Enamines
eMolecules 632-93-9 | 3,5-DIETHOXYCARBONYL-1,4-DIHYDRO-2,4,6-COLLIDINE | AstaTech | MFCD00005950 | 267.325 | C14H21NO4 | 95.000 | CCOC(=O)C1=C(C)NC(C)=C(C1C)C(=O)OCC | 100g | 449760138
3,5-DIETHOXYCARBONYL-1,4-DIHYDRO-2,4,6-COLLIDINE | AstaTech | 632-93-9 | MFCD00005950 | 267.325 | C14H21NO4 | 95.000 | CCOC(=O)C1=C(C)NC(C)=C(C1C)C(=O)OCC | 100g | 449760138
Medchemexpress LLC (S)-Nimodipine | 77940-93-3 | 99.9% | 418.44 | 10 MG
(S)-Nimodipine is an enantiomer of Nimodipine, an orally active, well-tolerated, and light-sensitive dihydropyridine calcium antagonist. It is suitable for the research of cerebrovascular disorders.
- Functions as a calcium channel antagonist
- Inhibits membrane transporter and neuronal signaling pathways
- Orally active compound
- Light-sensitive properties
- Suitable for cerebrovascular disorder research
Selleck Chemical LLC Amlodipine S1905-1g
Amlodipine (UK-48340) is a long-acting calcium channel blocker used to lower blood pressure and prevent chest pain
Medchemexpress LLC Mirogabalin besylate | 1138245-21-2 | MFCD31631215 | 99.6% | 367.46 | C18H25NO5S | 50 MG
Mirogabalin besylate is a research-grade small molecule that acts as a selective, orally available ligand for the α2δ subunit of voltage-gated calcium channels. It is supplied as a high-purity solid with manufacturer documentation supporting identity, purity, and safe handling for laboratory research.
- High purity (99.6%) suitable for research applications.
- Molecular formula C18H25NO5S; molecular weight 367.46.
- Solid powder formulation supplied in a 50 MG unit.
- Store solid sealed at 4°C, away from moisture; in solution store at -80°C (6 months) or -20°C (1 month).
- Documentation available: datasheet, certificate of analysis, and safety data sheet.
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
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 Methyl but-3-enoate 100g
Methyl but-3-enoate is a drug intermediate for synthesis of various active compounds
Medchemexpress LLC TO-1187 (TFA) | 98.4% | 795.72 | 25 MG
TO-1187 TFA is a selective PROTAC degrader designed to target HDAC6, effectively promoting its ubiquitination and subsequent degradation. It is a valuable tool for research into hematological malignancies and solid tumors, composed of an HDAC6 ligand, a CRBN ligase ligand, and a linker.
- Selective PROTAC degrader for HDAC6
- Promotes ubiquitination and degradation of HDAC6
- Useful for studying hematological malignancies and solid tumors
- Provided as a light yellow to yellow solid
- Soluble in DMSO at 100 mg/mL
Medchemexpress LLC Amlodipine besylate | 111470-99-6 | 99.7% | 5 G
Amlodipine besylate | 111470-99-6 | 99.7% | 5 G
Medchemexpress LLC Mirogabalin besylate | 1138245-21-2 | MFCD31631215 | 99.6% | 367.46 | C18H25NO5S | 10 MG
Mirogabalin besylate is the besylate salt of a selective, orally available ligand for the α2δ subunit of voltage-gated calcium channels, provided for research use with manufacturer-specified purity, solubility, and storage recommendations.
- Selective α2δ ligand with low-nanomolar binding affinity to human α2δ-1 and α2δ-2.
- High purity: 99.57% (manufacturer stated).
- White to off-white solid suitable for analytical and preparative workflows.
- Available as small research packs and as DMSO solutions ready for use.
- Soluble in DMSO at 100 mg/mL; may require sonication and use of fresh DMSO.
- Storage: solid at 4°C sealed, solutions at -20°C to -80°C per stability guidance.
- For research use only; not for human or veterinary use and subject to territorial restrictions.
eMolecules 91-56-5 | 2,3-Indolinedione | Oakwood Chemical | MFCD00005718 | 147.133 | C8H5NO2 | 98.000 | O=C1Nc2ccccc2C1=O | 1g | 537699447
2,3-Indolinedione | Oakwood Chemical | 91-56-5 | MFCD00005718 | 147.133 | C8H5NO2 | 98.000 | O=C1Nc2ccccc2C1=O | 1g | 537699447
Medchemexpress LLC (S)-Nimodipine | 77940-93-3 | 99.9% | 418.44 | 25 MG
(S)-Nimodipine is an enantiomer of Nimodipine. This orally active dihydropyridine calcium antagonist is well-tolerated and light-sensitive, making it suitable for research into cerebrovascular disorders.
- Enantiomer of Nimodipine
- Orally active
- Well-tolerated
- Light-sensitive dihydropyridine calcium antagonist
- Used for research of cerebrovascular disorders
- Targets Calcium Channel
- Involved in Membrane Transporter/Ion Channel pathway
- Involved in Neuronal Signaling pathway