Ametryn is a methylthiotriazine based herbicide which inhibits photosynthesis and other enzymatic processes. Ametryn is used to control broadleaf weeds and annual grasses in pineapple, sugarcane and bananas.

Mirodenafil belongs to the drug class PDE5 inhibitors, which includes avanafil, sildenafil, tadalafil, udenafil, and vardenafil, and is the first-line treatment for erectile dysfunction.

JNJ-10191584 maleate is a highly selective histamine H4 receptor silent antagonist.

Salicyl-AMS is a MbtA Inhibitors and Antimycobacterial Agent. salicyl-AMS [5'-O-(N-salicylsulfamoyl)adenosine] inhibits M. tuberculosis growth in vitro under iron-limited conditions.

SNJ-1945 is a calpain inhibitor with more favorable retinal penetration, high oral bioavailability, and long half-life. SNJ1945 rescued defective function in lissencephaly. SNJ-1945 protects SH-SY5Y cells against MPP(+) and rotenone. SNJ-1945 reduces murine retinal cell death in vitro and in vivo. SNJ-1945 has good aqueous solubility, can prevents the heart from KCl arrest-reperfusion injury associated with the impairment of total Ca(2+) handling by inhibiting the proteolysis of alpha-fodrin as a cardioplegia.

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.