Drug Standards
Medchemexpress LLC Metoprolol (Standard) | 51384-51-1 | 99.99% | 267.36 | 1 G
Metoprolol is an orally active, selective β1-adrenoceptor antagonist. It exhibits anti-inflammation, antitumor, and anti-angiogenic properties, making it suitable for various research applications.
- Acts as a selective β1-adrenoceptor antagonist
- Exhibits anti-inflammatory effects
- Demonstrates antitumor activity
- Shows anti-angiogenic properties
- Cytotoxic to U937 and MOLT-4 cells in vitro
- Reduces proinflammatory cytokines and atherosclerosis in ApoE-/- mice
- Provides anti-inflammatory and antiviral effects in viral myocarditis models
- Inhibits myocardial apoptosis in coronary microembolization models
Sigma Aldrich Fine Chemicals Biosciences Trandolapril Related Compound E United States Pharmacopeia (USP) Reference Standard | 87679-71-8 | 25MG
Trandolapril Related Compound E United States Pharmacopeia (USP) Reference Standard | Mol Wt: 402.48 | 87679-71-8 | 25MG
Sigma Aldrich Fine Chemicals Biosciences Buflomedil impurity B European Pharmacopoeia (EP) Reference Standard | 79967-07-0 |
Buflomedil impurity B European Pharmacopoeia (EP) Reference Standard | Mol Wt: 293.36 | 79967-07-0 |
Sigma Aldrich Fine Chemicals Biosciences Loratadine Related Compound C United States Pharmacopeia (USP) Reference Standard | 31251-41-9 | 15MG
Loratadine Related Compound C United States Pharmacopeia (USP) Reference Standard | Mol Wt: 243.69 | 31251-41-9 | 15MG
Selleck Chemical LLC Doxycycline Hyclate S4163-500mg
Doxycycline Hyclate is a member of the tetracycline antibiotics group and is commonly used to treat a variety of infections It is also an inhibitor of matrix metallo-proteinases (MMP)
Med Vet International Fluconazole Tablets (Diflucan), 50mg, 30ct
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Fluconazole is a generic version of Diflucan. It belongs to a class of drugs called azole antifungals and should be stored at room temperature away from light and moisture.
Medchemexpress LLC Mogroside IV-E | 88915-64-4 | 1 ML
Mogroside IV-E is a triterpenoid glycoside and a nonsugar sweetener. Mogrosides are known to be sweeter than sucrose and exhibit antioxidant, antidiabetic, and anticancer activities.
- Triterpenoid glycoside and nonsugar sweetener
- Sweeter than sucrose
- Exhibits antioxidant activity
- Exhibits antidiabetic activity
- Exhibits anticancer activity
Medchemexpress LLC (2S)-2-(6-Methoxy-2-naphthyl)propanoic acid sodium salt | 26159-34-2 | C14H13NaO3 | 25 G
Naproxen sodium is a nonsteroidal anti-inflammatory drug (NSAID) and a potent inhibitor of both COX-1 and COX-2 enzymes. It demonstrates anti-inflammatory and antifibrotic effects, downregulating TGF-β levels and Smad3/4 complex formation, and inhibiting pain, fever, and PGE2 time-courses.
- Purity of 99.74%
- White to off-white solid appearance
- Store at 4°C, sealed, away from moisture
- When in solvent, store at -80°C for 6 months or -20°C for 1 month, sealed and away from moisture
- Inhibits COX-1 (IC50 of 9.55 μM in intact cells)
- Inhibits COX-2 (IC50 of 5.65 μM in intact cells)
![Medchemexpress LLC 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, sodium salt (1:1), (2S,5R,6R)- | 343-55-5 | 98.0% | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000413355-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, sodium salt (1:1), (2S,5R,6R)- | 343-55-5 | 98.0% | 5 MG
Dicloxacillin sodium is a β-lactam antibiotic belonging to the penicillin family. It is effective against Gram-positive bacteria, including β-lactamase-producing organisms such as *Staphylococcus aureus*.
- β-lactam antibiotic.
- Active against Gram-positive bacteria.
- Effective against β-lactamase-producing organisms like *Staphylococcus aureus*.
Medchemexpress LLC Ethacrynic acid | 58-54-8 | MFCD00056693 | 98.8% | 303.14 g/mol | C13H12Cl2O4 | 10 MG
Ethacrynic acid analytical standard supplied for research and analytical use. The compound is a loop diuretic and bioactive small molecule reported to modulate glutathione S-transferases and NF-κB signaling, affect calcium channels, and show anti-inflammatory activity; it is provided as a purified solid standard for biochemical and pharmacological studies.
- Intended for research and analytical applications.
- Purity approximately 98.8%.
- Molecular weight 303.14 g/mol.
- CAS number 58-54-8 for unambiguous identification.
- Available in small package sizes, including 10 mg.
- Supplied as a solid powder suitable for analytical preparation.
U.S. Pharmacopeia Norphenylephrine hydrochloride, 4779-94-6, MFCD00012879, 25 mg
Linear Formula: HOC6H4CH(CH2NH2)OH · HCl, Molecular Weight: 189.64, mp: 162-164 °C, Synonym: α-Aminomethyl-3-hydroxybenzyl alcohol hydrochloride, 3,α-Dihydroxyphenethylamine hydrochloride, Norfenefrine hydrochloride.
Sigma Aldrich Fine Chemicals Biosciences Ropivacaine United States Pharmacopeia (USP) Reference Standard | 84057-95-4 | 200MG
Ropivacaine United States Pharmacopeia (USP) Reference Standard | Mol Wt: 274.4 | 84057-95-4 | 200MG
Cayman Chemical Salbutamol-d9 500ug
An internal standard for the quantification of salbutamol by GC- or LC-MS
Cayman Chemical Olanzapine-related Compound B
A potential impurity found in commercial preparations of olanzapine; a degradation product formed by exposure to oxidative stress
AdipoGen Ketoconazole
Chemical. CAS 65277-42-1. Formula C26H28Cl2N4O4. MW 531.43. Ketoconazole is a broad-spectrum triazole antifungal agent that has activity against C. albicans, C. krusei, C. tropicalis, C. glabrata, C. parapsilosis, C. neoformans and A. fumigatus strains IC50s = 0.031-8 µg/ml. It inhibits the fungal cytochrome P450 CYP isoform CYP51, also known as lanosterol 14alpha-demethylase, which arrests ergosterol biosynthesis at the fungal membrane. This interaction inhibits ergosterol synthesis and results in increased fungal cellular permeability. Ketoconazole also inhibits human CYP3A4 IC50 = 0.54 µM. Formulations containing ketoconazole have been used in the treatment of fungal infections. Ketoconazole blocks in humans activity of several enzymes necessary for the conversion of cholesterol to steroid hormones such as testosterone and cortisol.