Réactifs synthétiques

<p>Applications ABT-888 is a potent, orally bioavailable PARP-1/-2 inhibitor shown to potentiate DNA damaging agents. The ability to potentiate temozolomide (TMZ) and develop a biological marker for PARP inhibition was evaluated in vivo. Potent PARP inhibitor.<br>References Virag, L., et al.: Pharmacol. Rev., 54, 375 (2002), Tentori, L., et al.: Clin. Cancer Res., 9, 5370 (2003), Kim, M., et al.: Cell, 119, 803 (2004), Tentori, L., et al.: Pharmacol. Res., 52, 25 (2005),<br></p>

<p>Applications Ammonium iron(III) citrate (cas# 1185-57-5) is a useful research chemical.<br>Chemical Name: Ammonium iron(III) citrate (cas# 1185-57-5) is a useful research chemical.<br></p>

<p>Applications YM155 is a novel small-molecule survivin suppressant that suppressed expression of survivin and induced apoptosis in PC-3 and PPC-1 human HRPC. cell lines. Potent Survivin Inhibitor.<br>References Takhito, N., et al.: Cancer. Res., 67, 8014 (2007); Kita, A., et al.: J. Pharmacol. Exper. Therap., 343, 178 (2012); Kumar, B., et al.: Molec. Cancer. Therap., 11, 1988 (2012);<br></p>

<p>Applications Analogue of Papaverine. Antispasmodic.<br>References Lalla, J., et al.: J. Pharm. Biomed. Anal., 11, 385 (1993), Bolaji, O.O., et al.: Eur. J. Drug Metab. Pharmacokinet., 21, 217 (1996), Kraemer, T., et al.: Drug Metab. Dispos., 28, 339 (2000)<br></p>

<p>Applications Sodium Phosphate Monobasic Monohydrate is often used in foods and in water treatment. it can be used as a buffer to adjust pH. In medicine, it is sometimes used as a stimulant laxative before certain operations and medical procedures.<br>References Krajewska, B., et al.: Biocat. Biotrans., 23, 225 (2005); Aliabadi, H., et al.: Am. J. Health-System Pharm., 65, 441 (2008); Henderson, J., et al. Gastrointestinal endoscopy 42, 238 (1995)<br></p>

<p>Applications Ethyl 3-Phenylpropionate is also used in the synthesis pyrimidine based inhibitors of cyclin-dependant kinases. It is also used to preparation of inhibitor BB-3497.<br>References Markwalder, J. et al.: J. Med. Chem., 47, 5894 (2004); Davies, S. et al.: Bioorg. Med. Chem. Lett., 13, 2709 (2003);<br></p>

<p>Stability Hygroscopic<br>Applications Bafilomycin A1 is a specific inhibitor of vacuolar type H+-ATPase (V-ATPase) in animal cells, plant cells and microorganisms.<br>References Bownman, E., et al.: PNAS, 85, 7972 (1988); Umata, T., et al.: J. Biol. Chem., 265, 21940 (1990); Saurin, A., et al.: Biochem.<br></p>

<p>Applications 1-(3-DIMETHYLAMINOPROPYL)-3-ETHYLCARBODIIMIDE (cas# 1892-57-5) is a useful research chemical.<br></p>

<p>Applications Mitoquinol is an antioxidant mitochondrial-targeted coenzyme Q analog with neuroprotective effects.<br>References Fink, B.D., et. al.: J. Pharmacol. Exp. Ther., 342, 709 (2012); Hobbs, C.E., et. al.: Pediatr. Int., 50, 481 (2008)<br></p>

<p>Applications Adamantoic Acid is an inhibitor of chorismate mutase activity and hydroxyphenylpyruvate synthase. It inhibits TTR conformational changes facilitating amyloid fibril formation.<br>References Baures, P. et al.: Bioorg. Med. Chem., 6, 1389 (1998); Christopherson, R. et al.: Biochem., 24, 1116 (1985); Chao, Herbert S. &amp; Berchtold, G.: Biochem., 21, 2778 (1982)<br></p>

