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宮本 洋子, 石田 寿昌, 井上 正敏
1981 年 29 巻 12 号 p.
3427-3432
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
As a model study of the intramolecular interaction between the adenine and pyridinium rings of nicotinamide adenine dinucleotide (NAD
+), conformational analysis of 1-[3-(adenin-9-yl) propyl]-3-carbamoylpyridinium cation was carried out by means of semiempirical energy calculation. The extended conformation of the molecule, which was observed in the crystal structure, was found to be energetically a metastable one. The most energetically stable conformations seem to be folded forms, especially forms in which the two aromatic rings are stacked ; four kinds of stacking modes were observed.
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山田 敏廣, 信原 陽一, 嶋村 浩, 吉原 和生, 山口 東, 大木 正彦
1981 年 29 巻 12 号 p.
3433-3439
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
The pyridine ring of 2-phenyl-2-(2-pyridyl) thioacetamide (Ia), the lead compound for the present study, was replaced by a pyridazine ring in the hope of obtaining more potent and less toxic drugs with long-lasting action, and a series of 2-phenyl-2-(3-pyridazinyl) thioacetamide derivatives (II) was synthesized from halopyridazines (III) and phenyl-acetonitriles via the key intermediates, 2-phenyl-2-(3-pyridazinyl) acetonitrile derivatives (IV). The chemical structure of II appears to be in equilibrium between the pyridazine form and the pyridazinone-methide form on the basis of nuclear magnetic resonance (NMR) and ultraviolet (UV) spectral data. The antisecretory activity and acute toxicity of II were investigated and the structure-activity relationships are discussed. Among the compounds tested, 2-Phenyl-2-(3-pyridazinyl) thioacetamide (IIa) and 2-(6-methyl-3-pyridazinyl)-2-phenylthioacetamide (IIb) possessed long-lasting, potent activity when administered to rats at 20 mg/kg. The acute toxicities of IIa and IIb were about half to one-third of that of Ia in mice.
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大塚 栄子, 柴原 進, 池原 森男
1981 年 29 巻 12 号 p.
3440-3448
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
p-Chlorophenyl N-(p-methoxyphenyl) chlorophosphoramidate was used to phosphorylate the 3'-hydroxyl groups of N, 5'-O-protected deoxyribonucleosides. These nucleotides served as the 3'-terminal unit in the synthesis of fully protected oligonucleotides, and the p-anisidine was readily removed by treatment with isoamyl nitrite to generate the 3'-phosphodiester for condensations. This approach was suitable for complete purification of fully protected oligonucleotides by chromatography, which was essential to obtain products. Deoxyoligonucleotides complementary to the anticodon loop of E. coli tRNA
Metf were synthesized by condensation of di-, tri- and tetranucleotide blocks (dATp, dTATp and dTTATp) with protected dGAG. The products (dA-T-G-A-G, d-T-A-T-G-A-G and d-T-T-A-T-G-A-G) were isolated by anion-exchange or reverse phase high pressure liquid chromatography.
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村岡 全子
1981 年 29 巻 12 号 p.
3449-3454
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
2, 6-Diamino-9-β-D-ribofuranosylpurine (I) was brominated with saturated bromine-water to the 8-bromo compound (II), which was tosylated at the 2'-hydroxygroup via the 2', 3'-O-dibutylstannylene compound (III). The resulting 2, 6-diamino-8-bromo-9-(2'-O-tosyl-β-D-ribofuranosyl)-purine (IV) was cyclized with thiourea in n-propanol or 40% sodium hydrogen sulfide to give 2, 6-diamino-8, 2'-anhydro-8-mercapto-9-β-D-arabinofuranosylpurine (V) in yields of 40% and 80%, respectively. Alternatively, 8, 2'-anhydro-8-mercapto-9-β-D-arabinofuranosylguanine (VI) was acetylated and chlorinated with phosphoryl chloride to give the 2-amino-6-chloropurine-8, 2'-S-cyclonucleoside derivative (VIII), which was aminated with ammonia in methanol to afford the 2, 6-diaminopurine cyclonucleoside (V) in a yield of 45%. Catalytic desulfurization of the cyclonucleoside (V) gave 2, 6-diamino-9-(2'-deoxy-β-D-ribofuranosyl)-purine (IX). Some physical properties of these compounds were elucidated by ultraviolet (UV), nuclear magnetic resonance (NMR) and circular dichroism (CD) spectroscopy. The CD spectra of these nucleosides and cyclonucleoside were similar to those of the corresponding adenine nucleosides and cyclonucleoside in general.
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田中 信壽, 村上 孝夫, 斎木 保久, 陳 秋明 /, LUIS D. GOMEZ P
1981 年 29 巻 12 号 p.
3455-3463
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
The constituents of five Costa Rican ferns of Preridaceae were investigated. The ferns and isolated compounds are as follows. Acrostichum aureum : quercetin 3-O-β-D-glucoside (I), ponasterone A (III). Neurocallis praestantissima : 2-deoxy-D-glucose (IV), 3, 6-anhydro-2-deoxy-D-glucose (V). Pteris podophylla : 6-(2-chloroethyl)-2 (S)-hydroxy-methyl-5, 7-dimethylindan-1-one (X), pterosin G (XI), kaempferol 3, 7-di-O-α-L-rhamnoside (II), apigenin 7-O-β-D-glucoside (VI), luteolin 7-O-β-D-glucoside (VII). Pteris livida : pterosin C (VIII), pterosin S (IX), 9-hydroxy-15-oxo-ent-kaur-16-en-19-oyl-β-D-glucoside (XII), 6β, 11β-dihydroxy-15-oxo-ent-kaur-16-en-19-oyl-β-D-glucoside (XIII), 6β, 9-dihydroxy-15-oxo-ent-kaur-16-en-19-oyl-β-D-glucoside (XIV), paniculoside III (XV), ptero-kaurene L
1 (XVI), 11β-hydroxy-15-oxo-ent-kaur-16-en-19-oic acid (XIX). Pteris altissima : VII, XI, XII, XIII, XV. Among the above products, X, XII, XIII and XIV are new compounds and their structures were elucidated by chemical and physicochemical methods.
