Enamines
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%)
Medchemexpress LLC Nimodipine | 66085-59-4 | MFCD00153848 | 99.9% | 500 MG
Nimodipine is an orally active, well-tolerated, and light-sensitive dihydropyridine calcium antagonist used for the research of cerebrovascular disorders.
- Orally active and well-tolerated dihydropyridine calcium antagonist.
- Light-sensitive compound.
- Molecular formula: C21H26N2O7.
- Molecular weight: 418.44.
- Appearance: Solid, light yellow to yellow.
- Shipping at room temperature.
- Storage at 4°C, protected from light.
- In solvent, store at -80°C for 6 months or -20°C for 1 month, protected from light.
- Soluble in DMSO: 100 mg/mL.
Matrix Scientific Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate, 1149-23-1, MFCD00005951, 25g
Molecular Formula C13H19NO4, Purity 95+%, Molecular Weight 253.30, Melting Point 178-183°
eMolecules 164648-76-4 | 4-(Aminomethyl)-N,N-dimethylbenzamide | Combi-Blocks | MFCD07186282 | 178.235 | C10H14N2O | 97.000 | CN(C)C(=O)c1ccc(CN)cc1 | 1g | 117570899
4-(Aminomethyl)-N,N-dimethylbenzamide | Combi-Blocks | 164648-76-4 | MFCD07186282 | 178.235 | C10H14N2O | 97.000 | CN(C)C(=O)c1ccc(CN)cc1 | 1g | 117570899
Apexbio Technology LLC Amlodipine 88150-42-9 5g
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
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.
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 Amlodipine | 88150-42-9 | 99.87% | 5 G
Amlodipine is an antianginal agent and an orally active dihydropyridine calcium channel blocker. It functions by blocking voltage-dependent L-type calcium channels, thereby inhibiting the initial influx of calcium. It can be used in the research of high blood pressure and cancer.
- Functions as an antianginal agent
- Orally active dihydropyridine calcium channel blocker
- Blocks voltage-dependent L-type calcium channels
- Inhibits initial influx of calcium
- Suitable for research on high blood pressure
- Suitable for research on cancer
Sigma Aldrich Fine Chemicals Biosciences Amlodipine besylate >=98% (HPLC) | 111470-99-6 | MFCD00887594 | 50MG
Amlodipine besylate >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 567.05 | 111470-99-6 | MFCD00887594 | 50MG
Apexbio Technology LLC Mesoridazine Besylate 32672-69-8 10mM (in 1mL DMSO)
Mesoridazine besylate (CAS 32672-69-8) is a phenothiazine derivative that functions primarily as a dopamine receptor antagonist demonstrating notable inhibitory activity against dopamine D2 and D4 receptors The molecule has particularly high affinity toward the dopamine D4 receptor subtype By modulating dopamine receptor activity Mesoridazine besylate has potential relevance in neuroscience research aimed at understanding dopamine-mediated neurological pathways and disorders Frequently utilized in studies of psychotic conditions the compound serves as an important tool for investigating receptor-specific pharmacological mechanisms
Medchemexpress LLC NCC-149 | 1316652-41-1 | 98.7% | 326.37 g/mol | C16H14N4O2S | 1 ML
NCC-149 is a selective HDAC8 inhibitor intended for in vitro research applications, including neural differentiation studies. It is supplied as either a 10 mM solution in DMSO or as a solid for reconstitution, and is characterized by reported high purity and a defined molecular weight.
- Selective HDAC8 inhibition suitable for mechanistic and cellular studies.
- Useful for neural differentiation research and related assays.
- Available as 10 mM solution in DMSO or as solid for preparation of stock solutions.
- High reported purity supports reproducible experimental results.
- Defined molecular weight and formula simplify calculation of working concentrations.
Medchemexpress LLC Methyl but-3-enoate 100g
Methyl but-3-enoate is a drug intermediate for synthesis of various active compounds
TARGETMOL CHEMICALS INC Mesoridazine Besylate 10MG
Also available in 1 mL, 5 mg and bulk. Please contact Fisher for quotes.Mesoridazine Besylate (Serentil) is a piperidine neuroleptic drug belonging to the class of drugs called phenothiazines, used in the treatment of schizophrenia. It is a metabolite of thioridazine. Purity 99.58%
Medchemexpress LLC Amlodipine besylate | 111470-99-6 | 99.7% | 5 G
Amlodipine besylate | 111470-99-6 | 99.7% | 5 G