[(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl dihydrogen diphosphate (non-preferred name)

Base Information

• Chemical Name: [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl dihydrogen diphosphate (non-preferred name)
• CAS No.: 21401-20-7
• Molecular Formula: C₁₄H₂₂N₂O₁₆P₂
• Molecular Weight: 536.28

Synonyms:

Chemical Property of [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl dihydrogen diphosphate (non-preferred name)

Chemical Property:

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Technology Process of [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl dihydrogen diphosphate (non-preferred name)

There total 24 articles about [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl dihydrogen diphosphate (non-preferred name) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

UDP-glucuronic acid (2616-64-0) → UDP-xylose (3616-06-6,21401-20-7,30329-30-7,38-57-3,97905-92-5,7164-64-9) + 5'-Uridylic Acid (58-97-9,27416-86-0)

Guidance literature:

With UDP-api/UDP-xylose synthase from Arabidopsis thaliana; nicotinamide adenine dinucleotide; In aq. phosphate buffer; at 25 ℃; for 8h; pH=8; Enzymatic reaction;

DOI:10.1016/j.carres.2019.03.011

Reference yield:

UDP-glucuronic acid (2616-64-0) → UDP-xylose (3616-06-6,21401-20-7,30329-30-7,38-57-3,97905-92-5,7164-64-9) + 5'-Uridylic Acid (58-97-9,27416-86-0) + diphosphoric acid 1-((3R)-α-D-apiofuranosyl) ester 2-uridin-5'-yl ester (20230-91-5,36020-60-7)

Guidance literature:

With UDP-api/UDP-xylose synthase from Arabidopsis thaliana; In aq. phosphate buffer; at 25 ℃; for 8h; pH=8; Enzymatic reaction;

DOI:10.1016/j.carres.2019.03.011

Reference yield:

C35H40N2O16P2 → UDP-arabinose (21401-20-7,30329-30-7,38-57-3,97905-92-5,7164-64-9)

Guidance literature:

With hydrogen; palladium dihydroxide; In methanol; Yield given; Ambient temperature;

DOI:10.1021/jo00106a007

upstream raw materials:

UDP-glucuronic acid

α-D-xylose 1-phosphate, free acid

uridine 5’-monophosphate-imidazole

5'-Uridylic Acid

Downstream raw materials:

astragaloside III

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