|M9091||A-779||A-779 is a specific antagonist of G-protein coupled receptor (Mas receptor).|
|M9079||Angiotensin-(1-7)||Angiotensin (1-7) is a synthetic heptapeptide identical to endogenous angiotensin-(1-7), inhibits purified canine angiotensin converting enzyme (ACE) activity with an IC50 of 0.65 μM.|
|M9056||Losartan||Losartan is an angiotensin II receptor antagonist, competing with the binding of angiotensin II to AT1 receptors with IC50 of 20 nM.|
|M8987||EMA401||EMA401 (also known as Olodanrigan and PD-126055) is a highly selective angiotensin AT2 antagonist.|
|M6240||Angiotensin II human||Angiotensin II human is converted by Angiotensin I through removal of two C-terminal residues by the enzyme angiotensin-converting enzyme (ACE). Angiotensin II is mediated by AT1 and AT2 receptors, which are seven transmembrane glycoproteins with 30% sequence similarity.|
|M6025||Tranilast||Tranilast is an antiallergic agent.|
|M3917||PD 123319||PD 123319 is a potent, selective AT2 angiotensin II receptor antagonist with IC50 of 34 nM.|
|M3511||Olmesartan Medoxomil||Olmesartan Medoxomil is a compound which is hydrolyzed to olmesartan that is a selective AT1 subtype angiotensin II receptor antagonist.|
|M3507||Valsartan||Valsartan is an angiotensin II receptor antagonist with IC50 of ranging from 39.5 to 116 μM|
|M3265||Olmesartan||Olmesartan is an angiotensin II receptor antagonist with an IC50 of 7.7 nM.|
|M2258||Losartan potassium||Losartan potassium is a selective non-peptide angiotensin AT1 receptor antagonist.|
|M2164||PD 123319 ditrifluoroacetate||PD 123319 ditrifluoroacetate is a potent, selective, non-peptide angiotensin AT2 receptor antagonist.|
|M2106||Azilsartan||Azilsartan (TAK-536) is an angiotensin II type 1 (AT1) receptor antagonist with IC50 of 2.6 nM.|
|M2105||Azilsartan medoxomil||Azilsartan medoxomil is an orally administered angiotensin II receptor type 1 antagonist.|
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