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SIJ1777 is a pyrimidopyrimidinone class type II pan-BRAF inhibitor, optimized as a derivative of GNF-7. It exerts anti-tumor effects by simultaneously inhibiting the phosphorylation and activation of the MAPK pathway (MEK/ERK) and the PI3K/AKT pathway.
Research Areas: Cancer
Targets: MEK; ERK; Akt; Apoptosis

MSU-44147 is a small-molecule inhibitor that targets the membrane transport protein MmpL3 in Mycobacterium abscessus. MSU-44147 exhibits selective anti-mycobacterial activity and low cytotoxicity toward eukaryotic cells.
Research Areas: Infection

LN-439A is a novel tetrahydro-β-carboline small molecule that acts as a potent catalytic inhibitor of the BAP1 deubiquitinase. It induces ubiquitination and degradation of the KLF5 transcription factor by binding to the catalytic pocket of BAP1.
Research Areas: Cancer
Targets: KLF; RAD51

LLS30 is an allosteric inhibitor of Galectin-1 (Gal-1). LLS30 inhibits the downstream MEK/ERK signaling pathway and also inhibits Akt phosphorylation. LLS30 exhibits potent proliferation-inhibitory activity against various prostate cancer cell lines.
Research Areas: Cancer
Targets: MEK; ERK

LG-121071 is an orally active selective androgen receptor modulator (SARM) with a Ki of approximately 17 nM for the androgen receptor. It is commonly used in studies of androgen receptor-related diseases, such as prostate cancer.
Research Areas: Cancer
Targets: Androgen Receptor

IA65 is a selective small molecule agonist that enhances Orai1 channel-mediated calcium influx and activates calcium-dependent inactivation mechanisms.
Research Areas: Cardiovascular Research
Targets: Orai1 agonist

Frevecitinibum is a Janus kinase (JAK) inhibitor with activity against multiple JAK isoforms, including JAK1, JAK2, JAK3, and TYK2, thereby suppressing activation of the JAK-STAT signaling pathway.
Research Areas: Immunology & Inflammation
Targets: JAK/Pan-JAK

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