Literature for TMC-95 (XT01.001 inhibitor)
(Topics flags: S Structure, I Inhibitor, V Review. To select only the references relevant to a single topic, click the link above. See explanation.)
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Wilson,D.L., Meininger,I., Strater,Z., Steiner,S., Tomlin,F., Wu,J., Jamali,H., Krappmann,D. and Gotz,M.G.
Synthesis and evaluation of macrocyclic peptide aldehydes as potent and selective inhibitors of the 20S proteasome
ACS Med Chem Lett7, 250-255. PubMed Europe PubMed DOI I -
Xu,K., Wang,K., Yang,Y., Yan,D.A., Huang,L., Chen,C.H. and Xiao,Z.
Discovery of novel non-covalent inhibitors selective to the beta5-subunit of the human 20S proteasome
Eur J Med Chem98, 61-68. PubMed Europe PubMed DOI I -
Desvergne,A., Genin,E., Marechal,X., Gallastegui,N., Dufau,L., Richy,N., Groll,M., Vidal,J. and Reboud-Ravaux,M.
Dimerized linear mimics of a natural cyclopeptide (TMC-95A) are potent noncovalent inhibitors of the eukaryotic 20S proteasome
J Med Chem56, 3367-3378. PubMed Europe PubMed DOI I -
Groll,M., Gallastegui,N., Marechal,X., Le Ravalec,V., Basse,N., Richy,N., Genin,E., Huber,R., Moroder,L., Vidal,J. and Reboud-Ravaux,M.
20S Proteasome inhibition: designing noncovalent linear peptide mimics of the natural product TMC-95A
ChemMedChem5, 1701-1705. PubMed Europe PubMed DOI I -
Groll,M., Gotz,M., Kaiser,M., Weyher,E. and Moroder,L.
TMC-95-Based inhibitor design provides evidence for the catalytic versatility of the proteasome
Chem Biol13, 607-614. PubMed Europe PubMed DOI I -
[YEAR:29-11-2004]Groll,M. and Huber,R.
Inhibitors of the eukaryotic 20S proteasome core particle: a structural approach
Biochim Biophys Acta1695, 33-44. PubMed Europe PubMed DOI V I -
[YEAR:9-2-2004]Inoue,M., Zhai,H., Sakazaki,H., Furuyama,H., Fukuyama,Y. and Hirama,M.
TMC-95A, a reversible proteasome inhibitor, induces neurite outgrowth in PC12 cells
Bioorg Med Chem Lett14, 663-665. PubMed Europe PubMed DOI I -
Kaiser,M., Milbradt,A.G., Siciliano,C., Assfalg-Machleidt,I., Machleidt,W., Groll,M., Renner,C. and Moroder,L.
TMC-95A analogues with endocyclic biphenyl ether group as proteasome inhibitors
Chem Biodivers1, 161-173. PubMed Europe PubMed DOI I -
[YEAR:6-9-2004]Kaiser,M., Groll,M., Siciliano,C., Assfalg-Machleidt,I., Weyher,E., Kohno,J., Milbradt,A.G., Renner,C., Huber,R. and Moroder,L.
Binding mode of TMC-95A analogues to eukaryotic 20S proteasome
Chembiochem5, 1256-1266. PubMed Europe PubMed DOI S I -
[YEAR:17-8-2001]Groll,M., Koguchi,Y., Huber,R. and Kohno,J.
Crystal structure of the 20 S proteasome:TMC-95A complex: a non-covalent proteasome inhibitor
J Mol Biol311, 543-548. PubMed Europe PubMed DOI S I -
Koguchi,Y., Kohno,J., Nishio,M., Takahashi,K., Okuda,T., Ohnuki,T. and Komatsubara,S.
TMC-95A, B, C, and D, novel proteasome inhibitors produced by Apiospora montagnei Sacc. TC 1093. Taxonomy, production, isolation, and biological activities
J Antibiot (Tokyo)53, 105-109. PubMed Europe PubMed I
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