3258-02-4

基本信息
N-羟基胞苷(NHC(EIDD-1931))
Uridine, 4-oxime
N-Hydroxycytidine
N(4)-hydroxycytidine
β-D-N4-Hydroxycytidine
Beta-d-N4-hydroxycytidine
EIDD2801 ,β-D-N4-hydroxycytidine
Beta-d-N4-hydroxycytidine (NHC)
3,4-Dihydro-1-β-D-ribofuranosyl-4-(hydroxyimino)pyrimidin-2(1H)-one
1-[(2R)-3α,4α-Dihydroxy-5β-(hydroxymethyl)oxolane-2β-yl]-4-(hydroxyamino)pyrimidine-2(1H)-one
物理化学性质
报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
2025/02/08 | HY-125033 | N-羟基胞苷 EIDD-1931 | 3258-02-4 | 5mg | 250元 |
2025/02/08 | HY-125033 | N-羟基胞苷 EIDD-1931 | 3258-02-4 | 10mg | 350元 |
2025/02/08 | HY-125033 | N-羟基胞苷 EIDD-1931 | 3258-02-4 | 25mg | 700元 |
常见问题列表
Beta-d-N4-hydroxycytidine is an anti-VEEV (venezuelan equine encephalitis virus) agent with EC 50 , EC 90 , and EC 99 are 0.426, 1.036, and 2.5 μM, respectively.Beta-d-N4-hydroxycytidine inhibits CHIKV replicon activity and the 50% effective concentration (EC 50 ) s 0.8 μM in the Huh-7–CHIKV replicon cell line. Similar results is presented with the replicon in BHK-21 cells (EC 50 =1.8 μM). NHC has no cytotoxicity for NHC in the Huh-7 cell culture system until up to 100 μM using MTT assays. The 50% cytotoxic concentration (CCsub>50) values for NHC are determined to be 30.6 μM, 7.7 μM, and 2.5 μM in peripheral blood mononuclear (PBM), Vero, and CEM cells, respectively.NHC behaves as a pyrimidine analog, NHC-mediated inhibition of the CHIKV replicon can be abrogated by the addition of exogenous nucleosides, such as pyrimidines C and U, but dA, dC, dG, dU, or T has no impact on the replicon. Pyrimidines A and G contributes to replicon inhibition both in the presence and in the absence of NHC.