Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Tetsuko Hase"'
Publikováno v:
Chemischer Informationsdienst. 14
In order to study the structure-activity relationship of sparsomycin, an antitumor antibiotic, 26 sparsomycin-related compounds (3-5) were synthesized and their antibacterial activities and lytic actions on Ehrlich ascites carcinoma cells were tested
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edf0fb53998f050221c610009ba4e0ec
https://doi.org/10.1002/chin.198333246
https://doi.org/10.1002/chin.198333246
Publikováno v:
Chemicalpharmaceutical bulletin. 32(11)
In order to study the structure-activity relationship of sparsomycin, an antitumor antibiotic, 26 sparsomycin analogs (3-5) were synthesized and their antibacterial activities and lytic actions on Ehrlich ascites carcinoma cells were tested. It was f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5edeb54e0ee2f7a266ecd9fbc493bcf3
https://pubmed.ncbi.nlm.nih.gov/6532561
https://pubmed.ncbi.nlm.nih.gov/6532561
Sparsomycin analogs. II. Synthesis and biological activities of 5-carboxy-6-methyluracil derivatives
Publikováno v:
Chemicalpharmaceutical bulletin. 31(1)
In order to study the structure-activity relationship of sparsomycin, an antitumor antibiotic, 26 sparsomycin-related compounds (3-5) were synthesized and their antibacterial activities and lytic actions on Ehrlich ascites carcinoma cells were tested
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ce7d3da9c146eb1ab2476e0fd72931f
https://pubmed.ncbi.nlm.nih.gov/6850930
https://pubmed.ncbi.nlm.nih.gov/6850930
Autor:
Akimori Wada, S. Kanatomo, S. Fukuda, M. Yomei, Sotoo Nagai, M. Tanaka, Tetsuko Hase, Takuma Sasaki
Publikováno v:
ChemInform. 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ad50e39bc3088db78402396c72cfd05
https://doi.org/10.1002/chin.198903282
https://doi.org/10.1002/chin.198903282
Autor:
Sotoo Nagai, Takuma Sasaki, Motohiro Tanaka, Kazuhiro Ohki, Shoichi Kanatomo, Tetsuko Hase, Akimori Wada
Publikováno v:
Chemicalpharmaceutical bulletin. 37(3)
Five sparsomycin analogs (9-13) were prepared and examined for their ability to inhibit deoxyribonucleic acid (DNA) synthesis in L5178Y lymphoma cells. All of the compounds showed significant activity in the DNA synthesis assay. The compounds having
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::200c42a8dd2797a8fad626bdec8f782c
https://pubmed.ncbi.nlm.nih.gov/2752478
https://pubmed.ncbi.nlm.nih.gov/2752478
Publikováno v:
Chemischer Informationsdienst. 12
Methods for the synthesis of 5-carboxy-6-methyluracil (9), which is expected to be useful as an intermediate for the preparation of sparsomycin analogs, were investigated. A new route that leads to 9 from cyanoacetylurea (5) via 2-cyano-3-oxobutanoyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efc3161cb8e22f134f2e787491c7111b
https://doi.org/10.1002/chin.198125258
https://doi.org/10.1002/chin.198125258
Autor:
Tetsuko Hase, Sotoo Nagai, Shizuo Fukuda, Motohiro Tanaka, Masakatsu Yomei, Akimori Wada, Takuma Sasaki, Shoichi Kanatomo
Publikováno v:
Chemicalpharmaceutical bulletin. 36(6)
Synthese et etude biologique des composes du titre N-substitues par carboxy-1'-, methoxycarbonyl-1'- ou hydroxymethyl-1' alkyl, la partie pyrimidine etant elle-meme substituee par dimethoxy-2,4 methyl-6 ou dioxo-1,3 tetrahydro-1,2,3,4 trimethyl-1,3,6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::886a9f072efee57ba79c7b5379560c81
https://pubmed.ncbi.nlm.nih.gov/3240439
https://pubmed.ncbi.nlm.nih.gov/3240439
Publikováno v:
Synthesis. 1986:555-556
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54cdbc83e0c6a75699cec3192cd2bdf9
https://doi.org/10.1055/s-1986-31699
https://doi.org/10.1055/s-1986-31699