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Featured researches published by Iwao Miura.


Tetrahedron Letters | 1982

Constitution of two coloring matters in the flower petals of Carthamus Tinctorius L.

Yoshiyuki Takahashi; Nobutoshi Miyasaka; Shigeo Tasaka; Iwao Miura; Shiro Urano; Mitsuo Ikura; Kunio Hikichi; Takeshi Matsumoto; Mizu Wada

Abstract Structures of the safflower red pigment carthamin and the yellow pigment safflor yellow A are shown to be expressed by 3 and 4 respectively, mainly on the basis of spectroscopic evidence.


Phytochemistry | 1985

Drimane-type sesqui- and norsesquiterpenoids from polygonum hydropiper

Yoshiyasu Fukuyama; Tsuneo Sato; Iwao Miura; Yoshinori Asakawa

Abstract Polygonic acid, which shows weak anticomplement activity, has been isolated from leaves of Polygonum hydropiper together with four drimane-type sesquiterpenes, 11-ethoxycinnamolide, polygodial acetal, valdiviolide and fuegin and two drimane-type norsesquiterpenes, isopolygonal and polygonone.


Phytochemistry | 1984

Phthalides from the rhizome of Ligusticum wallichii

Wang Pushan; Gao Xuanliang; Wang Yixiong; Yoshiyasu Fukuyama; Iwao Miura; Michiharu Sugawara

Abstract Three phthalides, 3-butylidene-7-hydroxyphthalide, and cis and trans -6,7-dihydroxyligustilides, along with a dimeric phthalide wallichilide have been isolated from the hot water extract of the rhizome of Ligusticum wallichii . Their structures were established mainly on the basis of spectroscopic data. 3-Butyl-4,5-dihydro-3-hydroxy phthalide and adenosine were identified as active principles of the extract which are responsible for increase of coronary blood flow in the dog heart.


Phytochemistry | 1981

Jinkohol, a prezizane sesquiterpene alcohol from agarwood

Tsutomu Nakanishi; Etsuko Yamagata; Kaisuke Yoneda; Iwao Miura

Abstract A new tricyclic sesquiterpene, jinkohol, has been isolated from an agarwood ( Aquillaria sp.) which is different from that obtained from Aquillaria agallocha . Its structure was shown to be 2β-hydroxy-(+)-prezizane by spectroscopic methods and by chemical transformation. The two kinds of agarwood are readily identified from their sesquiterpene components.


Tetrahedron Letters | 1983

Isolation, structure and synthesis of maesanin, a host defense stimulant from an African medicinal platn maesa lanceolata

Isao Kubo; T. Kamikawa; Iwao Miura

Abstract The isolation, characterization and an efficient synthesis of maesanin 1 , a host defense stimulant isolated from an African medicinal plant Maesa lanceolata is reported.


Phytochemistry | 1984

Sesquiterpenoids in two different kinds of agarwood

Kaisuke Yoneda; Etsuko Yamagata; Tsutomu Nakanishi; Tsukasa Nagashima; Ichiro Kawasaki; Toshio Yoshida; Hideo Mori; Iwao Miura

Abstract Sesquiterpenoids of an agarwood originating from Aquilaria agallocha and of the other kind of agarwood (Aquilaria sp.; probably Aquilaria malaccensis) were investigated by a combination of GLC and GC/MS. The differences in sesquiterpene composition between the two kinds of agarwood are discussed.


Tetrahedron Letters | 1983

A first total synthesis of Germacrone by intramolecular alkylation of protected cyanohydrin

Takashi Takahashi; Kyoko Kitamura; Hisao Nemoto; Jiro Tsuji; Iwao Miura

Abstract A total synthesis of Germacrone by the intramolecular alkylation of a carbanion generated from protected cyanohydrin is presented.


Phytochemistry | 1985

Azedarachol, a steroid ester antifeedant from Melia azedarach var. japonica

Munehiro Nakatani; Hideki Takao; Iwao Miura; Tsunao Hase

Abstract A new steroid ester, azedarachol, from the root bark of Melia azedarach has been identified as an antifeedant against a Japanese insect pest and the structure has been assigned as 2α,3α,16β-trihydroxy-5α-pregnane 20 R -methacrylate.


Biochemical and Biophysical Research Communications | 1988

Observation of fatigue unrelated to gross energy reserve of skeletal muscle during tetanic contraction ― an application of 31P-MRS

Shinjiro Takata; Hiroaki Takai; Takaaki Ikata; Iwao Miura

The mechanism of muscle fatigue was studied by 31P-MRS. During tetanic contraction for 2 minutes(min), the tension measured with a strain gauge and Phosphocreatine(PCr)/Inorganic phosphate(Pi)+ Phosphomonoester(PME) ratio decreased to 31.5 +/- 4.4% of the control value and 0.6 +/- 0.1, respectively. The intracellular pH(pH) also decreased to 6.62 +/- 0.04. Toward the end of the stimulation, the tension decreased to 25.3 +/- 1.9% of the control value. However, during 20min stimulation, the PCr/(Pi+PME) ratio increased to 2.5 +/- 0.5 and the pH to 6.91 +/- 0.04. These results show that muscular fatigue is ascribable not to a decreased level of high energy metabolites required for actomyosin ATPase, but to an increase in the threshold intensity of excitation in excitation-contraction coupling.


Phytochemistry | 1982

Aristoloside, an aristolochic acid derivative from stems of Aristolochia manshuriensis

Tsutomu Nakanishi; Kyoko Iwasaki; Masao Nasu; Iwao Miura; Kaisuke Yoneda

Abstract Aristoloside, a new companion aristolochic acid derivative isolated from stems of Aristolochia manshuriensis has been shown to be 6- O -β- d -glucopyranoside of aristolochic acid-D on chemical and physicochemical evidence. Three known acids, aristolochic acids I, IV (both as their corresponding methyl esters), and -D have also been characterized from stems of the plant.

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Chuichi Kawai

Takeda Pharmaceutical Company

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