Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Benzethonium chloride European Pharmacopoeia (EP) Reference Standard | 121-54-0 | MFCD00011742 |
Benzethonium chloride European Pharmacopoeia (EP) Reference Standard | Mol Wt: 448.08 | 121-54-0 | MFCD00011742 |
Med Vet International Zoetis Amoxi-Tabs, 200mg, 500ct.
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Amoxi-Tabs (amoxicillin) is a semisynthetic antibiotic with a broad spectrum of activity. It provides bactericidal activity against a wide range of common Gram-positive and Gram-negative pathogens. DOGS Indicated in the treatment of susceptible strains of the organisms causing the following infections in dogs: Respiratory tract infections (tonsillitis, tracheobronchitis), Genitourinary tract infections (cystitis). Gastrointestinal tract infections (bacterial gastroenteritis), Bacterial dermatitis due to Staphylococcus aureus, Streptococcus spp. , and Proteus mirabilis Soft tissue infections (abscesses, lacerations, and wounds) CATS Indicated in the treatment of susceptible strains of the organisms causing the following infections in cats: Upper respiratory tract infections, Genitourinary tract infections (cystitis), Gastrointestinal tract infections, Skin and soft tissue infections
Sigma Aldrich Fine Chemicals Biosciences Docusate sodium United States Pharmacopeia (USP) Reference Standard | 577-11-7 | MFCD00012455 | 1G
Docusate sodium United States Pharmacopeia (USP) Reference Standard | Mol Wt: 444.56 | 577-11-7 | MFCD00012455 | 1G
Cayman Chemical Methocarbamol 5g
An orally bioavailable skeletal muscle relaxant; inhibits the ability of mice to remain on a vertical ladder for 1 minute (ED50 = 15 mg/kg) and decreases forelimb grip strength by 35.9% (500 mg/kg); abolishes femoral nerve-stimulated polysynaptic reflex contractions of the cat tibialis anterior muscle and prolongs the mean refractory period of directly or indirectly stimulated skeletal muscle (200 mg/kg); inhibits human CAI over CAII (IC50s = 70 and ~80,000 μM, respectively)
Apexbio Technology LLC Sarafloxacin HCl 91296-87-6 5g
Sarafloxacin hydrochloride (91296-87-6) is a small-molecule inhibitor targeting bacterial DNA gyrase (topoisomerase II) and topoisomerase IV It is designed to inhibit these essential enzymes thereby disrupting bacterial DNA replication Sarafloxacin hydrochloride exerts its biological activity primarily through stabilization of enzyme-DNA complexes leading to interference with bacterial DNA synthesis and cell death It demonstrates anti-microbial activity against various Gram-positive and Gram-negative bacterial strains with reported IC50 values against bacterial enzyme targets in the submicromolar range Based on these pharmacological properties sarafloxacin hydrochloride holds research potential in studies of bacterial resistance mechanisms susceptibility profiling and the pharmacodynamics of quinolone antibiotics
Medchemexpress LLC Fostamatinib (disodium hexahydrate) | 914295-16-2 | 99.5% | 100 MG
Fostamatinib (disodium hexahydrate) is a chemical compound commonly used as a laboratory chemical and for the manufacture of substances. It appears as a white to gray solid with a high purity of 99.5%. It is recommended for sealed storage away from moisture at 4°C, or at -80°C for 6 months (-20°C for 1 month) when in solvent.
- Used in laboratory research
- Suitable for substance manufacturing
- High purity (99.5%)
- Recommended sealed storage at 4°C, away from moisture
- Storage in solvent: -80°C for 6 months, -20°C for 1 month
- Shipping at room temperature if less than 2 weeks
- White to gray solid appearance
Medchemexpress LLC Ketoconazole | 65277-42-1 | 99.6% | C26H28Cl2N4O4 | 25 MG
Ketoconazole (R-41400) is an imidazole anti-fungal agent and an inhibitor of CYP3A4 and CYP24A1. It is for research use only. In studies, it has been observed to inhibit hepatic CYP450 and CYT b5 activities, enhance antiproliferative effects, and promote caspase-independent apoptosis pathways. It is also a potent exosome biogenesis and/or secretion inhibitor.