<p>Applications Hydrobromic acid is a strong acid that is used in conjunction with Phenol (P318005) to carry out rapid cleavage of sulfonamides. Hydrobromic acid is primarily used in chemistry to produce inorganic bromides, and is also used in isomerization reactions.<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 Aida, T., et al.: Tetrahedron Lett., 14, 39 (1973); Elliott, J., et al.: J. Agr. Food Chem., 8, 111 (1960); Nozaki, K. &amp; Ogg Jr., R.: J. Am. Chem. Soc., 63, 2583 (1941); Snyder, H. &amp; Geller, H.: J. Am. Chem. Soc., 74, 4864 (1952)<br></p>

<p>Applications A tankyrase (TNKS) inhibitor that antagonizes Wnt signaling via stimulation of β-catenin degradation and stabilization of axin. XAV 939 inhibits proliferation of the μ-catenin-dependent colon carcinoma cell line DLD-1.<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 Huang, S. et al.: Nature, 461, 614 (2009); Wang, H. et al.: ACS Chem. Biol., 6, 192 (2011); Adles, M.E. et al.: Sci. Signal., 91, ec326 (2009);<br></p>

<p>Applications Iron(III) Chloride is commonly employed as a Lewis acid for catalysing reactions such as chlorination of aromatic compounds and Friedel-Crafts reaction of aromatics. In industrial application, iron(III) chloride is used in sewage treatment and drinking water production. It is also used as a leaching agent in chloride hydrometallurgy.<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 Cox, D., et al.: J. Am. Chem. Soc., 110, 8085 (1988); Tauxe-Wuersch, A., et al.: Water Res., 39, 1761 (2005); Trebouet, D., et al.: Water Res., 35, 2935 (2001)<br></p>

<p>Applications Forskolin is a diterpene isolated from Coleus forskohlii, possessing vasodilating and cardiostimulatory properties. Forskolin resensitizes cell receptors by activating the enzyme adenylyl cyclase and increasing the intracellular levels of cAMP.<br>References Lindner, E., et al.: Arzneim.-Forsch., 28, 284 (1984), Hoever, G., et al.: J. Med. Chem., 48, 1256 (2005), Lai, S., et al.: Eur. J. Clin. Microbiol. Infect. Dis., 24, 5831 (2005),<br></p>

<p>Stability Very Hygroscopic<br>Applications Magnesium Chloride is used in magnesium replacement therapy for those deficient in magnesium. Effective anaesthetic for cephalopods.<br>References Iezhitsa, I. et al.: Nutr. Neurosci., 14, 10 (2011); Culloty, S. et al.: Aquaculture., 107, 249 (1992);<br></p>

<p>Stability Moisture Sensitive<br>Applications 2-Furanone is a heterocyclic organic compound that is used widely in the synthetic preparation of pharmaceutical goods.<br>References Kim, H.K., et al.: Plant. Pathol. J., 28, 259 (2012); Nam, S., et al.: J. Agr. Food. Chem., 60, 9097 (2012); Durchschein, K., et al.: Eur. J. Org. Chem., 2012, 4963 (2012);<br></p>

<p>Applications Cetyltrimethylammonium hydrogensulfate 99% (cas# 68214-07-3) is a useful research chemical.<br></p>

<p>Applications Tris(triphenylphosphine)rhodium Chloride is also known as Wilkinson's catalyst and is commonly used to catalyze the hydrogenation of alkenes. Tris(triphenylphosphine)rhodium(I) Chloride is also used in the catalytic hydroboration of alkenes with catecholborane and pinacolborane and the selective 1,4-reduction of α, β-unsaturated carbonyl compounds.<br>References Evans, D.A. et al.: J. Am. Chem. Soc., 110, 6917 (1988); Ojima, I. et al.: Tetrahedron Lett., 13, 5035 (1972); Birch, A.J. et al.: Org. React., 24 (1976);<br></p>

