Enamines
Accela Chembio Inc Isopropyl 3-aminocrotonate | 25g | 14205-46-0 | MFCD00134272 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4
Isopropyl 3-aminocrotonate | 25g | 14205-46-0 | MFCD00134272 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4
Medchemexpress LLC (R)-Amlodipine | 103129-81-3 | 99.5% | 5 MG
(R)-Amlodipine is the R-enantiomer of Amlodipine. This compound is intended for research use only and is not suitable for patient use.
- High purity: 99.45%
- Documentation available: data sheet, COA, SDS, handling instructions, HNMR, LCMS
- Detailed solubility information provided for in vitro and in vivo dissolution
- Related research tools, antibodies, and screening libraries are available
- Classified under membrane transporter/ion channel, neuronal signaling, and calcium channel
- Related to disease areas such as blood or cardio-cerebrovascular disease, cancer, and cardiovascular disease
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.
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
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.
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