
Farampator
CAS No. 211735-76-1
Farampator( Farampator | Org-24448 | CX-691 )
Catalog No. M17430 CAS No. 211735-76-1
Farampator (CX-691;Org24448) is an AMPA receptor positive modulator.
Purity : >98% (HPLC)






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2MG | 45 | In Stock |
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5MG | 72 | In Stock |
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10MG | 105 | In Stock |
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25MG | 214 | In Stock |
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50MG | 372 | In Stock |
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100MG | 554 | In Stock |
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500MG | 1188 | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameFarampator
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NoteResearch use only, not for human use.
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Brief DescriptionFarampator (CX-691;Org24448) is an AMPA receptor positive modulator.
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DescriptionFarampator, also known as Org-24448; CX-691, is an AMPA receptor positive allosteric modulator potentially for the treatment of schizophrenia.(In Vivo):Farampator has potential in treating disorders characterised by cognitive deficits such as Alzheimer's disease and schizophrenia. CX691 attenuates a scopolamine-induced impairment of cued fear conditioning following acute administration (0.1 mg/kg p.o.) and a temporally induced deficit in novel object recognition following both acute (0.1 and 1.0 mg/kg p.o.) and sub-chronic (bi-daily for 7 days) administration (0.01, 0.03, 0.1 mg/kg p.o.). It also improves attentional set-shifting following sub-chronic administration (0.3 mg/kg p.o.). Farampator (500 mg) unequivocally improves short-term memory but appeares to impair episodic memory. Furthermore, it tends to decrease the number of switching errors in the CTMT. Drug-induced side effects (SEs) included headache, somnolence and nausea. Subjects with SEs has significantly higher plasma levels of farampator than subjects without SEs.
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In Vitro——
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In VivoFarampator has potential in treating disorders characterised by cognitive deficits such as Alzheimer's disease and schizophrenia. CX691 attenuates a scopolamine-induced impairment of cued fear conditioning following acute administration (0.1 mg/kg p.o.) and a temporally induced deficit in novel object recognition following both acute (0.1 and 1.0 mg/kg p.o.) and sub-chronic (bi-daily for 7 days) administration (0.01, 0.03, 0.1 mg/kg p.o.). It also improves attentional set-shifting following sub-chronic administration (0.3 mg/kg p.o.). Farampator (500 mg) unequivocally improves short-term memory but appeares to impair episodic memory. Furthermore, it tends to decrease the number of switching errors in the CTMT. Drug-induced side effects (SEs) included headache, somnolence and nausea. Subjects with SEs has significantly higher plasma levels of farampator than subjects without SEs.
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SynonymsFarampator | Org-24448 | CX-691
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PathwayImmunology/Inflammation
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TargetAntiviral
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RecptorAMPA
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Research Area——
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Indication——
Chemical Information
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CAS Number211735-76-1
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Formula Weight231.26
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Molecular FormulaC12H13N3O2
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Purity>98% (HPLC)
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SolubilityDMSO : ≥ 34 mg/mL; 147.03 mM
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SMILESO=C(N1CCCCC1)c1cc2nonc2cc1
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Chemical Name1-(2,1,3-Benzoxadiazol-5-ylcarbonyl)piperidine
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. Woolley ML, et al.Psychopharmacology (Berl). 2009 Jan;202(1-3):343-54.
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