Literature for peptidase C01.032: cathepsin L
(References are filtered for relevance to Inhibitor. To remove the filter click here. See explanation.)
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Ciaglia,T., Vestuto,V., Di Sarno,V., Musella,S., Smaldone,G., Di Matteo,F., Napolitano,V., Miranda,M.R., Pepe,G., Basilicata,M.G., Novi,S., Capolupo,I., Bifulco,G., Campiglia,P., Gomez-Monterrey,I., Snoeck,R., Andrei,G., Manfra,M., Ostacolo,C., Lauro,G. and Bertamino,A.
Peptidomimetics as potent dual SARS-CoV-2 cathepsin-L and main protease inhibitors: In silico design, synthesis and pharmacological characterization
Eur J Med Chem266, 116128-116128. PubMed Europe PubMed DOI I -
Deng,W., Hu,X., Tian,X., Zhang,Y., Shang,W., Zhang,L. and Shang,L.
Peptidomimetic Analogues Act as Effective Inhibitors against SARS-CoV-2 by Blocking the Function of Cathepsin L
J Med Chem67, 17124-17143. PubMed Europe PubMed DOI I -
Falke,S., Lieske,J., Herrmann,A., Loboda,J., Karnicar,K., Gunther,S., Reinke,P.Y.A., Ewert,W., Usenik,A., Lindic,N., Sekirnik,A., Dretnik,K., Tsuge,H., Turk,V., Chapman,H.N., Hinrichs,W., Ebert,G., Turk,D. and Meents,A.
Structural Elucidation and Antiviral Activity of Covalent Cathepsin L Inhibitors
J Med Chem67, 7048-7067. PubMed Europe PubMed DOI I -
Jangra,S., Raghav,N., Wadhwa,D., Kumar,A., Bhattacharyya,S., Kumar,V. and Sheokand,J.
Biological evaluation of trans-2,3-dihydrofuro[3,2-c]coumarins as potential cathepsin inhibitors and anticancer agents
J Biomater Sci Polym Ed1-19. PubMed Europe PubMed DOI I -
Mao,L., Shaabani,N., Zhang,X., Jin,C., Xu,W., Argent,C., Kushnareva,Y., Powers,C., Stegman,K., Liu,J., Xie,H., Xu,C., Bao,Y., Xu,L., Zhang,Y., Yang,H., Qian,S., Hu,Y., Shao,J., Zhang,C., Li,T., Li,Y., Liu,N., Lin,Z., Wang,S., Wang,C., Shen,W., Lin,Y., Shu,D., Zhu,Z., Kotoi,O., Kerwin,L., Han,Q., Chumakova,L., Teijaro,J., Royal,M., Brunswick,M., Allen,R., Ji,H., Lu,H. and Xu,X.
Olgotrelvir, a dual inhibitor of SARS-CoV-2 M(pro) and cathepsin L, as a standalone antiviral oral intervention candidate for COVID-19
Med5, 42-61. PubMed Europe PubMed DOI I -
Mao,L., Shaabani,N., Zhang,X., Jin,C., Xu,W., Argent,C., Kushnareva,Y., Powers,C., Stegman,K., Liu,J., Xie,H., Xu,C., Bao,Y., Xu,L., Zhang,Y., Yang,H., Qian,S., Hu,Y., Shao,J., Zhang,C., Li,T., Li,Y., Liu,N., Lin,Z., Wang,S., Wang,C., Shen,W., Lin,Y., Shu,D., Zhu,Z., Kotoi,O., Kerwin,L., Han,Q., Chumakova,L., Teijaro,J., Royal,M., Brunswick,M., Allen,R., Ji,H., Lu,H. and Xu,X.
Olgotrelvir, a dual inhibitor of SARS-CoV-2 M(pro) and cathepsin L, as a standalone antiviral oral intervention candidate for COVID-19
Med5, 169-171. PubMed Europe PubMed DOI I -
Xie,X., Lan,Q., Zhao,J., Zhang,S., Liu,L., Zhang,Y., Xu,W., Shao,M., Peng,J., Xia,S., Zhu,Y., Zhang,K., Zhang,X., Zhang,R., Li,J., Dai,W., Ge,Z., Hu,S., Yu,C., Wang,J., Ma,D., Zheng,M., Yang,H., Xiao,G., Rao,Z., Lu,L., Zhang,L., Bai,F., Zhao,Y., Jiang,S. and Liu,H.
