Labware Detergents and Cleaners
Medchemexpress LLC CYM50358, Solution, 10 mM * 1 mL in DMSO
CYM50358 is a potent and selective S1PR4 antagonist, with an IC50 of 25 nM. CYM50358 can be used for the research of influenza infection.
Medchemexpress LLC (-)-JNJ-A07 | 2135640-92-3 | 98.0% | 578.96 g/mol | C28H26ClF3N2O6 | 5 MG
(-)-JNJ-A07 is the (-) enantiomer of JNJ-A07, a potent and selective dengue virus (DENV) inhibitor that disrupts viral replication by targeting the NS3-NS4B interaction. It exhibits low-nanomolar antiviral activity (EC50 = 31 nM) and is supplied for research use. Chemical identifiers include CAS 2135640-92-3, formula C28H26ClF3N2O6, molecular weight 578.96 g/mol; typical purity is ~98%.
- Potent DENV inhibitor (EC50 31 nM).
- Chiral (-) enantiomer for stereospecific studies.
- High chemical purity (~98%).
- Available as solid and 10 mM solution in DMSO across multiple sizes.
- Well-defined chemical identity: CAS 2135640-92-3; formula C28H26ClF3N2O6.
- For research use only, not for human or veterinary use.
Enterprise Technology Solutions Betco Corporation Detergent,Dye/Fragrance-free,Concentrated,5 Gal,Clear
Count on the same great cleaning performance as Betco's Symplicity Detergent but without dyes and fragrance that cause allergies and sensitivities in some customers. Concentrated synthetic detergent with powerful surfactants and anti-redeposition agents release heavy soils from the linen, preventing dulling and leaving linen fresh and white. Blended surfactant technology means it is effective on a variety of soil types. Use as a standalone detergent or with Symplicity Break Alkaline Booster for the worst soils and stains. Detergency is Cold Water Effective, saving energy by getting the job done in cold water. For low environmental impact, it contains no phosphorous, APE, NPE or EDTA.
BRANSON ULTRASONICS CORPORATION (3P) QT. CASE INDSTRL STRNGTH 12/CS
Branson Ultrasonics Ultrasonic Industrial Cleaning Solutions, Size: 1 qt., Concentration: 8 to 10%, For Use With: Cutting Oils, Metal Carbon, pH Range: 11 to 12, Recommended Applications: Safety
Selleck Chemical LLC JNJ-A07-E1422-1G
JNJ-A07 is a highly potent inhibitor of Dengue virus (DENV) with an EC50 of 0 1 nM in the DENV-2 strain (16681) in Vero cells It exhibits antiviral activity by preventing the formation of the viral replication complex through blocking the interaction between two viral proteins NS3 and NS4B
Medchemexpress LLC (+)-JNJ-A07 | 2135640-93-4 | 98.5% | 578.96 | 25 MG
(+)-JNJ-A07 is a highly potent, orally active pan-serotype dengue virus inhibitor that targets the NS3-NS4B interaction. It demonstrates nanomolar to picomolar activity against a panel of 21 clinical isolates. The compound possesses a favorable pharmacokinetic profile, leading to outstanding efficacy against dengue virus infection in mouse infection models.
- Exhibits a high barrier to resistance
- Prevents the formation of the viral replication complex by blocking the interaction between two viral proteins (NS3 and NS4B)
- Potent and orally active pan-serotype dengue virus inhibitor
- Effective against a panel of 21 clinical isolates
- Favorable pharmacokinetic profile
- Outstanding efficacy against dengue virus infection in mouse models
Medchemexpress LLC Butanoic acid, 4-[3-[[1-(4-chlorophenyl)-2-[2,3-dihydro-6-(trifluoromethoxy)-1H-indol-1-yl]-2-oxoethyl]amino]-5-methoxyphenoxy]-, (-)- | 2135640-92-3 | 99.35% | 578.96 | 1 MG
(-)-JNJ-A07 is a potent and selective DENV inhibitor with an EC50 value of 31 nM. It is for research use only and not sold to patients.
- For research use only
- Potent and selective DENV inhibitor with an EC50 value of 31 nM
- Appearance: white to light yellow solid
- Powder storage: -20°C for 3 years
- In solvent storage: -80°C for 6 months, -20°C for 1 month
Anatech Ltd EZ Green, 1 qt
A stain specially created for use with EZ Mucicarmine as a contrast-enhancing green counterstain.
Medchemexpress LLC LYG-409 GSPT1 degrader | 3053857-55-6 | 98.1% | 515.44 | 50 MG
LYG-409 is an orally active degrader of GSPT1. It demonstrates excellent anti-acute myeloid leukemia and prostate cancer activity in vivo, with TGI of 94.34% and 104.49% respectively. LYG-409 inhibits KG-1 cells through the degradation of GSPT1 with an IC50 of 9.50 nM, and a DC50 of 7.87 nM in vitro.
- Orally active degrader of GSPT1.
- Exhibits anti-acute myeloid leukemia and prostate cancer activity in vivo.
- Inhibits KG-1 cells by degrading GSPT1.