Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0196 |
Diclofenac
双氯芬酸,奥尔芬,Diclofenacum,Voltaren |
Apoptosis; COX | Apoptosis; Immunology/Inflammation; Neuroscience |
Diclofenac (Diclofenacum) 是一种具有抗炎活性的非甾体苯乙酸衍生物,是 COX 抑制剂,在 CHO 细胞中,对人 COX-1 和 COX-2 的 IC50值分别为 4 和 1.3 nM。它对绵羊 COX-1 和 COX-2 的 IC50值分别为 5.1 μM,0.84 μM。它通过活化 caspase 级联反应来诱导神经干细胞凋亡。 | |||
T22307 |
Diclofenac Epolamine
diclofenac hydroxyethylpyrrolidine,DHEP,2-((2,6-二氯苯基)氨基)苯乙酸 1-吡咯烷乙醇盐,DIEP |
Others | Others |
Diclofenac Epolamine (DHEP) 是一种非甾体抗炎药 (NSAID),具有镇痛和解热作用。 | |||
T0432 |
Diclofenac diethylamine
|
Apoptosis; COX | Apoptosis; Immunology/Inflammation; Neuroscience |
Diclofenac diethylamine 是非选择性抗炎剂,通过活化 caspase 级联反应来诱导神经干细胞凋亡。它是一种COX 抑制剂,在 CHO 细胞中,对人COX-1和COX-2的IC50值分别为 4 和 1.3 nM。它对绵羊COX-1和COX-2的IC50值分别为 5.1 μM 和0.84 μM。 | |||
T0643 |
Diclofenac Amide
|
Others | Others |
Diclofenac Amide 用作Diclofenac 的中间体。 | |||
T6470 |
Diclofenac Potassium
双氯芬酸钾,CGP-45840B,Cataflam,Voltfast |
Apoptosis; Others; COX | Apoptosis; Immunology/Inflammation; Neuroscience; Others |
Diclofenac Potassium (CGP-45840B) 是一种非甾体抗炎药,用于减轻炎症并在某些情况下作为镇痛剂减轻疼痛。它通过活化 caspase 级联反应来诱导神经干细胞凋亡。它是一种COX 抑制剂,在 CHO 细胞中,对人 COX-1 和 COX-2 的IC50值分别为 4 和 1.3 nM。它对绵羊 COX-1 和 COX-2 的IC50值分别为 5.1 μM 和0.84 μM。 | |||
T37482 |
Diclofenac methyl ester
|
Others | Others |
Diclofenac methyl ester 是双氯芬酸(diclofenac)的疏水性前药形式,它是一种非甾体抗炎药 (NSAID)。它比双氯芬酸更易溶于肉豆蔻酸异丙酯,但毒性更高。 | |||
T1555 |
Diclofenac sodium
GP 45840,双氯芬酸钠 |
Apoptosis; COX | Apoptosis; Immunology/Inflammation; Neuroscience |
Diclofenac sodium (GP 45840) 是一种非选择性抗炎剂,是 COX 抑制剂,在 CHO 细胞中,对人 COX-1 和 COX-2 的 IC50值分别为 4 和 1.3 nM。它对绵羊 COX-1 和 COX-2 的 IC50值分别为 5.1 μM,0.84 μM。它通过活化 caspase 级联反应来诱导神经干细胞凋亡。 | |||
T37481 |
Diclofenac ethyl ester
|
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Diclofenac ethyl ester 可用于生命科学领域的相关研究。其产品编号为 T37481,CAS号为 15307-77-4。 | |||
T37917 |
5-hydroxy Diclofenac
|
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5-hydroxy Diclofenac is a metabolite of the NSAID diclofenac formed by the cytochrome P450 (CYP) isoform CYP3A4. Diclofenac is a non-selective COX inhibitor. It inhibits human COX-1 and -2 with IC50 values of 0.9-2.7 and 1.5-20 μM, respectively. Diclofenac inhibits ovine COX-1 and -2 with IC50 values of 60 and 220 nM, respectively. | |||
T19819 |
4'-Hydroxy diclofenac
4′-羟基双氯芬酸,4'-Hydroxydiclofenac |
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4'-Hydroxydiclofenac is a diclofenac metabolite. | |||
T27167 |
Diclofenac Acyl Glucuronide
|
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Diclofenac Acyl Glucuronide is a major biliary metabolite of Diclofenac (GLXC-07892), a nonsteroidal antiinflammatory drug and COX inhibitor. | |||
T68640 |
Diclofenac deanol
|
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Diclofenac deanol is a nonsteroidal anti-inflammatory drug (NSAID) of the phenylacetic acid class with anti-inflammatory, analgesic, and antipyretic properties. Contrary to the action of many traditional NSAIDs, diclofenac inhibits cyclooxygenase (COX)-2 enzyme with greater potency than it does COX-1. | |||
T38240 |
2,6-Dichlorodiphenylamine
|
Antibacterial | Microbiology/Virology |
2,6-Dichlorodiphenylamine 是双氯芬酸钠的一种结构类似物,显示出抗白色念珠菌活性。2,6-Dichlorodiphenylamine 是非选择性抗炎剂,为COX 的抑制剂,在 CHO 细胞中,对人 COX-1 和 COX-2 的IC50分别为 4 和 1.3 nM。 | |||
T22037 |
AS 1892802
|
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
AS 1892802是一种强效和选择性的ROCK 抑制剂。AS 1892802 用于人ROCK2、大鼠ROCK2和人ROCK1的 IC50值分别为52nM、57nM 和122nM。AS 1892802的镇痛作用起效速度与曲马多和双氯芬酸的起效速度一样快。 | |||
T21939 |
ATB-337
|
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S-Diclofenac 的分子结构由 H2S 供体和非甾体类抗炎药双氯芬酸组合而成。S-Diclofenac 显著抑制前列腺素的合成,并且不会损伤胃粘膜。 |