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Á¦¸ñ [MedChemExpress ; MCE] New Bioactive Molecules for April 2022
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ÀÛ¼ºÀÏÀÚ 2022-04-06
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MCE (MedChemExpress) provides a wide range of lifescience biochemicals, including more than 30,000 bioactive compounds, dye reagents, peptides and natural compounds for laboratory and scientific use. If you need these products, please do not hesitate to contact us via sales@MedChemExpress.com.
CAS No.: 2711006-67-4
ZXH-4-130 TFA

Research Area: PROTAC CRBN Degrader/Multiple Myeloma

ZXH-4-130 TFA structure
Potent and highly selective PROTAC CRBN degrader which is a CRBN-VHL compound (hetero-PROTAC).
Induces ~80% CRBN degradation at 10 nM in MM1.S cells.

Solubility: DMSO : 170 mg/mL (172.57 mM; Need ultrasonic)

DSM705 hydrochloride

Research Area: DHODH Inhibitor/Malaria

DSM705 hydrochloride structure
Potent antimalarial and orally active, selective Plasmodium DHODHs inhibitor.
Shows inhibitory activity against P. falciparum DHODH (PfDHODH, IC50=95 nM), P. vivax DHODH (PvDHODH, IC50=52 nM) and Pf3D7 cells (EC50=12 nM), with no inhibition of the human enzyme.

Solubility: DMSO : 100 mg/mL (226.83 mM; Need ultrasonic)

CAS No.: 1312547-19-5

Samatasvir

Research Area: NS5A Inhibitor/HCV Infection

Potent and orally active NS5A inhibitor of HCV replication, with EC50s of 2 to 24 pM in genotype 1 through 5 replicons.
Selective for HCV and is not active against other DNA and RNA viruses.
Effectively combined with other classes of direct-acting HCV antivirals, as well as IFN-¥á and Ribavirin.

Solubility: DMSO : 50 mg/mL (56.49 mM; Need ultrasonic)

Hcyb1

Research Area: PDE2 Inhibitor/Depression

Hcyb1 structure
Highly selective, orally active PDE2 inhibitor with an IC50 of 0.57 ¥ìM for PDE2A.
Shows over 250-fold selectivity against other recombinant PDE family members.
Has neuroprotective and antidepressant‐like effects.

Solubility: DMSO : 62.5 mg/mL (164.28 mM; Need ultrasonic)

CAS No.: 2097117-06-9

Lu AF27139

Research Area: P2X7 Receptor Antagonist/Neuroinflammation and CNS Diseases

Lu AF27139 structure
Orally active, rodent-active, and CNS-penetrant P2X7 receptor antagonist (IC50s=12 and 2.4 nM for human and rat P2X7 receptor, respectively; Kis=22, 54, and 13 nM for mouse, human and rat P2X7 receptor, respectively).
Has the potential for the research of CNS disease.

Solubility: DMSO : 125 mg/mL (251.04 mM; Need ultrasonic)

Apoptosis Detection Kit
KitDescription
Annexin V-FITC/PI Apoptosis Detection KitMCE Annexin V-FITC/PI Apoptosis Detection Kit provides a rapid and convenient method to detect cell apoptosis and necrosis.
After staining, live cells show little or no fluorescence (Annexin V-/PI-), early apoptosis cells show green fluorescence (Annexin V+/PI-), late apoptosis cells and necrosis cells show red and green fluorescence (Annexin V+/PI+).
Cell Cycle and Apoptosis Analysis Kit (PI staining)MCE Cell Cycle and Apoptosis Analysis Kit (PI staining) provides a convenient method to detect cell cycle and cell apoptosis.
The content of DNA is changed with the process of cell cycle. DNA can be stained by fluorescent dye, such as Propidium Iodide (PI), to measure its intensity by flow cytometry to monitor the cell cycle distribution in G1/S/G2/M phase as well as apoptosis cells with signals at sub-G1 region.
Flavonoids
Flavonoids refer to a series of compounds synthesized by connecting two benzene rings (often referred to as A ring and B ring) with three central carbons. They are called flavonoids because their structure contains ketone groups, and their color is often yellow. Flavonoids widely exists in nature. Most of them combine with saccharides to form flavonoid glycosides in plants, and few of these exist as aglycones. Generally, flavonoids can be divided into several subgroups such as flavones, dihydroflavones, chalcone and isoflavones.
Flavonoids have a wide range of activities. For example, Rutin, a common flavonoid in nature, has antioxidant, anti-inflammatory, and antiviral activities, and Silymarin derived from Silybum marianum has antiviral and anti-tumor effects.
Cat. No.Drug NameStructureDescription
HY-N18603-O-MethylquercetinMangiferin structureInhibits total cAMP and cGMP-phosphodiesterase (PDE) of guinea pig trachealis. Exhibits IC50s ranging from 1.6-86.9 ¥ìM for PDE isozymes (PDE1-5).
HY-N6896IsoviolanthinAlpha-Mangostin structureMarkedly inhibits TGF-¥â1-mediated migration and invasion by deactivating epithelial-mesenchymal transition (EMT) via the TGF-¥â/Smad and PI3K/Akt/mTOR pathways in HCC cells. Exhibits no cytotoxic effects on normal liver LO2 cells.
HY-N70127,3',4'-Tri-O-methylluteolinGambogic Acid structurePossesses potent anti-inflammatory effects in LPS-induced macrophage cell line mediated by inhibition of release of inflammatory mediators, NO, PGE2, and pro-inflammatory cytokines.
Significantly induces reduction in the mRNA __expression__s of inducible nitric oxide synthase and cyclooxygenase-2.
HY-N2412IrisolidoneGarcinone D structureShows the high efficacy for volume-regulated anion channels (VRAC) blockade (IC50=9.8 ¥ìM). Hepatoprotective activity.
Latest Publications Citing Use of MCE Products
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2022 Mar;603(7899):138-144.
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