Indoles

<p>Applications 3-Methyl-d3-indole has been used to prove that bioactivation of the pulmonary toxin 3-methylindole requires methyl carbon-hydrogen bond breakage in mice. 3-Methyl-d3-indole is the labeled analogue of 3-Methylindole (M313470), A naturally abundant pneumotoxin, found primarily in mammalian feces providing its strong fecal odor.<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 Huijzer, J., et. al.: Toxicol. Appl. Pharm., 90, 60 (1987); Nakashima, T., et al.: Biol. Pharm. Bull., 32, 832 (2009); Xu, H., et al.: Chem. Pharm. Bull., 57, 321 (2009); Bodoor, K., et al.: J. Med. Chem., 52, 3753 (2009); Naskar, S., et al.: J. Chem. Res., 3, 174 (2009); Sollner, K., et al.: J. Agric. Food Chem., 57, 4319 (2009)<br></p>

<p>M04074 - 5-Bromo-6-chloro-3-indolyl beta-D-glucuronide cyclohexylammonium salt</p>

<p>M03452 - Fmoc-Tryptophanol</p>

<p>Applications Indole-3-acetonitrile is an indole derivative involved in the biosynthesis of the plant hormone indole acetic acid (I577340) via the indole-3-acetaldoxime pathway.<br>References Kong, W., et al.: Plant Cell Physiol, 56, 715-726 (2015)<br></p>

<p>Applications A phytohormone.<br>References Quittenden, L., et al.: Plant Physiol., 151, 1130 (2009), Jiraskova, D., et al.: J. Phycol., 45, 108 (2009),<br></p>

<p>Impurity Solifenacin EP impurity A<br>Applications Solifenacin (S676700) intermediate.<br>References Andersson, K., et al.: Drugs, 35, 477 (1988), Wallis, R., et al.: Life Sci., 64, 395 (1999), Mitsuya, M., et al.: J. Med. Chem., 43, 5017 (2000), Ohtake, A., et al.: Eur. J. Pharmacol., 492, 243 (2004),<br></p>