Building Blocks

<p>Versatile small molecule scaffold</p>

<p>D-Cysteine is the L-cysteine stereoisomer. It has been shown to inhibit the response of nicotinic acetylcholine receptors and toll-like receptor 4, which are proteins that play a role in inflammation. D-Cysteine also inhibits the production of nitric oxide by inhibiting NADPH oxidase. This inhibition leads to decreased inflammation, as well as decreased oxidation of proteins and DNA. D-Cysteine has been shown to be a specific inhibitor of wild type strains of Escherichia coli, but not mutant strains with defects in iron homeostasis. The enzyme activity for d-cysteine is also inhibited by l-cysteine, which may result in drug interactions. D-Cysteine can be found naturally in foods such as garlic, onions, broccoli, and cauliflower.</p>

<p>Artificial sweetener</p>

<p>1-Cyanoimidazole is a phosphodiester that is used in the chemical ligation of nucleic acids. It reacts with terminal alkynes to form covalent linkages between DNA molecules, and can be used as a crosslinker for dna duplexes. 1-Cyanoimidazole can be used as a phosphate group replacement in DNA replication. This compound has been shown to react with terminal alkyne groups on DNA templates, forming stable covalent linkages between strands in the presence of an appropriate nucleophile. 1-Cyanoimidazole has been shown to have sequence specificity and efficient method for linking strands of DNA.</p>

<p>3-Methylbenzophenone is a fatty acid that has been used as an analytical reagent in organic synthesis. It can be synthesized by acylation of benzoic acid with methylchloroformate. 3-Methylbenzophenone is also a chlorinated derivative of benzophenone, and its structure can be rationalized by the protonation and deprotonation of the chloride ion. The acidic properties of 3-methylbenzophenone are due to the presence of carbonyl group.</p>

<p>4-Chloroindole-3-acetic acid is a plant hormone that belongs to the group of auxins. It has been shown to stimulate root formation in plants by increasing the amount of auxin present in the plant's tissues. 4-Chloroindole-3-acetic acid is an intramolecular hydrogen donor and can form hydrogen bonds with other molecules. It also has a receptor binding site and cyclic peptide backbone, which allow it to act as a transcription factor or enzyme inhibitor. This molecule has been shown to be an optimum concentration for root formation in physiology experiments, and can be used as a model system for auxin research.</p>

<p>Radiosensitiser in hypoxic tumours</p>

<p>Please enquire for more information about 3-Chloro-5-hydroxybenzoic acid ethyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Methylbenzamide is a palladium complex that has been used in the synthesis of imatinib, a drug used to treat chronic myeloid leukemia. 4-Methylbenzamide has been shown to form a hydrogen bond with water molecules and also exhibits cavity effects. The cavity effect can be explained by intermolecular hydrogen bonding and the deuterium isotope effect. The deuterium isotope effect is observed when an atom of deuterium replaces an atom of hydrogen in a molecule. This substitution leads to reduced boiling point and increased solubility for the compound. 4-Methylbenzamide is also known for its inhibitory effects on p38 kinase, which are seen through titration calorimetry.</p>

<p>4-Methoxybenzamide is a small molecule that has been shown to have anticancer activity in vitro and in vivo. It is a hydroxylated benzamide with an intramolecular hydrogen bond, which allows it to selectively bind to DNA at the C4' position of cytosine. The compound's anticancer effects are due to its ability to inhibit the transcription of genes involved in cancer cell proliferation and its ability to induce apoptosis via caspase activation. 4-Methoxybenzamide has been shown to be synergistic when used with other chemotherapeutics, such as cisplatin, doxorubicin or 5-fluorouracil. This drug also inhibits the uptake of these drugs by cancer cells, limiting their therapeutic effects on healthy tissues.</p>

<p>2'-Methoxyacetophenone is a member of the class of halogenated phenols that exhibits anti-inflammatory activities. It inhibits protease activity in vitro and has been shown to have anti-inflammatory effects in vivo. 2'-Methoxyacetophenone is a ruthenium complex with hydrochloride salt that has been shown to be an efficient catalyst for acylation reactions. This compound also inhibits the transfer of the nerve impulse from the trigeminal nerve to the brain, which may be due to its ability to inhibit lipid peroxidation and protein autoxidation. 2'-Methoxyacetophenone has also been shown to have antimicrobial activity against gram-negative bacterial species, such as Proteus vulgaris, Escherichia coli, Pseudomonas aeruginosa, and Salmonella enterica.</p>

