201792-91-8Relevant articles and documents
The amido-pentadienoate-functionality of the rakicidins is a thiol reactive electrophile - Development of a general synthetic strategy
Clement, Lise L.,Tsakos, Michail,Schaffert, Eva S.,Scavenius, Carsten,Enghild, Jan J.,Poulsen, Thomas B.
, p. 12427 - 12430 (2015)
We demonstrate that a unique class-defining functionality (mc-APD) found in macrocyclic natural products with potent anti-cancer activity, imparts these compounds with electrophilic reactivity. The mc-APD group represents an interesting structural hybrid between canonical biologically relevant Michael-acceptors. Further, a novel thiol-elimination method for preparation of the mc-APD group is outlined.
Synthesis and CB1 receptor activities of novel arachidonyl alcohol derivatives
Parkkari, Teija,Savinainen, Juha R.,Rauhala, Anu L.,Tolonen, Tiina L.,Nevalainen, Tapio,Laitinen, Jarmo T.,Gynther, Jukka,Jaervinen, Tomi
, p. 3231 - 3234 (2007/10/03)
Novel derivatives of arachidonyl alcohol were synthesized and evaluated for their CB1 receptor activity by [35S]GTPγS assay using rat cerebellar membranes.