high affinity. This binding leads to an inhibition of release of neurotransmitters such as dopamine, serotonin, and acetylcholine by neurons.</p>

<p>Bexagliflozin is a drug that is used to treat type II diabetes in adults. It helps to control blood sugar levels by inhibiting the enzyme DPP-IV and increasing insulin release from the pancreas. Bexagliflozin has been shown to be effective in lowering blood sugar levels in patients with chronic kidney disease and cancer, as well as those with a body mass index (BMI) of 30 or higher. This drug is an oral hypoglycaemic agent that can be used for diagnostic purposes. It has also been shown to be clinically effective for the treatment of diabetic nephropathy and diabetic retinopathy. The enantiomers of bexagliflozin can be differentiated according to their pharmacological properties, which may allow for more targeted therapy.</p>

<p>Please enquire for more information about Fmoc-a-Me-D-Asp(OtBu)-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Aloc-DL-Orn (Boc)-OH·DCHA including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>D-Ala2,N-Me-Phe4,methionin(O)-ol5)-Enkephalin trifluoroacetate salt H-Tyr-D-Ala-Gly-N-Me-Phe-methionin(O)-ol trifluoroacetate salt is an analog of the endocannabinoid neurotransmitter, anandamide. It has been shown to be effective in the treatment of autoimmune diseases such as multiple sclerosis and inflammatory bowel disease. D-(3R)-3-[(1S,2R,3R,5R) -3-[2-(2,6 dichlorophenyl)ethenyl] -1H -indole]-1 -butanamine trifluoroacetate salt has been shown to inhibit the replication of a number of viruses including human immunodeficiency virus type 1 (HIV). This drug also inhibits the growth of organisms that are resistant</p>

<p>Please enquire for more information about Neuropeptide Y (free acid) (human, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about H-Ser-AMC hydrochloride salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Prepro VIP (156-170) (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Suc-Val-Pro-Phe-4MbNA including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-DL-Val-Leu-Arg-pNA acetate salt is a natriuretic that is used to treat chronic kidney failure. It has an inhibitory effect on serine protease and epidermal growth factor, which are enzymes involved in the production of atrial natriuretic peptide (ANP). The drug also reduces blood pressure by inhibiting the activity of angiotensin II, which is a potent vasoconstrictor. H-DL-Val-Leu-Arg-pNA acetate salt has been shown to increase urea nitrogen levels by inhibiting the activity of alkaline phosphatase, which breaks down ammonia in the liver.</p>

<p>H-Met-Arg-OH acetate salt is a metabolite of the amino acid L-methionine. It is also a dipeptide, which consists of two amino acids that are linked by an amide bond. The linkage between the amino acids in this compound is clockwise instead of the usual left to right orientation. This means that H-Met-Arg-OH acetate salt is not an essential amino acid and can be synthesized by the body. Salmonella typhimurium uses H-Met-Arg-OH acetate salt as a precursor for its synthesis of L-arginine and L-methionine, which are essential to bacterial growth and survival. Residues have been found in foods such as milk and eggs, and it has been shown that cotransduction can lead to resistance against antibiotics such as streptomycin and tetracycline.</p>

<p>H-Gly-Arg-Gly-Asp-D-Ser-Pro-OH trifluoroacetate salt (HGGDS) is a collagen gel that is used in the treatment of autoimmune diseases, such as arthritis and lupus. HGGDS inhibits the production of fibrinogen, which is a protein involved in blood clotting, by binding to its receptor on human fibroblasts. It also inhibits the production of basic proteins needed for the generation of collagen and activation of integrin receptors, which are involved in cell adhesion and migration. HGGDS also blocks transcription polymerase chain reactions (PCRs), which are necessary for the synthesis of DNA. This can lead to a decrease in cell proliferation and an increase in apoptosis.</p>

