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Volumn 2, Issue 7, 2005, Pages 529-532

Synthesis and anti-breast cancer activity of tetrasubstituted pyrrole derivatives

Author keywords

Breast cancer; Diversity oriented synthesis; Privileged structure; Pyrroles; SU11248; Tyrosine kinase inhibitors

Indexed keywords

2,4 DIMETHYL 5 (2 OXO 1H INDOL 3 YLMETHYLENE) 3 PYRROLEPROPIONIC ACID; 3 [4 METHYL 2 (2 OXO 3 INDOLINYLMETHYLIDENYL) 3 PYRROLYL]PROPIONIC ACID; AMINE; ANTINEOPLASTIC AGENT; PHA 665752; PROTEIN TYROSINE KINASE INHIBITOR; PYRROLE DERIVATIVE; SEMAXANIB; SUNITINIB; UNCLASSIFIED DRUG;

EID: 28344458097     PISSN: 15701808     EISSN: None     Source Type: Journal    
DOI: 10.2174/157018005774479122     Document Type: Article
Times cited : (4)

References (24)
  • 9
    • 0033775563 scopus 로고    scopus 로고
    • and references therein
    • (c) O'Hagan, D. Nat. Prod. Rep. 2000, 17, 435 and references therein;
    • (2000) Nat. Prod. Rep. , vol.17 , pp. 435
    • O'Hagan, D.1
  • 24
    • 28444499747 scopus 로고    scopus 로고
    • note
    • Pure compounds were initially dissolved in DMSO at 400 times the desired final maximum test concentration, i.e. 100 μM. Control cells were exposed to an equivalent concentration of DMSO. Each agent was tested in duplicates at five different ten-fold dilutions. Drug incubation times were 48 h, after which cells were precipitated with 25 μL ice-cold 50% (w/v) trichloroacetic acid and fixed for 60 min at 4 °C. Then the SRB assay was performed. The optical density (OD) of each well was measured at 490 nm using Bio-Tek's Elx800 NB 96-well plate reader. The percentage growth was calculated at each of the drug concentration levels based on the difference in OD at the start and end of drug exposure. Values were corrected for background OD from wells only containing medium.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.