Aminoácidos (AA)

<p>Applications Mono(3-methylpentyl) Phthalate, is a phthalate monoester, which can be used as plasticizers (substances added to plastics to increase their flexibility, transparency, durability, and longevity). It has been also shown to have effects on peroxisomal fatty acid β-oxidation in rats.<br>References Peterson, J.C., et al.: Int. J. Envrion. Anal. Chem., 18, 237 (1984); Gharagheizi, F., et al.: Indust. Engin. Chem. Res., 49, 12685 (2010); Lake, B. G., et al.: Arch. Toxic. Supplem., 9, 386 (1986);<br></p>

<p>Stability Hygroscopic<br>Applications 1-(2-Amino-7H-purin-6-yl)-1-methylpyrrolidinium Chloride (cas# 680622-68-8) is a compound useful in organic synthesis.<br>References Pauly, G., et al.: J. Med. Chem., 51, 7144 (2008),<br></p>

<p>Applications 1-Amino-3-methylisoquinoline-4-carbonitrile (cas# 161468-33-3) is a compound useful in organic synthesis.<br></p>

<p>Applications D-Alanine methyl ester is a derivative of D-Alanine (A480995). D-Alanine is an amino acid that is commonly found in bacteria, such as Streptococcus faecalis. It is essential for the biosynthesis of peptidoglycan crosslinking sub-units that are used for bacterial cell walls. D-Alanine is also known to cause cytotoxic oxidative stress in brain tumour cells.<br>References Ellsworth, B., et al.: Chem. Biol., 3, 37 (1996); Ferrari, E. et al.: Nat. Biotech., 3, 1003 (1985); Stegman, L., et al.: Human Gene Ther., 9, 185 (1998); Wood, W. &amp; Gunsalus, I.: J. Biol. Chem., 190, 403 (1951)<br></p>

<p>Applications Intermediate for the synthesis of 1-Naphthol β-D-Glucuronide.<br></p>

<p>Applications An optically active amino acid derivative as intermediate for making drugs.<br></p>

<p>Applications Intermediate in the preparation of Indomethacin<br>References Kalgutkar, A.S., et al.: Bioorg. Med. Chem., 13, 6810 (2005),<br></p>

<p>Applications 1-(azidomethyl)-3-methoxybenzene (cas# 123767-44-2) is a useful research chemical.<br></p>

<p>Applications Diethyl 3,7-Bis(formyloxy)-25-methyl-cholestane-26,27-dioic Acid Ester-d3 is an intermediate used in the synthesis of 3α,7α-Dihydroxycoprostanic Acid-d3 (D452517), which is a labelled analogue of 3α,7α-Dihydroxycoprostanic Acid (D452515), a precursor of Cholic Acid (C432600), it undergoes side chain oxidation during the synthesis of bile acids. It was found that Zellweger’s syndrome patients have abnormal mitochondrial structure, the organelle that is responsible for the side chain oxidation, and as a consequence, excess amounts of 3α,7α-Dihydroxycoprostanic Acid.<br>References Hanson, R. F., et al.: Science (Washington, DC, U. S.), 203, 1107 (1979)<br></p>

<p>Applications 2-Methoxycarbonylphenylboronic acid<br></p>

<p>Applications (4R)-6-Methoxycarbonyl-4-phenyl-3,4-dihydrocoumarin is an intermediate in the synthesis of (R)-5-Hydroxymethyl Tolterodine Formate (H949480), a metabolite of Tolterodine (T535800), a muscarinic receptor antagonist used in the treatment of urinary incontinence.<br>References Palmer, L., et al.: J. Pharm. Biomed. Anal., 16, 155 (1997); Hills, C., et al.: Drugs, 55, 813 (1998); Wefer, J., et al.: World J. Urol., 19, 312 (2001)<br></p>

<p>Applications D-Leucine methyl ester hydrochloride is a protected form of D-Leucine (L330150). D-Leucine is an unnatural isomer of L-Leucine (L330110) that acts as an auto-inhibitor of lactic streptococci in culture. D-Leucine causes analgesia in humans and also exhibits inhibitory activity in bacterial cell cultures.<br>References Chuan, Y., et al.: Chin. J. Anim. Vet. Sci., 4, 003 (1985); Fox, S., et al.: J. Biol. Chem., 155, 465 (1944); Gillillad, S. &amp; Speck, M.: J. Dairy Sci., 51, 1573 (1968); Schoenheimer, R., et al.: J. Biol. Chem., 130, 703 (1939); Seltzer, S., et al.: Pain, 11, 141 (1981)<br></p>

<p>Applications Indole-2-carboxylic Acid-13C (cas# 1216839-31-4) is a compound useful in organic synthesis.<br></p>

<p>Applications Fmoc-d-3-pyridylalanine, is an amino acid building block used in peptide synthesis. With a growing peptide drug market the fast, reliable synthesis of peptides is of great importance.<br></p>