NS9283
CAS No. 913830-15-6
NS9283( NS 9283 | NS-9283 )
Catalog No. M27906 CAS No. 913830-15-6
NS9283, a positive allosteric modulator selective for the α4β2 form, reduces ethanol consumption.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 87 | Get Quote |
|
| 10MG | 132 | Get Quote |
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| 25MG | 282 | Get Quote |
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| 50MG | 444 | Get Quote |
|
| 100MG | 651 | Get Quote |
|
| 500MG | 1368 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameNS9283
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NoteResearch use only, not for human use.
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Brief DescriptionNS9283, a positive allosteric modulator selective for the α4β2 form, reduces ethanol consumption.
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DescriptionNS9283, a positive allosteric modulator selective for the α4β2 form, reduces ethanol consumption.(In Vitro):NS9283 increased the potency of varenicline to activate and desensitize α4β2 nAChRs in vitro without affecting other known targets of varenicline.(In Vivo):In male and female C57BL/6J mice, NS9283 (10 mg/kg) reduced ethanol intake in a two-bottle choice, intermittent drinking procedure without affecting saccharin intake, ethanol-induced incoordination or ethanol-induced loss of the righting reflex. Subthreshold doses of NS9283 (2.5 mg/kg) plus varenicline (0.1 mg/kg) synergistically reduced ethanol intake in both sexes. Finally, despite having no aversive valence of its own, NS9283 enhanced ethanol-conditioned place aversion.
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In Vitro——
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In Vivo——
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SynonymsNS 9283 | NS-9283
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PathwayCell Cycle/DNA Damage
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TargetAChR
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Recptorlignostilbene-α,β-dioxygenase
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Research Area——
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Indication——
Chemical Information
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CAS Number913830-15-6
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Formula Weight248.245
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Molecular FormulaC14H8N4O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 16.67 mg/mL (67.15 mM)
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SMILESN#Cc1cccc(c1)-c1nc(no1)-c1cccnc1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Cai S, et al. Synthesis, structure-activity relationships and preliminary mechanism study of N-benzylideneaniline derivatives as potential TLR2 inhibitors. Bioorg Med Chem. 2018 May 1;26(8):2041-2050.
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