Phenylhydrazines
Sigma Aldrich Fine Chemicals Biosciences Carbonyl cyanide 3-chlorophenylhydrazone | 555-60-2 | MFCD00001848 | 100 mg
Carbonyl cyanide 3-chlorophenylhydrazone | Purity: ≥97% | Mol Wt: 204.62 | 555-60-2 | MFCD00001848 | 100 mg
Aobchem (3-Bromo-2-fluoro-5-methylphenyl)(piperidin-1-yl)methanone | 95% | CAS 2918897-70-6 | C13H15BrFNO | 250mg
(3-Bromo-2-fluoro-5-methylphenyl)(piperidin-1-yl)methanone | 95% | CAS 2918897-70-6 | C13H15BrFNO | 250mg
Aobchem 4-Fluorophenylhydrazine | ≥95% | CAS 371-14-2 | C6H7FN2 | 5g
4-Fluorophenylhydrazine | ≥95% | CAS 371-14-2 | C6H7FN2 | 5g
Aobchem 6-Chloro-2-fluoro-3-methylphenol | ≥97% | CAS 261762-91-8 | C7H6ClFO | 25g
6-Chloro-2-fluoro-3-methylphenol | ≥97% | CAS 261762-91-8 | C7H6ClFO | 25g
eMolecules 100-63-0 | Phenylhydrazine | Oakwood Chemicals | MFCD00007573 | 108.144 | C6H8N2 | 97.000 | NNc1ccccc1 | 50g | 480149105
Phenylhydrazine | Oakwood Chemicals | 100-63-0 | MFCD00007573 | 108.144 | C6H8N2 | 97.000 | NNc1ccccc1 | 50g | 480149105
Medchemexpress LLC M-PEG3-0-benzaldehyde | 153364-63-7 | C14H20O5 | 5 G
M-PEG3-0-benzaldehyde is a PEG-based PROTAC linker. PROTACs contain two different ligands connected by a linker, with one ligand for an E3 ubiquitin ligase and the other for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Can be used in the synthesis of PROTACs
- Utilizes the ubiquitin-proteasome system for selective protein degradation
Medchemexpress LLC Saccharopine hydrochloride | 99.8% | 312.75 | C11H21ClN2O6 | 5 MG
Saccharopine hydrochloride is a lysine degradation intermediate that acts as a mitochondrial toxin and can disrupt mitochondrial homeostasis. It is supplied for research use in biochemical and cellular studies of lysine metabolism and mitochondrial function.
- Lysine degradation intermediate and mitochondrial toxin.
- Useful for research on lysine metabolism and mitochondrial function.
- Molecular formula: C11H21ClN2O6.
- Molecular weight: 312.75.
- Purity: 99.8%.
- Available in small milligram quantities for bench-scale experiments.
Medchemexpress LLC Hydroxylamine, O-methyl-, hydrochloride (1:1) | 593-56-6 | MFCD00012951 | 98.0% | 83.52 | CH6ClNO | 100g
Methoxyamine (O-Methylhydroxylamine) hydrochloride is an orally active and potent base excision repair (BER) inhibitor Methoxyamine hydrochloride binds to 3 hydroxyl groups that are left behind by 3-methylpurine-DNA glycosylase (MPG) following excision of the damaged base and thus inhibits BER activity Methoxyamine hydrochloride binds directly to the apyrimidinic (AP) sites Methoxyamine hydrochloride synergistically enhances the therapeutic efficacy of DNA-damaging agents[1][2]
Medchemexpress LLC Pexidartinib hydrochloride | 2040295-03-0 | 99.77% | 454.28 | 1 ML
Pexidartinib hydrochloride is a potent, orally active, selective, and ATP-competitive inhibitor of colony stimulating factor 1 receptor (CSF1R or M-CSFR) and c-Kit. It exhibits high selectivity for c-Kit and CSF1R over other related kinases, induces cell apoptosis, and demonstrates anti-cancer activity.
- Potent, orally active, selective, and ATP-competitive inhibitor
- Induces cell apoptosis
- Demonstrates anti-cancer activity
- High selectivity for c-Kit and CSF1R over other related kinases
- Can be used to deplete microglia cells in mice
- Reduces tissue macrophage levels