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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Ancitabine

OC[C@H]1O[C@@H]2[C@H]([C@@H]1O)Oc1n2ccc(=N)n1 Request for Quotation
Chemical Name: Ancitabine
CAS Number: 31698-14-3
Product Number: AG01EFQR(AGN-PC-0WAIHU)
Synonyms:
MDL No:
Molecular Formula: C9H11N3O4
Molecular Weight: 225.20134

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Chemical Structure


Ancitabine, also known as 2',5'-dideoxy-5-fluorocytidine, is a nucleoside analog that has shown significant potential in chemical synthesis applications. This compound plays a crucial role in the field of medicinal chemistry, particularly in the development of new antiviral and anticancer agents. Ancitabine's unique structure and properties make it a valuable building block for the synthesis of novel nucleoside analogs with improved pharmacological profiles.In chemical synthesis, Ancitabine can be used as a key starting material for the preparation of various modified nucleosides. Through selective chemical modifications of its functional groups, researchers can create a diverse library of analogs with enhanced therapeutic activities and improved metabolic stability. By incorporating Ancitabine into synthetic pathways, scientists can access a wide range of nucleoside derivatives that may exhibit potent antiviral or antitumor properties.Furthermore, Ancitabine's fluorine substitution at the 5-position confers unique pharmacological properties that can be further optimized through structural modifications. This fluorinated nucleoside analog has demonstrated promising activity against a variety of viral infections and cancer types, making it a valuable asset in drug discovery and development efforts. By leveraging Ancitabine's chemical versatility and biological activity, researchers can design innovative nucleoside-based compounds with enhanced efficacy and reduced toxicity for potential therapeutic applications.