<p>Please enquire for more information about 4,6-Dichloro-2-methylnicotinic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Boc-Asn-Phe-Pro-aldehyde is a cytosolic proteolytic target enzyme that hydrolyzes peptides with an aliphatic amino acid residue at the carboxy terminus. It is localized in the cytoplasm, where it is activated by serine proteases. Boc-Asn-Phe-Pro-aldehyde has been shown to be effective in cell culture and supernatant. This enzyme can also be used to demonstrate the presence of a particular peptide by releasing a reactive chloride, which can be detected using tetrazolium chloride. This protease has been shown to exacerbate inflammation when administered in vivo.</p>

<p>H-Leu-Pro-Pro-OH is a synthetic tripeptide that has been shown to increase endothelial function in humans. The peptide is thought to work by increasing nitric oxide production and by inhibiting angiotensin II production. H-Leu-Pro-Pro-OH also reportedly increases uptake of glucose in the intestine and decreases blood pressure. In placebo-controlled, crossover studies, H-Leu-Pro-Pro-OH increased plasma concentrations of angiotensin I and II, suggesting that it may be a potent inhibitor of angiotensin converting enzyme (ACE).</p>

<p>H-Arg-Arg-Arg-OH acetate salt is a polycarboxylic acid that is found in human immunoglobulins. It has been used as a synthetic substrate for the study of radiation enhancement. H-Arg-Arg-Arg-OH acetate salt is also an allergen and can cause allergic reactions, such as itching and swelling. This compound can be used to study the neutral pH, chemical reactions, protein synthesis, and the hydroxyl group.</p>

<p>Hippocampal Cholinergic Neurostimulating Peptide Ac-Ala-Ala-Asp-Ile-Ser-Gln-Trp-Ala-Gly-Pro-Leu is a peptide hormone that has been found in the hippocampus. It is a cholinergic neurotransmitter that is synthesized and secreted by neurons in the brain. It has been shown to have an effect on bowel disease, locomotor activity, and hippocampal formation. Hippocampal Cholinergic Neurostimulating Peptide Ac-Ala-Ala-Asp-Ile-Ser-Gln-Trp was first identified through biochemical analysis of rat brain tissue.</p>

<p>H-Gly-DL-Thr-OH is an organic compound that is a component of natural phenolic compounds. This compound is generated by the pyrolysis of biomass, and it has been shown to have selective properties for GC-MS analysis. H-Gly-DL-Thr-OH can be used as a sustainable chemical component in the production of biofuels and other chemicals. The optimal conditions for this synthesis are potassium hydroxide, temperature, pressure, and irradiation time. The separation parameters for H-Gly-DL-Thr-OH are based on its GC retention time and mass spectra.</p>

<p>Please enquire for more information about H-Thr(tBu)-pNA including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fmoc-Cys(NPys)-OH is a disulfide with a cyclic structure that can be used in the synthesis of peptides. It reacts efficiently with thiols to form stable, covalent bonds and can be used as an efficient ligation reagent for cyclic peptides. Fmoc-Cys(NPys)-OH is also useful for the synthesis of biomolecules because it has a systematic nature and does not react with other reactive groups on the molecule. It has been shown to have high reactivity towards oxytocin, which is important for its function in triggering labor contractions.</p>

<p>Z-Gly-Leu-NH2 is a synthetic peptide that has been designed to mimic the amino acid sequence of casein. It is a metalloendopeptidase inhibitor and can be used in the synthesis of proteins. Z-Gly-Leu-NH2 inhibits the activity of subtilisin, which is a proteolytic enzyme. The inhibition of subtilisin by Z-Gly-Leu-NH2 prevents the hydrolysis of peptide bonds in protein substrates. This inhibition leads to an increase in molecular weight and molecular weight distribution, as well as an increase in the number of high molecular weight peaks on chromatograms. This peptide also has serine protease inhibitory activity and can be used as a synthetic substrate for kinetic studies.</p>

<p>P-hydroxyhippuryl-His-Leu-OH is a natriuretic that has been shown to have beneficial effects on diabetic patients. It can be used to prevent and treat proliferative diabetic retinopathy, which is a complication of diabetes. P-hydroxyhippuryl-His-Leu-OH increases the glomerular filtration rate and decreases the ventricular mass index, which may be due to its ability to inhibit angiotensin II receptors in the brain. P-hydroxyhippuryl-His-Leu-OH also inhibits angiotensin converting enzyme, an enzyme that converts angiotensin I into angiotensin II. This inhibition leads to an increase in levels of atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), and the downstream effectors of these peptides, namely nitric oxide synthase and cyclooxygenase</p>

