000 01393 a2200385 4500
005 20250514023745.0
264 0 _c20030731
008 200307s 0 0 eng d
022 _a0960-894X
024 7 _a10.1016/s0960-894x(01)00816-2
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBeevers, Rebekah
245 0 0 _aSolution and solid-phase synthesis of potent inhibitors of hepatitis C virus NS3 proteinase.
_h[electronic resource]
260 _bBioorganic & medicinal chemistry letters
_cFeb 2002
300 _a641-3 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAmino Acids
650 0 4 _aCombinatorial Chemistry Techniques
650 0 4 _aEnzyme Inhibitors
_xchemical synthesis
650 0 4 _aFluorenes
650 0 4 _aHepacivirus
_xenzymology
650 0 4 _aHumans
650 0 4 _aInhibitory Concentration 50
650 0 4 _aOligopeptides
_xchemical synthesis
650 0 4 _aStructure-Activity Relationship
650 0 4 _aViral Nonstructural Proteins
_xantagonists & inhibitors
700 1 _aCarr, Maria G
700 1 _aJones, Philip S
700 1 _aJordan, Steven
700 1 _aKay, Paul B
700 1 _aLazell, Robert C
700 1 _aRaynham, Tony M
773 0 _tBioorganic & medicinal chemistry letters
_gvol. 12
_gno. 4
_gp. 641-3
856 4 0 _uhttps://doi.org/10.1016/s0960-894x(01)00816-2
_zAvailable from publisher's website
999 _c11753361
_d11753361