首页 工具
登录
购物车
COX

COX

Cyclooxygenase (COX), officially known as prostaglandin-endoperoxide synthase (PTGS), is an enzyme (specifically, a family of isozymes) that is responsible for formation of prostanoids, including thromboxane and prostaglandins such as prostacyclin, from arachidonic acid. A member of the animal-type heme peroxidase family, it is also known as prostaglandin G/H synthase.
1 2 3 4 5 ... 20
Cat. No. Product Name CAS No. Purity Chemical Structure
T3P2855 Chamigrenal
恰米醛
19912-84-6
β-Chamigrenal has anti-inflammatory activity, it has inhibitory effects on lipopolysaccharide-induced nitric oxide and prostaglandin E2 production in RAW 264.7 m...
TN4592 Murrangatin
化合物 TN4592
37126-91-3 98%
Murrangatin may be a valuable anti-tumor-promoting agent, it can significantly inhibit Epstein-Barr virus early antigen (EBV-EA) activation, and preserve the hig...
TN5248 Voleneol
化合物 TN5248
70389-88-7 98%
1β,6α-Dihydroxyeudesm-4(15)-ene (Voleneol,DE) can attenuate the lipopolysaccharide (LPS)-induced inflammation in BV2 microglial cells, it also can dose-dependent...
T22346 Indomethacin sodium hydrate
吲哚美辛钠
74252-25-8 98%
Indomethacin Sodium is the sodium salt of indomethacin, which is a non-selective, competitive, and reversible, inhibitor of cyclooxygenases 1 and 2 with analgesi...
T12800 (S)-(+)-Ibuprofen D3
化合物 T12800
1329643-44-8 98%
(S)-(+)-Ibuprofen D3 is a deuterium labeled (S)-(+)-Ibuprofen. (S)-(+)-Ibuprofen is the S(+)-enantiomer of Ibuprofen ,it is an inhibitor of COX-1 and COX-2 activ...
TN3366 Ailanthoidol
化合物 TN3366
156398-61-7 98%
Ailanthoidol has anti-inflammatory activity, it inhibits inflammatory reactions by macrophages and protects mice from endotoxin shock. It also possesses potentia...
TN1694 Gliotoxin
胶霉毒素
67-99-2 98%
Gliotoxin 是一种次生代谢产物,由A. fumigatus 分泌,可以抑制巨噬细胞的吞噬作用和其他免疫细胞的免疫功能。它通过阻止 IκB 降解来抑制诱导型NF-κB 活性,从而诱导宿主细胞凋亡。它可以激活PKA 并增加细胞内 cAMP 浓度,调节肌动蛋白细胞骨架重排以促进A. fumigatus 内化到肺上皮细胞...
TN4938 Samidin
化合物 TN4938
477-33-8 98%
Samidin has anti-inflammatory properties through suppression of NF-κB and AP-1-mediated-genes in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells.
T78705 COX-2-IN-30
化合物 COX-2-IN-30
1160498-08-7 98%
COX-2-IN-30 是苯磺酰胺衍生的口服活性 COX/5-LOX 双重抑制剂,其 IC50 值为 COX 同源物为 49 nM、5-LOX 同源物为 10.4 μM。此化合物还能纳摩尔级别 Ki 值抑制 hCA IX 与 hCA XII 亚型。COX-2-IN-30 具备镇痛、抗炎、致溃疡作用,不引发急性胃部反应。
T78706 COX-2-IN-31
化合物 COX-2-IN-31
98%
COX-2-IN-31(化合物7b)是一种COX/5-LOX双重抑制剂,口服活性显著,对COX-2的IC50为60 nM,对5-LOX的IC50为0.9 μM。此外,COX-2-IN-31对跨膜蛋白hCA IX和hCA XII具有抑制作用,其Ki值分别为48.9 nM和5.8 nM,显示出镇痛和抗炎的生物活性。
T78754 COX-2-IN-33
化合物 COX-2-IN-33
98%
COX-2-IN-33(化合物5f)作为一种COX-2抑制剂(IC50=45.5 nM),同样具备潜在抗炎作用。该化合物能抑制促炎细胞因子的生成,同时确保胃部安全。
T79592 COX-1/2-IN-4
化合物 COX-1/2-IN-4
98%
COX-1/2-IN-4 为COX-1与COX-2酶的抑制剂,其IC50值分别为0.239 μM与0.191 μM。此化合物在对COLO205与B16F1癌细胞系表现出中等程度的抗癌活性,对应IC50值分别为30.79 μM与74.15 μM。
T79594 COX-1/2-IN-5
化合物 COX-1/2-IN-5
98%
COX-1/2-IN-5 (compound 2a) 为 COX1/2 双抑制剂,IC50 分别为 2.650 μM 和 0.958 μM,展现抗癌功效。针对肝癌细胞株 HepG2,其抑制作用的 IC50 值为 60.75 μM。
T79598 Anti-inflammatory agent 52
化合物 Anti-inflammatory agent 52
98%
Anti-inflammatory agent 52 (compound 7j) 是一种口服有效的选择性COX-2抑制剂,它不仅抑制HT29细胞迁移并诱导G2/M期的细胞周期停滞,而且在大鼠胃肠道安全性良好,并对炎症具有中等程度的抑制作用。此外,Anti-inflammatory agent 52 在携带艾利希实体癌的小...
