Indoles

<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>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>

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

<p>M04070 - 5-Bromo-6-chloro-3-indolyl-Å-D-galactopyranoside</p>

<p>Applications Indoleacetic Acid is the most common and naturally occuring plant hormone in the auxin class of hormones. It effects cell elongation, cell division as well as plant growth and development.<br></p>

<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>M03452 - Fmoc-Tryptophanol</p>