
Tinoridine hydrochloride
CAS No. 25913-34-2
Tinoridine hydrochloride ( Y-3642 hydrochloride )
产品货号. M18320 CAS No. 25913-34-2
Tinoridine (Y-3642) 是一种非甾体抗炎药。 Tinoridine (5-100 μM) 对肾素颗粒部分中 50 μM 抗坏血酸诱导的脂质过氧化物形成和肾素释放同时增加产生浓度依赖性抑制。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥389 | 有现货 |
![]() ![]() |
5MG | ¥648 | 有现货 |
![]() ![]() |
10MG | ¥1037 | 有现货 |
![]() ![]() |
25MG | ¥1920 | 有现货 |
![]() ![]() |
50MG | ¥3102 | 有现货 |
![]() ![]() |
100MG | ¥4496 | 有现货 |
![]() ![]() |
200MG | 获取报价 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称Tinoridine hydrochloride
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述Tinoridine (Y-3642) 是一种非甾体抗炎药。 Tinoridine (5-100 μM) 对肾素颗粒部分中 50 μM 抗坏血酸诱导的脂质过氧化物形成和肾素释放同时增加产生浓度依赖性抑制。
-
产品描述Tinoridine (Y-3642) is a non-steroidal anti-inflammatory drug. Tinoridine (5-100 μM), produced a concentration-dependent inhibition on the simultaneous increases in lipid peroxide formation and renin release induced by 50 μM ascorbic acid in the renin granule fraction. On the other hand, indomethacin, hydrocortisone, and prednisolone, which had no ability to inhibit the lipid peroxidation in the renin granule fraction, did not influence the release of renin from the granules. These results suggest that tinoridine suppresses renin release by inhibiting the oxidative disintegration of membranes of renin granules.(In Vitro):Tinoridine reduces a stable free radical, diphenyl-p-picrylhydrazyl, in the molar ratio of about 1:2, indicating its free radical scavenging ability. Tinoridine inhibits the lipid peroxidation in rat liver microsomes induced by xanthine-xanthine oxidase system in the presence of ADP and Fe2+, in which hydroxyl radical is formed. Tinoridine is demonstrated to be oxidized in the course of the lipid peroxidation by following the fluorescence derived from the oxidation product of tinoridine. It is also oxidized by the xanthine-xanthine oxidase system in the presence of Fe2+, but its oxidation is slow in the absence of Fe2+ and almost completely inhibited by catalase. Tinoridine is also oxidized by H2O2-Fe2+ system producing OH (Fenton reaction), but it does not affect the reduction of cytochrome c caused by superoxide radical.(In Vivo):CCl4 aministration produces a marked decrease in the concentrations of liver microsomal cytochrome P-450 and G6Pase, indicating that hepatic endoplasmic reticulum function is disrupted. Prior treatment of the animals with tinoridine (100 mg/kg) significantly reduces the CCl4-induced alterations in the enzyme activities, and a rapid recovery toward the normal values is observed.
-
体外实验Tinoridine reduces a stable free radical, diphenyl-p-picrylhydrazyl, in the molar ratio of about 1:2, indicating its free radical scavenging ability. Tinoridine inhibits the lipid peroxidation in rat liver microsomes induced by xanthine-xanthine oxidase system in the presence of ADP and Fe2+, in which hydroxyl radical is formed. Tinoridine is demonstrated to be oxidized in the course of the lipid peroxidation by following the fluorescence derived from the oxidation product of tinoridine. It is also oxidized by the xanthine-xanthine oxidase system in the presence of Fe2+, but its oxidation is slow in the absence of Fe2+ and almost completely inhibited by catalase. Tinoridine is also oxidized by H2O2-Fe2+ system producing OH (Fenton reaction), but it does not affect the reduction of cytochrome c caused by superoxide radical.
-
体内实验CCl4 aministration produces a marked decrease in the concentrations of liver microsomal cytochrome P-450 and G6Pase, indicating that hepatic endoplasmic reticulum function is disrupted. Prior treatment of the animals with tinoridine (100 mg/kg) significantly reduces the CCl4-induced alterations in the enzyme activities, and a rapid recovery toward the normal values is observed.
-
同义词Y-3642 hydrochloride
-
通路Others
-
靶点Other Targets
-
受体COX
-
研究领域Inflammation/Immunology
-
适应症——
化学信息
-
CAS Number25913-34-2
-
分子量352.88
-
分子式C17H21ClN2O2S
-
纯度>98% (HPLC)
-
溶解度DMSO : ≥ 31 mg/mL; 87.85 mM
-
SMILESO=C(C1=C(N)SC2=C1CCN(CC3=CC=CC=C3)C2)OCC.Cl
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Kalariya PD, etal. J Mass Spectrom. 2015 Nov;50(11):1222-33
产品手册




关联产品
-
2,6-Dihydroxyacetoph...
The herbs of Phyllanthus urinaria L.
-
LQZ-7I
LQZ-7I 是一种存活靶向抑制剂。它口服可有效抑制异种移植肿瘤的生长并诱导肿瘤中生存素的丧失。
-
Beta-Tocotrienol
Beta-Tocotrienol to serve as a new anticancer agent for treating human lung and brain cancers. It inhibits the growth of both A549 (GI50=1.38±0.334μM) and U87MG (GI50=2.53±0.604μM) cells at rather low concentrations.