Building Blocks

<p>Applications 2-(Bromomethyl)benzonitrile is an intermediate in the synthesis of Alogliptin (A575425), an oral antihyperglycemic agent that is a selective inhibitor of the enzyme dipeptidyl peptidase-4 (DPP-4). Antidiabetic agent.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Lai, Z., et. al.: Eur. J. Med. Chem., 83, 547 (2014); Lynn, F., et al.: Diabetes, 50, 1004 (2001); Trumper, A., et al.: J. Endocrinol., 174, 233 (2002); Vollmer, K., et al.: J. Clin. Endocrinol. Metab., 94, 1379 (2009)<br></p>

<p>Applications 3-Bromothiofuran is a compound used as a corrosion inhibitor in mild steel. It also shows antimicrobial activity against common bacterium types such as Escherichia coli and Bacillus subtillis.<br>References Sawkar, A. et al.: Proc. Nat. Acad. Sci., 99, 15428 (2002); Cox, T. et al.: Lancet, 355, 1481 (2000);<br></p>

<p>Applications Budesonide (B689490) epimer S. Budesonide 22R epimer is more active than 22S epimer. Used as an antiinflammatory agent.<br>References Ryrfeldt., A., et a.: J. Steroid Biochem., 10, 317 (1979), Roth, G., et al.: J. Pharm. Sci., 69, 766 (1980), Clissold, S.P., et al.: Drugs, 28, 485 (1984),<br></p>

<p>Applications cis-1-Butene-1,4-diol is used in the synthesis of bezoxazinyl-oxazolidinones as promising antbacterial agents. Also used in the preparation of AMF-26, an antitumor agent for inhibition of the golgi system, targeting a specific ribosylation factor.<br>References Guo, B. et al.: J. Med. CHem., 56, 2642 (2013); Shiina, I. et al.: J. Med. CHem., 56, 150 (2013);<br></p>

<p>Applications 1,4-Butane Sultone is an alkylating agent with weak carcinogenic activity.<br>References Van Duuren, B.L. et al.: J. Nat. Cancer Inst., 53, 696 (1974); Druckrey, H. et al.: Zeitsch. Krebsforsch.,75, 69 (1970);<br></p>

<p>Applications Pramoxine impurity. Phenol derivatives induced tumor cell apoptosis.<br>References Li, B., et al.: J. Biochem., 138, 679 (2005), Peltason, L., et al.: J. Med. Chem., 50, 5571 (2007),<br></p>

<p>Please enquire for more information about Tocinoic acid trifluroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Cyanopiperidine is an organic compound that belongs to the class of medicines and has a cyclohexane ring with two functional groups. It is a part of the compound class of dehydrating agents. 4-Cyanopiperidine is most commonly used as an intermediate in the synthesis of other compounds, but can also be used as a medicine. 4-Cyanopiperidine has been shown to be effective against pain, cancer, and seizures. The inhibitory effect of 4-cyanopiperidine on cyclic AMP causes it to have potent inhibitory activity against cb1 receptor, which is responsible for the psychoactive effects caused by tetrahydrocannabinol (THC). This drug also has potent antagonistic effects on pethidine and related drugs such as fentanyl, morphine, and oxycodone.</p>

<p>5-Chloro-2-mercaptobenzimidazole is an inorganic base that is used as a microscopy reagent. It has been shown to have a transfer mechanism that is similar to the hydrogen ion transfer mechanism. 5-Chloro-2-mercaptobenzimidazole has been used in vivo assays and has functional groups that are important for its use in coatings and aluminum oxide. The molecule also contains chlorine atoms, which are important for its use in chlorination reactions. 5-Chloro-2-mercaptobenzimidazole can be used in voltammetry to test samples of organic compounds (e.g., casein) and has been shown to be effective against the Gram positive bacterium Staphylococcus aureus.</p>

<p>Pyridine 4-acetic acid HCl is a synthetic, fluorescent probe with reactive and luminescence properties. It is used for the detection of hydrogen bond formation in organic compounds. It is also used as a probe to study the molecular interactions between metal ions and β-unsaturated aldehydes. Pyridine 4-acetic acid HCl has been shown to be useful for transduction of light energy into chemical energy. The pyridine ring makes this compound an excellent candidate for molecular modeling studies due to its rigid structure.</p>

