Aminoácidos (AA)

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

<p>Z-L-Asp-OH is a protease inhibitor that inhibits the activity of serine proteases, including trypsin and chymotrypsin. Z-L-Asp-OH binds to the active site of these enzymes and prevents them from cleaving their substrates. The optimal pH for this enzyme is 8.0, which corresponds to its maximum level of activity. Z-L-Asp-OH also has apoptotic activities in cells by causing cellular pathway changes, leading to cell death via programmed cell death or apoptosis. This agent is activated by hydrolysis at ester linkages and polymerizes into films in aqueous solution at physiological pH. It has been shown to inhibit the growth of human ovarian carcinoma cells in vitro, but not normal cells.</p>

<p>1-Methyl-1H-indole-3-carbohydrazide (MZ) is a potential anticancer drug that inhibits the growth of cancer cells. It binds to the colchicine binding site on the DNA, which prevents doxorubicin from binding and causing damage to the DNA. MZ has been shown to be effective against breast cancer and has been shown to inhibit tumor growth in mice by targeting cancer cells lines. MZ also inhibits proliferation of MDA-MB-231 cells in culture, as well as inhibiting cell cycle progression, leading to apoptosis. The molecular docking studies show that 1MZ binds to colchicine site on DNA with high affinity and specificity.</p>

<p>Diethyl 2-methylenemalonate is an ester compound that is used in the production of film-forming polymers. The polymer can be activated by exposing it to a reactive substance, such as hydrogen chloride or water. This reaction produces a film-forming polymer with properties that can be tailored for specific applications. Diethyl 2-methylenemalonate has been shown to react efficiently with ethyl ethoxymethylenecyanoacetate and diethyl ketomalonate to produce the desired product in an efficient manner.</p>

<p>2-(2-Nitroanilino)-5-methylthiophene-3-carbonitrile is a crystalline compound that belongs to the group of small molecules. It has a molecular weight of 153.2 g/mol and a melting point of 281 °C. The compound has three different crystalline forms, including a monoclinic form, which is thermodynamically stable at room temperature. 2-(2-Nitroanilino)-5-methylthiophene-3-carbonitrile can be used as a model system for studying influenza virus and as an inhibitor of influenza virus replication. 2-(2-Nitroanilino)-5-methylthiophene-3-carbonitrile also inhibits the activity of carbamazepine, which is an anti epileptic drug, by binding to its active site on the molecule.</p>

<p>mPEG6-OH is a PEG polymer categorised as monofunctional (OH-PEG-X). Used as a linker, mPEG6-OH is used to attached PEG to proteins, peptides, oligonucleotides, nanoparticles and small molecules via pegylation, a bioconjugation technique.</p>

<p>Ethyl 5-acetoxy-6-bromo-2-(bromomethyl)-1-methyl-1H-indole-3-carboxylate is a chemical compound that has been shown to have anti viral activity in vitro. The structure of the compound suggests that it may inhibit the production of inflammatory cytokines. This drug inhibits the activity of enzymes such as hydroxylases and lipases, which are important for the inflammatory process. Ethyl 5-acetoxy-6-bromo-2-(bromomethyl)-1-methyl-1H-indole-3 carboxylate may be an effective treatment for bowel disease and other inflammatory conditions.</p>

<p>Please enquire for more information about [(4-Methyl-1H-imidazol-5-yl)methyl]amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Boc-Gly-Arg-Arg-AMC trifluoroacetate is a potent inhibitor of kinases, which are enzymes that play a crucial role in various cellular processes. It has been shown to effectively inhibit the activity of both Chinese and human kinases. This inhibitor has also demonstrated its efficacy as an anticancer agent by inducing apoptosis in cancer cells. Boc-Gly-Arg-Arg-AMC trifluoroacetate is a medicinal protein analog that can be used for the development of novel inhibitors with improved potency and selectivity. Its potential therapeutic applications make it a promising candidate for cancer treatment. Additionally, this compound can be detected in urine, making it an excellent biomarker for kinase activity in vivo.</p>

<p>Please enquire for more information about 8-Ethyl-1,3,4,9-tetrahydro-1-(1-methylethyl)pyrano[3,4-b]indole-1-acetic acid 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 Ethyl 6-bromo-5-hydroxy-1-methyl-2-(phenylsulfanylmethyl)indole-3-carboxylate 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)-OBzl.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 L-Phenylalaninol 2-chlorotrityl resin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Phenoxybutyric acid is a molecule that is produced by filamentous fungi. It has been shown to inhibit the growth of many bacteria, including Staphylococcus aureus, Salmonella typhimurium, and Enterobacter aerogenes. 4-Phenoxybutyric acid binds to the receptor on the surface of the bacterial cell membrane and prevents it from functioning correctly. It also prevents the production of proteins necessary for growth and survival. This inhibition leads to a loss of energy in the cell, which eventually leads to death. The molecule has been shown to be effective in inhibiting bacteria even if they are resistant to antibiotics. 4-Phenoxybutyric acid has been shown to be more efficient than other methods for microbial biotransformation, such as dispersive solid-phase extraction or liquid-liquid extraction.</p>

<p>3-(2-Aminoethyl)-N-methyl-1H-indole-5-methanesulfonamide (AMIS) is an intermediate in the preparation of medicaments. It is a stable process and can be used as an intermediate for other compounds. AMIS is prepared by reacting methanesulfonic acid with methanol and ammonium carbonate, which produces methanesulfonamide, succinic acid and ammonium hydroxide. The reaction liquid is then heated to produce a crystalline solid. The crystals are then recrystallized to yield AMIS as a white solid.</p>

<p>Please enquire for more information about 1-Methylindole-3-boronic acid pinacol ester 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 1,1,1-Trichloro-3-(1-methyl-1H-benzimidazol-2-yl)propan-2-ol 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-(3-Methoxyphenyl)piperazine dihydrochloride 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-Amino-6,7-dimethoxy-2-methylquinazolin-4(3H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fmoc-PAL is an amino acid that can be used in the synthesis of peptides with a free amine group. It is prepared as an amide and can be immobilized on solid phase for preparative purposes. Fmoc-PAL has a labile functional group, which means it can be cleaved from the peptide once the synthesis is complete. The presence of nitro groups on Fmoc-PAL makes it susceptible to oxidation by trifluoroacetic acid (TFA). This amino acid is used in solid-phase chemistry and sequences are typically synthesized by adding one molecule of Fmoc-PAL at a time to the growing chain until the desired sequence is complete.</p>