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Merck
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Documentos clave

F1503

Sigma-Aldrich

Fructosazine

Sinónimos:

2,5-bis(D-Arabinotetrahydroxybutyl)pyrazine

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About This Item

Fórmula empírica (notación de Hill):
C12H20N2O8
Número de CAS:
13185-73-4
Peso molecular:
320.30
UNSPSC Code:
12352200

storage temp.

−20°C

InChI

1S/C12H20N2O8/c15-3-7(17)11(21)9(19)5-1-13-6(2-14-5)10(20)12(22)8(18)4-16/h1-2,7-12,15-22H,3-4H2/t7-,8-,9-,10-,11-,12-/m1/s1

InChI key

NPWQIVOYGNUVEB-PAUJSFGCSA-N

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Tomoko Shimamura et al.
Bioscience, biotechnology, and biochemistry, 67(2), 295-299 (2003-05-06)
XTT (3'-[1-[(phenylamino)-carbonyl]-3,4-tetrazolium]-bis(methoxy-6-nitro)benzenesulfonic acid hydrate) was reduced by incubated glucosamine hydrochloride. The XTT reducibility by incubated glucosamine was linearly related with the DNA-breaking activity. In order to elucidate the reaction mechanism, the glucosamine derivatives formed during the incubation process were separated
K Sumoto et al.
Chemical & pharmaceutical bulletin, 39(3), 792-794 (1991-03-01)
Two pyrazine derivatives [fructosazine (3) and deoxyfructosazine (6)] were simultaneously formed in a solution of D-glucosamine hydrochloride under various conditions. They showed deoxyribonucleic acid (DNA) strand breakage activity in plasmid pBR322 comparable to that of D-glucosamine. The DNA strand breakage
Nathaly Henry et al.
Talanta, 99, 816-823 (2012-09-13)
Fructosazine and 2,5-deoxyfructosazine are two natural chemicals with various applications as flavoring agents in food and tobacco industry; the 2,5-deoxyfructosazine has also anti-diabetic and anti-inflammatory activities. In order to quantify these compounds in natural samples such as plant or food
G Candiano et al.
Carbohydrate research, 184, 67-75 (1988-12-31)
The reaction of 2-amino-2-deoxy-D-glucose with lysine in water under simulated physiological conditions gave several browning products, with characteristic optical (lambda max 340 nm) and fluorescent properties (emission at 430 nm for excitation at 362 nm). The major product was isolated

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