V-0219
CAS No. 878453-71-5
V-0219( —— )
Catalog No. M28512 CAS No. 878453-71-5
V-0219 is a positive allosteric modulator of GLP-1 and can be used in studies about obesity-associated diabetes.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 191 | In Stock |
|
| 10MG | 327 | In Stock |
|
| 25MG | 604 | In Stock |
|
| 50MG | 906 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameV-0219
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NoteResearch use only, not for human use.
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Brief DescriptionV-0219 is a positive allosteric modulator of GLP-1 and can be used in studies about obesity-associated diabetes.
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DescriptionV-0219 is a positive allosteric modulator of GLP-1 and can be used in studies about obesity-associated diabetes.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayGPCR/G Protein
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TargetGlucagon Receptor
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number878453-71-5
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Formula Weight410.43
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Molecular FormulaC20H25F3N4O2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (243.65 mM)
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SMILESFC(F)(F)C=1C=CC(=CC1)C2=NOC(=N2)CN3CCCC(C3)CN4CCOCC4
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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
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MK-3577
A potent, oral active glucagon receptor antagonist blocking the glucagon effect for the treatment of T2DM.
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Semaglutide Acetate
Semaglutide Acetate is an agonist of a glucagon-like peptide 1 (GLP-1) receptor and can be used in studies about the treatment of type 2 diabetes.
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Bay 55-9837
Selective VPAC2 receptor agonist (EC50 values are 0.4, 100 and >1000 nM for VPAC2, VPAC1 and PAC1, respectively in a cAMP accumulation assay; IC50 values are 60, 8700 and >10000 nM for VPAC2, VPAC1 and PAC1, respectively in a competition binding assay). Stimulates glucose-dependent insulin secretion in isolated human pancreatic islets. Reduces HIV-1 viral replication and shows cooperative effects when given in conjunction with VPAC1 agonists.
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