Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Tetsuji Nunozawa"'
Autor:
Tetsuji Nunozawa, Shigeo Nozoe, Tomihisa Ohta, Tsutomu Agatsuma, Tadashi Endo, Atsushi Takahashi
Publikováno v:
ChemInform. 25
Five new chlorinated phenyl ethers, russuphelins B (2), C (3), D (4), E (5) and F (6) have been isolated from the mushroom Russula subnigricans Hongo, and their structures were elucidated by spectroscopic and chemical means. Russuphelins B (2), C (3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00c8c83cd1ba6d1bb8ddf9e5aa1f71d1
https://doi.org/10.1002/chin.199419307
https://doi.org/10.1002/chin.199419307
Russuphelins B, C, D, E and F, new cytotoxic substances from the mushroom Russula subnigricans Hongo
Autor:
Tetsuji Nunozawa, Tadashi Endo, Shigeo Nozoe, Tsutomu Agatsuma, Tomihisa Ohta, Atsushi Takahashi
Publikováno v:
Chemicalpharmaceutical bulletin. 41(10)
Five new chlorinated phenyl ethers, russuphelins B (2), C (3), D (4), E (5) and F (6) have been isolated from the mushroom Russula subnigricans Hongo, and their structures were elucidated by spectroscopic and chemical means. Russuphelins B (2), C (3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eec62a0417d183de4d93abe4fd70ff7f
https://pubmed.ncbi.nlm.nih.gov/8281571
https://pubmed.ncbi.nlm.nih.gov/8281571
Autor:
Tetsuji Nunozawa, Shigeo Nozoe, Tomihisa Ohta, Mamoru Matsuda, Tsutomu Agatsuma, Takeshi Endo, Akira Takahashi
Publikováno v:
Chemicalpharmaceutical bulletin. 40(12)
A new cytotoxic substance, designated russuphelin A (1), has been isolated from the mushroom Russula subnigricans HONGO(Basidiomycetes). The structure was elucidated as 2, 6-bis(2, 6-dichloro-4-hydroxyphenyloxy)-1, 4-dimethoxy-benzene on the basis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f136f919f164f437b65177fc44f51d3
https://pubmed.ncbi.nlm.nih.gov/1294320
https://pubmed.ncbi.nlm.nih.gov/1294320
Publikováno v:
Chemical and Pharmaceutical Bulletin. 40:1313-1314
1-β-D-Arabinofuranosylcytosine (ara-C), an anticancer drug, has been isolated for the first time from a natural source, the mushroom Xerocomus nigromaculatus HONGO.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::362e14f0740c0f0429acdcdca4229d2a
https://doi.org/10.1248/cpb.40.1313
https://doi.org/10.1248/cpb.40.1313
Publikováno v:
Tetrahedron Letters. 20:1683-1686
Asymmetric reduction of α-ketoester with a chiral dihydronicotinamide was significantly affected by chiral aromatic additives, capable of exerting an attractive interaction with dihydropyridine ring, which was further consolidated through with magne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f34ea39f885a9b618fcb0b53bc1952c
https://doi.org/10.1016/s0040-4039(01)93623-8
https://doi.org/10.1016/s0040-4039(01)93623-8
Autor:
Takashi Honda, Hiroshi Murasaki, Eiichi Nakajima, Toru Komai, Yukio Matsubara, Hiroshi Kozuka, Tetsuji Nunozawa, Shigeto Fujishita
Publikováno v:
Drug Metabolism and Pharmacokinetics. 3:275-285
The blood and plasma levels, distribution and excretion of S-adenosyl-L-methionine sulfate tosylate (FO-1561) were studied in rats afer intravenous administration of [CH3-14C] FO-1561. 1. After intravenous administration of 10 mg/kg to rats, the bloo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9284029641967e9b08482ea4347592d4
https://doi.org/10.2133/dmpk.3.275
https://doi.org/10.2133/dmpk.3.275
Autor:
Tetsuji Nunozawa, Toru Komai, Takashi Honda, Yukio Matsubara, Hiroshi Murasaki, Hiroshi Kozuka, Shigeto Fujishita
Publikováno v:
Drug Metabolism and Pharmacokinetics. 3:287-300
The biotransformation of S-adenosyl-L-methionine sulfate tosylate (FO-1561) was studied in rats after intravenous administration of 14C-labeled FO-1561 at a dose of 10 mg (as S-adenosyl-L-methionine)/kg. 1. After intravenous administration of [Ade-8-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9ce9db240b95c9046e217b6e9b158cf
https://doi.org/10.2133/dmpk.3.287
https://doi.org/10.2133/dmpk.3.287
Publikováno v:
Chemical and Pharmaceutical Bulletin. 28:920-925
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8a6ebbdb8d33112a31e9d7b6cbfc8d7
https://doi.org/10.1248/cpb.28.920
https://doi.org/10.1248/cpb.28.920
Publikováno v:
Chemical and Pharmaceutical Bulletin. 28:3223-3231
Grignard reaction of 2, 3, 4-tri-O-benzyl-D-xylopyranose yielded a single product with very high stereoselectivity. A threo relationship of the newly created chiral center with respect to C2 was established by converting the product into the δ-lacto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7dcf132df0f66482531a4046a5d1734
https://doi.org/10.1248/cpb.28.3223
https://doi.org/10.1248/cpb.28.3223
Publikováno v:
Chemical and Pharmaceutical Bulletin. 34:4859-4861
4-Acetylamino-2-hydroxylaminotoluene (4AA2HAT) and 2-hydroxylamino-6-nitrotoluene (2HA6NT) were prepared from 4-acetylamino-2-nitrotoluene (4AA2NT) and 2, 6-dinitrotoluene (2, 6-DNT), respectively, by reduction with zinc dust and NH4Cl. 2, 6-Dinitrob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44bce9b47714c70cc50ff2660524b5d9
https://doi.org/10.1248/cpb.34.4859
https://doi.org/10.1248/cpb.34.4859