Ac-Phe-NH2 is a non-competitive inhibitor (Ki = 8 ± 1.2 mM) of polyubiquitin chain elongation by destabilizing the active trimer.

Betaine Aldehyde Chloride is an inhibitor of anaerobic choline metabolism by human gut bacteria.

ADX10059 Hydrochloride is a metabotropic glutamate receptor 5 (mGluR5) negative allosteric modulator.

360A is a stabilizing G-Quadruplex ligand which has potent selectivity toward G-quadruplex structures of the telomeric 3'-overhang.

Grifolic acid is a natural inhibitor of the alpha-linolenic acid (LA)-induced ERK and [Ca(2+)](i) responses in GPR120-expressing cells, and a promotor of ERK and [Ca(2+)](i) responses in GPR120-expressing cells.

20-HETE is a lipid mediator which activates the transcription of ACE via NFkB translocation and promoter binding. This causes detrimental effects in cerebral circulation, and modulating KCa3.1 channels.

CyPPA is a positive modulator of SK3 and SK2, which reduces the activity of dopaminergic neurons. CyPPA inhibits dopamine release, and counteracts hyperdopaminergic behaviors induced by methylphenidate.

Myxothiazol is an inhibitor of mitochondrial respiratory chain complexes III. Myxothiazol induces transcription of the p53-responsive SESN2 gene that plays an important role in stress response and homeostatic regulation.

MS0015203 is a potent and selective agonist of the neuropeptide receptor GPR171.

C8 Ceramide is a cell-permeable analog of naturally occurring ceramides.

Ranitidine-N-oxide is a metabolite of Ranitidine. Ranitidine is a histamine H2-receptor antagonist, inhibiting the normal and meal-stimulated secretion of stomach acid. Ranitidine, sold under the trade name Zantac among others, is a medication which decreases stomach acid production.

5-CFDA is a cell membranes permeatable non-fluorescent prodrug of 5-carboxyfluorescein. It shows strongly fluorescent to differentiate viable cells from apoptotic cells after being enzymatically hydrolyzed inside cells.

XRP44X is a potent Ras-Net (Elk-3) pathway inhibitor.

MB-3 is a histone acetyltransferase GCN5 inhibitor.

BVT.13 is a selective PPAR-gamma activator.

YN1 is a PFKFB3 inhibitor.

Rubone is a modulator of the tumor suppressor miRNA-34a. It acts by inhibiting the growth of hepatocellular carcinoma.

Quinpirole dihydrochloride is a D2-like dopamine receptor agonist.

Lovastatin Sodium is an inhibitor of HMG-CoA reductase.

SKF-10047 is a sigma-1 receptor agonist.

Trimosulfa is a fixed antibiotic combination. It is widely used for mild-to-moderate bacterial infections and as prophylaxis against opportunistic infections.

NDM-1 inhibitor-1 is an inhibitor of new delhi metallo-β-lactamase-1 (NDM-1). New Delhi Metallo-β-Lactamase-1 (NDM-1) has drawn great attention due to its diverse antibiotic resistant activity.

FSBA is a covalent inhibitor of anthrax edema factor.

Doxazosin Mesylate is an alpha-Adrenergic receptor blocker.

Acriflavine Hydrochloride is an inhibitor of HIF-1α. It acts by inducing cell death and apoptosis in several glioma cell lines, targeting HIF-1α-mediated pathways, and decreasing the level of PGK1, VEGF and HIF-1α in vitro and in vivo.

Tetramethrin is a potent insecticide that acts on the insect's nervous system.

Tobramycin Sulfate is a broad-spectrum antibiotic. It is effective against gram-negative bacteria, and especially potent against the Pseudomonas species.

Phenolphthalein is a laxative agent. It stimulates the intestinal mucosa and constricts smooth muscles. It also acts as an acid-base indicator.

Gibberellic acid is a hormone found in plants and fungi that promotes the growth and elongation of cells.

Biotin alkyne for the preparation of various biotinylated conjugates via Click Chemistry. This alkyne reacts with various azides, including biomolecules containing azide groups. Biotinylated conjugates can be used for various assays and applications requiring affinity binding. Our recommended protocol can be used for the conjugation.