Simple exploration of 4-(2,5-Dioxo-2,5-dihydro-pyrrol-1-yl)-benzoicacid

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Formula: C11H7NO4, you can also check out more blogs about17057-04-4

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Formula: C11H7NO4. Introducing a new discovery about 17057-04-4, Name is 4-(2,5-Dioxo-2,5-dihydro-pyrrol-1-yl)-benzoicacid

Acute effects of alkylating agents on canine renal function: Specifically designed synthetic maleimides

Maleimidohippurates and maleimidobenzoates were synthesized that possess a carboxy group for active uptake into renal proximal tubular cells and a reactive maleimide moiety to covalently bond with proximal tubular components. The reactivity of the maleimide moiety in each series was progressively reduced by substitution of methyl groups in place of the vinyl hydrogens. In contrast to N-ethylmaleimide (NEM), the resulting maleimidohippurates and maleimidobenzoates did not possess significant diuretic activity in the dog following renal arterial administration. However, as predicted, the nephrotoxicity of the maleimidohippurates paralleled their in vitro alkylating ability and was quite specifically located in the proximal portion of the canine renal tubule.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Formula: C11H7NO4, you can also check out more blogs about17057-04-4

Reference£º
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem