NGI-1
CAS No. 790702-57-7
NGI-1 ( ML414 )
产品货号. M20759 CAS No. 790702-57-7
NGI-1是一种细胞渗透性寡糖转移酶(OST)抑制剂,可有效降低病毒感染性而不影响细胞活力。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥253 | 有现货 |
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| 5MG | ¥397 | 有现货 |
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| 10MG | ¥626 | 有现货 |
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| 25MG | ¥1004 | 有现货 |
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| 50MG | ¥1516 | 有现货 |
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| 100MG | ¥2178 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥437 | 有现货 |
|
生物学信息
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产品名称NGI-1
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述NGI-1是一种细胞渗透性寡糖转移酶(OST)抑制剂,可有效降低病毒感染性而不影响细胞活力。
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产品描述NGI-1 is a a cell-permeable inhibitor of oligosaccharyltransferase (OST).can effectively reduce virus infectivity without affecting cell viability.
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体外实验NGI-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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体内实验——
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同义词ML414
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通路Others
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靶点Other Targets
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受体oligosaccharyltransferase
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研究领域——
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适应症——
化学信息
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CAS Number790702-57-7
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分子量394.51
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分子式C17H22N4O3S2
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纯度>98% (HPLC)
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溶解度DMSO: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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化学全称5-(dimethylsulfamoyl)-N-(5-methyl-13-thiazol-2-yl)-2-(pyrrolidin-1-yl)benzamide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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2-Hydroxychalcone B
2'-Hydroxychalcone is a drug synthesis intermediate for the synthesis of flavonoids. 2'-Hydroxychalcone loaded in nanoemulsion showed fungicidal activity against Coccidioides parapsilosis in Danio rerio model.2'-Hydroxychalcone induced cytotoxicity through oxidative stress in lipid-loaded Hepg2 cells.2'-Hydroxychalcone inhibited the induction of ICAM-1, VCAM-α, tumor necrosis factor-α, and tumor necrosis factor-alpha as determined by reverse transcription-polymerase chain reaction determined by tumor necrosis factor-alpha induces steady-state transcript levels of ICAM-1, VCAM-1, and E-selectin, and therefore may interfere with the transcription of their genes.
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Aristololactam IIIa
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Naringin dihydrochal...
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