Steric hindrance from the increased side-chain volume of E14 Cagri and R17 Cagri promotes a shift of the -helix of Cagri away from ECL2 and a slight expansion of the peptide binding pocket at the extracellular side of the CTR TM domain, relative to those observed with rAmy/San385-bound AMYR complexes
Su frmula molecular es C14H21CuN6O4 y su masa molecular terica es 404.9 Da
Patients reported, in interview forms, using the following drugs: brinzolamide, latanoprost, ripasudil, travoprost, carteolol, isopropyl unoprostone, tafluprost, timolol, bunazosin, bimatoprost, brimonidine, bromfenac, gatifloxacin, levofloxacin, phenylephrine and tropicamide
Plant Physiol 176(1):930945