Lactims
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.
Sigma Aldrich Fine Chemicals Biosciences Cycloheximide | 66-81-9 | MFCD00082346 | 1g
Cycloheximide | Purity: 94% | MW: 281.35 | 66-81-9 | MFCD00082346 | 1g
Medchemexpress LLC 10-(6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanoyl)-4,7,13,16-tetraoxa-10-azanonadecanedioic acid | 3026691-12-0 | 98.0% | 530.57 g·mol-1 | C24H38N2O11 | 50mg
Mal-C5-N-bis(PEG2-C2-acid) is an ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]
Cayman Chemical CyclohexImIde 100mg
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
Medchemexpress LLC Complement C5/C5a C 100ug | 100ug
Complement C5 is activated by C5 convertase inducing C5-C9 assembly to form the membrane attack complex The transient C6 binding site on C5b is critical for the formation of the cleavage complex Complement C5/C5a Protein Cynomolgus is the recombinant cynomolgus-derived Complement C5/C5a protein expressed by E coli with tag free
Apexbio Technology LLC Cycloheximide 10mM (in 1mL DMSO)
Cycloheximide (CAS 66-81-9) is a small molecule inhibitor that specifically disrupts protein biosynthesis in eukaryotic cells by interfering with translational elongation at the ribosomal level It is widely employed in biomedical research to transiently block protein synthesis in vitro facilitating the study of cellular processes dependent on active translation Due to its cytotoxicity teratogenic potential and capacity to induce DNA damage cycloheximide is exclusively utilized for experimental research applications and inappropriate for clinical therapeutic use
Medchemexpress LLC HA/Hemagglutinin H7 50ug
The hemagglutinin (HA) protein attaches viral particles to host cells by binding to sialic acid-containing receptors and induces viral particle internalization through clathrin-dependent endocytosis HA also promotes an alternative clathrin- and caveolin-independent pathway for some virions HA/Hemagglutinin Protein H7N9 (AGI60301 sf9 His) is the recombinant Virus-derived HA/Hemagglutinin protein expressed by Sf9 insect cells with C-His labeled tag
Medchemexpress LLC Dibromomaleimide-C5-COOH | 1443214-97-8 | 99.4% | 369.01 | C10H11Br2NO4 | 5 MG
Dibromomaleimide-C5-COOH is a bifunctional dibromomaleimide (DBM) linker used in antibody-drug conjugate (ADC) synthesis. It provides a C5 carboxylic acid handle for conjugation to payloads such as MMAF and is supplied for research use only.
- Bifunctional dibromomaleimide linker for ADC synthesis.
- Suitable for conjugation to MMAF and similar payloads.
- High purity (99.4%) to support reproducible chemistry.
- Molecular weight 369.01; formula C10H11Br2NO4.
- Intended for research use only; not for human or clinical use.
Cayman Chemical CyclohexImIde 1g
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
Chem-Impex International, Inc. Cycloheximide (from Streptomyces griseus) | 66-81-9 | MFCD00082346 | 5G
Cycloheximide (from Streptomyces griseus), 66-81-9, MFCD00082346, 5G
Medchemexpress LLC 3-Quinolinecarboxylic acid, 4-hydroxy-8-nitro- | 35973-25-2 | 98.5% | 1 MG
DNA2 inhibitor C5 is a potent, competitive, and specific DNA2 nuclease inhibitor with an IC50 of 20 μM. It inhibits the nuclease, DNA-dependent ATPase, helicase, and DNA-binding activities of DNA2. It can be used in breast cancer and colorectal cancer research.
- Potent, competitive, and specific DNA2 nuclease inhibitor
- Inhibits nuclease, DNA-dependent ATPase, helicase, and DNA-binding activities of DNA2
- Useful in breast cancer and colorectal cancer research
- Shows strong synergistic effect in inhibiting MCF7 cell survival with MK4827
Chem-Impex International, Inc. Cycloheximide (from Streptomyces griseus) | 66-81-9 | MFCD00082346 | 1G
Cycloheximide (from Streptomyces griseus), 66-81-9, MFCD00082346, 1G
Sigma Aldrich Fine Chemicals Biosciences Cycloheximide | 66-81-9 | MFCD00082346 | 5g
Cycloheximide | Purity: ≥95% | Mol Wt: 281.35 | 66-81-9 | MFCD00082346 | 5g
AG Scientific Inc Cycloheximide 5 G
Cycloheximide is an antibiotic produced by Streptomyces sp. that activates against yeasts and fungi. It inhibits protein synthesis thru DNA translation arrest in eukaryotes. Cycloheximide also inhibits chain initiation and chain elongation by acting on 60S subunits of eukaryote ribosome.