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Dive into the research topics where Morifusa Eto is active.

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Featured researches published by Morifusa Eto.


Bioorganic & Medicinal Chemistry | 2002

Three-dimensional common-feature hypotheses for octopamine agonist 2-(arylimino)imidazolidines

Akinori Hirashima; Masako Morimoto; Eiichi Kuwano; Eiji Taniguchi; Morifusa Eto

Three-dimensional pharmacophore hypotheses were built from a set of 10 octopamine (OA) agonist 2-(Arylimino)imidazolidines (AIIs), 2-(Arylimino)thiazolidines (AITs) and 2-(Arylimino)oxazolidines (AIOs). Among the 10 common-featured models generated by program Catalyst/HipHop, a hypothesis including a ring aromatic (RA), a positive ionizable (PI) and three hydrophobic aliphatic (HpAl) features was considered to be important in evaluating the OA-agonist activity. Active OA agonist 2,6-Et2 AII mapped well onto all the RA, PI and HpAl features of the hypothesis. On the other hand, less active compounds were shown to be difficult to achieve the energetically favorable conformation which is found in the active molecules in order to fit the 3-D common-feature pharmacophore models. Taken together, 2,6-Et2-Ph and foramidine structures are important as OA agonists. The present studies on OA agonists demonstrate that a RA, a PI and three HpAl sites located on the molecule seem to be essential for OA-agonist activity.


Journal of Molecular Graphics & Modelling | 2002

Three-dimensional common-feature hypotheses for octopamine agonist arylethanolamines

Akinori Hirashima; Masako Morimoto; Eiichi Kuwano; Eiji Taniguchi; Morifusa Eto

Three-dimensional pharmacophore hypotheses were built from a set of 12 octopamine (OA) agonist arylethanolamines (AEAs). Among the 10 common-featured models generated by program catalyst/HipHop, a hypothesis including a hydrogen-bond donor (HBD) and a hydrogen-bond acceptor lipid (HBA1) features was considered to be important in evaluating the OA activity. OA mapped well onto all the HBD and HBA1 features of the hypothesis. On the other hand, for some inactive compounds, their lack of affinity is primarily due to their inability to achieve an energetically favorable conformation shared by the active compounds. Taken together, structures of a 4-OH-Ph, alpha-OH, and a primary amine are important for OA activities. The present studies on OA agonists demonstrate that an HBD and an HBA1 sites located on the molecule seem to be essential for OA activity.


Pest Management Science | 2001

Identification of novel inhibitors of calling and in vitro [14C]acetate incorporation by pheromone glands of Plodia interpunctella

Akinori Hirashima; Tomohiko Eiraku; Yasuyuki Watanabe; Eiichi Kuwano; Eiji Taniguchi; Morifusa Eto


International Journal of Molecular Sciences | 2002

Three-Dimensional Common-Feature Hypotheses for Octopamine Agonist 1-Arylimidazolidine-2-Thiones

Akinori Hirashima; Masako Morimoto; Hiroto Ohta; Eiichi Kuwano; Eiji Taniguchi; Morifusa Eto


Archive | 1987

1,5-Disubstituted imidazoles as inhibitors of juvenile hormone

Eiichi Kuwano; Ryuko Takeya; Morifusa Eto; Shoji Asano


Pest Management Science | 2002

Three‐dimensional common‐feature hypotheses of inhibitors of calling behaviour and in vitro [14C]acetate incorporation by pheromone glands of Plodia interpunctella

Akinori Hirashima; Tomohiko Eiraku; Yoko Shigeta; Eiichi Kuwano; Eiji Taniguchi; Morifusa Eto


講演要旨集 | 2002

B309 フェロモン分泌阻害剤の pharmacophore モデリング

明法 平島; 智彦 永楽; 陽子 茂田; 栄一 桑野; Eiji Taniguchi; Morifusa Eto


九州大学農学部紀要 | 1991

Effects of 1,5-Disubstituted Imidazoles on the Growth of Lettuce and Rice Seedlings

Masamichi Kikuchi; Eiichi Kuwano; Yukiko Nakashima; Morifusa Eto; 政道 菊池; 榮一 桑野; 守総 江藤


Archive | 1987

1,5-disubstituierte imizadole. 1,5-disubstituted imizadole.

Eiichi Kuwano; Ryuko Takeya; Morifusa Eto; Shoji Asano


Archive | 1987

1,5-di-substituted imizadole.

Eiichi Kuwano; Ryuko Takeya; Morifusa Eto; Shoji Asano

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