Page last updated: 2024-10-21

urea and Anochlesia

urea has been researched along with Anochlesia in 6 studies

pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.

Research Excerpts

ExcerptRelevanceReference
"ACP-103 also attenuated catalepsy produced by haloperidol or risperidone."1.34ACP-103, a 5-hydroxytryptamine 2A receptor inverse agonist, improves the antipsychotic efficacy and side-effect profile of haloperidol and risperidone in experimental models. ( Anderson, GT; Barido, R; Bonhaus, DW; Brann, MR; Brunmark, P; Davis, RE; Dyssegaard, A; Gardell, LR; Hacksell, U; Johnson, RW; Pounds, L; Tabatabaei, A; Vanover, KE; Veinbergs, I, 2007)
"Because catalepsy is thought to be a good predictor of extrapyramidal symptoms in humans, treatment with orexin-1 antagonists might decrease the occurrence or severity of antipsychotic treatment-emergent extrapyramidal symptoms in humans."1.34The orexin-1 antagonist SB-334867 blocks antipsychotic treatment emergent catalepsy: implications for the treatment of extrapyramidal symptoms. ( Hemrick-Luecke, SK; Hsu, MA; Johnson, BG; Noone, S; Rasmussen, K; Thompson, LK, 2007)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's0 (0.00)18.2507
2000's3 (50.00)29.6817
2010's2 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kumari, N1
Agrawal, S1
Luthra, PM1
Azam, F2
Alkskas, IA1
Ahmed, MA1
Prasad, MV1
Thangavel, N1
Shrivastava, AK1
Mohan, G1
Gardell, LR1
Vanover, KE1
Pounds, L1
Johnson, RW1
Barido, R1
Anderson, GT1
Veinbergs, I1
Dyssegaard, A1
Brunmark, P1
Tabatabaei, A1
Davis, RE1
Brann, MR1
Hacksell, U1
Bonhaus, DW1
Rasmussen, K1
Hsu, MA1
Noone, S1
Johnson, BG1
Thompson, LK1
Hemrick-Luecke, SK1
Pieri, M1
Schaffner, R1
Pieri, L1
Da Prada, M1
Haefely, W1

Other Studies

6 other studies available for urea and Anochlesia

ArticleYear
Pharmacological assessments of potent A
    Neuroscience letters, 2017, 04-24, Volume: 647

    Topics: Adenosine A2 Receptor Antagonists; Adenosine-5'-(N-ethylcarboxamide); Animals; Antiparkinson Agents;

2017
Synthesis of some urea and thiourea derivatives of 3-phenyl/ethyl-2-thioxo-2,3-dihydrothiazolo[4,5-d]pyrimidine and their antagonistic effects on haloperidol-induced catalepsy and oxidative stress in mice.
    European journal of medicinal chemistry, 2009, Volume: 44, Issue:10

    Topics: Animals; Anti-Dyskinesia Agents; Antiparkinson Agents; Brain; Catalepsy; Glutathione; Glutathione Pe

2009
Structure-based design, synthesis and molecular modeling studies of thiazolyl urea derivatives as novel anti-parkinsonian agents.
    Medicinal chemistry (Shariqah (United Arab Emirates)), 2012, Volume: 8, Issue:6

    Topics: Animals; Antiparkinson Agents; Catalepsy; Chemistry Techniques, Synthetic; Drug Design; Haloperidol;

2012
ACP-103, a 5-hydroxytryptamine 2A receptor inverse agonist, improves the antipsychotic efficacy and side-effect profile of haloperidol and risperidone in experimental models.
    The Journal of pharmacology and experimental therapeutics, 2007, Volume: 322, Issue:2

    Topics: Amphetamine; Amphetamines; Animals; Antipsychotic Agents; Behavior, Animal; Brain Chemistry; Catalep

2007
The orexin-1 antagonist SB-334867 blocks antipsychotic treatment emergent catalepsy: implications for the treatment of extrapyramidal symptoms.
    Schizophrenia bulletin, 2007, Volume: 33, Issue:6

    Topics: Animals; Antipsychotic Agents; Basal Ganglia Diseases; Behavior, Animal; Benzodiazepines; Benzoxazol

2007
Turning in MFB-lesioned rats and antagonism of neuroleptic-induced catalepsy after lisuride and LSD.
    Life sciences, 1978, May-08, Volume: 22, Issue:18

    Topics: 5,7-Dihydroxytryptamine; Animals; Apomorphine; Behavior, Animal; Brain Injuries; Catalepsy; Ergoline

1978