Design, synthesis, and biological activity of potent and selective inhibitors of mast cell tryptase
CR Hopkins, M Czekaj, SS Kaye, Z Gao… - Bioorganic & medicinal …, 2005 - Elsevier
A new series of novel mast cell tryptase inhibitors is reported, which features the use of an
indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The …
indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The …
[引用][C] Design, synthesis, and biological activity of potent and selective inhibitors of mast cell tryptase
CR HOPKINS, M CZEKAJ, Y LUO… - Bioorganic & …, 2005 - pascal-francis.inist.fr
Design, synthesis, and biological activity of potent and selective inhibitors of mast cell tryptase
CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple search …
CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple search …
Design, synthesis, and biological activity of potent and selective inhibitors of mast cell tryptase
CR Hopkins, M Czekaj, SS Kaye… - Bioorganic and …, 2005 - experts.nebraska.edu
A new series of novel mast cell tryptase inhibitors is reported, which features the use of an
indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The …
indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The …
Design, synthesis, and biological activity of potent and selective inhibitors of mast cell tryptase
CR Hopkins, M Czekaj, SS Kaye, Z Gao… - Bioorganic & Medicinal …, 2005 - infona.pl
A new series of novel mast cell tryptase inhibitors is reported, which features the use of an
indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The …
indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The …
[PDF][PDF] Design, synthesis, and biological activity of potent and selective inhibitors of mast cell tryptase
CR Hopkins, M Czekaj, SS Kaye, Z Gao… - … & Medicinal Chemistry …, 2005 - academia.edu
A new series of novel mast cell tryptase inhibitors is reported, which features the use of an
indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The …
indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The …
Design, synthesis, and biological activity of potent and selective inhibitors of mast cell tryptase
CR Hopkins, M Czekaj, SS Kaye… - Bioorganic & …, 2005 - pubmed.ncbi.nlm.nih.gov
A new series of novel mast cell tryptase inhibitors is reported, which features the use of an
indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The …
indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The …
Design, synthesis, and biological activity of potent and selective inhibitors of mast cell tryptase.
CR Hopkins, M Czekaj, SS Kaye, Z Gao… - Bioorganic & …, 2005 - europepmc.org
A new series of novel mast cell tryptase inhibitors is reported, which features the use of an
indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The …
indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The …