diphenylamine

Fenamic acid (N-Phenylanthranilic acid) is a chloride channel blocker that causes renal papillary necrosis in rats. Fenamic acid serves as a parent structure for several nonsteroidal anti-inflammatory drugs (NSAIDs), including flufenamic acid, tolfenamic acid, mefenamic acid, and meclofenamic acid.

Diphenylamine hydrochloride, isolated from coriander, has antioxidant properties. In agriculture, it can be used as a fungicide and antibacterial agent; in industry, it can be used as an antioxidant and dye mordant.

2,6-Dichlorodiphenylamine, an analogue of Diclofenac Sodium, exhibits anti-Candida albicans activity. Diclofenac Sodium, a potent and nonselective COX inhibitor, has IC50 values of 4 and 1.3 nM for human COX-1 and COX-2 in CHO cells. [1]. Makoto Urai, et al. Potent Drugs That Attenuate anti-Candida albicans Activity of Fluconazole and Their Possible Mechanisms of Action. J Infect Chemother. 2014 Oct;20(10):612-5.

4,4'-Iminodiphenol (Leucoindophenol) is an inactive estrogen receptor ligand with a diphenylamine backbone.

3-Cl-DPA, a cardiac troponin activator, acts by a mechanism distinct from bepridil or TFP.

4-Nitrodiphenylamine is an aromatic amine antioxidant that can be used as a stabilizing additive and ozone inhibitor in rubber.

N-Nitrosodiphenylamine-d6 is a deuterated compound of N-Nitrosodiphenylamine. N-Nitrosodiphenylamine has a CAS number of 86-30-6.