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Merck
CN

475254

2-Amino-6-bromopurine

95%

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About This Item

Empirical Formula (Hill Notation):
C5H4BrN5
CAS Number:
Molecular Weight:
214.02
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
95%
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InChI

1S/C5H4BrN5/c6-3-2-4(9-1-8-2)11-5(7)10-3/h1H,(H3,7,8,9,10,11)

SMILES string

Nc1nc(Br)c2nc[nH]c2n1

InChI key

HPGBGNVPUMCKPM-UHFFFAOYSA-N

assay

95%

mp

>350 °C (lit.)

functional group

bromo

Quality Level

General description

2-Amino-6-bromopurine is a 2-amino-6-halogenopurine. It can be synthesized by reaction between 2-amino-6-chloropurine and KX (X=Br). It has been reported to be a substrate for the adenine deaminase. Orientations of 2-amino-6-bromopurine (ABPu) in the docking conformations of guanine riboswitch complexed with ABPu have been analyzed.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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D A Jankowska et al.
Journal of applied microbiology, 115(5), 1134-1146 (2013-08-02)
Construction of a transgenic Arxula adeninivorans strain that produces a high concentration of adenine deaminase and investigation into the application of the enzyme in the production of food with low purine content. The A. adeninivorans AADA gene, encoding adenine deaminase
Synthesis of Some Biologically Active Halogenopurines.
Hu YL, et al.
J. Korean Chem. Soc., 54(4), 429-436 (2010)
Theoretical studies on the interaction of guanine riboswitch with guanine and its closest analogues.
Ling B, et al.
Molecular Simulations, 36(12), 929-938 (2010)

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