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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Aprepitant Related Compound A United States Pharmacopeia (USP) Reference Standard | 1148113-53-4 | 10MG
Aprepitant Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 534.43 | 1148113-53-4 | 10MG
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Sigma Aldrich Fine Chemicals Biosciences Amitriptyline Related Compound B United States Pharmacopeia (USP) Reference Standard | 1159-03-1 | 25MG
Amitriptyline Related Compound B United States Pharmacopeia (USP) Reference Standard | Mol Wt: 295.42 | 1159-03-1 | 25MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000723888 METHYLPREDNISOLONE I 25MG
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Medchemexpress LLC Propyl gallate | 121-79-9 | 212.20 | 1 ML
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Propyl gallate is a common food antioxidant that can inhibit the production of acrolein, glyoxal, and methylglyoxal. It also exhibits anti-inflammatory, antitumor, and cardioprotective activities. This product is for research use only and not sold to patients.
- Common food antioxidant
- Inhibits the production of acrolein, glyoxal, and methylglyoxal
- Exhibits anti-inflammatory, antitumor, and cardioprotective activities
- Increases ROS level and decreases glutathione (GSH) in vitro
- Inhibits cancer cell growth (e.g., Calu-6 and A549), arrests the cell cycle at G1 phase, and induces apoptosis via mitochondrial and cell death receptor pathways
- Inhibits cardiac enlargement in dilated cardiomyopathy (DCM) mice
- Prevents left ventricular dilatation and systolic dysfunction
- Increases myocardial contractility by enhancing myofilament sensitivity to Ca2+ in myocardial fibers
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Alkali Scientific Augmentin [Amoxicillin, Sodium Salt/Potassium Clavulanate 5:1], 2 G
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Amoxicillin and Clavulanate is a combination antibiotic formulation widely used in microbiological and pharmaceutical research. Amoxicillin is a beta lactam antibiotic that inhibits bacterial cell wall synthesis, while clavulanate acts as a beta lactamase inhibitor that protects amoxicillin from enzymatic degradation by resistant bacteria. This combination provides broad spectrum antibacterial activity against both Gram positive and Gram negative organisms. In laboratory applications, it is used to study bacterial resistance mechanisms, antimicrobial susceptibility, and enzyme inhibition. The formulation is also used in cell culture and microbiology research where reliable inhibition of resistant bacterial strains is required.
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Medchemexpress LLC Ethyl gallate | 831-61-8 | 198.17 | 1 ML
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Ethyl gallate is a nonflavonoid phenolic compound and a scavenger of hydrogen peroxide. It has a cytotoxic effect on HL-60 cells, leading to changes in morphology, shrinkage of the cell membrane, development of apoptotic bodies, and decreased cell viability. It is suitable for laboratory research applications.
- Nonflavonoid phenolic compound
- Scavenger of hydrogen peroxide
- Has cytotoxic effect on HL-60 cells
- Leads to changes in morphology, shrinkage of the cell membrane, development of apoptotic bodies, and decreased cell viability
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eMolecules 1263166-91-1 | Ambeed | rel-((1R8S9s)-Bicyclo[6.1.0]non-4-yn-9-yl)methyl (4-nitrophenyl) carbonate | 25mg | 682931751 | A756306 | 315.325 | C17H17NO5
Ambeed | Fmoc-Glu-OMe | 5g | 525085874 | A169419 | 145038-49-9 | MFCD22200617 | 383.400 | C21H21NO6
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eMolecules Building Block Tool<|a>
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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
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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.
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Cayman Chemical R-CrIzotInIb 250mg
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A dual inhibitor of c-Met and ALK (IC50s = 8 and 20 nM, respectively, in a cell-based assay); selective for c-Met and ALK over several other receptor and non-receptor tyrosine kinases, including Ron, Tie2, Abl, LCK, and VEGFR2 (IC50s = 0.08, 0.448, 1.159, 2.741, and >10 µM, respectively); selectively inhibits the proliferation of cancer cell lines with MET amplifications over cancer cell lines with MET or EGFR mutations (IC50s = 5-10, 472-1,284, and 767-787 nM, respectively); induces apoptosis in MET-amplified EBC-1 and NCI H1993 cells at 100 nM; reduces tumor volume in an EBC-1 mouse xenograft model at 25 mg/kg
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Selleck Chemical LLC Carprofen-50mg
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Carprofen inhibits canine COX2 with IC50 of 30 nM.
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Selleck Chemical LLC Pantoprazole S2105-500mg
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Pantoprazole (SKF96022 BY-1023) is a proton pump inhibitor drug that inhibits gastric acid secretion It works on gastric parietal cells to irreversibly inhibit (H /K )-ATPase function and suppress the production of gastric acid
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Medchemexpress LLC 1H-Benzimidazole, 6-methoxy-2-[(S)-[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-, sodium salt (1:1) | 161796-78-7 | MFCD00870347 | 99.4% | 367.40 | 5 MG
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Esomeprazole sodium is a potent and orally active proton pump inhibitor. It reduces acid secretion by inhibiting the H+, K+-ATPase in gastric parietal cells. Additionally, it acts as an exosome inhibitor by blocking exosome release through the inhibition of V-H+-ATPases. It has potential for research related to symptomatic gastroesophageal reflux disease and for suppressing the growth of triple-negative breast cancer cells.
- Potent and orally active proton pump inhibitor
- Reduces acid secretion
- Acts as an exosome inhibitor
- Potential for symptomatic gastroesophageal reflux disease research
- For research use only
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Selleck Chemical LLC Betamethasone Valerate 25mg 2152-44-5
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Betamethasone Valerate is a moderately potent glucocorticoid steroid with anti-inflammatory and immunosuppressive properties. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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Medchemexpress LLC Pantoprazole (sodium) | 138786-67-1 | 99.8% | 405.35 | 1 ML
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Pantoprazole sodium (BY1023 sodium) is an orally active and potent proton pump inhibitor (PPI). This substituted benzimidazole acts as a strong H+/K+-ATPase inhibitor with an IC50 of 6.8 μM. It enhances pH stability and exhibits anti-secretory and anti-ulcer properties. When combined with Doxorubicin, Pantoprazole sodium significantly increased tumor growth delay.
- Potent H+/K+-ATPase inhibitor
- Improved pH stability
- Anti-secretory activity
- Anti-ulcer activity
- Potential in cancer therapy
- Blocks exosome release
- Impairs tumor cell acidification
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U.S. Pharmacopeia 2-tert-Butyl-4-hydroxyanisole, 88-32-4, MFCD00057667, 200mg
Molecular Formula C11H16O2, Molecular Weight 180.245, Boiling Point 507.2 °F (264 °C), Flash point 312.80 °F (156.00 °C), Synonyms: 3-tert-Butyl-4-methoxyphenol, 2-BHA
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