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Volumn 20, Issue 16, 2010, Pages 4855-4857

Morroniside cinnamic acid conjugate as an anti-inflammatory agent

Author keywords

7 O Cinnamoylmorroniside; Anti inflammatory activity; Morroniside

Indexed keywords

7 O CINNAMOYLMORRONISIDE; CINNAMIC ACID DERIVATIVE; ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE 1; HARPAGOSIDE; IRIDOID; MORRONISIDE; TUMOR NECROSIS FACTOR ALPHA; UNCLASSIFIED DRUG; ANTIINFLAMMATORY AGENT; CINNAMIC ACID; GLYCOSIDE; PHENYLPROPIONIC ACID DERIVATIVE; PYRAN DERIVATIVE;

EID: 77955421460     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2010.06.095     Document Type: Article
Times cited : (22)

References (31)
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    • 77955413059 scopus 로고    scopus 로고
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    • 77955414838 scopus 로고    scopus 로고
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    • 77955429508 scopus 로고    scopus 로고
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    • 4 cells of HUVEC were seeded into a 96-well microtiter plate-and grown with EBM-2 overnight. Medium was replaced to DMEM before the cells were pretreated with 10 ng/ml of TNF-α. Two hours after the addition of TNF-α, the medium was removed and the cell layer was washed three times with ice-cold PBS/1% BSA and fixed with 4% paraformaldehyde phosphate buffer. After being washed with PBS five times, the cells were incubated with PBS/1% BSA for 60 min. After being washed with PBS three times, the cells were incubated with an anti-E-selectin antibody at 4 °C overnight (1:1000 in PBS/1% BSA). After being washed with PBS three times, the AP-conjugated secondary antibody (1:500 in PBS/1% BSA) was added for 120 min. After the addition of p-nitrophenyl phosphate (pNPP) solution, the enzymatic reaction was allowed to proceed for 60 min at room temperature; the optical density (OD: 405 nm) was measured using the ELISA plate reader. At least three independent experiments (each performed in triplicate) were used for the statistical interpretation of the data (means ± SEM).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.