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米田 利夫, 松野 富雄, 深津 俊三
1981 年 29 巻 12 号 p.
3464-3468
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
A new deoxygenation of kanamycin A leading to 3', 4'-dideoxykanamycin A and 4'-deoxykanamycin A is described. The key stage in the syntheses involves the formation of the 3', 4'-anhydro-4'-epi derivative (5) followed by its conversion to the 3'Δ and 4'-deoxy derivative through the iodohydrin. Compound 5 was prepared by the treatment of 2', 3', 2"-tri-O-benzoyl-4", 6"-O-cyclohexylidene-4'-O-methylsulfonyl-tetra-N-tert-butyloxycar-bonylkanamycin A (4) with sodium methoxide.
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米田 利夫, 松野 富雄, 七星 日出隆, 深津 俊三
1981 年 29 巻 12 号 p.
3469-3473
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
A new synthetic route has been exploited for the large-scale production of 3'-deoxykanamycin A. The key stage in the synthesis involves the formation of the 3', 4'-anhydro-3'-epi derivative (9) or 2', 3'-anhydro-3'-epi derivative (10) followed by conversion to the 3'-deoxy derivative by reduction with Raney-nickel or sodium borohydride. Compound (9) or (10) was prepared by the treatment of 2', 2"-di-O-benzoyl-3'-O-methylsulfonyl-tetra-N-ethoxycarbonylkanamycin A with sodium methoxide.
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(±)-3β, 6β-Dihydroxy-10βHfuranoeremophilan-9-one, and (±)-3β, 6β-Dihydroxy-10αH-furanoeremophilan-9-one
山川 浩司, 佐藤 毅
1981 年 29 巻 12 号 p.
3474-3485
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
The total syntheses of several highly oxygenated, 1, 10-dehydrofuranoeremophilanes [(±)-6β-hydroxy-1, 10-dehydrofuranoeremophilan-9-one (1a), (±)-decompositin (1b), (±)-dihydrodecompositin (3), (±)-adenostylone (1c), (±)-3β, 6β-dipropionyleuryopsin-9-one (2b)] and polyoxy compounds [(±)-3β, 6β-dihydroxy-10βH-furanoeremophilan-9-one (4), (±)-3β, 6β-dihydroxy-10αH-furanoeremophilan-9-one (5), and 3β-acetoxy-6β-isobutyroxy-furanoeremophilan-9-one (28b)] from a bicyclic enone (6a) are described. Treatment of 10α-hydroxy-6, 9-dioxo compounds (8a, 18 and 23) with SOCl
2-pyridine gave the corresponding 1, 10-dehydro-6, 9-dioxo compounds (11, 20 and 24, respectively). NaBH
4 reduction of 11, 20 and 24 afforded the 6β-hydroxy derivatives (12a, 1a and 2a, respectively) regio- and stereoselectively. (±)-1a was converted into (±)-1b, (±)-1c, and (±)-3. (±)-2a was also converted into (±)-2b. Catalytic reduction of 12a with H
2/Pd gave the 10α-H and 10β-H compounds (25 and 26a). Deketalization of 25 and 26a with aq. AcOH followed by reduction with NaBH
4 gave (±)-5 and (±)-4, respectively. Esterification of 26a with 2-methylbutyric anhydride-pyridine gave the ester (26b), which was converted to (±)-28a and 28b.
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野沢 幸平, 山田 美紀子, 津田 貴子, 河合 賢一, 仲嶋 正一
1981 年 29 巻 12 号 p.
3486-3493
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Various cis- and trans-3-aryl-3, 4-dihydro-8-(hydroxy or methoxy) isocoumarin-4-carboxylic acids (3-16) and their methyl esters (21-29) were prepared. In addition, cis- and trans-3, 4-dihydro-8-(hydroxy or methoxy)-4-hydroxyacetyl-3-phenylisocoumarins (33 or 32, and 35 or 34), cis- and trans-4-diazoacetyl-3, 4-dihydro-8-methoxy-3-phenylisocoumarins (30 and 31), trans-4-acetoxyacetyl-3, 4-dihydro-8-methoxy-3-phenylisocoumarin (36), and trans-4-acetyl-3, 4-dihydro-8-(hydroxy or methoxy)-3-phenylisocoumarins (38 or 37) were prepared. All the 3, 4-dihydroisocoumarins thus prepared were examined in vitro for antifungal activity. The introduction of a carboxyl, carbomethoxy, acetyl, diazoacetyl or hydroxyacetyl group at the 4-position of the 3, 4-dihydroisocoumarin nucleus resulted in the disappearance of the activity.
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大和 正利, 橋垣 国子, 津々 美明, 田坂 賢二
1981 年 29 巻 12 号 p.
3494-3498
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Structural modification of the isocoumarin moiety (A and B rings) of 1'-benzylspiro-[isocoumarin-piperidines] (1a and 2a), which inhibit the compound 48/80-induced release of histamine from isolated rat peritoneal mast cells, was undertaken to clarify the structure-activity relationship. Chromanone (3), chroman (4), 1, 3-benzoxazine (5), 1, 3-benzothiazine (6), and 4-quinazolinone (7) analogs were active, although there were differences in potency. Substituent effects on the benzene moiety (A ring) of 3 were examined.
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金子 孝夫, 松尾 光芳, 飯高 洋一
1981 年 29 巻 12 号 p.
3499-3506
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
When indole reacted with titanium (III)- or iron (II)-hydrogen peroxide systems, the products varied widely, depending on the pH of the reaction solutions. Under acidic conditions, indole gave rise to oxindole, 2, 3'-biindole and a novel indole trimer, diindolo-[2, 3-a : 2', 3'-c] carbazole. Under neutral conditions, indole was converted to oxindole, hydroxyindoles and 3, 3'-biindole. The structure of the trimer was determined by X-ray diffraction analysis of its monoacetyl derivative. A possible mechanism for the formation of the products is proposed.
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岡村 信幸, 八木 晟, 西岡 五夫
1981 年 29 巻 12 号 p.
