Design of noncovalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides

SF Chowdhury, J Sivaraman, J Wang… - Journal of medicinal …, 2002 - ACS Publications
A novel series of noncovalent inhibitors of cathepsin L have been designed to mimic the
mode of autoinhibition of procathepsin L. Just like the propeptide, these peptide-based …
被引用次数：95 相关文章

[引用][C] Design of noncovalent inhibitors of human cathepsin L from the 96-residue proregion to optimised tripeptides

SF CHOWDHURY - J. Med. Chem., 2002 - cir.nii.ac.jp
Design of noncovalent inhibitors of human cathepsin L from the 96-residue proregion to
optimised tripeptides | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] …

[引用][C] Design of noncovalent inhibitors of human cathepsin L. from the 96-residue proregion to optimized tripeptides

SF CHOWDHURY, J SIVARAMAN… - Journal of medicinal …, 2002 - pascal-francis.inist.fr
Design of noncovalent inhibitors of human cathepsin L. from the 96-residue proregion to
optimized tripeptides CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic …

Design of noncovalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides.

SF Chowdhury, J Sivaraman, J Wang… - Journal of Medicinal …, 2002 - europepmc.org
A novel series of noncovalent inhibitors of cathepsin L have been designed to mimic the
mode of autoinhibition of procathepsin L. Just like the propeptide, these peptide-based …

Design of noncovalent inhibitors of human cathepsin L. from the 96-residue proregion to optimized tripeptides

SF Chowdhury, J Sivaraman… - Journal of …, 2002 - mdanderson.elsevierpure.com
A novel series of noncovalent inhibitors of cathepsin L have been designed to mimic the
mode of autoinhibition of procathepsin L. Just like the propeptide, these peptide-based …

[引用][C] DESIGN OF NONCOVALENT INHIBITORS OF HUMAN CATHEPSIN L. FROM THE 96-RESIDUE PROREGION TO OPTIMIZED TRIPEPTIDES.

S CHOWDHURY, J SIVARAMAN, J WANG… - PROC NATL ACAD SCI …, 2002 - osti.gov
DESIGN OF NONCOVALENT INHIBITORS OF HUMAN CATHEPSIN L. FROM THE 96-RESIDUE
PROREGION TO OPTIMIZED TRIPEPTIDES. (Journal Article) | OSTI.GOV skip to main …

Design of noncovalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides

SF Chowdhury, J Sivaraman… - Journal of …, 2002 - pubmed.ncbi.nlm.nih.gov
A novel series of noncovalent inhibitors of cathepsin L have been designed to mimic the
mode of autoinhibition of procathepsin L. Just like the propeptide, these peptide-based …

[引用][C] Design of Noncovalent Inhibitors of Human Cathepsin L. From the 96-Residue Proregion to Optimized Tripeptides

SF Chowdhury, J Sivaraman, J Wang… - Journal of Medicinal …, 2002 - infona.pl
Design of Noncovalent Inhibitors of Human Cathepsin L. From the 96-Residue Proregion to
Optimized Tripeptides × Close The Infona portal uses cookies, ie strings of text saved by a …

[引用][C] Design of noncovalent inhibitors of human cathepsin L. from the 96-residue proregion to optimized tripeptides

SF CHOWDHURY, J SIVARAMAN… - Journal of …, 2002 - American Chemical Society