Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Tiaprofenic acid impurity C European Pharmacopoeia (EP) Reference Standard | 78239-47-1 |
Tiaprofenic acid impurity C European Pharmacopoeia (EP) Reference Standard | Mol Wt: 260.31 | 78239-47-1 |
Medchemexpress LLC Atazanavir sulfate | 229975-97-7 | 99.7% | 802.93 | 5 MG
Atazanavir (BMS-232632) sulfate is a highly selective and orally active HIV-1 protease inhibitor with blood-brain barrier permeability. Atazanavir sulfate is a substrate and inhibitor of CYP3A4, and an inhibitor of P-glycoprotein (P-gp). Atazanavir sulfate is also a SARS-CoV 3CLpro inhibitor with an IC50 of 3.49 μM. Atazanavir sulfate inhibits cardiac fibrosis, hyperlipidemia and induces malignant glioma death.
- Highly selective and orally active HIV-1 protease inhibitor with blood-brain barrier permeability.
- Functions as a substrate and inhibitor of CYP3A4.
- Acts as an inhibitor of P-glycoprotein (P-gp).
- Inhibits SARS-CoV 3CLpro with an IC50 of 3.49 μM.
- Inhibits cardiac fibrosis.
- Inhibits hyperlipidemia.
- Induces malignant glioma death.
AdipoGen Rosiglitazone,Chemical. CAS: 122320-73-4
Rosiglitazone, AdipoGen Life Sciences. Chemical. CAS: 122320-73-4. Formula: C18H19N3O3S. MW: 357.4. Antidiabetic, hypoglycemic agent. Potent and selective peroxisome proliferator-activated receptor gamma (PPAR-gamma) agonist. Potent insulin sensitizing agent binding to the PPAR receptors in fat cells and making the cells more responsive to insulin. Ameliorates insulin resistance. Improves blood pressure and vascular function. Enhances proliferation of endogenous neural progenitor cells (NPCs). Anti-inflammatory compound. Has controversial therapeutic effects on the cardiovascular system. Promotes adipocyte differentiation of mesenchymal stem cells (MSCs).
Apexbio Technology LLC Doxycycline hyclate 24390-14-5 10mM (in 1mL DMSO)
Doxycycline hyclate is a semisynthetic antibiotic derivative of tetracycline exhibiting antibacterial antiviral and anti-inflammatory activities It functions primarily as an inhibitor of matrix metalloproteinases (MMPs) notably reducing expression and activity of MMP-2 MMP-8 and MMP-9 thus applicable in research involving inflammatory conditions and vascular pathologies such as intracranial aneurysms Its antiviral properties include inhibition of dengue virus replication by targeting viral NS2B-NS3 serine protease experimental conditions at 37 C and 40 C yielded IC50 values of 52 3 M and 26 7 M respectively Additionally doxycycline hyclate demonstrates antimalarial activity with in vivo experiments showing an IC50 of 320 nM at 96 hours facilitating potential use in parasitology research models
![Medchemexpress LLC 2-[(4-chloro-3,5-dimethyl-2-pyridinyl)methylsulfanyl]-6-methoxy-1H-benzimidazole | 220757-74-4 | MFCD09840353 | 5mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000266909.png-250.jpg)
Medchemexpress LLC 2-[(4-chloro-3,5-dimethyl-2-pyridinyl)methylsulfanyl]-6-methoxy-1H-benzimidazole | 220757-74-4 | MFCD09840353 | 5mg
Omeprazole impurity 13 is an impurity ofOmeprazole (HY-B0113)
Cayman Chemical D-a-Tocopheryl QuInon 50mg
An oxidative metabolite of vitamin E; has antioxidant activity in ORAC and radical trapping assays at 25 µM; inhibits (1S,3R)-RSL3-induced ferroptosis in Q7 cells (EC50 = 0.233 µM); decreases serum MDA and blood glucose levels and restores the number and diversity of intestinal microflora in a rat model of high cholesterol and cholate diet-induced NASH at 20 mg/kg
Medchemexpress LLC Sumatriptan succinate | 103628-48-4 | 99.5% | 25 MG
Sumatriptan succinate is an orally active 5-HT1 receptor agonist, with IC50 values of 7.3 nM, 9.3 nM, and 17.8 nM for 5-HT1D, 5-HT1B, and 5-HT1F receptors, respectively. This compound is suitable for migraine headache research and has been shown to reverse nitroglycerin-induced thermal hypersensitivity in mice.
