Gimeracil enhances the antitumor activity of fluoropyrimidines by competitively and reversibly inhibiting the enzyme dihydropyrimidine dehydrogenase causing decreased degradation of the fluoropyrimidines
While the antiviral drug 3TC is not highly active on K65R and M184V mutant strains
Formula: C20H17NO6
and ameliorates impaired subcellular structure in rats treated with Aβ oligomers
5-tetrahydro-2-benzofuran-1-one
(3S, 4S, 5R)-1, 3, 4, 5, 6-Pentahydroxyhexan-2-one Catalog No.:M20939-C Gimeracil enhances the antitumor activity(3S,4S,5R) 1,3,4,5,6 Pentahydroxyhexan 2 one is an endogenous metabolite. Product information CAS Number: 87 81 0 Molecular Weight: 180. 16 Formula: C6H12O6 Chemical Name: (3S,4S,5R) 1,3,4,5,6 pentahydroxyhexan 2 one Smiles: O[C@H](CO)[C@H](O)[C@H](O)C(=O)CO InChiKey: BJHIKXHVCXFQLS PQLUHFTBSA N InChi: InChI=1S C6H12O6 c7 1 3(9)5(11)6(12)4(10)2 8 h3,5 9,11 12H,1 2H2 t3 ,5+,6 m1 s1 Technical Data Appearance: Solid Power Purity: 98% (or refer to the