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Fast garnet GBC sulfate salt, 90% is an azo diazonium dye used as a chromogenic substrate for alkaline phosphatase in histochemical staining and related enzymatic assays. It is supplied as a sulfate salt with high dye content suitable for laboratory staining protocols.
Chromogenic substrate for alkaline phosphatase staining
High dye content, formulated at 90.0% purity
Suitable for histochemistry and enzyme activity assays
Available in small laboratory-scale quantities
Solid form with molecular formula C14H14N4O4S
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Also available in 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. GPR40/FFAR1 modulator 1 is a Gq-coupled free fatty acid receptor 1 (GPR40/FFAR1) agonist and allosteric modulator. purity: 99%
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COP1-ATGL modulator 1 is an orally active small-molecule research reagent that modulates the COP1-ATGL pathway. It increases ATGL protein expression, reduces ATGL and COP1 ubiquitination, and diminishes lipid accumulation in hepatocytes at nanomolar concentrations. Supplied as a white to off-white solid with high purity and defined storage recommendations for powder and solution.
Orally active modulator of COP1-ATGL signaling.
Increases ATGL protein expression at nanomolar concentrations.
Reduces ATGL and COP1 ubiquitination in cellular assays.
High purity suitable for research applications.
Stable solid with recommended low-temperature storage.
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CXCR7 modulator 2 is a modulator of C-X-C Chemokine Receptor Type 7 (CXCR7), with a Ki of 13 nM. It is for research use only and not sold to patients. This modulator offers protection against cardiac injury.
Potent CXCR7-binding affinity (Ki=13 nM).
β-arrestin activity (EC50=11 nM).
Improved selectivity in the GPCR panel.
Improved therapeutic index in the hERG patch-clamp assay.
Moderate to high in vitro turnover in NADPH-supplemented mouse-liver microsomes (MLM, 93 μL/min/mg) and hepatocytes (28 μL/min per million cells).
Good aqueous solubility.
Rapidly absorbed with a mean maximal plasma concentration (Cmax) of 682 ng/mL at 0.25 h (Tmax).
Reduces cardiac fibrosis in an isoproterenol-induced cardiac injury model in mice.
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Elafibranor sulfoxide is the sulfoxide metabolite of elafibranor supplied as a research-grade powder for in vitro and preclinical studies. It is intended for laboratory research use only and can be used to investigate PPAR-related pathways and metabolic disease models such as primary biliary cholangitis.
Chemical formula C22H24O5S, molecular weight 400.49.
Supplied as a powder; pack sizes include 10 MG.
Purity (NMR): 95.0%.
Target: PPAR; drug metabolite.
Storage: powder -20°C for 3 years, 4°C for 2 years; in solvent -80°C for 6 months, -20°C for 1 month.
Provided for research use only; not for human therapeutic use.
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GLP-1R modulator L7-028 is an allosteric modulator that enhances GLP-1 binding to GLP-1R via a transmembrane site (EC50 11.01 ± 2.73 μM). It is intended for research use only.
Available as a solid, white to off-white in color.
Soluble in DMSO at 100 mg/mL.
Shipped at room temperature in continental US.
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Mutant p53 modulator-1 is a compound that modulates mutant p53. It has been shown to reduce the progression of various cancers characterized by p53 mutations.
Functions as a modulator for mutant p53.
Aids in reducing the progression of cancers with p53 mutations.
Available in both solid and solution forms for research applications.
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Sulforaphane is an orally active inducer of the Keap1/Nrf2/ARE pathway. It promotes the transcription of tumor-suppressing proteins and effectively inhibits the activity of HDACs. It protects the heart through the activation of the Keap1/Nrf2/ARE pathway and further induction of HO-1 expression. Sulforaphane suppresses high glucose-induced pancreatic cancer through AMPK-dependent signal transmission and exhibits both anticancer and anti-inflammatory properties.