(2R,3R,4S,5R)-2-(4-Amino-5-bromo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol

97%

Reagent Code: #36478
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CAS Number 21193-80-6

science Other reagents with same CAS 21193-80-6

blur_circular Chemical Specifications

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Weight 345.1493 g/mol
Formula C₁₁H₁₃BrN₄O₄
badge Registry Numbers
MDL Number MFCD22124434
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. The presence of the pyrrolo[2,3-d]pyrimidine moiety makes it particularly valuable for designing molecules that can interact with enzymes or nucleic acids, potentially inhibiting viral replication or cancer cell proliferation. Additionally, its structural features allow for further modifications, enabling researchers to optimize drug candidates for improved efficacy, selectivity, and pharmacokinetic properties. This compound is also explored in biochemical studies to understand nucleotide metabolism and enzyme mechanisms.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,062.00

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(2R,3R,4S,5R)-2-(4-Amino-5-bromo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. The presence of the pyrrolo[2,3-d]pyrimidine moiety makes it particularly valuable for designing molecules that can interact with enzymes or nucleic acids, potentially inhibiting viral replication or cancer cell proliferation. Additionally, its structural features allow for further modifications, enabling researchers to optimize drug candidates for improved efficacy, selectivity, and pharmacokinetic properties. This compound is also explored in biochemical studies to understand nucleotide metabolism and enzyme mechanisms.
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