3507-3514
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
New glycosides, zizybeoside I (I) and II (II), zizyvoside I (IV) and II (V), and a mixture of 6, 8-di-C-glucosyl-2 (S)-naringenin and 6, 8-di-C-glucosyl-2 (R)-naringenin (compound A), together with vomifoliol and roseoside, were isolated from the ethanol extract of Zizyphi Fructus. On the basis of spectral and chemical evidence the structures of the new glycosides were determined as benzyl β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside (I), benzyl β-D-glucopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-β-D-glucopyranoside (II), vomifoliol 9-O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside (IV), vomifoliol 9-O-β-glucopyranosyl-(1→2)-[β-glucopyranosyl-(1→3)]-β-glucopyranoside (V), 6, 8-di-C-glucosyl-2 (S)-naringenin (VII) and 6, 8-di-C-glucosyl-2 (R)-naringenin (VIII).
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田川 博昭, 久保 志郎, 石川 文義
1981 年 29 巻 12 号 p.
3515-3521
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
As part of a search for new antiinflammatory agents, some new tricyclic compounds and their acetic acid derivatives were prepared. Pyrido [2, 3-c] [1] benzoxepin-5 (11H)-one (4a) and pyrido [3, 2-c] [1] benzoxepin-11 (5H)-one (10a) and their thiepin analogs (4b, 10b) were synthesized by cyclization of the corresponding pyridinecarboxylic acid derivatives (3a, 3b, 9a and 9b) with polyphosphoric acid (PPA). The acetic acid derivatives (12a-b) of 4a-b were prepared via methyl derivatives (14a-b) of 4a-b. Their antiinflammatory activities were less potent than those of the corresponding dibenz [b, e] oxepin- and dibenz-[b, e] thiepinacetic acids.
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植田 泰誠, 間瀬 英志, 織田 範一, 伊藤 磯雄
1981 年 29 巻 12 号 p.
3522-3528
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Syntheses of pyrano [2, 3-c] pyrazoles by means of the reaction of 3-ethoxycarbonyl-5-hydroxy-1-methyl (or phenyl) pyrazole (Ia, b) and acetylenecarboxylates or ethyl acetoacetate were examined. The reactions of Ia, b with acetylenecarboxylates gave 3-ethoxycarbonyl-4-substituted-1-methyl (or phenyl) pyrano [2, 3-c] pyrazol-6 (1H)-ones (IIa-c) in 5.9-23.9% yields. The Pechmann-Duisberg reaction of Ia-c with ethyl acetoacetate gave 3-ethoxycarbonyl-4-methyl-1-substitutedpyrano [2, 3-c] pyrazol-6 (1H)-ones (VIIa-c) in 33.1-46.2% yields. Similar reactions of 5-hydroxy-3-methylcarbamoyl-1-phenyl (or m-chlorophenyl) pyrazoles (IXa, b) with ethyl acetoacetate gave 4-methyl-3-methylcarbamoyl-1-phenyl (or m-chlorophenyl) pyrano [2, 3-c] pyrazol-6 (1H)-ones (Xa, b) in 17.4-30% yields. The newly synthesized pyrano [2, 3-c] pyrazoles (Xa, Xb, XII) showed analgesic activity in mice when tested by two methods.
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太刀川 隆次, 和智 一之, 佐藤 定男, 寺田 敦祐
1981 年 29 巻 12 号 p.
3529-3535
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
A novel S-N bond formation through 3, 3-sigmatropic rearrangement in the reaction of imidoyl chlorides of 1, 3-benzoxazines (1) with 2-mercaptopyridine N-oxide (8) is described. Treatment of the imidoyl chlorides (1a-f) with 2-hydroxypyridine N-oxide (2) afforded the corresponding pyridone derivatives (3a-f). When 2-mercaptopyridine N-oxide (8) was used instead of 2, the thiopyridones (7) or N-oxides (9) were obtained and both compounds were transformed to 3-(2-pyridylthio)-4-oxo-2, 3-dihydro-1, 3-benzoxazines (13) through electrocyclic rearrangement on heating in a suitable solvent.
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三川 潮, 嶋田 寿男, 佐藤 俊次, 木下 武司, 山崎 和男
1981 年 29 巻 12 号 p.
3536-3542
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
The biosynthesis of scytalone, a simple derivative of tetralone, has been studied by using [1, 2-
13C
2] and [2-
13C, 2-
2H
3]-acetate. Scytalone labelled by [1, 2-
13C
2]-acetate showed an unusual coupling pattern in the
13C-nuclear magnetic resonance (NMR) spectrum, indicating that all the carbon atoms coupled to both of the adjacent carbons. The results clearly demonstrate that scytalone is biosynthesized via a symmetrical aromatic intermediate, 1, 3, 6, 8-tetrahydroxynaphthalene. Incorporation of
2H into C-4 and -5 from [2-
13C, 2-
2H
3]-acetate was demonstrated by
1H and
2H decoupled
13C-NMR. In contrast,
2H was not observed on the other potential sites of labelling, C-2 and C-7. It has been shown that the use of [2-
13C, 2-
2H
3]-acetate is effective in tracing the fate of acetate hydrogen in polyketide biosynthesis.
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山中 宏, 白岩 雅文, 山本 恵津子, 坂本 尚夫
1981 年 29 巻 12 号 p.
3543-3547
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
3, 5-Dimethyl-4-iodoisoxazole (1a) reacted with phenylacetylene with catalysis by palladium (II) chloride-triphenylphosphine complex to give 3, 5-dimethyl-4-phenylethynyl-isoxazole (2a). When 1a was treated with styrene under similar conditions, 3, 5-dimethyl-4-trans-styrylisoxazole (3a) was obtained. In contrast, the palladium-catalyzed crosscoupling reaction of 3-phenyl-5-bromoisoxazole (4) with styrene afforded 3, 3'-diphenyl-5, 5'-biisoxazole (6) as the main product, instead of the desired styryl compound (5a). However, 3-phenyl-5-phenylethynylisoxazole (7a) was obtained, as in the case of 1a, by the reaction of 4 with phenylacetylene. Some additional examples of these coupling reactions are also described.