- Orally active 5-HT1 receptor agonist
- Suitable for migraine headache research
- Reverses nitroglycerin-induced thermal hypersensitivity in mice
- Exhibits IC50 values of 7.3 nM for 5-HT1D receptors
- Exhibits IC50 values of 9.3 nM for 5-HT1B receptors
- Exhibits IC50 values of 17.8 nM for 5-HT1F receptors
Sigma Aldrich Fine Chemicals Biosciences Telmisartan European Pharmacopoeia (EP) Reference Standard | 144701-48-4 | MFCD00918125 |
Telmisartan European Pharmacopoeia (EP) Reference Standard | Mol Wt: 514.62 | 144701-48-4 | MFCD00918125 |
Sigma Aldrich Fine Chemicals Biosciences Finasteride United States Pharmacopeia (USP) Reference Standard | 98319-26-7 | MFCD00869737 | 200MG
Finasteride United States Pharmacopeia (USP) Reference Standard | Mol Wt: 372.54 | 98319-26-7 | MFCD00869737 | 200MG
Medchemexpress LLC Mogroside I A1 | 88901-46-6 | 1 MG
Mogroside I A1 is a triterpenoid glycoside and a nonsugar sweetener. It is known for being sweeter than sucrose and exhibits antioxidant, antidiabetic, and anticancer activities.
- Triterpenoid glycoside
- Nonsugar sweetener, sweeter than sucrose
- Exhibits antioxidant, antidiabetic, and anticancer activities
- Store at 4°C, protected from light
- In solvent, store at -80°C for 6 months or -20°C for 1 month, protected from light
Med Vet International Ketoconazole Tablets (Nizoral), 200mg, 100ct
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Ketoconazole a generic version of Nizoral is used to treat fungal and yeast infections on skin, hair, nails, and blood.
Medchemexpress LLC Lidocaine impurity 1 | 39084-88-3 | 99.9% | 232.11 | 50 MG
Lidocaine impurity 1 is an impurity of Lidocaine. It is for research use only and not sold to patients. The appearance is solid, and the formula is C10H11Cl2NO.
- Appearance: Solid
- Formula: C10H11Cl2NO
- Shipping: Room temperature in continental US; may vary elsewhere
- Storage (powder): -20°C for 3 years, 4°C for 2 years
- Storage (in solvent): -80°C for 6 months, -20°C for 1 month
- Usage: For research use only
Medchemexpress LLC Aprepitant impurity 1 | 170729-76-7 | 100 MG
Defluoro aprepitant is an analytical standard intended for research and analytical applications. This product is for research use only.
- Analytical and reference standard for assay
- Suitable for qualitative, quantitative, and methodological research
- Applicable in HPLC, GC, and MS experiments
Sigma Aldrich Fine Chemicals Biosciences Ifosfamide impurity F European Pharmacopoeia (EP) Reference Standard | 40722-73-4 |
Ifosfamide impurity F European Pharmacopoeia (EP) Reference Standard | Mol Wt: 218.02 | 40722-73-4 |
Apexbio Technology LLC Diphemanil Methylsulfate 62-97-5 10mM (in 1mL DMSO)
Diphemanil Methylsulfate (CAS 62-97-5) is a synthetic quaternary ammonium compound that acts as an anticholinergic agent by competitively inhibiting muscarinic acetylcholine receptors This blockade reduces the activity of the parasympathetic nervous system leading to decreased secretory and smooth muscle activity Diphemanil Methylsulfate is utilized in biomedical research to investigate cholinergic pathways autonomic nervous system modulation and the physiological regulation of glandular secretions or gastrointestinal motility Its defined mechanism makes it a useful tool in studies of receptor pharmacology and neurotransmitter-mediated signaling