NNC 0756 (odapipam)
8
relevant articles (1 outcomes,
1 trials/studies)
found for this Bio-Agent
Description:
structure given in first source; NNC 0756 is the (acetate,(+))-isomer and NNC 0772 is the (HCl,(-))-isomer; NNC 0756 is a potent dopamine D-1 receptor antagonist; odapipam is the (S)-isomer
Also Known As:
odapipam; 8-chloro-7-hydroxy-5-(2,3-dihydrobenzofuran-7-yl)-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine; NNC 0756, (R)-isomer; NNC 0756, (S)-isomer; NNC 0756, (S)-isomer,C11-labeled; NNC 0772; NNC 756; NNC-0756; NNC-0772; NNC-756; 1H-3-Benzazepin-7-ol, 8-chloro-5-(2,3-dihydro-7-benzofuranyl)-2,3,4,5-tetrahydro-3-methyl-, (S)-, acetate (salt)
Relationship Network
Bio-Agent Context: Research Results
Related Diseases
| 1. | Schizophrenia (Dementia Praecox)
|
| 2. | Narcolepsy
|
| 3. | Movement Disorders (Movement Disorder)
|
| 4. | Dystonia (Limb Dystonia)
04/01/1994
- " NNC 756 induced no dystonia, while marked dystonia was induced by raclopride" 10/01/2001
- " RESULTS: SKF 83959 acted as a DA D1 agonist (induced oral dyskinesia given alone, counteracted DA D1 antagonist [NNC 756], induced dystonia, and did not inhibit AMP induced behaviors)" 11/01/1998
- " NNC 756 (0.004 and 0.01 mg/kg), raclopride (0.004 and 0.01 mg/kg), SKF 81297 (0.3 and 0.6 mg/kg), quinpirole (0.1 and 0.2 mg/kg), amphetamine (0.25 and 0.5 mg/kg), and biperiden (0.125 and up to 1.0 mg/kg), had no significant effect on MK-801-induced dystonia" 11/01/1998
- " MK-801 (dizocilpine), a noncompetitive N-methyl-D-aspartate antagonist, induces dystonia in monkeys at doses of 0.08 mg/kg. This syndrome was tested with the dopamine D1 receptor antagonist NNC 756, the DA D2 receptor antagonist raclopride, the atypical antipsychotic clozapine, the dopamine D1 receptor agonist SKF 81297, the dopamine D2/D3 receptor agonist quinpirole, the anticholinergic biperiden, amphetamine, and the benzodiazepine midazolam in 7 Cebus apella monkeys previously treated with dopaminergic agents"
Order ALL the reference details at left...
|
| 5. | Dyskinesias (Dyskinesia)
04/01/1994
- " Concomitant treatment with NNC 756 tended to reduce the D1 agonist SKF 81297-induced dyskinesia and grooming, while concomitant treatment with raclopride increased SKF 81297-induced dyskinesia and tended to decrease SKF 81297-induced grooming" 04/01/1994
- " No significant dyskinesia was induced by NNC 756, while raclopride significantly induced both acute and tardive oral dyskinesia" 10/01/2001
- " SKF 83822, unlike previously studied DA D1 agonists, did not induce dyskinesia, but resulted in a state of extreme arousal and locomotor activation without stereotypy, effectively counteracted by NNC 756, but not by SKF 83959 nor raclopride (DA D2 antagonist).CONCLUSIONS: It is hypothesized that: 1) dyskinesia is linked to PLC stimulation; 2) DA D1 agonism can play a role in the induction of psychosis, via a mechanism linked neither to AC nor PLC, and 3) DA D1 antagonists differ in antipsychotic potential, possibly via this unidentified mechanism."
Order ALL the reference details at left...
|
|
Related Drugs and Biologics