Amino Acids (AA)

<p>1,2,3,4-Tetrahydro-4,6-dihydroxy-2-methyl-isoquinoline is a useful building block in the synthesis of various compounds such as pharmaceuticals and pesticides. It is an intermediate for the preparation of other valuable chemicals such as the antihistamine diphenhydramine, which is used to treat allergies. Tetrahydroisoquinoline can also be used as a reagent to synthesize other chemical compounds. This compound has been used in research as well as commercial applications. Tetrahydroisoquinoline is also a versatile scaffold that can be modified to produce different derivatives with different properties.</p>

<p>Fmoc-Thr-OPAC is a solid-phase peptide synthesis reagent. It is used to synthesize α-amino acid peptides. Fmoc-Thr-OPAC has been used in the preparation of various peptides, including polypeptide hormones such as insulin and vasopressin. The compound has also been used in the crystalline form for the synthesis of α-amino acid derivatives.</p>

<p>4-Chloro-2-methoxy-5-methylaniline is a dye molecule that is used in the synthesis of other molecules, such as diketene. It is also used as a solvent, coupling agent, and a dye molecule. This compound can be synthetically prepared by reacting naphthylamine with pyrazolone. The reaction requires catalytic amounts of polyvalent metal salts, such as zinc chloride or iron(III) chloride. The halogenation of 4-chloro-2-methoxy-5-methylaniline to produce 2,4,5-trichlorophenol can be achieved by diazotising the molecule with sodium nitrite and potassium dichromate. 4-Chloro-2-methoxy-5 methylaniline's substituents are methyl groups on the phenyl ring (Cl) and chlorine atoms (C1). Derivatives of this</p>

<p>Fmoc-O-trityl-L-serine is a synthetic molecule that is not naturally occurring. It has been shown to have inhibitory effects on the growth of cancer cells in vitro and in vivo, but does not affect healthy cells. Fmoc-O-trityl-L-serine binds to the membrane of cancer cells and inhibits protein synthesis by binding to ribosomes. This drug also inhibits cell growth by interfering with the membrane interactions necessary for cellular metabolism. Fmoc-O-trityl-L-serine is toxic to red blood cells, which may be due to its ability to induce hemolysis.</p>

<p>Please enquire for more information about tert-Butyl 4-(2-methoxy-2-oxoethyl)piperazine-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Abrine is a plant toxin that belongs to the group of abrinoids. It is a chiral molecule and can exist as an L-form or D-form. The L-form is used in some analytical methods, such as gas chromatography, while the D-form is used in medical purposes. L-Abrine has been shown to have anti-HIV effects by inhibiting reverse transcriptase and deoxyribonuclease activity. It has also been shown to inhibit colony stimulating factor production and decrease bacterial growth in vitro. L-Abrine inhibits the replication of bacteria by binding to adenylate cyclase and blocking the enzyme's ability to synthesize cAMP from ATP. This inhibition prevents protein synthesis, leading to cell death.</p>

<p>Z-NH-PEG2-CH2COOH is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Z-NH-PEG2-CH2COOH is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>3-Methylglutaric acid is an organic compound that belongs to the group of alkanocarboxylic acids. It has been shown to reduce the formation of malonic acid, which can be toxic to the heart and cause congestive heart failure. 3-Methylglutaric acid also inhibits oxidation catalysts and increases the production of energy in cells by providing electrons. The kinetic data for 3-methylglutaric acid have been determined using a gas chromatography technique on a high-temperature conversion reactor at a pH of 7.0 with a concentration of 0.1 M potassium phosphate buffer (pH 7) and a temperature of 70°C. 3-Methylglutaric acid has been shown to inhibit monoclonal antibody cationic polymerization, which may be due to its reactive nature and its ability to donate hydrogen ions or electrons.</p>

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

<p>N-[1-(4-Fluorophenyl)propan-2-Yl]-N-methylprop-2-Yn-1-amine is a synthetic molecule that has been shown to be an inhibitor of the enzyme nitroethane reductase. This drug is also capable of inhibiting the activity of other enzymes and is being investigated for its potential use in the treatment of various types of cancer. N-[1-(4-Fluorophenyl)propan-2-Yl]-N-methylprop-2-Yn-1-amine inhibits nitroethane reductase by binding reversibly to the active site and competitively inhibiting the substrate. The potency of this drug against nitroethane reductase has been shown to be increased by alkylation.br&gt;<br>The inhibition of nitroethane reductase by N-[1-(4-fluorophenyl)propan-2-Yl]-</p>

