Enamines
Medchemexpress LLC Amlodipine maleate | 88150-47-4 | 99.9% | 1 ML
Amlodipine maleate is a dihydropyridine calcium channel blocker that acts as an orally active antianginal agent. It blocks voltage-dependent L-type calcium channels, thereby inhibiting the initial influx of calcium.
- Acts as an orally active antianginal agent
- Blocks voltage-dependent L-type calcium channels
- Inhibits the initial influx of calcium
- Used for research on high blood pressure
- Used for research on cancer
Medchemexpress LLC Amlodipine maleate | 88150-47-4 | 99.9% | 1 G
Amlodipine maleate is a dihydropyridine calcium channel blocker that acts as an orally active antianginal agent. It blocks voltage-dependent L-type calcium channels, inhibiting the initial influx of calcium. It can be used for the research of high blood pressure and cancer.
- Calcium channel blocker
- Orally active
- Blocks voltage-dependent L-type calcium channels, inhibiting the initial influx of calcium
- Used for research related to high blood pressure and cancer
- High purity (99.87%)
Apexbio Technology LLC Cisatracurium Besylate 96946-42-8 25mg
Cisatracurium Besylate (CAS 96946-42-8) is a non-depolarizing neuromuscular blocking agent that acts by competitively inhibiting acetylcholine at nicotinic receptors on the neuromuscular junction This inhibition prevents depolarization of the muscle cell membrane resulting in skeletal muscle relaxation Cisatracurium Besylate is utilized in biomedical research to study neuromuscular transmission skeletal muscle function and mechanisms underlying muscle paralysis It is also frequently used as an adjunct in anesthesia research to model conditions requiring controlled muscle relaxation such as intubation or mechanical ventilation
![Medchemexpress LLC N-hydroxy-3-[1-(phenylsulfanylmethyl)triazol-4-yl]benzamide | 1316652-41-1 | MFCD21363002 | 99.3% | 326.37 g/mol | C16H14N4O2S | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000227588.png-250.jpg)
Medchemexpress LLC N-hydroxy-3-[1-(phenylsulfanylmethyl)triazol-4-yl]benzamide | 1316652-41-1 | MFCD21363002 | 99.3% | 326.37 g/mol | C16H14N4O2S | 100 MG
NCC-149 (CAS 1316652-41-1) is a selective histone deacetylase 8 (HDAC8) inhibitor used in neural differentiation and other HDAC8-targeted research. The compound has molecular formula C16H14N4O2S and a molecular weight of 326.37 g/mol. Certificate of analysis lists purity ~99.3%. Store powder at -20°C for long-term stability. For research use only.
- Selective HDAC8 inhibitor suitable for target validation and neural differentiation assays.
- Validated molecular identity: C16H14N4O2S; MW 326.37 g/mol.
- High purity reported by COA (≈99.3%).
- Available in multiple pack sizes, including 100 MG.
- Powder storage at -20°C extends shelf life; follow SDS for solvent storage recommendations.
- Supporting documentation available: SDS and COA for handling and quality verification.
Selleck Chemical LLC PF-562271 Besylate S2672-50mg
PF-562271 Besylate is the benzenesulfonate salt of PF-562271 which is a potent ATP-competitive reversible inhibitor of FAK with IC50 of 1 5 nM 10-fold less potent for Pyk2 than FAK and 100-fold selectivity against other protein kinases except for some CDKs Phase 1
Medchemexpress LLC PF-562271 besylate | 939791-38-5 | 99.2% | 665.66 g·mol⁻¹ | C27H26F3N7O6S2 | 100 MG
PF-562271 besylate is an ATP-competitive, reversible inhibitor of focal adhesion kinase (FAK) and Pyk2 that exhibits low-nanomolar potency and is used in biochemical and cellular research to probe FAK/Pyk2 signaling pathways.
- Potent inhibition of FAK and Pyk2 with IC50s of 1.5 nM and 13 nM.
- High purity suitable for research applications.
- Chemical formula C27H26F3N7O6S2; molecular weight 665.66 g·mol⁻¹.
- Available in multiple package sizes, including 100 mg.
- Storage: sealed at 4°C; in solvent: -80°C (6 months), -20°C (1 month).
Medchemexpress LLC PF-562271 besylate | 939791-38-5 | MFCD14105612 | 99.2% | 665.66 g·mol⁻¹ | C27H26F3N7O6S2 | 25 MG
PF-562271 besylate is a small-molecule, ATP-competitive and reversible inhibitor of focal adhesion kinase (FAK) and proline-rich tyrosine kinase 2 (Pyk2). It exhibits low-nanomolar potency in biochemical assays and is used in biochemical and cell-based studies to investigate FAK/Pyk2 signaling, cell migration, and cancer-related pathways. Supplied as a high-purity solid for research use.
- Potent ATP-competitive, reversible inhibition of FAK and Pyk2.
- Low-nanomolar biochemical potency (FAK IC50 ≈ 1.5 nM; Pyk2 IC50 ≈ 13 nM).
- Suitable for biochemical and cell-based assays investigating signaling and migration.
- High purity appropriate for research applications.
- Soluble in DMSO and largely insoluble in water.
- Available in small research pack sizes for laboratory studies.
Sigma Aldrich Fine Chemicals Biosciences Adrenochrome | 54-06-8 | MFCD00069732 | 25g
Adrenochrome | Purity: >95% | Mol Wt: 179.17 | 54-06-8 | MFCD00069732 | 25g