Structure-based design of pan-coronavirus inhibitors targeting host cathepsin L and calpain-1
Signal Transduct Target Ther9, 54-54. PubMed Europe PubMed DOI I -
Zhou,W., You,B., Zhao,X., Si,S., Li,Y. and Zhang,J.
Establishment, optimization and validation of a fluorescence polarization-based high-throughput screening assay targeting cathepsin L inhibitors
SLAS Discov29, 100153-100153. PubMed Europe PubMed DOI I -
Doijen,J., Temmerman,K., Van den Eynde,C., Diels,A., Van den Broeck,N., Van Gool,M., Heo,I., Jaensch,S., Zwaagstra,M., Diosa Toro,M., Chiu,W., De Jonghe,S., Leyssen,P., Bojkova,D., Ciesek,S., Cinatl,J., Verschueren,L., Buyck,C., van Kuppeveld,F., Neyts,J., Van Loock,M. and Van Damme,E.
Identification of Z-Tyr-Ala-CHN(2), a Cathepsin L Inhibitor with Broad-Spectrum Cell-Specific Activity against Coronaviruses, including SARS-CoV-2
Microorganisms11, PubMed Europe PubMed DOI I -
Huang,H., Zhang,Y., Xu,X., Liu,Y., Zhao,J., Ma,L., Lei,J., Ge,W., Li,N., Ma,E., Li,Y. and Yuan,L.
Design and synthesis of dual cathepsin L and S inhibitors and antimetastatic activity evaluation in pancreatic cancer cells
Bioorg Med Chem Lett80, 129087-129087. PubMed Europe PubMed DOI I -
Li,Y., Wang,K., Sun,H., Wu,S., Wang,H., Shi,Y., Li,X., Yan,H., Yang,G., Wu,M., Li,Y., Ding,X., Si,S., Jiang,J., Du,Y., Li,Y. and Hong,B.
Omicsynin B4 potently blocks coronavirus infection by inhibiting host proteases cathepsin L and TMPRSS2
Antiviral Res214, 105606-105606. PubMed Europe PubMed DOI I -
Tang,T.T., Li,S.M., Pan,B.W., Xiao,J.W., Pang,Y.X., Xie,S.X., Zhou,Y., Yang,J. and Wei,Y.
Identification of Flavonoids from Scutellaria barbata D. Don as Inhibitors of HIV-1 and Cathepsin L Proteases and Their Structure-Activity Relationships
Molecules28, PubMed Europe PubMed DOI I -
Wang,C., Ye,X., Ding,C., Zhou,M., Li,W., Wang,Y., You,Q., Zong,S., Peng,Q., Duanmu,D., Chen,H., Sun,B. and Qiao,J.
Two Resveratrol Oligomers Inhibit Cathepsin L Activity to Suppress SARS-CoV-2 Entry
J Agric Food Chem71, 5535-5546. PubMed Europe PubMed DOI I -
Kwon,C.W., Yeo,S. and Chang,P.S.
Characterization and molecular docking study of cathepsin L inhibitory peptides (SnuCalCpIs) from Calotropis procera R. Br
Sci Rep12, 5825-5825. PubMed Europe PubMed DOI I -
Meewan,I., Kattoula,J., Kattoula,J.Y., Skinner,D., Fajtova,P., Giardini,M.A., Woodworth,B., McKerrow,J.H., Lage de Siqueira-Neto,J., O'Donoghue,A.J. and Abagyan,R.
Discovery of Triple Inhibitors of Both SARS-CoV-2 Proteases and Human Cathepsin L
Pharmaceuticals (Basel)15, PubMed Europe PubMed DOI I -
Mondal,S., Chen,Y., Lockbaum,G.J., Sen,S., Chaudhuri,S., Reyes,A.C., Lee,J.M., Kaur,A.N., Sultana,N., Cameron,M.D., Shaffer,S.A., Schiffer,C.A., Fitzgerald,K.A. and Thompson,P.R.
Dual Inhibitors of Main Protease (M(Pro)) and Cathepsin L as Potent Antivirals against SARS-CoV2
J Am Chem Soc144, 21035-21045. PubMed Europe PubMed DOI K I -
Yang,W.L., Li,Q., Sun,J., Huat Tan,S., Tang,Y.H., Zhao,M.M., Li,Y.Y., Cao,X., Zhao,J.C. and Yang,J.K.
