Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Pantoprazole Related Compound A United States Pharmacopeia (USP) Reference Standard | 127780-16-9 | 25MG
Pantoprazole Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 399.37 | 127780-16-9 | 25MG
Sigma Aldrich Fine Chemicals Biosciences Nateglinide Related Compound A United States Pharmacopeia (USP) Reference Standard | 7077-05-6 | 10MG
Nateglinide Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 170.25 | 7077-05-6 | 10MG
Sigma Aldrich Fine Chemicals Biosciences Oxitropium bromide European Pharmacopoeia (EP) Reference Standard | 30286-75-0 |
Oxitropium bromide European Pharmacopoeia (EP) Reference Standard | Mol Wt: 412.32 | 30286-75-0 |
Medchemexpress LLC Pantoprazole sodium hydrate | 164579-32-2 | 99.93% | 432.37 | 250 MG
Pantoprazole sodium hydrate is an orally active and potent proton pump inhibitor (PPI) and a substituted benzimidazole. It is a potent H+/K+-ATPase inhibitor with an IC50 of 6.8 μM. It improves pH stability and possesses anti-secretory and anti-ulcer activities. It also significantly increased tumor growth delay when combined with Doxorubicin.
- Orally active and potent proton pump inhibitor
- Substituted benzimidazole
- Potent H+/K-ATPase inhibitor with an IC50 of 6.8 μM
- Improves pH stability
- Anti-secretory and anti-ulcer activities
- Increases tumor growth delay in combination with Doxorubicin
Cayman Chemical SalInomycIn 100mg
An antibacterial and coccidiostat compound that shows selective toxicity for HMLER breast cancer stem cells (IC50 = ~24 μM); 8 μM treatment of 4T1 and MCF-7-Ras breast cancer cell lines decreases cancer stem cell growth ~2-fold and ~3-fold, respectively; 5 mg/kg inhibits mammary tumor growth and induces increased epithelial differentiation of tumor cells in mice implanted with SUM159 human breast cancer cells
Medchemexpress LLC Citalopram | 59729-33-8 | 99.8% | 1 ML
Citalopram is an orally active selective serotonin reuptake inhibitor (SSRI) provided for research use. This product is supplied as a 10 mM solution in DMSO (1 mL) and is intended for in vitro pharmacology and neuroscience studies.
- Orally active selective serotonin reuptake inhibitor for research use.
- Supplied as a 10 mM solution in DMSO, 1 mL volume.
- High purity (99.8%) suitable for biochemical and cell-based assays.
- Molecular formula C20H21FN2O and molecular weight 324.39.
- Suitable for in vitro pharmacology and neuroscience research applications.
Selleck Chemical LLC Lidocaine hydrochloride S4667-500mg
Lidocaine hydrochloride (Lidothesin Lignocaine Xyloneural) is an inhibitor of epidermal growth factor receptor (EGFR) and has antiproliferative effect on human tongue cancer cells Lidocaine hydrochloride is a local anesthetic and cardiac depressant used as an antiarrhythmia agent
Cayman Chemical SynthetIc OuabaIn-d3 1mg
An internal standard for the quantification of ouabain by GC- or LC-MS
Cayman Chemical Abnormal Cannabidiol
An analytical reference standard that is structurally similar to known phytocannabinoids; not found in Cannabis; has been used as an internal standard for the detection of cannabinoids in hemp extracts; intended for research and forensic applications
Sigma Aldrich Fine Chemicals Biosciences Plastic Additive 11 | 2082-79-3 | MFCD00017498 | 300mg
Plastic Additive 11 | Mol Wt: 530.86 | 2082-79-3 | MFCD00017498 | 300mg
Sigma Aldrich Fine Chemicals Biosciences Choline chloride United States Pharmacopeia (USP) Reference Standard | 67-48-1 | MFCD00011721 | 500MG
Choline chloride United States Pharmacopeia (USP) Reference Standard | Mol Wt: 139.62 | 67-48-1 | MFCD00011721 | 500MG
Echelon Biosciences Research Labs PIK-93 5 mg
PIK-93 is the first reported PI4-kinase inhibitor, which is able to inhibit PI4KIII at low-nanomolar range (IC50=19 nM). In addition, this compound is a potent inhibitor of PI3K in vitro (IC50=16 nM). This compound inhibits p110, p110, p110 with IC50s of 0.039, 0.59, 0.12 M respectively. PIK-93 hydrogen bonds to the backbone amide and carbonyl of Val882 and between its sulphonamide and Asp964. PI4KIII is esential for replication of numerous viruses P. falciparum. Inhibition of plasmodial PI4KIII has been proposed as an anti-malaria treatment. This item is non returnable
![Medchemexpress LLC 6-Heptenoic acid, 7-[4-(4-fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]-3,5-dihydroxy-, sodium salt (1:1), (3R,5S,6E)- | 147098-18-8 | 99.9% | 503.52 | 200 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000386888-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 6-Heptenoic acid, 7-[4-(4-fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]-3,5-dihydroxy-, sodium salt (1:1), (3R,5S,6E)- | 147098-18-8 | 99.9% | 503.52 | 200 MG
Rosuvastatin Sodium is a competitive HMG-CoA reductase (HMGCR) inhibitor, with an IC50 of 11 nM. It potently blocks hERG current with an IC50 of 195 nM. This compound effectively lowers low-density lipoprotein (LDL) cholesterol, triglycerides, and C-reactive protein levels.
- Reduces the expression of mature hERG and the interaction of heat shock protein 70 (Hsp70) with the hERG protein.
- Effectively lowers low-density lipoprotein (LDL) cholesterol.
- Reduces triglyceride levels.
- Decreases C-reactive protein levels.