Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Naomi Daikuhara"'
Autor:
Takatoshi Kawai, Takashi Owa, Rie Ushijima-Sugano, Naomi Daikuhara, Masashi Yokoya, Kornvika Charupant, Naoki Saito, Khanit Suwanborirux
Publikováno v:
Marine Drugs, Vol 7, Iss 4, Pp 483-494 (2009)
Renieramycin M and jorunnamycin C, two isoquinolinequinone compounds differing only at the C-22 ester side chain, were evaluated for their cytotoxic effects on human colon (HCT116) and breast (MDA-MB-435) cancer cell lines. These two compounds displa
Externí odkaz:
https://doaj.org/article/1ab5f9a6bb3a4e7f906338e16e12f16a
Autor:
Surattana Amnuoypol, Emi Saito, Kornvika Charupant, Naomi Daikuhara, Khanit Suwanborirux, Naoki Saito, Takashi Owa
Publikováno v:
Bioorganic & Medicinal Chemistry. 17:4548-4558
Twenty-four ester analogues of renieramycin M (1m) were prepared from jorunnamycin A (3a), which was easily transformed from marine natural 1m in three steps. These analogues, along with 1m itself, cyanojorumycin (2b), and jorunnamycins A (3a) and C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52454db5b4119ca98d43b90bbae2f9e6
https://doi.org/10.1016/j.bmc.2009.05.009
https://doi.org/10.1016/j.bmc.2009.05.009
Autor:
Kornvika Charupant, Khanit Suwanborirux, Naoki Saito, Sachiyo Yamaki, Surattana Amnuoypol, Yumiko Tada, Naomi Daikuhara
Publikováno v:
Tetrahedron Letters. 50:4276-4278
Two new bistetrahydroisoquinoline marine natural products, renieramycins T ( 1 ) and U ( 2 ), were isolated from the Thai blue sponge Xestospongia sp. and their structures were elucidated by comparing spectral data with those of renieramycin M ( 3a )
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68bead2a99245fc71a45e8478cb0efad
https://doi.org/10.1016/j.tetlet.2009.05.014
https://doi.org/10.1016/j.tetlet.2009.05.014
Autor:
Naoki Saito, Naomi Daikuhara, Rie Ushijima-Sugano, Masashi Yokoya, Kornvika Charupant, Takatoshi Kawai, Takashi Owa, Khanit Suwanborirux
Publikováno v:
Marine Drugs
Marine Drugs, Vol 7, Iss 4, Pp 483-494 (2009)
Marine Drugs, Vol 7, Iss 4, Pp 483-494 (2009)
Renieramycin M and jorunnamycin C, two isoquinolinequinone compounds differing only at the C-22 ester side chain, were evaluated for their cytotoxic effects on human colon (HCT116) and breast (MDA-MB-435) cancer cell lines. These two compounds displa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8033349a81f6e5f820304ca99bd8fda8
https://pubmed.ncbi.nlm.nih.gov/20098592
https://pubmed.ncbi.nlm.nih.gov/20098592
Publikováno v:
ChemInform. 39
The two-step transformation of saframycin G (9) into saframycin F (1b) and renieramycin O (11) into renieramycin Q (2) is described, along with the results of cytotoxicity studies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfc1db95ed4ec8605eb462e6b2cd1b11
https://doi.org/10.1002/chin.200826217
https://doi.org/10.1002/chin.200826217
Publikováno v:
HETEROCYCLES. 86:317
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::704ee5a45cfcea95eaf1eae8fc4e295f
https://doi.org/10.3987/com-12-s(n)12
https://doi.org/10.3987/com-12-s(n)12
Publikováno v:
HETEROCYCLES. 74:411
The two-step transformation of saframycin G (9) into saframycin F (1b) and renieramycin O (11) into renieramycin Q (2) is described, along with the results of cytotoxicity studies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1f5eb78412399813b6b28aaf9ceaddb
https://doi.org/10.3987/com-07-s(w)20
https://doi.org/10.3987/com-07-s(w)20