52145-93-4

Upstream product

• 126582-32-9 2-(4-benzyloxyphenyl)-3-(4-methoxyphenyl)cyclopropane 
• 104-01-8 4-Methoxyphenylacetic acid 
• 123-11-5 4-methoxy-benzaldehyde 
• 99-93-4 4-Hydroxyacetophenone 
• 6338-81-4 (E)-1-(4-hydroxyphenyl)-3-(4-methoxyphenyl)-2-propen-1-one 
• 126582-22-7 C₂₂H₂₀O₂ 
• 126582-19-2 (E)-3-(4-Benzyloxy-phenyl)-2-(4-methoxy-phenyl)-acrylic acid 
• 126582-26-1 C₂₃H₂₀Cl₂O₂ 

Relevant academic research and scientific papers

Synthesis, biological evaluation, and docking studies of gigantol analogs as calmodulin inhibitors

Several analogs of gigantol (1) were synthesized to evaluate their effect on the complexes Ca2+-calmodulin (CaM) and Ca2+-CaM-CaM sensitive phosphodiesterase 1 (PDE1). The compounds belong to four structural groups including, 1,2-dip

SYNTHESIS OF ATR AND LIGHT SENSITIVE CIS-PHENOLIC CYCLOPROPANE DERIVATIVES

The synthesis of several cis-phenolic cyclopropanes, 6, 7, 8 and 13 is described.These cyclopropanes are new potential antiestrogens.A hydrogenolysis study of precursors, 5b, 5c, 5d, 10, 11, and 12, and a novel method for the prevention of gem-dichlorocyclopropane ring-opening during hydrogenolysis are discussed.