<p>Applications 1,4-Dihydropyridine calcium antagonist with antihypertensive and diuretic effects. A potential candidate in the treatment of patients with renal parenchymal hypertension.<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 Ohya, Y. et al.: Int. J. Clin. Pharmacol. Therap., 38, 304 (2000); Huh, W. S. et al.: Curr. Therap. Res., 61, 395 (2000); Katoh, M. et al.: Eur. J. Clin. Pharmacol., 55, 843 (2000);<br></p>

<p>Applications PAC-1 is a caspase 3 activator. Caspase activation is a key strategy in cancer therapy. Caspase 3 is a key executioner caspase and direct effector of apoptosis. Hallmark of many cancers is the circumvention of signal in the activation of executioner caspases and loss of apoptotic response. EC50 for caspase 3 activation = 0.33 μM and caspase 7= 4.5 μM. The IC50 for apoptosis induction = 0.92 μM. Elevated caspase 3 level in cancerous cell lines and tissues allows PAC-1 to selectively induce apoptosis in tissues.<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 Slee, E., et al.: J. Biol. Chem., 276, 7320 (2001), Pop, C., et al.: Biochemistry, 42, 12311 (2003), Li, L., et al.: Science, 305, 1471 (2004), Green, D., et al.: J. Clin. Invest., 115, 2610 (2005), Satoh, T., et al.: Clin. Cancer Res., 15, 3872 (2009),<br></p>

<p>Applications Foscarnet inhibits viral DNA polymerase and reverse transcriptase. Foscarnet is used as an antiviral.<br>References Helgstrand, E., et al.: Science, 201, 819 (1978), Reno, J.M., et al.: Antimicrob. Agents Chemother., 13, 188, (1978), Alenius, S., et al.: Arch. Virol., 60, 197 (1979),<br></p>

<p>Stability Hygroscopic<br>Applications Perindopril L-Arginine, is a complex compound of Perindopril (P287500), having the antihypertensive, cardiovascular protective and antithrombotic properties, and has been shown to exists as a neutral complex.<br>References Remko, M., et al.: Euro. J. Med. Chem., 44, 101 (2009); Morgan, T., et al.: J. Cardiovasc. Pharmacol., 10, Supp. 7, S116, (1987);<br></p>

<p>Applications Cupriethylenediamine Hydroxide is used as a solvent for cellulose.<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 Yang, L., et al.: J. Applied Polym. Sci., 126, E244 (2012); Shi, W., et al.: Ind. Eng. Chem. Res., 52, 586 (2013); Cyrot, J., et al.: Bulletin de l'Institut Textile de France, 18, 211 (1964)<br></p>

<p>Applications Sulbactam Pivoxil is a prodrug of the semi-synthetic β-lactamase inhibitor Sulbactam (S699195).<br>References Foulds, G. et al.: Curr. Chemother. Infect. Dis., Proc. Int. Congr. Chemother., 11, 353 (1980); Pei, Q. et al.: J. Chrom. B Anal. Technol. Biomed. Life Sci., 879, 2000 (2011);<br></p>

<p>Applications AHR 11652 is a metabolite of Bromfenac sodium (B678550).<br>References Walsh, D.A., et al.: J. Med. Chem., 25, 446 (1982),<br></p>

<p>Applications 2-Pyrrolidinylphosphonic Acid, is an impurity of Alendronate (A521250), a bisphosphonate used as a bone reabsoption inhibitor.<br>References Wang, X.M., et al.: Clin. J. Dent. Res., 3, 26 (2000), Woo, T., et al.: Best Pract. Res. Clin. Rheumatol., 15, 469 (2001), Benford, H.L., et al.: Bone, 28, 465 (2001),<br></p>

