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N6-Methyl-ATP is a methylated derivative of adenosine triphosphate (ATP) designed to function as a selective agonist for purinergic P2 receptors Due to structural modifications including methylation at the N6 position of the adenine moiety this compound displays specificity for interaction with distinct subtypes of P2 purinergic receptors In cellular and molecular research N6-Methyl-ATP is utilized as a pharmacological tool to investigate receptor-mediated signaling pathways particularly ion channel activation calcium influx and associated intracellular signaling cascades modulated through P2 receptors Furthermore it serves as a molecular probe in characterizing purinergic receptor-mediated neurotransmission physiological regulatory processes and receptor subtype distribution in both normal physiological states and pathological conditions contributing to the foundational understanding necessary for receptor-targeted drug discovery
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7-Methylguanosine 5'-diphosphate sodium (m7GDP sodium) is a nucleotide cap analog used in RNA and mRNA research. Supplied as a solid sodium salt with high purity, it serves as a reagent or standard in studies of mRNA capping, cap-binding proteins, and enzymatic assays involving guanine nucleotides.
Used as a cap analog in mRNA cap-analogue synthesis and biochemical assays.
Supplied as a solid sodium salt suitable for laboratory use.
High purity (97.1%) for consistent experimental performance.
Available in small research pack sizes for low-quantity applications.
Store sealed at -20°C; in solution, store at -80°C for longer-term stability.
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Vapendavir diphosphate (BTA798 diphosphate) is a potent enteroviral capsid binder (CB) Vapendavir diphosphate (BTA798 diphosphate) possesses potent antiviral activity for enterovirus 71 (EV71) replication with EC50 values of 0 5-1 4 M in different EV71 strains[1 [2
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Also available in 5 mg 10 mg 25 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Adenosine Dialdehyde (Periodate-oxidized adenosine) is a purine nucleoside analogue. Adenosine Dialdehyde is a potent inhibitor of S-Adenosylhomocysteine hydrolase (SAHH) (Ki=3.3 nM). Adenosine Dialdehyde exhibits potent anti-tumor activity in vivo. purity: 95%
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