-
15249-50An inhibitor of LAT1 that blocks the uptake of L-leucine with an IC<sub>50</sub> value of 131.5 µM and can inhibit all members of the LAT family at a concentration of 10 mM suppresses mTORC1 signaling that drives DNA synthesis and cell
-
B0150-100 mg
Thomas Scientific
BChE inhibitor and 2-adrenergic receptor agonist that decreases bronchoconstriction. It is also a terbutaline prodrug. (C08-0488-567)
Price: $164.05List Price: $182.28Bambuterol is a long-acting ß2-adrenergic agonist and inhibitor of butylcholinesterase (BChE). Bambuterol is a prodrug of terbutaline and exhibits bronchodilatory and anti-asthma activities. -
B0150-500 mg
Thomas Scientific
BChE inhibitor and 2-adrenergic receptor agonist that decreases bronchoconstriction. It is also a terbutaline prodrug. (C08-0489-166)
Price: $383.71List Price: $426.35Bambuterol is a long-acting ß2-adrenergic agonist and inhibitor of butylcholinesterase (BChE). Bambuterol is a prodrug of terbutaline and exhibits bronchodilatory and anti-asthma activities. -
B0150-1 g
Thomas Scientific
BChE inhibitor and 2-adrenergic receptor agonist that decreases bronchoconstriction. It is also a terbutaline prodrug. (C08-0489-386)
Price: $547.74List Price: $608.60Bambuterol is a long-acting ß2-adrenergic agonist and inhibitor of butylcholinesterase (BChE). Bambuterol is a prodrug of terbutaline and exhibits bronchodilatory and anti-asthma activities. -
B0150-5 g
Thomas Scientific
BChE inhibitor and 2-adrenergic receptor agonist that decreases bronchoconstriction. It is also a terbutaline prodrug. (C08-0489-853)
Price: $1,867.79List Price: $2,075.32Bambuterol is a long-acting ß2-adrenergic agonist and inhibitor of butylcholinesterase (BChE). Bambuterol is a prodrug of terbutaline and exhibits bronchodilatory and anti-asthma activities. -
10006309-10A potent TRPV1 antagonist that inhibits capsaicin-induced and acid-induced activation of rat TRPV1 with IC50 values of 35 and 6 nM, respectively.
-
10006309-5A potent TRPV1 antagonist that inhibits capsaicin-induced and acid-induced activation of rat TRPV1 with IC50 values of 35 and 6 nM, respectively.
-
10006309-50A potent TRPV1 antagonist that inhibits capsaicin-induced and acid-induced activation of rat TRPV1 with IC50 values of 35 and 6 nM, respectively.
-
11426-1A mycotoxin which is cytotoxic against insect cells, killing the insect cell line SF-9 with a 50% cytotoxic concentration of 2.5 &muM induces apoptosis in mammalian cells with an IC50 value of 4.5 &muM.
-
11426-10A mycotoxin which is cytotoxic against insect cells, killing the insect cell line SF-9 with a 50% cytotoxic concentration of 2.5 &muM induces apoptosis in mammalian cells with an IC50 value of 4.5 &muM.
-
11426-5A mycotoxin which is cytotoxic against insect cells, killing the insect cell line SF-9 with a 50% cytotoxic concentration of 2.5 &muM induces apoptosis in mammalian cells with an IC50 value of 4.5 &muM.
-
10170-1L-Arginine serves as a common substrate for both NOS and arginase in the cell. NOS catalyzes the oxidation of arginine to citrulline and NO with N&omega-hydroxy-L-arginine (NOHA) formed as an intermediate.