Amino Acids (AA)

<p>Please enquire for more information about Boc-Met-PAM 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 3'-methoxy apiin;Chrysoeiol-7-(2-O-apiosylglucoside) 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-N-Me-Homocys (Trt)-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-2,6-Difluoro-Phe-OH·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The CD4 molecule is a major component of the human immune system. It interacts with other cells, such as T-cells, and plays an important role in the immune response. The CD4 molecule is a glycoprotein that consists of two subunits, (Cys(Bzl)84)-CD4 and (81-92) H-Thr-Tyr-Ile-Cys(Bzl)-Glu-Val-Glu-Asp-Gln-Lys-Glu-. The sequence of this molecule is important for its function, as it has been shown to be essential for binding to HIV particles. This protein may also play a role in regulating the growth of T cells. It was found that the amino acid sequence of CD4 is not conserved among different species. The amino acid sequence specificity in the CD4 molecule is due to the cysteine residues. These residues are able to form disulfide bridges with other cyste</p>

<p>Please enquire for more information about Sperm Peptide P10G trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dynorphin A (1-9) H-Tyr-Gly-Gly-Phe-Leu-Arg-Arg-Ile-Arg-OH is a substrate binding inhibitor that blocks potassium channels. Dynorphin A (1-9) H-Tyr-Gly-Gly-Phe-Leu Arg Arg Ile Arg OH binds to the d -alanine site of the potassium channel and inhibits glutamate release from presynaptic terminals. Dynorphin A (1 9) H Tyr Gly Gly Phe Leu Arg Arg Ile Arg OH has been shown to be a potent inhibitor of aminopeptidase activity in vitro, which may be due to its affinity for the substrate binding site on the enzyme. Its inhibition of aminopeptidase activity may lead to an increase in opioid peptides such as dynorphins and enkephalins. Dynorphin A (1 9) H Tyr Gly Gly Phe</p>

<p>H-Arg-Gly-Tyr-Ala-Leu-Gly-OH is a synthetic, competitive inhibitor of the aminopeptidase that cleaves the amino acid Arg from peptide chains. This compound has been shown to inhibit kinases in vitro and block viral replication in cell culture. H-Arg-Gly-Tyr-Ala-Leu-Gly-OH is reversibly inhibited by endogenous aminopeptidases, which have been shown to be involved in the regulation of cell proliferation and apoptosis.</p>

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

<p>2-Methylacetophenone is an organic compound that has a molecular weight of 100.12 g/mol, and a chemical formula of C10H14O2. The compound is a colorless liquid at room temperature and pressure, with a sweet odor. It is soluble in nonpolar solvents such as hexane, ether, benzene, and toluene. 2-Methylacetophenone has been used as a solvent for the chemical study of benzyl groups, hydroxyl group activation energies, hydrogen bond, carbonyl group proton and intramolecular hydrogen bonding. It has also been used to study the reaction mechanism of fatty acid with benzyl groups in cryogenic conditions.</p>

<p>Please enquire for more information about Phylloseptin-L2 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Ala-Leu-Ala-OH is a synthetic peptide that has been shown to be an effective inhibitor of the human aminopeptidase. It is synthesized on a solid phase and then purified from the resin. The H-Ala-Leu-Ala-OH peptide was found to have a ph optimum of 7 and can be used for the treatment of skin infections caused by fungi such as Metarhizium anisopliae, which are resistant to conventional treatments. This peptide inhibits the synthesis of proteins in fungal cells and prevents the growth of the fungus.</p>

<p>H-Leu-Gly-bNA is a chromogenic, dipeptide, which has been shown to react with 2-naphthylamine in the presence of condensation agents and carboxylic acid to form a carboxy group. The amino group on the terminal Leu residue reacts with the carboxy group to form an amide bond. This reaction is used as a method for detecting bNA.</p>

<p>Please enquire for more information about Fmoc-Pro-Pro-Pro-Pro-Pro-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-Met-Wang resin (100-200 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 Fluorescein-6-carbonyl-Tyr-Val-Ala-DL-Asp(OMe)-fluoromethylketone 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-Arg(Mtr)-Wang resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>FITC-Tyr-Val-Ala-Asp-OH (Contains FITC isomer I) is a bioactive molecule that has been shown to inhibit the growth of filamentous fungi. This compound binds to the tyrosine kinase, which is an enzyme involved in the regulation of cell division and differentiation. It also inhibits neutrophil recruitment by dectin-1, a protein that recognizes fungal cell walls on neutrophils. The FITC isomer I has been shown to impair macrophages and fungus aspergillus fumigatus infiltration in tissues with impaired immune function.<br>FITC-Tyr-Val-Ala-Asp-OH (Contains FITC isomer I) has also been shown to decrease the production of caspase 1, which activates inflammatory responses and stimulates phagocytic cells.</p>

