Chemistry Heterocyclic Building Blocks Purines 9-((3As,4R,6Ar)-Tetrahydrofuro[3,4-D][1,3]Dioxol-4-Yl)-9H-Purine

9-((3As,4R,6Ar)-Tetrahydrofuro[3,4-D][1,3]Dioxol-4-Yl)-9H-Purine

Phosphorylation: 4'-O-Methyl Adenosine can be phosphorylated by kinases to form nucleoside monophosphates. For example, adenosine kinases can phosphorylate it to form 4'-O-Methyl Adenosine-5'-monophosphate (4'-O-Me-AMP). Nucleotide Formation: The nucleoside can be further phosphorylated to form nucleoside diphosphates (NDPs) or nucleoside triphosphates (NTPs) by sequential phosphorylation reactions involving kinases. Base Modification: The purine base in 4'-O-Methyl Adenosine can undergo various chemical modifications, such as N-alkylation or N-oxidation, depending on reaction conditions and reagents used. Hydrolysis: Nucleosides can undergo hydrolysis reactions, especially under acidic or enzymatic conditions, leading to the release of the purine base and ribose or its derivatives. Glycosidic Bond Cleavage: The glycosidic bond between the purine base and the ribose can be cleaved under specific conditions, yielding the isolated purine or its derivatives. Enzymatic Reactions: Various enzymes in biological systems can interact with 4'-O-Methyl Adenosine, potentially leading to further modifications or degradation. Chemical Modifications: Organic chemistry techniques can be employed to modify the compound further, including the introduction of functional groups or chemical reactions at specific positions on the molecule.

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(R)-N-(9-(Tetrahydrofuran-2-Yl)-9H-Purin-6-Yl)Benzamide 2-(Acetoxymethyl)-5-(9H-Purin-9-Yl)Tetrahydrofuran-3,4-Diyl Diacetate 2-(Hydroxymethyl)-5-(9H-Purin-9-Yl)Tetrahydrofuran-3,4-Diol 2-Chloro-7H-Purine 2-Chloro-9H-Purine 7H-Purin-2-Amine 7H-Purin-6-Amine 9-((3As,4R,6Ar)-Tetrahydrofuro[3,4-D][1,3]Dioxol-4-Yl)-9H-Purine 9-(Tetrahydrofuran-2-Yl)-9H-Purin-6-Amine 9-(Tetrahydrofuran-2-Yl)-9H-Purin-6-Ol 9-(Tetrahydrofuran-2-Yl)-9H-Purine 9H-Purin-6-Amine

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    (3aS,4S,6R,6aR)-6-(6-Amino-2-chloro-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carboxylic acid

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    A14820372209-19-997%

    (3aS,4S,6R,6aR)-6-(6-Amino-2-chloro-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carboxylic acid

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    6-Chloro-9-[2,3-O-(1-methylethylidene)-beta-D-ribofuranosyl]-9H-Purine

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    6-Chloro-9-[2,3-O-(1-methylethylidene)-beta-D-ribofuranosyl]-9H-Purine

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    2',3'-O-Isopropylideneadenosine

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    2',3'-O-Isopropylideneadenosine

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    2′,3′-Isopropylideneinosine

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    A1801952140-11-697%

    2′,3′-Isopropylideneinosine

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    9-((3aR,4R,6R,6aR)-6-(Aminomethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amine

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    A11219721950-36-798%

    9-((3aR,4R,6R,6aR)-6-(Aminomethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amine

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    ((3AR,4R,6R,6aR)-6-(6-amino-2-chloro-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol

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    A25273624639-06-397%

    ((3AR,4R,6R,6aR)-6-(6-amino-2-chloro-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol

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    5’-Acetyl-2’,3’-isopropylidene Adenosine

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    5’-Acetyl-2’,3’-isopropylidene Adenosine

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