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S-(4-NITROBENZYL)-6-THIOINOSINE

S-(4-NITROBENZYL)-6-THIOINOSINE Structure
  • ₹7231.1 - ₹43754.65
  • Product name: S-(4-NITROBENZYL)-6-THIOINOSINE
  • CAS: 38048-32-7
  • MF: C17H17N5O6S
  • MW: 419.41
  • EINECS:253-753-4
  • MDL Number:MFCD00005745
  • Synonyms:S-(P-NITROBENZYL)-6-THIOINOSINE;S-(4-NITROBENZYL)-6-THIOINOSINE;NBTI;4-nitrobenzylthioinosine ;6-(((4-nitrophenyl)methyl)thio)-9-beta-d-ribofuranosyl-9h-purin ;6-(((4-nitrophenyl)methyl)thio)-9-beta-d-ribofuranosyl-9h-purine ;6-(p-nitrobenzylthio)inosine ;6-[(4-NITROBENZYL)THIO]-9-BETA-D-RIBOFURANOSYLPURINE
3 prices
Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 25MG
  • 100MG
  • 250MG
  • ManufacturerSigma-Aldrich(India)
  • Product numberN2255
  • Product descriptionS-(4-Nitrobenzyl)-6-thioinosine ≥98%, solid
  • Packaging25MG
  • Price₹7231.1
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product numberN2255
  • Product descriptionS-(4-Nitrobenzyl)-6-thioinosine ≥98%, solid
  • Packaging100MG
  • Price₹19874.7
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product numberN2255
  • Product descriptionS-(4-Nitrobenzyl)-6-thioinosine ≥98%, solid
  • Packaging250MG
  • Price₹43754.65
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) N2255 S-(4-Nitrobenzyl)-6-thioinosine ≥98%, solid 25MG ₹7231.1 2022-06-14 Buy
Sigma-Aldrich(India) N2255 S-(4-Nitrobenzyl)-6-thioinosine ≥98%, solid 100MG ₹19874.7 2022-06-14 Buy
Sigma-Aldrich(India) N2255 S-(4-Nitrobenzyl)-6-thioinosine ≥98%, solid 250MG ₹43754.65 2022-06-14 Buy

Properties

Melting point :187-190 °C(lit.)
Boiling point :770.2±70.0 °C(Predicted)
Density :1.3904 (rough estimate)
refractive index :1.6460 (estimate)
storage temp. :2-8°C
solubility :0.1 M HCl: slightly soluble
form :solid
pka :13.08±0.70(Predicted)
color :white
CAS DataBase Reference :38048-32-7(CAS DataBase Reference)

Safety Information

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Description

S-(4-Nitrobenzyl)-6-thioinosine is a nucleoside analog that competitively inhibits the equilibrative nucleoside transporter 1 (Kd = 0.1-1.0 nM; IC50s = 4.6 and 3.6 nM in rat and human, respectively). It blocks adenosine flux across the plasma membrane, thereby potentiating the interaction of extracellular adenosine with purinoreceptors, which can affect cardiac signaling associated with adenosine.

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