Drug Standards
Medchemexpress LLC Clevudine (L-FMAU) | 163252-36-6 | 99.8% | 260.22 | 50 MG
Clevudine (L-FMAU) is a nucleoside analog of the unnatural L-configuration with potent anti-HBV activity, long half-life, and low toxicity. It acts as a non-competitive inhibitor that binds to the polymerase rather than being incorporated into the viral DNA. Clevudine is also active against cowpox virus respiratory infection in mice.
- Potent anti-HBV activity
- Long half-life
- Low toxicity
- Acts as a non-competitive inhibitor
- Active against cowpox virus respiratory infection in mice
Medchemexpress LLC Moxifloxacin (Standard) | 151096-09-2 | 99.7% | C21H24FN3O4 | 25 MG
Moxifloxacin is an analytical standard for research and analytical applications. This orally active 8-methoxyquinolone antimicrobial is utilized in the treatment of acute bacterial sinusitis, acute bacterial exacerbations of chronic bronchitis, and community-acquired pneumonia.
- Intended for research and analytical applications
- Analytical standard for assay
- Used in qualitative, quantitative, and methodological research experiments
- Suitable for HPLC, GC, and MS applications
AdipoGen Imiquimod,Chemical. CAS: 99011-02-6. Formula: C14H
Imiquimod, AdipoGen Life Sciences. Chemical. CAS: 99011-02-6. Formula: C14H16N4. MW: 240.3. Immune response modulator. Anti-inflammatory. TLR7 agonist. Stimulates proinflammatory cytokine production interferon-alpha (IFN-alpha), interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-alpha) and activates NF-kappaB. Caspase-3 activator that directly induces procaspase-3 cleavage. Anti-cancer compound. Apoptosis inducer. Antiproliferative, independent of immune system activation or function. Antiviral and anti-angiogenic. Approved treatment for external genital warts caused by human papillomavirus infection.
Sigma Aldrich Fine Chemicals Biosciences Rauwolfia Serpentina United States Pharmacopeia (USP) Reference Standard | 8063-17-0 | 15G
Rauwolfia Serpentina United States Pharmacopeia (USP) Reference Standard | 8063-17-0 | 15G
Cayman Chemical Mevastatin Inhibitors
An HMG-CoA reductase inhibitor (Ki = 0.1 µM); inhibits cholesterogenesis in the liver and ileum of normolipidemic rats, as well as enhances suppression of cholesterogenesis in cholesterol-fed rats or rats administered cholestyramine at 50 mg/kg; suppresses TNF-induced NF-κB activation (IC50 = ~17 µM) and potentiates apoptosis in human myeloid leukemia cells; suppresses induced ferroptosis in HT-1080 cells
Medchemexpress LLC N-Acetyl mesalazine | 51-59-2 | 99.9% | C9H9NO4 | 100 MG
N-Acetyl mesalazine (N-Acetyl-5-aminosalicylic acid) is the primary intestinal metabolite of 5-Aminosalicylic Acid and serves as a biomarker for evaluating the efficacy of 5-Aminosalicylic Acid. It can scavenge free radicals, reduce DNA base hydroxylation, and ameliorate mucosal inflammation. N-Acetyl mesalazine can be used in the study of diseases such as colitis and colon cancer.
- Primary intestinal metabolite of 5-Aminosalicylic Acid.
- Serves as a biomarker for evaluating the efficacy of 5-Aminosalicylic Acid.
- Scavenges free radicals.
- Reduces DNA base hydroxylation.
- Ameliorates mucosal inflammation.
- Can be used in the study of diseases such as colitis and colon cancer.
