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Filtered Search Results
eMolecules Medchem Express / Chlormethiazole hydrochloride / 10mg / 482204521 / HY-A0296 / / 6001-74-7 / MFCD00673948 / 198.110 / C6H9Cl2NS
Medchem Express / Chlormethiazole hydrochloride / 10mg / 482204521 / HY-A0296 / / 6001-74-7 / MFCD00673948 / 198.110 / C6H9Cl2NS
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Medchemexpress LLC Coblopasvir dihydrochloride | 1966138-53-3 | MFCD00007349 | 99.2% | 855.81 | C41H52Cl2N8O8 | 10 MG
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Coblopasvir dihydrochloride is a research-grade pangenotypic inhibitor of hepatitis C virus non-structural protein 5A (NS5A), supplied as the dihydrochloride salt for laboratory studies on chronic HCV infection.
- High purity suitable for research use.
- Targets NS5A for antiviral mechanism studies.
- Provided as the dihydrochloride salt to improve handling and stability.
- Available in small, milligram-scale quantities for preclinical and in vitro experiments.
- Molecular formula and weight documented for experimental planning.
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![Medchemexpress LLC 2,2'-[1,2-phenylenebis(oxy)]bis[N-phenyl-N-(phenylmethyl)acetamide] | 61595-77-5 | >98.0% | 556.65 | C36H32N2O4 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000222615.png-250.jpg)
Medchemexpress LLC 2,2'-[1,2-phenylenebis(oxy)]bis[N-phenyl-N-(phenylmethyl)acetamide] | 61595-77-5 | >98.0% | 556.65 | C36H32N2O4 | 5 MG
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ETH 157 (Sodium ionophore II) is a neutral sodium (Na+) ionophore used in research to induce Na+/Ca2+ selectivity in membranes. It is employed in analytical chemistry and membrane electrode applications to selectively transport or detect sodium ions. Chemical formula C36H32N2O4; molecular weight 556.65; supplied as a solid.
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Medchemexpress LLC KL-11743 | 1369452-53-8 | 99.4% | C30H30N6O3 | 100 MG
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KL-11743 is a potent, orally active, and glucose-competitive inhibitor of class I glucose transporters (GLUT1, GLUT2, GLUT3, and GLUT4), with IC50s of 115, 137, 90, and 68 nM respectively. It specifically blocks glucose metabolism and can synergize with electron transport inhibitors to induce cell death, additionally inducing cellular disulfidptosis by forming disulfide bonds in actin cytoskeletal proteins.
- Potent, orally active glucose-competitive inhibitor
- Inhibits class I glucose transporters (GLUT1, GLUT2, GLUT3, GLUT4)
- Blocks glucose metabolism
- Synergizes with electron transport inhibitors to induce cell death
- Induces cellular disulfidptosis
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Medchemexpress LLC Carvacrol methyl ether | 6379-73-3 | 99.9% | 164.25 | C11H16O | 1 ML
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Carvacrol methyl ether is a methyl ether derivative of carvacrol supplied as a research-grade reagent and analytical standard. It exhibits antibacterial activity and is available as a 10 mM solution in DMSO (1 mL) or as solids in multiple sizes for laboratory research purposes.
- Antibacterial activity observed in vitro.
- Available as 10 mM solution in DMSO (1 mL) and as solids (100 mg, 250 mg, 1 g, larger sizes on request).
- High purity (approximately 99.9%).
- Molecular formula C11H16O; molecular weight 164.25.
- Recommended storage: solids at -20°C (long term); solutions at -80°C for extended storage.
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Medchemexpress LLC trans-4-aminocrotonic acid | 38090-53-8 | MFCD00673818 | 99.3% | 101.10 g/mol | C4H7NO2 | 10 MG
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TACA (trans-4-aminocrotonic acid) is a research chemical and GABA receptor agonist used in neuroscience and pharmacology studies. Supplied as a high-purity solid, it is intended for laboratory use in assay development, receptor pharmacology, and biochemical experiments.
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Medchemexpress LLC γ-Linolenic acid ethyl ester | 31450-14-3 | 99.1% | 306.48 | 5 G
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γ-Linolenic acid ethyl ester, also known as Ethyl γ-linolenate, functions as a leukotriene B4 receptor 4 (LTB4) antagonist. It is intended for research use only.
