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 |
| 2MG | 32 | In Stock |
|
| 5MG | 51 | In Stock |
|
| 10MG | 84 | In Stock |
|
| 50MG | 210 | In Stock |
|
| 100MG | 311 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameNGI-1
-
NoteResearch use only, not for human use.
-
Brief DescriptionNGI-1 is a a cell-permeable inhibitor of oligosaccharyltransferase (OST).can effectively reduce virus infectivity without affecting cell viability.
-
DescriptionNGI-1 is a a cell-permeable inhibitor of oligosaccharyltransferase (OST).can effectively reduce virus infectivity without affecting cell viability.
-
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.
-
In Vivo——
-
SynonymsML414
-
PathwayOthers
-
TargetOther Targets
-
Recptoroligosaccharyltransferase
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number790702-57-7
-
Formula Weight394.51
-
Molecular FormulaC17H22N4O3S2
-
Purity>98% (HPLC)
-
SolubilityDMSO:160 mg/mL (405.57 mM)
-
SMILESCN(C)S(=O)(=O)c1ccc(N2CCCC2)c(c1)C(=O)Nc1ncc(C)s1
-
Chemical Name5-(dimethylsulfamoyl)-N-(5-methyl-13-thiazol-2-yl)-2-(pyrrolidin-1-yl)benzamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Lopez-Sambrooks C Shrimal S Khodier C et al. Oligosaccharyltransferase inhibition induces senescence in RTK-driven tumor cells[J]. Nature Chemical Biology 2016.
molnova catalog
related products
-
RLX-33
RLX-33 is a potent and selective antagonist of relaxin family peptide 3 (RXFP3) that crosses the blood-brain barrier and also blocks relaxin 3-induced ERK1/2 phosphorylation.
-
WSB1 Degrader 1
WSB1 Degrader 1 is a poten and orally active?WD repeat and SOCS box-containing 1 degrader. WSB1 Degrader 1 has anticancer metastatic effects.
-
5-Bromo-4-chloro-3-i...
5-Bromo-4-chloro-3-indoxyl-beta-D-cellobioside is a chromogenic compound used to detect cellobiohydrolases.
Cart
sales@molnova.com