Flavine Adenine Dinucleotide Disodium Salt

CAS: 84366-81-4

Ref. TR-F371500

Produktinformation

• Name: Flavine Adenine Dinucleotide Disodium Salt
• Synonyme: FAD sodium salt, 5'-Ester with adenosine riboflavin 5'-(trihydrogen diphosphate) sodium salt (1:2), Benzo[g]pteridine, riboflavin 5′-(trihydrogen diphosphate) deriv., Flavin adenine dinucleotide disodium salt, Flavin adenine dinucleotide sodium salt, Riboflavin 5'-(trihydrogen diphosphate), 5'.5'-ester with adenosine, disodium salt, Riboflavin 5′-(trihydrogen diphosphate), P′→5′-ester with adenosine, disodium salt, Riboflavin 5′-(trihydrogen diphosphate), P′→5′-ester with adenosine, sodium salt (1:2), disodium [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl [[(2R,3S,4S)-5-(7,8-dimethyl-2,4-dioxo-benzo[g]pteridin-10-yl)-2,3,4-trihydroxy-pentoxy]-oxido-phosphoryl] phosphate, disodium [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl [[5-(7,8-dimethyl-2,4-dioxo-benzo[g]pteridin-10-yl)-2,3,4-trihydroxy-pentoxy]-oxido-phosphoryl] phosphate
• CAS: 84366-81-4

Beschreibung

Stability Hygroscopic
Applications The prosthetic group of certain flavoproteins including D-amino acid oxidase, glucose oxidase, glycine oxidase, fumaric hydrogenase, histaminase, and xanthine oxidase. Riboflavin kinase tumor necrosis factor receptor 1 NADPH oxidase.
References DeLuca, K., et al.: J. Biol. Chem., 223, 569 (1956), Yagi, K., et al.: Biochemistry, 19, 1553 (1980), Li, G., et al.: J. Phys. Chem., 112, 4573 (2008),

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 829.51
• Formel: C₂₇H₃₁N₉Na₂O₁₅P₂
• Farbe/Form: Neat
• InChl: InChI=1S/C27H33N9O15P2.2Na/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36;;/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43);;/q;2*+1/p-2/t14-,15+,16+,19-,20+,21+,26+;;/m0../s1
• SMILES: Cc1cc2nc3c([O-])nc(=O)nc-3n(C[C@H](O)[C@H](O)[C@H](O)COP(=O)([O-])OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)c2cc1C.O.[Na+].[Na+]