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山中 宏, 白岩 雅文, 坂本 尚夫, 今野 昌悦
1981 年 29 巻 12 号 p.
3548-3553
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Hydration of 5-isoxazolyl-phenyl (or -butyl) acetylenes (1a, b) in dilute sulfuric acid in the presence of mercuric sulfate afforded 5-isoxazolylmethyl phenyl (or butyl) ketones (3a, b), predominantly. In contrast, the hydration of 4-isoxazolyl-phenyl (or -butyl)-acetylenes (2a-d) under identical conditions gave 4-isoxazolyl benzyl (or pentyl) ketones (5a-d) as the main products. The structure of one of these products, 3, 5-dimethyl-4-isoxazolyl benzyl ketone (5a), was determined by Beckmann rearrangement. Isoxazoles containing a cis-alkene or alkane chain were obtained by the catalytic reduction of the above acetylenes without cleaving the isoxazole nucleus.
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今野 昌悦, 白岩 雅文, 山中 宏
1981 年 29 巻 12 号 p.
3554-3560
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Studies were carried out on the hydration and hydrogenation of the triple bond in quinoline and isoquinoline derivatives containing an ethynyl substituent linked directly to the pyridine moiety. Fourteen kinds of ethynyl quinolines and isoquinolines such as 2-, 3-, 4-phenylethynylquinoline, 2-, 3-, 4-(1-hexynyl) quinoline, 2-(1-propynyl) quinoline, 1-, 3-, 4-phenylethynylisoquinoline, 1-, 3-, 4-(1-hexynyl) isoquinoline, and 1-(1-propynyl)-isoquinoline were converted into the corresponding acylmethyl derivatives with high selectivity, when they were heated in dilute sulfuric acid in the presence of mercuric sulfate. In all cases, no products due to reverse hydration were isolated. Partial catalytic reduction of the ethynyl linkage of the above compounds is possible, while exhaustive reduction afforded quinolines and isoquinolines with a saturated side chain.
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宮瀬 敏男, 川崎 宏子, 野呂 忠敬, 上野 明, 福島 清吾, 竹本 常松
1981 年 29 巻 12 号 p.
3561-3564
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Two new furanoid diterpenes, teucjaponin A (II) and teucjaponin B (V), have been isolated from Teucrium japonicum HOUTT. together with teucvin (I) and their structures were determined on the basis of chemical and spectral data. Teucjaponin A showed antifeedant activity for Prodenia litura.
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田中 博道, 早川 弘之, 宮坂 貞
1981 年 29 巻 12 号 p.
3565-3572
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
6-Aroyluridines, a hitherto unknown class of uridine derivatives, were synthesized from 2', 3'-O-isopropylidene-5'-O-methoxymethyluridine via regiospecific lithiation.
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上杉 晴一, 志田 敏夫, 池原 森男
1981 年 29 巻 12 号 p.
3573-3585
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
To elucidate the conformational properties and their chain length dependency in solution of oligodeoxyribonucleotides containing an alternating C-G sequence, which have been shown to take a left-handed duplex structure in crystals, d (C-G), d (C-G-C-G) and d (C-G-C-G-C-G) were synthesized by a modified triester method and characterized by ultraviolet (UV) circular dichroism (CD) and
1H-nuclear magnetic resonance (NMR) spectroscopy. The effects of salt concentration (0.1 M and 4 M NaCl), oligomer strand concentration (10
-5-10
-2M) and temperature (0°-90°C) on the oligomer conformation were investigated. The dimer does not form a duplex under any conditions studied. The tetramer does form a right-handed duplex in 0.1M NaCl even at 3×10
-5M strand concentration. In 4M NaCl, however, it does not form any duplex at the same strand concentration, and left-handed duplex formation is observed at 10-fold higher concentration. The hexamer forms a duplex in either salt concentration even at 2×10
-5M strand concentration. The melting temperatures of these duplexes were measured by UV and CD methods. The CD-temperature profile in 4M NaCl, which is not sigmoidal when monitored at the λ
min of the characteristic negative band, suggests that melting of the high salt duplex is a rather complex process that involves more than two species. The results of
1H-NMR-temperature studies support left-handed duplex formation in a high salt solution.
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二階堂 保, 大本 太一, 木下 武司, 三川 潮, / , SUEO HISADA
1981 年 29 巻 12 号 p.
3586-3592
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Cyclic adenosine monophosphate (AMP) phosphodiesterase inhibitors contained in Forsythia suspensa were identified as lignans, (+)-pinoresinol (Ja) and (+)-pinoresinol-β-D-glucoside (Id), and their structure-activity relationship was investigated. In pinoresinol congeners, the configuration of the two phenyl rings is very important in relation to the activity. When both of the p-hydroxyl groups in matairesinol congeners are substituted by methyl or glucose, the activities are decreased as compared with those of the unsubstituted compounds.
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津田 喜典, 吉本 公浩, 西川 照美
1981 年 29 巻 12 号 p.
3593-3600
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
A practical synthetic route to optically active [2R]- and [2S]-1-alkylamino-3-aryloxy-2-propanols (β-blockers) from [2R]-2, 3-O-isopropylideneglyceraldehyde ([R]-1) was developed. Synthesis of the [S]-isomers was carried out as follows. Borohydride reduction of [R]-1 in the presence of excess alkylamine followed by alkoxycarbonylation, acid hydrolysis, and cyclization under K
2CO
3 catalysis gave [5S]-3-alkyl-5-hydroxymethyl-1, 3-oxazolidin-2-ones, the tosylates of which were coupled with various phenols then hydrolyzed by alkali treatment to give [S]-(-)-β-blockers (e. g., propranolol, carteolol) in satisfactory yields. [R]-, [S]-, and rac-pindolol were synthesized from the corresponding 3-isopropyl-5-(2-methyl-3-nitrophenoxymethyl)-1, 3-oxazolidin-2-one by application of the Leimgruber-Batcho method.
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三川 潮, 嶋田 寿男, 山崎 和男
1981 年 29 巻 12 号 p.
