Life Science

The RPI brilliant green [ethyl green] is suitable for use in research facilities and chemical laboratories to conduct wide range of experiments. It is available in sturdy bottle that endures heavy and rigorous usage.

A selective &alpha2-adrenergic receptor agonist (Ki = 183 nM) that lowers intraocular pressure by decreasing aqueous humor synthesis and increasing drainage through uveoscleral outflow protects rat retinal ganglion cells against glutamate

A selective &alpha2-adrenergic receptor agonist (Ki = 183 nM) that lowers intraocular pressure by decreasing aqueous humor synthesis and increasing drainage through uveoscleral outflow protects rat retinal ganglion cells against glutamate

A selective &alpha2-adrenergic receptor agonist (Ki = 183 nM) that lowers intraocular pressure by decreasing aqueous humor synthesis and increasing drainage through uveoscleral outflow protects rat retinal ganglion cells against glutamate

A selective &alpha2-adrenergic receptor agonist (Ki = 183 nM) that lowers intraocular pressure by decreasing aqueous humor synthesis and increasing drainage through uveoscleral outflow protects rat retinal ganglion cells against glutamate

A potent inhibitor of carbonic anhydrases (IC50s = 3.2 and 45.3 nM for CAII and CAIV, respectively) that lowers intraocular pressure by locally inhibiting carbonic anhydrase in the ciliary processes and suppressing aqueous humor secretion.

A potent inhibitor of carbonic anhydrases (IC50s = 3.2 and 45.3 nM for CAII and CAIV, respectively) that lowers intraocular pressure by locally inhibiting carbonic anhydrase in the ciliary processes and suppressing aqueous humor secretion.

A potent inhibitor of carbonic anhydrases (IC50s = 3.2 and 45.3 nM for CAII and CAIV, respectively) that lowers intraocular pressure by locally inhibiting carbonic anhydrase in the ciliary processes and suppressing aqueous humor secretion.

A potent inhibitor of carbonic anhydrases (IC50s = 3.2 and 45.3 nM for CAII and CAIV, respectively) that lowers intraocular pressure by locally inhibiting carbonic anhydrase in the ciliary processes and suppressing aqueous humor secretion.

A selective agonist of &beta3-adrenergic receptors with Ki values of 0.43, 9.17, and 37.9 &microM for &beta3, &beta2, and &beta1, respectively.

A selective agonist of &beta3-adrenergic receptors with Ki values of 0.43, 9.17, and 37.9 &microM for &beta3, &beta2, and &beta1, respectively.

A selective agonist of &beta3-adrenergic receptors with Ki values of 0.43, 9.17, and 37.9 &microM for &beta3, &beta2, and &beta1, respectively.