Thiophenes
Aobchem 5-(2-Methylphenyl)-2-thiophenecarboxylic acid | 95% | CAS 893733-30-7 | C12H10O2S | 250mg
5-(2-Methylphenyl)-2-thiophenecarboxylic acid | 95% | CAS 893733-30-7 | C12H10O2S | 250mg
Aobchem 5-(2-Methylphenyl)-2-thiophenecarboxylic acid | 95% | CAS 893733-30-7 | C12H10O2S | 1g
5-(2-Methylphenyl)-2-thiophenecarboxylic acid | 95% | CAS 893733-30-7 | C12H10O2S | 1g
Aobchem (6-Bromo-2-fluoro-3-(methylthio)phenyl)(4-ethylphenyl)methanol | 97% | CAS 3002517-64-5 | C16H16BrFOS | 1g
(6-Bromo-2-fluoro-3-(methylthio)phenyl)(4-ethylphenyl)methanol | 97% | CAS 3002517-64-5 | C16H16BrFOS | 1g
Aobchem 2-Chloro-6-fluoro-3-(methylthio)benzaldehyde | 97% | CAS 2807471-52-7 | C8H6ClFOS | 250mg
2-Chloro-6-fluoro-3-(methylthio)benzaldehyde | 97% | CAS 2807471-52-7 | C8H6ClFOS | 250mg
Medchemexpress LLC Bisantrene dihydrochloride | 71439-68-4 | MFCD01743164 | >98.0% | 471.39 g/mol | C22H24Cl2N8 | 50 MG
Bisantrene dihydrochloride is the dihydrochloride salt of bisantrene, an anthracycline-class antitumor agent that intercalates DNA and inhibits topoisomerase. It is supplied as a research-grade solid for in vitro and cellular studies of DNA damage and cell-cycle pathways, and requires sealed, moisture-free storage with low-temperature solvent storage for extended stability.
- Anthracycline-class mechanism: DNA intercalation and topoisomerase inhibition.
- Research applications: cellular assays, DNA damage, and cell-cycle studies.
- High purity suitable for analytical and biological assays.
- Solid form supplied in sealed quantities for laboratory use.
- Storage guidance: sealed at 4°C short term; in solvent -20°C (1 month) and -80°C (up to 6 months).
- Molecular formula C22H24Cl2N8; molecular weight 471.39 g/mol.
Apexbio Technology LLC Pramipexole dihydrochloride 104632-25-9 50mg
Pramipexole dihydrochloride is a small-molecule agonist targeting dopamine receptors exhibiting selective affinity toward the D3 dopamine receptor subtype and lower affinity for the D2L D2S and D4 subtypes It is designed to stimulate dopamine receptor-mediated signaling thereby modulating dopaminergic pathways involved in motor function Pramipexole dihydrochloride exerts its biological activity primarily through dopamine receptor agonism and also demonstrates receptor-independent neuroprotective effects by attenuating mitochondrial reactive oxygen species (ROS) production and decreasing apoptosis-related signaling cascades Based on these pharmacological properties pramipexole dihydrochloride holds research potential in exploring dopaminergic system involvement and neuroprotective mechanisms relevant to neurodegenerative conditions such as Parkinson s disease and restless legs syndrome
Medchemexpress LLC Way-100135 dihydrochloride | 149055-79-8 | 98.1% | 468.46 g/mol | C24H35Cl2N3O2 | 10 MG
WAY-100135 dihydrochloride is a selective 5-HT1A receptor antagonist supplied as the dihydrochloride salt for research use. It is typically used in pharmacology studies to probe serotonergic signaling and in models of mood and anxiety disorders.
- Selective antagonist of presynaptic and postsynaptic 5-HT1A receptors.
- Reported activity with an IC50 of approximately 34 nM in rat hippocampal tissue.
- Dihydrochloride salt form enhances solubility for biological assays.
- High chemical purity suitable for laboratory research.
- Available in small-format quantities for dose-response and pilot studies.
eMolecules 848472-61-7 | tert-Butyl (2-methylthiazol-4-yl)carbamate | Ambeed | MFCD27923451 | 214.280 | C9H14N2O2S | 97.000 | Cc1nc(NC(=O)OC(C)(C)C)cs1 | 100mg | 837401996
tert-Butyl (2-methylthiazol-4-yl)carbamate | Ambeed | 848472-61-7 | MFCD27923451 | 214.280 | C9H14N2O2S | 97.000 | Cc1nc(NC(=O)OC(C)(C)C)cs1 | 100mg | 837401996
Medchemexpress LLC Ensartinib dihydrochloride | 2137030-98-7 | 99.7% | 634.36 | C26H29Cl4FN6O3 | 10 MG
Ensartinib dihydrochloride is the dihydrochloride salt of ensartinib (X-396), a potent small-molecule inhibitor targeting anaplastic lymphoma kinase (ALK) and MET for research use. It is provided as a high-purity solid for in vitro and preclinical studies and is not intended for human use.
- Potent dual ALK/MET inhibitor with IC50s of <0.4 nM (ALK) and 0.74 nM (MET).
- High purity (99.73%).
- Molecular weight 634.36 g/mol.
- Molecular formula C26H29Cl4FN6O3.
- Solid, white to light yellow powder.
- Supplied as a 10 mg research quantity.
- Store sealed, away from moisture; in solvent: -80°C for 6 months, -20°C for 1 month.
Apexbio Technology LLC GSK-LSD1 2HCl 2102933-95-7 25mg
GSK-LSD1 2HCl (CAS 2102933-95-7) is a selective irreversible inhibitor of lysine-specific demethylase 1A (LSD1) a flavin-dependent histone demethylase that modulates mono- and dimethylated lysine residues and is implicated in processes such as oocyte growth and tissue-specific differentiation GSK-LSD1 2HCl inhibits LSD1 with an IC50 of 16 nM and exhibits over 1000-fold selectivity against related FAD-utilizing enzymes including LSD2 MAO-A and MAO-B In cancer cell lines it demonstrates EC50 values below 5 nM for both gene expression modulation and growth inhibition GSK-LSD1 2HCl serves as a valuable chemical probe in epigenetics and cancer research
Medchemexpress LLC Histamine dihydrochloride (Standard) | 56-92-8 | 100.0% | 250 MG
Histamine dihydrochloride (Standard) | 56-92-8 | 100.0% | 250 MG
Accela Chembio Inc Methyl 3-aminothiophene-2-carboxylate | 100g | 22288-78-4 | MFCD00009765 | 98% | Shelf Life: 1260 Days | Light Sensitive/nitrogen Or Argon
Methyl 3-aminothiophene-2-carboxylate | 100g | 22288-78-4 | MFCD00009765 | 98% | Shelf Life: 1260 Days | Light Sensitive/nitrogen Or Argon
Accela Chembio Inc Methyl 3-amino-4-methylthiophene-2-carboxylate | 100g | 85006-31-1 | MFCD00051822 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4
Methyl 3-amino-4-methylthiophene-2-carboxylate | 100g | 85006-31-1 | MFCD00051822 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4