16-Phenoxy tetranor prostaglandin F2α is a metabolically stable analog that selectively binds to the FP receptor. This compound demonstrates significantly enhanced affinity for the FP receptor on ovine luteal cells, exhibiting a 440% increase compared to PGF2α. Its robust interaction profile makes it a valuable tool for investigating prostaglandin signaling pathways and their role in reproductive biology and endocrine functions.
16-Phenoxy tetranor prostaglandin F2α is a metabolically stable analog that selectively binds to the FP receptor. This compound demonstrates significantly enhanced affinity for the FP receptor on ovine luteal cells, exhibiting a 440% increase compared to PGF2α. Its robust interaction profile makes it a valuable tool for investigating prostaglandin signaling pathways and their role in reproductive biology and endocrine functions.
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