Lactims
Sigma Aldrich Fine Chemicals Biosciences Cycloheximide | 66-81-9 | MFCD00082346 | 1g
Cycloheximide | Purity: 94% | MW: 281.35 | 66-81-9 | MFCD00082346 | 1g
Medchemexpress LLC 7030B-C5 | 370871-42-4 | 99.8% | 359.38 g/mol | C17H21N5O4 | 10 MG
7030B-C5 is a small-molecule PCSK9 inhibitor intended for preclinical research. It shows in vitro activity (IC50 = 1.61 μM) and has been reported to reduce plasma cholesterol and triglyceride levels in vivo. The compound is identified by CAS No. 370871-42-4 and is supplied at high purity for laboratory studies.
- Small-molecule PCSK9 inhibitor with reported IC50 of 1.61 μM.
- Demonstrated in vivo activity reducing plasma cholesterol and triglyceride levels.
- High purity (99.78%), suitable for preclinical studies.
- Characterized molecular weight 359.38 g/mol and formula C17H21N5O4.
- Supplied as a 10 mg quantity for laboratory use.
Crescent Chemical Co Inc CYCLOHEXIMIDE CRYST. PURE
Cycloheximide cryst. pure Glutarimide antibiotic isolated from Streptomyces griseus; active against fungi and yeasts, but not against bacteria. Inhibits eukaryotic protein synthesis by blocking the translocation step in the elongation cycle (1,3,8). Blocks tra
Chem-Impex International, Inc. Cycloheximide (from Streptomyces griseus) | 66-81-9 | MFCD00082346 | 1G
Cycloheximide (from Streptomyces griseus), 66-81-9, MFCD00082346, 1G
Cayman Chemical Cycloheximide, Purity: ≥95%, CAS: 66-81-9, 100 mg
An inhibitor of protein synthesis in eukaryotes (IC50 = 5-50 μM) that functions by interfering with translational elongation; can either induce or inhibit apoptosis depending on cell type
Cayman Chemical Cycloheximide, Purity: ≥95%, CAS: 66-81-9, 1 g
An inhibitor of protein synthesis in eukaryotes (IC50 = 5-50 μM) that functions by interfering with translational elongation; can either induce or inhibit apoptosis depending on cell type
TARGETMOL CHEMICALS INC Cycloheximide 500MG
Also available in 200 mg and bulk. Please contact Fisher for quotes. Cycloheximide (Naramycin A) is a natural product that reversibly inhibits translation elongation, is an antimitotic compound, and is an inhibitor of DNA and protein synthesis.
Chem-Impex International, Inc. Cycloheximide (from Streptomyces griseus) | 66-81-9 | MFCD00082346 | 5G
Cycloheximide (from Streptomyces griseus), 66-81-9, MFCD00082346, 5G
Sigma Aldrich Fine Chemicals Biosciences InSolution Cytochalasin D
A cell-permeable fungal toxin that is approximately 10 times more potent than cytochalasin B (Cat. No. 250233) in inhibiting actin filament function. Does not inhibit monosaccharide transport across cell membranes. Inhibits cytoplasmic division by blocking the formation of contractile microfilaments at 10 181M. Inactivates low conductance K channels. Also modulates CD4 cross-linking in T lymphocytes and increases intracellular Ca2 levels. Cytochalasin D also exhibits antibiotic and anti-tumor properties.