<p>N-Acetyl-D-proline is a ligand that binds to the calcium ion. It has been shown to enhance the cross-linking of collagen, elastin, and other proteins. N-Acetyl-D-proline is also used as a crosslinking agent for polymers such as silicone rubber and epoxy resin. This compound can be found in devices such as connectors, valves, and pipes. N-Acetyl-D-proline can be used as a ligand to bind cphpc (carbon paste), which is an important component of membranes in fuel cells.</p>

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

<p>1-Methylimidazole-2-sulfonyl chloride is a synthetic estrogen that is used for the treatment of estrogen deficiency in women. It has been shown to increase plasma estradiol levels and reduce plasma testosterone levels. This drug is not active at physiological levels, but was found to have biological relevance when administered at higher doses. 1-Methylimidazole-2-sulfonyl chloride has been found to be effective in the treatment of cancer in humans, with a specific effect on breast cancer cells.</p>

<p>Please enquire for more information about Boc-(4-pyridyl)-L-beta-homoalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Methyl-5-propyl-2-dioxanone is a polymer that has reactivities similar to those of dioxane. It can be polymerized by an azobenzene catalyze or polymerization. 5-Methyl-5-propyl-2-dioxanone can also be polymerized into an alternating, cyclic structure with moieties of esters. This polymer is chemically inert and insoluble in water.</p>

<p>Please enquire for more information about Fmoc-(S)-3-amino-3-(2-naphthyl)propionic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Indole-7-methanol is a flavin cofactor that catalyses the formylation of indole-7-carboxylic acid. Indole-7-methanol can be synthesized by the conversion of indole-7-carboxaldehyde with formaldehyde and ammonium acetate. The macrocyclic, isomeric, and formylated forms of indole-7-methanol have been shown to have utilisation activity in the synthesis of various compounds. These reactions are catalyzed by flavins such as FAD or FMN. Mutant, unsymmetrical derivatives of indole-7-methanol are also known to undergo these types of reactions. The most common derivative is indirubin, which has been shown to inhibit DNA polymerase III and IV in vitro.</p>

<p>S-Aminoethyl-L-cysteine hydrochloride is an amino acid that is used in the diagnosis of metabolic disorders. It has been found to have a high concentration in plasma and can be used to measure the activity of bowel disease. S-Aminoethyl-L-cysteine hydrochloride is also used as a diagnostic marker for inflammatory diseases. It is extensively metabolized by acidic hydrolysis, which results in the release of chloride ions and amines.</p>

<p>6-Methoxy-2-(4-methoxyphenyl)benzo[b]thiophene (6MBT) is a mesomorphic, acid catalyst that has been used to synthesize polyphosphoric acid. It reacts with chloride to form 6-chloro-2-(4-methoxyphenyl)benzo[b]thiophene, which can be converted to the desired product by sulfoxide. The reaction time for this process is relatively short and the yield is high. 6MBT can also be used as a semiconductor in devices such as solar cells and electronic displays. The photoelectric effect of 6MBT was demonstrated in 1972, when it was found that electron emission from a photocurrent could be obtained at room temperature. This property has been shown to be due to the molecule's absorption of light energy and subsequent conversion into electrical energy.</p>

<p>Please enquire for more information about (1S,2R)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenyl-1-propanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>9-Methyl-b-carboline is a phytochemical that belongs to the class of protonated carbon disulphide. It has been shown to inhibit monoamine oxidase and is used in some medications. 9-Methyl-b-carboline has been shown to have physiological function, including growth factor activity and epidermal growth properties. It also inhibits hydroxylase, which is an enzyme that catalyzes the stepwise oxidation of tyrosine and phenylalanine. This compound can be found in plants belonging to the families of Fabaceae, Lamiaceae, and Solanaceae. The compound has been found to act as a secondary messenger in mitochondria by transferring electrons from NADH to coenzyme Q10.</p>

