62691-17-2

Upstream product

• 13742-23-9 (1R,4aS,10aR)-6-Hydroxy-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-phenanthrene-1-carboxylic acid methyl ester 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 

Downstream Products

• 37866-99-2 royleanone 
• 62393-78-6 12-Benzoyloxyabieta-8,12-dien-11,14-dion 
• 62691-19-4 12-Benzyloxyabieta-8,11,13-trien 
• 62751-55-7 8β-Benzoyloxy-12-oxoabieta-9(11),13-dien 
• 62691-21-8 11-Acetoxy-12-benzoyloxyabieta-8,11,13-trien 
• 62691-23-0 11-Acetoxy-12-benzoyloxyabieta-6,8,11,13-tetraen 
• 62691-22-9 (+)-11-acetoxy-12-benzoyloxy-8,11,13-abietatrien-7-one 
• 62393-73-1 12-benzoyloxy-11-hydroxyabieta-8,11,13-triene 
• 62716-37-4 13α-Benzoyloxy-12-oxoabieta-8(14),9(11)-dien 
• 62691-20-7 13β-Benzoyloxy-12-oxoabieta-8(14),9(11)-dien 
• 514-62-5 ferruginol 
• 1082940-39-3 C₂₇H₃₄O₃ 
• 62691-18-3 12-(benzyloxy)abieta-8,11,13-trien-18-al 

Relevant academic research and scientific papers

Novel BK channel openers containing dehydroabietic acid skeleton: Structure-activity relationship for peripheral substituents on ring C

A series of dehydroabietic acid (DHAA, 2) derivatives was synthesized and evaluated as BK channel openers in an assay system of CHO-K1 cells expressing hBKα channels. Systematic modifications of the peripheral functionality of ring C of DHAA showed that t