Potent inhibitors of lipoprotein-associated phospholipase A2: Benzaldehyde O-heterocycle-4-carbonyloxime = 강력한 Lp-PLA2의 억제제인 벤즈알데히드 O-헤테로사이클-4-카르보닐옥심의 개발

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dc.contributor.authorHyung Jae Jung-
dc.contributor.authorYong-Dae Park-
dc.contributor.authorHo Yong Park-
dc.contributor.authorI Y Jeong-
dc.contributor.authorTae Sook Jeong-
dc.contributor.authorWoo Song Lee-
dc.date.accessioned2017-04-19T09:05:04Z-
dc.date.available2017-04-19T09:05:04Z-
dc.date.issued2006-
dc.identifier.issn0960-894X-
dc.identifier.uri10.1016/j.bmcl.2006.08.031ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/7565-
dc.description.abstractA series of multi-substituted oximes were prepared and their potencies for inhibiting lipoprotein-associated phospholipase A2 (Lp-PLA2) activity were evaluated in vitro. Among them, compounds 3a, 3b, and 3m were identified to display a micromolar potency for inhibiting Lp-PLA2 in whole human plasma and isolated human LDL. Based on these results, structure-activity relationship was studied on modification of three parts of R1, R2, and R3 to identify a potent pharmacophore for Lp-PLA2. In an attempt to introduce various functional groups at R2 and R3, we discovered that replacement of less lipophilic groups led to an increase of inhibitory activity. Among the tested oxime derivatives, cyano- and morpholino-substituted analogue 4f at R2 and R3 had the highest potency with an IC50 value of 0.05 μM in whole human plasma.-
dc.publisherElsevier-
dc.titlePotent inhibitors of lipoprotein-associated phospholipase A2: Benzaldehyde O-heterocycle-4-carbonyloxime = 강력한 Lp-PLA2의 억제제인 벤즈알데히드 O-헤테로사이클-4-카르보닐옥심의 개발-
dc.title.alternativePotent inhibitors of lipoprotein-associated phospholipase A2: Benzaldehyde O-heterocycle-4-carbonyloxime-
dc.typeArticle-
dc.citation.titleBioorganic & Medicinal Chemistry Letters-
dc.citation.number21-
dc.citation.endPage5579-
dc.citation.startPage5576-
dc.citation.volume16-
dc.contributor.affiliatedAuthorHyung Jae Jung-
dc.contributor.affiliatedAuthorYong-Dae Park-
dc.contributor.affiliatedAuthorHo Yong Park-
dc.contributor.affiliatedAuthorTae Sook Jeong-
dc.contributor.affiliatedAuthorWoo Song Lee-
dc.contributor.alternativeName정형재-
dc.contributor.alternativeName박용대-
dc.contributor.alternativeName박호용-
dc.contributor.alternativeName정일윤-
dc.contributor.alternativeName정태숙-
dc.contributor.alternativeName이우송-
dc.identifier.bibliographicCitationBioorganic & Medicinal Chemistry Letters, vol. 16, no. 21, pp. 5576-5579-
dc.identifier.doi10.1016/j.bmcl.2006.08.031-
dc.subject.keywordLp-PLA2 inhibitor-
dc.subject.localLp-PLA2 inhibitor-
dc.description.journalClassY-
Appears in Collections:
Jeonbuk Branch Institute > Functional Biomaterial Research Center > 1. Journal Articles
Division of Biomedical Research > Microbiome Convergence Research Center > 1. Journal Articles
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