(3S, 4S, 5R)-1, 3, 4, 5, 6-Pentahydroxyhexan-2-one Catalog No.:M20939-C 25)13-31-21/h2-3

25)13-31-21/h2-3

It blocks transformation of 24-methylendihydrolanosterol to desmethylsterol in fungi together with inhibition of HMG-CoA

2H2O/c1-11-8-17-6-3-7-19(11)22(20

InChi: InChI=1S/C24H26N2O5/c1-29-23-13-16(27)9-10-21(23)30-12-11-25-14-17(28)15-31-22-8-4-7-20-24(22)18-5-2-3-6-19(18)26-20/h2-10

Gimeracil enhances the antitumor activity of fluoropyrimidines by competitively and reversibly inhibiting the enzyme dihydropyrimidine dehydrogenase causing decreased degradation of the fluoropyrimidines

(3S, 4S, 5R)-1, 3, 4, 5, 6-Pentahydroxyhexan-2-one Catalog No.:M20939-C 25)13-31-21/h2-3(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