69839-83-4

中文名稱 3,4-二羥基苯甲羥肟酸

英文名稱 dido

CAS 69839-83-4

分子式 C7H7NO4

分子量 169.13

MOL 文件 69839-83-4.mol

更新日期 2026/07/08 16:27:09

69839-83-4 結(jié)構(gòu)式

基本信息物理化學(xué)性質(zhì) 安全數(shù)據(jù) 圖譜信息 3,4-二羥基苯甲羥肟酸價(jià)格(試劑級(jí)) 常見問題列表

基本信息

中文別名

4-二羥基苯甲羥肟酸
3,4-二羥基苯甲羥肟酸

英文別名

dido
Didox
NSC-324360
Didox, NSC-324360
Didox Exclusive
4-Trihydroxybenzamide
N,3,4-trihydroxybenzamide
Benzamide, N,3,4-trihydroxy-
3,4-dihydroxybenzohydroxamic acid

所屬類別

生物化工：激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

熔點(diǎn)207 °C

密度1.571±0.06 g/cm3(Predicted)

儲(chǔ)存條件Inert atmosphere,Store in freezer, under -20°C

溶解度DMSO:60.0(Max Conc. mg/mL);354.76(Max Conc. mM)
DMF:20.0(Max Conc. mg/mL);118.25(Max Conc. mM)
Ethanol:20.0(Max Conc. mg/mL);118.25(Max Conc. mM)
PBS (pH 7.2):10.0(Max Conc. mg/mL);59.13(Max Conc. mM)

酸度系數(shù)(pKa)8.16±0.20(Predicted)

形態(tài)結(jié)晶固體

顏色Light yellow to khaki

InChIInChI=1S/C7H7NO4/c9-5-2-1-4(3-6(5)10)7(11)8-12/h1-3,9-10,12H,(H,8,11)

InChIKeyQJMCKEPOKRERLN-UHFFFAOYSA-N

SMILESC(NO)(=O)C1=CC=C(O)C(O)=C1

安全數(shù)據(jù)

毒性LD10 unreported in mouse: 643mg/kg

圖譜信息

3,4-二羥基苯甲羥肟酸(69839-83-4)核磁圖(¹HNMR)

3,4-二羥基苯甲羥肟酸價(jià)格(試劑級(jí))

報(bào)價(jià)日期	產(chǎn)品編號(hào)	產(chǎn)品名稱	CAS號(hào)	包裝	價(jià)格
2026/06/05	HY-19387R	3,4-二羥基苯甲羥肟酸 Didox (Standard)	69839-83-4	5 mg	1200元
2026/06/05	HY-19387R	3,4-二羥基苯甲羥肟酸 Didox (Standard)	69839-83-4	10 mg	1800元
2026/06/05	HY-19387R	3,4-二羥基苯甲羥肟酸 Didox (Standard)	69839-83-4	25 mg	3500元

常見問題列表

生物活性

Didox (NSC-324360) 是一種合成的核糖核苷酸還原酶 (ribonucleotide reductase, RR) 抑制劑。

靶點(diǎn)

Ribonucleotide reductase

體外研究

Didox (NSC-324360) suppresses LPS-induced mRNA levels of iNOS, IL-6, IL-1, TNF-α, NF-κβ (p65), and p38-α, after 24 h of treatment. Treatment with Didox also suppresses the secretion of nitric oxide (NO), IL-6, and IL-10. Using mitochondrial dehydrogenase activity as a measure of cytotoxicity, the effects of Didox on cellular respiration in RAW264.7 are examined over a range of concentrations for 24 h. Cells exposures to 200 μM and below Didox, with and without LPS, do not exhibit significant cellular toxicity. Didox (NSC-324360) is active against all human and murine acute myeloid leukemia (AML) lines tested with IC ₅₀ values in the low micromolar range (mean IC ₅₀ 37 μM [range 25.89-52.70 μM]).

體內(nèi)研究

Once engraftment is established by bioluminescent imaging, the animals receive daily administrations of Didox at 425 mg/kg via IP injection over 5 days. Didox (NSC-324360) treatment significantly reduces leukemic burden compared to vehicle treated controls (p=0.0026 and p=0.0342). More importantly, Didox (NSC-324360) provides a significant survival benefit (p<0.0001 and p=0.0094).