PIPERAZINE - A BIOLOGICALLY ACTIVE SCAFFOLD

被引:29
作者
Singh, Kuldeep [1 ]
Siddiqui, H. H. [1 ]
Shakya, Pragati [1 ]
Bagga, Paramdeep [1 ]
Kumar, Arun [1 ]
Khalid, M. [1 ]
Arif, M. [1 ]
Alok, Shashi [2 ]
机构
[1] Integral Univ, Fac Pharm, PO Basha,Kursi Rd, Lucknow 226026, UP, India
[2] Bundelkhand Univ, Inst Pharm, Dept Pharmacognosy, Jhansi, UP, India
关键词
Piperazine; synthesis; Spectral studies; Stereochemistry; Biological activity;
D O I
10.13040/IJPSR.0975-8232.6(10).4145-58
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The broad and potent activity of piperazine has established it as one of the biologically important scaffolds. This article is an effort to highlight the importance of the piperazine in the present context and promise they hold for the future. This review mainly focused the updated information on the most active piperazine derivatives that have been reported to show significant biological actions for instance anti-microbial, anti-depressant, anticonvulsant, anti-parkinson, anti-inflammatory, antipsychotic, antioxidant, antidiabetic, antiarrhythmic, antiproliferative, anxiolytic, antialzheimer, antimalarial, antihypertensive, antiplatelet aggression and anti-histaminic activity. This review would take on benzylpiperazine (BZP) and trifluoromethylpiperazine (TFMPP), benzhydryl piperazine, diphenylalkyl piperazine, phenyl piperazine as the most popular member of the piperazines, focusing the discussion on their origins, pharmacokinetics and pharmacodynamics, and their effects on the human body. From these outcomes, information for future molecular modifications leading to compounds with greater positive pharmacological properties may be derived.
引用
收藏
页码:4145 / 4158
页数:14
相关论文
共 34 条
[1]  
Acri JB, 1996, J PHARMACOL EXP THER, V277, P198
[2]   Complete experimental and theoretical proton and carbon nuclear magnetic resonance spectral assignments, molecular structure and conformational study of 1-cyclohexylpiperazine and 1-(4-pyridyl)piperazine [J].
Alver, Oezguer .
MAGNETIC RESONANCE IN CHEMISTRY, 2010, 48 (01) :53-60
[3]  
Aytemir MD, 2010, ARZNEIMITTELFORSCH, V60, P22, DOI 10.1055/s-0031-1296244
[4]   Synthesis, evaluation and computational studies on a series of acetophenone based 1-(aryloxypropyl)-4-(chloroaryl) piperazines as potential atypical antipsychotics [J].
Bali, Alka ;
Sharma, Komal ;
Bhalla, Abhishek ;
Bala, Suman ;
Reddy, Dinesh ;
Singh, Anant ;
Kumar, Anil .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2010, 45 (06) :2656-2662
[5]   Investigation of various N-heterocyclic substituted piperazine versions of 5/7-{[2-(4-aryl-piperazin-1-yl)-ethyl]-propyl-amino}-5,6,7,8-tetrahydro-naphthalen-2-ol: Effect on affinity and selectivity for dopamine D3 receptor [J].
Brown, Dennis A. ;
Mishra, Manoj ;
Zhang, Suhong ;
Biswas, Swati ;
Parrington, Ingrid ;
Antonio, Tamara ;
Reith, Maarten E. A. ;
Dutta, Aloke K. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2009, 17 (11) :3923-3933
[6]   Mechanism of 2,5-dioxopiperazine formation [J].
Capasso, S ;
Vergara, A ;
Mazzarella, L .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (09) :1990-1995
[7]   (1,4-benzothiazinyloxy)alkylpiperazine derivatives as potential antihypertensive agents [J].
Cecchetti, V ;
Schiaffella, F ;
Tabarrini, O ;
Fravolini, A .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2000, 10 (05) :465-468
[8]  
Cunica W, Z KRYSTALLOGRAPHIE, V224, P461
[9]   SYNTHESIS AND SOME CNS ACTIVITIES OF NEW BENZOFURANYLACRYLOYLPIPERAZINES [J].
DAUZONNE, D ;
GILLARDIN, JM ;
LEPAGE, F ;
POINTET, R ;
RISSE, S ;
LAMOTTE, G ;
DEMERSEMAN, P .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1995, 30 (01) :53-59
[10]  
Dayalan A, 2007, SULPHONYL NAPHTHALEN, V19, P5041