VUN65671
CAS No. 2479465-67-1
VUN65671( —— )
Catalog No. M28888 CAS No. 2479465-67-1
VUN65671is a Potent Entry Inhibitor of Ebola and Marburg Virus Infections. VUN65671 was reported in Journal of Medicinal Chemistry (2020), 63(13), 7211-7225. This product has no formal name at the moment.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 112 | In Stock |
|
| 5MG | 169 | In Stock |
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| 10MG | 257 | In Stock |
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| 25MG | 426 | In Stock |
|
| 50MG | 586 | In Stock |
|
| 100MG | 792 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 1572 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameVUN65671
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NoteResearch use only, not for human use.
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Brief DescriptionVUN65671is a Potent Entry Inhibitor of Ebola and Marburg Virus Infections. VUN65671 was reported in Journal of Medicinal Chemistry (2020), 63(13), 7211-7225. This product has no formal name at the moment.
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DescriptionVUN65671is a Potent Entry Inhibitor of Ebola and Marburg Virus Infections. VUN65671 was reported in Journal of Medicinal Chemistry (2020), 63(13), 7211-7225. This product has no formal name at the moment.
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In VitroEBOV/MARV-IN-1 (12.5 μM; 48 h) inhibits HIV/EBOV-GP (EC50=12 nM) and HIV/MARV-GP (EC50=180 nM) pseudotype virus in A549 cells containing a luciferase reporter gene, with low cytotoxicity (SI =2088).
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorSGLT2
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Research Area——
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Indication——
Chemical Information
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CAS Number2479465-67-1
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Formula Weight461.52
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Molecular FormulaC25H30F3N3O2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (216.68 mM)
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SMILESCC1CCN(CC1)C1=CC=C(NC(=O)C2=CC=C(CN3CCOCC3)C=C2)C=C1C(F)(F)F
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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.Hussey EK, et al. Multiple-dose pharmacokinetics and pharmacodynamics of sergliflozin etabonate, a novel inhibitor of glucose reabsorption, in healthy overweight and obese subjects: a randomized double-blind study. J Clin Pharmacol. 2010 Jun;50(6):636-46.
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