<p>Please enquire for more information about Fmoc-4-(7-hydroxy-4-coumarinyl)-Abu-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Kemptide is a substrate molecule that has been shown to inhibit the enzyme activity of some protein kinases. Kemptide is a 3-amino acid peptide that contains the amino acids L-leucine, L-arginine, and L-arginine. It was originally isolated from an extract of human brain tissue and has been shown to inhibit the activity of protein kinase C (PKC), phosphorylase kinase, and glycogen synthase kinase 3β in vitro assays. Kemptide also inhibits the expression of genes encoding PKCα1, PKCα2, PKCδ, PKCε, PKCγ1, PKCγ2, PKCζ in t84 cells. The inhibition of these genes suggests that kemptide may be useful as a drug candidate for inhibiting protein kinases in vivo.</p>

<p>(2R,3S)-3-Amino-2-hydroxy-3-phenylpropanoic acid hydrochloride is an organic compound that is used in the manufacture of taxol, an anticancer drug. It is synthesized by reacting chloroacetic acid with a metal hydroxide, such as sodium hydroxide or potassium hydroxide. The reaction proceeds spontaneously to form the enantiomerically pure (2R,3S) form and unreacted (2S,3R) form. The (2R,3S) enantiomer has been found to be more reactive than the (2S,3R) form. Quaternary ammonium salts are formed when the (2R,3S) enantiomer reacts with quaternary ammonium compounds such as benzyltrimethylammonium chloride. This compound can also be used in catalytic reactions to produce drugs such as carbapenems and pen</p>

Please enquire for more information about Boc-Lys(Z)-Lys(Z)-Lys(Z)-Lys(Z)-OBzl including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Please enquire for more information about Fmoc-Trp(Boc)-Thr(Psi(Me,Me)pro)-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 (Cys(Acm)2·7)-a-CGRP (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methyl-6-(trifluoromethyl)aniline is a colorless, oily liquid with a sulfurous odor. It is soluble in water and alcohol. The reaction rate of 2-methyl-6-(trifluoromethyl)aniline with sulfoxides is faster than that of benzyl anilines, but slower than that of anilino derivatives. The addition of hydrophobic groups to the 2-methyl-6-(trifluoromethyl)aniline molecule increases the reaction rate. 2-Methyl-6-(trifluoromethyl)aniline can be used as an anesthetic agent because it is a potent inhibitor of nerve conduction in sciatic nerves. It also has been shown to be effective in desulfurizing propylene, which is important for the production of polypropylene plastics and synthetic rubber. 2-Methyl-6-(triflu</p>

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

<p>2-Amino-5-methoxypyridine (2AM5MP) is a synthetic compound that is used to study the nicotinic acetylcholine receptor. It has been shown that 2AM5MP can be used as an agonist for the nicotinic acetylcholine receptor, which may be due to its ability to act as a substrate for amine oxidase. This compound has been shown to have anti-cancer properties and fluoresce when exposed to positron emission tomography (PET) scans. The anti-cancer effects of 2AM5MP are thought to be due to its ability to inhibit cancer cell proliferation and induce cancer cell apoptosis.</p>

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

<p>H-Asp-Trp-OH is a peptide that has been shown to have antioxidative activity and neuroprotective effects. It has also been shown to be a reactive compound that can interact with other molecules, such as thiobarbituric acid. H-Asp-Trp-OH has been shown to increase the number of neurons in the brain and may be helpful in reducing neuronal damage by apoptotic cell death. This peptide also has potential use in treating neurodegenerative diseases, such as Alzheimer's disease.</p>

<p>H-Met-Arg-Phe-Ala-OH is a synthetic peptide that has been shown to be an effective inhibitor of protein synthesis in mammalian cells. It binds to the active site of protein translation machinery, thereby inhibiting the production of proteins vital for cell division. H-Met-Arg-Phe-Ala-OH is stable in aqueous solution and resistant to proteolytic degradation. It also has a high detection sensitivity and can be detected by FTIR spectroscopy, which makes it suitable for use in a variety of applications. H-Met-Arg-Phe-Ala-OH can be used as a tool for studying protein synthesis inhibition or as an antiobiotic agent against cancer cells.</p>

