Design and synthesis of aryl sulfonamide-based nonsteroidal mineralocorticoid receptor antagonists
摘要:
Hit-to-lead medicinal chemistry efforts are described starting from a screening hit 1, leading to a new class of aryl sulfonamide-based MR antagonist, exemplified by 17, that possesses favourable MR binding affinity, selectivity profile against closely related NHRs, physicochemical properties and metabolic stability. (C) 2013 Elsevier Ltd. All rights reserved.
Design and synthesis of aryl sulfonamide-based nonsteroidal mineralocorticoid receptor antagonists
摘要:
Hit-to-lead medicinal chemistry efforts are described starting from a screening hit 1, leading to a new class of aryl sulfonamide-based MR antagonist, exemplified by 17, that possesses favourable MR binding affinity, selectivity profile against closely related NHRs, physicochemical properties and metabolic stability. (C) 2013 Elsevier Ltd. All rights reserved.