메뉴 건너뛰기




Volumn 19, Issue 8, 2011, Pages 2726-2741

7-Azabicyclo[2.2.1]heptane as a structural motif to block mutagenicity of nitrosamines

Author keywords

Ames test; Bond dissociation energy; Mutagenicity; Nitrosamines

Indexed keywords

7 AZABICYCLO[2.2.1]HEPTANE; DIMETHYLNITROSAMINE; NITROSAMINE; UNCLASSIFIED DRUG;

EID: 79954425141     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2011.02.049     Document Type: Article
Times cited : (12)

References (46)
  • 22
    • 0026321495 scopus 로고
    • D.A. Wink, K.S. Kasprzak, C.M. Maragos, R.K. Elespuru, M. Misra, T.M. Dunams, T.A. Cebula, W.H. Koch, A.W. Andrews, J.S. Allen, and L.K. Keefer Science 254 1991 1001 In this pathway, the formation of nitric oxide (NO), which may cause lethal cell injury, is possible. While some involvement of this alternative metabolic pathway of N-nitrosamines cannot be ruled out, the present observation that most of these bicyclic nitrosamines showed no cytotoxicity in the presence of S9 mix may exclude a significant contribution of denitrosation in the present cases
    • (1991) Science , vol.254 , pp. 1001
    • Wink, D.A.1    Kasprzak, K.S.2    Maragos, C.M.3    Elespuru, R.K.4    Misra, M.5    Dunams, T.M.6    Cebula, T.A.7    Koch, W.H.8    Andrews, A.W.9    Allen, J.S.10    Keefer, L.K.11
  • 27
    • 79954425248 scopus 로고    scopus 로고
    • 2-Nitronapthalene was reported to be positive in the Ames test (Ref. 21). It may be assumed that the olefin derivative 11 can undergo homoallylic conjugation, which may lead to electronically equivalent 2-nitronaphthalene
    • 2-Nitronapthalene was reported to be positive in the Ames test (Ref. 21). It may be assumed that the olefin derivative 11 can undergo homoallylic conjugation, which may lead to electronically equivalent 2-nitronaphthalene.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.