
SLV319
CAS No. 362519-49-1
SLV319( (±)-SLV319 | (±)-BMS6462 )
Catalog No. M18476 CAS No. 362519-49-1
SLV319 has been used in trials studying the treatment of Obesity and Obesity and Type 2 Diabetes.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 40 | In Stock |
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5MG | 65 | In Stock |
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10MG | 125 | In Stock |
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25MG | 250 | In Stock |
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50MG | 462 | In Stock |
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100MG | 669 | In Stock |
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500MG | 1341 | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameSLV319
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NoteResearch use only, not for human use.
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Brief DescriptionSLV319 has been used in trials studying the treatment of Obesity and Obesity and Type 2 Diabetes.
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DescriptionSLV319 has been used in trials studying the treatment of Obesity and Obesity and Type 2 Diabetes.(In Vitro):Cannabinoid receptor 1 (CB1R) antagonists appear to be promising drugs for the treatment of obesity, however, serious side effects have hampered their clinical application. Ibipinabant is a new, potent [Ki (CB1)=7.8 nM] and selective [Ki (CB2)=7.943 nM] CB1 antagonist [pA2 for arachidonic acid release in CHO cells=9.9] with in vitro pharmacological characteristics similar to rimonabant including inverse agonism and brain penetrance.(In Vivo):(±)-Ibipinabant ((±)-SLV319) (3 mg/kg) reduces unfasted glucose to a significantly greater degree than rimonabant at the same dose on days 17, 28 and 38. Chronic treatment with (±)-Ibipinabant ((±)-SLV319) significantly attenuates the progression of diabetes in ZDF rats, blunting the increase in blood glucose and HbA1c over time. Ibipinabant also reduces the hyperinsulinemia apparent at 6-8 weeks of age and attenuates the dramatic reduction in insulin levels observed 1-2 weeks later.
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In VitroCannabinoid receptor 1 (CB1R) antagonists appear to be promising drugs for the treatment of obesity, however, serious side effects have hampered their clinical application. Ibipinabant is a new, potent [Ki (CB1)=7.8 nM] and selective [Ki (CB2)=7.943 nM] CB1 antagonist [pA2 for arachidonic acid release in CHO cells=9.9] with in vitro pharmacological characteristics similar to rimonabant including inverse agonism and brain penetrance.
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In Vivo(±)-Ibipinabant ((±)-SLV319) (3 mg/kg) reduces unfasted glucose to a significantly greater degree than rimonabant at the same dose on days 17, 28 and 38. Chronic treatment with (±)-Ibipinabant ((±)-SLV319) significantly attenuates the progression of diabetes in ZDF rats, blunting the increase in blood glucose and HbA1c over time. Ibipinabant also reduces the hyperinsulinemia apparent at 6-8 weeks of age and attenuates the dramatic reduction in insulin levels observed 1-2 weeks later.
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Synonyms(±)-SLV319 | (±)-BMS6462
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PathwayOthers
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TargetOther Targets
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RecptorCB1
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Research Area——
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Indication——
Chemical Information
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CAS Number362519-49-1
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Formula Weight487.4
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Molecular FormulaC23H20Cl2N4O2S
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Purity>98% (HPLC)
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SolubilityDMSO : ≥ 31 mg/mL; 63.60 mM
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SMILESO=S(=O)(N=C(NC)N1CC(C(=N1)c2ccc(Cl)cc2)c3ccccc3)c4ccc(Cl)cc4
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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.Chorvat RJ, et al.Bioorg Med Chem Lett. 2012 Oct 1;22(19):6173-80.
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