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ChemicalBook--->CAS DataBase List--->14675-48-0

14675-48-0

14675-48-0 Structure

14675-48-0 Structure
IdentificationBack Directory
[Name]

6-METHYLPURINE RIBOSIDE
[CAS]

14675-48-0
[Synonyms]

6-D-MPR
Nsc101619
6-METHYLPURINE RIBOSIDE
6-Methylpurine-β-D-riboside
6-Methylpurine ribonucleoside
6-Methylpurine-beta-D-riboside
6-Methylpurine-9-beta-D-ribofuranoside
6-Methyl-9.beta.-D-ribofuranosylpurine
6-Methyl-9-(1-β-D-ribofuranosyl)purine
9H-Purine, 6-methyl-9-b-D-ribofuranosyl-
9H-Purine, 6-methyl-9-β-D-ribofuranosyl-
6-Methyl-9-(beta-D-ribofuranosyl)-9H-purine
9H-Purine, 6-methyl-9-.beta.-D-ribofuranosyl-
(2R,3S,4R,5R)-2-(HydroxyMethyl)-5-(6-Methyl-9H-purin-9-yl)tetrahydrofuran-3,4-diol
(2r,3s,4r,5r)-2-(hydroxymethyl)-5-(6-methyl-1H-purin-9-yl)tetrahydrofuran-3,4-diol
[Molecular Formula]

C11H14N4O4
[MDL Number]

MFCD00056009
[MOL File]

14675-48-0.mol
[Molecular Weight]

266.25
Chemical PropertiesBack Directory
[Melting point ]

209-210 °C
[Boiling point ]

590.4±60.0 °C(Predicted)
[density ]

1.81±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Store in freezer, under -20°C
[form ]

Solid
[pka]

13.13±0.70(Predicted)
[color ]

White to off-white
[InChI]

InChI=1/C11H14N4O4/c1-5-7-10(13-3-12-5)15(4-14-7)11-9(18)8(17)6(2-16)19-11/h3-4,6,8-9,11,16-18H,2H2,1H3/t6-,8-,9-,11-/s3
[InChIKey]

FIGBCBGMUIGJBD-SOMIAQKHNA-N
[SMILES]

N1(C=NC2C(C)=NC=NC1=2)[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 |&1:10,11,13,15,r|
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H312-H332
[Precautionary statements ]

P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P403+P233-P501
[Hazard Codes ]

T
[Risk Statements ]

23/24/25
[Safety Statements ]

36/37/39-45
Hazard InformationBack Directory
[Description]

6-Methylpurine-β-D-riboside (β-D-MPR; 6-methylpurine riboside), an antibiotic isolated from culture broths of the basidiomycetes fungi Collybia dryophilia and Collybia maculata, has antifungal, antiviral and antitumor activity. β-D-MPR is an excellent substrate of mammalian adenosine deaminase (ADA), and its mechanism of activation in tumor cells presumably relates to its interaction with this enzyme [1].
[References]

[1] Sufrin, J . "Improved Synthesis of β-D-6-Methylpurine Riboside and Antitumor Effects of the β-D- and α-D-Anomers." Molecules 10(2005).
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