ADPS is a water-soluble modified trinder reagent.

dtBHQ is a non-arylating oxidizable phenol as the source of reactive oxygen species (ROS).

Quinaprilat is an angiotensin converting enzyme inhibitor.

AG-17724 is a potent peptidyl-prolyl isomerase (PPIase) Pin1 inhibitor.

RF9 is a potent and selective neuropeptide FF receptor antagonist, targeting both NPFF1 and NPFF2 receptors.

JAK3 Inhibitor VI is a cell-permeable, potent, and reversible inhibitor of Janus kinase 3 (JAK3).

LAP is a photocrosslinker for hydrogels.

FAD-Na2 is a redox cofactor (electron carrier) by flavoproteins including succinate dehydrogenase (complex), α-ketoglutarate dehydrogenase, apoptosis-inducing factor 2 (AIF-M2, AMID), folate/FAD-dependent tRNA methyltransferases, and N-hydroxylating flavoprotein monooxygenases.

(-)-Quinpirole HCl is the most widely used D2 agonist in in vivo and in vitro studies.

R(+)-SKF-38393A is a D1 dopamine receptor agonist. It is also a more active enantiomer of (±)-SKF-38393A.

MAL2-11B is an inhibitor of Simian Virus 40 replication. It acts by targeting the molecular chaperone function and ATPase activity of T antigen. MAL2-11B is also a MAL3-101 precursor.

AMPK activator D942 is a cell-permeable activator of AMPK.

MDK5466, also known as Flt3 Inhibitor III, is a Flt3 inhibitor that acts by preventing glutamate-induced cell death. MDK5466 has CAS#852045-46-6. For the convenience of scientific communication, we temporally name it as MDK5466. The last four digit of the CAS# was used in the name.

GPBAR-A is a bile acid receptor TGR5 (GPBA) agonist.

LT175 is a PPARα/γ ligand with potent insulin sensitizing effects and reduced adipogenic properties.

SG-209 is a potassium channel opener.

ARDP0006 is a NS2B-NS3 protease inhibitor.

Ridaifen-B is a tamoxifen derivative. It acts by inducing Bcl-2 independent autophagy without estrogen receptor involvement.

NSC-33994 is a selective inhibitor of JAK2.

Naloxonazine Dihydrochloride is a potent and selective antagonist for μ1 opioid receptors.

NLRP3-IN-9 is an inhibitor of caspase-1 and NLRP3 ATPase activities. It acts by irreversibly trapping thiol nucleophiles, which prevents both ATP- and nigericin-triggered pyroptosis of human THP-1 cells in a time- and concentration-dependent manner.

Ritanserin is a selective and potent serotonin-2 antagonist. Ritanserin acts as a selective 5-HT2A (Ki = 0.45 nM) and 5-HT2C receptor (Ki = 0.71 nM) antagonist.

Sodium D-Pantothenate is a vitamin that performs an important role in the oxidation of fats and carbohydrates and certain amino acids. It is also a precursor in the biosynthesis of coenzyme A.

Cefpirome is a broad-spectrum, fourth-generation cephalosporin. It binds to and inactivates penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall.

Delapril is an angiotensin-converting enzyme (ACE) inhibitor that blocks the conversion of angiotensin I to angiotensin II.

Acetrizoic Acid is a high-osmolality, iodine-based radiographic contrast medium.

CTP disodium dihydrate is a P2X4 purinergic receptor agonist.

GSK983 is a potent broad-spectrum antiviral. It blocks cell proliferation and dengue virus replication by inhibiting the pyrimidine biosynthesis enzyme dihydroorotate dehydrogenase (DHODH).

Ingenol 3-Hexanoate novel potent reactivator of latent HIV-1.

N106 directly activates the SUMO-activating enzyme, E1 ligase, and triggers intrinsic SUMOylation of SERCA2a. Decreased activity and expression of the cardiac sarcoplasmic reticulum calcium ATPase (SERCA2a), a critical pump regulating calcium cycling in cardiomyocyte, are hallmarks of heart failure.