T79599 Anti-inflammatory agent 53
化合物 Anti-inflammatory agent 53
98%
Anti-inflammatory agent 53(compound 7c)是口服有效及选择性的COX-2抑制剂。Anti-inflammatory agent 52展现了抗HT29细胞迁移的特性,能够促使细胞周期在S期与G2/M期停滞。此外,该化合物对大鼠胃肠道安全,对炎症具有中等程度的抑制效应。在携带艾利希实体瘤的...
T79670 Anti-inflammatory agent 56
化合物 Anti-inflammatory agent 56
2413127-32-7 98%
Anti-inflammatory agent 56 (Compound 9) 是一种选择性COX-2抑制剂,IC50值为0.54 μM。该化合物展现出显著的抗氧化和抗炎效果,并能有效抑制氧化应激引起的细胞死亡。通过抑制Keap1、COX-2和iNOS,Anti-inflammatory agent 56减轻氧化应激及神...
T79760 COX-2-IN-35
化合物 COX-2-IN-35
98%
COX-2-IN-35(化合物7),作为选择性COX-2抑制剂,表现出4.37 nM的IC50,并展现抗炎活性。
T79915 Antioxidant agent-15
化合物 Antioxidant agent-15
596-38-3 98%
Antioxidant agent-15 (Compound 4) 显示出显著的抗氧化抑制活性,其 IC50 为 15.44 nM。在细胞水平上,Antioxidant agent-15 对Hela、Hep G2 和 Caco-2肿瘤细胞生长的抑制作用各自具有不同的 IC50 值,分别为 395.26 nM、4000.4...
T79944 2-O-Sinapoyl makisterone A
化合物 2-O-Sinapoyl makisterone A
98%
2-O-Sinapoyl makisterone A(化合物2)为芥子酸-蜕皮甾酮杂合体,具有选择性抑制COX-2的作用。该化合物能显着降低COX-2蛋白的表达。
TN4465 Luvangetin
化合物 TN4465
483-92-1 98%
Luvangetin may have anti-inflammatory activity, it can inhibit NO and PGE2 production in LPS-stimulated BV2 cells. Luvangetin shows significant protection agains...
Chamigrenal
T3P2855
β-Chamigrenal has anti-inflammatory activity, it has inhibitory effects on lipopolysaccharide-induced nitric oxide and prostaglandin E2 production in RAW 264.7 m...
Murrangatin
TN4592
Murrangatin may be a valuable anti-tumor-promoting agent, it can significantly inhibit Epstein-Barr virus early antigen (EBV-EA) activation, and preserve the hig...
Voleneol
TN5248
1β,6α-Dihydroxyeudesm-4(15)-ene (Voleneol,DE) can attenuate the lipopolysaccharide (LPS)-induced inflammation in BV2 microglial cells, it also can dose-dependent...
Indomethacin sodium hydrate
T22346
Indomethacin Sodium is the sodium salt of indomethacin, which is a non-selective, competitive, and reversible, inhibitor of cyclooxygenases 1 and 2 with analgesi...
(S)-(+)-Ibuprofen D3
T12800
(S)-(+)-Ibuprofen D3 is a deuterium labeled (S)-(+)-Ibuprofen. (S)-(+)-Ibuprofen is the S(+)-enantiomer of Ibuprofen ,it is an inhibitor of COX-1 and COX-2 activ...
Ailanthoidol
TN3366
Ailanthoidol has anti-inflammatory activity, it inhibits inflammatory reactions by macrophages and protects mice from endotoxin shock. It also possesses potentia...
