Drug Standards
Apexbio Technology LLC Losartan Potassium (DuP 753) 124750-99-8 10mM (in 1mL DMSO)
Losartan Potassium (DuP 753 CAS 124750-99-8) is a small molecule antagonist selective toward angiotensin AT receptors By competitively blocking AT receptors it inhibits angiotensin II-mediated vasoconstriction demonstrated by antagonism of contractile responses in isolated rabbit aortic and jugular vein tissues (pA 8 27) As an orally bioavailable agent losartan potassium is frequently utilized in cardiovascular research notably in studies investigating hypertension and associated mechanisms of angiotensin II signaling
Sigma Aldrich Fine Chemicals Biosciences Clozapine United States Pharmacopeia (USP) Reference Standard | 5786-21-0 | MFCD00153785 | 100MG
Clozapine United States Pharmacopeia (USP) Reference Standard | Mol Wt: 326.82 | 5786-21-0 | MFCD00153785 | 100MG
Sigma Aldrich Fine Chemicals Biosciences Isradipine United States Pharmacopeia (USP) Reference Standard | 75695-93-1 | MFCD00153820 | 200MG
Isradipine United States Pharmacopeia (USP) Reference Standard | Mol Wt: 371.39 | 75695-93-1 | MFCD00153820 | 200MG
Medchemexpress LLC Benazepril | 86541-75-5 | 99.9% | C24H28N2O5 | 25 MG
Benazepril is an orally active angiotensin-converting enzyme (ACE) inhibitor that reduces angiotensin-II production. It inhibits oxidative stress and apoptosis via the PI3K/Akt signaling pathway. This compound improves diabetic nephropathy and decreases proteinuria, making it suitable for studies of hypertension, heart failure, and diabetic nephropathy.
- Alleviates oxidative stress and inhibits cell apoptosis.
- Improves diabetic nephropathy in Wistar male rats.
- Decreases proteinuria, urea, creatinine, triglycerides, and total cholesterol levels.
- Increases albumin level, diminishes kidney volume, and ameliorates pathological changes.
Medchemexpress LLC Stearyl arachidate 50mg
Stearyl arachidate is a biochemical reagent that can be used as a biological material or organic compound for life science related research
Sigma Aldrich Fine Chemicals Biosciences D-(+)-Maltose monohydrate|6363-53-7 | MFCD00149343 | 100g
D-(+)-Maltose monohydrate | 99.90% | MW: 360.31 | 6363-53-7 | MFCD00149343 | 100g
Sigma Aldrich Fine Chemicals Biosciences Salbutamol European Pharmacopoeia (EP) Reference Standard | 18559-94-9 | MFCD00148978 |
Salbutamol European Pharmacopoeia (EP) Reference Standard | Mol Wt: 239.31 | 18559-94-9 | MFCD00148978 |
Sigma Aldrich Fine Chemicals Biosciences Dichlorphenamide United States Pharmacopeia (USP) Reference Standard | 120-97-8 | MFCD00148948 | 200MG
Dichlorphenamide United States Pharmacopeia (USP) Reference Standard | Mol Wt: 305.16 | 120-97-8 | MFCD00148948 | 200MG
Sigma Aldrich Fine Chemicals Biosciences Zomepirac sodium salt | 64092-48-4 | MFCD00057223 | 250mg
Zomepirac sodium salt | MW: 313.71 | 64092-48-4 | MFCD00057223
Medchemexpress LLC Tivantinib | 905854-02-6 | 99.6% | C23H19N3O2 | 200 MG
Tivantinib is a highly selective, low-molecular-weight, and orally available c-Met tyrosine kinase inhibitor. It selectively inhibits c-Met activity in both cell-free and cell-based assays, leading to a dose-dependent loss of proliferative capacity or caspase-dependent apoptosis in c-Met-expressing cancer cell lines.
- Highly selective c-Met tyrosine kinase inhibitor
- Inhibits c-Met activity in cell-free and cell-based assays
- Causes dose-dependent loss of proliferative capacity or apoptosis in c-Met-expressing cancer cells
- Orally available
- Inhibits constitutive c-Met phosphorylation
- Inhibits HGF-induced c-Met phosphorylation
Medchemexpress LLC Tivantinib | 905854-02-6 | 99.6% | C23H19N3O2 | 100 MG
Tivantinib is a highly selective c-Met tyrosine kinase inhibitor, notable for its low molecular weight and as the first orally available selective inhibitor of c-Met. It selectively inhibits c-Met activity in cell-free and cell-based assays, leading to dose-dependent loss of proliferative capacity or caspase-dependent apoptosis in c-Met-expressing cancer cell lines.
- Highly selective c-Met tyrosine kinase inhibitor
- First orally available selective inhibitor of c-Met
- Inhibits c-Met activity in cell-free and cell-based assays
- Induces dose-dependent loss of proliferative capacity or caspase-dependent apoptosis in c-Met-expressing cancer cell lines
- Inhibits human recombinant c-Met with a Ki of approximately 355 nM
Medchemexpress LLC Norfloxacin | 70458-96-7 | 99.8% | 250 MG
Norfloxacin (Standard) is the analytical standard of Norfloxacin. This product is intended for research and analytical applications. Norfloxacin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria, functioning by inhibiting DNA gyrase. It is commonly used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
- Analytical standard
- Broad-spectrum antibiotic
- Active against Gram-positive and Gram-negative bacteria
- Inhibits DNA gyrase
- Suitable for research and analytical applications
- Used in HPLC, GC, and MS research experiments