Lactims
![Medchemexpress LLC 4-[4-(1H-Imidazol-1-yl)phenyl]-N-2-propyn-1-yl-2-pyrimidinamine | 2234272-10-5 | 98.1% | C16H13N5 | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000258861.png-250.jpg)
Medchemexpress LLC 4-[4-(1H-Imidazol-1-yl)phenyl]-N-2-propyn-1-yl-2-pyrimidinamine | 2234272-10-5 | 98.1% | C16H13N5 | 10MG
AP-C5 is a selective small-molecule inhibitor of cGMP-dependent protein kinase II (cGKII) used in cellular and biochemical research, including studies of diarrheal disease. It also contains an alkyne functional group that enables copper-catalyzed azide-alkyne cycloaddition (click chemistry) for probe conjugation.
- Selective cGKII inhibition suitable for biochemical and cellular assays.
- Click-chemistry compatible alkyne for facile probe conjugation.
- High purity (>98%) for consistent experimental performance.
- Solid, light yellow to light brown physical form for straightforward handling.
- Stable when stored under recommended conditions for long-term use.
- Good solubility in DMSO for preparation of screening solutions.
Medchemexpress LLC Glutarimide-isoindolinone-NH-PEG4-COOH | 2927334-86-7 | 99.5% | 507.53 | 100 MG
Glutarimide-Isoindolinone-NH-PEG4-COOH is a synthesized E3 ligase ligand-linker conjugate that incorporates a cereblon ligand and a linker used in PROTAC technology. Proteolysis Targeting Chimeras (PROTACs) consist of two different ligands connected by a linker; one ligand targets an E3 ubiquitin ligase, and the other targets the protein of interest. PROTACs function by leveraging the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- Synthesized E3 ligase ligand-linker conjugate
- Incorporates a cereblon ligand
- Used in PROTAC technology
- Leverages the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
Chem-Impex International, Inc. Cycloheximide (from Streptomyces griseus) | 66-81-9 | MFCD00082346 | 5G
Cycloheximide (from Streptomyces griseus), 66-81-9, MFCD00082346, 5G