Pharmaceutical Standards

Applications 7-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-hydroxy-2-naphthalenesulfonic Acid is an intermediate used in the synthesis of 7-[[4-[Bis(3-Amino-3-oxopropyl)amino]-6-chloro-1,3,5-triazin-2-yl]amino]-4-hydroxy-3-[(4-methoxyphenyl)azo]-2-naphthalenesulfonic Acid (B426265), which acts as a non-peptide hormone receptor antagonist affecting physiological homeostasis and reproduction. Hormone antagonist.
References Arey, B. et al.: Endocrinol., 143, 3822 (2002); Wrobel, J. et al.: Synth. Comm., 32, 2695 (2002)

Applications 4-BROMO-1,8-NAPHTHYRIDINE (cas# 54569-28-7) is a useful research chemical.

Applications Cholera Autoinducer 1: (3S)-3-Hydroxy-4-tridecanone is an extracellular quorum-sensing molecule which is responsible for the virulence production factor and biofilm development of Vibrio cholerae.
References Kelly, R. et al.: Nat. Chem. Biol., 12, 891 (2009);

Applications 4-(chloromethyl)-2-(4-nitrophenyl)-1,3-oxazole (cas# 39867-96-4) is a useful research chemical.

Applications 3,3'-Bis(methylthio)-2,2'-bithiophene is a useful reagent for organic synthesis and other chemical processes.
References Smie, A., et al.: J. Electroanal. Chem., 452, 87 (1998), Di C. N., et al.: Chem. Phys. Lett., 275, 533 (1997),

Applications H-D-Phe-Homopro-Arg-pNA.2 Acetate is a useful organic reagent.

Applications 3-Methoxy Acetaminophen-d3 is deuterium labeled 3-Methoxy Acetaminophen (M226050). 3-Methoxy Acetaminophen is a metabolite of Acetaminophen (A161220), an analgesic and antipyretic agent used as a pain reliever to treat headache, muscle aches, and arthritis (1,2,3).
References (1) McGill, M. R. and Jaeschke, H. Pharm Res. 30, 2174 (2013)(2) Fairbrother, J.E., et al.: Anal. Profiles Drug Subs., 3, 1 (1974) (3) Hinson, J.A., et al.: Rev. Biochem. Toxicol., 2, 103 (1980)

Applications N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine is an intermediate used to prepare 4-[2-(Di-n-propylamino)ethyl]-2(3H)-indolone and related compounds as a prejunctional dopamine receptor agonist.
References Gallagher, G., et al.: J. Med. Chem., 28, 1533 (1985); DeMarinis, R., et al.: J. Med. Chem., 29, 939 (1986)