<p>Applications Phosphomolybdic Acid Hydrate functions as catalyst, and also use in the preparation of other catalyst, e.g. the preparation of highly active deep HDS catalysts prepared using Mo and W heteropolyacids supported on SBA-15. It is also a reagent for the preparation of molybdophosphate complexes of rare earth elememts. Dyes and metabolites.<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 Lizama, L., et al.: Appl. Catal., B: Env., 82, 139 (2008); Xiao, Z., et al.: Fujian Shifan Daxue Xuebao, Ziran Kexueban, 2, 77 (1986)<br></p>

<p>Stability Light Sensitive<br>Applications Gallic Acid is a phenolic acid with antioxidant activity. Gallic acid was found to protect human cells against oxidative damage and showed cytotoxicity against cancer cells. Gallic Acid and its esters also show antiviral and antifungal activities.<br>References Yen, G. et al.: Food Chem., 79, 307 (2002); Chen, C. et al.: Mol. Nutrit. Food Res., 51, 962 (2007); Kratz, J. et al.: Mem. Inst. Oswaldo Cruz, 103, 437 (2008); Osborne, L. et al.: Infect. Immun., 33, 769 (1981);<br></p>

<p>Applications 2-Chlorophenylboronic Acid used in the preparation of imidazo[1,2-a]pyridine amides which has tuberculostatic activity.<br>References Kang, S., et al.: J. Med. Chem., 57, 5293 (2014);<br></p>

<p>Applications β-Cyclodextrin is a cyclic oligosaccharide produced from starch via enzymatic conversion. β-Cyclodextrin is commonly used to produce HPLC columns allowing chiral enantiomers separation.<br>References Motoyama, A. et al.: J. Pharmac. Biomed. Anal., 28, 97 (2002); Nakamura, N. et al. Biotechnol. Bioeng., 19, 87 (1977); Riddle, L. A. et al.: J. Chrom. Sci., 45, 330 (2007);<br></p>

<p>Stability Moisture Sensitive<br>Applications Ethyl Malonyl Chloride is used as a reagent in the synthesis of novel thiadiazoloacrylamide analogs as inhibitors of dengue-2 virus NS2B/NS3 protease. Ethyl Malonyl Chloride is also used as a reagent in the synthesis of quinolone-benzylpiperidine derivatives as acetylcholinesterase inhibitors and antioxidant hybrids for Alzheimer disease.<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 Liu, H., et al.: Bioorg. Med. Chem., 22, 6344 (2014); Pudlo, M., et al.: Bioorg. Med. Chem., 22, 2496 (2014)<br></p>

<p>Applications Alkaloid naturally occurring in the d-form. Shows GABA antagonist activity.<br>References Curtis, et al.: Nature, 226, 1222 (1970), Avoli, M., et al.: J. Physiol. Pharmacol., 75, 526 (1997), Chebib, M., et al.: Clin. Exp. Pharmacol. Physiol., 26, 927 (1999),<br></p>

<p>Applications 2-Amino-6-fluorobenzothiazole is a useful research chemical. An intermediate for the synthesis of benzothiazoles and aminobenzothiazoles with antimicrobial activity.<br>References Defrenza, I., et al.: J. Heterocycl. Chem., 52, 1705 (2015); Catalano, A., et al.: Eur. J. Med. Chem., 64, 357 (2013)<br></p>

<p>Stability Moisture Sensitive<br>Applications 1,1,1-Trifluoro-N-((trifluoromethyl)sulfonyl)methanesulfonamide (cas# 82113-65-3) is a useful research chemical.<br></p>

<p>Applications A mitotic kinesin inhibitor as novel anti-cancer agent. Used in the study of neurodegenerative diseases.<br>References Brown, K., et al.: J. Cell Biol., 125, 1303 (1994), Sharp, D., et al.: Nature, 407, 41 (2000), Sueishi, M., et al.: J. Biol. Chem., 275, 28888 (2000), Lee, Y., et al.: Biochem. J., 360, 549 (2001),<br></p>

