t 2525

Cefteram (T-2525), an orally active ester of the cephalosporin class, is the free acid form of Cefteram pivoxil. This compound exhibits potent activity against enteropathogenic families Enterobacteriaceae and Vibrionaceae [1].

Alosetron hydrochloride (GR 68755) is the hydrochloride salt form of alosetron, a potent and selective 5-HT3 receptor antagonist. Alosetron blocks the actions of serotonin at 5-HT3 sites in the peripheral nervous system, particularly on enteric and nociceptive sensory neurons, thereby affecting the regulation of visceral pain, decreasing gastrointestinal contraction and motility, and decreasing gastrointestinal secretions.

Clazuril is an anticoccidial drug that inhibits both asexual and sexual developmental stages of Eimeria labbeana and E. columbarum, disrupting their life cycles.

CID-7309015 is a human tyrosyl-DNA phosphodiesterase 1 (TDP1) inhibitor, delayed death of the malarial parasite plasmid, the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-1, ROR gamma transcriptiona

Cimoxatone (MD 780515) is a reversible, orally active inhibitor of type A monoamine oxidase (MAO-A) that can enhance the anorexic effect of MAO-A.

Cinnamtannin B-1 (LDN 0022358) is an A-type proanthocyanidin contained in several plant species such as Vaccinium vitis-idaea, Laurus nobilis L., Cinnamomum zeylanicum, and Lindera umbellata. It is a potent antioxidant and protective agent against oxidative stress and apoptosis in human platelets. It is a Cox-2 inhibitor.

CL67 is a hypoxia-inducible factor pathway inhibitor. It acts by binding to a G-quadruplex higher-order structure in the HIF promoter sequence in vitro.

Clathrin-IN-1 is a selective clathrin inhibitor that acts by addressing clathrin function in cell physiology with potential applications as an inhibitor of virus and pathogen entry and as a modulator of cell signaling.

Clathrin-IN-25 is the most effective clathrin terminal domain-amphiphysin inhibitor reported to date.