Zobrazeno 1 - 10
of 68
pro vyhledávání: '"SHUNSAKU NOGUCHI"'
Autor:
Shunsaku Noguchi, Takashi Ishizu
Publikováno v:
Chemical and Pharmaceutical Bulletin. 46:1303-1307
Cyclo(Phe-Pro) 4 (1) formed a 1:1 complex with noradrenaline hydrochloride (NAd.HCl) through intermolecular hydrogen bonds and a hydrophobic effect. The formation constant of the 1:1 complex of 1 with l-NAd.HCl was approximately 12.3 times that of th
Publikováno v:
Chemical and Pharmaceutical Bulletin. 42:1567-1570
Steroid-17α-hydroxy-17-carboxylic acids (2) were allowed to react with carbodiimides (DCCI, DPCI, DTCI, EDCI) to afford 17-spiro-5'-[2'-imino-4'-oxazolidinones] (3-5, 11), 17-spiro-5'-[2', 4'-oxazolidinediones] (7-9)and N-acylureas (10), depending o
Publikováno v:
ChemInform. 26
Steroid-17α-hydroxy-17-carboxylic acids (2) were allowed to react with carbodiimides (DCCI, DPCI, DTCI, EDCI) to afford 17-spiro-5'-[2'-imino-4'-oxazolidinones] (3-5, 11), 17-spiro-5'-[2', 4'-oxazolidinediones] (7-9)and N-acylureas (10), depending o
Publikováno v:
ChemInform. 29
The ginseng tetrapeptide H-L-Val-γ-D-Gly-D-Arg-Gly-OH (1) was synthesized using a solution-phase methodology, and its solution conformation in dimethyl sulfoxide (DMSO)-d 6 was determined by a combination of NMR and computational techniques with the
Autor:
Shunsaku Noguchi, Takashi Ishizu
Publikováno v:
Chemical and Pharmaceutical Bulletin. 45:1202-1204
The formation constant of the 1 : 1 complex of cyclo(L-Phe-L-Pro)4 (1) with L-PheOMe·HCl was about 13.2 times that of the complex with D-PheOMe·HCl. The 1 : 1 complex of 1 with L-PheOMe·HCl formed three intermolecular hydrogen bonds between Pro2 C
Publikováno v:
Chemical and Pharmaceutical Bulletin. 42:1146-1148
The 13C-NMR spectrum of cyclo(L-Phe-L-Pro)4 (1) and DL-noradrenaline hydrochloride (DL-NA·HCl) in a mixture of CDCl3 and CD3OD suggested the formation of a complex, which was demonstrated to be 1 : 1 from examination of the titration curves. The com
Autor:
Jungo Hirayama, Takashi Ishizu, Shunsaku Noguchi, Hiroyuki Iwamoto, Junzo Hirose, Keitaro Hiromi
Publikováno v:
Chemical and Pharmaceutical Bulletin. 41:2029-2031
Cyclic octapeptides, cyclo[L-Tyr(Bzl)-L-Pro]4 (2) and cyclo(L-Tyr-L-Pro)4 (3), were prepared and their conformations investigated. A C2-symmetric conformation containing two cis peptide bonds was found in 2 in CDCl3 and 3 in CD3OD. Cyclo(L-Phe-L-Pro)
Publikováno v:
Chemical and Pharmaceutical Bulletin. 39:1617-1619
The 13C-NMR spectrum (Fig. 2,1) of cyclooctapeptide cyclo(L-phe-L-Pro-Gly-L-Pro)2 (A) in CDC13 suggested that its conformation involved the coexistence of two kinds of C2-symmetric conformation with trans-trans-trans-trans and cis-trans-trans-trans f
Publikováno v:
Planta medica. 62(2)
The configurations of the component amino acids in ginseng tetrapeptide 1 isolated from Panax ginseng were determined by HPLC with an optical resolution column and the structure of 1 was established to be H-L-Val-gamma-D-Glu-D-Arg- Gly-OH. Synthesis
Publikováno v:
Chemicalpharmaceutical bulletin. 41(2)
Analyses of the 1H- and 13C-nuclear magnetic resonance (1H- and 13C-NMR) spectra of the cyclooctapeptide cyclo (L-Phe-L-Pro-Gly-L-Pro)2 (3) in CDCl3 with the aid of the C-H correlated spectroscopy (C-H COSY) two-dimensional NMR spectrum (Fig. 2) sugg