Medchemexpress LLC Butyl 3-(butylamino)-4-phenoxy-5-sulfamoylbenzoate | 32643-00-8 | MFCD09838330 | 25mg
Bumetanide impurity 2 is an impurity of Bumetanide (HY-17468)
Selleck Chemical LLC Ciclopirox 200mg 29342-05-0
Ciclopirox is a broad-spectrum antifungal agent working as an iron chelator. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Sigma Aldrich Fine Chemicals Biosciences Chlorzoxazone|95-25-0 | MFCD00005717 | 100g
Chlorzoxazone | Purity: 98% | 169.57 | 95-25-0 | MFCD00005717 | 100g
Medchemexpress LLC BMS-232632 sulfate | 229975-97-7 | 99.1% | 802.93 | 100 MG
Atazanavir sulfate is a highly selective and orally active HIV-1 protease inhibitor with blood-brain barrier permeability. It functions as both a substrate and inhibitor of CYP3A4 and an inhibitor of P-glycoprotein (P-gp). This compound also acts as a SARS-CoV 3CLpro inhibitor with an IC50 of 3.49 μM and has demonstrated efficacy in inhibiting cardiac fibrosis, hyperlipidemia, and inducing malignant glioma cell death.
- Targets HIV-1 protease, CYP3A4, P-glycoprotein, and SARS-CoV 3CLpro.
- Shows an IC50 of 3.49 μM for SARS-CoV 3CLpro.
- Attenuates hypoxia-induced cardiac fibroblast proliferation.
- Inhibits collagen I and III expression in cardiac fibroblasts.
- Induces endoplasmic reticulum stress response in glioma cells.
- Reduces collagen deposition and cardiac remodeling in MI models.
Medchemexpress LLC Dabigatran impurity 75 | 1408238-36-7 | 479.57 | 10 MG
Dabigatran impurity 75 is a laboratory chemical for research use only, intended for experienced personnel. This product is for the manufacture of substances and requires handling by suitably qualified scientists in equipped facilities. It is stable under recommended storage conditions but is harmful if swallowed, causes skin and serious eye irritation, and may cause respiratory irritation.
- Appearance: Off-white to yellow solid
- Purity: ≥97.0% (NMR)
- Melting point: 119-135 °C
- Recommended storage: 4°C, protect from light
- In solvent storage: -80°C for 6 months, -20°C for 1 month, protect from light
- Intended for research use only
Alkali Scientific Dicloxacillin Sodium Salt, 1 G
Dicloxacillin Sodium Salt, 1g, is an antibiotic used in laboratory research to study its effects on bacterial infections. It is particularly effective against penicillin-resistant Gram-positive bacteria, including strains of Staphylococcus aureus. In microbiological experiments, Dicloxacillin is used to test bacterial resistance and evaluate new antimicrobial agents. The 1g volume allows for more extensive testing, making it suitable for larger-scale experiments or studies where higher dosages are required. Dicloxacillin is frequently used in combination therapy research to enhance the effectiveness of other antibiotics in combating bacterial resistance.
Sigma Aldrich Fine Chemicals Biosciences Celecoxib impurity B European Pharmacopoeia (EP) Reference Standard | 331943-04-5 |
Celecoxib impurity B European Pharmacopoeia (EP) Reference Standard | Mol Wt: 381.37 | 331943-04-5 |
Sigma Aldrich Fine Chemicals Biosciences Fenbufen British Pharmacopoeia (BP) Reference Standard | 36330-85-5 | MFCD00056701 |
Fenbufen British Pharmacopoeia (BP) Reference Standard | Mol Wt: 254.28 | 36330-85-5 | MFCD00056701 |
Medchemexpress LLC Febantel | 58306-30-2 | 99.9% | 446.48 | 1 ML
Febantel is an oral dewormer used to treat gastrointestinal nematodes in sheep, as well as roundworm and tapeworm infections in poultry and livestock. It also inhibits the embryonic development of mouse hairworms and whipworm eggs.
- Oral dewormer
- Treats gastrointestinal nematodes in sheep
- Treats roundworm and tapeworm infections in poultry and livestock
- Inhibits embryonic development of mouse hairworms and whipworm eggs
- High purity: 99.91%
- Available in solid and solution forms