Topilutamide is a topical nonsteroidal antiandrogen (NSAA) that is used in the treatment of metastatic prostate cancer.

JJKK 048 is an ultrapotent and highly selective inhibitor of Monoacylglycerol lipase (MAGL).

Methyl Green is a potent fluorescent dye. Methyl Green is a DNA stains of cells and electrophoretic gels. Methyl Green can be used as a stain for direct measuring of viability by both microscopy and flow cytometry, with peaks at 633 and 677 nm.

Cycloartenyl ferulate (Cycloartenol ferulate) is one of the typical triterpene alcohols and possesses several biological activities including anti-oxidative activity, antiallergic activity, anti-inflammatory and anticancer activities.

2-Furoyl-LIGRLO-amide is a potent and selective proteinase-activated receptor 2 (PAR2) agonist with a pD2 value of 7.0..

Nicotinamide-d4 is the deuterium labeled Nicotinamide. Nicotinamide is a form of vitamin B3 that plays essential roles in cell physiology through facilitating NAD+ redox homeostasis and providing NAD+ as a substrate to a class of enzymes that catalyze non-redox reactions. Nicotinamide is an inhibitor of SIRT1.

(R)-Ketorolac ((+)-Ketorolac) is the R-enantiomer of ketorolac that functions as a selective allosteric inhibitor of the small GTPases Cdc42 and Rac1, blocking GTP binding and downstream signaling pathways like PAK activation. It exhibits the potential for repurposing as an anti-metastatic agent in ovarian cancer.

Caerulomycin A (Cerulomycin; Caerulomycin), an antifungal compound, induces generation of T cells, enhances TGF-β-Smad3 protein signaling via suppressing interferon-γ-induced STAT1 signaling. Antifungal and antibiotic activity, and used in autoimmune diseases.

Nourseothricin sulfate (Streptothricin sulfate) is a broad-spectrum antibiotic that destroys the outer membrane of Gram-negative bacteria and is a dominant selective marker for Fonsecaea pedrosoi. Nourseothricin sulfate inhibits protein biosynthesis in prokaryotic cells and strongly inhibits the growth of eukaryotes like fungi and can also be used as a elective marker for a wide range […]

Roluperidone (CYR-101; MIN-101) is a cyclic amide derivative with antagonistic activity against serotonergic 5-HT2A, sigma-2, and α1A-adrenergic receptors. It exhibits Ki of 7.53 nM for 5-HT2A and 8.19 nM for sigma-2 receptors, with potential for the treatment of schizophrenia.