<p>Proline is a non-essential amino acid that is found in the basic structure of collagen. Proline has been shown to have physiological effects, including a protective effect on the myocardium, and can be used as an analytical method for detecting proline residues in biological samples. Trans-4-Hydroxy-L-proline is a proline derivative that has been shown to inhibit collagenase activity in vitro. It was also shown to have an optimum concentration of 1 mM and a matrix effect at pH 6.5. The model system used to study trans-4-hydroxy-l-proline was the enzyme extracted from rat liver.</p>

<p>4-Azidopiperidine hydrochloride is a chemical compound that is used as a versatile building block in the synthesis of complex chemical compounds. It is also used as a reagent or speciality chemical, and has many applications in research, such as being an intermediate for the synthesis of other chemicals. 4-Azidopiperidine hydrochloride can be used to make useful building blocks, reaction components, and scaffolds for chemical reactions.</p>

<p>6-Methylheptanol is a chemical compound that belongs to the group of imidazole hydrochlorides. It is used as a catalyst for the treatment of wastewater. 6-Methylheptanol has been shown to catalyze the reaction of malonic acid with glycol ethers and hydroxyl groups in water, which produces high values of phosphorus pentoxide. The kinetic data and reaction mechanism for this process have been elucidated by using a model system and reaction solution. 6-Methylheptanol also has an effect on polymerase chain reactions (PCR) due to its ability to increase the temperature at which the enzyme works.</p>

2-Chloro-3-nitropyridine is a nucleophilic compound that reacts with amines to form substituted amines. It can be synthesized by hydrolysis of chloroacetamide with hydrochloric acid and reacting the resulting ammonium chloride with nitrobenzene. The reactions are nucleophilic substitutions, which means it reacts at an electron rich atom such as the nitrogen in the ammonium chloride. This reaction is exothermic, meaning it releases heat, and the products are 2-chloro-3-nitropyridine and water. 2-Chloro-3-nitropyridine has been shown to inhibit α subunit of protein kinase C (PKCα) activity by binding to the PKCα ATP site. It also has been shown to react with proteins containing reactive sulfhydryl groups such as cysteine residues, forming sulfonamides or sulfoxides that may inhibit enzyme activity or

<p>2-Hydroxy-4-bromopyridine (2HBP) is a product with genotoxic activity that can be used for research. 2HBP has been shown to inhibit the synthesis of DNA by inhibiting the enzymatic reaction or binding to DNA. 2HBP is also an inhibitor of virus replication and causes monolayer cell death through radiation or chemical structures. It can be used as an anti-tumor agent and has been shown to have inhibitory properties on dna replication.</p>

<p>6-Chloro-2-cyano-3-nitropyridine is a modified pyridine derivative that has been shown to be an antagonist of the adenosine receptors. 6-Chloro-2-cyano-3-nitropyridine blocks the binding of adenosine to A1 and A2A receptors, which leads to increased levels of cyclic AMP in cells. This compound can be used as an antiviral agent or as a component in the development of a new generation of drugs for the treatment of malaria. 6-Chloro-2-cyano-3-nitropyridine has also been shown to be active against HIV, inhibiting its replication and preventing viral assembly. The drug’s mechanism of action is not yet fully understood, but it may involve interference with viral replication by binding to sulfinyl groups on proteins required for virus assembly.</p>

<p>6-Chloropurine is an isothiouronium salt that is metabolized by the enzyme thiopurine methyltransferase to its active form, 6-methylthioinosine. It has been shown to inhibit the growth of bacterial cells in culture by binding to their adenine nucleotide. 6-Chloropurine inhibits the synthesis of purines and pyrimidines, which are involved in DNA replication and RNA synthesis. 6-Chloropurine has been shown to have cytotoxic effects on certain human carcinoma cell lines and may be used as a chemotherapeutic agent for these types of cancer. The drug has also been shown to have high values with aerobacter aerogenes, which is a bacterium that can cause lung infections.</p>