Valproic Acid b-D-Glucuronide

Product Description
CAT No.
ALN-V009024
CAS No.
60113-83-9
Mol. F.
C14H24O8
Mol. Wt.
320.3
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Technical Data
Reference
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Product Overview
Chemical Name : (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-((2-propylpentanoyl)oxy)tetrahydro-2H-pyran-2-carboxylic acid
Smiles : O=C(C(CCC)CCC)O[C@@H]([C@@H]([C@H]1O)O)O[C@@H]([C@H]1O)C(O)=O
Inchi : InChI=1S/C13H17N3O4/c1-10(17)14-12(9-20-2)13(18)16(15-19)8-11-6-4-3-5-7-11/h3-7,12H,8-9H2,1-2H3,(H,14,17)/t12-/m1/s1
Technical Data
Reference
Behavioral alterations in autism model induced by valproic acid and translational analysis of circulating microRNA
Mauro Mozael Hirsch, Iohanna Deckmann, Mellanie Fontes-Dutra, Guilherme Bauer-Negrini, Gustavo Della-Flora Nunes, Walquiria Nunes, Bruna Rabelo, Rudimar Riesgo, Rogerio Margis, Victorio Bambini-Junior, Carmem GottfriednFood and Chemical Toxicology Volume 115, May 2018, Pages 336-343
Bioactivation of a Toxic Metabolite of Valproic Acid, (E)-2-Propyl-2,4-pentadienoic Acid, via Glucuronidation. LC/MS/MS Characterization of the GSHu2212Glucuronide Diconjugates
Wei Tang and Frank S. Abbott – Chem. Res. Toxicol. 1996, 9, 2, 517–526
Chromatographic approaches for the characterization and quality control of therapeutic oligonucleotide impurities
N. M. El Zahar\xa0 N. Magdy\xa0 A. M. El?Kosasy\xa0 Michael G. Bartlett – Biomedical Chromatography Volume32, Issue1 Special Issue: 2018 Special Review Issue January 2018 e4088
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