Merck, SML1374-5MG, Alamandine trifluoroacetate salt

Biochem/physiol Actions
Alamandine is an endogenous heptapeptide that can be formed from angiotensin A by angiotensin converting enzyme-2 or directly from angiotensin-(1–7) by decarboxylation of its aspartate residue. Alamandine′s activity is similar to Ang-(1–7) rather than that of angiotensin II or angiotensin A. However, Alamandine acts at a different receptor, the Mas-related receptor, MrgD. Alamandine causes vasodilation, and has antifibrosis and antihypertensive activity.
Alamandine is an endogenous heptapeptide with similar activity to Angitensin (1-7), but acting at a different receptor, the Mas-related receptor, MrgD.