3601-3605
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Biosynthetic incorporation of
2H from [2-
13C, 2-
2H
3]-acetate into 2-hexyl-5-propylresorcinol was investigated in Pseudomonas. The
13C nuclear magnetic resonance spectrum of labelled 2-hexyl-5-propylresorcinol showed
13C-
2H signals of expected methylene and methyl carbons in the side chains, but no
2H was found on the aromatic carbons. The main species of methyl groups labelled with
2H were
13C-
2H
3 and
13C-
2H
21H. The incorporation experiments unambiguously demonstrate that 2-hexyl-5-propylresorcinol is biosynthesized from two polyketide chains.
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細田 宏, 小林 典裕, 宮入 伸一, 南原 利夫
1981 年 29 巻 12 号 p.
3606-3610
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
The specificity in heterogeneous enzyme immunoassays for cortisol has been investigated. Enzyme labeling of cortisol was accomplished by the N-succinimidyl ester method at an appropriate molar ratio of steroid to enzyme. Three cortisol derivatives possessing different bridges at C-4 were covalently linked to β-galactosidase. The anticortisol antisera used were those elicited in rabbits by immunization with the conjugates of these haptenic derivatives with bovine serum albumin. With the aim of obtaining high sensitivity, enzyme immunoassays were carried out in the bridge heterologous combinations of antiserum and enzyme-labeled cortisol. The specificity of these assay systems was assessed by measuring the amount of cortisol in biological fluids, and by comparison of the results with those of radioimmunoassays. The cross-reactivities were also tested with fifteen kinds of closely related steroids. The assay using the antiserum raised against the 4-(2-carboxyethylthio) cortisol-protein conjugate was found to be relatively specific and applicable to the determination of cortisol in human plasma and urine.
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宮崎 利夫, 西島 基弘
1981 年 29 巻 12 号 p.
3611-3616
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
A water-soluble, antitumor polysaccharide GL-1, [α]
20D+26°(c=1, water), M.W. 40000, was isolated from the fruit bodies of Ganoderma lucidum (Rokkakushi, a kind of Reishi). GL-1 consists of glucose, xylose and arabinose in the molar ratio of 18.8 : 1.5 : 1.0. Structural examination was carried out by periodate oxidation, Smith degradation, methylation analysis, partial acid hydrolysis and α-amylase treatment. It is concluded that (1) GL-1 is a branched arabinoxyloglucan, (2) GL-1 contains backbone and side-chains involving D-glucopyranosyl (1→4)-α- and -β-, (1→6)-β- and (1→3)-β-linkages, (3) arabinose is present as a part of the non-reducing terminal residues, and (4) xylose may be present as a part of the side-chain. GL-1 strongly inhibited the growth of Sarcoma 180 solid-type tumor (inhibition ratio, 95.6-98.5%) when injected i. p. (20 mg/kg) for 10 days. Mild acid hydrolysis and α-amylase treatment of GL-1 had no effect on the antitumor activity. These results suggest that the essential structure for the antitumor activity of GL-1 is a branched glucan core (GL-3) involving (1→3)-β-, (1→4)-β-and (1→6)-β-linkages.
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松本 善雄, 須賀 哲弥
1981 年 29 巻 12 号 p.
3617-3623
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
The effects of 3-amino-1, 2, 4-triazole (AT) on the uptake of tritiated p-biphenylmethyl-(dl-tropyl-α-tropinium) bromide (
3H-BTTB) into the subcellular fractions of livers of carbon tetrachloride (CCl
4)-treated mice were studied. The uptake of
3H-BTTB into the liver of CCl
4-treated mice was decreased to 50% of that in the control group. Pretreatment with AT resulted in an effective restoration of the decrease caused by CCl
4 treatment up to the AT group's level, though AT itself lowered the uptake of
3H-BTTB to 61% of that of the control group. The subcellular distribution of
3H-BTTB in the liver of CCl
4-treated mice was different from that of the control : the ratio of the radioactivity in the lysosomal fraction to that of the supernatant fraction (the L/S ratio) was decreased by CCl
4 treatment from 1.85 to 1.66. This decrease was almost completely reversed to the control value by the pretreatment with AT and there was a similar change in the distribution of acid phosphatase. Furthermore, the cross-points of the lysosomes of the liver in mice which had been treated with CCl
4, AT and AT-CCl
4 were determined by means of cross-partition in aqueous polymer two-phase systems. CCl
4 made the surface charge of the lysosomal membrane more acidic, though AT reversed this change. There may be an important relationship between the uptake of BTTB into lysosomes and the characteristics of the lysosomal membranes.
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沢田 英夫, 篠田 道夫, 丸山 仁美, 中山 俊裕
1981 年 29 巻 12 号 p.
3624-3629
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Acid phosphatase (orthophosphoric monoester phosphohydrolase, EC 3. 1. 3. 2) isozyme 4 (pI 6.1) has been isolated from human prostate tissue. The enzyme showed a single protein band when examined by polyacrylamide gel disc electrophoresis. The purification coefficient was approximate 3.2 and the recovery of enzyme activity was 0.1% from the supernatant fraction. The molecular weight of the enzyme obtained by gel filtration was 100000, whereas that obtained by polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate was 79000. The enzyme was not cross-reactive with acid phosphatase isozyme (pI 5.3) in immunodiffusion. Isozyme 4 had almost the same enzymic properties (K
m, K
i, and optimum pH) as isozyme 2, but the specific activity of isozyme 4 was one-fourth of that of the latter.
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品川 進, 藤野 政彦, 石井 治光, 川井 清尚
1981 年 29 巻 12 号 p.
3630-3638
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Thirty tetrapeptide hydrazide analogs of enkephalin, H-Tyr-D-Ala-Gly-Phe-NHN-(R
1)-R
2 (R
1, R
2=H, alkyl or acyl), were synthesized. The analgesic activities of these peptides were tested in mice after intravenous or subcutaneous injection, and compared with that of morphine. Among the analogs synthesized, the tetrapeptide acyl-hydrazide analog, H-Tyr-D-Ala-Gly-Phe-NHNH-CO-R (R=lower alkyl), was the most active and showed analgesic activity ten times more potent than that of the tetrapeptide amide analog, H-Tyr-D-Ala-Gly-Phe-NH
2 and half as potent as that of morphine. On the basis of these results, structure-activity relations in the hydrazide part of enkephalin analogs of this new type are discussed.