<p>Applications A nonspecific inhibitor of phosphodiesterases.<br>References Beavo., J.A., et al.: Mol. Pharmacol., 6, 597 (1970), Scamps, F., et al.: Eur. J. Pharmacol., 224, 119 (1993)<br></p>

<p>Applications Zinc dibutyldithiocarbamate (CAS# 136-23-2) is a useful research chemical compound.<br></p>

<p>Applications A highly potent (IC50=4.3 nM) and uniquely specific tyrosine kinase inhibitor of a rationally engineered v-Src tyrosine kinase.<br>References Bishop, A.C., et al.: J. Am. Chem. Soc., 121, 627 (1999), Davies, S., et al.: Biochem. J., 351, 95 (2000), Regan, J., et al.: J. Med. Chem., 45, 2994 (2002), Bain, J., et al.: Biochem. J., 371, 199 (2003), Kuma, Y., et al.: J. Biol. Chem., 280, 19472 (2005),<br></p>

<p>Applications Ammonium Formate is an intermediate used to prepare AZD0530 as a highly selective, orally available, dual-specific c-Src/Abl kinase inhibitor. It is also used to synthesize inhibitors of human cyclophilin A.<br>References Hennequin, L., et al.: J. Med. Chem., 49, 6465 (2006); Li, J., et al.: Bioorg. Med. Chem., 14, 2209 (2006)<br></p>

<p>Applications Methyl (S)-(+)-3-hydroxybutyrate<br></p>

<p>Applications Tigogenin is a saponin structurally similar to Diosgenin (D484700) and acts as a natural plant steroid which induces apoptosis in rheumatoid arthritic fibroblast-like synoviocytes.<br>References Liagre B. et al.: Int. J. Mol. Med., 20, 451 (2007);<br></p>

<p>Stability Hygroscopic<br>Applications Clothiapine, is a atypical antipsychotic of the dibenzothiazepine chemical class. It has shown efficacy in treatment-resistant schizophrenic patients.<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 Schmutz, J., et al.: Helvetica Chimica Acta 50, 245 (1967); Geller, V., et al.: Schizophrenia Research 80 (2-3), 343 (2005);<br></p>

<p>Applications Cyclosporin is an immunosuppressant that has revolutionized organ transplantation through its use in the prevention of graft rejection.A group of nonpolar cyclic oligopeptides with immunosupppressant activity.<br>References van Wartburg, A., et al.: Prog. Med. Chem., 25, 1 (1988), Jorgensen, K.A., et al.: Scand. J. Imunol., 57, 93 (2003), Vollenbroeker, et al.: Transplant. Proc., 37, 1741 (2005),<br></p>

<p>Applications Hydrogen Tetrafluoroborate(1-) is a useful building block for organic synthesis.<br>References Ohkuma, T., et al.: Journal of the American Chemical Society., 218, 8724 (2006)<br></p>

<p>Applications 2-Hydroxybutanoic Acid is an analyte used in the diagnoses of colorectal cancer as well as Type II diabetes. It is also used in the purification of the major Vibrio autoinducer and the study of its role in virulence factor production for cholera.<br>References Qiu, Y. et al.: J. Proteome Res., 8, 4844 (2009); Salek, R.. et al.: Phys. Genom., 29, 99, (2007); Higgins, D. et al.: Nature, 450, 883 (2007);<br></p>

<p>Applications ABT 199 (&gt;99%) is a potent and selective BCL-2 inhibitor that achieves potent antitumour activity while sparing platelets. It’s practical application is to treat chronic lymphocytic leukaemic cells and estrogen receptor-positive breast cancer.<br>References Davids, M. &amp; Letai, A.: Cancer Cell, 23, 139 (2013); Souers, A.,et al.: Nat. Med., 19, 202 (2013); Vaillant, F., et al.: Cancer Cell, 24, 120 (2013); Vogler, M., et al.: Brit. J. Haematol., 163, 139 (2013);<br></p>

