TY - JOUR
T1 - Solid-phase synthesis of FKBP12 inhibitors
T2 - N-sulfonyl and N-carbamoylprolyl/pipecolyl amides
AU - Wei, Ling
AU - Wu, Yong Qian
AU - Wilkinson, Douglas E.
AU - Chen, Yi
AU - Soni, Raj
AU - Scott, Chad
AU - Ross, Douglas T.
AU - Guo, Hong
AU - Howorth, Pamela
AU - Valentine, Heather
AU - Liang, Shi
AU - Spicer, Dawn
AU - Fuller, Mike
AU - Steiner, Joseph
AU - Hamilton, Gregory S.
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2002/5/20
Y1 - 2002/5/20
N2 - In parallel with our work on solution-phase parallel synthesis of ligands for the rotamase enzyme FKBP12, we herein report a methodology for the solid-phase synthesis of two classes of inhibitor, N-sulfonyl and N-carbamoylprolyl and pipecolyl amides along with their in vitro/in vivo biological results.
AB - In parallel with our work on solution-phase parallel synthesis of ligands for the rotamase enzyme FKBP12, we herein report a methodology for the solid-phase synthesis of two classes of inhibitor, N-sulfonyl and N-carbamoylprolyl and pipecolyl amides along with their in vitro/in vivo biological results.
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U2 - 10.1016/S0960-894X(02)00146-4
DO - 10.1016/S0960-894X(02)00146-4
M3 - Article
C2 - 11992791
AN - SCOPUS:18344393965
SN - 0960-894X
VL - 12
SP - 1429
EP - 1433
JO - Bioorganic and Medicinal Chemistry Letters
JF - Bioorganic and Medicinal Chemistry Letters
IS - 10
ER -