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irtemazole

Known as: 1H-Benzimidazole, 5-(1H-imidazol-1-ylphenylmethyl)-2-methyl-, (+-)-, 5-((1H-imidazol-1-yl)phenylmethyl)-2-methyl-1H-benzimidazole 
National Institutes of Health

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Related topics

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Broader (1)

Benzimidazoles

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Composés 2-(1h-pyrazol-1-yl)-1h-benzimidazole substitués
La presente invention concerne des composes 2-(pyrazol-1-yl)-benzimidazole substitues de formule generale (I) : dans laquelleR 2… 
2006
2006
Carbodiimide-based benzimidazole library method.
Using carbodiimide reagents [1,3-diisopropylcarbodiimide or N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC… 
2006
2006
Uricosuric effect of different doses of irtemazole in normouricaemic subjects
SummaryIrtemazole 12.5 to 50 mg in 6 healthy, normouricaemic subjects caused a maximal decrease in plasma uric acid (after 8 to… 
2005
2005
Efficient white organic light-emitting device based on a thin layer of hole-transporting host with rubrene dopant
Review
1990
Review
1990
New initiatives in the control of helminths.
1989
1989
Uricosuric effect of irtemazole in hyperuricemic patients without and with renal insufficiency.
A single oral dose of 50 mg irtemazole exhibited a clear cut uricosuric effect in five patients with hyperuricemia and normal… 
1989
1989
Uricosuric effect of irtemazole in healthy subjects
SummaryFollowing a single dose of 50 mg irtemazole per os, plasma uric acid levels decreased after 1 h and fell to 53.5% of the… 
1989
1989
A new uricosuric substance, 5-[(1H-lmidazol-1-yl)phenylmethyl]-2-methyl-1H-benzimidazole (C18H16N4)
5 [( 1Himidazol1 yl)phenylmethyl] 2methyl 1tt benzimid azole (C18H16N4; generic name: irtemazole) has been tested for its… 
1975
1975
The molecular mechanism of benzimidazole mutagenicity: In vitro studies on transcription and translation
Benzimidazoles are weak mutagens acting through base substitutions; they are incorporated into nucleic acids. Experiments with… 
1961
1961
Structure of cobamide coenzymes: influence of pH on absorption spectra and ionophoretic mobilities.
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