<p>H-Phe-Ser-OH is a molecule that is present in the bacterial strain. It can be used in diagnosis, where it can be detected by messenger RNA profiling and kinetic analysis of uptake. In vitro synthesis of H-Phe-Ser-OH was performed using caco-2 cells and metabolic profiles were obtained from this experiment. Hydroxyl groups are found on the molecule, which are important for diagnostic purposes. This molecule has been shown to form hydrogen bonds with other molecules, which may also be useful for diagnostic tests.</p>

<p>Disulfide bond is a protein that regulates muscle cell assembly and interactions. Disulfide bonds are formed by the oxidation of two cysteine molecules, which can be found in the extracellular matrix (ECM). The protein is an important regulator of metalloproteinases, which are enzymes that regulate ECM turnover. When disulfide bond lacks, it causes a deficiency in collagen production. Disulfide bond also has interactions with MMP-2, which plays a role in the regulation of arteriosclerosis and genetic disorders such as muscular dystrophy.</p>

<p>Please enquire for more information about (H-Cys-Ala-OH)2 (Disulfide bond) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Insulin B (22-25) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Boc-Glu(Lys-OH)-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-Oleoyl-3-palmitoyl-rac-glycero-2-phosphoethanolamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about For-Ala-Ala-Pro-Abu-SBzl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (Des-Gly10,D-Leu6,[13C6]Leu7,Pro-NHEt 9)-LHRH trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(4-Hydroxy-3-methoxyphenyl)-2-nitroethene is an experimental molecule that was not previously known to exist. The intramolecular reaction of 1,4-dihydroxynitrobenzene and glyoxylic acid yields the product. It is a phenolic compound with biological activity, which has been shown to inhibit glycosidases and alkaloids.</p>

<p>Fmoc-rink amide resin is a synthetic, radionuclide, and constant polymer. It is used in chemical ligation to produce peptides from amines and growth factors. Fmoc-rink amide resin also has antimicrobial properties due to its ability to inhibit the growth of bacteria and fungi by binding to their cell membranes. This polymer can be conjugated with growth factor or antimicrobial peptides for use as a therapeutic agent or used in the production of antibodies against a particular protein. Fmoc-rink amide resin has been shown to increase epidermal growth factor (EGF) uptake into cells by targeting EGF receptors on the cell surface.</p>

<p>Please enquire for more information about Neuronostatin-13 (human, canine, porcine) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Bz-DL-Arg-AMC·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Z-Leu-Leu-4,5-dehydro-Leu-aldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 6-methylnicotinate is a synthetic compound that has been shown to have cholinergic properties. It is an oxidation catalyst that can be used in the synthesis of methyl nicotinate, which is a drug for the treatment of influenza virus. Methyl 6-methylnicotinate also has been shown to inhibit the replication of influenza virus in vitro and in vivo. Methyl 6-methylnicotinate inhibits viral growth by binding to the antigenic site on hemagglutinin, preventing it from attaching to host cells. This compound also has been shown to inhibit the release of chloride ions in animal models and inhibits neuromuscular transmission. The molecular modeling studies revealed that methyl 6-methylnicotinate binds with high affinity to the active site of acetylcholinesterase enzyme and is able to form a covalent bond with its serine residue, thereby inhibiting its activity.</p>

<p>Please enquire for more information about Z-Asp(OtBu)-ONp including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about H-Lys-Leu-Lys-OH triacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-Boc-pyrrolidine-2,4-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Cyclo(-D-Trp-Tyr) is a cyclic peptide that is produced by the fungus Microbispora sp. It has been shown to inhibit the growth of Staphylococcus aureus, as well as other bacteria, fungi and cancer cells. Cyclo(-D-Trp-Tyr) binds to the ribosomal RNA in these cells and inhibits protein synthesis. The peptide does not bind to subtilisin or bgc-823, but does bind to lung fibroblasts and leukemia cells.</p>

