000 01462 a2200409 4500
005 20250515045257.0
264 0 _c20070409
008 200704s 0 0 eng d
022 _a0960-894X
024 7 _a10.1016/j.bmcl.2006.10.047
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aImbach, Patricia
245 0 0 _aNovel beta-lactam derivatives: potent and selective inhibitors of the chymotrypsin-like activity of the human 20S proteasome.
_h[electronic resource]
260 _bBioorganic & medicinal chemistry letters
_cJan 2007
300 _a358-62 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aChymotrypsin
_xantagonists & inhibitors
650 0 4 _aCrystallography, X-Ray
650 0 4 _aDrug Design
650 0 4 _aHumans
650 0 4 _aModels, Molecular
650 0 4 _aPeptides
_xchemistry
650 0 4 _aProteasome Inhibitors
650 0 4 _aStructure-Activity Relationship
650 0 4 _aTrypsin Inhibitors
_xchemical synthesis
650 0 4 _abeta-Lactams
_xchemical synthesis
700 1 _aLang, Marc
700 1 _aGarcía-Echeverría, Carlos
700 1 _aGuagnano, Vito
700 1 _aNoorani, Maria
700 1 _aRoesel, Johannes
700 1 _aBitsch, Francis
700 1 _aRihs, Grety
700 1 _aFuret, Pascal
773 0 _tBioorganic & medicinal chemistry letters
_gvol. 17
_gno. 2
_gp. 358-62
856 4 0 _uhttps://doi.org/10.1016/j.bmcl.2006.10.047
_zAvailable from publisher's website
999 _c16668036
_d16668036