Amino Acids (AA)

<p>Applications 4-Chloro-2-fluoro-N-methylbenzamide<br></p>

<p>Applications (2Z,4E)-5-[(1S)-3-(Hexylthio)-1-hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl]-3-methyl-2,4-pentadienoic Acid-d13 is the isotope labelled analog of (2Z,4E)-5-[(1S)-3-(Hexylthio)-1-hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl]-3-methyl-2,4-pentadienoic Acid (H298050); an analog of Abscisic Acid (A110000) designed as an antagonist of PYL-PP2C receptor interactions.<br>References Takeuchi, J., et al.: Nat. Chem. Biol., 10, 477 (2014)<br></p>

<p>Applications (αR)-7,8-Dihydro-α-methyl-N-[3-[3-(trifluoromethyl)phenyl]propyl]-1-naphthalenemethanamine is synthetically prepared though a double bond migration in Heck reaction during the preparation of cinacalcet congeners. This enantiomerically pure material is seperated from its counter part, (αR)-5,6-Dihydro-α-methyl-N-[3-[3-(trifluoromethyl)phenyl]propyl]-1-naphthalenemethanamine (D455335) using HPLC.<br>References Wang, X., et al.: Tetrahedron Lett., 45, 8355 (2004)<br></p>

<p>Applications 2-methylquinoline-4,6-diamine (cas# 5443-31-2) is a useful research chemical.<br></p>

<p>Applications 2-Bromo-5-methylbenzoic acid<br></p>

<p>Applications 2-Methyl-propanoic acid 3-Hydroxy-2,2,4-trimethylpentyl Ester is a plasticizer. It can also be used to synthesize hard and flexible nanocomposite coatings.<br>References Dieckmann, D., et al.:J. Vinyl Addit. Technol., 12, 217 (1990); Fogelstroem, L., et al.: ACS Appl. Mater. Interfaces, 2, 1679 (2010)<br></p>

<p>Applications 3-Bromo-4-methoxybenzoyl Chloride is an intermediate in the synthesis of (3-Bromo-4-hydroxyphenyl)(2-ethyl-3-benzofuranyl)-methanone (B685230), which is an impurity of benzbromarone (B185200) and is currently being investigated as a potent human uric acid (U829200) transporter I inhibitor.<br>References Wempe, M, et al.: Drug Des. Devel. Ther., 6, 323 (2012)<br></p>

<p>Applications 2-Amino-5-methoxybenzoic Acid is used in the synthesis of quinazolinone class of histamine H3 receptor inverse agonists. It is also used in the synthesis of Alogliptin, a selective inhibitor of the serine protease dipeptidyl peptidase IV.<br>References Feng, J. et al.: J. Med. Chem., 50, 2297 (2007); Nagase, T. et al.: J. Med. Chem., 51, 4780 (2008);<br></p>

<p>Applications N-(5-formylpyrimidin-2-yl)-N-methylglycine (cas# 915921-77-6) is a useful research chemical.<br></p>

<p>Applications 1-Bromo-3-methyl-2-butene is used to prepare xanthine dipeptidyl peptidase inhibitors for treatment of type 2 diabetes. It can also be used to synthesize natural and non-natural prenylated chalcones with antitumor, antioxidant activities.<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 Eckhardt, M., et al.: J. Med. Chem., 50, 6450 (2007); Vogel, S., et al.: Bioorg. Med. Chem., 16, 4286 (2008)<br></p>

<p>Stability Hygroscopic<br>Applications L-3-(4-Hydroxy-3-methoxy-d3-phenyl)alanine (CAS# 586954-09-8) is a useful isotopically labeled research compound.<br></p>

<p>Stability Hygroscopic<br>Applications N-Acetyl-L-α-aspartyl-L-α-glutamyl-L-valyl-N-(4-nitrophenyl)-L-asparagine TFA Salt is an para-nitro aniline chromophore cleaved by caspase.<br></p>

<p>Applications 3-(5-amino-2-methyl-4-oxoquinazolin-3(4H)-yl)piperidine-2,6-dione (cas# 1015474-32-4) is a useful research chemical.<br></p>

<p>Applications 2-(4-methoxybenzyl)isothiazolidine 1,1-dioxide (cas# 158089-76-0) is a useful research chemical.<br></p>

<p>Applications 8-Bromo-3,9-dihydro-3-methyl-1H-purine-2,6-dione, is a substituted derivative of Xanthine (X499950), found in animal organs, yeast, potatoes, coffee beans, tea. It can also be used for the synthesis of Linagliptin (L465900), which is a novel potent and selective dipeptidyl peptidase-4 (DPP-4) inhibitor with potential use in the treatment of type 2 diabetes.<br>References Mueller, C. et. al: Handbook Exp. Pharmacol. 200,151(2011); Prabavathy, N. et al.: Int. J. Pharm. Bio. Sci., 2, 438 (2011); Deacon, C.F.: Diab. Obes. Metab., 13, 7 (2011); Mtthias E., et. al: J. Med. Chem., 50, 6450 (2007);<br></p>