Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Vinpocetine United States Pharmacopeia (USP) Reference Standard | 42971-09-5 | MFCD00211233 | 100MG
Vinpocetine United States Pharmacopeia (USP) Reference Standard | Mol Wt: 350.45 | 42971-09-5 | MFCD00211233 | 100MG
Selleck Chemical LLC Ivermectin 50mg 70288-86-7 MK933
Ivermectin (MK-933, IVM) is a glutamate-gated chloride channel (GluCls) activator, used as a broad-spectrum antiparasitic drug. Ivermectin (MK-933, IVM) is a specific positive allosteric effector of P2X4 and ?7 nicotinic acetylcholine receptors (nAChRs). Ivermectin has potent antiviral activity towards both HIV-1 and dengue virus. Ivermectin induces autophagy through the AKT/mTOR signaling pathway and mitophagy. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Sigma Aldrich Fine Chemicals Biosciences Tyloxapol United States Pharmacopeia (USP) Reference Standard | 25301-02-4 | MFCD00149002 | 3X200MG
Tyloxapol United States Pharmacopeia (USP) Reference Standard | 25301-02-4 | MFCD00149002 | 3X200MG
Medchemexpress LLC Aminopterin | 54-62-6 | 98.7% | C19H20N8O5 | 50 MG
Aminopterin, also known as 4-Aminofolic acid, is a powerful folic acid antagonist. It operates by catalyzing the reduction of folic acid to tetrahydrofolic acid and competitively inhibits dihydrofolate reductase (DHFR) with a high affinity (Ki of 3.7 pM). This compound is recognized for its significant anticancer and immunosuppressive activities, making it a valuable agent in medical applications, particularly in the treatment of pediatric leukemia.
- Acts as a folic acid antagonist
- Competitively inhibits dihydrofolate reductase (DHFR)
- Exhibits anticancer properties
- Possesses immunosuppressive activities
- Used in the treatment of pediatric leukemia
Medchemexpress LLC Diphenhydramine (Standard) | 58-73-1 | MFCD00274173 | 98.7% | 100 MG
Diphenhydramine (Standard) is an analytical standard intended for research and analytical applications. It is a first-generation histamine H1-receptor antagonist with an anti-cholinergic effect and can cross the ovine blood-brain barrier (BBB). This compound is supplied as a reference standard assay and is commonly used in qualitative, quantitative, and methodological research experiments.
- First-generation histamine H1-receptor antagonist
- Anti-cholinergic effect
- Can cross the ovine blood-brain barrier (BBB)
- Used in HPLC, GC, and MS experiments
- Molecular weight: 255.35
- Formula: C17H21NO
- Appearance: liquid
- Color: colorless to light yellow
- Classified as an alkaloid
- Initial source: endogenous metabolite
- For research use only
Medchemexpress LLC Felodipine | 72509-76-3 | 99.83% | 5 MG
Felodipine is a potent, vasoselective dihydropyridine calcium channel antagonist. It lowers blood pressure by selectively acting on vascular smooth muscle, particularly in the resistance vessels. This anti-hypertensive agent also induces autophagy and can cross the blood-brain barrier. It is intended for research use only and not for sale to patients.
- Potent, vasoselective calcium channel antagonist
- Lowers blood pressure by acting on vascular smooth muscle
- Induces autophagy
- Can cross the blood-brain barrier
U.S. Pharmacopeia Phytonadione, 84-80-0, MFCD00214063, 100 mg x 5 ampules
Molecular formula C31H46O2, Molecular weight 450.7, Melting point -4 °F (-20 °C), Boiling point 284 - 293 °F (140 - 145 °C), Flash point > 235.4 °F (> 113.0 °C) Closed Cup, Synonyms: Vitamin K1, Phylloquinone, Phytomenadione
Sigma Aldrich Fine Chemicals Biosciences Calcitriol European Pharmacopoeia (EP) Reference Standard | 32222-06-3 | MFCD00867079 |
Calcitriol European Pharmacopoeia (EP) Reference Standard | Mol Wt: 416.64 | 32222-06-3 | MFCD00867079 |
Medchemexpress LLC Mogroside III | 130567-83-8 | MFCD00238648 | ≥98.0% | 963.15 g/mol | C48H82O19 | 10 MG
Mogroside III is a triterpenoid glycoside sold as a purified research reagent and used in studies of carbohydrate metabolism and related pharmacology.
- Purity ≥98.0%.
- Molecular weight 963.15 g/mol.
- Chemical formula C48H82O19.
- CAS number 130567-83-8.
- Supplied as a small white to off-white powder in 10 mg packaging.
- Used in biochemical and pharmacological research, including maltase inhibition studies.
Medchemexpress LLC Risperidone | 106266-06-2 | 99.9% | 410.48 | 50 MG
Risperidone | 106266-06-2 | 99.9% | 410.48 | 50 MG
Bioworld Streptalon (Steptavidin Magnetic Beads) Kit, 2 mL
bioWorld's Streptalon (Streptavidin magnetic beads) Kit is designed for convenient and quick purification of biotinylated proteins and nucleic acids inimmunoprecipitation, protein interaction studies, immunoassays and cell isolation, etc.Streptalon (Streptavidin Magnetic Beads)Kit providessuperparamagnetic beads of approximately 10 μm in size, covalently coated with highly purified streptavidin.Kit Contents:• Streptalon™ (25mg/ml magnetic beads), 2ml• Binding/Wash Buffer • Elution Buffer• Neutralization BufferThis kit requires MagneZoom™ paramagnetic bead station (20160000-1)for separation of beads.
Sigma Aldrich Fine Chemicals Biosciences Tinidazole Related Compound A United States Pharmacopeia (USP) Reference Standard | 696-23-1 | MFCD00151322 | 100MG
Tinidazole Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 127.1 | 696-23-1 | MFCD00151322 | 100MG
Apexbio Technology LLC Manidipine 89226-50-6 200mg
Manidipine (CAS 89226-50-6) is a dihydropyridine derivative functioning as a calcium channel blocker This compound specifically inhibits voltage-dependent calcium channels impairing calcium influx into vascular smooth muscle cells resulting in systemic arterial vasodilation Due to this mechanism manidipine is used mainly in research involving cardiovascular regulation hypertension models and investigations into calcium-mediated smooth muscle signaling pathways
Sigma Aldrich Fine Chemicals Biosciences Aloin United States Pharmacopeia (USP) Reference Standard | 1415-73-2 | MFCD00151160 | 25MG
Aloin United States Pharmacopeia (USP) Reference Standard | Mol Wt: 418.39 | 1415-73-2 | MFCD00151160 | 25MG
Medchemexpress LLC Taprenepag isopropyl | 1005549-94-9 | 99.0% | 520.60 | 1 ML
Taprenepag isopropyl is a highly selective EP2 receptor agonist. It reduces intraocular pressure (IOP) in the right (dosed) eye in a dose-dependent manner in cynomolgus monkeys. In a high-dose group (0.75 mg/day), IOP was reduced to less than 4 mm Hg on Days 22 and 29. No clinical signs or changes in body weight were observed with any dose, and no ocular findings occurred in the low-dose group (0.75 mg/day).
- Highly selective EP2 receptor agonist.
- Reduces intraocular pressure (IOP) in a dose-dependent manner.
- Achieved IOP reduction to less than 4 mm Hg in high-dose group.
- No clinical signs or changes in body weight observed.
- No ocular findings occurred in the low-dose group.
- Target: EP2.