<p>Please enquire for more information about Acetyl-(Cys(Acm)33·42)-EGF (33-42) amide (mouse) 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 (3,5-Dibromo-Tyr1)-Leu-Enkephalin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(R)-(+)-2-Methyl-CBS-oxazaborolidine is a dpp-iv inhibitor that is a β-unsaturated ketone. It has been shown to inhibit the enzyme histone lysine demethylase, which may be involved in the regulation of bone mass. This compound also has a pharmacokinetic profile that is characterized by high oral bioavailability, low plasma protein binding, and rapid metabolism by liver enzymes. The reaction mechanism for this compound is based on the formation of an enolate carbanion. (R)-(+)-2-Methyl-CBS-oxazaborolidine can be synthesized with high stereoselectivity and yields from reactions with simple starting materials. This synthetic route also has a number of advantages over other methods: it does not require any protecting groups, it does not use toxic solvents such as dichloromethane or chloroform, and it can be performed in anhydrous conditions</p>

<p>Please enquire for more information about (Cys39)-Tissue Factor (33-53) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ac-Pro-Leu-Gly-OH is a synthetic peptide that has been shown to be an effective crosslinker for thiols. Ac-Pro-Leu-Gly-OH is a water soluble, acidic peptide and can be used in biological systems as a crosslinker.</p>

<p>Please enquire for more information about (Leu13-psi(CH2NH)Leu14)-Bombesin 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-Ala-Phe-NH2·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Please enquire for more information about Boc-D-His(3-Bom)-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Suc-Ala-Ala-Pro-Phe-SBzl is a synthetic peptide with a sequence similar to the signal peptide of procarboxypeptidase B2. It has been shown that Suc-Ala-Ala-Pro-Phe-SBzl can be used as a diagnostic tool for pancreatic cancer, because it is found in higher concentrations in the blood of patients with pancreatic cancer. This peptide also has an affinity for metal ions, which allows it to be used as a probe to detect the presence of these ions in solution. Suc-Ala-Ala-Pro-Phe-SBzl binds to human immunoglobulin G (IgG) and can be used in analytical methods that use x ray diffraction data.</p>

<p>Please enquire for more information about Mast Cell Degranulating (MCD) Peptide HR-1 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 8·21,Tyr34)-pTH (1-34) amide (rat) 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 Nps-Val-OH·DCHA 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 (Arg17)-Amyloid b-Protein (1-42) 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 (Tyr0)-C-Peptide (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 Z-Val-Arg-Pro-DL-Arg-fluoromethylketone trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Boc-beta-cyclohexyl-L-alanine is a synthetic peptide that has been shown to bind to the thrombin receptor and inhibit the activity of this enzyme. It blocks the interaction between thrombin and its receptor, thereby inhibiting thrombin’s ability to convert fibrinogen into fibrin. This inhibition prevents the formation of a blood clot, which is essential for hemostasis. Boc-beta-cyclohexyl-L-alanine has also been shown to be an anticoagulant with antiplatelet properties. It binds to chloride ions in the blood and prevents platelets from binding together, thus preventing aggregation and adhesion.</p>

<p>Azilsartan medoxomil is an antihypertensive drug, which is a prodrug of the angiotensin II receptor blocker azilsartan. It is synthesized through a chemical process involving the modification of the medoxomil ester, converting it into its active form upon absorption in the gastrointestinal tract. The primary mode of action of azilsartan medoxomil involves selective antagonism of the angiotensin II type 1 (AT1) receptor. By blocking the effects of angiotensin II—a potent vasoconstrictor—azilsartan medoxomil effectively reduces vascular resistance, leading to decreased blood pressure.</p>

<p>H-beta-Ala-Val-OH is a synthetic amino acid that has been positioned in the beta helix of a crystallographic protein. It has a helical structure with an alpha carbon backbone. The dipeptide is water soluble and dipeptides are found in helices, which are hydrogen bonded to other helices. H-beta-Ala-Val-OH also has supramolecular properties, which means it can form structures on its own that are not dependent on other molecules.</p>

<p>Please enquire for more information about 17-alpha,21-Dihydroxy-16-a-methylpregna-1,4,9(11)-triene-3,20-dione 21-acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Apelin-36 is a human apelin protein. It is involved in the regulation of appetite and energy expenditure. Apelin-36 has been shown to be an independent predictor of body mass index and insulin resistance in women with polycystic ovary syndrome. Apelin-36 is also an indicator of the risk for cardiovascular disease, stroke, and type 2 diabetes mellitus. This molecule can be measured using a Western blot assay method on ovary homogenates. The level of apelin-36 can be used as a diagnostic tool for determining insulin resistance and overweight status.</p>