Gliotoxin
TN1694
Gliotoxin 是一种次生代谢产物,由A. fumigatus 分泌,可以抑制巨噬细胞的吞噬作用和其他免疫细胞的免疫功能。它通过阻止 IκB 降解来抑制诱导型NF-κB 活性,从而诱导宿主细胞凋亡。它可以激活PKA 并增加细胞内 cAMP 浓度,调节肌动蛋白细胞骨架重排以促进A. fumigatus 内化到肺上皮细胞...
Samidin
TN4938
Samidin has anti-inflammatory properties through suppression of NF-κB and AP-1-mediated-genes in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells.
COX-2-IN-30
T78705
COX-2-IN-30 是苯磺酰胺衍生的口服活性 COX/5-LOX 双重抑制剂,其 IC50 值为 COX 同源物为 49 nM、5-LOX 同源物为 10.4 μM。此化合物还能纳摩尔级别 Ki 值抑制 hCA IX 与 hCA XII 亚型。COX-2-IN-30 具备镇痛、抗炎、致溃疡作用,不引发急性胃部反应。
COX-2-IN-31
T78706
COX-2-IN-31(化合物7b)是一种COX/5-LOX双重抑制剂,口服活性显著,对COX-2的IC50为60 nM,对5-LOX的IC50为0.9 μM。此外,COX-2-IN-31对跨膜蛋白hCA IX和hCA XII具有抑制作用,其Ki值分别为48.9 nM和5.8 nM,显示出镇痛和抗炎的生物活性。
COX-2-IN-33
T78754
COX-2-IN-33(化合物5f)作为一种COX-2抑制剂(IC50=45.5 nM),同样具备潜在抗炎作用。该化合物能抑制促炎细胞因子的生成,同时确保胃部安全。
COX-1/2-IN-4
T79592
COX-1/2-IN-4 为COX-1与COX-2酶的抑制剂,其IC50值分别为0.239 μM与0.191 μM。此化合物在对COLO205与B16F1癌细胞系表现出中等程度的抗癌活性,对应IC50值分别为30.79 μM与74.15 μM。
COX-1/2-IN-5
T79594
COX-1/2-IN-5 (compound 2a) 为 COX1/2 双抑制剂,IC50 分别为 2.650 μM 和 0.958 μM,展现抗癌功效。针对肝癌细胞株 HepG2,其抑制作用的 IC50 值为 60.75 μM。
Anti-inflammatory agent 52
T79598
Anti-inflammatory agent 52 (compound 7j) 是一种口服有效的选择性COX-2抑制剂,它不仅抑制HT29细胞迁移并诱导G2/M期的细胞周期停滞,而且在大鼠胃肠道安全性良好,并对炎症具有中等程度的抑制作用。此外,Anti-inflammatory agent 52 在携带艾利希实体癌的小...
Anti-inflammatory agent 53
T79599
Anti-inflammatory agent 53(compound 7c)是口服有效及选择性的COX-2抑制剂。Anti-inflammatory agent 52展现了抗HT29细胞迁移的特性,能够促使细胞周期在S期与G2/M期停滞。此外,该化合物对大鼠胃肠道安全,对炎症具有中等程度的抑制效应。在携带艾利希实体瘤的...
Anti-inflammatory agent 56
T79670
Anti-inflammatory agent 56 (Compound 9) 是一种选择性COX-2抑制剂,IC50值为0.54 μM。该化合物展现出显著的抗氧化和抗炎效果,并能有效抑制氧化应激引起的细胞死亡。通过抑制Keap1、COX-2和iNOS,Anti-inflammatory agent 56减轻氧化应激及神...
COX-2-IN-35
T79760
COX-2-IN-35(化合物7),作为选择性COX-2抑制剂,表现出4.37 nM的IC50,并展现抗炎活性。
Antioxidant agent-15
T79915
Antioxidant agent-15 (Compound 4) 显示出显著的抗氧化抑制活性,其 IC50 为 15.44 nM。在细胞水平上,Antioxidant agent-15 对Hela、Hep G2 和 Caco-2肿瘤细胞生长的抑制作用各自具有不同的 IC50 值,分别为 395.26 nM、4000.4...
2-O-Sinapoyl makisterone A
T79944
2-O-Sinapoyl makisterone A(化合物2)为芥子酸-蜕皮甾酮杂合体,具有选择性抑制COX-2的作用。该化合物能显着降低COX-2蛋白的表达。
Luvangetin
TN4465
Luvangetin may have anti-inflammatory activity, it can inhibit NO and PGE2 production in LPS-stimulated BV2 cells. Luvangetin shows significant protection agains...
1 2 3 4 5 ... 20
联系我们
400-820-0310

上海市静安区江场三路238号8楼