Enamines
Medchemexpress LLC Nimodipine (BAY-e 9736) | 66085-59-4 | 99.9% | 1 G
Nimodipine (BAY-e 9736) is an orally active, well-tolerated, and light-sensitive dihydropyridine calcium antagonist. It can be used for the research of cerebrovascular disorders.
- Orally active
- Well-tolerated
- Light-sensitive
- Dihydropyridine calcium antagonist
- Used for the research of cerebrovascular disorders
Medchemexpress LLC (R)-Nimodipine ((R)-BAY-e 9736) | 77940-92-2 | 99.9% | 5 MG
(R)-Nimodipine ((R)-BAY-e 9736) | 77940-92-2 | 99.9% | 5 MG
Medchemexpress LLC Amlodipine benzenesulfonate | 111470-99-6 | 99.7% | 500 MG
Amlodipine besylate (Amlodipine benzenesulfonate) is an orally active dihydropyridine calcium channel blocker and antianginal agent. It functions by blocking voltage-dependent L-type calcium channels, inhibiting initial calcium influx. This compound can be used for research into high blood pressure and cancer.
- Blocks voltage-dependent L-type calcium channels
- Inhibits initial influx of calcium
- Useful for high blood pressure research
- Useful for cancer research
Medchemexpress LLC Amlodipine besylate | 111470-99-6 | 99.7% | 1 ML
Amlodipine besylate is an antianginal agent and an orally active dihydropyridine calcium channel blocker. It functions by blocking voltage-dependent L-type calcium channels, which inhibits the initial influx of calcium. This product is for research use only and not sold to patients.
- Used for high blood pressure and cancer research
- Inhibits initial influx of calcium by blocking L-type channels
- Available as 10 mM in 1 mL solution in DMSO
Medchemexpress LLC (R)-Amlodipine | 103129-81-3 | MFCD06809924 | 99.5% | 408.88 g/mol | C20H25ClN2O5 | 10 MG
(R)-Amlodipine is the R-enantiomer of amlodipine, a dihydropyridine L-type calcium channel inhibitor supplied as an off-white to light yellow solid for research use. It is commonly used in pharmacological and formulation studies that require the isolated enantiomer.
- High purity (99.45%).
- Molecular weight 408.88 g/mol.
- Chemical formula C20H25ClN2O5.
- Soluble in DMSO at 100 mg/mL; ultrasonic recommended.
- In vivo formulation protocols yield ≥2.5 mg/mL solubility in listed vehicles.
- Available in small research sizes (e.g., 10 mg).
- Storage: powder -20°C for up to 3 years; in solvent -80°C for 6 months or -20°C for 1 month.
Medchemexpress LLC Methyl but-3-enoate 25g
Methyl but-3-enoate is a drug intermediate for synthesis of various active compounds
Apexbio Technology LLC Amlodipine 88150-42-9 10mM (in 1mL DMSO)
Amlodipine (CAS 88150-42-9) is a dihydropyridine-based small molecule that functions as a long-acting calcium channel blocker It selectively inhibits L-type calcium channels on vascular smooth muscle and cardiac myocytes thereby reducing intracellular calcium influx This action leads to vasodilation and decreased vascular resistance Amlodipine is widely utilized in biomedical research to investigate calcium signaling pathways vascular tone modulation and cardiovascular pharmacology Its mechanistic profile also makes it a reference compound in studies evaluating novel antihypertensive or vasodilatory agents
Medchemexpress LLC ALLO-2 | 1316652-41-1 | 98.7% | 326.37 g·mol⁻¹ | C16H14N4O2S | 25 MG
NCC-149 is a selective histone deacetylase 8 (HDAC8) inhibitor used in research on neural differentiation and HDAC8-related signaling pathways. It is supplied as a high-purity solid for laboratory use and is commonly prepared as a DMSO stock for cellular and biochemical assays.
- Selective HDAC8 inhibition for targeted epigenetic studies.
- Suitable for neural differentiation experiments and mechanistic research.
- High reported purity for reproducible experimental results.
- Available in small milligram pack sizes for screening and assay development.
- Soluble in DMSO for preparation of concentrated stock solutions.
![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.
Medchemexpress LLC TO-1187 (TFA) | 98.4% | 795.72 | 25 MG
TO-1187 TFA is a selective PROTAC degrader designed to target HDAC6, effectively promoting its ubiquitination and subsequent degradation. It is a valuable tool for research into hematological malignancies and solid tumors, composed of an HDAC6 ligand, a CRBN ligase ligand, and a linker.
- Selective PROTAC degrader for HDAC6
- Promotes ubiquitination and degradation of HDAC6
- Useful for studying hematological malignancies and solid tumors
- Provided as a light yellow to yellow solid
- Soluble in DMSO at 100 mg/mL