- Antagonist of leukotriene B4 receptor 4 (LTB4)
- Liquid appearance
- Colorless to light yellow
- Molecular weight: 306.48
- Purity: 99.14%
- Storage conditions at 4°C, protected from light and under nitrogen
- Soluble in DMSO at concentrations of 250 mg/mL or higher
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Medchemexpress LLC Acoramidis hydrochloride | 2242751-53-5 | 98.7% | 328.77 | 50 MG
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Acoramidis (AG10) hydrochloride is an orally active and selective kinetic stabilizer of WT and V122I-TTR (transthyretin). It is utilized in the study of transthyretin amyloidosis. This compound demonstrates equal efficacy in stabilizing V122I- and WT-TTR and surpasses tafamidis in stabilizing both WT and mutant TTR in whole serum. Additionally, it exhibits minimal inhibition of common drug discovery off-targets like the hERG potassium ion channel and cytochrome P450 isozymes, indicating low toxicity.
- Stabilizes WT and V122I-TTR.
- Used in the study for transthyretin amyloidosis.
- Shows minimal inhibition of hERG and cytochrome P450 isozymes, suggesting low toxicity.
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![eMolecules ChemScene / (2S3aS6aS)-Octahydrocyclopenta[b]pyrrole-2-carboxylic acid / 100mg / 572180440 / CS-0055787 / 0.000 / 109428-53-7 / [null] / 155.197 / C8H13NO2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502463898.JPG-250.jpg)
eMolecules ChemScene / (2S3aS6aS)-Octahydrocyclopenta[b]pyrrole-2-carboxylic acid / 100mg / 572180440 / CS-0055787 / 0.000 / 109428-53-7 / [null] / 155.197 / C8H13NO2
ChemScene / (2S3aS6aS)-Octahydrocyclopenta[b]pyrrole-2-carboxylic acid / 100mg / 572180440 / CS-0055787 / 0.000 / 109428-53-7 / [null] / 155.197 / C8H13NO2
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Medchemexpress LLC ETH 157 | 61595-77-5 | 556.65 | 50 MG
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ETH 157 is a Na+ ionophore that induces a Na+/Ca2+ selectivity in membranes. It is intended for research use only.
- Na+ ionophore
- Induces Na+/Ca2+ selectivity in membranes
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Medchemexpress LLC Eth 157 | 61595-77-5 | 556.65 | 100 MG
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ETH 157 is a Na+ ionophore that induces a Na+/Ca2+ selectivity in membranes.
- Solid appearance
- Soluble in DMSO (100 mg/mL)
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Medchemexpress LLC Valecobulin hydrochloride | 1240321-53-2 | MFCD19311027 | 98.5% | C26H29ClN6O5S | 10MG
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Valecobulin hydrochloride is a valine prodrug of S516 and a vascular disrupting agent that inhibits β-tubulin polymerization. It has reported antitumor activity against murine and human solid tumors and is supplied for laboratory research use in both solid and solution forms.
- Potent β-tubulin polymerization inhibitor with antitumor activity.
- Valine prodrug of S516, suitable for tubulin-targeted studies.
- Vascular disrupting agent activity relevant to tumor biology research.
- High purity (≈98.5%), appropriate for in vitro and in vivo experiments.
- Available in small research pack sizes and solution formats.
- Stable when sealed; long-term storage recommended at -80°C in solvent.
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Medchemexpress LLC 2,5-Dibromothiazole | 4175-78-4 | 99.9% | C3HBr2NS | 5 G
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2,5-Dibromothiazole is a heterocyclic compound that serves as a key intermediate in organic synthesis. It is intended for research use only.
- Molecular weight of 242.92
- Appears as an off-white to yellow solid
- Store powder at -20°C for 3 years or 4°C for 2 years
- Store in solvent at -80°C for 6 months or -20°C for 1 month
- Soluble in DMSO at 100 mg/mL
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eMolecules 2-(4-Hydroxy-phenyl)-thiazole-4-carboxylic acid ethyl ester | 113334-60-4 | MFCD06738354 | 5g
J & W PharmLab LLC | 2-(4-Hydroxy-phenyl)-thiazole-4-carboxylic acid ethyl ester | 5g | 289356919 | 90R0026 | 96.000 | 113334-60-4 | MFCD06738354 | 249.280 | C12H11NO3S
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eMolecules THIAZOLE-4-CARBOXALDEHYDE 5G
5000160734 THIAZOLE-4-CARBOXALDEHYDE 5G
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