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Volumn 15, Issue 22, 2005, Pages 4936-4943

Synthesis and in vitro cytotoxicity of novel hydrophilic chiral 2-alkoxy-1,4-butanediamine platinum (II) complexes

Author keywords

Antitumor drugs; Chiral 2 alkoxy 1,4 butanediamine; Platinum (II) complexes

Indexed keywords

CARBOPLATIN; CISPLATIN; CYCLOBUTANE 1,1 DICARBOXYLATO(ETHOXY 1,4 BUTANEDIAMINE)PLATINUM; CYCLOBUTANE 1,1 DICARBOXYLATO(METHOXY 1,4 BUTANEDIAMINE)PLATINUM; DICHLORO(ETHOXY 1,4 BUTANEDIAMINE)PLATINUM; DICHLORO(METHOXY 1,4 BUTANEDIAMINE)PLATINUM; DICHLOROACETATE(ETHOXY 1,4 BUTANEDIAMINE)PLATINUM; DIGLYCOLATO(ETHOXY 1,4 BUTANEDIAMINE)PLATINUM; DIGLYCOLATO(METHOXY 1,4 BUTANEDIAMINE)PLATINUM; GLYCOLATO(ETHOXY 1,4 BUTANEDIAMINE)PLATINUM; GLYCOLATO(METHOXY 1,4 BUTANEDIAMINE)PLATINUM; MALONATO(ETHOXY 1,4 BUTANEDIAMINE)PLATINUM; MALONATO(METHOXY 1,4 BUTANEDIAMINE)PLATINUM; OXALATO(ETHOXY 1,4 BUTANEDIAMINE)PLATINUM; OXALATO(METHOXY 1,4 BUTANEDIAMINE)PLATINUM; PLATINUM COMPLEX; UNCLASSIFIED DRUG;

EID: 25844481568     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2005.08.025     Document Type: Article
Times cited : (4)

References (38)
  • 27
    • 25844493025 scopus 로고    scopus 로고
    • note
    • 2: C, 54.28; H, 5.92. Found: C, 54.30; H, 6.04. (R)-2-Ethoxy-1,4-ditosylbutane was prepared in a similar manner and spectral data were identical with that of (S)-2-ethoxy-1,4- ditosylbutane.
  • 29
    • 25844442327 scopus 로고    scopus 로고
    • note
    • 2O).
  • 33
    • 25844434254 scopus 로고    scopus 로고
    • note
    • 2O (100 ml) was stirred at 60°C in the dark overnight. The resulting silver iodide was filtered through a pad of Celite. The filtrate was concentrated under a reduced pressure and white precipitate was collected and dried in vacuum.
  • 34
    • 25844462815 scopus 로고    scopus 로고
    • note
    • 2O (20 ml). Under the nitrogen atmosphere the mixture was heated at 40°C for 24 h in the dark and filtered though a pad of Celite. Then disodium glycolate (2.0 mmol), sodium chloride (4.0 mmol) or sodium glycolate (4.0 mmol) aqueous solution was added to the above filtration. The resultant solution was then mixed with the above filtration and stirred at 40°C for 24 h. The reaction mixture was concentrated and ethanol was added before filtration. The filtrate was concentrated to afford yellow syrup, which gave a precipitate after addition of ether. The resulting precipitate was then filtered quickly to give a very hygroscopic solid.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.