cx 5

Anti-Mouse NKG2D/CD314 Antibody (CX5) is a rat-derived inhibitory antibody targeting mouse NKG2D/CD314. It can reduce the cytotoxicity of natural killer cells and is used in research on cancer, infection, inflammation, immunology, and metabolic diseases, including colitis and diabetes.

AM6701 is an effective dual inhibitor of FAAH (fatty acid amide hydrolase) and MAGL (monoacylglycerol lipase), with an IC50 of 1.2 nM. It exhibits neuroprotective effects by modulating endogenous cannabinoids and inhibiting calpain-mediated excitotoxic brain injury.

Lasalocid sodium (Lasalocid-A sodium) is a cationic ionophore antibiotic derived from Streptomyces lasaliensis that disrupts calcium fluxes in muscle fibers. It is primarily used as a coccidiostat, particularly in poultry.

Lasalocid (Lasalocid-A) is an ion carrier antibiotic produced by Streptomyces, which has antimicrobial and parasitic properties and is often added to feed.

CX516 (Ampalex), an ampakine and nootropic, acts as an AMPA receptor positive allosteric modulator as a therapy for Alzheimer's disease, schizophrenia and mild cognitive impairment (MCI).

CX5461 is an rRNA synthesis inhibitor with oral activity that inhibits Pol I-driven rRNA transcription. CX5461 activates the DNA damage response and has antitumor activity in tumors such as ovarian cancer.

NCX-530 is a compound formed by the partial chemical bonding of the Indomethacin molecule with nitric oxide (NO). It releases NO, inhibits cancer cell proliferation, and induces apoptosis. NCX-530 is applicable in research related to cancer and inflammation.

CX-5279 is a potent and selective CK2 inhibitor, exhibiting IC50 values of 2.73 nM for nCK2 and 0.91 nM for CK2α. It shows sensitivity to mutations Val66, Ile174, and V66I174AA, with IC50 values of 13.8 nM, 12.5 nM, and 23.35 nM, respectively, and demonstrates weak inhibitory activity against PIM1 with an IC50 of 8.52 μM. CX-5279 displays antiproliferative activity across various cancer cell lines and can be used in research on cancers such as pancreatic cancer and leukemia.

CX-5461 dihydrochloride is a potent, orally active inhibitor of Pol I-mediated rRNA synthesis that acts on HCT-116 cells (IC50: 142 nM), A375 cells (IC50: 113 nM) and MIA PaCa-2 cells (IC50: 54 nM), and to a lesser extent on Pol II (IC50 ≥ 25 μM).

EML-405 is a small-molecule inhibitor of SPIN1 ( Kd of 14 uM).

CX-5011, a CK2 inhibitor, induces Rac1 activation and promotes apoptosis, effectively causing cancer cell death [1] [2].

CX546 is an AMPA receptor modulator. CX546 enhances cognitive function in rats. It has also been proposed as a treatment for schizophrenia.

CX-6258 is an orally valid Pim 1/2/3 kinase(IC50=5 nM/25 nM/16 nM) inhibitor. It has good biological activity and kinase specificity.

CX-6258 hydrochloride (Pim-Kinase Inhibitor X) is an effective, orally efficacious Pim1/2/3 kinase inhibitor (IC50: 5/25/16 nM).

CX-6258 hydrochloride hydrate is a potent, selective inhibitor of pan-Pim kinase, targeting Pim-1 (IC50: 5 nM), Pim-2 (IC50: 25 nM), and Pim-3 (IC50: 16 nM).