Pin1 inhibitors: Pitfalls, progress and cellular pharmacology
JD Moore, A Potter - Bioorganic & medicinal chemistry letters, 2013 - Elsevier
Compelling data supports the hypothesis that Pin1 inhibitors will be useful for the therapy of
cancer: Pin1 deficient mice resist the induction of breast cancers normally evoked by …
cancer: Pin1 deficient mice resist the induction of breast cancers normally evoked by …
Mechanisms that increase stability of estrogen receptor alpha in breast cancer
AC Tecalco-Cruz, JO Ramírez-Jarquín - Clinical breast cancer, 2017 - Elsevier
Estrogen receptor alpha (ER) is a transcriptional regulator that controls the expression of
genes related to cellular proliferation and differentiation in normal mammary tissue …
genes related to cellular proliferation and differentiation in normal mammary tissue …
Structure and function of the human parvulins Pin1 and Par14/17
A Matena, E Rehic, D Hönig, B Kamba… - Biological chemistry, 2018 - degruyter.com
Parvulins belong to the family of peptidyl-prolyl cis/trans isomerases (PPIases) assisting in
protein folding and in regulating the function of a broad variety of proteins in all branches of …
protein folding and in regulating the function of a broad variety of proteins in all branches of …
A selective, cell-permeable nonphosphorylated bicyclic peptidyl inhibitor against peptidyl–prolyl isomerase Pin1
Pin1 regulates the levels and functions of phosphoproteins by catalyzing phosphorylation-
dependent cis/trans isomerization of peptidyl–prolyl bonds. Previous Pin1 inhibitors …
dependent cis/trans isomerization of peptidyl–prolyl bonds. Previous Pin1 inhibitors …
Structure-based design of novel human Pin1 inhibitors (III): optimizing affinity beyond the phosphate recognition pocket
C Guo, X Hou, L Dong, J Marakovits, S Greasley… - Bioorganic & medicinal …, 2014 - Elsevier
The design of potent Pin1 inhibitors has been challenging because its active site specifically
recognizes a phospho-protein epitope. The de novo design of phosphate-based Pin1 …
recognizes a phospho-protein epitope. The de novo design of phosphate-based Pin1 …
Recent advances of Pin1 inhibitors as potential anticancer agents
Y Bai, Z Yuan, S Yuan, Z He - Bioorganic Chemistry, 2024 - Elsevier
Pin1 (proline isomerase peptidyl-prolyl isomerase NIMA-interacting-1), as a member of
PPIase family, catalyzes cis–trans isomerization of pThr/Ser-Pro amide bonds of its substrate …
PPIase family, catalyzes cis–trans isomerization of pThr/Ser-Pro amide bonds of its substrate …
[HTML][HTML] Polyubiquitination inhibition of estrogen receptor alpha and its implications in breast cancer
AC Tecalco-Cruz… - World journal of clinical …, 2018 - ncbi.nlm.nih.gov
Estrogen receptor alpha (ERα) is detected in more than 70% of the cases of breast cancer.
Nuclear activity of ERα, a transcriptional regulator, is linked to the development of mammary …
Nuclear activity of ERα, a transcriptional regulator, is linked to the development of mammary …
Pin1 WW Domain Ligand Library Synthesized with an Easy Solid-Phase Phosphorylating Reagent
XR Chen, AY Mercedes-Camacho, KA Wilson… - Biochemistry, 2024 - ACS Publications
Cell cycle regulatory enzyme Pin1 both catalyzes pSer/Thr-cis/trans-Pro isomerization and
binds the same motif separately in its WW domain. To better understand the function of Pin1 …
binds the same motif separately in its WW domain. To better understand the function of Pin1 …
[HTML][HTML] Transient domain interactions enhance the affinity of the mitotic regulator Pin1 toward phosphorylated peptide ligands
A Matena, C Sinnen, J van den Boom, C Wilms… - Structure, 2013 - cell.com
The mitotic regulator Pin1 plays an important role in protein quality control and age-related
medical conditions such as Alzheimer disease and Parkinson disease. Although its cellular …
medical conditions such as Alzheimer disease and Parkinson disease. Although its cellular …
Design, synthesis and biological evaluation of benzimidazole derivatives as novel human Pin1 inhibitors
T Ma, M Huang, A Li, F Zhao, D Li, D Liu… - Bioorganic & Medicinal …, 2019 - Elsevier
In this work, a series of novel benzimidazole derivatives were designed and synthesized as
Pin1 inhibitors. Protease-coupled assay was used to investigate the Pin1 inhibitory potency …
Pin1 inhibitors. Protease-coupled assay was used to investigate the Pin1 inhibitory potency …