1,4-二氧代-2,3-二溴甲基喹啉
| 中文名称 | 1,4-二氧代-2,3-二溴甲基喹啉 |
|---|---|
| 中文同义词 | 1,4-二氧代-2,3-二溴甲基喹啉;1,4-二氧代-2,3-二溴甲基喹喔啉;1,4-二氧代-2,3-二溴甲基喹啉,10 MM DMSO 溶液;Conoidin A /抗氧化蛋白Prx I&II抑制剂/Peroxiredoxins,Prxs/18080-67-6;Conoidin A /抗氧化蛋白Prx I&II抑制剂/Peroxiredoxins,Prxs/18080-67-6;2,3-二溴甲基喹喔啉1,4-二氧化物;Conoidin A【CAS:18080-67-6】【规格:100mg】【纯度:98%】;Conoidin A【CAS:18080-67-6】【规格:100mg】【纯度:98%】 |
| 英文名称 | 2,3-BIS(BROMOMETHYL)QUINOXALINE 1,4-DIOXIDE |
| 英文同义词 | 2,3-BIS(BROMOMETHYL)QUINOXALINE 1,4-DIOXIDE;2,3-bis(broMoMethyl)-1-oxoquinoxalin-1-iuM-4(1H)-olate;Conoidin A;Quinoxaline, 2,3-bis(bromomethyl)-, 1,4-dioxide;antioxidative,antioxidant,heart disease,Parasite,Inhibitor,Peroxiredoxin II,hyperperoxidation,Conoidin A,ischaemic,inhibit,neuroprotective;Conoidin A, 10 mM in DMSO;Peroxiredoxin Inhibitor, Conoidin A;1,4-Dioxo-2,3-dibromomethylquinoline |
| CAS号 | 18080-67-6 |
| 分子式 | C10H8Br2N2O2 |
| 分子量 | 347.99 |
| EINECS号 | |
| 相关类别 | |
| Mol文件 | 18080-67-6.mol |
| 结构式 | ![]() |
1,4-二氧代-2,3-二溴甲基喹啉 性质
| 熔点 | 180-190 °C (decomp) |
|---|---|
| 沸点 | 512.3±60.0 °C(Predicted) |
| 密度 | 1.95±0.1 g/cm3(Predicted) |
| 储存条件 | -20°C |
| 溶解度 | DMF:25mg/mL; DMF:PBS(pH 7.2)(1:1):0.5 mg/ml;二甲基亚砜:20mg/mL |
| 形态 | 结晶固体 |
| 酸度系数(pKa) | 1.91±0.30(Predicted) |
| 颜色 | 白色至黄色 |
| InChI | 1S/C10H8Br2N2O2/c11-5-9-10(6-12)14(16)8-4-2-1-3-7(8)13(9)15/h1-4H,5-6H2 |
| InChIKey | DQKNFTLRMZOAMG-UHFFFAOYSA-N |
| SMILES | BrCC1=C(N(c2c(cccc2)[N+]1=O)[O-])CBr |
IC50: 23 µM ( T. gondii enzyme peroxiredoxin II (TgPrxII))
Peroxiredoxins are a widely conserved family of enzymes that function in antioxidant defense and signal transduction. And the changes in PrxII expression are associated with a variety of human diseases, including cancer.Conoidin A binds to the peroxidatic cysteine of TgPrxII, inhibiting its enzymatic activity in vitro. Conoidin A also shown to alkylate or crosslink catalytic cysteines of wild type AcePrx-1 in Ancylostoma ceylanicum and human PrxII and PrxIV with similar efficiency. But it is ineffective to mitochondrial hPrxIII.Conoidin A (5 µM) can inhibit the glucose oxidase-mediated hyperoxidation of mammalian peroxiredoxin I and II.
Conoidin A (intraperitoneal injection; 5 mg/kg; for three successive days before MI/R injury) blocks the effect of Luteolin (HY-N0162) on the ST‐segment elevation. Furthermore, an increase in the infarct size presented of the MI/R group can be reduced by Luteolin. But pre‐treatment with conoidin A abolishs the effect of Luteolin. Pre‐treatment with conoidin A also prevents Luteolin-reduced activities of CK‐MB, AST and LDH in vivo .
| Animal Model: | Rat myocardial I/R model |
| Dosage: | 5 mg/kg |
| Administration: | Intraperitoneal injection; 5 mg/kg; for three successive days before MI/R injury |
| Result: | Significantly reversed the antioxidative effect of Luteolin. Impaired the protective effects of luteolin. |
安全信息
| WGK Germany | WGK 3 |
|---|---|
| 存储类别 | 11 - 可燃固体 |
| 危险性类别 | 危害水生环境-长期危害 类别4 |
| 更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
|---|---|---|---|---|---|
| 2026/06/05 | HY-116090 | 1,4-二氧代-2,3-二溴甲基喹啉 Conoidin A | 18080-67-6 | 10 mg | 323元 |
| 2026/06/05 | HY-116090 | 1,4-二氧代-2,3-二溴甲基喹啉 Conoidin A | 18080-67-6 | 10mM * 1mLin DMSO | 355元 |
