Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN320931 Azilsartan 147403-03-0
Azilsartan is an angiotensin II type 1 (AT1) receptor antagonist with IC50 of 2.6 nM.
YN321210 Elisartan 149968-26-3
Elisartan is an orally active non-peptide pro-drug ofangiotensin II AT1 receptorantagonist HN-12206, and shows anti-hypertension activities.
YN320152 Pratosartan 153804-05-8
Pratosartan is a selectiveangiotensin II receptorantagonist.
L162441 is anAngiotensin type 1 receptorantagonist.
YN320730 Olmesartan impurity 154709-18-9
Olmesartan impurity is an Olmesartan impurity. Olmesartan (RNH-6270) is anangiotensin II receptor (AT1R)antagonist has the potential for high blood pressure study.
L-159282 is a highly potent, orally active, nonpeptideangiotensin II receptorantagonist, with anti-hypertensive activity.
A 779 is a specific antagonist of G-protein coupled receptor (Mas receptor), which is anAng1-7 receptordistinct from the classical AngII.
LY285434 is a suitableangiotensin II receptorantagonist.
L162389 is a potent antagonist ofangiotensin AT1 receptor with Kiof 28nM.
YN320698 Dehydro Olmesartan 172875-98-8
Dehydro Olmesartan is a derivative of Olmesartan. Olmesartan is anangiotensin II receptor (AT1R)antagonist and has the potential for high blood pressure study.
YN321577 Fimasartan 247257-48-3
Fimasartan is a non-peptide angiotensin II receptor antagonist (ARB) with noncompetitive, insurmountable binding with the AT1 receptor. It is used for the treatment of hypertension and heart failure.
YN321170 Sparsentan 254740-64-2
Sparsentan is a dual endothelin type A receptor(ETA) and angiotensin II type 1 receptor antagonist.
AVE 0991 is a nonpeptide and orally activeangiotensin-(1-7) receptoragonist with an IC50 of 21nM.
YN321033 AVE 0991 sodium salt 306288-04-0
AVE 0991 sodium salt is a nonpeptide and orally activeAng-(1-7) receptor Masagonist. AVE 0991 competes for high-affinity binding of [125I]-Ang-(1-7) to bovine aortic endothelial cell membranes with IC50 of 21nM.
YN320004 AT2 receptor agonist C21 477775-14-7
AT2 receptor agonist C21 is a druglike selectiveangiotensin II AT2 receptoragonist with Ki values of 0.4nM and >10µM for the AT2 receptor and AT1 receptor, respectively.
YN320697 Olmesartan lactone impurity 849206-43-5
Olmesartan lactone impurity is a cyclic ester impurity of Olmesartan. Olmesartan is anangiotensin II receptor (AT1R)antagonist and has the potential for high blood pressure study.
YN320903 Azilsartan medoxomil 863031-21-4
Azilsartan Medoxomil is a potent angiotensin II type 1 (AT1) receptor antagonist, inhibits the RAAS, with an IC50 of 2.6 nM, exhibits >10,000-fold selectivity over AT2.
YN320696 Olmesartan medoxomil impurity... 879562-26-2
Olmesartan medoxomil impurity C is an Olmesartan medoxomil impurity. Olmesartan medoxomil is a potent and selectiveangiotensin AT1 receptorinhibitor with IC50 of 66.2μM.
LCZ696 (Sacubitril/Valsartan), comprised Valsartan (an ARB) and Sacubitril (AHU377) in 1:1 molar ratio, is a first-in-class, orally bioavailable, and dual-actingangiotensin receptor-neprilysin (ARN)inhibitor for hyperten...
YN321158 Losartan D4 1030937-27-9
Losartan D4 (DuP-753 D4) is the deuterium labeled Losartan. Losartan is anangiotensin II receptorantagonist, competing with the binding of angiotensin II to AT1 receptors with IC50 of 20nM.
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