(±)-Liquiritigenin is a flavonoid that has anticancer activity.

GSK 2239633A, is a potent CCR4 antagonist.

MB-0223 is a novel potent and selective STING agonist.

ST 045849 is an O-GlcNAc transferase (OGT) inhibitor, it can reduce proliferation and viability of prostate cancer cells in vitro.

Quazinone, is a phosphodiesterase 3 (PDE3) inhibitor and novel cardiotonic agent with vasodilating properties.

Nepodin, also know as Musizin; is a naphthol that has been found in Rumex and has diverse biological activities

L-778123 is an inhibitor of FPTase and GGPTase-I, which was developed in part because it can completely inhibit Ki-Ras prenylation. The combination of L-778,123 and radiotherapy at dose level 1 showed acceptable toxicity in patients with locally advanced pancreatic cancer. Radiosensitization of a patient-derived pancreatic cancer cell line was observed.

Diflapolin is a potent dual soluble epoxide hydrolase (sEH)/5-lipoxygenase-activating protein (FLAP) inhibitor

VH032-linker 5 is a derivative of the proteolysis-targeting chimera technology (PROTAC) for PROTAC research and development; by incorporating an E3 ligase ligand and an alkyl C4 linker with terminal carboxylic acid, it is ready for conjugation to a target protein ligand.

VH 032 Linker 6 is a derivative of the proteolysis-targeting chimera technology (PROTAC) for PROTAC research and development; by incorporating an E3 ligase ligand and a PEG2 linker with terminal alkyne, it is ready for conjugation to a target protein ligand

VH 032 Linker 3 is a derivative of the proteolysis-targeting chimera technology (PROTAC) for PROTAC research and development; by incorporating an E3 ligase ligand and a short alkyl linker, it is ready for conjugation to a target protein ligand.

Pimprinine is an alkaloid. It is a potent inhibitor of MAO (monoamine oxidase). More recently, pimprinine showed promising anticonvulsant activity in electric seizure threshold.

Ciclopirox olamine is a synthetic, broad-spectrum antifungal agent with additional antibacterial, anti-inflammatory and also recently antitumor activities.

Succinylacetone is an inhibitor of δ-aminolevulinic acid dehydratase

MDR-652 is a nonpungent transient receptor potential vanilloid 1 (TRPV1) agonist discovered to be a strong topical analgesic.

Sclerotiorin is a compound isolated from the fermented broth of Penicillium frequentans that exhibited potent inhibition against human polymorphonuclear leukocytes 5-lipoxygenase and human platelet aggregation.

Diacetoxyscirpenol is a mycotoxin from the group of type A trichothecenes. It is a secondary metabolite product of fungi of the genus Fusarium.

Schisantherin B is one bioactive of lignans isolated from Schisandra chinensis (Turcz.) Baill which has been commonly used as a traditional herbal medicine for thousands of years.

Desmedipham is a carbamate herbicide.

Flunixin is a nonsteroidal anti-inflammatory drug (NSAID), analgesic, and antipyretic used in horses, cattle and pigs.

Viridicatumtoxin is a fungus-derived tetracycline-like antibiotic.

Menbutone is an oxobutyric acid derivative and acts as a choleretic.

Sulcotrione is a triketone herbicide used to control dicotyledonous weeds in maize culture.

Thiobencarb is a thiocarbamate cholinesterase inhibitor that is used as a pre-emergence herbicide.

Sari 59-801 is a novel, orally effective hypoglycemic compound.

Sarcophine is a natural cembranoid from the Red Sea soft coral Sarcophyton glaucum.

Chlorfenvinphos is an organophosphorous compound that possesses acaricidal and insecticidal properties.

Pyridaben is a pyridazinone derivative, is a new acaricide and insecticide for control of mites and some insects such as white flies, aphids and thrips. It acts as a complex I inhibitor.

Flusilazole is an organosilicon fungicide which is used to control fungal infections on a variety of fruit and vegetable crops. It is moderately toxic to animals and has been shown to produce birth defects and embryotoxicity at high doses.

Dipropetryn is a triazine herbicide.