T8173

Delafloxacin meglumine (RX-3341 meglumine) is a broad-spectrum fluoroquinolone antibiotic.

Myristoyl hexapeptide-16, a bioactive peptide known for stimulating eyelash growth, is reported to be used as a cosmetic ingredient [1].

Myosin light chain kinase fragment 11-19 amide (MLCK(11-19) amide) acts as a substrate-specific peptide inhibitor of MLCK and inhibits hypotonicity-induced Ca2+ entry, with applications in human cervical cancer research [1] [2].

Myelin Oligodendrocyte Glycoprotein (40-54), Rat, Mouse (MOG (40-54)) is a self-antigenic epitope associated with the CD8 class of proteins within the MOG protein, presented in conjunction with H-2Db [1].

Myelin Basic Protein (1-11), an encephalitogenic epitope of MBP, facilitates the induction of experimental autoimmune encephalomyelitis (EAE) [1] [2].

Mycestericin C, isolated from Mycelia sterilia ATCC 20349 culture broth, inhibits lymphocyte proliferation in the mouse allogeneic mixed lymphocyte reaction [1].

Muzastotug (ADG126) is a humanized monoclonal antibody targeting CTLA-4/CD152 that selectively inhibits CTLA-4-mediated regulatory T cells (Tregs) in the tumor microenvironment, demonstrating anti-tumor immunotherapy efficacy.

MurF-IN-1 is an antibacterial agent and a potent inhibitor of S. pneumoniae MurF ligase (pIC50 = 5.19). It disrupts cell wall assembly by interfering with peptidoglycan synthesis.

Murabutide, a safe synthetic immunomodulator, diminishes the expression of CD4 and CCR5 receptors and promotes the secretion of high levels of beta-chemokines, thereby enhancing nonspecific resistance to viral infections. It does not impact virus entry, reverse transcriptase activity, or the formation of early proviral DNA in the cytoplasm of infected cells [1].

Compound 5K (Multi-target kinase inhibitor 2) is a multi-targeted kinase inhibitor demonstrating activity against EGFR, Her2, VEGFR2, and CDK2 with IC50 values between 40 to 204 nM. It exhibits cytotoxic effects on HepG2, HeLa, MDA-MB-231, and MCF-7 cell lines, with IC50 values of 41, 57, 51, and 59 μM, respectively. Additionally, it induces cell cycle arrest and apoptosis specifically in HepG2 cells.