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Sudoxicam is a reversible and orally active COX antagonist and a non-steroidal anti-inflammatory drug (NSAID) from the enol-carboxamide class Sudoxicam has potent anti-inflammatory anti-edema and antipyretic activity[1 [2 [3
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Oxypeucedanin hydrate is a natural product isolated from D. anethifolia. It exhibits mild toxicity on fibroblasts and parental lymphoma cells. This product is for research use only.
Isolated from D. anethifolia
Exhibits mild toxicity on fibroblasts and parental lymphoma cells
Molecular weight of 304.29
Chemical formula is C16H16O6
Appears as an off-white to light yellow solid
Purity of 98.0%
Soluble in DMSO at 100 mg/mL
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(R)-5,7-Dimethoxyflavanone exhibits potent antimutagenic activity against MeIQ mutagenesis in Ames test utilizing S. typhimurium TA100 and TA98 strains. Additionally, it significantly and dose-dependently inhibits inflammatory mediators.
Potent antimutagenic activity
Inhibits inflammatory mediators
Molecular weight of 284.31
Chemical formula C17H16O4
Appears as a white to off-white solid
Classified as a flavonoid and flavanone
Initially sourced from plants
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(R)-5,7-Dimethoxyflavanone is a compound that demonstrates potent antimutagenic activity against MeIQ mutagenesis in Ames tests using S. typhimurium TA100 and TA98 strains. It also significantly and dose-dependently inhibits inflammatory mediators. This product is for research use only.
Potent antimutagenic activity
Inhibits inflammatory mediators
Molecular weight: 284.31
Formula: C17H16O4
Appearance: solid
Color: white to off-white
Classified under flavonoids and flavanones
Initial source from plants
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Oxypeucedanin hydrate is a naturally occurring furanocoumarin isolated from D. anethifolia, supplied for laboratory research. It is provided as a small, high-purity powder suitable for analytical and biological studies.
Natural furanocoumarin isolated from D. anethifolia.
High purity (98.0%) suitable for analytical and biological assays.
Small 10 mg pack size for screening and method development.
Documented mild cytotoxicity in fibroblasts and parental lymphoma cells.
Stable as powder when stored at -20°C (up to 3 years) or 4°C (up to 2 years).
Solvent aliquots recommended to be stored at -80°C (up to 6 months) or -20°C (up to 1 month).
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Ker047 (ALK2-IN-4) is a potent activin receptor-like kinase-2 (ALK2) inhibitor. It is utilized in the research of metabolic diseases, including fibrodysplasia ossificans progressiva (FOP).
High purity of 98.8%
Soluble in DMSO at 10 mg/mL
Stable as powder for up to 3 years at -20°C
Stable in solvent for up to 2 years at -80°C
Documentation available for data, safety, and handling
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KER047 (ALK2-IN-4) is a potent activin receptor-like kinase-2 (ALK2) inhibitor. It can be used for research into metabolic diseases such as fibrodysplasia ossificans progressiva (FOP).