Potential drug discovery for COVID-19 treatment targeting Cathepsin L using a deep learning-based strategy
Comput Struct Biotechnol J20, 2442-2454. PubMed Europe PubMed DOI I -
Yu,F., Pan,T., Huang,F., Ying,R., Liu,J., Fan,H., Zhang,J., Liu,W., Lin,Y., Yuan,Y., Yang,T., Li,R., Zhang,X., Lv,X., Chen,Q., Liang,A., Zou,F., Liu,B., Hu,F., Tang,X., Li,L., Deng,K., He,X., Zhang,H., Zhang,Y. and Ma,X.
Glycopeptide Antibiotic Teicoplanin Inhibits Cell Entry of SARS-CoV-2 by Suppressing the Proteolytic Activity of Cathepsin L
Front Microbiol13, 884034-884034. PubMed Europe PubMed DOI I -
Breidenbach,J., Lemke,C., Pillaiyar,T., Schakel,L., Al Hamwi,G., Diett,M., Gedschold,R., Geiger,N., Lopez,V., Mirza,S., Namasivayam,V., Schiedel,A.C., Sylvester,K., Thimm,D., Vielmuth,C., Phuong Vu,L., Zyulina,M., Bodem,J., Gutschow,M. and Muller,C.E.
Targeting the Main Protease of SARS-CoV-2: From the Establishment of High Throughput Screening to the Design of Tailored Inhibitors
Angew Chem Int Ed Engl PubMed Europe PubMed DOI I -
Hu,Y., Ma,C., Szeto,T., Hurst,B., Tarbet,B. and Wang,J.
Boceprevir, Calpain Inhibitors II and XII, and GC-376 Have Broad-Spectrum Antiviral Activity against Coronaviruses
ACS Infect Dis7, 586-597. PubMed Europe PubMed DOI I -
Li,Y., Ai,X., Zou,C., Liu,Y., Ma,L., Men,J., Liu,D., Sheng,L., Ruan,X., Liu,H., Li,W., Ma,E. and Yuan,L.
Discovery of a novel and selective cathepsin L inhibitor with anti-metastatic ability in vitro and in vivo against breast cancer cells
Bioorg Chem115, 105256-105256. PubMed Europe PubMed DOI I -
Mellott,D.M., Tseng,C.T., Drelich,A., Fajtova,P., Chenna,B.C., Kostomiris,D.H., Hsu,J., Zhu,J., Taylor,Z.W., Kocurek,K.I., Tat,V., Katzfuss,A., Li,L., Giardini,M.A., Skinner,D., Hirata,K., Yoon,M.C., Beck,S., Carlin,A.F., Clark,A.E., Beretta,L., Maneval,D., Hook,V., Frueh,F., Hurst,B.L., Wang,H., Raushel,F.M., O'Donoghue,A.J., de Siqueira-Neto,J.L., Meek,T.D. and McKerrow,J.H.
A Clinical-Stage Cysteine Protease Inhibitor blocks SARS-CoV-2 Infection of Human and Monkey Cells
ACS Chem Biol16, 642-650. PubMed Europe PubMed DOI I -
Munikishore,R., Wang,L.L., Zhang,S., Zhao,Q.S. and Zuo,Z.
An efficient and concise synthesis of a selective small molecule non-peptide inhibitor of cathepsin L: KGP94
Bioorg Chem116, 105317-105317. PubMed Europe PubMed DOI I -
Phan,H.A.T., Giannakoulias,S.G., Barrett,T.M., Liu,C. and Petersson,E.J.
Rational design of thioamide peptides as selective inhibitors of cysteine protease cathepsin L
Chem Sci12, 10825-10835. PubMed Europe PubMed DOI I -
Abhinand,C.S., Nair,A.S., Krishnamurthy,A., Oommen,O.V. and Sudhakaran,P.R.
Potential protease inhibitors and their combinations to block SARS-CoV-2
J Biomol Struct Dyn1-15. PubMed Europe PubMed DOI I -
Arafet,K., Gonzalez,F.V. and Moliner,V.
Quantum mechanics/molecular mechanics studies of the mechanism of cysteine proteases inhibition by dipeptidyl nitroalkenes
Chemistry26, 2002-2012. PubMed Europe PubMed DOI I -
Ashhurst,A.S., Tang,A.H., Fajtova,P., Yoon,M., Aggarwal,A., Stoye,A., Larance,M., Beretta,L., Drelich,A., Skinner,D., Li,L., Meek,T.D., McKerrow,J.H., Hook,V., Tseng,C.K., Turville,S., Gerwick,W.H., O'Donoghue,A.J. and Payne,R.J.