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品川 進, 藤野 政彦, 石井 治光, 川井 清尚
1981 年 29 巻 12 号 p.
3639-3645
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
In order to study the effect of N-methylation of a potent enkephalin analog, H-Tyr-D-Ala-Gly-Phe-NHNH-CO-CH
2CH
3, on analgesic activity, six new analogs were synthesized in which one or more of amino acid residues and the acyl-hydrazide constituting the tetrapeptide acyl-hydrazide were N-methylated. N-Methylation of both Tyr at position 1 and Phe at position 4 of the analog led to a derivative which was twice as potent as morphine. On the other hand, N-methylation of D-Ala at position 2, Gly at position 3 or NHNH-CO-CH
2CH
3 at position 5 markedly decreased the analgesic potency. Five analogs with a modified tyrosine residue at position 1 of the tetrapeptide acyl-hydrazide were also synthesized in order to assess the role of the N-terminal Tyr residue in the biological activity.
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品川 進, 藤野 政彦, 脇舛 光広, 石井 治光, 川井 清尚
1981 年 29 巻 12 号 p.
3646-3659
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Thirty-five tetrapeptide acyl-hydrazide analogs of enkephalin substituted at position 2 were synthesized. Substitution of D-Ala at position 2 of H-Tyr-D-Ala-Gly-Phe-NHNH-CO-R (R=lower alkyl), by D-Met (O), D-Gln, D-Glu (NH-CH
3) or D-Thr enhanced the analgesic potency, but substitution by D-Glu or Ser resulted in an analog with no antinociceptive activity. Among the analogs synthesized, the D-Met (O)-analog was the most potent and H-Tyr-D-Met (O)-Gly-Phe-NHNH-CO-CH
2CH
3 exhibited analgesic activtiy four times more potent than that of morphine in mice following subcutaneous injection. Structure-activity relations for position 2 of the enkephalin-like tetrapeptide are discussed.
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杉浦 衛, 平野 和行, 飯泉 祐一, 宮崎 純, 三木 一正, 飯野 四郎, 鈴木 宏, 織田 敏次
1981 年 29 巻 12 号 p.
3660-3666
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Human alkaline phosphatase was purified from meconium by treatment with cetylpyridinium chloride, followed by diethylaminoethyl (DEAE)-cellulose and CM-cellulose chromatography, Sephadex G-200 gel filtration and DEAE-Sephadex A-50 chromatography. The homogeneity of the purified enzyme was demonstrated by disc electrophoresis and immunological investigation. The molecular weight of the purified meconial alkaline phosphatase was 155000 and the enzyme was composed of two subunits of equal molecular weight. The optimum pH was found to be 10.0 and the enzyme was stable over the pH range of 4-10. The Km value was 2.2mM for p-nitrophenylphosphate as a substrate. The isoelectric point was pH 4.0, and the purified enzyme was inhibited by N-bromosuccinimide (NBS), o-phenanthroline, ethylenediaminetetraacetic acid (EDTA) and L-phenylalanine. Meconial alkaline phosphatase obtained by our method contained 2 g-atoms of zinc/mole of enzyme. The enzymic properties of the purified meconial alkaline phosphatase were compared with those of adult intestinal alkaline phosphatase.
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溝尻 顕爾, 山本 恵津子, 中島 善次, 岡部 博, 菅野 浩一, 渡辺 淳
1981 年 29 巻 12 号 p.
3667-3670
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Perisoxal glucuronides were isolated from rabbit urine after repeated subcutaneous administration of dl-perisoxal citrate. Optical rotatory analysis of free bases obtained from the glucuronides indicated that about twice as much d-perisoxal glucuronide as l-isomer was formed. Stereoselective metabolism was observed in rabbit urine after d- or l-perisoxal administration. d-Perisoxal glucuronide was excreted predominantly at doses of 1.8 and 9.0 mg/kg. The excretions of d- and l-isomers of p-hydroxyperisoxal glucuronides were similar at the dose of 9.0 mg/kg, but a larger value was obtained for the l-isomer at the dose of 1.8 mg/kg.
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草井 章, 田中 誠二, 上田 省吾
1981 年 29 巻 12 号 p.
3671-3679
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
The kinetics and mechanisms of the degradation of 2, 5-diethylenimino-1, 4-benzoquinone (EB) in aqueous solution were investigated as a function of pH (4-11), temperature (20-50°C), buffer concentration (0.01-0.1M) and ionic strength (0.1-0.5) by means of high pressure liquid chromatography. The reaction followed pseudo first-order kinetics. The pH-rate profile showed slopes of -1 at pH below 7.5 and +1 at pH over 7.5. Thus, the degradation of EB is subjected to specific acid-base catalysis. No effect of buffer concentration on the degradation rate of EB was apparent in the range of pH 4-11, though some effect of ionic strength on it was observed below pH 7. The apparent activation energies for the degradation of EB at pH 4 or 5 and pH 10 or 11 were 14 and 19 kcal/mol, respectively. In the range of pH 4-6, EB was degraded to 2, 5-diethanolamino-1, 4-benzoquinone with sequential hydrolytic cleavage of two ethylenimine rings. In the range of pH 10-11, EB was degraded to 2, 5-dihydroxy-1, 4-benzoquinone with sequential substitution of the two ethylenimine rings by hydroxyl ion (radical). In the range of pH 7-9, EB was degraded to 2, 5-diethanolamino-1, 4-benzoquinone, 2, 5-dihydroxy-1, 4-benzoquinone and 2-ethanol-amino-5-hydroxy-1, 4-benzoquinone by the two mechanisms described above.
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関 裕充, 加々美 剛, 林 泰三, 大草 直也
1981 年 29 巻 12 号 p.
