Ácidos Grasos y Derivados Lipídicos

<p>Atorvastatin hemicalcium trihydrate, an oral HMG-CoA reductase inhibitor, lowers blood lipids and inhibits SV-SMC with IC50s: 0.39/2.39 μM.</p>

<p>Arundic Acid (ONO 2506) is an astrocyte-modulating agent, delays the expansion of cerebral infarcts by modulating the activation of astrocytes.</p>

<p>Octanoic acid (Caprylic acid) is found naturally in coconuts and breast milk. Caprylic acid is used in the production of esters used in perfumery.</p>

<p>Imeglimin hydrochloride (EMD 387008 hydrochloride） is an oral hypoglycemic agent. Imeglimin improves insulin sensitivity.Cost-effective and quality-assured.</p>

<p>Regaloside H, a glyceryl phenylpropionate glycoside, is a gluconeogenesis inhibitor.</p>

<p>ONO-RS-082 is a Ca2+-independent phospholipase A2 inhibitor. </p>

<p>SW033291 is a small-molecule inhibitor of 15-PGDH (Ki=0.1 nM) that increases prostaglandin PGE2 levels in bone marrow and other tissues.</p>

<p>Vardenafil hydrochloride is a New Phosphodiesterase Type 5(PDE5) Inhibitor, in the Treatment of Erectile Dysfunction in Men With Diabetes</p>

<p>Disodium succinate is a sodium salt of succinate, key in metabolism and reactive oxygen species regulation.</p>

<p>Stability Light Sensitive<br>Applications Important polyunsaturated fatty acid of the marine food chain that serves as a precursor for the prostaglandin-3 and thromboxane-3 families. It differs from arachidonic acid (the eicosatetraenoic acid that is a precursor for the prostaglandin and thromboxane-2 families) by the extra double bond between the third and fourth carbons from the “methyl end” of the molecule. Antilipemic.<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 Bergstrom, S., et al.: J. Biol. Chem., 239, PC 4006 (1964), Srivastava, K.C., et al.: Biochem. Exp. Biol., 16, 317 (1980), Kremer, J.M., et al.: Ann. Intern. Med., 106, 497 (1987), DiGiacomo, R.A., et al.: Am. J. Med., 86, 158 (1989),<br></p>

<p>Applications Labelled Choleretic produced by, and isolated from liver cells.<br>References Nomoto, M., et al.: Biol. Pharm. Bull., 32, 172 (2009), Simonsen, H., et al.: J. Agric. Food Chem., 57, 2056 (2009), Miyata, M., et al.: Drug Metab. Disposition, 37, 338 (2009),<br></p>

<p>Applications 2-(4-Hydroxybenzyl)-N,5-bis-(4-fluorophenyl)-5-hydroxypentanamide is an ring-opened impurity of Ezetimibe (E975000).<br>References Raman, B. et al.: J. Pharmac. Biomed. Anal., 52, 73 (2010);<br></p>

<p>Applications 3-Methyl Salicylic Acid is a toxic compound, it’s toxicity is similar to salicylic acid. Reagent used in manufacturing and preparation of dyes.<br>References Egorova, T. V., et al.: Tekstil'naya Promyshlennost , 3, 48 (1987); Keshavarz, M. H., et al.: J. Hazard. Mater., 237, 79 (2012)<br></p>

<p>Applications Orlistat isomer. Used in the asymmetric synthesis of Orlistat (O686500).<br>References Barbier, P., et al.: Helv. Chimica Acta, 70, 196 (1987),<br></p>

<p>Applications Orlistat is an antiobesity agent. Orlistat is an pancreatic lipase inhibitor.<br>References Borgstrom, B., et al.: Biochim. Biophys. Acta, 962, 308 (1988), Hauptman, J.B., et al.: Am. J. Clin. Nutr., 55, 309S (1992), McNeely, W., et al.: Drugs, 56, 241 (1998), Hauptman, J. B., et al.: Arch. Fam. Med., 9, 160 (2000),<br></p>

<p>Applications 7-Despropyl 7-Methyl Vardenafil is an impurity of Vardenafil (V098001, 2HCl); a selective phosphodiesterase type 5 (PDE5) inhibitor.<br>References Bischoff, E., et al.: J. Urol., 165, 1316 (2001); Kim, N.N., et al.: Life Sci., 69, 2249 (2001); Kendirci, M., et al.: Expert Opin. Pharmacother., 5, 923 (2004)<br></p>

<p>Applications (3S,4S,3’S)-Ezetimbe is a 3-epimer impurity of Ezetimibe (E975000), a cholesterol absorption inhibitor.<br>References van Heek, M., at al.: J. Pharmacol. Exp. Ther., 283, 157 (1997), van Heek, M., at al.: Brit. J. Pharmacol., 129, 1748 (2000)<br></p>

<p>Applications N-Desmethyl Sildenafil Hemicitrate is an impurity of Sildenafil (S435000), an orally active selective type 5 cGMP phosphodiesterase inhibitor.<br>References Terrett, N.K., et al.: Bioorg. Med. Chem. Lett., 6, 1819 (1996); Goldstein, I., et al.: N. Engl. J. Med., 338, 1397 (1998)<br></p>