Gallic Acid
Medchemexpress LLC Demethylwedelolactone | 6468-55-9 | MFCD09264645 | 99.9% | 300.22 g/mol | C15H8O7 | 10 MG
Demethylwedelolactone is a coumestan-class bioactive small molecule supplied for laboratory research as a milligram-scale reagent. It acts as a trypsin inhibitor and is used in biochemical and cell-based studies. The compound has molecular formula C15H8O7, molecular weight 300.22 g/mol, and CAS number 6468-55-9, and is provided as a 10 mg quantity for research use only.
- High reported purity of 99.89%.
- Milligram-scale quantity suitable for assay development and analytical studies.
- Molecular weight 300.22 g/mol and formula C15H8O7 for exact stoichiometry.
- Trypsin inhibitor activity useful in protease-related research.
- CAS number 6468-55-9 for unambiguous identification.
eMolecules Chem-Impex Gallic acid anhydrous 5kg 369602086 22784 0 000 149-91-7 MFCD00002510 170 120 C7H6O5
Chem-Impex Gallic acid anhydrous 5kg 369602086 22784 0 000 149-91-7 MFCD00002510 170 120 C7H6O5
![Medchemexpress LLC Ethanone, 1-(2-pyridinyl)-, 2-(6-methyl-5H-1,2,4-triazino[5,6-b]indol-3-yl)hydrazone | 327031-55-0 | MFCD01305422 | 99.8% | 317.35 g/mol | C17H15N7 | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000235143.png-250.jpg)
Medchemexpress LLC Ethanone, 1-(2-pyridinyl)-, 2-(6-methyl-5H-1,2,4-triazino[5,6-b]indol-3-yl)hydrazone | 327031-55-0 | MFCD01305422 | 99.8% | 317.35 g/mol | C17H15N7 | 10MG
VLX600 is an iron-chelating inhibitor of oxidative phosphorylation used as a research tool to induce mitochondrial dysfunction, shift cellular metabolism toward glycolysis, and trigger autophagy and selective cytotoxicity in malignant cells. It is supplied for research use and is characterized by CAS 327031-55-0, molecular formula C17H15N7, and molecular weight 317.35 g/mol.
- Iron-chelating inhibitor of oxidative phosphorylation that disrupts mitochondrial function.
- Induces a metabolic shift toward glycolysis in treated cells.
- Promotes autophagy and selective cytotoxicity in malignant or quiescent cancer cells.
- High chemical purity, typically 99.8%.
- Supplied in small pack sizes suitable for in vitro research (for example, 10 mg).
Medchemexpress LLC Tigulixostat | 1287766-55-5 | 99.2% | C16H14N4O2 | 10MG
Tigulixostat is an orally active, non-purine selective xanthine oxidase inhibitor used in preclinical and biochemical research to investigate uric acid metabolism and potential treatments for gout and hyperuricemia. It is provided as a solid suitable for preparation of stock solutions for in vitro and in vivo studies.
- High purity (99.2%).
- Non-purine selective xanthine oxidase inhibitor.
- Suitable for biochemical and preclinical research applications.
- Provided as a solid for solution preparation.
- Available in small research pack sizes for convenience.
eMolecules Chem-Impex Gallic acid anhydrous 2 5kg 205001990 22784 0 000 149-91-7 MFCD00002510 170 120 C7H6O5
Chem-Impex Gallic acid anhydrous 2 5kg 205001990 22784 0 000 149-91-7 MFCD00002510 170 120 C7H6O5
Medchemexpress LLC Tegoprazan | 942195-55-3 | MFCD30533430 | 99.8% | 387.38 g/mol | C20H19F2N3O3 | 10 MG
Tegoprazan is a potassium-competitive acid blocker (P-CAB) provided as a high-purity research reagent for studies of gastric acid regulation and related pharmacology. It is intended for in vitro assays and preclinical investigations and is supplied with analytical characterization to support research use.
- High-purity reference compound for biochemical and cellular assays.
- Potassium-competitive acid blocker mechanism relevant to acid suppression studies.
- Suitable for in vitro and preclinical pharmacology investigations.
- Comes with analytical documentation including purity and structural identifiers.
- Stable solid form convenient for handling and storage.
- Available in small research quantities for dose-ranging experiments.
