NGI-1
CAS No. 790702-57-7
NGI-1( ML414 )
Catalog No. M20759 CAS No. 790702-57-7
NGI-1 is a a cell-permeable inhibitor of oligosaccharyltransferase (OST).can effectively reduce virus infectivity without affecting cell viability.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 60 | In Stock |
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| 2MG | 34 | In Stock |
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| 5MG | 54 | In Stock |
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| 10MG | 88 | In Stock |
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| 25MG | 148 | In Stock |
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| 50MG | 217 | In Stock |
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| 100MG | 322 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameNGI-1
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NoteResearch use only, not for human use.
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Brief DescriptionNGI-1 is a a cell-permeable inhibitor of oligosaccharyltransferase (OST).can effectively reduce virus infectivity without affecting cell viability.
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DescriptionNGI-1 is a a cell-permeable inhibitor of oligosaccharyltransferase (OST).can effectively reduce virus infectivity without affecting cell viability.
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In VitroNGI-1 inhibits the glycosylation of LASV GP mediated by STT3A-OST (in STT3B- and MAGT1-TUSC3- cells) or STT3B-OST (in STT3A- cells) and impaires its proteolytic cleavage in a dose-dependent manner.NGI-1 blocks EGFR N-linked glycosylation in lung adenocarcinoma cells as assessed. In controls EGFR is biotinylated, consistent with its plasma membrane expression, but in NGI-1 treated cells the EGFR is predominantly found in the non-biotinylated intracellular fraction suggesting a change in cellular localization. Western Blot Analysis Cell Line:STT3A-, STT3B- and MAGT1-TUSC3- cellsConcentration:1, 2, 5 μM Incubation Time:36 hours Result:Inhibited the glycosylation of LASV GP mediated by STT3A-OST (in STT3B- and MAGT1-TUSC3- cells) or STT3B-OST (in STT3A- cells) and impaired its proteolytic cleavage in a dose-dependent manner.
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In Vivo——
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SynonymsML414
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PathwayOthers
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TargetOther Targets
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Recptoroligosaccharyltransferase
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Research Area——
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Indication——
Chemical Information
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CAS Number790702-57-7
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Formula Weight394.51
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Molecular FormulaC17H22N4O3S2
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Purity>98% (HPLC)
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SolubilityDMSO:160 mg/mL (405.57 mM)
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SMILESCN(C)S(=O)(=O)c1ccc(N2CCCC2)c(c1)C(=O)Nc1ncc(C)s1
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Chemical Name5-(dimethylsulfamoyl)-N-(5-methyl-13-thiazol-2-yl)-2-(pyrrolidin-1-yl)benzamide
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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Rosuvastatin lactone
Rosuvastatin lactone is the lactone form of the HMG-CoA reductase inhibitor rosuvastatin. It is found in vivo following rosuvastatin administration.
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Betulinic acid methy...
Betulinic acid methyl ester showed antiplasmodial activity against chloroquine-resistant Plasmodium falciparum parasites in vitro.It also inhibited B16 2F2 cell proliferation by induction of apoptosis.
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