ツロブテロールの生体内運命(第4報)ラット日齢と生体内動態について
スポンサーリンク
概要
- 論文の詳細を見る
The absorption, excretion and metabolism of tulobuterol were studied in various aged rats after oral administration of ^<14>C-tulobuterol. The blood levels of ^<14>C after oral dosing in various aged rats, decreased gradually according to a biphasic process, that is, the first peak appeared at 30-40 min and the second one at 1-2 hr. The excretion of ^<14>C after oral dosing was generally rapid and the radioactivities in the urine and feces for 7 days after oral dosage in various aged rats were 59-66% and 33-36% of the dose, respectively. The biliary excretion of ^<14>C until 24 hr was estimated to be 59-66% of the dose in all aged rats studied, but the rate of excretion in 21-day-old rats was slower than those of 49- and 150-day-old rats. Furthermore, the excretion amount of the ring hydroxylated metabolites, such as 4-hydroxy form (II) and 4-hydroxy-5-methoxy form (IV) into the bile of the 21-day-old-rats was different from those of the 49- and 150-day-old rats. The relation between the activity of metabolizing enzymes in the liver and the age of rats was also studied. The metabolic activity of tulobuterol in the rat liver gradually increased until the 28th day, and thereafter decreased with an increase in the age.
- 社団法人日本薬学会の論文
- 1980-12-25
著者
-
桐山 典城
Faculty of Pharmaceutical Sciences, Hokuriku University
-
桐山 典城
北陸大学薬学部
-
加藤 日出男
北陸製薬株式会社
-
西出 和憲
北陸製薬株式会社中央研究所
-
荒谷 隆幸
Research Laboratories, Hokuriku Seiyaku Co., Ltd.,
-
高原 義男
北陸製薬株式会社 中央研究所
-
松村 阜子
北陸製薬株式会社中央研究所
-
桐山 典城
Faculty Of Pharmaceutical Sciences Hokuriku University
-
荒谷 隆幸
Research Laboratories Hokuriku Seiyaku Co. Ltd.
関連論文
- FOUR NEW METABOLITES OF ASPERGILLUS TERREUS
- キンミズヒキAgrimonia pilosa LEDEB.の成分研究(第1報)n-Hexane可溶性酸性画分の生物活性について
- 気管支喘息治療薬ツロブテロールの経皮吸収型製剤の開発
- 232 新規TXA_2/LTD_4デュアル拮抗薬RS-601の抗喘息作用
- Benzenesulfonamide誘導体の合成とThromboxane A_2及びLeukotriene D_4に対するDual拮抗作用
- Amphoteric Drugs. II. Synthesis and Antiallergic Activity of [4-(5H-Dibenzo[a, d]cycloheptan-5-ylidene)piperidino]alkanoic Acid Derivatives and Related Compounds
- Amphoteric Drugs. I. Synthesis and Antiallergic Activity of [4-(Diphenylmethoxy)piperidino]-, [4-(Diphenylmethyl)piperazinyl]-and [4-(Diphenylmethylene)piperidino]alkanoic Acid Derivatives
- Transport Mechanism of an H_1-Antagonist at the Blood-Brain Barrier : Transport Mechanism of Mepyramine Using the Carotid Injection Technique
- 医薬品の両性イオン化(第3報)1,2,3,4,10,14b-Hexahydrodibenzo-[c, f]pyrazino[1,2-α]azepine及び2,3,4,9-Tetrahydro-1H-dibenzo[3,4 : 6,7]cyclohepta[1,2-c]pyridineのN-Alkylcarboxylic Acid誘導体の合成とその薬理作用
- Study on Zwitter-Ionization of Drugs. II. Synthesis and Pharmacological Activity of Some N-[3-(5H-Dibenzo[a, d]cyclohepten-5-ylidene)propyl]-N-methylamino- and N-[3-(6H-Dibenz[b, e]oxepin-11-ylidene)propyl]-N-methylamino-alkanoic Acid Derivatives and Rela
- INTER-INDIVIDUAL DIFFERENCES OF (+)-4-[4-(4-METHYLPHENYL)PHENYLMETHOXY-1-PIPERIDINYL]BUTYRIC ACID ((+)-MPPB) DISPOSITION IN RATS