<p>Dolasetron mesylate is a mesylate of the biologically active form of dolasetron, which is an octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester. Dolasetron has been shown to be effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy or radiation therapy. It has been approved for use in adults with cancer who have not responded to other treatments. Dolasetron is rapidly absorbed from the gastrointestinal tract and is then distributed throughout the body, including into the brain. The elimination half life of dolasetron mesylate is about 2 hours and it binds to plasma proteins. Dolasetron mesylate specifically binds to serotonin receptors, which are found on cells in the gut. This binding inhibits serotonin induced contraction of bowel smooth muscle cells.</p>

<p>Please enquire for more information about (R,S)-Z-3-Amino-7-chloro-2-oxo-5-phenyl-1,4-benzodiazepine 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-Methylindole-3-acetonitrile 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-Formyl-3-methoxy-phenyloxymethyl polystyrene resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Arg-Pro-OH sulfate salt is a synthetic peptide that binds to the receptor for filtrates. It is used to treat skin conditions such as dermatitis, eczema, and psoriasis. H-Arg-Pro-OH sulfate salt has been shown to be effective in inhibiting clostridium from producing proteins. This drug also inhibits the uptake of these proteins by blocking the binding of phosphorylated lysine residues to their receptors on the cell membrane. It has been shown to hydrolyze amide bonds and can be used as a catalyst for bond cleavage reactions.</p>

<p>Please enquire for more information about 1-tert-Butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Phenylcyclohexanol (1-PC) is an organic compound that is used as a reagent in the synthesis of other compounds. It is a colorless liquid with a pleasant odor. 1-PC has been shown to have synergic effects when reacted with various types of oxidizing agents, such as magnesium and boron trichloride. The reaction products are cyclohexanol, dehydration, and modifiers. When 1-PC reacts with phenylcyclohexene, it forms the antigen hemiketal.</p>

<p>Gamma-Methylleucine (2-Amino-3-tert-butylpropionic acid) is an auxiliary for copper-catalyzed asymmetric Michael reactions.</p>

<p>mGlu receptor antagonist</p>

<p>Allylglycine is a glutamate decarboxylase inhibitor and a GAMMA-AMINOBUTYRIC ACID antagonist. It is used to induce convulsions in experimental animals.</p>

<p>N-alpha-Tosyl-L-lysine chloromethyl ketone hydrochloride inhibits trypsin-like proteases and IFN-γ activities.</p>

<p>N-Monoacetylcystine is a paracetamol poisoning antidote. It is used in the treatment of influenza A virus pandemic.</p>

<p>N-Oleoyl Leucine (Oleoyl-L-leucine) is an N-fatty acyl amino acid present in plasma.</p>

<p>Boc-Glu(OBzl)-OSu can be used for the synthesis of solid phase peptides containing benzyl glutamate residues.</p>

<p>Alitame is a high-intensity sweetener and sugar substitute widely used in biochemical experiments and drug synthesis research.</p>

<p>L-4FPG is a Glycine derivative, inhibits the neutral amino acid transporters ASCT1 and ASCT2.</p>

<p>Fmoc-5-aminopentanoic acid: alkane, Fmoc-protected amine, carboxyl group, PROTAC linker, deprotects to free amine, forms amides with activators.</p>

<p>L-5-BromoTryptophan (5-BrW) is an analog of the tryptophan (Trp) effector and inhibits the gelation of hemoglobin S.</p>

<p>Lombricine, as a phosphodiester of 2-guanidinoethanol and D-serine in structure, is a phosphagen that is unique to earthworms.</p>

<p>Indoleacetyl phenylalanine is an indole-acetyl-amino acid involved in regulating auxin activity.</p>

<p>Please enquire for more information about 8-Chloro-1-methyl-6-phenyl-4H-Imidazo[1,5-a][1,4]benzodiazepine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Acetylserine (N-Acetyl-L-serine) serves as the physiological inducer of cysteine biosynthesis by binding to the CysB apoprotein and stimulating cysJIH</p>

<p>A 924 is an amino acid derivative with antineoplastic activity.</p>

<p>Certain chronic neurologic disorders, such as Parkinson's disease, are caused by an insufficiency of the neurotransmitter dopamine secondary to the degeneration</p>

<p>Thialysine HCl is a cytotoxic cysteine derivative that inhibits Escherichia coli, acting as a protein synthesis inhibitor and metabolite.</p>