3680-3687
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
For the quality control of drug products, it is usually necessary to predict the coloration of parenteral solutions under marketing conditions. This paper presents a new method for the prediction of coloration of parenteral solutions using as examples thiamine hydrochloride injection, reserpine injection, ascorbic acid injection and ATP injection. The time course of decrease of percent transmittance at 430 nm for each parenteral solution was measured spectrophotometrically. When the decreases at elevated temperatures were plotted against time on Weibull probability paper, straight lines were obtained at all temperatures. The temperature dependence of the decrease in each parenteral solution was obtained as a straight regression line on plotting (1/m) In k vs. 1/T. The predicted decreases of percent transmittance for each parenteral solution at 25°C were in good agreement with those observed at 25°C except in the case of reserpine injection. Thus, this method proved to be satisfactory for the quality control of the other three injections and may also be applicable to other injections.
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栗田 城治, 小島 弘一, 土屋 隆
1981 年 29 巻 12 号 p.
3688-3695
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Thermolysis of various 4- and/or 6-methyl-1, 2-diazepines (12a, b and 18a-e), prepared from pyridine and lutidine N-imides (11 and 17a-d) having a methyl group in the 3-position, gave the corresponding 1, 3-diazepines (13 and 19) and the 2-aminopyridine derivatives (14 and 20), whereas 1, 2-diazepines (9a-d) having no methyl group in the 4- or 6-position gave only the parent N-imides (8) and no 1, 3-diazepines. Heating of the 2, 3-diazabicyclo [3. 2. 0] hepta-3, 6-dienes (21a, b) formed from the corresponding 1, 2-diazepines by irradiation also gave the 1, 3-diazepines (13a and 19b).
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栗田 城治, 小島 弘一, 円角 美智子, 土屋 隆
1981 年 29 巻 12 号 p.
3696-3705
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
The thermolysis of 1, 2-diazepines (7a-f and 11) having an electron-donating substituent in the 4- or 6-position resulted in the formation of the 1, 3-diazepines (9 and 12) and 2-aminopyridines (10), whereas 1, 2-diazepines (7g-k) having an electron-withdrawing substituent in the same position gave only 2-aminopyridines (10) and no 1, 3-diazepines. However, the thermolysis of 3-, 5-, or 7-substituted 1, 2-diazepines with either an electron-donating or-withdrawing substituent did not give 1, 3-diazepines. Heating of the bicyclic compounds (8) also gave the corresponding 1, 3-diazepines. Based on these results, we concluded that the presence of an electron-donating substituent is essential for this ring-conversion of 1, 2-diazepines into 1, 3-diazepines. These substituent effects and the reaction mechanism are discussed.
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久野 拓造, 松岡 俊和, 堤 一博, 村岡 敬治, 市川 正孝
1981 年 29 巻 12 号 p.
3706-3712
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Pyridine 1-oxide was subjected to 1, 3-dipolar cycloaddition with phenyl isocyanates having an ortho, meta or para substituent group. The reaction conducted at 90°C in dimethylformamide gave the 2, 3-dihydropyridine-form cycloadduct, although the reaction of pyridine 1-oxide with phenyl isocyanate directly affords 2-anilinopyridine. An increase of the reaction time led to increases in the yields of 2-anilinopyridine and 1-phenyl-carbamoyl-2-phenylimino-1, 2-dihydropyridine, while the yield of the cycloadduct tended to decrease. The reaction at 150°C resulted in an increased yield of 2-anilinopyridine. The reactions of 2-anilinopyridine and 5-methyl-2-anilinopyridine with phenyl isocyanate at room temperature afforded the corresponding 1-phenylcarbamoyl-2-phenylimino-1, 2-dihydropyridines, whereas the reactions of 3-methyl- and 3, 5-dimethyl-2-anilinopyridines with phenyl isocyanate at 90°C afforded 2-(N-phenylcarbamoylanilino) pyridine derivatives.
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有富 治郎, 上田 昇三, 西村 温樹
1981 年 29 巻 12 号 p.
3712-3715
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Two ethyl 1, 2-dimethyl-1, 4-dihydroquinoline-3-carboxylate derivatives (I, III) were subjected to the Mannich reaction to give 1-methyl-2-(2-disubstituted aminoethyl) derivatives (II, IV). They are additional examples of the Mannich reaction at the γ-carbon atom of enaminoester compounds.
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千葉 卓男, 土屋 享, 加藤 鉄三
1981 年 29 巻 12 号 p.
3715-3720
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Photoreaction of diketene with N-phenylmaleimide (2) and its dimethyl derivative 3 gave rel-(4R, 5S, 6S)- and rel-(4R, 5R, 6R)-2-oxo-1-oxaspiro [3. 3] heptane-5, 6-dicarboximides (4a and 4b) and their dimethyl derivatives 5a and 5b, respectively. Alcoholysis of compounds 4a and 4b with alcoholic hydrogen chloride gave 5-alkoxycarbonyl-4-oxo-N-phenyl-1, 2-pentanedicarboximides 7 and 8, which were transformed to the corresponding 5-alkoxycarbonyl-3-oxoheptanedioates 9 and 10 by further alcoholysis. Compounds 4a and 4b were hydrolyzed with 10% hydrochloric acid to give 3-carboxy-5-oxohexanoic acid (11). Thermolysis of compounds 4a and 4b gave 3-methylenecyclobutane-1, 2-dicarboximide (12).
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正山 征洋, 森元 聡, 西岡 五夫
1981 年 29 巻 12 号 p.
3720-3723
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Two new neutral propyl cannabinoids, cannabicyclovarin and Δ
7-cis-iso-tetrahydrocannabivarin have been isolated from Thai cannabis, "Meao strain."This is the first report of isolation of the latter, which has a novel skeleton, from natural sources.
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松原 真知子, 古屋 しう子, 黒田 久寅
1981 年 29 巻 12 号 p.
3723-3726
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Soluble trehalase (EC 3.2.1.28) was isolated and purified from the conidia of Cochliobolus miyabeanus by diethylaminoethyl Sephadex A-50 column chromatography and polyacrylamide gel electrophoresis. The molecular weight of this enzyme was estimated to be 160000 by the gel filtration method. Although the purified trehalase hydrolyzed both trehalose and maltose, this enzyme showed higher activity toward trehalose than maltose (the K
m values were 7.3×10
-4M for trehalose and 1.5×10
-2M for maltose). The optimal pH and temperature for the enzyme reaction were 4.0 and 37°C respectively. The enzyme became unstable at 50°C. This enzyme was competitively inhibited by fructose-6-phosphate and Na-pyruvate.
