COX(环氧合酶)
COX (cyclooxygenase) is an enzyme that is responsible for formation of important biological mediators called prostanoids, including prostaglandins, prostacyclin and thromboxane.
Products for COX
- Cat.No. 产品名称 Information
-
GC16508
Salicylic acid
水杨酸; 2-Hydroxybenzoic acid
An Analytical Reference Standard -
GC74187
Salicylic acid-13C6
2-Hydroxybenzoic acid-13C6
Salicylic acid-13C6是13c标记的水杨酸。 -
GC49480
Salicylic Acid-d4
水杨酸-D4
An internal standard for the quantification of salicylic acid -
GC64032
Salicylic acid-d6
水杨酸-D6; 2-Hydroxybenzoic acid-d6
Salicylic acid-D6 (2-Hydroxybenzoic acid-D6) 是 Salicylic acid 的一种氘代化合物。Salicylic acid 抑制 COX-2 活性,抑制作用与转录因子 (NF-κB) 激活无关。 -
GC49363
Salicyluric Acid
2-羟基马尿酸
A major metabolite of aspirin and salicylic acid -
GC10973
SC 236
4-(5-(4-氯苯基)-3-(三氟甲基)-1H-
A potent, selective COX-2 inhibitor -
GC15634
SC 560
5-(4-氯苯基)-1-(4-甲氧基苯基)-3-(三氟甲基)-1H-吡唑
A selective inhibitor of COX-1 -
GC17817
SC 58125
1-[(4-甲基磺酰基)苯基]-3-三氟甲基-5-(4-氟苯基)吡唑
A selective COX-2 inhibitor -
GC31960
SC57666
SC57666是选择性的COX2抑制剂,IC50值为26nM。
-
GC31985
SC58451
SC58451是一个强效的,有选择性的COX-2抑制剂。
-
GC12013
Sodium salicylate
水杨酸钠; Salicylic acid sodium salt; 2-Hydroxybenzoic acid sodium salt
水杨酸钠(水杨酸钠盐)抑制环加氧酶 2(COX-2)活性,与转录因子(NF-κB)激活无关。 -
GC60345
Sphondin
牛防风素
Sphondin可从Heracleumlaciniatum中分离,对IL-1β诱导的A549细胞中COX-2蛋白和PGE2释放水平的升高具有抑制作用。 -
GC64940
Sudoxicam
舒多昔康
Sudoxicam 是一种可逆的口服活性的 COX 拮抗剂,是烯醇-羧酰胺类的非甾体抗炎药 (NSAID)。Sudoxicam 具有有效的抗炎,抗浮肿和退热作用。 -
GC16716
Sulindac
舒林酸; MK-231
A non-selective COX inhibitor -
GC15059
Sulindac sulfide
cis-Sulindac sulfide
An active metabolite of sulindac -
GC11721
Sulindac sulfone
磺基舒林,Exisulind
A metabolite of sulindac -
GC48677
Sulindac-d3
MK-231-d3
An internal standard for the quantification of sulindac -
GC31440
Syringaldehyde
丁香醛
A polyphenol with diverse biological activities -
GC39040
Taraxerol acetate
醋酸蒲公英霜
Taraxerol acetate 是 COX-1 和 COX-2 抑制剂, IC50 值分别为 116.3 μM 和 94.7μM。Taraxerol acetate 具有抗癌作用并诱导细胞凋亡(apoptosis)。 -
GC64025
Tazofelone
LY 213829
Tazofelone (LY 213829) 是一种环氧合酶-II (COX-II) 抑制剂。Tazofelone 转化为亚砜和喹啉代谢物主要由 CYP3A 介导。Tazofelone 可用于炎症性肠病的研究。 -
GC11853
Tenidap
替尼达普,CP-66248
A COX-1 selective NSAID -
GC10006
Tenoxicam
替诺昔康; Ro-12-0068
An NSAID and COX-1 inhibitor -
GC49386
Tepoxalin
替泊沙林
A dual inhibitor of COX and 5-LO -
GC61764
Teriflunomide impurity 3
4-Amino-N-(4-trifluoromethylphenyl)benzamide