<p>Please enquire for more information about (Cys26)-Amyloid b-Protein (1-40) 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 Z-D-Arg(Z)2-OSu including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Pro-Asp-Val-Asp-His-Val-Phe-Leu-Arg-Phe is a peptide that is synthesized from proctolin. It has been shown to have gland cell receptor activity and physiological effects in animals. HPAVH has been shown to inhibit the binding of specific antibody to its antigen and can be used as a receptor for various applications, such as a cation channel. This peptide has also been shown to inhibit the binding of carboxy terminal of the alpha subunit of the acetylcholine receptor and can be used for research in animals.</p>

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

<p>Senktide is a substance P analog that has been shown to produce tail-flick responses in animals. The maximum response of the tail-flick test can be enhanced by the administration of either dopamine or serotonin. Inhibition of metabolism is likely to be responsible for these effects, as demonstrated by experiments in Sprague-Dawley rats. Senktide is an experimental model for studying the role of substance P in the regulation of blood pressure and locomotor activity. This compound also has pressor properties that are similar to those of dopamine and serotonin, which may be due to its ability to stimulate alpha-adrenergic receptors and inhibit dopaminergic neurons via a presynaptic mechanism.</p>

<p>Z-Gly-Ser-OH is a peptidase that hydrolyzes glycoproteins. It is found in a number of microorganisms and has been isolated from the bacterium, Bacillus subtilis. Z-Gly-Ser-OH hydrolyzes β-galactosidase substrates with the most common acceptor being lactose. This enzyme also has an o-glycosylation activity with a preference for n-substituted glycans. Z-Gly-Ser-OH is able to cleave lactose as well as other sugars, such as maltose, cellobiose, and sucrose.</p>

<p>Muramyl dipeptide (MDP) is a cell-wall constituent of Mycobacterium tuberculosis, which induces an antibody response. Muramyl tripeptide (MTP) is a modified form of MDP that has been used as a vaccine adjuvant. Ac-muramyl-Thr-D-Glu-NH2 is a specific antibody to MDP, which can be reconstituted by mixing with water and sodium chloride. It binds to the influenza virus, enhancing the immune response. The flu virus contains an antigen that stimulates the production of antibodies against influenza virus, and it also contains amphipathic molecules that are responsible for receptor binding and fusion with cells in the respiratory system. Ac-muramyl-Thr-D-Glu-NH2 binds to these molecules and enhances their function by increasing the efficiency of antibody binding. This leads to increased viral clearance from the body and reduced symptoms associated with infection with influenza</p>

<p>Trifluoroacetate salt</p>

<p>DL-Phenylalaninol is a chemical compound with the molecular formula CHNO. It is a white to pale yellow solid that is soluble in water and methanol, but not in diethyl ether. DL-Phenylalaninol has been synthesized by reacting cycloleucine with l-phenylalaninol. The reaction solution was heated at a temperature of 140°C for six hours, which yielded DL-Phenylalaninol as a hydroxy methyl compound. The synthesis of DL-Phenylalaninol was achieved through an asymmetric synthesis with sodium dodecyl sulfate surfactant. A detection sensitivity of 1 ppm and an enhancement at 260 nm were observed when analyzing the product by high performance liquid chromatography (HPLC).</p>

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

<p>1-Phenyl-4,5-dihydro-1H-pyrazol-3-amine is an organic compound that is used as a reagent in the synthesis of other compounds. It is a dimeric compound that can be synthesized by electrolysis. It has been shown to have kinetic and potential properties, which are determined by its anilines and pyridines. 1-Phenyl-4,5-dihydro-1H-pyrazol-3-amine can also be synthesized from ethanolamine and copper (II) salts. This technique involves the electrochemical oxidation of copper, followed by reduction with acetonitrile. The resulting 1-(aminomethyl)-4,5 dihydro pyrazole 3 amine can then be used for further reactions.</p>

<p>Please enquire for more information about (1S, 2R)-1-Phenyl-2-(1-pyrrolidinyl)-1-propanol 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-D-His(1-Me)-OH hydrochloride salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Procollagen type I (212-216) H-Lys-Thr-Thr-Lys-Ser-OH is a tetrapeptide that is the most abundant component of human skin. It has been shown to have biological properties and can be synthesized in vitro. Procollagen type I (212-216) H-Lys-Thr-Thr-Lys-Ser-OH has an absorption maximum at 265 nm, which makes it suitable for use in uv protection creams. It also has a high chemical stability and can be stored for up to two years without degradation. Procollagen type I (212-216) H-Lys-Thr-Thr-Lys-Ser-OH is used as a substrate in cell culture to study protein synthesis and transcription, or polymerase chain reaction, technique. This peptide also inhibits the activity of proteases such as trypsin and chymotrypsin, making</p>

