Results for Nucleotides ( 1306 )
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N4-Acetyl-2'-Deoxycytidine is a nucleoside analogue that acts as an inhibitor of DNA synthesis. N4-Acetyl-2'-Deoxycytidine blocks the conversion of ribonucleotides to deoxyribonucleotidesbinds by binding to the active site of the enzyme ribonucleotide reductase. This leads to cell death by preventing DNA synthesis and replication. N4-Acetyl-2'-Deoxycytidine has been shown to be more efficient than other analogues in terms of energy efficiency, control levels, and constant linear model. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
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5'-O-DMT-N4-Acetyl-2'-Deoxycytidine is a potent and selective inhibitor of the receptor tyrosine kinases Cck-A, which is overexpressed in certain tumour cells. 5'-O-DMT-N4-Acetyl-2'-Deoxycytidine blocks the activation of Cck-A by endothelin, thereby inhibiting the proliferation of tumour cells. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
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N2-Isobutyryl-2'-Deoxyguanosine is an inhibitor of bacterial translocation, prostaglandin synthesis, and adenosine triphosphate (ATP) synthesis of several bacterial species. N2-Isobutyryl-2'-Deoxyguanosine can bind to fatty acids, which are important for maintaining the integrity of the cell membrane and preventing bacterial translocation. The inhibition of prostaglandin synthesis may be due to its ability to form acid conjugates with fatty acids and dicarboxylic acids. N2-Isobutyryl-2'-Deoxyguanosine inhibits the synthesis of ATP in bacteria, which decreases bacterial growth rate. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
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5'-O-DMT-N2-Isobutyryl-2'-Deoxyguanosine is a synthetic nucleoside and can be used as a building block in the synthesis of oligonucleotides. 5'-O-DMT-N2-Isobutyryl-2'-Deoxyguanosine has a higher electronegativity value than guanine. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
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5'-O-DMT-Thymidine is a key deoxynucleoside building block that is protected with a dimethoxytrityl group in the 5-O-position of the deoxy-ribose moiety, leaving the 3-hydroxyl free for modification. 5'-O-DMT-Thymidine can be used a starting point for nucleotide synthesis. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.