<p>Statine is a protease inhibitor that is active against pepsin and other acid proteases.</p>

<p>Fmoc-Phe-Phe-OH is a supramolecular compound that has been synthesized and characterized. It is a carboxylic acid with an amino group at the end of the side chain. Fmoc-Phe-Phe-OH has been shown to be an effective antioxidant, which is due to its ability to regenerate other antioxidants in the body. It also has regenerative properties, as it can be used for cell culture, skin cells, and optical properties. Fmoc-Phe-Phe-OH also has antidiabetic effects, as it can inhibit glucose production by pancreatic beta cells.</p>

<p>Please enquire for more information about HIV Protease Substrate III-B (Native Sequence) 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-Val-Leu-Lys-AMC 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 5-(H-Gly-Pro-Gly-Pro-amido)-9-[di-(3-sulfonylpropyl)amino]-benzo[a]phenoxazonium perchlorate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Gly-Cys-Gly-OH is an amino acid sequence that has been evaluated for its interactions with other amino acids and proteins. It is a tripeptide heterocycle and can be found in the tissues of many organisms, including humans. H-Gly-Cys-Gly-OH can be found in bovine serum and has been shown to have reversed phase high performance liquid chromatography activity. This molecule also interacts with reversed phase high performance liquid chromatography, ion exchange, and tripeptides.</p>

<p>H-Lys(Abz)-Pro-Pro-pNA is a potent and selective DPP-IV inhibitor that has been shown to be active in humans. This drug binds to the DPP-IV enzyme and prevents it from breaking down the incretin hormone, GLP-1, which is released by the intestine in response to food intake. This leads to increased insulin production and an improved glycemic profile in people with type 2 diabetes. H-Lys(Abz)-Pro-Pro-pNA also inhibits endoproteolysis of dipeptidyl peptidase IV (DPPIV), which reduces its activity against other enzymes such as amyloid beta protein precursor protein (APP) and angiotensin II receptor type 1 (AT1R).</p>

<p>Pz-Pro-Leu-Gly-Pro-D-Arg-OH trifluoroacetate salt is a synthetic substrate that can be used for the synthesis of cyclic peptides. It has been shown to act as a competitive inhibitor of the serine protease, chymotrypsin, and cytochalasin B. Pz-Pro-Leu-Gly-Pro-D-Arg is a soluble substrate that can be used in tissue culture experiments with caco2 cells. This compound also has high solubility and is stable at pH values between 5 and 12. The optimum pH for this compound is 8.</p>

<p>H-Gly-His-Gly-OH is an amino acid that belongs to the class of peptide science. It is a protonated molecule with a histidine side chain, which has been shown to have enzyme inhibition properties. This amino acid has been used in model studies to determine the effect of acidic and basic ternary mixtures on the stability of proteins. H-Gly-His-Gly-OH has also been found to be effective as a chelate ring, which is a ring that binds metals such as iron and copper. Enzymes can form when this amino acid is present in solution with metal ions.</p>

<p>Please enquire for more information about Human CMV pp65 (495-503) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Sauvagine is a trifluoroacetate salt of Pyr-Gly-Pro-Pro-Ile-Ser-Ile-Asp-Leu-Ser-Leu-Glu-Leu-Leu-Arg. It has been used as a model system to study the effects of trifluoroacetic acid on brain functions. Sauvagine has also been shown to have inhibitory effects on cyclase enzymes, which are involved in the synthesis of steroids and other hormones. This compound has also been found to have an effect on locomotor activity and receptor activity.</p>

<p>Please enquire for more information about H-Gly-Phe-NH2·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 C-Peptide 1 (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 Ovokinin 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-Ala-Phe-NH2·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Pro-Gly-Pro-OH is a peptide that is derived from the sequence of human proline-glycine-proline (HGP). It has been shown to have a number of physiological activities, including anti-inflammatory effects. This peptide can be used as a model compound for inflammatory genes and proteins. H-Pro-Gly-Pro-OH has been shown to inhibit the synthesis of inflammatory cytokines in mouse splenocytes and neutrophil recruitment in wild type mice. HGP also suppresses chemotactic activity and inhibits neutrophil migration in an experimental model. HGP has also been shown to reduce intracellular calcium concentration in cerebellar granule cells, which may be due to its ability to inhibit protein synthesis.</p>

