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264 0 _c20010510
008 200105s 0 0 eng d
022 _a0960-894X
024 7 _a10.1016/s0960-894x(00)00644-2
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLevin, J I
245 0 0 _aHeteroaryl and cycloalkyl sulfonamide hydroxamic acid inhibitors of matrix metalloproteinases.
_h[electronic resource]
260 _bBioorganic & medicinal chemistry letters
_cJan 2001
300 _a239-42 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAnimals
650 0 4 _aCombinatorial Chemistry Techniques
650 0 4 _aHumans
650 0 4 _aHydroxamic Acids
_xchemical synthesis
650 0 4 _aInhibitory Concentration 50
650 0 4 _aMatrix Metalloproteinase 13
650 0 4 _aMatrix Metalloproteinase Inhibitors
650 0 4 _aProtease Inhibitors
_xchemical synthesis
650 0 4 _aStructure-Activity Relationship
650 0 4 _aSulfonamides
_xchemical synthesis
650 0 4 _aortho-Aminobenzoates
_xchemical synthesis
700 1 _aGu, Y
700 1 _aNelson, F C
700 1 _aZask, A
700 1 _aDiJoseph, J F
700 1 _aSharr, M A
700 1 _aSung, A
700 1 _aJin, G
700 1 _aCowling, R
700 1 _aChanda, P
700 1 _aCosmi, S
700 1 _aHsiao, C L
700 1 _aEdris, W
700 1 _aWilhelm, J
700 1 _aKillar, L M
700 1 _aSkotnicki, J S
773 0 _tBioorganic & medicinal chemistry letters
_gvol. 11
_gno. 2
_gp. 239-42
856 4 0 _uhttps://doi.org/10.1016/s0960-894x(00)00644-2
_zAvailable from publisher's website
999 _c11144485
_d11144485