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6-METHYLMERCAPTOPURINE RIBOSIDE

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6-METHYLMERCAPTOPURINE RIBOSIDE Basic information

Product Name:
6-METHYLMERCAPTOPURINE RIBOSIDE
Synonyms:
  • 6-METHYLMERCAPTOPURINE RIBONUCLEOSIDE
  • 6-METHYLMERCAPTOPURINE RIBOSIDE
  • 6-(METHYLTHIO)-9-BETA-D-RIBOFURANOSYLPURINE
  • 6-METHYLTHIOPURINE RIBOSIDE
  • 6-MMPR
  • 6-(methylthio)-9-beta-d-ribofuranosyl-9h-purin
  • METHYLTHIOINOSINE
  • 6-(methylthio)-inosin
CAS:
342-69-8
MF:
C11H14N4O4S
MW:
298.32
EINECS:
206-442-2
Product Categories:
  • Nucleotides and Nucleosides
  • Bases & Related Reagents
  • Nucleotides
Mol File:
342-69-8.mol
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6-METHYLMERCAPTOPURINE RIBOSIDE Chemical Properties

Melting point:
166°C
Density 
1.4113 (rough estimate)
refractive index 
1.6270 (estimate)
storage temp. 
-20°C
solubility 
DMSO (Slightly), Methanol (Slightly), Water (Slightly, Sonicated)
form 
Solid
color 
White to Off-White
Stability:
Incompatible with strong oxidizing agents.
EPA Substance Registry System
6-Methylmercaptopurine riboside (342-69-8)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
RTECS 
UO8985000
HS Code 
29349990

MSDS

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6-METHYLMERCAPTOPURINE RIBOSIDE Usage And Synthesis

Chemical Properties

white powder

Uses

6-Methylmercaptopurine Riboside (cas# 342-69-8) is a compound useful in organic synthesis.

Uses

6-Methylmercaptopurine riboside (6MMPr) is used in studies on thiopurine metabolism by enzymes such as inosine-5′-monophosphate dehydrogenase and thiopurine methyltransferase. 6MMPr may also be used to study mechanisms of bovine viral diarrhea virus (BVDV) inhibition.

Definition

ChEBI: A thiopurine that is inosine in which the aromatic hydroxy group is replaced by a methylsulfanediyl group.

General Description

White powder.

Air & Water Reactions

Slightly soluble in water.

Biochem/physiol Actions

6-Methylmercaptopurine riboside (6MMPR) is a modified thiopurine nucleoside involved in the inhibition of purine synthesis. It exhibits anti-viral effects against various viruses. 6MMPR is an analog of purine and an inhibitor of nerve growth factor-activated protein kinase N.

Safety Profile

Poison by intraperitoneal route. Experimental teratogenic effects. Questionable carcinogen with experimental tumorigenic data. Mutation data reported. When heated to decomposition it emits very toxic fumes of SO, and NOx.

6-METHYLMERCAPTOPURINE RIBOSIDESupplier

J & K SCIENTIFIC LTD.
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