L-Aspartic acid, 4-(phenylmethyl) ester, 5′-ester with 5-hydroxy-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamide, 2,2,2-trifluoroacetate (1:1)

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L-Aspartic acid, 4-(phenylmethyl) ester, 5′-ester with 5-hydroxy-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamide, 2,2,2-trifluoroacetate (1:1) Basic information
Product Name:L-Aspartic acid, 4-(phenylmethyl) ester, 5′-ester with 5-hydroxy-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamide, 2,2,2-trifluoroacetate (1:1)
Synonyms:L-Aspartic acid, 4-(phenylmethyl) ester, 5′-ester with 5-hydroxy-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamide, 2,2,2-trifluoroacetate (1:1);Mizoribine prodrug-2 trifluoroacetate
CAS:2237237-32-8
MF:C20H24N4O9.C2HF3O2
MW:578.45
EINECS:
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Mol File:2237237-32-8.mol
L-Aspartic acid, 4-(phenylmethyl) ester, 5′-ester with 5-hydroxy-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamide, 2,2,2-trifluoroacetate (1:1) Structure
L-Aspartic acid, 4-(phenylmethyl) ester, 5′-ester with 5-hydroxy-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamide, 2,2,2-trifluoroacetate (1:1) Chemical Properties
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MSDS Information
L-Aspartic acid, 4-(phenylmethyl) ester, 5′-ester with 5-hydroxy-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamide, 2,2,2-trifluoroacetate (1:1) Usage And Synthesis
UsesMizoribine prodrug-2 trifluoroacetate (compound 20) is a oral active mizoribine (HY-17470) prodrug (amino acid conjugate). Mizoribine prodrug-2 displays a prolonged inhibition of IL-2 production[1].
References[1] Gao LJ, et al. Synthesis of mizoribine prodrugs and their in vivo evaluation as immunosuppressive agents. Bioorg Med Chem Lett. 2023;95:129490. DOI:10.1016/j.bmcl.2023.129490
L-Aspartic acid, 4-(phenylmethyl) ester, 5′-ester with 5-hydroxy-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamide, 2,2,2-trifluoroacetate (1:1) Preparation Products And Raw materials
Tag:L-Aspartic acid, 4-(phenylmethyl) ester, 5′-ester with 5-hydroxy-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamide, 2,2,2-trifluoroacetate (1:1)(2237237-32-8) Related Product Information
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