120 related articles for article (PubMed ID: 20150627)
1. Quantitative structure-cytotoxicity relationship of newly synthesized tropolones determined by a semiempirical molecular-orbital method (PM5).
Ishihara M; Wakabayashi H; Motohashi N; Sakagami H
Anticancer Res; 2010 Jan; 30(1):129-33. PubMed ID: 20150627
[TBL] [Abstract][Full Text] [Related]
2. Estimation of relationship between the structure of trihaloacetylazulene derivatives determined by a semiempirical molecular-orbital method (PM5) and their cytotoxicity.
Ishihara M; Wakabayashi H; Motohashi N; Sakagami H
Anticancer Res; 2010 Mar; 30(3):837-41. PubMed ID: 20393004
[TBL] [Abstract][Full Text] [Related]
3. Estimation of relationship between structure of newly synthesized dihydroimidazoles determined by a semiempirical molecular-orbital method and their cytotoxicity.
Takekawa F; Sakagami H; Ishihara M
Anticancer Res; 2009 Dec; 29(12):5019-22. PubMed ID: 20044611
[TBL] [Abstract][Full Text] [Related]
4. Quantitative structure-cytotoxicity relationship analysis of 5-trifluoromethyloxazole derivatives by a semiempirical molecular-orbital method with the concept of absolute hardness.
Ishihara M; Kawase M; Sakagami H
Anticancer Res; 2008; 28(2A):997-1003. PubMed ID: 18507047
[TBL] [Abstract][Full Text] [Related]
5. Estimation of relationship between descriptors and cytotoxicity of newly synthesized 1,2,3,4-tetrahydroisoquinoline derivatives.
Ishihara M; Hatano H; Takekawa F; Kawase M; Sakagami H
Anticancer Res; 2009 Oct; 29(10):4077-82. PubMed ID: 19846954
[TBL] [Abstract][Full Text] [Related]
6. Quantitative structure-cytotoxicity relationship analysis of coumarin and its derivatives by semiempirical molecular orbital method.
Ishihara M; Yokote Y; Sakagami H
Anticancer Res; 2006; 26(4B):2883-6. PubMed ID: 16886609
[TBL] [Abstract][Full Text] [Related]
7. Quantitative structure-activity relationship analysis of 4-trifluoromethylimidazole derivatives with the concept of absolute hardness.
Ishihara M; Kawase M; Sakagami H
Anticancer Res; 2007; 27(6B):4047-51. PubMed ID: 18225569
[TBL] [Abstract][Full Text] [Related]
8. Estimation of relationship between the structure of 1,2,3,4-tetrahydroisoquinoline derivatives determined by a semiempirical molecular-orbital method and their cytotoxicity.
Ishihara M; Hatano H; Kawase M; Sakagami H
Anticancer Res; 2009 Jun; 29(6):2265-71. PubMed ID: 19528491
[TBL] [Abstract][Full Text] [Related]
9. Quantitative structure-cytotoxicity relationship analysis of 3-formylchromone derivatives by a semiempirical molecular-orbital method with the concept of absolute hardness.
Ishihara M; Sakagami H
Anticancer Res; 2008; 28(1A):277-81. PubMed ID: 18383857
[TBL] [Abstract][Full Text] [Related]
10. QSAR of molecular structure and cytotoxic activity of vitamin K2 derivatives with concept of absolute hardness.
Ishihara M; Sakagami H
Anticancer Res; 2007; 27(6B):4059-63. PubMed ID: 18225571
[TBL] [Abstract][Full Text] [Related]
11. Quantitative structure-cytotoxicity relationship of newly synthesised trihaloacetylazulenes determined by a semi-empirical molecular-orbital method (PM5).
Ishihara M; Wakabayashi H; Motohashi N; Sakagami H
Anticancer Res; 2011 Feb; 31(2):515-20. PubMed ID: 21378332
[TBL] [Abstract][Full Text] [Related]
12. Relationship between electronic structure and cytotoxic activity of tropolones.
Kurihara T; Mine H; Satoh Y; Wakabayashi H; Motohashi N; Sakagami H
In Vivo; 2006; 20(3):391-5. PubMed ID: 16724677
[TBL] [Abstract][Full Text] [Related]
13. Estimation of gas-phase reaction rate constants of alkylnaphthalenes with chlorine, hydroxyl and nitrate radicals.
Long X; Niu J
Chemosphere; 2007 May; 67(10):2028-34. PubMed ID: 17239921
[TBL] [Abstract][Full Text] [Related]
14. QSPR study on the bioconcentration factors of nonionic organic compounds in fish by characteristic root index and semiempirical molecular descriptors.
Saçan MT; Erdem SS; Ozpinar GA; Balcioglu IA
J Chem Inf Comput Sci; 2004; 44(3):985-92. PubMed ID: 15154766
[TBL] [Abstract][Full Text] [Related]
15. Quantitative structure-activity relationship analysis of cytotoxicity and anti-UV activity of 2-aminotropones.
Sekine S; Shimodaira C; Uesawa Y; Kagaya H; Kanda Y; Ishihara M; Amano O; Sakagami H; Wakabayashi H
Anticancer Res; 2014 Apr; 34(4):1743-50. PubMed ID: 24692705
[TBL] [Abstract][Full Text] [Related]
16. Quantitative structure-cytotoxicity relationship analysis of phenoxazine derivatives by semiempirical molecular-orbital method.
Ishihara M; Kawase M; Westman G; Samuelsson K; Motohashi N; Sakagami H
Anticancer Res; 2007; 27(6B):4053-7. PubMed ID: 18225570
[TBL] [Abstract][Full Text] [Related]
17. QSPR analysis of the toxicity of aromatic compounds to the algae (Scenedesmus obliquus).
Saçan MT; Ozkul M; Erdem SS
Chemosphere; 2007 Jun; 68(4):695-702. PubMed ID: 17360023
[TBL] [Abstract][Full Text] [Related]
18. Quantitative structure-activity relationship (QSAR) analysis of tumor-specificity of 1,2,3,4-tetrahydroisoquinoline derivatives.
Uesawa Y; Mohri K; Kawase M; Ishihara M; Sakagami H
Anticancer Res; 2011 Dec; 31(12):4231-8. PubMed ID: 22199286
[TBL] [Abstract][Full Text] [Related]
19. Quantitative structure-activity relationship for cyclic imide derivatives of protoporphyrinogen oxidase inhibitors: a study of quantum chemical descriptors from density functional theory.
Wan J; Zhang L; Yang G; Zhan CG
J Chem Inf Comput Sci; 2004; 44(6):2099-105. PubMed ID: 15554680
[TBL] [Abstract][Full Text] [Related]
20. Synthesis, antitumor evaluation, molecular modeling and quantitative structure-activity relationship (QSAR) of some novel arylazopyrazolodiazine and triazine analogs.
El-Shafei A; Fadda AA; Khalil AM; Ameen TA; Badria FA
Bioorg Med Chem; 2009 Jul; 17(14):5096-105. PubMed ID: 19527933
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
