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Aromatic organic heterocyclic compounds that consist of a six-membered ring with four carbon atoms and two nitrogen atoms at opposite positions of the ring, making this ring symmetrical.
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MCB-22-174 is a deuterated Piezo1 agonist with an EC50 value of 6.28 μM. It activates the CaMKII/ERK signaling pathway and initiates Ca2+ influx in rMSCs. It decreases the expression of chondrogenesis markers (Comp, Acan) and adipogenesis markers (Lpl, Fabp4) in MSCs. This compound can improve bone quality in hind-limb unloading (HU) model rats and can be used for the study of disuse osteoporosis (OP).
Deuterated Piezo1 agonist
Activates the CaMKII/ERK signaling pathway
Initiates Ca2+ influx in rMSCs
Decreases expression of chondrogenesis markers (Comp, Acan) in MSCs
Decreases expression of adipogenesis markers (Lpl, Fabp4) in MSCs
Effectively improves bone quality in hind-limb unloading (HU) model rats
Can be used for the study of disuse osteoporosis (OP)
Can be used as a tracer
Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
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Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Pacritinib (SB1518) (SB1518) is an effective and specific inhibitor of JAK2 and FLT3 (IC50 23/22 nM in cell-free assays). purity: 99%
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ICA-121431 (22-Diphenyl-N-[4-(thiazol-2-ylsulfamoyl) is a nanomolar potent small molecule Nav1.7 channel inhibitor with IC50 of 19 nM for rat Nav1.7 with little or no activity against human Nav1.5 or Nav1.7 channels. purity: 98%
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More