eMolecules 19146-55-5 | Ambeed | Ac-D-Glu-OH | 100g | 491675237 | A607464 | MFCD00063196 | 189.167 | C7H11NO5
Ambeed | 22-(99-Dioctyl-9H-fluorene-27-diyl)bis(132-dioxaborinane) | 250mg | 598443842 | A474547 | 317802-08-7 | MFCD03701607 | 558.420 | C35H52B2O4
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eMolecules 477-73-6 | Ambeed | 37-Diamino-28-dimethyl-5-phenylphenazin-5-ium chloride | 100g | 642081069 | A645497 | MFCD00011759 | 350.85 | C20H19ClN4
Ambeed | (4R5S)-2-(6-(Dicyclohexylmethyl)pyridin-2-yl)-45-diphenyl-45-dihydrooxazole | 100mg | 721743954 | A1519867 | | 478.680 | C33H38N2O
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![eMolecules 35202-55-2 | (3,4-DIMETHOXYBICYCLO[4.2.0]OCTA-1,3,5-TRIEN-7-YL)METHANAMINE HCL | AstaTech | MFCD28038688 | 229.700 | C11H16ClNO2 | 97.000 | Cl.COc1cc2CC(CN)c2cc1OC | 0.1g | 771348148](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502470572.JPG-250.jpg)
eMolecules 35202-55-2 | (3,4-DIMETHOXYBICYCLO[4.2.0]OCTA-1,3,5-TRIEN-7-YL)METHANAMINE HCL | AstaTech | MFCD28038688 | 229.700 | C11H16ClNO2 | 97.000 | Cl.COc1cc2CC(CN)c2cc1OC | 0.1g | 771348148
(3,4-DIMETHOXYBICYCLO[4.2.0]OCTA-1,3,5-TRIEN-7-YL)METHANAMINE HCL | AstaTech | 35202-55-2 | MFCD28038688 | 229.700 | C11H16ClNO2 | 97.000 | Cl.COc1cc2CC(CN)c2cc1OC | 0.1g | 771348148
Medchemexpress LLC Vlx600 | 327031-55-0 | MFCD01305422 | 99.8% | 317.35 | C17H15N7 | 100MG
VLX600 is a small-molecule oxidative phosphorylation (OxPhos) inhibitor and iron chelator used in cancer and mitochondrial metabolism research. It impairs mitochondrial respiration, induces autophagy, and shows selective cytotoxicity in quiescent or nutrient-starved tumor cells. Molecular formula C17H15N7; molecular weight 317.35; CAS 327031-55-0.
- Inhibits mitochondrial oxidative phosphorylation.
- Functions as an iron chelator.
- Induces autophagy and promotes tumor cell death under nutrient limitation.
- Useful as a reference compound for cancer metabolism studies.
- Crystalline solid with reported DMSO solubility around 25 mg/mL.
- Recommended storage at -20°C as a powder.
Medchemexpress LLC Maohuoside A | 128988-55-6 | 1 MG
Maohuoside A is a single compound isolated from E. koreanum that potently promotes osteogenesis. It enhances the osteogenesis of bone marrow-derived mesenchymal stem cells via bone morphogenetic protein (BMP) and MAPK signaling pathways.
- For research use only
- Not sold to patients
![Medchemexpress LLC 2,6-dichloro-4-[2-(1-piperazinyl)-4-pyridinyl]-N-(trimethylpyrazol-4-yl)-benzenesulfonamide | 1215010-55-1 | 99.7% | 495.43 g/mol | C21H24Cl2N6O2S | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000246455.png-250.jpg)
Medchemexpress LLC 2,6-dichloro-4-[2-(1-piperazinyl)-4-pyridinyl]-N-(trimethylpyrazol-4-yl)-benzenesulfonamide | 1215010-55-1 | 99.7% | 495.43 g/mol | C21H24Cl2N6O2S | 25 MG
DDD85646 (IMP-366) is an orally active inhibitor of N-myristoyltransferase (NMT) with potent enzymatic activity against Trypanosoma brucei (TbNMT IC50 = 2 nM) and measurable activity versus human NMT (hNMT IC50 = 4 nM). It is supplied as a high-purity research compound for in vitro and in vivo pharmacology studies targeting NMT.
- Potent N-myristoyltransferase inhibition (TbNMT IC50 = 2 nM; hNMT IC50 = 4 nM).
- High purity suitable for research (reported ≥99.7%).
- Soluble in DMSO (100 mg/mL); recommended in vivo formulations provided for dosing.
- Available in small research pack sizes, suitable for preclinical studies.
- Powder stable at -20°C for long-term storage; solutions should be aliquoted and stored cold.
Apexbio Technology LLC Gallic acid 149-91-7 10mM (in 1mL DMSO)
Gallic acid (CAS 149-91-7) is a naturally occurring polyphenolic compound widely distributed in the plant kingdom with substantial levels identified in sources such as gallnuts grapes tea hops and oak bark It exerts biological effects primarily through antioxidant and anti-inflammatory mechanisms including scavenging free radicals and modulating cellular oxidative stress pathways Gallic acid has been investigated for its capacity to inhibit enzymes involved in inflammation and carcinogenesis influencing cell proliferation and apoptosis in various in vitro models Due to these properties it serves as a valuable tool for studies on oxidative damage inflammation and cancer biology
![eMolecules 1257535-55-9 | AstaTech | 1H-PYRROLO[23-C]PYRIDIN-3-AMINE 2HCL | 0.25g | 112532801 | BL001287 | 95 | MFCD16628054 | 206.07 | C7H9Cl2N3](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502453523.PNG-250.jpg)
eMolecules 1257535-55-9 | AstaTech | 1H-PYRROLO[23-C]PYRIDIN-3-AMINE 2HCL | 0.25g | 112532801 | BL001287 | 95 | MFCD16628054 | 206.07 | C7H9Cl2N3
ChemScene | 3-Iodo-6-methylquinoline | 100mg | 779526078 | CS-0628358 | 1424246-00-3 | 269.085 | C10H8IN
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Selleck Chemical LLC OT-82-5mg
OT-82 is a novel nicotinamide phosphoribosyltransferase (NAMPT) inhibitor with average IC50s of 13.03 nM in non-HP cancer cells and 2.89 nM in HP cancer cells, respectively.