- Inhibits hepatic CYP450 and CYT b5 activities
- Enhances antiproliferative effects and increases systemic calcitriol exposure
- Promotes activation of caspase-independent apoptosis pathways
- Potent exosome biogenesis and/or secretion inhibitor
- Used in histological imaging/staining, cell proliferation/viability assays, and in vivo efficacy studies
- Assesses lipid peroxidation and cell viability
- Pre-treats primary mouse hepatocytes to measure PEPCK1 protein levels
Sigma Aldrich Fine Chemicals Biosciences AMITRAZ RELATED COMPOUND B United States Pharmacopeia (USP) Reference Standard | 33089-74-6 | MFCD00225755 | 40MG
AMITRAZ RELATED COMPOUND B United States Pharmacopeia (USP) Reference Standard | Mol Wt: 162.23 | 33089-74-6 | MFCD00225755 | 40MG
Selleck Chemical LLC Salbutamol
Salbutamol (Albuterol) is a short-acting selective beta2-adrenergic receptor agonist used to treat or prevent bronchospasm in patients with asthma bronchitis emphysema and other lung diseases
Medchemexpress LLC Betahistine dihydrochloride | 5579-84-0 | 99.8% | 10 G
Betahistine dihydrochloride is an orally active histamine H1 receptor agonist and a H3 receptor antagonist. It is used for the study of rheumatoid arthritis (RA). In vitro, Betahistine dihydrochloride inhibits [125I]iodoproxyfan binding to membranes of CHO (rH3(445)R) and CHO (hH3(445)R) cells with IC50 values of 1.9 μM and 3.3 μM, respectively, leading to Ki values of 1.4 μM and 2.5 μM. It has a regulating function on cAMP formation in CHO cells, acting as an apparent inverse agonist at low concentrations (EC50 values of 0.1 nM, 0.05 nM, and 0.3 nM) and inhibiting cAMP formation at higher concentrations with an EC50 value of 0.1 μM in CHO (rH3(445)R). In vivo, acute administration of Betahistine dihydrochloride (0.1-30 mg/kg intraperitoneal or oral) increased tele-methylhistamine (t-MeHA) levels with an ED50 of 0.4 mg/kg. Oral administration of 1 and 5 mg/kg daily for 3 weeks attenuated the severity of arthritis and reduced pro-inflammatory cytokines in CIA mice.
Medchemexpress LLC Cimetidine (SKF-92334) | 51481-61-9 | 99.7% | C10H16N6S | 1 ML
Cimetidine (SKF-92334) is an orally active, inverse, and BBB-permeable histamine H2 receptor antagonist. It is primarily known as a gastric acid reducer and can be used for duodenal and gastric ulcers research. Additionally, Cimetidine demonstrates anti-cancer and anti-inflammatory activities.
- Orally active histamine H2 receptor antagonist
- Gastric acid reducer
- Anti-cancer and anti-inflammatory activity
- For research use only
Sigma Aldrich Fine Chemicals Biosciences Esculetin European Pharmacopoeia (EP) Reference Standard | 305-01-1 | MFCD00006874 |
Esculetin European Pharmacopoeia (EP) Reference Standard | Mol Wt: 178.14 | 305-01-1 | MFCD00006874 |
Selleck Chemical LLC Bufexamac S3023-1g
Bufexamac(Bufexamic acid) is a COX inhibitor for IFN- release with EC50 of 8 9 M
Sigma Aldrich Fine Chemicals Biosciences Dapsone British Pharmacopoeia (BP) Reference Standard | 80-08-0 | MFCD00007887 |
Dapsone British Pharmacopoeia (BP) Reference Standard | Mol Wt: 248.3 | 80-08-0 | MFCD00007887 |