Oxazoles
Medchemexpress LLC (2S,4S)-Sacubitril | 149709-63-7 | C24H29NO5 | 1 ML
(2S,4S)-Sacubitril is an impurity of Sacubitril, a potent NEP inhibitor used for heart failure research. This compound is also a stereoisomer derived from Sacubitril.
- Impurity of sacubitril
- Stereoisomer derived from sacubitril
- Appears as colorless to light yellow oil
- Molecular weight: 411.49
Medchemexpress LLC Pomalidomide-C6-O-C5-O-C4-COOH | 2375774-54-0 | 98.6% | 559.65 | 50 MG
Pomalidomide-C6-O-C5-O-C4-COOH is an E3 ligase ligand-linker conjugate composed of a Pomalidomide-based cereblon ligand and linker. It can be used for the synthesis of PROTACs.
- E3 ligase ligand-linker conjugate
- Comprises a Pomalidomide-based cereblon ligand and linker
- Can be used for the synthesis of PROTACs
Selleck Chemical LLC Y-27632
Y-27632 is a selective ROCK1 and ROCK2 inhibitor with a Ki of 140 nM and 300nM in a cell-free assay exhibits 200-fold selectivity over other kinases including PKC cAMP-dependent protein kinase MLCK and PAK
Medchemexpress LLC (S)-1-t-butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate | 756486-14-3 | 97.0% | 257.29 g/mol | C12H19NO5 | 100 MG
AN-12-H5 intermediate-2 is a synthetic chemical intermediate used to prepare the viral inhibitor AN-12-H5 and as a building block for antibody-drug conjugates (ADCs). The compound is supplied as a solid with reported purity of 97.0%, molecular formula C12H19NO5, and molecular weight 257.29 g/mol.
- Used as a synthetic intermediate for antiviral compound synthesis.
- Suitable for antibody-drug conjugate (ADC) synthesis.
- Reported purity 97.0% (typical analytical grade).
- Solid form; recommended storage -20°C.
eMolecules Pharmablock / tert-butyl N-(13-oxazol-4-yl)carbamate / 25mg / 586142266 / PB92463 / 0.000 / 1314931-66-2 / MFCD18533643 / 184.195 / C8H12N2O3
Pharmablock / tert-butyl N-(13-oxazol-4-yl)carbamate / 25mg / 586142266 / PB92463 / 0.000 / 1314931-66-2 / MFCD18533643 / 184.195 / C8H12N2O3
FUJIFILM BIOSCIENCES INC Y-27632 GMP-compliant
Y-27632 is reagent for cell culture applications including human ES/iPS cell culture It enhances cell viability and reduces cell death during passaging and cryopreservation It is a selective and potent inhibitor of ROCK Rho-associated coiled-coil forming kinase/Rho binding kinase Y-27632 has a variety of activities including vascular smooth muscle contraction through the ROCK signaling Ki 140 nmol/L p160ROCK This product has been reported to suppress death of human ES/iPS cells at the time of cell dispersion and improves viability of the cells after cryopreservation This product complies with ICH-Q7 GMP for APIs as a raw material for commercial production of regenerative medicine products
Medchemexpress LLC 4-(Chloromethyl)-7-hydroxycoumarin | 25392-41-0 | 98.01% | C10H7ClO3 | 1 ML
4-(Chloromethyl)-7-hydroxycoumarin is a hydroxycoumarin derivative exhibiting potent antioxidant effects and high hydroxyl radical-scavenging properties. It contains a methyl group and a chlorine group within its heterocyclic ring and has been investigated as a potent inhibitor of zinc enzyme carbonic anhydrase isoforms CA IX and XII.
- Potent antioxidant effect
- High hydroxyl radical-scavenging property
- Investigated as inhibitors of tumor-associated carbonic anhydrase isoforms CA IX and XII