<p>Please enquire for more information about (D-Ser6,Azagly10)-LHRH acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>C-Cys-Asp-Pro-Gly-Tyr-Ile-Gly-Ser-Arg is a cyclic peptide that is synthesized from the amino acid sequence of human epidermal growth factor (EGF). It has been shown to have in vitro and in vivo antitumor activity against melanoma cells. C-Cys-Asp-Pro-Gly-Tyr-Ile-Gly-Ser-Arg has also been shown to activate EGF receptors with physiological levels of EGF and to inhibit tumor metastasis.</p>

<p>Please enquire for more information about 2-(Aminomethyl)-2-methyl-1,3-propanediamine trihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (H-Cys-allyl ester)2·2 p-tosylate (Disulfide bond) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Neuropeptide Y (3-36) (porcine) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (D-Tyr5,D-Ser(tBu)6,Azagly10)-LHRH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Neuropeptide W-30 (rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about H-Pro-Phe-Lys-OH acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-His-Tyr-OH is a histidine-containing compound that has been synthesized and structurally characterized. H-His-Tyr-OH was shown to be a competitive inhibitor of the enzyme histidine decarboxylase in a rat liver microsomal preparation. The kinetic constants for the inhibition of the enzyme were determined, and the binding site on the enzyme was identified by molecular modeling. This study also showed that H-His-Tyr-OH binds to monoclonal antibodies with high affinity and specificity, which may be useful for therapy.</p>

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

<p>Please enquire for more information about H-beta-Ala-Lys-OH·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>BQ-610 is a novel peptide that has been shown to reduce the severity of mucosal inflammation in animal models of inflammatory bowel disease. It functions by binding to myofibroblasts, which are cells that produce an extracellular matrix and collagen. BQ-610 also blocks signalling pathways that are responsible for the production of TNF-α, MMP-2, and other molecules involved in the pathogenesis of inflammatory bowel disease. BQ-610 is effective at reducing inflammation in animal models of colitis, but not in human colonic epithelial cells or human colonic tissue.</p>

<p>DABCYL-TNF-alpha-EDANS (-4 to +6) (human) trifluoroacetate salt is a fine chemical that has been shown to be useful in research. It is a versatile building block for the synthesis of complex compounds and can be used as a reaction component for the synthesis of speciality chemicals. The compound is a high quality reagent, which can be used as an intermediate for the synthesis of other chemical compounds.</p>

<p>Z-Leu-Leu-Nle (ZLL) is a small molecule that selectively inhibits the activity of the aspartyl protease, BACE1, which is an enzyme that cleaves amyloid precursor protein (APP) to produce amyloid beta peptides. The inhibition of this enzyme has been shown to be effective in preventing or delaying the onset of Alzheimer's disease. ZLL also inhibits estrogen receptor alpha and has antiestrogenic effects in breast cancer cells. This compound induces apoptosis by binding to apoptotic proteins, such as tumor necrosis factor receptor 1, Fas ligand, and TRAIL receptors. It also inhibits cell growth and induces chemoresistance in breast cancer cells.</p>

<p>Z-Phe-Val-OH is an optical isomer of the molecule Z-Val-OH. It can be synthesized from the reactants Isobutyl, Chloroformate, and Hydrophobic. This synthetic product has been shown to have high yields and specificities. The chiral center in this molecule causes it to rotate light in one direction or another, which means that it can be used to create a spectrum of colors. The synthesis of this molecule takes place in a kinetically controlled manner. When mixed with amines, carboxylic acids, and tripeptides, this compound will form a tripeptide bond with two amino acids on either side of the peptide chain.</p>

<p>Angiotensin I/II (4-8) H-Tyr-Ile-His-Pro-Phe-OH is a peptide that contains the sequence of angiotensin I and II. It has been shown to have proton transport properties, which may be related to its sequence. The amino acid sequence of this peptide is similar to other pentapeptides such as insulin and vasopressin. This peptide has been linked to a vector that can cross the blood brain barrier, allowing it to act on the central nervous system.</p>

