Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Flavolipin"'
Autor:
Yannik K.-H. Schneider, Kine Ø. Hansen, Johan Isaksson, Sara Ullsten, Espen H. Hansen, Jeanette Hammer Andersen
Publikováno v:
Molecules, Vol 24, Iss 21, p 3991 (2019)
Two bacterial isolates from the Barents Sea, both belonging to the genus Algibacter, were found to yield extracts with anti-bacterial bioactivity. Mass spectrometry guided dereplication and purification of the active extracts lead to the isolation of
Externí odkaz:
https://doaj.org/article/b6b5882bd1594551a3af4dc63c4e8200
Akademický článek
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Publikováno v:
Tetrahedron. 54:15701-15710
Topostins B567 (2b) and D654 (3b) (WB-3559D, flavolipin) have been efficiently synthesized from 1, 10-decanediol (5) in 11 and 13 steps, respectively, involving an asymmetric hydrogenation of the β-keto ester14 using(R)-BINAP ruthenium bromide and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e65fe37f8ecf230fcf504b521685f1d0
https://doi.org/10.1016/s0040-4020(98)00984-3
https://doi.org/10.1016/s0040-4020(98)00984-3
Autor:
Yohko Kawai, Noriko Deguchi, Hideyuki Haruyama, Masahiro Nishijima, Masao Shiozaki, Tomio Ishikawa
Publikováno v:
Tetrahedron Letters. 39:4497-4500
The proposed structure of natural flavolipin was revised as N-[N-[(3R)-15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]glycyl]-L-serine as a result of synthetic study and biological activity test.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::701d68d9e9c3d4fc5643b9c7776f7567
https://doi.org/10.1016/s0040-4039(98)00798-9
https://doi.org/10.1016/s0040-4039(98)00798-9
Publikováno v:
ChemInform. 27
All four stereoisomers of flavolipin were synthesized from d -glucose in a stereocontrolled manner. None of them was identical with the reported natural product.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03451818d90507dcb008f092fea9dd80
https://doi.org/10.1002/chin.199638234
https://doi.org/10.1002/chin.199638234
Autor:
Noriko Deguchi, Yohko Kawai, Masao Shiozaki, Hideyuki Haruyama, Tomio Ishikawa, Masahiro Nishijima
Publikováno v:
ChemInform. 29
The proposed structure of natural flavolipin was revised as N-[N-[(3R)-15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]glycyl]-L-serine as a result of synthetic study and biological activity test.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c4e69e88e0acdd847055e7aa849d3d5
https://doi.org/10.1002/chin.199836277
https://doi.org/10.1002/chin.199836277
Autor:
Masahiro Nishijima, Noriko Deguchi, Masao Shiozaki, Yohko Kawai, Tomio Ishikawa, Hideyuki Haruyama, Takashi Mochizuki, Takanori Wakabayashi
Publikováno v:
ChemInform. 30
The proposed structure of natural flavolipin was revised as N-[N-[(3R)-15-methyl-3- (13-methyltetradecanoyloxy)hexadecanoyl]glycyl]-L-serine as a result of a synthetic study and biological activity tests, and its isomers were synthesized in a stereoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7367d39f26b58a1003218d484f1ecc6d
https://doi.org/10.1002/chin.199902245
https://doi.org/10.1002/chin.199902245
Publikováno v:
ChemInform. 30
Topostins B567 (2b) and D654 (3b) (WB-3559D, flavolipin) have been efficiently synthesized from 1, 10-decanediol (5) in 11 and 13 steps, respectively, involving an asymmetric hydrogenation of the β-keto ester14 using(R)-BINAP ruthenium bromide and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58976e441a8caf9950261a79029cb047
https://doi.org/10.1002/chin.199918223
https://doi.org/10.1002/chin.199918223
Publikováno v:
Journal of endotoxin research. 9(5)
We previously reported that Taxol™, which mimics the action of LPS on murine macrophages, induces signals via mouse TLR4/MD-2, but not via human TLR4/MD-2. Here we investigated the molecular basis for this species-specific action of Taxol™. Expre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::427d77faf0d3f58d99e61220f2f8a358
https://pubmed.ncbi.nlm.nih.gov/14577846
https://pubmed.ncbi.nlm.nih.gov/14577846
Autor:
Yannik Karl-Heinz Schneider, Jeanette Hammer Andersen, Sara Ullsten, Kine Østnes Hansen, Johan Isaksson, Espen Hansen
Publikováno v:
Molecules, Vol 24, Iss 21, p 3991 (2019)
Molecules
Volume 24
Issue 21
Molecules
Volume 24
Issue 21
Two bacterial isolates from the Barents Sea, both belonging to the genus Algibacter, were found to yield extracts with anti-bacterial bioactivity. Mass spectrometry guided dereplication and purification of the active extracts lead to the isolation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e46f5eec5e2073a8d3dcb61ee9ab749