An inducer of NRF2 that selectively activates NRF2 signaling with CD value (The concentration that doubles the specific activity) of 0.18 uM.

An indirubin derivative that potently blocks constitutive STAT3 signaling in human breast and prostate cancer cells, directly inhibits Src kinase activity (IC50=0.43 uM) in vitro.

An impurity of Roflumilast, which is a selective and long-acting inhibitor of PDE-4 with IC50 value of 0.8 nM..

An imidazolinone herbicide that effectively controls a broad spectrum of weed species..

An imidazoacridinone analogue with potent in vivo antitumour activity, inhibits the catalytic activity of Topoisomerase II.

An endogenous DHA metabolite that promotes neurite growth, synaptogenesis, and synaptic function both in vitro and in vivo.

An enantiomer of Ibuprofen that more potently inhibits COX activity, thromboxane formation, and platelet aggregation than the (R)-form.

An efficient prodrug of ampicillin with enhanced absorption and decreased side effects..

An antiviral compound that inhibits attachment to cells, inhibits human rhinovirus type 14 (HRV14) replication..

An antitrypansomal drug that also possesses antitumor activity.

An antipsychotic agent with serotonin-S2 and dopamine-D2 antagonistic properties.

An antipsychotic agent with serotonin-S2 and dopamine-D2 antagonistic properties.

An antiprotozoal, antirheumatic and intrapleural sclerosing agent.

An antimalarial candidate that demonstrates potent blood-stage and transmission-blocking activity, shows potent ABS activity (IC50 <25 nM) against drug-sensitive 3D7 and multidrug-resistant Dd2 parasites.

An anti-inflammatory agent used in the treatment of osteoarthritis.

An anti-inflammation agent..

An anti-infective, anti-bacterial agent.

An antifungal antibiotic that inhibits fatty acid synthase (FASN), also blocks cellular proliferation of KRAS-associated lung cancer cells.

An antifungal agent that works by altering the permeability of the fungal cell wall.

An anticestodal agent, fungicide, germicide, and antimicrobial agent.

An anticancer phytochemical commonly found in black cumin.

An antibiotic used to treat a number of bacterial infections..

An antibiotic used to treat a number of bacterial infections that acts by inhibiting proper cell wall synthesis..

An antiaggressive agent that acts as an agonist at the 5-HT1A and 5-HT1B receptors and as an antagonist at the 5-HT2C receptor..

An antiaggressive agent that acts as an agonist at the 5-HT1A and 5-HT1B receptors and as an antagonist at the 5-HT2C receptor..

An anthelmintic that has antibacterial and anthelmintic properties along with algaecide activity.

An anthelmintic that has antibacterial and anthelmintic properties along with algaecide activity.

An analogue of deoxyspergualin that has immunostimulating activity, promotes resistance to Candida albicans infection in mice..

An analog of the natural compound Fumagillin that functions as a highly potent methionine aminopeptidase 2 (MetAP2) inhibitor.

An analog of adenosine 5’-monophosphate that potently and selectively inhibits NEDD8-activating enzyme (NAE) with IC50 of 4.7 nM.