ChemicalBook--->CAS DataBase List--->13153-27-0

13153-27-0

13153-27-0 Structure

13153-27-0 Structure
IdentificationBack Directory
[Name]

NBTGR
[CAS]

13153-27-0
[Synonyms]

NBTG
NBTGR
6-(4-nitrobenzylthio)guanosine
S-(4-NITROBENZYL)-6-THIOGUANOSINE
S-(P-NITROBENZYL)-6-THIOGUANOSINE
S-(4-Nitrobenzyl)-6-thioguanosine,99%
2-Amino-6-[(4-nitrobenzyl)thio]-9-β-D-ribofuranosylpurine
2-AMINO-6-[(4-NITROBENZYL)THIO]-9-BETA-D-RIBOFURANOSYLPURINE
S-(4-NITROBENZYL)-6-THIOGUANOSINE (NBTG) POTENT ADENOSINE TRAN
NBTG, NBTGR, 2-Amino-6-[(4-nitrobenzyl)thio]-9-β-D-ribofuranosylpurine
[Molecular Formula]

C17H18N6O6S
[MDL Number]

MFCD00005737
[MOL File]

13153-27-0.mol
[Molecular Weight]

434.43
Chemical PropertiesBack Directory
[Appearance]

yellow powder
[Melting point ]

203-205 °C
[Boiling point ]

858.3±75.0 °C(Predicted)
[density ]

1.3888 (rough estimate)
[refractive index ]

1.7000 (estimate)
[storage temp. ]

0-6°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[pka]

13.07±0.70(Predicted)
[color ]

Off-white to yellow
Hazard InformationBack Directory
[Chemical Properties]

yellow powder
[Uses]

NBTGR (p-Nitrobenzylthioguanosine) is a potent inhibitor of nucleoside transport; inhibits adenosine uptake with a Ki of 70 nM.
[References]

[1] Turnheim K, et al. Inhibition of adenosine uptake in human erythrocytes by adenosine-5'-carboxamides, xylosyladenine, dipyridamole, hexobendine, and p-nitrobenzylthioguanosine. Biochem Pharmacol. 1978;27(18):2191-7. DOI:10.1016/0006-2952(78)90076-x
[2] Parterson A, et al. Nucleoside Transport II Inhibition by p-Nitrobeazylthiogoanosine and Related Compounds. Can. J. Biochem. 49,271-274 (1971)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[Safety Statements ]

24/25
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