Enamines
Medchemexpress LLC VU6004256 | 1316652-41-1 | 98.7% | 326.37 | C16H14N4O2S | 50 MG
NCC-149 is a selective histone deacetylase 8 (HDAC8) inhibitor for laboratory research, described for use in neural differentiation studies. It is supplied as a solid powder and is also offered as a 10 mM solution in DMSO. Typical purity is approximately 98.7%, and the molecular weight is 326.37 g·mol⁻¹.
- Selective HDAC8 inhibitor for neural differentiation research.
- Available as solid powder and 10 mM solution in DMSO.
- Typical purity approximately 98.7%.
- Molecular weight 326.37 g·mol⁻¹ and formula C16H14N4O2S.
- Intended for laboratory research use only.
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.
Sigma Aldrich Fine Chemicals Biosciences Nilvadipine >=98% (HPLC) | 75530-68-6 | 50MG
Nilvadipine >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 385.37 | 75530-68-6 | 50MG
Apexbio Technology LLC Cisatracurium Besylate 96946-42-8 100mg
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 Amlodipine maleate
Amlodipine (Amvaz UK-48340) maleate is a long-acting calcium channel blocker used to lower blood pressure and prevent chest pain
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 Mirogabalin besylate | 1138245-21-2 | 99.6% | 367.46 g·mol⁻¹ | C18H25NO5S | 100 MG
Mirogabalin besylate is a research-grade small molecule ligand for the α2δ subunit of voltage-gated calcium channels, provided as a solid and in solution formats for in vitro and preclinical studies. It is supplied with supporting documents (COA, SDS) and is intended for laboratory research use.
- Selective α2δ subunit ligand for calcium channels.
- High reported purity suitable for biochemical assays.
- White to off-white solid, supplied in multiple package sizes.
- Available as 10 mM solution in DMSO for ready-to-use assays.
- Certificate of analysis and safety data sheet available.
- Store sealed at 4°C; in solvent store at -80°C or -20°C as specified.
Sigma Aldrich Fine Chemicals Biosciences Potassium indigotrisulfonate ozone-scavenging reagent | 67627-18-3 | MFCD00013160 | 1G
Potassium indigotrisulfonate ozone-scavenging reagent | Purity: >60% (HPLC) | Mol Wt: 616.72 | 67627-18-3 | MFCD00013160 | 1G
Medchemexpress LLC Molibresib besylate | 1895049-20-3 | 97.0% | 100 MG
Molibresib besylate is an orally active pan-BET inhibitor. It targets BRD2, BRD3, BRD4, and BRDT, disrupting their interaction with chromatin by occupying acetylated lysine binding sites. This inhibits MYC expression and target gene transcription. It exhibits broad antiproliferative activity, useful for research in acute myeloid leukemia, multiple myeloma, triple-negative breast cancer, small-cell lung cancer, and other advanced refractory solid tumors.
- Disrupts BET protein-chromatin interaction
- Inhibits MYC expression and target gene transcription
- Exhibits broad antiproliferative activity
- Induces growth arrest and downregulates mitosis-related genes
- Upregulates p-ERK1/2 levels
- Shows synergistic effects with MEK inhibitors
- Modulates immune microenvironment and prolongs survival in models
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 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
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 Methyl but-3-enoate 1g
Methyl but-3-enoate is a drug intermediate for synthesis of various active compounds