<p>Please enquire for more information about Ac-muramyl-Ala-Glu-NH2 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Cyclo(-Gly-Asn-Trp-His-Gly-Thr-Ala-Pro-Asp)-Trp-Val-Tyr-Phe-Ala-His-Leu-Asp-Ile-Ile-Trp-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about N-Me-D-Ala-OMe·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Polistes mastoparan is a peptide that was extracted from the venom of the European beewolf. It has been shown to have high affinity for tumor cells and can be used as a diagnostic agent. Polistes mastoparan has also been shown to have anti-inflammatory properties and inhibit the formation rate of glycopeptide antibiotics. This peptide can bind to calmodulin, which may be due to its β-amino acid sequence. Polistes mastoparan inhibits the growth of Stenotrophomonas maltophilia in vitro by binding to fatty acids on the cell membrane.</p>

<p>Please enquire for more information about H-Gly-Gly-b-Ala-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>H-Gly-Cys-OH is an amide that is structurally related to the nonapeptide, Gly-Pro-Cys. H-Gly-Cys-OH has been shown to be an efficient method for preparation of 3-mercaptopropionic acid. The nucleophilic attack of the thiol group on the carbonyl carbon atom in the amide bond leads to cleavage and formation of a disulfide bond. This reaction occurs spontaneously at room temperature with high efficiency and can be used for synthesis of 3-mercaptopropionic acid. H-Gly-Cys-OH has low bioavailability, which may be due to its primary amino group, which is not well absorbed by the intestinal epithelium.</p>

<p>Glutamine is a non-essential amino acid that is found in the cell in large amounts. It functions as a precursor of glutamate, an important neurotransmitter and intermediate in protein synthesis. Glutamine also has antioxidant properties, which may be due to its ability to donate hydrogen atoms or act as a reducing agent. Glutamine can be synthesized by glutaminase from glutamate and ammonia, but it can also be obtained from dietary sources. The uptake of glutamine is rapid at low concentrations, but becomes slower at higher concentrations. Glutamine is catabolized by the liver and kidney into glutamate and ammonia.<br>Glutamate dehydrogenase (GLDH) catalyzes the conversion of glutamate to α-ketoglutarate, producing NADH and H+.<br>The genetic mechanisms underlying the synthesis of glutamine are not well understood; however, one hypothesis states that glutamine could be synthesized from alpha-ketoglutarate via the reverse transamination reaction during periods when glucose</p>

<p>Please enquire for more information about H-Glu(Ala-Gly-pNA)-OH trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Fmoc-p-phenyl-D-phenylalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The peptide z-Gly-Gly-Leu-pNA is a synthetic substrate that is used in the study of metalloendopeptidases. The peptide is composed of four amino acids and has an acidic, monoclonal antibody, dodecyl, proteolytic, peptide hormones, extracellular, inactivated, serine protease. It is synthesized from wheat leaves and can be used as a substrate for the enzyme.</p>

<p>H-D-Tyr-Val-Gly-OH is a catalyst that is used in the synthesis of phenylhydrazones. It catalyses the condensation of an aromatic aldehyde and hydrazine, which leads to the formation of a phenylhydrazone. The reaction occurs at neutral pH and high temperature. H-D-Tyr-Val-Gly-OH has been shown to inhibit protein synthesis in rat liver cells, with its inhibitory effect increasing with increased pH.</p>

<p>Cholecystokinin octapeptide (CCK-8) is a peptide hormone that is secreted from the pancreas. It is a conjugate of CCK and desulfated cholinesterase, which has been shown to have surfactant properties. The concentration-response curves for CCK-8 are biphasic, with an initial increase in contractility followed by a decrease. This response is caused by activation of both the B2 and B1 receptors in the paraventricular nucleus of the hypothalamus and subsequently release of pancreatic enzymes into the bloodstream. CCK-8 has also been shown to stimulate protein synthesis in gland cells such as those found in the pancreas.</p>

<p>Trifluoroacetate salt</p>

<p>Please enquire for more information about Galanin (1-19) (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>