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Volumn 11, Issue 21, 2009, Pages 4894-4897

9-Amino acridines undergo reversible amine exchange reactions in water: Implications on their mechanism of action in vivo

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; AMINOACRIDINE DERIVATIVE; WATER;

EID: 70350686736     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol9019925     Document Type: Article
Times cited : (28)

References (36)
  • 9
    • 0035758620 scopus 로고    scopus 로고
    • Acridines lacking a 9-amino substituent (e.g., DACA) have also been reported as potent anticancer drugs. For example, see: Bridewell, D. J.; Finlay, G. J.; Baguley, B. C. Anti-Cancer Drug Des. 2001, 16, 317.
    • (2001) Anti-Cancer Drug Des. , vol.16 , pp. 317
    • Bridewell, D.J.1    Finlay, G.J.2    Baguley, B.C.3
  • 19
    • 70350658245 scopus 로고    scopus 로고
    • 9-Amino-4-carboxylic acid acridines were chosen as a model system because of their high solubility in water at near-physiological pH and because of their structural analogy with drugs from the AHMA and DACA families.
    • 9-Amino-4-carboxylic acid acridines were chosen as a model system because of their high solubility in water at near-physiological pH and because of their structural analogy with drugs from the AHMA and DACA families.
  • 24
    • 70350629551 scopus 로고    scopus 로고
    • No amine exchange reaction was observed with spermidine or other primary amines that are protonated in solution at near-physiological pH of 7.4.
    • No amine exchange reaction was observed with spermidine or other primary amines that are protonated in solution at near-physiological pH of 7.4.
  • 33
    • 68149096934 scopus 로고    scopus 로고
    • For recent examples of novel reversible covalent chemistries suitable for DCC, see: (a) Saiz, C.; Wipf, P.; Manta, E.; Mahler, G. Org. Lett. 2009, 11, 3170.
    • (2009) Org. Lett. , vol.11 , pp. 3170
    • Saiz, C.1    Wipf, P.2    Manta, E.3    Mahler, G.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.