6-METHYLMERCAPTOPURINE RIBOSIDE

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
6-METHYLMERCAPTOPURINE RIBOSIDE Structure
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 System6-Methylmercaptopurine riboside (342-69-8)
Safety Information
Safety Statements 22-24/25
WGK Germany 3
RTECS UO8985000
HS Code 29349990
MSDS Information
ProviderLanguage
SigmaAldrich English
6-METHYLMERCAPTOPURINE RIBOSIDE Usage And Synthesis
Chemical Propertieswhite powder
Uses6-Methylmercaptopurine Riboside (cas# 342-69-8) is a compound useful in organic synthesis.
Uses6-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.
DefinitionChEBI: A thiopurine that is inosine in which the aromatic hydroxy group is replaced by a methylsulfanediyl group.
General DescriptionWhite powder.
Air & Water ReactionsSlightly soluble in water.
Biochem/physiol Actions6-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 ProfilePoison 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 RIBOSIDE Preparation Products And Raw materials
2-AMINO-9-(2,3,5-TRI-O-ACETYL-BETA-D-RIBOFURANOSYL)-6-THIOPURINE 1,9-DIHYDRO-6H-PURINE-6-THIONE 6-N-HEPTYLMERCAPTOPURINE 2-Amino-6-mercaptopurine-13C2,15N 6,8-DIHYDROXY-2-METHYLMERCAPTOPURINE 6-(Methylthio)purine S-(2-HYDROXY-5-NITROBENZYL)-6-THIOGUANOSINE 6-METHYLMERCAPTOPURINE RIBOSIDE S-(2-HYDROXY-5-NITROBENZYL)-6-THIOINOSINE 2-AMINO-6-CHLORO-[(4-METHYLPHENYL)THIO]-9-(2',3',5'-TRI-O-ACETYL-BETA-D-RIBOFURANOSYL)PURINE 6-(2-PYRIDYLMETHYLTHIO)-9-BETA-D-RIBOFURANOSYL-9H-PURINE 6-[(4-NITROBENZYL)THIO]-9-BETA-D-RIBOFURANOSYLPURINE-5'-MONOPHOSPHATE, DISODIUM SALT NBTGR 6-(ETHYLTHIO)-9-BETA-D-RIBOFURANOSYLPURINE NITROBENZYLTHIOINOSINE, [BENZYL-3H]- S-(4-NITROBENZYL)-6-THIOINOSINE 6-THIO-G CEP S-(P-NITROBENZYL)-6-THIOINOSINE, [3H]-

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