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Search Results for " celecoxib "

Targets Recommended: COX

15

抑制剂 & 化合物

1

化合物库

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Cat. No.	Product Name
L4710	非甾体类抗炎化合物库		530 compounds
	530 种非甾体类的抗炎相关化合物，可用于高通量和高内涵筛选；

化合物库

非甾体类抗炎化合物库

Cat.No: L4710

Compounds: 530

Cat. No.	Product Name	Target	Signaling Pathways
T0466	Celecoxib 塞来西布,塞来昔布,SC 58635	COX	Immunology/Inflammation; Neuroscience
	Celecoxib (SC 58635) 是一种非甾体抗炎剂，是一种 COX-2 抑制剂 (IC50=40 nM)，具有选择性。Celecoxib 具有抗炎和止痛活性，可以用于治疗骨关节炎、类风湿性关节炎、急性疼痛等。
T35610	2,5-dimethyl Celecoxib	Apoptosis; Wnt/beta-catenin; Prostaglandin Receptor	Apoptosis; Cytoskeletal Signaling; GPCR/G Protein; Immunology/Inflammation; Stem Cells
	2,5-dimethyl Celecoxib 是塞来昔布衍生物和微粒体前列腺素 E 合酶 1 (mPGES-1) 的靶向抑制剂，mPGES-1 是炎症介质 PGE2 合成途径中的关键酶。
T11005	Desmethyl Celecoxib	COX	Immunology/Inflammation; Neuroscience
	Desmethyl Celecoxib 是一种选择性的环氧化酶 2 (COX-2) 抑制剂，IC50为 32 nM，具有抗炎活性。
T36187	Celecoxib Carboxylic Acid	Others	Others
	Celecoxib carboxylic acid is an inactive metabolite of the COX-2 inhibitor celecoxib .1,2It is formed from celecoxib primarily by the cytochrome P450 (CYP) isoform CYP2C9. 1.Liu, H., Huang, X., Shen, J., et al.Inhibitory mode of 1,5-diarylpyrazole derivatives against cyclooxygenase-2 and cyclooxygenase-1: Molecular docking and 3D QSAR analysesJ. Med. Chem.45(22)4816-4827(2002) 2.Kim, S.-H., Kim, D.-H., Byeon, J.-Y., et al.Effects of CYP2C9 genetic polymorphisms on the pharmacokinetics of celecox...
T37251	Celecoxib Carboxylic Acid Acyl-β-D-Glucuronide	Others	Others
	Celecoxib carboxylic acid acyl-β-D-glucuronide is a phase II metabolite of celecoxib . Celecoxib is an anti-inflammatory compound from the diaryl heterocycle class that selectively inhibits cyclooxygenase-2 (COX-2; IC50s = 22.9 and 0.05 μM for COX-1 and COX-2, respectively). Celecoxib carboxylic acid acyl-β-D-glucuronide is a minor metabolite, accounting for 2% of the administered dose in human urine and rat bile.
T84997	Hydroxy Celecoxib	Others	Others
	Hydroxy celecoxib, an inactive metabolite of celecoxib, is synthesized through the metabolism of celecoxib by cytochrome P450 (CYP) isoforms CYP2C9, CYP3A4, and CYP2D6 in human liver microsomes.
T2466	Osu03012 Osu-03012,Osu 03012,AR-12	PDK	PI3K/Akt/mTOR signaling
	Osu03012 (AR-12) 是一种口服生物可利用的小分子塞来昔布衍生的磷酸肌醇依赖性激酶 1(PDK1) 抑制剂，具有潜在的抗肿瘤活性。
T62175	COX-2-IN-8	Others	Others
	COX-2-IN-8 (compound 6a) 是一种有效的、选择性的、口服具有活力的 COX-2 抑制剂 (IC50: 6.585 μM)。COX-2-IN-8 的 COX-2 选择性比 Celecoxib 高。COX-2-IN-8 在体内表现出良好的抗炎活性和低致溃疡效果。
T60978	COX-2-IN-7	Others	Others
	COX-2-IN-7 (compound 4a) 是口服有效的COX-2 选择性抑制剂，其选择性高于 Celecoxib，IC50值为6.585 uM。COX-2-IN-7 在体内具有良好的抗炎和低致溃疡活性。
T61760	COX-2-IN-18	Others	Others
