Zobrazeno 1 - 10
of 246
pro vyhledávání: '"Morifusa Eto"'
Publikováno v:
International Journal of Molecular Sciences, Vol 3, Iss 2, Pp 56-68 (2002)
Abstract: Three-dimensional pharmacophore hypotheses were built from a set of 10 octopamine (OA) agonist 1-arylimidazole-2(3H)-thiones (AIHTs) and 1-arylimidazolidine-2-thiones (AITs). Among the ten common-featured models generated by program Catalys
Externí odkaz:
https://doaj.org/article/a079a05af16a497db8d82eedf5002785
Publikováno v:
Journal of Insect Science, Vol 3, p 10 (2003)
The compounds 1-(2,6-diethylphenyl)imidazolidine-2-thione and 2-(2,6-diethylphenyl)imidazolidine showed the almost same activity as octopamine in stimulating adenylate cyclase of cockroach thoracic nervous system among 70 octopamine agonists, suggest
Externí odkaz:
https://doaj.org/article/3aaac26e6317474c98116d7da39a8d55
Autor:
Gunter Zweig, Morifusa Eto
In order to get a general concept of organophosphorus pesticides with such a variety in structure and biological activities, consideration of each aspect of chemistry, biochemistry, and the applied sciences is necessary. This book consists of these t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9acd138622ba01ecdad4e47c55c660a
https://doi.org/10.1201/9781351075305
https://doi.org/10.1201/9781351075305
Autor:
Rong Tsao, Morifusa Eto
Publikováno v:
Aquatic and Surface Photochemistry ISBN: 9781351069847
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b37fe256f2bfebc2f739130a3050b11
https://doi.org/10.1201/9781351069847-12
https://doi.org/10.1201/9781351069847-12
Autor:
Morifusa Eto
In order to get a general concept of organophosphorus pesticides with such a variety in structure and biological activities, consideration of each aspect of chemistry, biochemistry, and the applied sciences is necessary. This book consists of these t
Publikováno v:
Bioscience, biotechnology, and biochemistry. 62(6)
3-(Substituted phenyl)imidazolidine-2-thiones (SPITs) and related compounds were synthesized by cyclizing monoethanolamine hydrogen sulfate with arylisothiocyanates in the presence of sodium hydroxide. The activity for stimulating adenylate cyclase p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76a10a605021d4a837a8a038cfe9a743
https://pubmed.ncbi.nlm.nih.gov/27388644
https://pubmed.ncbi.nlm.nih.gov/27388644
Autor:
Akinori Hirashima, Morifusa Eto
Publikováno v:
Bioscience, biotechnology, and biochemistry. 57(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa15ed44fd386fc92d464625de6cf2e2
https://pubmed.ncbi.nlm.nih.gov/27316902
https://pubmed.ncbi.nlm.nih.gov/27316902
Publikováno v:
Bioscience, biotechnology, and biochemistry. 57(2)
Diisopropyl dithiolanylidenemalonate (isoprothiolane) was oxidized with m-chloroperbenzoic acid to give a monosulfoxide, disulfoxide, and disulfone. The monosulfoxide was subjected to addition reactions with such nucleophiles as methanol, thiols, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f970a36bd211b50fcd93fccb1db95c6
https://pubmed.ncbi.nlm.nih.gov/27314784
https://pubmed.ncbi.nlm.nih.gov/27314784
Publikováno v:
Bioscience, biotechnology, and biochemistry. 56(5)
A number of N-acyl-L-proline derivatives were synthesized and their biological activities were investigated by using lettuce (Lactuca sativa L. cv. Sacramento) seedling test. A wide variety of these compounds promoted root growth at 25°C both under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::353d5ff97c6a962e94fc1bd8de04a9e4
https://pubmed.ncbi.nlm.nih.gov/27286207
https://pubmed.ncbi.nlm.nih.gov/27286207
Publikováno v:
Journal of Insect Physiology. 53:1242-1249
Tyramine (TA) increased significantly after mating, whereas there were no significant differences in octopamine (OA) and dopamine (DA) levels in the brain-suboesophageal ganglion (SOG) complexes between virgin and mated females. The effects of variou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2edcc41e7c16119f5b27be82b82d365
https://doi.org/10.1016/j.jinsphys.2007.06.018
https://doi.org/10.1016/j.jinsphys.2007.06.018