Teriflunomideimpurity3(4-Amino-N-(4-trifluoromethylphenyl)benzamide)是一种选择性COX-1抑制剂,IC50为30µM,对COX-2的活性较低(IC50>100µM)。 -
GC19353
TFAP
N-(5-Aminopyridin-2-yl)-4-(trifluoromethyl)benzamide
A selective COX-1 inhibitor -
GC31826
Thioflosulide (L-745337)
L-745337
Thioflosulide (L-745337) (L-745337) 是一种选择性 cyclooxygenase-2 (COX2) 抑制剂,IC50 为 2.3 nM,具有抗炎活性。 -
GC45579
Tiaprofenic Acid
噻洛芬酸
A COX inhibitor and NSAID -
GC31956
Tilmacoxib (JTE522)
替马考昔; JTE522; JTP19605; RWJ57504
Tilmacoxib (JTE522) (JTE522) 是一种高度选择性、时间依赖性和不可逆的人 COX-2 抑制剂,在酶试验中 IC50 为 85 nM。 -
GC31965
Timegadine (SR1368)
替美加定; SR1368
Timegadine (SR1368) 是一种新型抗炎剂,被发现是一种有效的、竞争性的环加氧酶 (COX) 和脂加氧酶抑制剂,IC50 范围为 5 nM(洗涤过的兔血小板)至 20 μM(大鼠脑) ) 用于 COX 和 100 μ;M 用于马血小板匀浆的胞质溶胶部分和洗涤过的兔血小板中的脂加氧酶。 -
GC15395
Tolfenamic Acid
托芬那酸; GEA 6414
An NSAID with anticancer activity -
GC45965
Tolfenamic Acid-d4
托芬那酸 D4
An internal standard for the quantification of tolfenamic acid -
GC61337
Tolmetin
托麦汀;托美丁
Tolmetin (Tolectin) is a nonsteroidal anti-inflammatory drug of the heterocyclic acetic acid derivative class and also exhibits analgesic and antipyretic activity. -
GC16428
Tolmetin (sodium salt hydrate)
痛灭定
A non-selective NSAID -
GC13300
Triflusal
三氟柳
An inhibitor of platelet aggregation -
GC13402
Tryptanthrin
色胺酮,NSC 349447
An alkaloid with diverse actions -
GC14020
Valdecoxib
伐地考昔; SC 65872
A COX-2 inhibitor -
GC48232
Valdecoxib-d3
戊地昔布-D3,SC 65872-d3
An internal standard for the quantification of valdecoxib -
GC10335
Valeroyl Salicylate
戊酰基水杨酸,2-Valeryloxybenzoic Acid
A selective, irreversible inhibitor of COX-1 -
GC61371
Veratric acid
藜芦酸
Veratricacid(3,4-Dimethoxybenzoicacid)是从蔬菜和水果中得到的多酚物质,可口服,具有抗氧化、保护心血管和抗炎活性。当细胞受到UVB辐射时,Veratricacid能够减少上调的COX-2表达,降低PGE2和IL-6水平。 -
GC33632
Veratric acid (3,4-Dimethoxybenzoic acid)
藜芦酸; 3,4-Dimethoxybenzoic acid
Veratric acid (3,4-Dimethoxybenzoic acid), a simple benzoic acid derived from plants and fruits, has anti-oxidant, anti-inflammation, and blood pressure-lowering effects. Veratric acid reduces upregulated COX-2 expression, and levels of PGE2, IL-6 after UVB irradiation. -
GC12391
Xanthohumol
黄腐醇
A natural prenylated chalcone
-
GC13626
Zaltoprofen
扎托布洛芬; CN100
A non-selective COX inhibitor -
GC11203
ZLJ-6
Dual inhibitor of cyclooxygenase/5-lipoxygenase
-
GC63267
α-Chaconine
阿尔法卡茄碱
α-Chaconine 可在转录水平抑制 COX-2,IL-1β,IL-6 和 TNF-α 表达。α-Chaconine 作用于 RAW 264.7 巨噬细胞,在蛋白和 mRNA 水平上抑制 LPS 诱导的 iNOS 和 COX-2 表达及其启动子活性。α-Chaconine 具有抗炎作用。