<p>Please enquire for more information about H-DL-Met-bNA·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 Boc-Asp(OcHex)-Merrifield 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 1b-(4-Fluorophenyl)hexahydro-',7-dihydroxy-7-(1-methylethyl)-1a-phenyl-7a-[(phenylamino)carbonyl]-3H-oxireno[3,4]pyrrolo[2,1-b][1,3] oxazine-3-butanoic Acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Pro-Ser-Hyp-Gly-Asp-Trp-OH is a cyclic hexapeptide with a high activity against platelets. It is an antagonist of the cyclic RGD sequence, which is present in fibrinogen, fibronectin, vitronectin and other proteins. This peptide binds to the n-terminal residue of these proteins and prevents them from binding to their receptors on the surface of platelets. H-Pro-Ser-Hyp-Gly-Asp-Trp-OH has been shown to be specific for human platelets and does not bind to erythrocytes or leukocytes.</p>

<p>Bradykinin is a peptide that is released in response to injury and inflammation. It has two receptors, B1 and B2. Bradykinin binds to the B2 receptor which leads to vasodilation, increased vascular permeability, and bronchoconstriction. Lys-(Des-Arg9,Leu8)-Bradykinin trifluoroacetate salt H-Lys-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Leu (LBP) is a synthetic analogue of bradykinin that competes with bradykinin for binding sites on the bradykinin b2 receptor. LBP also inhibits lipoxygenase activity in vitro and in animals. This drug can be used as an antagonist against bradykinin b2 receptor or as an antiplatelet agent.</p>

<p>Please enquire for more information about (Met(O)35)-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>7-Diethylamino-4-methylcoumarin is a fluorescence probe that can be used in applications such as the study of hydrogen bonding interactions. It is excited by laser light and emits a red-shifted fluorescent light. 7-Diethylamino-4-methylcoumarin is a hydroxyl group analogue of coumarin, which has been shown to have physiological effects on the liver cells. The absorption spectrum of 7-Diethylamino-4-methylcoumarin is sensitive to changes in pH and chemical stability. A decrease in pH increases the intensity of the emission while an increase in pH decreases the intensity of the emission. This compound can also be used to label nucleic acids during polymerase chain reactions (PCR) or for sample preparation before analysis using nuclear magnetic resonance spectroscopy (NMR).</p>

<p>Ne-Fmoc-L-lysine is an amine with a homopolypeptide backbone. It is insoluble in water and has a low profile. Ne-Fmoc-L-lysine is synthesized using solid phase chemistry, which can be used for the synthesis of nanocarriers. It has been shown to interact with other molecules such as polymers and proteins. Ne-Fmoc-L-lysine can also be used in supramolecular architectures and oriented microscopy techniques.</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>Please enquire for more information about 3-Bromo-6-methylpicolinic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fmoc-glu(otbu)-thr(psi(Me,Me)pro)-OH is a c1-6 alkoxy, expressed, alkenyl, linker, c1-6 alkyl, efficiency, sequence that can be used for peptide synthesis. It is an efficient linker for the synthesis of peptides and has been shown to yield high yields with few side products. The hydroxyl group on the side chain of the amino acid residue provides an additional site for acylation. This product also contains an aralkyl and alkoxy group that can be used in further reactions.</p>

<p>Please enquire for more information about Proadrenomedullin (1-20) (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 Fmoc-Tyr(SO2(ONeopentyl))-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Lysyl-L-lysyl-L-lysyl-L-lysyl-L-lysine (LLLLLL) is an antibacterial agent that belongs to the class of pharmacological agents. LLLLLL has been shown to have antibacterial efficacy against oral pathogens, such as Streptococcus mutans and Porphyromonas gingivalis. LLLLLL binds to the bacterial cell wall by forming a covalent disulfide bond with cysteine residues on the peptidoglycan layer. This prevents cell wall synthesis, leading to cell death by inhibiting protein synthesis. LLLLLL has also been shown to have low toxicity in animal models for long periods of time, with high values in human serum.</p>

