Acides aminés (AA)

<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>

Z-Pro-Leu-Ala-NHOH is a potent inhibitor of stromal cells. It is a hydroxamic acid molecule that acts as an inhibitor of protein synthesis in the ribosome. Z-Pro-Leu-Ala-NHOH has been shown to have potent inhibitory activity against ethyl palmitate and lipiodol, which are used for therapeutic purposes. The molecule also inhibits viscosity in pharmaceutical preparations and pluripotent stem cells. This compound has shown inhibitory activities against stromal cells, which are responsible for growth, differentiation, and tissue repair. It also prevents the formation of embryoid bodies or pluripotent stem cells by suppressing the expression of proteins needed for early development.

4-Bromo-1-methyl-1H-imidazole is an organic compound that belongs to the group of imidazoles. It is a chiral molecule with two stereoisomers, 4-bromo-1H-imidazole and 1H-imidazole. This compound can be synthesized by reacting ethyl formate with α-amino acid and chlorides in the presence of magnesium, followed by reduction with lithium aluminum hydride. The yield of this reaction is low, so it is not used in industrial processes. The imidazoles are important for their pharmacological activity as they are a class of drugs such as nitrofurantoin or griseofulvin. The dinitrate derivatives are also important for their metallation reactions and use in organic synthesis.

<p>1-O-Octadecyl-2-O-benzyl-sn-glycerol (ODBG) is a novel antiviral drug that is being developed for the treatment of HIV. ODBG inhibits HIV by binding to the virus and preventing it from entering cells, which prevents the virus from replicating. ODBG has been shown to be effective against other viruses as well, such as herpes simplex virus and respiratory syncytial virus. ODBG is a lipid molecule that can cross cell membranes and has been shown to have low toxicity in animal studies. This drug also has potential to be used as an oral medication for patients with HIV.</p>

<p>Please enquire for more information about Boc-Thionoser(Bzl)-1-(6-nitro)benzotriazolide 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>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>(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>The peptide Z-Gly-Leu-Ala-OH is a reactive substance that is generated by the cleavage of casein kinase II. The peptide has been shown to have cytotoxic effects on Hodgkin's lymphoma cells, and also induces apoptosis in these cells. This peptide binds to mitochondria and causes mitochondrial damage, as well as generating reactive oxygen species (ROS) in the cell. ROS generation is dependent on oxygen species.</p>

<p>Z-Trp-Ala-OH is an imidazolide that is used as a potassium supplement. It has the potential to be used in the treatment of epilepsy, but more research is needed to determine its safety and efficacy.</p>

<p>3-Methylthiopropionic acid is a bacterial metabolite that can serve as an alternative carbon source for the production of amino acids. 3-Methylthiopropionic acid is used to study the effect of matrix on enzyme activities, and has been shown to have protein-binding properties. The compound also serves as a precursor in the synthesis of tiglic acid, which is a lysine precursor. 3-Methylthiopropionic acid has been found to be effective in slowing the growth of cancer cells. It has been shown to inhibit fatty acid synthesis, and may also inhibit methionine synthetase activity and cell proliferation.</p>

<p>Ranalexin is a peptide antibiotic that has been isolated from the fungus Penicillium patulum. It is an antimicrobial peptide and has shown antibacterial efficacy against gram-positive bacteria, including methicillin-resistant Staphylococcus aureus and Enterococcus faecalis. Ranalexin binds to bacterial membrane receptors, leading to rapid cell death. The biological properties of ranalexin are still being studied in order to determine its mechanism of action.</p>

<p>Please enquire for more information about H-Ala-D-Gln-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 4-{[4-(4-Methyloxyphenyl)-piperazin-1-yl]-phenyl}-2,4-dihydro-[1,2,4]-triazol-3-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trifluoroacetate salt</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>Please enquire for more information about Amyloid beta-Protein (1-40) (scrambled) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Met-Asn-OH is a peptide that is composed of the amino acids methionine, asparagine, and hydroxyproline. It has been found to be specific for influenza and has been proposed as a potential drug target for this virus. The constant and resonance energies of H-Met-Asn-OH have been determined by NMR spectroscopy. The amino acid composition of H-Met-Asn-OH is typical of many proteins. Structural isomers are molecules that differ only in their spatial arrangement but share the same chemical formula. H-Met-Asn-OH can be considered a structural isomer because it differs by its chirality, which means that it rotates plane polarized light in one direction while its mirror image, L-methionine asparagine hydroxyproline (LMAHP), rotates light in the opposite direction. Gene products are molecules that are responsible for converting information from DNA into proteins via</p>

<p>Please enquire for more information about (Des-Gly10,D-Ala6,Pro-NHEt 9)-LHRH (salmon) 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 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>N-Methylmorpholine N-oxide is an activated cellulose product. It is used for the treatment of autoimmune diseases and can be used as a reagent to synthesize fatty acid esters. This drug has been shown to have low water permeability, meaning it does not readily diffuse through membranes, which may be due to its high hydrochloric acid content.</p>

