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Givinostat (ITF2357)

    
98.3%

Givinostat (ITF2357)

源葉(MedMol)
S80922 一鍵復制產品信息
732302-99-7
C24H30ClN3O5
475.97
(6-((diethylamino)methyl)naphthalen-2-yl)methyl 4-(hydroxycarbamoyl)phenylcarbamate hydrochloride hydrate
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S80922-1mg
98.3% ¥290.00 4 - - -
S80922-2mg
98.3% ¥510.00 5 - - -
S80922-5mg
98.3% ¥800.00 6 - - -
S80922-10mg
98.3% ¥1200.00 5 - - -
S80922-25mg
98.3% ¥1740.00 6 - - -
S80922-50mg
98.3% ¥2150.00 5 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

Givinostat hydrochloride monohydrate (ITF-2357 hydrochloride monohydrate) is a HDAC inhibitor with an IC50 of 198 and 157 nM for HDAC1 and HDAC3, respectively.

產品描述:

Givinostat hydrochloride monohydrate (ITF-2357 hydrochloride monohydrate) is a HDAC inhibitor with an IC50 of 198 and 157 nM for HDAC1 and HDAC3, respectively.

靶點: hHDAC3:157 nM (IC50);hHDAC1:198 nM (IC50);hHDAC11:292 nM (IC50);hHDAC6:315 nM (IC50);hHDAC2:325 nM (IC50);hHDAC10:340 nM (IC50);hHDAC7:524 nM (IC50);hHDAC5:532 nM (IC50);hHDAC9:541 nM (IC50);hHDAC8:854 nM (IC50);hHDAC4:1059 nM (IC50);HD1-B:7.5 nM (IC50);HD1-A ;16 nM (IC50);HD2 ;10 nM (IC50);HDAC
體內研究: Givinostat (ITF2357) at 10 mg/kg is used as a positive control and, as expected, reduced serum TNFα by 60%. Strikingly, pretreatment of ITF3056 starting at 0.1 mg/kg significantly reduces the circulating TNFα by nearly 90%. To achieve a significant increase in serum IL-1β production, a higher dose of LPS is injected (10 mg/kg), and blood is collected after 4 h. Similarly, when pretreated with lower doses of Givinostat (ITF2357) (1 or 5 mg/kg), there is a 22% reduction for 1 mg/kg and 40% for 5 mg/kg
參考文獻: 1. Li S, et al. Specific inhibition of histone deacetylase 8 reduces gene expression and production of proinflammatory cytokines in vitro and in vivo. J Biol Chem. 2015 Jan 23;290(4):2368-78. 2. Wang YG, et al. Givinostat inhibition of hepatic stellate cell proliferation and protein acetylation. World J Gastroenterol. 2015 Jul 21;21(27):8326-39. 3. Leoni F, et al. The histone deacetylase inhibitor ITF2357 reduces production of pro-inflammatory cytokines in vitro and systemic inflammation in vivo. Mol Med. 2005 Jan-Dec;11(1-12):1-15.
溶解性: Soluble  in  DMSO、H2O
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.101 ml 10.505 ml 21.01 ml
5 mM 0.42 ml 2.101 ml 4.202 ml
10 mM 0.21 ml 1.05 ml 2.101 ml
50 mM 0.042 ml 0.21 ml 0.42 ml
注意: 部分產品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。

參考文獻

質檢證書(COA)

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請輸入貨號和一個與之匹配的批號。
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批號:JS298415 貨號:S20001-25g
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摩爾濃度計算器

質量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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