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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
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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
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Tocris
Product number
2666
Product name
JP1302dihydrochloride
Purity
≥99%(HPLC)
Packaging
10
Price
$233
Updated
2021/12/16
Tocris
Product number
2666
Product name
JP1302dihydrochloride
Purity
≥99%(HPLC)
Packaging
50
Price
$980
Updated
2021/12/16
Usbiological
Product number
255566
Product name
JP 1302 dihydrochloride
Packaging
10mg
Price
$480
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0008021
Product name
JP 1302 DIHYDROCHLORIDE
Purity
95.00%
Packaging
10MG
Price
$727.65
Updated
2021/12/16
ApexBio Technology
Product number
B7147
Product name
JP1302dihydrochloride
Packaging
10mg
Price
$338
Updated
2021/12/16
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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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JP1302 Suppliers

3B Pharmachem (Wuhan) International Co.,Ltd.
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3bsc@sina.com
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021-52996696,15000506266 15000506266
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021-61350663 13052117465
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021-61350662
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sales@zehanbiopharma.com
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15076683720
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022-23754520
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klq@cw-bio.com
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021-31433387 15618786686
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QQ:1369748377
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sales@rechemscience.com
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021-QQ:65489617 15618227136
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400-1647117 13681763483
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product02@bidepharm.com
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marketing@tsbiochem.com
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80259-18-3, JP1302Related Search:


  • JP1302
  • 9-Acridinamine, N-(4-(4-methyl-1-piperazinyl)phenyl)-
  • Brn 5117597
  • N-(4-(4-Methyl-1-piperazinyl)phenyl)-9-acridinamine
  • JP 1302 dihydrochloride
  • N-[4-(4-Methyl-1-piperazinyl)phenyl]-9-acridinaminedihydrochloride
  • JP1302(9-Acridinamine, N-[4-(4-methyl-1-piperazinyl)phenyl]-)
  • MMV006172
  • N-(4-(4-Methylpiperazin-1-yl)phenyl)acridin-9-amine
  • 80259-18-3
  • C24H24N42HCl
  • Potently antagonizes adrenalin-stimulated 35GTPγS binding in vitro (KB = 16 nM) and produces antidepressant and antipsychotic-like effects in vivo.