<p>Applications D-Citronellol is an monoterpene alcohol that is prevalent in essential oils of various aromatic plant species, such as Cymbopogon citratus.<br>References Brito, R.G., et al.: J. Nat. Med., 66, 637 (2012);<br></p>

<p>Applications RAD 140 is a potent, orally bio-available, and non-steroidal selective androgen receptor modulator (SARM).<br>References Miller, C.P., et al.: ACS Med. Chem. Lett., 2, 124-129 (2011)<br></p>

<p>Stability Moisture Sensitive<br>Applications Reagent used to produce many guanidine based pharmaceuticals<br></p>

<p>Applications Ethyl 3-Bromopyruvate is used in the preparation of 1,2,4-trisubstituted imidazoles as inhibitors of growth factor-β type I ALK5 inhibitors.<br>References Guo, C. et al.: Bioorg. Med. Chem. Lett., 23, 5850 (2013); Catarzi, D. et al.: Farmaco, 48, 447 (1993);<br></p>

<p>Applications (+)-Muscarine Chloride modulates calcium channel currents in rats.<br>References Stewart, A. E., et al.: J. Neurophysiol., 81, 72-84 (1999);<br></p>

<p>Stability Hygroscopic<br>Applications Gondadotropin-releasing hormone agonist, used to treat hormone-responsive cancers such as prostate and breast cancer. Synthetic nonapeptide agonist analog of LH-RH. Antineolpastic (hormonal).<br>References Lam, P., et al.: Gynecol. Endocrinol., 24, 674 (2008), Chi, K., et al.: J. Urol., 180, 565 (2008), Menchaca, A., et al.: Theriogenol., 72, 477 (2009), Harada, T., et al.: Fertility and Sterility, 91, 675 (2009),<br></p>

<p>Applications 1-Chloropentane is used for studies on the antimicrobial activity of some halogenated hydrocarbons and their derivatives, effect of chlorinated hydrocarbons on the myelin sheath of peripheral nerve tissues.<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 Kalatskaya, L. M., et al.: Fiziologicheski Aktivnye Veshchestva; 20, 77 (1988); Rumsby, M. G., et al.: J. Neurochem., 13, 1513 (1966)<br></p>

<p>Applications 1,5-Diazabicyclo[4.3.0]non-5-ene is used as a nucleophilic catalyst for the Freidel-Crafts C-acylation of pyrroles and indoles. 1,5-Diazabicyclo[4.3.0]non-5-ene is also an inhibitor of indoleamine-N-methyltransferase (II) of rabbit lung in vitro.<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 Mandel, L.: Biochem. Pharmacol., 25, 2251 (1976); Taylor, J., et al.: Org. Lett., 12, 5740 (2010)<br></p>

<p>Applications Atosiban is an oxytocin receptor blocking agent in the treatment of experimental endometriosis and was shown exhibit significant therapeutic efficiency.<br>References Simsek, Y., et al.: Arch. Gynecol. Obstet., 286, 777 (2012); Mak, P., et al.: J. Psychopharmacol., 26, 532 (2012); Simsek, Y., et al.: Arch. Gynecol. Obstet., 285, 655 (2012);<br></p>

<p>Applications (1S,2S,3R,5S)-(+)-2,3-Pinanediol is a bicyclic monoterpene diols that has been shown to induce differentiation of S91 melanoma and PC12 pheochromocytoma cells and thus provide possible therapeutic and sunless tanning use. It is also used in the transformation of isopinocampheol and caryophyllene oxide.<br>References Brown, D.A. et al.: Pigment Cell Res., 12, 36 (1999); Noma, Y. et al.: Flav. Frag. J., 25, 161 (2010);<br></p>

