Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Brinzolamide Related Compound A United States Pharmacopeia (USP) Reference Standard | 154127-19-2 | 50MG
Brinzolamide Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 383.51 | 154127-19-2 | 50MG
Medchemexpress LLC Diclofenac (Standard) | 15307-86-5 | C₁₄H₁₁Cl₂NO₂ | 100 MG
Diclofenac (Standard) is an analytical standard intended for research and analytical applications. It functions as a potent, nonselective anti-inflammatory agent and a COX inhibitor. It also induces apoptosis of neural stem cells (NSCs) through the activation of the caspase cascade.
- Analytical standard for research and analytical applications
- Potent and nonselective anti-inflammatory agent
- COX inhibitor
- Induces apoptosis of neural stem cells (NSCs)
- Used in qualitative, quantitative, and methodological research experiments
- Suitable for HPLC, GC, and MS
Medchemexpress LLC Diclofenac potassium | 15307-81-0 | C14H10Cl2KNO2 | 1 ML
Diclofenac potassium is a potent and nonselective anti-inflammatory agent that acts as a COX inhibitor.
- Potent and nonselective anti-inflammatory agent.
- Acts as a COX inhibitor.
- Induces apoptosis of neural stem cells (NSCs) via activation of the caspase cascade.
- Effectively blocks COX-1 mediated prostanoid production.
- Increases expression of cleaved (activated) caspase-3.
- Significantly increases fecal 51Cr excretion.
- Demonstrates in vivo anti-inflammatory activity.
Sigma Aldrich Fine Chemicals Biosciences Flumazenil Related Compound B United States Pharmacopeia (USP) Reference Standard | 131666-45-0 | 20MG
Flumazenil Related Compound B United States Pharmacopeia (USP) Reference Standard | Mol Wt: 301.3 | 131666-45-0 | 20MG
Sigma Aldrich Fine Chemicals Biosciences Flumazenil impurity B European Pharmacopoeia (EP) Reference Standard | 131666-45-0 |
Flumazenil impurity B European Pharmacopoeia (EP) Reference Standard | Mol Wt: 301.3 | 131666-45-0 |
Sigma Aldrich Fine Chemicals Biosciences Diphenhydramine N-oxide United States Pharmacopeia (USP) Reference Standard | 13168-00-8 | 25MG
Diphenhydramine N-oxide United States Pharmacopeia (USP) Reference Standard | Mol Wt: 307.82 | 13168-00-8 | 25MG
Medchemexpress LLC Lenalidomide-C4-NH2 25mg | 2435715-90-3 | 351.83 g/mol | C17H22ClN3O3 | 25 MG
Lenalidomide-C4-NH2 hydrochloride is a lenalidomide-derived cereblon ligand supplied as the hydrochloride salt for use as an E3 ligase recruiter in PROTAC synthesis and chemical biology research. It is provided as a solid suitable for conjugation to linkers and target ligands.
- Hydrochloride salt, solid form suitable for handling and storage.
- Functions as a cereblon (CRBN) ligand for PROTAC design and E3 ligase recruitment.
- High purity (HPLC 95.8%) consistent with research-grade material.
- Available in small research pack sizes, including 25 MG.
- Molecular formula C17H22ClN3O3; molecular weight ~351.83 g/mol.
Medchemexpress LLC Rosuvastatin | 287714-41-4 | 99.7% | 50 MG
Rosuvastatin | 287714-41-4 | 99.7% | 50 MG
Apexbio Technology LLC Fenoldopam 67227-56-9 10mg
Fenoldopam is a small-molecule partial agonist targeting dopamine D1-like receptors It is designed to selectively activate these receptors thereby mediating peripheral vasodilation and modulating vascular resistance Fenoldopam exerts its biological activity primarily through D1-like receptor activation In in vitro studies Fenoldopam demonstrates partial agonist activity with an EC50 value of approximately 57 nM Additionally it exhibits inhibitory activity against 2-adrenoceptors with a reported Ki of 15 25 nM Based on these pharmacological properties Fenoldopam holds research potential in studies of cardiovascular regulation receptor pharmacodynamics and selective receptor ligand profiling
Medchemexpress LLC Voriconazole | 137234-62-9 | 99.5% | C16H14F3N5O | 5 MG
Voriconazole (UK-109496) is a second-generation, broad-spectrum triazole antifungal agent. It inhibits fungal ergosterol biosynthesis by inhibiting 14-α-lanosterol demethylation, a process mediated by fungal cytochrome P450 enzymes. It is also capable of penetrating the blood-brain barrier (BBB).
- Inhibits fungal ergosterol biosynthesis.
- Inhibits 14-α-lanosterol demethylation.
- Penetrates the blood-brain barrier.
- Active against *S. apiospermum* (MIC 0.5 μg/mL) and *C. neoformans* (MIC 0.125-0.25 μg/mL).
- Disrupts fungal cell membranes and halts growth.