1290176-46-3Relevant academic research and scientific papers
Et3N-Prompted Efficient Synthesis of Anthracenyl Pyrazolines and Their Cytotoxicity Evaluation against Cancer Cell Lines
Merry, Thechano,Maddela, Prabhakar,Devaraya, Kiran,Kondapi, Anand K.,Pradeep, Chullikkattil P.
supporting information, p. 2469 - 2478 (2019/08/12)
A series of anthracenyl pyrazoline derivatives (3a–o) were synthesized with an aim to evaluate their in vitro anticancer activities. Anthracenyl pyrazoline compounds were prepared by the reaction between various anthracenyl chalcones (1a–o) and hydrazine
Facile One-Pot Synthesis Methodology for Nitrogen-Containing Heterocyclic Derivatives of 3,5-Disubstituted 4,5-Dihydro-1H-Pyrazole, Their Biological Evaluation and Molecular Docking Studies
Upadhyay, Savita,Tripathi, Avinash C.,Paliwal, Sarvesh,Saraf, Shailendra K.
, p. 564 - 575 (2017/11/10)
A series of 2-pyrazoline derivatives (PS-1 to PS-16) were synthesized by reacting different aromatic/heteroaromatic aldehydes and ketones, in a two-step reaction through Claisen – Schmidt condensation, followed by cyclization of the resulting chalcones wi
2-pyrazoline derivatives in neuropharmacology: Synthesis, adme prediction, molecular docking and in vivo biological evaluation
Upadhyay, Savita,Tripathi, Avinash C.,Paliwal, Sarvesh,Saraf, Shailendra K.
, p. 628 - 649 (2017/06/05)
A novel series of 1,3,5-trisubstituted-2-pyrazoline derivatives (PFC-1 to PFC-16) were synthesized in a three step reaction using conventional and microwave assisted green chemistry approach. The synthesized derivatives were characterized and their chemic
Development of selective and reversible pyrazoline based MAO-B inhibitors: Virtual screening, synthesis and biological evaluation
Mishra, Nibha,Sasmal
experimental part, p. 1969 - 1973 (2011/04/24)
In an effort to develop selective MAO (monoamine oxidase) B inhibitors, structure based virtual screening was initiated on an in-house library. Top 10 HITS were synthesized and evaluated for MAO (A and B) inhibitory activity, both against human and rat en
