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10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
MMP13-IN-2 is a potent, selective and orally active MMP-13 inhibitor. MMP13-IN-2 exhibits excellent potency for MMP-13 ( IC 50 =0.036 nM) and selectivities (greater than 1,500-fold) over MMP-1 , 3, 7, 8, 9, 14, and TACE. MMP13-IN-2 has the ability to block the release of collagen from cartilage in vitro. MMP13-IN-2 has the potential for collagenase related disease research
In Vitro
In a bovine nasal cartilage (BNC) assay, the chondrocyte-mediated degradation of cartilage was studied using bovine nasal cartilage slices cultured for up to 14 days. MMP13-IN-2 (0.01-1 µM) is effective at preventing the IL-1/OSM induced in vitro degradation of BNC (-17.6%, 48.4% and 70.8% inhibition of cartilage degradation, respectively).. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
MMP13-IN-2 (oral gavage; 1 mg/kg) shows the best combination of CYP3A4 inhibition risk and oral exposure at a dose of 1 mg/kg in rats and mice (F% = 33 and 38, respectively) . MCE has not independently confirmed the accuracy of these methods. They are for reference only.
IC50& Target:MMP-13 0.036 nM (IC 50 ) MMP-2 180 nM (IC 50 ) MMP-3 1100 nM (IC 50 )
Comprehensive hazard, handling, storage, and regulatory compliance document.
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