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3258-02-4

中文名稱 N-羥基胞苷
英文名稱 N(4)-hydroxycytidine
CAS 3258-02-4
分子式 C9H13N3O6
分子量 259.22
MOL 文件 3258-02-4.mol
更新日期 2024/10/28 17:06:20
3258-02-4 結(jié)構(gòu)式 3258-02-4 結(jié)構(gòu)式

基本信息

中文別名
N-羥基胞苷
N-羥基胞苷(NHC(EIDD-1931))
英文別名
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
所屬類別
生物化工:抑制劑

物理化學(xué)性質(zhì)

熔點169-172 °C(Solv: methanol (67-56-1))
密度1.93±0.1 g/cm3(Predicted)
儲存條件Inert atmosphere,Store in freezer, under -20°C
溶解度可溶于DMSO(高達25mg/ml)或水(加熱時高達15mg/ml)。
酸度系數(shù)(pKa)8.19±0.20(Predicted)
形態(tài)固體
顏色白色
穩(wěn)定性DMSO或蒸餾水中的溶液可在-20°下穩(wěn)定儲存3個月。
N-羥基胞苷價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2024/08/19HY-125033N-羥基胞苷
EIDD-1931
3258-02-45mg250元
2024/08/19HY-125033N-羥基胞苷
EIDD-1931
3258-02-410mg350元
2024/08/19HY-125033N-羥基胞苷
EIDD-1931
3258-02-425mg700元

常見問題列表

生物活性
EIDD-1931 (Beta-d-N4-hydroxycytidine, β-d-N4-hydroxycytidine, NHC)是EIDD-2801的活性代謝產(chǎn)物,它是一種很有前途的 COVID-19 抑制劑。 EIDD-1931(NHC)對 SARS-CoV-2、MERS-CoV、SARS-CoV 和 related zoonotic group 2b或2c Bat-CoVs,對應(yīng)的平均IC50值為0.15 μM,并且對帶有對核苷類似物抑制劑remdesivir耐藥性突變的冠狀病毒的效力增強。
體外研究

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.

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