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ROS

ROS

Reactive oxygen species (ROS) are chemically reactive chemical species containing oxygen. Examples include peroxides, superoxide, hydroxyl radical, singlet oxygen, and alpha-oxygen. The reduction of molecular oxygen (O2) produces superoxide (•O−2), which is the precursor of most other reactive oxygen species.In a biological context, ROS are formed as a natural byproduct of the normal metabolism of oxygen and have important roles in cell signaling and homeostasis. However, during times of environmental stress (e.g., UV or heat exposure), ROS levels can increase dramatically.
TargetMol
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Cat. No. Product Name CAS No. Purity Chemical Structure
TN3653 Cimidahurinine
化合物 TN3653
142542-89-0 98%
TargetMol Chemical Structure Cimidahurinine
Cimidahurinine can attenuate Doxorubicin (DOX)-induced cardiotoxicity in a dose-dependent manner with EC50 values of 45.79 uM; it protects against cardiotoxicity...
TMA0291 Dehydroglyasperin D
化合物 TMA0291
517885-72-2 98%
TargetMol Chemical Structure Dehydroglyasperin D
Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 h...
TN1241 3,8''-Biapigenin
化合物3,8'-Biapigenin
101140-06-1 98%
TargetMol Chemical Structure 3,8''-Biapigenin
3, 8''-Biapigenin can modulate intracellular ROS production.
TN4399 Kushenol C
化合物 TN4399
99119-73-0 98%
TargetMol Chemical Structure Kushenol C
Kushenol C is a good 1,1-diphenyl-2-picrylhydrazyl (DPPH) scavenger, and it exhibits inhibitory activity against Sodium-dependent glucose cotransporter 2(SGLT2)....
TN3726 Cudraflavone B
化合物 TN3726
19275-49-1 98%
TargetMol Chemical Structure Cudraflavone B
Cudraflavone B has anti-proliferative activity, mouse brain monoamine oxidase (MAO) inhibitory effects, apoptotic actions in human gastric carcinoma cells and mo...
TN3364 Agrimonolide
仙鹤草内酯
21499-24-1 98%
TargetMol Chemical Structure Agrimonolide
Agrimonolide 是一种来自异香豆素的化合物,主要存在于草药Agrimonia pilosa Ledeb 中,具有显著的生物活性。Agrimonolide 通过抑制脂多糖(LPS)诱导的JAK-STATs 和p38 MAPKs 信号通路的激活而发挥抗炎作用。Agrimonolide 及其衍生物去甲阿戈莫内德已显示...
TN3872 Diosbulbin D
化合物 TN3872
66756-57-8 98%
TargetMol Chemical Structure Diosbulbin D
Diosbulbin D shows direct toxic effect on hepatocytes, the mechanism could be associated with oxidative stress.
TN1821 Kaempferol 3-O-arabinoside
山奈酚-3-O-α-L-吡喃阿拉伯糖苷
99882-10-7 98%
TargetMol Chemical Structure Kaempferol 3-O-arabinoside
Kaempferol-3-O-α±-D-arabinoside displays cytotoxic and high antioxidant activity.Kaempferol-3-O-arabinoside and kaempferol-3-O-glucoside can function as antioxid...
TN5264 Xanthoxyletin
化合物 TN5264
84-99-1 98%
TargetMol Chemical Structure Xanthoxyletin
Xanthoxyletin shows potent antibacterial, fungicidal, and algicidal properties, it also has anticancer, and anti-inflammatory activities. It shows an inhibitory ...
T5526 Glycoborinine
化合物 T5526
233279-39-5 98%
TargetMol Chemical Structure Glycoborinine
Glycoborinine is a potential molecule against cancer cells, it can induce HepG2 apoptosis through the mitochondrial-dependent pathway. Glycoborinine has photo-ac...
