||Nimodipine, a 1, 4-dihydropyridine calcium channel blocker, acts primarily on vascular smooth muscle cells.
||Mexiletine Hydrochloride is the hydrochloride salt form of mexiletine, a local anesthetic and antiarrhythmic (Class IB) agent structurally related to lidocaine. Mexiletine exerts i
||Leflunomide is an immunomodulatory agent used in the therapy of rheumatoid arthritis and psoriatic arthritis.
||StemRegenin 1 is an aryl hydrocarbon receptor (AhR) inhibitor.
||YL-109, a novel anticancer agent, can inhibit breast Y cell growth and invasiveness in vitro and in vivo.
||CH-223191 is a potent and specific antagonist for aryl hydrocarbon receptor (AhR).
||Tapinarof is targeted as a topical cream treatment for psoriasis, a chronic autoimmune skin disease.
||Indoxyl sulfate potassium salt
||Indoxyl sulfate (potassium salt) is an agonist for the human aryl hydrocarbon receptor (AHR). The aryl hydrocarbon receptor (AhR) has recently emerged as a pathophysiological regul
||L-Kynurenine is a key intermediate in the breakdown pathway of tryptophan. L-Kynurenine is a substrate of kynureninase, KMO, and KAT associated with the suppression of antitumor im
||AHR antagonist 1
||AHR antagonist 1 is an aryl hydrocarbon receptor (AHR) antagonist , has an IC50 of 39.9 nM in human cell line.
||ITE is a potent endogenous agonist of aryl hydrocarbon receptor (AhR) (Ki : 3 nM), has immunosuppressive activity.
||PDM 11 is an antagonist of aryl hydrocarbon receptor (AhR)
||1,4-Chrysenequinone acts as an activator of aryl hydrocarbon receptor (AhR).