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Volumn 17, Issue 9, 2007, Pages 2581-2589

Identification of a series of tetrahydroisoquinoline derivatives as potential therapeutic agents for breast cancer

Author keywords

Agonist; Antagonist; Antiestrogen; Breast cancer; Estrogen receptor; Ligand binding domain; Progesterone receptor

Indexed keywords

4 (1,2 DIPHENYL 1 BUTENYL)CINNAMIC ACID; 4 HYDROXYTAMOXIFEN; ANILIDE; FULVESTRANT; N BUTYL 11 (3,17BETA DIHYDROXYESTRA 1,3,5(10) TRIEN 7ALPHA YL) N METHYLUNDECANAMIDE; PROGESTERONE RECEPTOR; RALOXIFENE; TAMOXIFEN; TETRAHYDROISOQUINOLINE DERIVATIVE; TRANSCRIPTION FACTOR AP 1;

EID: 33947727864     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2007.02.002     Document Type: Article
Times cited : (26)

References (31)
  • 17
    • 33947719636 scopus 로고    scopus 로고
    • note
    • 3(1 mL, 10 mmol), compound 1g was synthesized following the above procedure for compound 1f.
  • 18
    • 33947723148 scopus 로고    scopus 로고
    • note
    • 50 of test compound.
  • 19
    • 33947729891 scopus 로고    scopus 로고
    • note
    • 5 cells in 2 ml maintained medium per well. Cells were allowed to attach to the bottom for 24 h incubation, then the seeding medium was removed and replaced by the experimental medium (phenol red-free DMEM supplemented with 5% charcoal-stripped fetal bovine serum and penicillin (100 U/ml)/Streptomycin (100 μg/ml). After further 24 h incubation, the test molecules dissolved in DMSO were added in the wells. The final concentration of DMSO in the culture medium did not exceed 0.1%. The culture was continued for 2 days. The final relative cell viability was estimated with Cell Titer proliferation assay kit (Promega, Madison, WI) by measuring the absorbance at 570 nm, which is directly proportional to the number of living cells in the culture. The testing was performed by following the manufacturer's protocol. Experiments were triplicated for each compound.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.