<p>Please enquire for more information about DABCYL-Arg-Gly-Val-Val-Asn-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 H-Arg(NO2)-pNA·HBr including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Orcokinin H-Asn-Phe-Asp-Glu-Ile-Asp-Arg-Ser-Gly-Phe-Gly-Phe is a peptide that was synthesized in the laboratory. It has been shown to have receptor activity and to stimulate locomotor activity in experimental models. Orcokinin H is a member of the family of peptide hormones that are present in mammals. The peptide sequence contains six amino acids, four of which are hydrophobic and two polar, with a single hydroxyl group. These features make this molecule an excellent candidate for use as a model system for studying amyloid protein aggregation and its physiological function.</p>

<p>Please enquire for more information about (Des-Pyr 1,D-Ser(tBu)6,Azagly10)-LHRH acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,3-Bis(methoxycarbonyl)-2-methyl-2-thiopseudourea (BMTC) is a novel anticancer agent that has been synthesized to be water soluble and also has significant cytotoxicity. BMTC is believed to exert its anticancer activity by binding to the colchicine binding site on tubulin which is involved in microtubule dynamics. The antitubulin effect of BMTC results in inhibition of cell division and growth. BMTC also inhibits cancer cell proliferation and migration. It has shown significant cytotoxicity against human prostate cancer cells and ovarian cancer cells, as well as inhibiting tumor xenografts in mice.</p>

<p>Nle-Leu-Phe-OH is a potent colony-stimulating factor that binds to the receptor on the surface of cells and stimulates the production of white blood cells. Nle-Leu-Phe-OH has been shown to induce actin filament formation, which is necessary for cell movement. It also induces cytosolic calcium release and enhances protein synthesis. Nle-Leu-Phe-OH also binds to phosphatase and inhibits its activity, which may be due to a conformational change in the enzyme. This process is necessary for the synthesis of DNA and other proteins from amino acids. Nle-Leu-Phe-OH also causes an increase in the uptake of Ca2+ ions by cells.</p>

<p>Please enquire for more information about PAR-2 (1-6) (mouse, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Please enquire for more information about H-Arg-Lys-Gly-Asp-Ile-Lys-Ser-Tyr-pNA including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Please enquire for more information about (D-Pro7)-Angiotensin I/II (1-7) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Copeptin (rat) trifluoroacetate salt is a peptide that belongs to the group of protein inhibitors. It can inhibit the activity of the acetylcholine receptor, which leads to an increase in muscle tone and rigidity. Copeptin is also used as a research tool for studying protein interactions, antibody-antigen reactions, cell biology, ligand-receptor binding, pharmacology and life sciences. Copeptin has been shown to inhibit ion channels such as nicotinic receptors and potassium channels. The CAS number for copeptin (rat) trifluoroacetate salt is 86280-64-0.</p>

<p>(S,S)-2,2'-Isopropylidenebis(4-phenyl-2-oxazoline) is an asymmetric ligand that is chiral and has been shown to be useful in the preparation of enantiopure alcohols. The compound has been used as a catalyst to prepare aldehydes and ketones. It also has been used in reactions involving dehydration or alkylation. (S,S)-2,2'-Isopropylidenebis(4-phenyl-2-oxazoline) can be synthesized by reacting molybdenum with an alcohol and adding a base. This reaction produces the desired product with high selectivity, which is due to its chirality.</p>

<p>5-Bromo-2-methoxyphenyl)acetic acid (BMPEA) is a hydroxylated derivative of aspartic acid. It has been shown to induce apoptotic cell death in various cell lines, including human lung cells and rat hippocampal cells. BMPEA is synthesized by the solid-phase method and is characterized by a constant structure. It can be used to treat degenerative diseases and other conditions where apoptosis is desirable, such as Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, retinitis pigmentosa, and Duchenne muscular dystrophy.</p>