<p>Stability Air Sensitive<br>Applications Thioglycolic Acid is an organic compound containing both a thiol and a carboxylic acid. Thioglycolic Acid is a precursor to ammonium thioglycolate, a chemical used for permanents. Thioglycolic Acid is used in organic synthesis as a nucleophile in thioglycolysis reactions and is used as a S transfer agent for sulfonyl chloride synthesis.<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 Kim, T.R. et al.: Bull. Kor. Chem. Soc., 3, 162 (1982); Badr, M.Z.A. et al.: Bull. Chem. Soc. Jap., 56, 326 (1983); Langler, R.F. et al.: Can. J. Chem., 57, 3193 (1979);<br></p>

<p>Applications Azilsartan medoxomil is a long-acting angiotensin II receptor blocker (ARB) that is used to lower hypertension. When Azilsartan medoxomil enters the gastrointestinal tract, it is rapidly converted to its active form, Azilsartan (A926900).<br>References Baker, W. &amp; White, W.: Pharmacotherapy, 45, 1506 (2011); Cushman, W., et al.: Hypertension, 60, 310 (2012); Lastra, G., et al.: Cardio. Med. 3, 154 (2013); Miura, S., et al.: Hypertens. Res., 36, 134 (2012); Rakugi, H., et al.: Hypertens. Res., 35, 552 (2012)<br></p>

<p>Applications A novel pancreatic lipase inhibitor for the treatment of obesity in both diabetic and non-diabetic patients.<br>References Yamada, Y. et al.: Horm. Metab. Res., 40, 539 (2008); Kopelman, P. et al.: Int. J. Obes., 31, 494 (2007); Kopelman, P. et al.: Obesity, 18, 108 (2010);<br></p>

<p>Applications (1R)-(+)-α-Pinene is used in hydroboration reactions and the reduction of ketones.<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 Brown, H. et al.: J. Org. Chem., 50, 1384 (1985);<br></p>

<p>Applications Tacrolimus Hydrate is a disease-modifying antirheumatic drugs (DMARDs)<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 Ogasawara, M., et al.: Mod. Rheumatol., 22, 831-836 (2012)<br></p>

<p>Applications N-(2-Carboxy-2-hydroxycaproyl)hydrazobenzene is an impurity in the synthesis of pheylbutazone (P319570) derivatives.<br>References Fricoteaux, R., et al.: J. Pharm. Biomed. Anal., 7, 1585 (1989), Segrestaa, J., et al.: Chem. Pharm. Bull., 50, 744 (2002),<br></p>

<p>Stability Hygroscopic<br>Applications The R-enantiomer of Lansoprazole; a gastric proton pump inhibitor. An antiulcerative.<br>References Figgitt, D., et al.: Drugs, 60, 925 (2000), Katsuki, H., et al.: Eur. J. Clin. Pharmacol., 57, 709 (2001), Barradell, L.B., et al.: Drugs, 44, 225 (1992), Kim, K., et al.: Clin. Pharmacol. Ther., 72, 90 (2002), Niioka, T., et al.: Ther. Drug Monit., 28, 321 (2006),<br></p>

<p>Applications Iodine is used in ionic liquids in the preparation of dye-sensitized solar cells.<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 Wang, P. et al.: J. Phys. Chem. B, 107, 13280 (2003); Kubo, W. et al.: J. Phys. Chem. B. 105, 12809 (2001);<br></p>

<p>Applications Ethylenediamine-N,N'-diacetic Acid is a substance used in the preclinical evaluation of somatostatin analogs as new analogs in the detection of somatostatin receptor-positive tumors. Also acts as a reagent used in the synthesis of new class of aldehyde and aldose reductase inhibitors.<br>References Andleeb, H., et al.: RSC Advances, 6, 77688 (2016); Gandomkar, M., et al.: Nucl. Med. Biol., 34, 651 (2007)<br></p>