TN1910 Malvidin chloride
氯化锦葵色素
643-84-5 98%
TargetMol Chemical Structure Malvidin chloride
Malvidin chloride has anti-spermatogenic, and antioxidant activities. It can prevent endothelial dysfunction by inhibiting ROS and XO-1.
TN3517 Bisacurone
化合物 TN3517
120681-81-4 98%
TargetMol Chemical Structure Bisacurone
Bisacurone has anti-oxidant, anti-inflammatory, and anti-metastatic activities, it may have a protective effect against ethanol-induced liver injury by suppressi...
TN3614 Cearoin
化合物 TN3614
52811-37-7 98%
TargetMol Chemical Structure Cearoin
Cearoin has anti-inflammatory, and antiallergic activities, it can markedly inhibit inflammatory responses including LPS-induced NO production by suppressing the...
TN4785 Picrasidine I
化合物 TN4785
100234-59-1 98%
TargetMol Chemical Structure Picrasidine I
Picrasidine I has antiosteoclastogenic effect by inhibiting inflammation induced activation of MAPKs, NF-κB and ROS generation followed by suppressing the gene ...
TN3655 Cimiside E
化合物 TN3655
154822-57-8 98%
TargetMol Chemical Structure Cimiside E
Cimiside E has anti-inflammatory activity, it selectively inhibits TNF-α-induced expression of VCAM-1 at least by upregulation of PPAR-γ, and signals for ERK1/2,...
T22318 Taletrectinib
化合物DS-6051b
1505515-69-4 99.96%
TargetMol Chemical Structure Taletrectinib
Taletrectinib (AB-106) 是具有口服活力的、选择性的 ROS1/NTRK 抑制剂。它对重组 ROS1、NTRK1、NTRK2 和 NTRK3 有较强的抑制作用,IC50值分别为 0.207、0.622、2.28 和 0.98 nM。它还抑制 ROS1 G2032R 和其他抗 Crizotinib 的 ...
T0877 Gallic acid
没食子酸
149-91-7 99.95%
TargetMol Chemical Structure Gallic acid
Gallic acid (Benzoic acid) 是一种天然多羟基酚类化合物,具有抑制环氧合酶-2 的自由基清除作用,还具有抗菌、抗氧化、抗菌、抗炎和抗肿瘤活性。
T3061 Lorlatinib
劳拉替尼
1454846-35-5 99.93%
TargetMol Chemical Structure Lorlatinib
Lorlatinib (PF-6463922) 是一种具有口服活性,选择性,脑渗透性和 ATP 竞争性的ROS1/ALK 抑制剂,具有抗癌活性。它对 ROS1、野生型 ALK 和 ALKL1196M 的Ki 值分别为 <0.025 nM、<0.07 nM 和 0.7 nM。
T4309 CIL56
化合物CIL56
300802-28-2 99.91%
TargetMol Chemical Structure CIL56
CIL56 (CA3) 是一种选择性铁死亡诱导剂,可通过产生铁依赖性活性氧来诱导细胞铁死亡。
T1630 Tiopronin
硫普罗宁
1953-02-2 99.87%
TargetMol Chemical Structure Tiopronin
Tiopronin (Acadione) 是可扩散的抗氧化剂,是重金属中毒的解毒剂和辐射防护剂。它可控制胱氨酸沉淀和排泄的速度,有用于胱氨酸尿症、类风湿性关节炎和肝病的研究潜力。
Cimidahurinine
TN3653
Cimidahurinine can attenuate Doxorubicin (DOX)-induced cardiotoxicity in a dose-dependent manner with EC50 values of 45.79 uM; it protects against cardiotoxicity...
Dehydroglyasperin D
TMA0291
Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 h...
3,8''-Biapigenin
TN1241
3, 8''-Biapigenin can modulate intracellular ROS production.
Kushenol C
TN4399
Kushenol C is a good 1,1-diphenyl-2-picrylhydrazyl (DPPH) scavenger, and it exhibits inhibitory activity against Sodium-dependent glucose cotransporter 2(SGLT2)....