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久保 真百合, 加藤 喜昭, 森坂 勝昭, 稲森 善彦, 野本 享資, 竹本 常松, 坂井 道彦, 沢田 洋介, 谷山 兵三
1981 年 29 巻 12 号 p.
3727-3730
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Racemomycin-A, -C and -B, like racemomycin-D, exhibited insecticidal activity against the adults of Blattella germanica and Musca domestica. These racemomycin compounds, like racemomycin-D, also showed a delayed toxicity on the adult of Blattella germanica. The insecticidal effect of racemomycin-A, -C and -B on both insects was in the order of B>C>A. As the number of β-lysine residues increased, the antibacterial effect increased along with the insecticidal effect. However, racemomycinic A acid, produced by opening of the lactam ring of the streptolidine moiety of racemomycin-A, showed no insecticidal effect. This would suggest an intimate relationship between the streptolidine moiety in the molecule of streptothricin antibiotics and the activity. Citromycin, a streptothricin-like antibiotic, also exhibited an insecticidal effect against the adults of Blattella germanica and Musca domestica, like racemomycin series compounds.
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清水 忠順, 三渕 一二, 横倉 輝男
1981 年 29 巻 12 号 p.
3731-3734
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
The mitogenic activity of whole cells of 18 strains of lactobacilli toward splenocytes from C57BL/6 mice was studied. Although most of the strains showed no mitogenicity, L. fermentum and L. Plantarum were capable of increasing the incorporation of
3H-thymidine (
3H-TdR) into splenocytes. Both strains were also able to stimulate the incorporation of
3H-TdR into splenocytes that had been treated with rabbit antithymocyte serum in the presence of complement in order to kill T-lymphocytes, but did not stimulate the incorporation into thymocytes. These results indicate that L. fermentum and L. plantarum cells act on the B-lymphocyte population of splenocytes.
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成瀬 正織, 芳澤 久美子, 木村 皓俊, 榊原 俊平
1981 年 29 巻 12 号 p.
3734-3737
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Des-Pro
2-Bradykinin was synthesized by the classical solution method as a reference compound for a possible contaminant in synthetic bradykinins, and its behavior in various chromatographic analyses was examined. It showed almost the same Rf values as bradykinin under several different conditions in cellulose thin layer chromatography and in paper electrophoresis, but was clearly separable from bradykinin by reversed phase high performance liquid chromatography under specific conditions. Since des-Pro
2-bradykinin was found to have a potent bradykinin-potentiating activity, contamination by this material should be carefully avoided in bradykinin synthesis.
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田島 和男, 山本 健次, 水谷 民雄
1981 年 29 巻 12 号 p.
3738-3741
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
2, 6-Di-tert-butyl-4-methylene-2, 5-cyclohexadien-1-one (BHT-quinone methide, BHT-QM) was detected in the bile of rats given butylated hydroxytoluene (BHT). The biliary excretion of BHT-QM during 24 h after administration of BHT, 3, 5-di-tert-butyl-4-hydroxybenzyl alcohol (BHT-alcohol), or 2, 6-di-tert-butyl-4-hydroxy-4-methyl-2, 5-cyclohexadien-1-one (4-hydroxy-BHT) was determined by high-performance liquid chromatography. BHT-alcohol gave about 7 times as much BHT-QM as did BHT, but no BHT-QM was detected after administration of 4-hydroxy-BHT. This result suggests that the transformation of BHT to BHT-QM proceeds mainly through BHT-alcohol. Although 1, 2-bis (3, 5-di-tert-butyl-4-hydroxyphenyl) ethane (BHT-dimer) has been reported as a biliary metabolite of BHT in rats, most of the BHT-dimer seems to be formed artificially by dimerization of BHT-QM during the isolation process.
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八木 直美, 縣 功, 川村 多恵子, 田中 揚子, 坂本 美恵子, 伊藤 めぐみ, 関川 彬, 高田 昌彦
1981 年 29 巻 12 号 p.
3741-3747
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Plasma concentration profiles of sulfadimethoxine, sulfamethoxazole and their biotransformed products (N
4-acetate and N
1-glucuronide) in dogs were determined and their pharmacokinetic parameters were calculated by using a two-compartment open model. The apparent partition coefficients between chloroform and phosphate buffer were also determined. Decline in plasma levels of sulfadimethoxine and sulfamethoxazole was considerably accelerated by N
4-acetylation and N
1-glucuronidation. The elimination of sulfadimethoxine-N
1-glucuronide from plasma was more rapid than that of sulfadimethoxine-N
4-acetate, and a similar tendency was observed for sulfamethoxazole and its biotransformed products. N
4-Acetylation or N
1-glucuronidation of sulfadimethoxine and sulfamethoxazole decreased the lipid solubilities markedly in comparison with those of original sulfonamides.
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岡本 敏彦, 首藤 紘一, 高橋 惣四郎, 河内 恵美子, 磯谷 遙
1981 年 29 巻 12 号 p.
3748-3750
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Cytokinins initiate or promote cell division and cell differentiation of plants. N-(4-Pyridyl)-N'-phenylureas with an electronegative substituent (s) at positions 2 and 6 of the pyridine ring are the strongest cytokinins so far known. Structure-activity relationships between urea- and purine-cytokinins were discussed.
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黒崎 文也, 高橋 惣四郎, 首藤 紘一, 岡本 敏彦, 磯谷 遙
1981 年 29 巻 12 号 p.
3751-3753
発行日: 1981/12/25
公開日: 2008/03/31
ジャーナル
フリー
Structural and biological correlation between two classes of cytokinins, purine- and urea-cytokinins, were discussed. The biological response in the presence of competitive antagonists of cytokinins suggested that benzyladenine and N-(4-pyridyl)-N'-phenylurea have a common active site for the growth of tobacco callus.
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