18248-54-9Relevant academic research and scientific papers
Synthesis, characterization and antioxidant activities of semicarbazide and thiosemicarbazide derivatives
Alam, Faima,Ali, Basharat,Ali, Mahboob,Khan, Khalid Mohammed,Khan, Momin,Manaf, Abdul,Zaman, Khair
, p. 475 - 483 (2021/08/21)
In this research work Semicarbazide, thiosemicarbazide derivatives 3 to 25 were synthesized by conventional methods with high percentage yield and reaction rate. 1H-NMR and EIMS spectroscopic techniques were used to elucidate the structure of t
Discovery and SAR of a series of agonists at orphan G protein-coupled receptor 139
Shi, Feng,Shen, Jing Kang,Chen, Danqi,Fog, Karina,Thirstrup, Kenneth,Hentzer, Morten,Karlsson, Jens-Jakob,Menon, Veena,Jones, Kenneth A.,Smith, Kelli E.,Smith, Garrick
scheme or table, p. 303 - 306 (2011/06/21)
GPR139 is an orphan G-protein coupled receptor (GPCR) which is primarily expressed in the central nervous system (CNS). In order to explore the biological function of this receptor, selective tool compounds are required. A screening campaign identified compound 1a as a high potency GPR139 agonist with an EC50 = 39 nM in a calcium mobilization assay in CHO-K1 cells stably expressing the GPR139 receptor. In the absence of a known endogenous ligand, the maximum effect was set as 100% for 1a. Screening against 90 diverse targets revealed no cross-reactivity issues. Assessment of the pharmacokinetic properties showed limited utility as in vivo tool compound in rat with a poor whole brain exposure of 61 ng/g and a brain/plasma (b/p) ratio of 0.03. Attempts to identify a more suitable analogue identified the des-nitrogen analogue 1s with a reduced polar surface area of 76.7 A2 and an improved b/p ratio of 2.8. The whole brain exposure remained low at 95 ng/g due to a low plasma exposure.
An efficient synthesis of 1,3,4-oxadiazoles from N,N′-diacylhydrazines using Ph3P·Br2, Ph3P·CCl4 or Ph3P·CBr4 adducts as condensing agents
Mazurkiewicz,Grymel
, p. 77 - 82 (2007/10/03)
1,3,4-Oxadiazoles including 2-amino derivatives were effectively synthesized by treatment of N,N′-diacylhydrazines or N-acylsemicarbazides with Ph3P·Br2, Ph3P·CCl4 or Ph3P·CBr4 adducts in the presence of Et3N in CH2Cl2 under mild conditions.
