Showing 5041–5056 of 5741 results

Diphenhydramine HCl

Diphenhydramine HCl is a first-generation histamine H1 receptor antagonist, used in various allergic conditions such as rhinitis, urticaria and conjunctivitis.

Diltiazem HCl

Diltiazem HCl (Tiazac) is a benzothiazepine derivative with vasodilating action due to its antagonism of the actions of the calcium ion in membrane functions.


Diethylstilbestrol is a synthetic nonsteroidal estrogen, used to prevent miscarriage and other pregnancy complications.


Etidronate is a non-aminobisphosphonate, show protein tyrosine phosphatase (PTP) inhibitory activity, used for the treatment of Paget’s disease and the prevention of heterotopic ossification.

Metoprolol Tartrate

Metoprolol Tartrate is a selective β1 receptor blocker medication, used to treat hypertension and heart failure.

Pefloxacin Mesylate

Pefloxacin Mesylate is a synthetic chemotherapeutic agent and an antibacterial agent with IC50 of 6.7 nM.


Bifonazole is a substituted imidazole antifungal agent.


Penicillamine is used as an antirheumatic and as a chelating agent in Wilson’s disease.


Oxibendazole is a benzimidazole drug that interferes with metabolic pathways, used to protect against roundworms, strongyles, threadworms, pinworms and lungworm infestations in horses and some domestic pets.


Daidzein is a natural isoflavone phytoestrogen found in Leguminosae, used as a component of foods and dietary supplements.


Curcumin is the principal curcuminoid of the popular Indian spice turmeric, which is a member of the ginger family (Zingiberaceae). It is an inhibitor of p300 histone acetylatransferase(IC50~25 μM) and Histone deacetylase activates Nrf2 pathway and supresses the activation of transcription factor NF-κB.

Clemastine Fumarate

Clemastine Fumarate (Clemastine) is a selective histamine H1 receptor antagonist with IC50 of 3 nM.


Cimetidine, a histamine congener, competitively inhibits histamine binding to histamine H2 receptors.

Chenodeoxycholic Acid

Chenodeoxycholic Acid is a naturally occurring human bile acid, and inhibits production of cholesterol in the liver and absorption in the intestines.


Lomustine inhibits cancer cells by damaging the DNA and stops cells from dividing.