Potent in vitro anti-SARS-CoV-2 activity by gallinamide A and analogues via inhibition of cathepsin L
bioRxiv PubMed Europe PubMed DOI I -
Cianni,L., Rocho,F.D.R., Rosini,F., Bonatto,V., Ribeiro,J.F.R., Lameira,J., Leitao,A., Shamim,A. and Montanari,C.A.
Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases
Bioorg Chem101, 104039-104039. PubMed Europe PubMed DOI I -
Dana,D. and Pathak,S.K.
A review of small molecule inhibitors and functional probes of human cathepsin L
Molecules25, PubMed Europe PubMed DOI V I -
Mellott,D., Tseng,C.T., Drelich,A., Fajtova,P., Chenna,B.C., Kostomiris,D., Hsu,J.C., Zhu,J., Taylor,Z., Tat,V., Katzfuss,A., Li,L., Giardini,M.A., Skinner,D., Hirata,K., Beck,S., Carlin,A.F., Clark,A.E., Berreta,L., Maneval,D., Frueh,F., Hurst,B.L., Wang,H., Kocurek,K.I., Raushel,F.M., O'Donoghue,A., Siqueira-Neto,J.L., Meek,T.D. and McKerrow,J.H.
A cysteine protease inhibitor blocks SARS-CoV-2 infection of human and monkey cells
bioRxiv PubMed Europe PubMed DOI I -
Ribeiro,J.F.R., Cianni,L., Li,C., Warwick,T.G., De Vita,D., Rosini,F., Dos Reis Rocho,F., Martins,F.C.P., Kenny,P.W., Lameira,J., Leitao,A., Emsley,J. and Montanari,C.A.
Crystal structure of Leishmania mexicana cysteine protease B in complex with a high-affinity azadipeptide nitrile inhibitor
Bioorg Med Chem28, 115743-115743. PubMed Europe PubMed DOI I -
Sacco,M.D., Ma,C., Lagarias,P., Gao,A., Townsend,J.A., Meng,X., Dube,P., Zhang,X., Hu,Y., Kitamura,N., Hurst,B., Tarbet,B., Marty,M.T., Kolocouris,A., Xiang,Y., Chen,Y. and Wang,J.
Structure and inhibition of the SARS-CoV-2 main protease reveals strategy for developing dual inhibitors against M(pro) and cathepsin L
Sci Adv PubMed Europe PubMed DOI I -
Sacco,M.D., Ma,C., Lagarias,P., Gao,A., Townsend,J.A., Meng,X., Dube,P., Zhang,X., Hu,Y., Kitamura,N., Hurst,B., Tarbet,B., Marty,M.T., Kolocouris,A., Xiang,Y., Chen,Y. and Wang,J.
Structure and inhibition of the SARS-CoV-2 main protease reveals strategy for developing dual inhibitors against M(pro) and cathepsin L
bioRxiv PubMed Europe PubMed DOI I -
Boudreau,P.D., Miller,B.W., McCall,L.I., Almaliti,J., Reher,R., Hirata,K., Le,T., Siqueira-Neto,J.L., Hook,V. and Gerwick,W.H.
Design of gallinamide A analogs as potent inhibitors of the cysteine proteases human cathepsin L and Trypanosoma cruzi cruzain
J Med Chem62, 9026-9044. PubMed Europe PubMed DOI I -
Dana,D., Garcia,J., Bhuiyan,A.I., Rathod,P., Joo,L., Novoa,D.A., Paroly,S., Fath,K.R., Chang,E.J. and Pathak,S.K.
Cell penetrable, clickable and tagless activity-based probe of human cathepsin L
Bioorg Chem85, 505-514. PubMed Europe PubMed DOI L I -
Shockey,W.A., Kieslich,C.A., Wilder,C.L., Watson,V. and Platt,M.O.
Dynamic model of protease state and inhibitor trafficking to predict protease activity in breast cancer cells
Cell Mol Bioeng12, 275-288. PubMed Europe PubMed DOI I -
Weiss-Sadan,T., Itzhak,G., Kaschani,F., Yu,Z., Mahameed,M., Anaki,A., Ben-Nun,Y., Merquiol,E., Tirosh,B., Kessler,B., Kaiser,M. and Blum,G.