Cudraflavone B
TN3726
Cudraflavone B has anti-proliferative activity, mouse brain monoamine oxidase (MAO) inhibitory effects, apoptotic actions in human gastric carcinoma cells and mo...
Agrimonolide
TN3364
Agrimonolide 是一种来自异香豆素的化合物,主要存在于草药Agrimonia pilosa Ledeb 中,具有显著的生物活性。Agrimonolide 通过抑制脂多糖(LPS)诱导的JAK-STATs 和p38 MAPKs 信号通路的激活而发挥抗炎作用。Agrimonolide 及其衍生物去甲阿戈莫内德已显示...
Diosbulbin D
TN3872
Diosbulbin D shows direct toxic effect on hepatocytes, the mechanism could be associated with oxidative stress.
Kaempferol 3-O-arabinoside
TN1821
Kaempferol-3-O-α±-D-arabinoside displays cytotoxic and high antioxidant activity.Kaempferol-3-O-arabinoside and kaempferol-3-O-glucoside can function as antioxid...
Xanthoxyletin
TN5264
Xanthoxyletin shows potent antibacterial, fungicidal, and algicidal properties, it also has anticancer, and anti-inflammatory activities. It shows an inhibitory ...
Glycoborinine
T5526
Glycoborinine is a potential molecule against cancer cells, it can induce HepG2 apoptosis through the mitochondrial-dependent pathway. Glycoborinine has photo-ac...
Malvidin chloride
TN1910
Malvidin chloride has anti-spermatogenic, and antioxidant activities. It can prevent endothelial dysfunction by inhibiting ROS and XO-1.
Bisacurone
TN3517
Bisacurone has anti-oxidant, anti-inflammatory, and anti-metastatic activities, it may have a protective effect against ethanol-induced liver injury by suppressi...
Cearoin
TN3614
Cearoin has anti-inflammatory, and antiallergic activities, it can markedly inhibit inflammatory responses including LPS-induced NO production by suppressing the...
Picrasidine I
TN4785
Picrasidine I has antiosteoclastogenic effect by inhibiting inflammation induced activation of MAPKs, NF-κB and ROS generation followed by suppressing the gene ...
Cimiside E
TN3655
Cimiside E has anti-inflammatory activity, it selectively inhibits TNF-α-induced expression of VCAM-1 at least by upregulation of PPAR-γ, and signals for ERK1/2,...
Taletrectinib
T22318
Taletrectinib (AB-106) 是具有口服活力的、选择性的 ROS1/NTRK 抑制剂。它对重组 ROS1、NTRK1、NTRK2 和 NTRK3 有较强的抑制作用,IC50值分别为 0.207、0.622、2.28 和 0.98 nM。它还抑制 ROS1 G2032R 和其他抗 Crizotinib 的 ...
Gallic acid
T0877
Gallic acid (Benzoic acid) 是一种天然多羟基酚类化合物,具有抑制环氧合酶-2 的自由基清除作用,还具有抗菌、抗氧化、抗菌、抗炎和抗肿瘤活性。
Lorlatinib
T3061
Lorlatinib (PF-6463922) 是一种具有口服活性,选择性,脑渗透性和 ATP 竞争性的ROS1/ALK 抑制剂,具有抗癌活性。它对 ROS1、野生型 ALK 和 ALKL1196M 的Ki 值分别为 <0.025 nM、<0.07 nM 和 0.7 nM。
CIL56
T4309
CIL56 (CA3) 是一种选择性铁死亡诱导剂,可通过产生铁依赖性活性氧来诱导细胞铁死亡。
Tiopronin
T1630
Tiopronin (Acadione) 是可扩散的抗氧化剂,是重金属中毒的解毒剂和辐射防护剂。它可控制胱氨酸沉淀和排泄的速度,有用于胱氨酸尿症、类风湿性关节炎和肝病的研究潜力。
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