CAS 56964-73-9
:S-(2-hydroxy-5-nitrobenzyl)-6-*thioinosine
Description:
S-(2-hydroxy-5-nitrobenzyl)-6-thioinosine, identified by its CAS number 56964-73-9, is a chemical compound that belongs to the class of thioinosine derivatives. This substance features a thio group, which contributes to its unique reactivity and potential biological activity. The presence of a 2-hydroxy-5-nitrobenzyl moiety suggests that it may exhibit specific interactions with biological targets, potentially influencing enzymatic or receptor activities. The nitro group can also impart distinct electronic properties, which may affect the compound's solubility and stability. Typically, thioinosine derivatives are studied for their roles in nucleoside metabolism and potential therapeutic applications, particularly in the context of antiviral or anticancer research. The compound's structural characteristics may allow it to participate in various biochemical pathways, making it of interest in medicinal chemistry. However, detailed studies on its pharmacokinetics, toxicity, and specific biological effects would be necessary to fully understand its potential applications and safety profile.
Formula:C17H17N5O7S
InChI:InChI=1/C17H17N5O7S/c23-4-11-13(25)14(26)17(29-11)21-7-20-12-15(21)18-6-19-16(12)30-5-8-3-9(22(27)28)1-2-10(8)24/h1-3,6-7,11,13-14,17,23-26H,4-5H2/t11-,13-,14-,17-/m1/s1
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
S-(2-Hydroxy-5-nitrobenzoyl)-6-thioinosine
CAS:<p>S-(2-Hydroxy-5-nitrobenzoyl)-6-thioinosine is a population of endogenous inotropic agents that are transported by the uptake system. It interacts with benzodiazepine receptor and has been shown to act as an agonist. The uptake system is responsible for the uptake of S-(2-hydroxy-5-nitrobenzoyl)-6-thioinosine, which then binds to the benzodiazepine receptor. This binding causes an increase in cAMP levels and subsequent relaxation of smooth muscle cells. S-(2-hydroxynitrobenzoyl)-6-thioinosine has been shown to be a transport inhibitor, which affects the uptake of other drugs such as benzodiazepines and antiepileptics. It also modulates responsiveness through interaction with the transport system.</p>Formula:C17H17N5O7SPurity:Min. 95%Molecular weight:435.41 g/mol