<p>Endothelin-1 (11-21) trifluoroacetate salt H-Cys-Val-Tyr-Phe-Cys-His-Leu-Asp-Ile-Ile-Trp is a peptide that is derived from endothelin. It has been shown to have an inhibitory effect on insulin stimulated glucose uptake in Sprague Dawley rats. This peptide has also been shown to bind to the endothelin receptor and act as a nonselective agonist. Endothelin 1 (11–21) trifluoroacetate salt H-Cys Val Tyr Phe Cys His Leu Asp Ile Ile Trp, when incubated with cells, had a maximal response at micron concentrations.</p>

<p>Please enquire for more information about Galanin (1-13)-Neuropeptide Y (25-36) amide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Asp-Arg-Gly-Asp-Ser-OH is an amide with a molecular weight of 456.5 and a purity of 99.2%. This compound has been shown to inhibit tumor cell growth in vitro and in vivo, as well as the metastasis of tumor cells. H-Asp-Arg-Gly-Asp-Ser-OH is also capable of inhibiting tumor cells that are resistant to conventional anti cancer drugs such as 5FU, cisplatin, and doxorubicin.</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>Please enquire for more information about Fmoc-Lys(N-Me-Abz-Boc)-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 (Des-Gly2)-Exenatide 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-Glu(OtBu)-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>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>

<p>Please enquire for more information about H-Val-AMC 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 Orphan GPCR SP9155 Agonist P518 (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>13-mer connexin mimetic peptide, composed of residue numbers 63-75 of the first extracellular loop of connexin 43 (gap junction blocker), containing the SHVR amino acid motif.</p>

<p>Cholecystokinin octapeptide (CCK-8) is a peptide hormone that belongs to the enkephalinase inhibitor family. It is a desulfated molecule with an amidated C-terminus and has been shown to inhibit the activity of aminopeptidases, which are enzymes that break down peptides. Cholecystokinin octapeptide (CCK-8) is found in the brain where it acts as a neurotransmitter and has been shown to have anti-inflammatory effects. This molecule has also been found to be effective in the treatment of cerebral disorders such as Parkinson's disease, Alzheimer's disease, and Huntington's disease by inhibiting glutamate release from nerve cells.</p>

<p>Myeloblastin (142-150) (human, mouse) trifluoroacetate salt HVal-Leu-Gln-Glu-Leu-Asn-Val-Thr-Val-OH trifluoroacetate salt is an antigen that belongs to the class of serine proteinases. It is a soluble recombinant human proteinase that has been shown to have a tumor cell lysis activity in vitro and in vivo. Myeloblastin (142-150) (human, mouse) trifluoroacetate salt HVal-Leu-Gln-Glu-Leu-Asn-Val-Thr Val is also a leukocyte antigen and can be used for the development of cancer vaccines.</p>

<p>Please enquire for more information about H-Lys(retro-Glu-H)-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 Osteoblast-Adhesive Peptide 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-Leu7)-LHRH trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Gly-Gly-Sar is a synthetic peptide that acts as a substrate for the peptide transporter, which is part of the membrane of cells. It is an amide with a reactive group that can form a ternary complex with two hydroxyl ions and one proton. Gly-Gly-Sar has been shown to be taken up by caco-2 cells in an extravesicular manner and undergoes proteolysis by peptidases. This leads to bond cleavage and formation of free Gly-Gly and Sar. The free Gly and Gly are then transported across the cell membrane into the cell cytoplasm, where they are hydroxylated by enzymes such as glycyl-l-leucine hydroxylase to form glycolic acid and glyoxylic acid, respectively.</p>

<p>Please enquire for more information about Fmoc-Ile-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 CD36 (93-110)-Cys 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 Thrombospondin-1 (1016-1021) (human, bovine, mouse) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Leucokinin II is a fatty acid. It is a diagnostic agent that can be used to identify bacteria, such as Stenotrophomonas maltophilia, which produce β-amino acids. Leucokinin II can also be used for the diagnosis of cancer and inflammatory diseases. Its analogs are being studied for their potential use in diagnosing infectious diseases. Leucokinin II binds to the receptor and activates it, resulting in the production of biochemical or electrochemical signals that can be detected by a detector.</p>

<p>C-reactive protein (CRP) is a protein that is synthesized by the liver in response to inflammation. It has a variety of functions, including the regulation of energy metabolism and glycolysis. CRP also has a role in regulating production of neutrophil chemotactic factors, cytokines, and reactive oxygen species. In addition, it binds to zymosan and can be used as an inflammatory marker in medical diagnostics. The amino acid sequence for CRP was first determined in 1971. The primary structure for CRP consists of two alpha helices connected by two beta strands. Its tertiary structure consists of four alpha helices that are connected through loops and turns by three beta sheets with an additional loop connecting one helix to the other strand. CRP contains no disulfide bonds or hydrophobic interactions; instead, it relies on hydrogen bonds to maintain its shape.br&gt;br&gt;</p>

<p>Please enquire for more information about (D-Phe12)-Bombesin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>