Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Aika Kai"'
Autor:
Natsumi Inada, Yuki Hitora, Momona Sebe, Aika Kai, Mika Nagaki, Yuka Maeyama, Sachiko Tsukamoto, Robert M. Williams, Yukihiko Sugimoto, Tomoaki Inazumi, Jens Christian Frisvad, Ahmed H. El-Desoky, Keisuke Eguchi, Hikaru Kato
Publikováno v:
Journal of Natural Products. 84:2475-2485
Fifteen new isopimarane-type diterpenes, taichunins E-S (1-15), and a new 20-nor-isopimarane, taichunin T (16), together with four known compounds were isolated from Aspergillus taichungensis (IBT 19404). The structures of these new compounds were de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9471e7e7f03dbe0fca89445e7e2f2d1
https://doi.org/10.1021/acs.jnatprod.1c00486
https://doi.org/10.1021/acs.jnatprod.1c00486
Autor:
Ahmed H H, El-Desoky, Natsumi, Inada, Yuka, Maeyama, Hikaru, Kato, Yuki, Hitora, Momona, Sebe, Mika, Nagaki, Aika, Kai, Keisuke, Eguchi, Tomoaki, Inazumi, Yukihiko, Sugimoto, Jens C, Frisvad, Robert M, Williams, Sachiko, Tsukamoto
Publikováno v:
Journal of natural products. 84(9)
Fifteen new isopimarane-type diterpenes, taichunins E-S (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e03f6239c25aa63d8c54d125b4e66a04
https://pubmed.ncbi.nlm.nih.gov/34464116
https://pubmed.ncbi.nlm.nih.gov/34464116
Autor:
Sherman, David H., Williams, Robert M., Aika, Kai, Hikaru, Kato, David H., Sherman, Robert M. , Williams, Sachiko, Tsukamoto
Publikováno v:
Tetrahedron Letters. 59(48):4236-4240
A new prenylated indoxyl alkaloid, Amoenamide B (1), was isolated from Aspergillus amoenus NRRL 35600 along with Asperochramide A (2). Although many prenylated oxyindole alkaloids, containing bicyclo[2.2.2]diazaoctane cores, have been isolated from t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9a6ac8a3303cd157e4a34d02cf53584
http://hdl.handle.net/2298/00043534
http://hdl.handle.net/2298/00043534
Autor:
Sunderhaus, James D., McAfoos, Timothy J., Finefield, Jennifer M., Williams, Robert M., Hikaru, Kato, Aika, Kai, Tetsuro, Kawabata, ames D. , SunderhausJ, Timothy J. , McAfoos, Jennifer M. , Finefield, Yukihiko, Sugimoto, Robert M. , Williams, Sachiko, Tsukamoto
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 27(22):4975-4978
The marine-derived Aspergillus protuberus MF297-2 and the terrestrial A. amoenus NRRL 35600 produce enantiomeric prenylated indole alkaloids. Investigation of biological activities of the natural and synthetic derivatives revealed that (−)-enantiom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8da2fbb1bb1af4636d561fe78f2bdeda
http://hdl.handle.net/2298/00043544
http://hdl.handle.net/2298/00043544
Publikováno v:
Tetrahedron letters. 50(48)
A new prenylated indoxyl alkaloid, Amoenamide B (1), was isolated from Aspergillus amoenus NRRL 35600 along with Asperochramide A (2). Although many prenylated oxyindole alkaloids, containing bicyclo[2.2.2]diazaoctane cores, have been isolated from t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::39b8c0180147481902074802ae3658af
https://pubmed.ncbi.nlm.nih.gov/30765898
https://pubmed.ncbi.nlm.nih.gov/30765898
Autor:
Robert M. Williams, Aika Kai, Jennifer M. Finefield, Tetsuro Kawabata, Sachiko Tsukamoto, Yukihiko Sugimoto, James D. Sunderhaus, Hikaru Kato, Timothy J. McAfoos
Publikováno v:
Bioorganicmedicinal chemistry letters. 28(14)
The marine-derived Aspergillus protuberus MF297-2 and the terrestrial A. amoenus NRRL 35600 produce enantiomeric prenylated indole alkaloids. Investigation of biological activities of the natural and synthetic derivatives revealed that (−)-enantiom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cf227ce0c0d52677feca41bc321793d
https://pubmed.ncbi.nlm.nih.gov/29037945
https://pubmed.ncbi.nlm.nih.gov/29037945
Autor:
Hikaru Kato, Sachiko Tsukamoto, Nicole J. de Voogd, Esther D. Angkouw, Aika Kai, Yuki Hitora, Arina Fukumoto, Remy E. P. Mangindaan
Publikováno v:
HETEROCYCLES. 97:1219
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::402bdbf3552f6d263c8a1c3c0a0d62e8
https://doi.org/10.3987/com-18-s(t)73
https://doi.org/10.3987/com-18-s(t)73