Cathepsin L regulates metabolic networks controlling rapid cell growth and proliferation
Mol Cell Proteomics18, 1330-1344. PubMed Europe PubMed DOI I -
Yuan,L., Liu,J., He,W., Bao,Y., Sheng,L., Zou,C., Hu,B., Ge,W., Liu,Y., Wang,J., Lin,B., Li,Y. and Ma,E.
Discovery of a novel cathepsin inhibitor with dual autophagy-inducing and metastasis-inhibiting effects on breast cancer cells
Bioorg Chem84, 239-253. PubMed Europe PubMed DOI I -
Yuan,L., Zou,C., Ge,W., Liu,Y., Hu,B., Wang,J., Lin,B., Li,Y. and Ma,E.
A novel cathepsin L inhibitor prevents the progression of idiopathic pulmonary fibrosis
Bioorg Chem103417-103417. PubMed Europe PubMed DOI I -
Huisman,M., Kodanko,J.P., Arora,K., Herroon,M., Alnaed,M., Endicott,J., Podgorski,I. and Kodanko,J.J.
Affinity-enhanced luminescent Re(I)- and Ru(II)-based inhibitors of the cysteine protease cathepsin L
Inorg Chem57, 7881-7891. PubMed Europe PubMed DOI I -
Dos Santos,D.A., Deobald,A.M., Cornelio,V.E., Avila,R.M.D., Cornea,R.C., Bernasconi,G.C.R., Paixao,M.W., Vieira,P.C. and Correa,A.G.
Asymmetric synthesis and evaluation of epoxy-alpha-acyloxycarboxamides as selective inhibitors of cathepsin L
Bioorg Med Chem25, 4620-4627. PubMed Europe PubMed DOI I -
Giroud,M., Ivkovic,J., Martignoni,M., Fleuti,M., Trapp,N., Haap,W., Kuglstatter,A., Benz,J., Kuhn,B., Schirmeister,T. and Diederich,F.
Inhibition of the cysteine protease human cathepsin L by triazine nitriles: amide???heteroarene pi-stacking interactions and chalcogen bonding in the S3 pocket
ChemMedChem12, 257-270. PubMed Europe PubMed DOI I -
Hashimoto,Y.
Gelatin zymography using leupeptin for the detection of various cathepsin L forms
Methods Mol Biol1594, 243-254. PubMed Europe PubMed DOI L I -
Kikuta,S., Murai,Y. and Tanaka,E.
Activation of cathepsin L contributes to the irreversible depolarization induced by oxygen and glucose deprivation in rat hippocampal CA1 neurons
Neurosci Lett636, 120-126. PubMed Europe PubMed DOI I -
Kuhn,B., Tichy,M., Wang,L., Robinson,S., Martin,R.E., Kuglstatter,A., Benz,J., Giroud,M., Schirmeister,T., Abel,R., Diederich,F. and Hert,J.
Prospective evaluation of free energy calculations for the prioritization of cathepsin L inhibitors
J Med Chem60, 2485-2497. PubMed Europe PubMed DOI I -
Li,Y.Y., Fang,J. and Ao,G.Z.
Cathepsin B and L inhibitors: a patent review (2010 - present)
Expert Opin Ther Pat27, 643-656. PubMed Europe PubMed DOI V I -
Parker,E.N., Odutola,S.O., Wang,Y., Strecker,T.E., Mukherjee,R., Shi,Z., Chaplin,D.J., Trawick,M.L. and Pinney,K.G.
Synthesis and biological evaluation of a water-soluble phosphate prodrug salt and structural analogues of KGP94, a lead inhibitor of cathepsin L
Bioorg Med Chem Lett27, 1304-1310. PubMed Europe PubMed DOI I -
Burton,L.J., Dougan,J., Jones,J., Smith,B.N., Randle,D., Henderson,V. and Odero-Marah,V.A.
Targeting the nuclear cathepsin L- CCAAT-displacement protein/cut homeobox transcription factor-epithelial mesenchymal transition pathway in prostate and breast cancer cells with Z-FY-CHO inhibitor
Mol Cell Biol37, e00297-16.-e00297-16. PubMed Europe PubMed DOI I -
Giroud,M., Harder,M., Kuhn,B., Haap,W., Trapp,N., Schweizer,W.B., Schirmeister,T. and Diederich,F.
