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.

Latanoprostene, also known as PF-3187207, is a a nitric oxide (NO)-donating latanoprost with prostaglandin activity. It loweres intraocular pressure (IOP) more effectively than latanoprost in monkeys, dogs and rabbits.

MEDICA16 is a GPR40 agonist. MEDICA 16 is a β,β'-dimethyl hexadecanedioic acid which exhibits hypolipidemic and antidiabetogenic effects in the rat.

Mucochloric acid is an organic compound that consists of a dibrominated alkene with aldehyde and carboxylic acid functional groups. It is a bacterial mutagen and genotoxic compound.

alpha-Naphthylacetic acid is a rooting agent and plant hormone in the auxin family. It is an ingredient in many commercial plant rooting horticultural products.

Dicyclohexyl phthalate is a white granular solid. It is used as a plasticizer to modify the properties of synthetic resins, in alkyd resins and cellulose nitrate to increase their stability to light and weathering, and to improve the chemical and physical properties of plastics by preventing creep.

Diisobutyl phthalate is a phthalate plasticizer which can be used as a substitute of dibutyl phthalate.

2-Acetylthiophene is a fragrance agent. It has a sulfurous type odor and an onion type flavor.

2-Nonanone is a flavor and fragrance agents. It has a fruity type odor and an cheesy type flavor.

Rhodblock 3 is a small molecule and potent inhibitor of the Rho pathway.

Thiolutin, also known as Acetopyrrothin aand NSC-3927, is an antibiotic and anti-angiogenic agent, acting as a zinc chelator that inhibits the Rpn11 and other JAMM metalloproteases.