Chromatography Standards
Medchemexpress LLC Dabigatran impurity 29 | 1642853-67-5 | MFCD30741307 | 25mg
Dabigatran impurity 29 (Dabigatran impurity F) is an impurity of Dabigatran (HY-10163)
Sigma Aldrich Fine Chemicals Biosciences Phenylephrine Related Compound D United States Pharmacopeia (USP) Reference Standard | 1367567-95-0 | 30MG
Phenylephrine Related Compound D United States Pharmacopeia (USP) Reference Standard | Mol Wt: 257.33 | 1367567-95-0 | 30MG
Sigma Aldrich Fine Chemicals Biosciences Thioridazine for system suitability European Pharmacopoeia (EP) Reference Standard | 50-52-2 |
Thioridazine for system suitability European Pharmacopoeia (EP) Reference Standard | Mol Wt: 370.57 | 50-52-2 |
Medchemexpress LLC Haloperidol decanoate | 74050-97-8 | MFCD00866706 | 99.7% | 530.11 g·mol⁻¹ | C31H41ClFNO3 | 100 MG
Haloperidol decanoate is the decanoate ester of haloperidol supplied for research use. It is used in pharmacology and formulation studies as a long-acting depot prodrug to investigate dopamine D2 receptor activity and long-acting injectable formulations.
- Long-acting ester for depot formulations.
- Suitable for pharmacology and formulation studies.
- High purity: 99.7%.
- Molecular formula C31H41ClFNO3; molecular weight 530.11 g·mol⁻¹.
- Available as solid packs and 10 mM DMSO solution stocks.
- For research use only; not for human or veterinary use.
Medchemexpress LLC Lidocaine | 137-58-6 | 99.96% | 234.34 | 5 G
Lidocaine inhibits sodium channels involving complex voltage and dependence. It decreases growth, migration, and invasion of gastric carcinoma cells by up-regulating miR-145 expression and further inactivating MEK/ERK and NF-κB signaling pathways. As an amide derivative, it has potential for ventricular arrhythmia research.
- Inhibits sodium channels
- Decreases growth, migration, and invasion of gastric carcinoma cells
- Up-regulates miR-145 expression
- Inactivates MEK/ERK and NF-κB signaling pathways
- Causes reversible tail nerve block in rats
- Inhibits human TREK-1 in HEK293 cells
- Inhibits cell viability in human gastric cancer cell lines
- Increases apoptotic cell rate
- Down-regulates Cyclin D1 and up-regulates p21 expression
Medchemexpress LLC Ruxolitinib (Standard) | 941678-49-5 | 99.7% | C₁₇H₁₈N₆ | 50 MG
Ruxolitinib (Standard) is the analytical standard of Ruxolitinib, intended for research and analytical applications. It is a potent and selective JAK1/2 inhibitor, inducing autophagy and killing tumor cells through toxic mitophagy. This compound is commonly used in qualitative, quantitative, and methodological research experiments.
- Used as an analytical standard in reference assays
- Suitable for HPLC, GC, and MS research experiments
- Store at 4°C, sealed, away from light and moisture
Medchemexpress LLC Bumetanide | 28395-03-1 | 99.9% | 364.42 | 50 MG
Bumetanide (Standard) is the analytical standard of Bumetanide. It is a highly potent loop diuretic and a Na+-K+-Cl+ cotransporter (NKCC) blocker, commonly used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
- Analytical standard
- Highly potent loop diuretic
- Na+-K+-Cl+ cotransporter (NKCC) blocker
- Selective NKCC1 inhibitor
- Inhibits NKCC2
- Intended for research and analytical applications
- Used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS
Sigma Aldrich Fine Chemicals Biosciences Doxazosin Related Compound A United States Pharmacopeia (USP) Reference Standard | 70918-74-0 | 20MG
Doxazosin Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 284.74 | 70918-74-0 | 20MG
Medchemexpress LLC Stearyl Stearate 50g
Stearyl StearateIt is an organic compound belonging to esters It is formed from the reaction between stearyl alcohol and stearic acid and has a mild fatty odor Stearyl stearate has several applications in the cosmetic and personal care industries especially as an emollient and conditioning agent in skin and hair care products Additionally it is used as a lubricant and surfactant in industrial settings
Sigma Aldrich Fine Chemicals Biosciences Ciprofloxacin European Pharmacopoeia (EP) Reference Standard | 85721-33-1 | MFCD00185755 |
Ciprofloxacin European Pharmacopoeia (EP) Reference Standard | Mol Wt: 331.34 | 85721-33-1 | MFCD00185755 |
Apexbio Technology LLC Metoprolol Succinate 98418-47-4 50mg
Metoprolol Succinate (CAS 98418-47-4) is an orally active selective 1-adrenergic receptor antagonist By selectively inhibiting 1-receptors in cardiac tissue it modulates myocardial contractility and heart rate resulting in altered hemodynamic parameters In preclinical cardiovascular models this small molecule is utilized to investigate its effects on cardiac function and systemic blood pressure Owing to its receptor selectivity Metoprolol Succinate is commonly employed in studies exploring therapeutic strategies for chronic heart failure and hypertension
Medchemexpress LLC Clopidogrel impurity 3 | 1015247-87-6 | 1g
Clopidogrel impurity 3 is an impurity of Clopidogrel (HY-15283)
Alkali Scientific Oxytetracycline Hydrochloride, 5 G
Oxytetracycline Hydrochloride, available in a 5g laboratory-grade powder form, is a broad-spectrum antibiotic effective in treating a wide variety of bacterial infections. This compound works by inhibiting protein synthesis in bacteria, making it an essential tool in antimicrobial research. It is commonly used for testing bacterial susceptibility in clinical microbiology, particularly for organisms like Staphylococcus and Escherichia coli. In addition to medical applications, oxytetracycline is used in veterinary medicine and agriculture. The 5g powder format is ideal for preparing precise concentrations for use in bacteriological media or in solution for antimicrobial testing.
Cayman Chemical Temozolomide, Purity: ≥98%, CAS: 85622-93-1, 100 mg
A prodrug form of MTIC; selectively cytotoxic to MGMT-deficient U87 and D54 cells over MGMT-expressing T98G and U3054MG cells (IC50s = 51, 12, 660, and 370 µM, respectively); increases survival in a Br23c glioblastoma orthotopic mouse xenograft model at 15 mg/kg; decreases tumor volume and increases the number of tumor-infiltrating CD4+ and CD8+ T cells in a GL261 murine glioma model in combination with anti-CD47
Medchemexpress LLC l-Naproxen | 23979-41-1 | C14H14O3 | 1 ML
l-Naproxen is an enantiomer of (S)-Naproxen. It functions as an inhibitor of Cdc42 and Rac1, with EC50 values of 96 μM and 212 μM respectively, and exhibits anti-tumor activity. Additionally, l-Naproxen is classified as a nonsteroidal anti-inflammatory agent (NSAID).
- Enantiomer of (S)-Naproxen.
- Inhibits Cdc42 and Rac1 activity.
- Exhibits anti-tumor activity.
- Functions as a nonsteroidal anti-inflammatory agent (NSAID).
- Inhibits Rac1 and Cdc42 activity in HeLa cells.
- Inhibits migration of immortalized human ovarian cancer cells.
- Activity is via a COX-independent mechanism.