Enamines
Sigma Aldrich Diaminomaleonitrile
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich 5-Bromo-1,2,3-trifluorobenzene
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich 5-(Chloromethyl)-3-methyl-1H-1,2,4-triazole hydrochloride
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich Methyl 3-aminocrotonate
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Medchemexpress LLC (S)-Nimodipine | 77940-93-3 | 99.9% | 418.44 | 100 MG
(S)-Nimodipine is an enantiomer of Nimodipine, an orally active, well-tolerated, and light-sensitive dihydropyridine calcium antagonist. It is used in the research of cerebrovascular disorders, targeting the Calcium Channel and involving Membrane Transporter/Ion Channel; Neuronal Signaling pathways.
- Enantiomer of Nimodipine
- Orally active dihydropyridine calcium antagonist
- Used in research of cerebrovascular disorders
- Targets Calcium Channel
- Involves Membrane Transporter/Ion Channel; Neuronal Signaling pathway
Apexbio Technology LLC Cisatracurium Besylate 96946-42-8 10mM (in 1mL DMSO)
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
Selleck Chemical LLC PF-562271 Besylate S2672-1g
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 (S)-Nimodipine | 77940-93-3 | 99.9% | 418.44 | 50 MG
(S)-Nimodipine is an enantiomer of Nimodipine. Nimodipine is an orally active, well-tolerated, and light-sensitive dihydropyridine calcium antagonist. It can be used for the research of cerebrovascular disorders.
- Target: Calcium channel
- Pathway: Membrane transporter/ion channel; neuronal signaling
- Application: Research of cerebrovascular disorders
Selleck Chemical LLC Amlodipine Besylate S1813-1g
Amlodipine Besylate is a long-acting calcium channel blocker used to lower blood pressure and prevent chest pain
Medchemexpress LLC CDK2-IN-4 | 1316652-41-1 | 99.3% | 326.37 g/mol | C16H14N4O2S | 5 MG
NCC-149 is a selective histone deacetylase 8 (HDAC8) inhibitor used in cell biology research, including studies of neural differentiation. The product is provided with supporting documentation for purity, handling, and storage, and is available both as a solid and as a DMSO solution.
- Selective HDAC8 inhibitor for neural differentiation studies.
- Documented purity approximately 99.3% based on certificate of analysis.
- Available as a solid and as a 10 mM solution in DMSO.
- Datasheet, certificate of analysis, and safety data sheet provided for quality and safety information.
- Storage recommendations included for powdered material and solutions.
eMolecules 13887-51-9 | 2-BROMO-2-METHYL-1-MORPHOLINOPROPAN-1-ONE | AstaTech | MFCD12910756 | 236.109 | C8H14BrNO2 | 97.000 | CC(C)(Br)C(=O)N1CCOCC1 | 0.25g | 206677639
2-BROMO-2-METHYL-1-MORPHOLINOPROPAN-1-ONE | AstaTech | 13887-51-9 | MFCD12910756 | 236.109 | C8H14BrNO2 | 97.000 | CC(C)(Br)C(=O)N1CCOCC1 | 0.25g | 206677639
Apexbio Technology LLC Amlodipine 88150-42-9 1g
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 To-1187 (TFA) | 98.4% | 795.72 | 50 MG
TO-1187 TFA is a selective HDAC6 PROTAC degrader with a DC50 of 5.81 nM. It functions by promoting the ubiquitination and degradation of HDAC6. This compound is suitable for use in research studying hematological malignancies and solid tumors. The compound is composed of an HDAC6 ligand, a CRBN ligase ligand, and a linker.
- Selective HDAC6 PROTAC degrader, exhibits a DC50 of 5.81 nM, indicating potent and specific degradation of HDAC6.
- Promotes ubiquitination and subsequent degradation of HDAC6.
- Useful in the study of hematological malignancies and solid tumors.
- Consists of a specific HDAC6 ligand, a CRBN ligase ligand, and a linker.
- Purity of 98.41%.
Medchemexpress LLC 4-((((1-(2-(2-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)amino)ethoxy)ethyl)-1h-1, | 98.4% | 795.72 | 5 MG
TO-1187 TFA is a selective HDAC6 PROTAC degrader with a DC50 of 5.81 nM. It promotes the ubiquitination and degradation of HDAC6 and is used in the study of hematological malignancies and solid tumors. The compound is composed of an HDAC6 ligand, a CRBN ligase ligand, and a linker.
- Selective PROTAC degrader
- Promotes ubiquitination and degradation of HDAC6
- Applicable for studying hematological malignancies and solid tumors