Epiberberine Chloride is a natural anticancer agent which stabilizes telomeric G4s and inhibits telomerase, specifically recognizing the hybrid-2 telomeric G4 predominant in physiologically relevant K+ solution and converts other telomeric G4 forms to hybrid-2.

S1QEL is a suppressor of mitochondrial respiratory complex I site IQ electron leak which suppresses superoxide and/or H2O2 production without altering oxidative phosphorylation.

Tuftsin is a self-immunomodulatory molecule produced by the spleen by enzymatic cleavage of a leukophilic gamma-globulin which stimulates the phagocytic activity of blood polymorphonuclear leukocytes and neutrophils in particular. The peptide is located in the Fd fragment of the gamma-globulin molecule.

Fluvastatin Methyl Ester is a precursor for Fluvastatin, which is a blocker of the liver enzyme HMG-CoA reductase.

Momordicine I is a secondary metabolite from bitter melon (Momordica charantia L.) which significantly inhibits Spodoptera litura ovary cell line (SL-1 cell) proliferation.

Flobetapir is a blood-brain barrier crossing ligand of amyloid protein deposits in the brain.

NAGKi is an inhibitor of N-acetylglucosamine kinase (NAGK) and N-acetylmannosamine kinase (NAMK).

NPD8716 is a hepatitis B/D virus entry inhibitor, targeting sodium taurocholate cotransporting polypeptide (NTCP).

Imidafenacin HCl is a potent antimuscarinic agent, exhibiting selectivity toward muscarinic M3 receptors.

Neurodazine is a neurogenic inducer for converting pluripotent P19 cells into electrophysiologically active neurons.

Clofilium Tosylate is a K+ channel blocker, cardiac depressant, and anti-arrhythmic agent.

S3QEL-2 is a modulator of the retrograde signaling. It acts by strongly mitigating the oxidative stress-induced apoptosis that limits the yield of functional ?-cells from intact islets.

PQ1 Succinate is a gap junction enhancer. It acts by restoring GJIC and increasing connexin expression in breast cancer cell lines while not affecting normal mammary cells.

Rhodblock 6 is an inhibitor of the Rho pathway. It acts by specifically abrogating Rho kinase activity.

JMC-4 is a 5-LOX inhibitor.

HNHA is a histone deacetylase (HDAC) inhibitor.

TMCB is a dual-kinase inhibitor. It acts by inhibiting both casein kinase 2 (CK2) and extracellular-signal-regulated kinase 8 (ERK8).

Ractopamine HCl is a beta-Adrenergic agonist. It acts by being a full agonist at the TAAR1.

8-Oxo-dG is a key biomarker of oxidative stress induced carcinogenesis.

(-)-Sparteine is a natural anticonvulsant. It inhibits seizures, delays the onset of convulsive behavior, and activates the M2 and M4 subtypes of mAChRs.

Droxicam is a non-steroidal anti-inflammatory drug (NSAID) for the relief of pain and inflammation in musculoskeletal disorders such as rheumatoid arthritis and osteoarthritis.

(S)-Oxiracetam is a positive allosteric modulator of the AMPA receptors.

Tetracaine is a potent local anesthetic. It alters the function of calcium release channels (ryanodine receptors) that control the release of calcium from intracellular stores.

Flurbiprofen Axetil, also known as Ropion, is a prodrug of Flurbiprofen that provides better analgesia effects and few side effects.

Nifuroxazide is an antibiotic used for the treatment of colitis and diarrhea in humans and non-humans.

PS372424 HCl is a specific agonist of human CXCR3. It has been shown to induce phosphorylation of ERK and block CXCL11 induced migration of CD45+ cells to air pouches generated on humanized mice.

GLPG-0259 is a small-molecule inhibitor of mitogen-activated protein kinase-activated protein kinase 5 (MAPKAPK5), a kinase enzyme that plays a role in important inflammatory pathways.

Fasnall is a selective FASN inhibitor that acts through its co-factor binding sites. Fasnall also shows potent anti-tumor activity in the MMTV-Neu model of HER2(+) breast cancer, particularly when combined with carboplatin.

UCL2077 is a selective slow-afterhyperpolarization (sAHP) channel blocker. UCL2077 suppresses the sAHP present in hippocampal neurons in culture and in the slice preparation. UCL2077 is selective and has minimal effects on Ca(2+) channels, action potentials, input resistance and the medium afterhyperpolarization.

Inz-1 is a fungal-selective inhibitor of mitochondrial cytochrome bc1.