<p>Applications The R-enantiomer of Albuterol (A514500). A β2-adrenoceptor agonist. Bronchodilator; tocolytic.<br>References Han, et al.: Bioorg. Med. Chem., 14, 6043 (2006), Liyou, H., et al.: Biochem., 46, 1432 (2007), Agrawal, D., et al.: J. Allergy Clin. Immunol., 113, 503 (2004),<br></p>

<p>Stability Hygroscopic<br>Applications Sodium Sulfide Nonahydrate is used as a reagent in the synthesis of surface functionalized cadmium sulfide quantum dots.<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 Veinot, J.G.C., et al.: Chem. Mater., 9, 2117 (1997)<br></p>

<p>Applications Etidronic acid is used as a calcium regulator. Etidronic acid is a bisphosphonate antiresorptive agent.<br>References Francis, M.D., et al.: Science, 165, 1264 (1969), Jowsey, J., et al.: J. Lab. Clin. Med. , 76, 126 (1970), Altman, R.D.: N. Engl. J. Med., 79, 583 (1985)<br></p>

<p>Applications An anticonvulsant agent.<br>References Shimada, et al.: Anal. Biochem., 147, 174 (1975), Dzhagatspanyan. IA., et al.: Pharm. Chem. J., 25, 181 (1991),<br></p>

<p>Applications A selective 5-HT4 receptor agonist. Gastroprokinetic.<br>References Yoshida, N., et al.: Arch. Int. Pharmacodyn. Ther., 300, 51 (1989), Yatera, S., et al.: Japan. Pharmacol. Ther., 21, 21 (1993), Ruth, M., et al.: Aliment Pharmacol. Ther., 12, 35 (1998),<br></p>

<p>Applications 2-Methylisoborneol solution - (CAS# 2371-42-8) is a useful research chemical compound.<br></p>

<p>Applications A nucleotide analog, useful as an oral reverse transcriptase inhibitor (ntRTI).<br>References Fliri, A., et al.: J. Med. Chem., 52, 8038 (2009), Fourches, D., et al.: Chem. Res. Toxicol., 23, 171 (2010), Ming, X., et al.: Biochem. Pharmacol., 79, 455 (2010),<br></p>

<p>Applications Used in the synthesis of substituted terphenyls.<br>References Strukelj, M., et al.: Science, 267, 1969 (1995), Burroughes, J., et al.: Nature, 347, 589 (1990),<br></p>

<p>Applications LEE 011 can be used in biological study of kinome-wide RNA interference screen reveals a role for PDK1 in acquired resistance to CDK4/6 inhibition in ER-positive breast cancer.<br>References Jansen, V. M., et al.: Cancer Research, 77, 2488 (2017)<br></p>

<p>Impurity Ziprasidone EP Impurity A<br>Applications 3-(1-Piperazinyl)-1,2-benzisothiazole (Ziprasidone EP Impurity A) is a reagent used to synthesize Ziprasidone (Z485000, HCl salt, monohydrate), a combined serotonin (5HT2) and dopamine (D2) receptor antagonist.<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 Prakash, C., et al.: Brit. J. Clin. Pharmacol., 49, 35S (2000); Orjales, A., et al.: J. Med. Chem., 46, 5512 (2003); Graham, J., et al.: Bioorg. Med. Chem. Lett., 18, 489 (2008); Bench, C.J., et al.: Psychopharmacology, 112, 308 (1993), Goldstein, J.M.: Exp. Opin. Invest. Drugs, 4, 291 (1995)<br></p>

<p>Applications Flumazenil-D5 is a labelled analogue of Flumazenil (F500450), a benzodiazepine antagonist that can prevent or abolish (at the receptor level) the effects of a benzodiazepine.<br>References Brogden, R. &amp; Goa, K.: Drugs, 35, 448 (1988); Klotz, U. &amp; Kanto, J.: Clin. Pharmacokinet., 14, 1 (1988)<br></p>