<p>Please enquire for more information about C3a (72-77) (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Leu-Ser-Ala-Leu-OH is a chemical compound that has been shown to bind to 5-HT1B receptors. This receptor belongs to the 5HT1 family of serotonin receptors, which are G protein coupled receptors. The 5HT1B receptor has been shown to have a role in locomotor activity and dopamine release. HLSALLOH is also a specific antibody that reacts with the 5HT1B receptor in rats. The location of this receptor is on the dorsal raphe nucleus and other parts of the brainstem. HLSALLOH has a pH optimum of 6.0 and can be used as an immunogen for polyclonal antibodies against 5HT1B receptors.</p>

<p>Lysozyme C (46-61) (chicken) trifluoroacetate salt is a conjugated synthetic peptide that binds to the antigen. It is a reactive molecule with solubilized properties that has been shown to bind to the peptide in binding experiments. This synthetic peptide has been found to be efficacious in transfected murine bone cells and antigen-presenting cells. The binding of Lysozyme C (46-61) (chicken) trifluoroacetate salt to phospholipid membranes may be due to its reactivity with the membrane's hydrophobic surface.</p>

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

<p>Peptide WE-14 H-Trp-Ser-Lys-Met-Asp-Gln-Leu-Ala-Lys-Glu-Leu-Thr-Ala-Glu is a tetradecapeptide that is a candidate for the diagnosis of pancreatic cancer. It has been shown to localize to the pancreas and other tissues in immunohistochemical studies. This peptide was found to be present in chromaffin cells and ileal tissue, which are associated with pancreatic cancer. Peptide WE14 H Trp Ser Lys Met Asp Gln Leu Ala Lys Glu Leu Thr Ala Glu also binds to markers expressed at high levels in pancreatic cancers such as insulinoma, endocrine tumor, and neuroendocrine tumor.</p>

<p>Please enquire for more information about Boc-4-Abz-OSu 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 HIV (gp120) Fragment (318-327) 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-Ala2)-Dynorphin A (1-9) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Suc-Phe-pNA is a synthetic substrate that has been shown to be a proteolytic enzyme. It is used for the study of proteolytic enzymes and in pharmaceutical research because it can inhibit the activity of pancreatic enzymes such as trypsin or chymotrypsin. Suc-Phe-pNA has also been shown to have antiviral properties, which may be due to its ability to inhibit viral proteases. Suc-Phe-pNA is an inhibitor of serine protease, which is an enzyme that catalyzes reactions involving peptide bonds. The pH optimum for Suc-Phe-pNA is 8 and it has been shown to have a low inhibitory effect on trypsin activity at all pH levels.</p>

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

<p>Lysine(succinyl)-OH, also known as N6-(3-carboxypropanoyl)-L-lysine, is a research chemical that falls under the category of amino acids. It is a derivative of lysine and has been widely used in various research studies. Lysine(succinyl)-OH is commonly used as a substrate for dehydrogenase enzymes and has been found to play a role in metabolic pathways. In addition to its research applications, Lysine(succinyl)-OH has also shown potential benefits for external use. It has been found to have moisturizing properties that can help improve the appearance of dry or damaged cuticles. Its succinyl group enhances its ability to penetrate the skin, providing deep hydration and nourishment. Lysine(succinyl)-OH is encoded by specific genes and expressed in various organisms. Its presence in different biological systems suggests its significance in cellular processes. In addition to its use as a</p>

<p>ACV trifluoroacetate salt H-Aad (Cys-D-Val-OH)-OH trifluoroacetate salt is a nonheme iron that has been shown to be an oxidizing agent. It is used in the synthesis of antibiotics and other organic compounds. ACV trifluoroacetate salt H-Aad (Cys-D-Val-OH)-OH trifluoroacetate salt also has synthetase activity, which catalyzes the formation of a thiolate ligand from two molecules of acetyl coenzyme A (ACCOA) and one molecule of propionyl coenzyme A (PCCOA). This ligand binds to metal ions such as Fe2+, which are then reduced to Fe3+ by the metal cluster. The water ligands on the coordination sphere may be replaced by other ligands, such as lysine.</p>

<p>Please enquire for more information about ((Cys31, Nva 34)-Neuropeptide Y (27-36))2 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Amino-2-methoxy-4-methylpyridine is a small molecule that inhibits bromodomains. Bromodomains are protein domains that bind to acetylated lysine residues on histones. 5-Amino-2-methoxy-4-methylpyridine binds to the bromodomain, preventing the acetylated lysine residues from binding with other proteins and inhibiting transcription. This drug has been shown to be effective in treating prostate cancer by interacting with the androgen receptor. 5-Amino-2-methoxy-4-methylpyridine also interacts with ATPase, which may lead to increased levels of ATP production, and has been shown to have antitumor effects in vitro.</p>