Fluorine scan of inhibitors of the cysteine protease human cathepsin L: dipolar and quadrupolar effects in the pi-stacking of fluorinated phenyl rings on peptide amide bonds
ChemMedChem11, 1042-1047. PubMed Europe PubMed DOI I -
Raghav,N., Jangra,S., Kumar,A., Bhattacharyya,S., Wadhwa,D. and Sindhu,J.
Cathepsin B, H and L inhibitors as cell proliferating agents: design, synthesis, computational and pharmacological studies of some novel 2-(2-naphthoyl)-6,6-dimethyl-3-aryl-2,3,6,7-tetrahydrobenzofuran-4(5H)-ones
RSC Adv6, 34588-34599. DOI I -
Sudhan,D.R., Pampo,C., Rice,L. and Siemann,D.W.
Cathepsin L inactivation leads to multimodal inhibition of prostate cancer cell dissemination in a preclinical bone metastasis model
Int J Cancer138, 2665-2677. PubMed Europe PubMed DOI I -
Sudhan,D.R., Rabaglino,M.B., Wood,C.E. and Siemann,D.W.
Cathepsin L in tumor angiogenesis and its therapeutic intervention by the small molecule inhibitor KGP94
Clin Exp Metastasis33, 461-473. PubMed Europe PubMed DOI I -
Ueki,N., Wang,W., Swenson,C., McNaughton,C., Sampson,N.S. and Hayman,M.J.
Synthesis and preclinical evaluation of a highly improved anticancer prodrug activated by histone deacetylases and cathepsin L
Theranostics6, 808-816. PubMed Europe PubMed DOI I -
Zhou,N., Pan,T., Zhang,J., Li,Q., Zhang,X., Bai,C., Huang,F., Peng,T., Zhang,J., Liu,C., Tao,L. and Zhang,H.
Glycopeptide antibiotics potently inhibit cathepsin L in the late endosome/lysosome and block the entry of Ebola virus, Middle East Respiratory Syndrome Coronavirus (MERS-CoV), and Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV)
J Biol Chem291, 9218-9232. PubMed Europe PubMed DOI I -
Celis-Barros,C., Saavedra-Rivas,L., Salgado,J.C., Cassels,B.K. and Zapata-Torres,G.
Molecular dynamics simulation of halogen bonding mimics experimental data for cathepsin L inhibition
J Comput Aided Mol Des29, 37-46. PubMed Europe PubMed DOI I -
Parker,E.N., Song,J., Kishore Kumar,G.D., Odutola,S.O., Chavarria,G.E., Charlton-Sevcik,A.K., Strecker,T.E., Barnes,A.L., Sudhan,D.R., Wittenborn,T.R., Siemann,D.W., Horsman,M.R., Chaplin,D.J., Trawick,M.L. and Pinney,K.G.
Synthesis and biochemical evaluation of benzoylbenzophenone thiosemicarbazone analogues as potent and selective inhibitors of cathepsin L
Bioorg Med Chem23, 6974-6992. PubMed Europe PubMed DOI I -
Wang,H., Sang,N., Zhang,C., Raghupathi,R., Tanzi,R.E. and Saunders,A.
Cathepsin L mediates the degradation of novel APP C-terminal fragments
Biochemistry54, 2806-2816. PubMed Europe PubMed DOI I -
Yang,N., Wang,P., Wang,W.J., Song,Y.Z. and Liang,Z.Q.
Inhibition of cathepsin L sensitizes human glioma cells to ionizing radiation in vitro through NF-kappaB signaling pathway
Acta Pharmacol Sin36, 400-410. PubMed Europe PubMed DOI I -
Chua,K.C., Pietsch,M., Zhang,X., Hautmann,S., Chan,H.Y., Bruning,J.B., Gutschow,M. and Abell,A.D.
Macrocyclic protease inhibitors with reduced peptide character
Angew Chem Int Ed Engl53, 7828-7831. PubMed Europe PubMed DOI I -
Dana,D., De,S., Rathod,P., Davalos,A.R., Novoa,D.A., Paroly,S., Torres,V.M., Afzal,N., Lankalapalli,R.S., Rotenberg,S.A., Chang,E.J., Subramaniam,G. and Kumar,S.
Development of a highly potent, selective, and cell-active Inhibitor of cysteine cathepsin L - a hybrid design approach
Chem Commun (Camb)50, 10875-10878. PubMed Europe PubMed DOI I -
Elshabrawy,H.A., Fan,J., Haddad,C.S., Ratia,K., Broder,C.C., Caffrey,M. and Prabhakar,B.S.
