메뉴 건너뛰기




Volumn 19, Issue 5 B, 1999, Pages 3895-3899

Electronic structure and cytotoxic activity of 'half-mustard type' phenothiazines by MM3 and PM3 methods

Author keywords

'Half mustard type' phenothiazines; Cytotoxic activity; MM3 method; Multiple regression analysis; PM3 method

Indexed keywords

DNA; PHENOTHIAZINE DERIVATIVE;

EID: 0032763614     PISSN: 02507005     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (12)

References (11)
  • 1
    • 0345043563 scopus 로고    scopus 로고
    • Relationship between In vitro-in vivo antibacterial activity and theoretical calculation on "half-mustard type" phenothiazines
    • (Chakrabarty AN, Molnár J, Dastidar S and Motohashi N. eds). Chapter 21., New Delhi, NISCOM Publ.
    • Motohashi N, Kurihara T, Shampa G, Dastidar SG, Chakrabarti A, Chakrabarty AN and Molnár J. Relationship between In vitro-in vivo antibacterial activity and theoretical calculation on "half-mustard type" phenothiazines. In: Non Antibiotics: A new class of unrecognized antimicrobics(Chakrabarty AN, Molnár J, Dastidar S and Motohashi N. eds). Chapter 21., New Delhi, NISCOM Publ., 1998, pp246-261.
    • (1998) Non Antibiotics: A New Class of Unrecognized Antimicrobics , pp. 246-261
    • Motohashi, N.1    Kurihara, T.2    Shampa, G.3    Dastidar, S.G.4    Chakrabarti, A.5    Chakrabarty, A.N.6    Molnár, J.7
  • 3
    • 0344612611 scopus 로고    scopus 로고
    • Molecular orbital of cytotoxic "half-mustard type" phenothiazines
    • in press
    • Motohashi N, Kurihara T, Sakagami H and Molnár J: Molecular orbital of cytotoxic "half-mustard type" phenothiazines. Anti-cancer Res 19: in press, 1999.
    • (1999) Anti-cancer Res , vol.19
    • Motohashi, N.1    Kurihara, T.2    Sakagami, H.3    Molnár, J.4
  • 4
    • 0032763676 scopus 로고    scopus 로고
    • Relationship between cytotoxic activity and dipole moment for phthalimido- and chloroethyl-phenothiazines
    • in press
    • Kurihara T, Motohashi N, Sakagami H and Molnár J: Relationship between cytotoxic activity and dipole moment for phthalimido- and chloroethyl-phenothiazines. Anticancer Res 19: in press, 1999.
    • (1999) Anticancer Res , vol.19
    • Kurihara, T.1    Motohashi, N.2    Sakagami, H.3    Molnár, J.4
  • 6
    • 0029966193 scopus 로고    scopus 로고
    • Synthesis and antitumor activity of 1-(2-chloroethyl)-3-(2-substituted-10H-phenothiazin-10-yl)alkylurea as potential anticancer agents
    • Motohashi N, Kawase M, Kurihara T, Hevér A, Nagy S, Oscovski I, Tanaka M and Molnár J: Synthesis and antitumor activity of 1-(2-chloroethyl)-3-(2-substituted-10H-phenothiazin-10-yl)alkylurea as potential anticancer agents. Anticancer Res 16: 2525-2532, 1996.
    • (1996) Anticancer Res , vol.16 , pp. 2525-2532
    • Motohashi, N.1    Kawase, M.2    Kurihara, T.3    Hevér, A.4    Nagy, S.5    Oscovski, I.6    Tanaka, M.7    Molnár, J.8
  • 11
    • 84986492477 scopus 로고
    • Atomic charges derived from semi-empirical method
    • Berler BH, Merz KM and Kollman PA: Atomic charges derived from semi-empirical method. J Comp Chem 11: 431-439, 1990.
    • (1990) J Comp Chem , vol.11 , pp. 431-439
    • Berler, B.H.1    Merz, K.M.2    Kollman, P.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.