Enamines
Medchemexpress LLC PF-562271 besylate | 939791-38-5 | MFCD16038299 | 99.2% | 665.66 g·mol⁻¹ | C27H26F3N7O6S2 | 5 MG
PF-562271 besylate is a small-molecule, ATP-competitive, reversible inhibitor of focal adhesion kinase (FAK) and Pyk2 used in research to study FAK pathway modulation. It is supplied as the besylate salt for laboratory use and has been evaluated in preclinical and clinical studies.
- Potent ATP-competitive inhibitor of FAK and Pyk2 (IC50 1.5 nM and 13 nM).
- Reversible mechanism suitable for biochemical and cellular assays.
- Supplied as besylate salt for improved stability and handling.
- High chemical purity (99.17%) for reproducible results.
- Molecular weight 665.66 g·mol⁻¹, molecular formula C27H26F3N7O6S2.
- Intended for research use only; not for human or veterinary use.
Apexbio Technology LLC Mesoridazine Besylate 32672-69-8 50mg
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
Sigma Aldrich Fine Chemicals Biosciences Cisatracurium besylate Uni50MG
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.for further information and support please go to the website of the issuing Pharmacopoeia.
Accela Chembio Inc Isopropyl 3-aminocrotonate | 100g | 14205-46-0 | MFCD00134272 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4
Isopropyl 3-aminocrotonate | 100g | 14205-46-0 | MFCD00134272 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4
Apexbio Technology LLC Amlodipine Besylate 111470-99-6 10mM (in 1mL DMSO)
Amlodipine Besylate (CAS 111470-99-6) is a long-acting calcium channel blocker that reduces blood pressure primarily through inhibition of calcium ion influx via voltage-gated calcium channels Calcium channel modulation influences critical cellular signaling pathways In cortical neurons exposed to oxidative stress Amlodipine Besylate ( 5 M) preserves cellular viability by reducing oxidative damage enhancing pro-survival signals and suppressing apoptotic pathways It has also demonstrated proliferative effects on human epidermoid carcinoma (A431) cells Furthermore clinical studies indicate that Amlodipine Besylate decreases peripheral vascular resistance and myocardial oxygen demand in angina patients and effectively lowers arterial pressure in hypertensive feline models
Sigma Aldrich Fine Chemicals Biosciences Cilnidipine >=98% (HPLC), powder | 132203-70-4 | MFCD00865853 | 50MG
Cilnidipine >=98% (HPLC), powder | Purity: >=98% (HPLC) | Mol Wt: 492.52 | 132203-70-4 | MFCD00865853 | 50MG
Medchemexpress LLC Amlodipine Besylate, USP | 111470-99-6 | MFCD00887594 | >=98% | 1 G
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 compound is suitable for research related to high blood pressure and cancer.
- Antianginal agent: Used in research for angina.
- Orally active: Convenient for oral administration in research settings.
- Dihydropyridine calcium channel blocker: A specific type of calcium channel blocker with a well-defined mechanism of action.
- Mechanism of action: Blocks voltage-dependent L-type calcium channels, inhibiting calcium influx.
- Versatile research applications: Applicable for research concerning high blood pressure and cancer.
Medchemexpress LLC Nimodipine | 66085-59-4 | 99.9% | 1 ML
Nimodipine is an orally active, well-tolerated, and light-sensitive dihydropyridine calcium antagonist. It is primarily used for the research of cerebrovascular disorders and is intended for research use only.
- Orally active and well-tolerated
- Light-sensitive dihydropyridine calcium antagonist
- Used in research for cerebrovascular disorders
- Available as a light yellow to yellow solid
- For research use only
Sigma Aldrich Fine Chemicals Biosciences Adrenochrome | 54-06-8 | MFCD00069732 | 250mg
AdrenochromePurity: | MW: 179.17 | 54-06-8 | MFCD00069732 | 250mg
Sigma Aldrich Fine Chemicals Biosciences Indigo carmine for microscopy (Bact., Hist.), indicator (pH 11.5-14.0) | 860-22-0 | MFCD00005723 | 25G
Indigo carmine for microscopy (Bact., Hist.), indicator (pH 11.5-14.0) | Mol Wt: 466.35 | 860-22-0 | MFCD00005723 | 25G