Identification of a broad-spectrum antiviral small molecule against severe acute respiratory syndrome coronavirus and Ebola, Hendra, and Nipah viruses by using a novel high-throughput screening assay
J Virol88, 4353-4365. PubMed Europe PubMed DOI I -
Miller,B., Friedman,A.J., Choi,H., Hogan,J., McCammon,J.A., Hook,V. and Gerwick,W.H.
The marine cyanobacterial metabolite gallinamide A is a potent and selective inhibitor of human cathepsin L
J Nat Prod77, 92-99. PubMed Europe PubMed DOI I -
Ramalho,S.D., De Sousa,L.R., Nebo,L., Maganhi,S.H., Caracelli,I., Zukerman-Schpector,J., Lima,M.I., Alves,M.F., da Silva,M.F., Fernandes,J.B. and Vieira,P.C.
Triterpenoids as novel natural inhibitors of human cathepsin L
Chem Biodivers11, 1354-1363. PubMed Europe PubMed DOI I -
Baek,K.H., Karki,R., Lee,E.S., Na,Y. and Kwon,Y.
Synthesis and investigation of dihydroxychalcones as calpain and cathepsin inhibitors
Bioorg Chem51, 24-30. PubMed Europe PubMed DOI I -
Ehmke,V., Winkler,E., Banner,D.W., Haap,W., Schweizer,W.B., Rottmann,M., Kaiser,M., Freymond,C., Schirmeister,T. and Diederich,F.
Optimization of triazine nitriles as rhodesain inhibitors: structure-activity relationships, bioisosteric imidazopyridine nitriles, and X-ray crystal structure analysis with human cathepsin L
ChemMedChem8, 967-975. PubMed Europe PubMed DOI I -
Song,J., Jones,L.M., Chavarria,G.E., Charlton-Sevcik,A.K., Jantz,A., Johansen,A., Bayeh,L., Soeung,V., Snyder,L.K., Lade,S.D., Jr., Chaplin,D.J., Trawick,M.L. and Pinney,K.G.
Small-molecule inhibitors of cathepsin L incorporating functionalized ring-fused molecular frameworks
Bioorg Med Chem Lett23, 2801-2807. PubMed Europe PubMed DOI I -
Torkar,A., Lenarcic,B., Lah,T., Dive,V. and Devel,L.
Identification of new peptide amides as selective cathepsin L inhibitors: The first step towards selective irreversible inhibitors?
Bioorg Med Chem Lett23, 2968-2973. PubMed Europe PubMed DOI I -
Wang,Y.R., Qin,S., Han,R., Wu,J.C., Liang,Z.Q., Qin,Z.H. and Wang,Y.
Cathepsin L plays a role in quinolinic acid-induced NF-Kappab activation and excitotoxicity in rat striatal neurons
PLoS ONE8, e75702-e75702. PubMed Europe PubMed DOI I -
Chavarria,G.E., Horsman,M.R., Arispe,W.M., Kumar,G.D., Chen,S.E., Strecker,T.E., Parker,E.N., Chaplin,D.J., Pinney,K.G. and Trawick,M.L.
Initial evaluation of the antitumour activity of KGP94, a functionalized benzophenone thiosemicarbazone inhibitor of cathepsin L
Eur J Med Chem58, 568-572. PubMed Europe PubMed DOI I -
Ehmke,V., Quinsaat,J.E., Rivera-Fuentes,P., Heindl,C., Freymond,C., Rottmann,M., Brun,R., Schirmeister,T. and Diederich,F.
Tuning and predicting biological affinity: aryl nitriles as cysteine protease inhibitors
Org Biomol Chem10, 5764-5768. PubMed Europe PubMed DOI I -
Marques,E.F., Bueno,M.A., Duarte,P.D., Silva,L.R., Martinelli,A.M., Dos Santos,C.Y., Severino,R.P., Bromme,D., Vieira,P.C. and Correa,A.G.
Evaluation of synthetic acridones and 4-quinolinones as potent inhibitors of cathepsins L and V
Eur J Med Chem54, 10-21. PubMed Europe PubMed DOI I -
Na,Z., Li,L., Uttamchandani,M. and Yao,S.Q.
Microarray-guided discovery of two-photon (2P) small molecule probes for live-cell imaging of cysteinyl cathepsin activities
Chem Commun (Camb)48, 7304-7306. PubMed Europe PubMed DOI I -
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