	COX-2-IN-18 (Compound 3) is a highly effective COX-2 inhibitor with strong inhibitory activity against COX-2 (IC 50 = 0.775 μM). Its potency is comparable to the reference drug Celecoxib (IC 50 = 0.153 μM). This compound, COX-2-IN-18, shows promise in the field of cancer research [1].
T1780L	Parecoxib sodium SC 69124A,SC-69124A,帕瑞昔布钠,SC69124A,Dynastat	Others	Others
	Parecoxib is a cyclooxygenase-2 inhibitor used for the short-term treatment of postoperative pain in adults. Parecoxib is a water-soluble and injectable prodrug of valdecoxib. Parecoxib is a COX2 selective inhibitor in the same category as celecoxib and r
T61674	COX-2/5-LOX-IN-1	Others	Others
	COX-2/5-LOX-IN-1 (compound 3a), a benzothiophen-2-yl pyrazole carboxylic acid derivative, is a potent and dual inhibitor of COX-2 / 5-LOX. It exhibits superior analgesic and anti-inflammatory properties compared to Celecoxib and Indomethacin. COX-2/5-LOX-IN-1 displays strong inhibitory activity against COX-1, COX-2, and 5-LOX, with IC50 values of 12.13 μM, 0.4 μM, and 4.96 μM, respectively [1].
T69451	R-130823	Others	Others
	R-130823 is a ighly selective inhibition against mitogen-activated protein kinase p38alpha (IC50=22 nM). The release of tumor necrosis factor-alpha, interleukin-1beta, -6 and -8 was inhibited in lipopolysaccharide-stimulated human blood pretreated by R-130823 , with IC50 values of 0.089, 0.066, 0.95 and 0.16 microM, respectively. R-130823 reduced the established hind paw swelling in rat adjuvant-induced arthritis, while methotrexate showed no suppression. In the same model, R-130823 ameliorated ...
T61910	COX-2/5-LOX-IN-2	Others	Others
	COX-2/5-LOX-IN-2 是苯并噻吩-2-基吡唑羧酸衍生物。COX-2/5-LOX-IN-2 (5b) 对COX-2和5-LOX 均有抑制作用。COX-2/5-LOX-IN-2 抑制 COX-1、COX-2 和 5-LOX 的IC50s 分别为 5.40、0.01 和 1.78 μM。COX-2/5-LOX-IN-2 显示出超过塞来昔布和吲哚美辛的镇痛和抗炎活性。
T63646	COX-2-IN-9	Others	Others
	COX-2-IN-9 是选择性的、有效的、口服具有活力的 COX-2 抑制剂 (IC50: 10.17 μM)。COX-2-IN-9 的 COX-2 选择性比 Celecoxib 高。COX-2-IN-9 表现出良好的体内抗炎活性和低致溃疡效果。

化合物

Cat.No: T0466

Synonym: 塞来西布,塞来昔布,SC 58635

Target: COX

2,5-dimethyl Celecoxib

Cat.No: T35610

Target: Apoptosis, Wnt/beta-catenin, Prostaglandin Receptor

Desmethyl Celecoxib

Cat.No: T11005

Target: COX

Celecoxib Carboxylic Acid

Cat.No: T36187

Target: Others

Celecoxib Carboxylic Acid Acyl-β-D-Glucuronide

Cat.No: T37251

Target: Others

Hydroxy Celecoxib

Cat.No: T84997

Target: Others

Cat.No: T2466

Synonym: Osu-03012,Osu 03012,AR-12

Target: PDK

Cat.No: T62175

Target: Others

Cat.No: T60978

Target: Others

Cat.No: T61760

Target: Others

Parecoxib sodium

Cat.No: T1780L

Synonym: SC 69124A,SC-69124A,帕瑞昔布钠,SC69124A,Dynastat

Target: Others

COX-2/5-LOX-IN-1

Cat.No: T61674

Target: Others

Cat.No: T69451

Target: Others

COX-2/5-LOX-IN-2

Cat.No: T61910

Target: Others

Cat.No: T63646

Target: Others

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