<p>H-Leu-Val-Tyr-AMC is a model compound that belongs to the group of sulfonamides. It is synthesized and used as a chymotrypsin-like protease inhibitor. H-Leu-Val-Tyr-AMC has been shown to inhibit the activity of chymotrypsin, a serine protease, by binding to its active site. This inhibition leads to an increase in the time required for digestion of proteins and peptides, which may be due to the steric hindrance created by the bulky H-Leu-Val-Tyr. H-Leu-Val-Tyr amide also has antiinflammatory properties, which are thought to be caused by its ability to inhibit prostaglandin synthesis.</p>

<p>Please enquire for more information about pTH (53-84) (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,2-Dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) is a sodium salt that has the ability to form surfactant bilayers. DPPC is a model system for studying biochemical reactions and the phase transition of lipid bilayers. This compound has been used to study the effects of various drugs on cell membranes in biochemical research. In addition, DPPC has been shown to have hypoglycemic effects in animal models as well as having an anti-inflammatory effect.</p>

<p>Please enquire for more information about (Fmoc-Glu70,Ala71·72,Lys74)-C3a (70-77) 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 (Ala11,D-Leu15)-Orexin B (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-D-Leu-pNA including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fibronectin fragment (196-203) H-Ser-Arg-Asn-Arg-Cys-Asn-Asp-Gln, is a synthetic peptide that has been shown to have antiinflammatory properties. It can inhibit the inflammatory response by inhibiting the production of cytokines and chemokines. Fibronectin fragment (196-203) H-Ser-Arg-Asn-Arg-Cys-Asn, has also been shown to inhibit angiogenesis and tumor growth in vitro, as well as stabilize blood vessels and reduce the incidence of lymphatic vessel leakage. This peptide may be used in cancer therapy and for other diseases such as Kaposi's sarcoma, rheumatoid arthritis, autoimmune diseases, or infectious diseases.</p>

<p>Please enquire for more information about Fmoc-Tyr-Ala-diazomethylketone 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-Gly-Ala-His-AMC 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-Asn(Trt)-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 Glutaryl-Ala-Ala-Phe-4MbNA 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 Kininogen-Based Thrombin Inhibitor 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 Catestatin (human) trifluoroacetate 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 Neuromedin S (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(4-Methyl-2-phenyl-1-piperazinyl)-3-pyridinemethanol is an impurity in hexane that is generated during the reaction of pyridine with acetonitrile. The impurity is removed by crystallizing it from methanol. 2-(4-Methyl-2-phenyl-1-piperazinyl)-3-pyridinemethanol has a high efficiency, and can be used to synthesize hexamethyldisiloxane. This product can be used as a metal catalyst for reactions involving alkali metals or metal halides. It can also be used as an alcohol solvent, but not hydrogenated.</p>

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

<p>H-His-Phe-OH is a polypeptide that is used in the diagnosis of chronic kidney disease. It is synthesized by the chemical reaction between histidine and phenylalanine. H-His-Phe-OH has been shown to have a molecular weight of 4,000 Da, with a diameter of 5 nm. The binding constants for this molecule are 3.5 x 10^6 M^(-1), and its stability in biological fluids has been shown to be greater than 100 hours at pH 7.4, 37°C.</p>

<p>N-Methyl-2-fluoro-4-aminobenzamide is a toxic compound that is commonly used as a reagent in chemical synthesis and research. It has been studied for its potential use in medicine, particularly in the treatment of castration-resistant prostate cancer. N-Methyl-2-fluoro-4-aminobenzamide acts as a nucleophilic agent, participating in reactions that involve the addition of an acyl group to a target molecule. Its stable formyl group allows for efficient reaction yields and reliable results. However, due to its toxic nature, caution must be exercised when handling this compound.</p>

<p>Bombesin (8-14) acetate salt H-Trp-Ala-Val-Gly-His-Leu-Met-NH2 acetate salt is a bifunctional peptide that has been shown to inhibit the growth of prostate cancer cells. Bombesin (8-14) acetate salt H-Trp-Ala-Val-Gly-His-Leu-Met-NH2 acetate salt also has antiinflammatory properties and is used in treating inflammatory diseases. It inhibits collagen synthesis and fibrinogen activation, which may be important in the treatment of autoimmune diseases such as rheumatoid arthritis. Bombesin (8 14) acetate salt H Trp Ala Val Gly His Leu Met NH2 Acetate Salt has been shown to have no effect on healthy tissues when administered systemically.</p>