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Key Documents

G11802

Sigma-Aldrich

2-Guanidinobenzimidazole

95%

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About This Item

Empirical Formula (Hill Notation):
C8H9N5
CAS Number:
Molecular Weight:
175.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

95%

mp

242-244 °C (dec.) (lit.)

SMILES string

NC(=N)Nc1nc2ccccc2[nH]1

InChI

1S/C8H9N5/c9-7(10)13-8-11-5-3-1-2-4-6(5)12-8/h1-4H,(H5,9,10,11,12,13)

InChI key

JJWCTKUQWXYIIU-UHFFFAOYSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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In pursuit of an inhibitory drug for the proton channel.
Amaury Pupo et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(27), 9673-9674 (2014-06-13)
M L Flonta et al.
Archives internationales de physiologie, de biochimie et de biophysique, 99(4), 335-337 (1991-08-01)
Procaine has different effects on various ionic conductive pathways through the frog skin. We investigated the season and temperature dependence of the stimulation by mucosal procaine, of the Na-conductive pathway. For this stimulation, we found higher half-maximal saturation constants (KNa)
Is chloride transfer in frog skin localized to a special cell type?
P Kristensen
Acta physiologica Scandinavica, 113(1), 123-124 (1981-09-01)
M Fronius et al.
The Journal of membrane biology, 195(1), 43-51 (2003-09-23)
In the present study we investigated the effect of extracellular gadolinium on amiloride-sensitive Na(+) current across Xenopus alveolar epithelium by Ussing chamber experiments and studied its direct effect on epithelial Na(+) channels with the patch-clamp method. As observed in various
A Pinelli et al.
Arzneimittel-Forschung, 34(8), 890-894 (1984-01-01)
In this study 2-guanidinebenzimidazole (GBI) and 1-phenylbiguanide (PBG) appear to be capable of decreasing gastric acid secretion, while the compounds dimethylbiguanide and cyanoguanidine do not. Thus, the antisecretory effect is present when the biguanide groups are associated with lipophilic molecules.

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