Blogs | MedChemExpress

Namodenoson (CF-102) is a Selective A3 Adenosine Receptor (A3AR) Agonist

Namodenoson (CF-102) is a selective A3 adenosine receptor (A3AR) agonist.
Temoporfin is a Second‐generation Photosensitizer for Cancer

Temoporfin, a photosensitizer agent, can be used for the research of squamous cell carcinoma of the head and neck.
Seliciclib (Roscovitine) is an Orally Active and Selective CDKs Inhibitor

Seliciclib, a potent, selective and orally active CDKs inhibitor, preferentially inhibits CDK2, CDK7 and CDK9.
Vistusertib (AZD2014) is an ATP Competitive mTOR Inhibitor

Vistusertib is an ATP competitive mTOR inhibitor with an IC50 of 2.81 nM. AZD2014 inhibits both mTORC1 and mTORC2 complexes.
Epoxomicin is a Selective and Irreversible Inhibitor of Proteasome

Epoxomicin is an epoxyketone-containing natural product and a selective and irreversible proteasome inhibitor. Cross the blood-brain barrier.
5-Azacytidine, a Nucleoside Analogue of Cytidine, Inhibits DNA Methylation

5-Azacytidine is a DNMT inhibitor. 5-Azacytidine can be used for the research of myelodysplastic syndrome.
Pimasertib is a Highly Selective and ATP non-Competitive Allosteric Inhibitor of MEK1/2

Pimasertib is a highly selective, ATP non-competitive allosteric orally available MEK1/2 inhibitor with antitumor activies.
Epothilone B is a Microtubule Stabilizer

Epothilone B, a non-taxane-related and nonneurotoxic microtubule stabilizer, can be used for the research of breast cancer.
Bisantrene, an Antitumor Drug, Targets Eukaryotic Type II Topoisomerases

Bisantrene is topoisomerase II poisons and DNA intercalators. Bisantrene intercalates with and disrupts the configuration of DNA.
Splitomicin is a cell-permeable, potent SIR2 Inhibitor

Splitomicin is a cell-permeable, potent inhibitor of SIR2. Splitomicin inhibits the aggregation of human platelets.

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Blogs (13)