<p>Methyl 4-aminobenzoate is a chemical compound that is used as a fluorescence probe in the study of DNA replication. It can be used to detect the presence of viral RNA in cell culture, and has been shown to inhibit the replication of bacterial RNA. Methyl 4-aminobenzoate binds to guanine residues in DNA and forms an alkyl bond with them. This prevents the binding of other amino acids, which are essential for DNA replication. Methyl 4-aminobenzoate has also been shown to have pharmacokinetic properties that make it useful for intravenous administration and oral administration.</p>

<p>3-Chloro-5-hydroxybenzoic acid methyl ester is a fine chemical that can be used as a versatile building block and reaction component in the synthesis of complex compounds. It is soluble in organic solvents such as dichloromethane, chloroform, and acetone. 3-Chloro-5-hydroxybenzoic acid methyl ester has CAS No. 98406-04-3 and a molecular weight of 149. 2.</p>

<p>4-Nitrobenzenesulfonyl chloride is a versatile chemical compound. As a reagent in organic synthesis, it plays a crucial role in the preparation of pharmaceuticals, iminosugars, and oligosaccharides. Its ability to facilitate alpha-glucosylation makes it an essential component in the synthesis of complex carbohydrates. 4-Nitrobenzenesulfonyl chloride is also utilized in the preparation of N-nosyl-alpha-amino acids, which are essential building blocks in peptide synthesis. Additionally, it is widely used in the production of dyes and pigments.</p>

<p>Derivative of naphthalene; used in the synthesis of various chemicals and as a precursor in the production of dyes, pigments, and pharmaceuticals. It is particularly important in the manufacture of azo dyes, where it serves as a coupling agent in the diazo coupling reaction to produce colored compounds.</p>

<p>cis-N-(3-Chloroallyl)-1-(R)-aminoindan hydrochloride is a high quality, research chemical that is a versatile building block. It is used as a reagent and reaction component for the synthesis of fine chemicals, speciality chemicals, and complex compounds. cis-N-(3-Chloroallyl)-1-(R)-aminoindan hydrochloride has CAS number 1175018-80-0.</p>

<p>5-Nitroindole is a chemical used in wastewater treatment. It is an electron acceptor that can be used to reduce the cost of the process. 5-Nitroindole has significant cytotoxicity and polymerase chain activity in human pathogens, such as Escherichia coli, Salmonella enterica, Staphylococcus aureus, and Mycobacterium tuberculosis. The drug is stable under aerobic conditions and has shown no significant cytotoxicity to mammalian cells. 5-Nitroindole has been shown to hybridize with DNA duplexes containing guanine bases and form covalent bonds in a model system. The drug also has been shown to be present in colonies of colony-stimulating factor (CSF) cells that are found in the blood stream of healthy individuals.</p>

<p>2-Naphthaldehyde is an antimicrobial agent that has been shown to inhibit the growth of bacteria in vitro. It has been shown to inhibit the synthesis of DNA, RNA and protein. 2-Naphthaldehyde is an intramolecular hydrogen acceptor and a substrate for coumarin derivatives. The reaction mechanism of 2-napthalaldehyde is not yet fully understood, but it has been proposed that 2-napthalaldehyde reacts with sodium carbonate to form sodium phenolate and acetone. 2-Naphthaldehyde also shows genotoxic activity, as it has been shown to induce structural aberrations in bacterial DNA. This chemical compound also forms coordination geometry complexes with metal ions such as copper and zinc.</p>

<p>Cis-4-Chloro-3-nitrocinnamic acid is an aromatic organic compound with potential utility in biochemical research and synthesis. This compound is typically derived from synthetic chemical processes involving chlorination and nitration reactions on cinnamic acid derivatives. Its molecular structure, characterized by both chloro and nitro functional groups, allows it to interact in unique ways with various biochemical pathways and molecular frameworks.</p>

<p>5-Nitroso-2,4,6-triaminopyrimidine is a chemical compound that has been shown to have anticancer activity. It reacts with nucleophilic compounds such as hydroxides of metals and amides to form an amide bond. 5-Nitroso-2,4,6-triaminopyrimidine inhibits the enzyme glycosylase by reacting with it in a nucleophilic attack. This reaction leads to the formation of a stable nitrosamine intermediate that can be hydrolyzed by an acid or base. The inhibitory effect of 5-Nitroso-2,4,6-triaminopyrimidine on malonic acid decarboxylase (MAD) and anthranilic acid synthase (AAS) in animals is due to its ability to react with these enzymes in a similar way as for MAD and AAS in humans. Inhibition of MAD and AAS leads to reduced levels of malonic</p>