JP1302
- Product Name
- JP1302
- CAS No.
- 80259-18-3
- Chemical Name
- JP1302
- Synonyms
- JP1302;MMV006172;Brn 5117597;JP 1302 dihydrochloride;N-(4-(4-Methylpiperazin-1-yl)phenyl)acridin-9-amine;N-(4-(4-Methyl-1-piperazinyl)phenyl)-9-acridinamine;9-Acridinamine, N-(4-(4-methyl-1-piperazinyl)phenyl)-;JP1302(9-Acridinamine, N-[4-(4-methyl-1-piperazinyl)phenyl]-);N-[4-(4-Methyl-1-piperazinyl)phenyl]-9-acridinaminedihydrochloride
- CBNumber
- CB31075143
- Molecular Formula
- C24H24N4
- Formula Weight
- 368.47
- MOL File
- 80259-18-3.mol
JP1302 Property
- Boiling point:
- 550.9±50.0 °C(Predicted)
- Density
- 1.227±0.06 g/cm3(Predicted)
- storage temp.
- Desiccate at -20°C
- pka
- 9.03±0.10(Predicted)
- Water Solubility
- <44.14mg/ml in Water
N-Bromosuccinimide Price
- Product number
- 2666
- Product name
- JP1302dihydrochloride
- Purity
- ≥99%(HPLC)
- Packaging
- 10
- Price
- $233
- Updated
- 2021/12/16
- Product number
- 2666
- Product name
- JP1302dihydrochloride
- Purity
- ≥99%(HPLC)
- Packaging
- 50
- Price
- $980
- Updated
- 2021/12/16
- Product number
- 255566
- Product name
- JP 1302 dihydrochloride
- Packaging
- 10mg
- Price
- $480
- Updated
- 2021/12/16
- Product number
- API0008021
- Product name
- JP 1302 DIHYDROCHLORIDE
- Purity
- 95.00%
- Packaging
- 10MG
- Price
- $727.65
- Updated
- 2021/12/16
- Product number
- B7147
- Product name
- JP1302dihydrochloride
- Packaging
- 10mg
- Price
- $338
- Updated
- 2021/12/16
JP1302 Chemical Properties,Usage,Production
Uses
JP 1302 Dihydrochloride is an α2-adrenoceptor blocker and can be used for the treatment or prevention of nephropathy.
Biological Activity
α 2C -adrenoceptor antagonist that displays ~ 50-fold selectivity over other α 2 -adrenoceptor subtypes (K i values are 28, 1470, 1700 and 3150 nM for human α 2C , α 2B , α 2D and α 2A subtypes respectively). Potently antagonizes adrenalin-stimulated 35 GTP γ S binding in vitro (K B = 16 nM) and produces antidepressant and antipsychotic-like effects in vivo .
in vivo
JP1302 (1-10 μmol/kg) decreases immobility time in the FST to a level similar to that seen with 10-30 μmol/kg of the antidepressant Desipramine.html" class="link-product" target="_blank">Desipramine (HY-B1272A)[1].
JP1302 (5 μmol/kg, once) is capable of complete reversal of the impairment in PPI induced in Sprague-Dawley rats by the psychotomimetic NMDA receptor antagonist, phencyclidine and similar results are found in Wistar rats[1].
JP1302 (3 mg/kg, IV, once) significantly ameliorates renal dysfunction[3].
| Animal Model: | Male Sprague Dawley rats (8 weeks old)[3] |
| Dosage: | 3 mg/kg |
| Administration: | IV, pre-treatment: administered 5 min before the induction of ischemia, post-treatment: injected 45 min after the initiation of reperfusion |
| Result: | Significantly ameliorated renal dysfunction in the rats at 24 h after reperfusion. post-ischemic administration of JP-1302 significantly ameliorated renal dysfunction, histological damage and reduced apoptotic cells and pro-inflammatory cytokine mRNA expression. |
IC 50
human α2C-adrenoceptor: 28±2 nM (Ki); human α2B-adrenoceptor: 1470±130 nM (Ki); human α2A-adrenoceptor: 3150±50 nM (Ki); rodent α2D-adrenoceptor: 1700±200 nM (Ki)
JP1302 Preparation Products And Raw materials
Raw materials
Preparation Products
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