Page last updated: 2024-08-16

piperazine and carbamates

piperazine has been researched along with carbamates in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (14.29)18.2507
2000's1 (14.29)29.6817
2010's5 (71.43)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
DeGrado, WF; Jackson, S; Mousa, S; Olson, RE; Rafalski, M; Rockwell, A; Roderick, J; Xue, CB1
Albericio, F; Armand-Ugón, M; El-Faham, A; Esté, JA1
Beyad, Y; Burns, R; Conway, W; Fernandes, D; Lawrance, G; Maeder, M; Puxty, G1
Fine, NA; Goldman, MJ; Rochelle, GT1
Korhonen, J; Kuusisto, A; Laitinen, JT; Laitinen, T; Navia-Paldanius, D; Nevalainen, TJ; Parkkari, T; Patel, JZ; Savinainen, JR; van Bruchem, J1
Kumari, S; Mishra, CB; Tiwari, M1
Armirotti, A; Bandiera, T; Bottegoni, G; Cavalli, A; De Simone, A; Di Martino, RM; Ferraro, M; Micoli, A; Ottonello, G; Ruda, GF; Russo, D; Summa, M1

Other Studies

7 other study(ies) available for piperazine and carbamates

ArticleYear
Design, synthesis, and in vitro activities of benzamide-core glycoprotein IIb/IIIa antagonists: 2,3-diaminopropionic acid derivatives as surrogates of aspartic acid.
    Bioorganic & medicinal chemistry, 1997, Volume: 5, Issue:4

    Topics: Alanine; Alkylation; Animals; Aspartic Acid; Benzamides; Benzamidines; Benzoates; Benzoic Acid; beta-Alanine; Carbamates; Esterases; Humans; Liver; Magnetic Resonance Spectroscopy; Oligopeptides; Piperazine; Piperazines; Piperidines; Platelet Aggregation Inhibitors; Platelet Glycoprotein GPIIb-IIIa Complex; Structure-Activity Relationship; Sulfonamides; Swine

1997
Use of N-methylpiperazine for the preparation of piperazine-based unsymmetrical bis-ureas as anti-HIV agents.
    ChemMedChem, 2008, Volume: 3, Issue:7

    Topics: Anti-HIV Agents; Benzoxazoles; Carbamates; Cell Line; Cell Survival; HIV Protease; HIV Protease Inhibitors; Humans; Lymphocytes; Methylation; Piperazine; Piperazines; Structure-Activity Relationship; Urea

2008
Reactions of CO2 with aqueous piperazine solutions: formation and decomposition of mono- and dicarbamic acids/carbamates of piperazine at 25.0 °C.
    The journal of physical chemistry. A, 2013, Feb-07, Volume: 117, Issue:5

    Topics: Carbamates; Carbon Dioxide; Molecular Structure; Piperazine; Piperazines; Solutions; Temperature; Water

2013
Kinetics of N-nitrosopiperazine formation from nitrite and piperazine in CO2 capture.
    Environmental science & technology, 2013, Apr-02, Volume: 47, Issue:7

    Topics: Carbamates; Carbon Dioxide; Catalysis; Hydrogen-Ion Concentration; Kinetics; Models, Chemical; Nitrites; Nitrosamines; Nitrosation; Piperazine; Piperazines; Temperature

2013
Piperazine and piperidine carboxamides and carbamates as inhibitors of fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL).
    Bioorganic & medicinal chemistry, 2014, Dec-01, Volume: 22, Issue:23

    Topics: Amides; Amidohydrolases; Carbamates; Dose-Response Relationship, Drug; Enzyme Inhibitors; HEK293 Cells; Humans; Models, Molecular; Molecular Structure; Monoacylglycerol Lipases; Piperazine; Piperazines; Piperidines; Structure-Activity Relationship

2014
Design, synthesis and pharmacological evaluation of N-[4-(4-(alkyl/aryl/heteroaryl)-piperazin-1-yl)-phenyl]-carbamic acid ethyl ester derivatives as novel anticonvulsant agents.
    Bioorganic & medicinal chemistry letters, 2015, Mar-01, Volume: 25, Issue:5

    Topics: Animals; Anticonvulsants; Carbamates; Drug Design; Electroshock; Epilepsy; Mice; Pentylenetetrazole; Piperazine; Piperazines; Seizures

2015
Design, Synthesis, Structure-Activity Relationship Studies, and Three-Dimensional Quantitative Structure-Activity Relationship (3D-QSAR) Modeling of a Series of O-Biphenyl Carbamates as Dual Modulators of Dopamine D3 Receptor and Fatty Acid Amide Hydrolas
    Journal of medicinal chemistry, 2017, 03-23, Volume: 60, Issue:6

    Topics: Amidohydrolases; Animals; Biphenyl Compounds; Blood-Brain Barrier; Carbamates; CHO Cells; Cricetulus; Drug Design; HEK293 Cells; Humans; Male; Models, Molecular; Piperazine; Piperazines; Quantitative Structure-Activity Relationship; Rats, Sprague-Dawley; Receptors, Dopamine D3

2017