Zobrazeno 1 - 10
of 43
pro vyhledávání: '"SHOJI KISHIMOTO"'
Publikováno v:
Chemical and Pharmaceutical Bulletin. 43:588-593
The spiro-epoxy group of fumagillol (2) was selectively modified and several analogues of AGM-1470 (3) with a (dialkyl)-β-hydroxyethylsulfonium moiety were prepared. These analogues were found to inhibit angiogenesis induced by basic fibroblast grow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe25507974cb93005fd8f1e38a93f314
https://doi.org/10.1248/cpb.43.588
https://doi.org/10.1248/cpb.43.588
Autor:
Shoji, Kishimoto
Publikováno v:
Kyobu geka. The Japanese journal of thoracic surgery. 65(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f3b3f6aeecebde999c0cbf4a9d573179
https://pubmed.ncbi.nlm.nih.gov/22479724
https://pubmed.ncbi.nlm.nih.gov/22479724
Autor:
Norikazu Tamura, Yoshihiro Matsushita, Toshi Iwama, Katsumi Itoh, Shoji Kishimoto, Setsuo Harada
Publikováno v:
ChemInform. 23
(S)-2-Amino-3-(2,5-dihydro-5-oxo-4-isoxazolyl)propanoic acid (TAN-950 A (1)) is a novel amino acid antibiotic which shows a high affinity for glutamate receptors of the central nervous system. To improve the affinity for glutamate receptors, the stru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f416940f0797cfb3a3579bc88c75d8f
https://doi.org/10.1002/chin.199215315
https://doi.org/10.1002/chin.199215315
Publikováno v:
ChemInform. 26
Tripeptide analogues 2 and 3 containing a dioxoethylene moiety were designed based on the characteristic structure of the naturally occurring human immunodeficiency virus (HIV)-1 protease inhibitors RPI-856 A, B, C and D (1). The compounds (2, 3) pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad550566afcd1b92a239fdf91e511769
https://doi.org/10.1002/chin.199535245
https://doi.org/10.1002/chin.199535245
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f2ee59f7840f7973bcf524e4186f0dc
https://doi.org/10.1002/chin.199545266
https://doi.org/10.1002/chin.199545266
Autor:
Shoji Kishimoto, Shogo Marui
Publikováno v:
Chemical and Pharmaceutical Bulletin. 40:575-579
6-Amino-6-deoxyfumagillol (5) was synthesized by reductive amination of 6-oxo-6-deoxyfumagillol (4), which was obtained by oxidation of fumagillol (2). The reduction proceeded stereoselectively by the equatorial attack of hydride and 5 was found to h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43978bd3e90004c32cf7eccb0b18839d
https://doi.org/10.1248/cpb.40.575
https://doi.org/10.1248/cpb.40.575
Autor:
Judah Folkman, Shoji Kishimoto, Takeshi Fujita, Harold Brem, Katsuichi Sudo, Tsuneo Kanamaru, Donald E. Ingber
Publikováno v:
Nature. 348:555-557
Neovascularization is critical for the growth of tumours and is a dominant feature in a variety of angiogenic diseases such as diabetic retinopathy, haemangiomas, arthritis and psoriasis. Recognition of the potential therapeutic benefit of controllin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ede6acd4315158cad82bd8055d12b20
https://doi.org/10.1038/348555a0
https://doi.org/10.1038/348555a0
Publikováno v:
31st Joint Propulsion Conference and Exhibit.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3595aaaf34b87892e9054a2ee2c61707
https://doi.org/10.2514/6.1995-2872
https://doi.org/10.2514/6.1995-2872
Publikováno v:
Chemicalpharmaceutical bulletin. 40(1)
The hydroxy group of fumagillol (3), a degradation product of fumagillin (1), was acylated, sulfonylated, alkylated or carbamoylated, and the anti-angiogenic activity of the resulting products was examined. These compounds inhibited the angiogenesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85f29bdff9b8d3dee7104bedc5b9e527
https://pubmed.ncbi.nlm.nih.gov/1374294
https://pubmed.ncbi.nlm.nih.gov/1374294
Autor:
Toshi Iwama, Shoji Kishimoto, Setsuo Harada, Yoshihiro Matsushita, Katsumi Itoh, Norikazu Tamura
Publikováno v:
Chemicalpharmaceutical bulletin. 39(5)
(S)-2-Amino-3-(2,5-dihydro-5-oxo-4-isoxazolyl)propanoic acid (TAN-950 A (1)) is a novel amino acid antibiotic which shows a high affinity for glutamate receptors of the central nervous system. To improve the affinity for glutamate receptors, the stru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be75cafff310b739bea239a329e701a2
https://pubmed.ncbi.nlm.nih.gov/1655291
https://pubmed.ncbi.nlm.nih.gov/1655291