Product Name :
3-Hydroxyindole (CAS 480-93-3)
Synonym :
Indol-3-ol; Indoxyl
Application :
CAS:
480-93-3
Purity:
Molecular Weight:
133.15
Formula :
C8H7NO
Physical state:
Solid
solubility :
Shipping Condition :
Store at -20° C
Melting point:
SMILES:
References:
:Formation of indigo by recombinant mammalian cytochrome P450. | Gillam, EM., et al. 1999. Biochem Biophys Res Commun.835616-60-9 site 265: 469-72.5467-74-3 SMILES PMID: 10558891Sulfation of indoxyl by human and rat aryl (phenol) sulfotransferases to form indoxyl sulfate.PMID:33397127 | Banoglu, E. and King, RS. 2002. Eur J Drug Metab Pharmacokinet. 27: 135-40. PMID: 12064372Inhibition of amyloid fibril formation and cytotoxicity by hydroxyindole derivatives. | Cohen, T., et al. 2006. Biochemistry. 45: 4727-35. PMID: 16605241[Microbial biosynthesis and biotransformation of indigo and indigo-like pigments]. | Han, X., et al. 2008. Sheng Wu Gong Cheng Xue Bao. 24: 921-6. PMID: 18807970Consumption of pasteurized human lysozyme transgenic goats′ milk alters serum metabolite profile in young pigs. | Brundige, DR., et al. 2010. Transgenic Res. 19: 563-74. PMID: 19847666Antioxidant activity of an unusual 3-hydroxyindole derivative isolated from fruits of Aristotelia chilensis (Molina) Stuntz. | Céspedes, CL., et al. 2009. Z Naturforsch C J Biosci. 64: 759-62. PMID: 19957448A labeled substrate approach to discovery of biocatalytic reactions: a proof of concept transformation with N-methylindole. | Rogers, JL. and MacMillan, JB. 2012. J Am Chem Soc. 134: 12378-81. PMID: 22809085New pathway for the biodegradation of indole in Aspergillus niger. | Kamath, AV. and Vaidyanathan, CS. 1990. Appl Environ Microbiol. 56: 275-80. PMID: 2310183