- 医薬品の両性イオン化(第1報)4-(2-Chlorodibenz[b, f][1,4]oxazepin-11-yl)piaerazine, 4-(2-Chlorodibenzo[b, f][1,4]thiazepin-11-yl)-piperazine及び4-(11H-Dibenz[b, e]azepin-6-yl)piperazineのN-アルキルカルボン酸誘導体の合成とその薬理作用
- Novel Phenoxyalkylamine Derivatives. VII. Synthesis and Pharmacological Activities of 2-Alkoxy-5-[(Phenoxyalkylamino)alkyl]benzenesulfonamide Derivatives
- Synthesis, Gastrointestinal Prokinetic Activity and Structure-Activity Relationships of Novel N-[[2-(Dialkylamino)ethoxy)benzyl]benzamide Derivatives
- Quinolone系抗菌剤の研究(第3報)5-Amino-7-(2-aminoalkoxy)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic Acid及びその関連化合物の合成と抗菌活性
- Ouinolone系抗菌剤の研究(第2報)7-Aminoalkoxy-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic Acid及びその関連化合物の合成と抗菌活性
- 新規なPhenoxyalkylamine誘導体(第6報)α-[(Phenoxyethylamino)propyl]-α-phenylacetonitrile誘導体の合成とα-遮断作用
- Studies on Antiallergic Agents. II. : Quantitative Structure-Activity Relationships of Novel 6-Substituted N-(1H-Tetrazol-5-yl)-2-pyrazinecarboxamides
- Quinolone系抗菌剤の研究(第1報)7-(2-Aminoethoxy)-, 7-(2-Aminoethylthio)-及び7-(2-Aminoethylamino)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic Acid及びそれらの誘導体の合成と抗菌活性
- Studies on Antiallergic Agents. I. : Synthesis and Antiallergic Activity of Novel Pyrazine Derivatives
- Novel Phenoxyalkylamine Derivatives. V. : Synthesis, α-Blocking Activity and Quantitative Structure-Activity Analysis of α-[(Phenoxyethylamino)propyl]-α-phenylacetonitrile Derivatives
- Novel Phenoxyalkylamine Derivatives. IV. : Synthesis, Ca^-Antagonistic Activity and Quantitative Structure-Activity Analysis of α-Isopropyl-α-[3[3-(3-methoxyphenoxy)propylamino]propyl]-α-phenylacetonitrile Derivatives
- Metabolic Products of Aspergillus terreus. IV. Metabolites of the Strain IFO 8835. (2). The Isolation and Chemical Structure of Indolyl Benzoquinone Pigments
- ο-Chloro-α-(tert-butylaminomethyl)-benzyl Alcohol Hydrochloride(C-78)の生体内運命(第2報^)ラットにおける代謝物
- Synthesis and Histamine H_2-Antagonist Activity of 4-Quinazolinone Derivatives
- Novel Phenoxyalkylamine Derivatives. III. : Quantitative Structure-Activity Relationships of Ca^-Antagonistic α-Alkyla-α-[(phenoxypropylamino)propyl]-3,4,5-trimethoxy-benzeneacetonitrile Derivatives
- Novel Phenoxyalkylamine Derivatives. II. : Synthesis and Ca^-Antagonistic Activities of α-Alkyl-α-[(phenoxypropylamino)propyl]-benzeneacetonitrile Derivatives
- Novel Phenoxyalkylamine Derivatives. I. : Synthesis and Pharmacological Activities of α-Isopropyl-α-[(phenoxyalkylamino)alkyl]-benzeneacetonitrile Derivatives
- (2-Pyrimidinylamino)phenylacetic Acid誘導体の合成と抗炎症作用
- Dexamethasone valerate (DV-17) と他の副腎皮質ステロイド外用剤のラット比較毒性試験
- Dexamethasone valerate (DV-17)と他の副腎皮質ステロイド外用剤のウサギにおける刺激性試験 : 皮膚および眼粘膜一次刺激性試験ならびに皮膚累積刺激性試験
- Study on Zwitter-Ionization of Drugs. II. Synthesis and Pharmacological Activity of Some N-[3-(5H-Dibenzo[a, d]cyclohepten-5-ylidene)propyl]-N-methylamino- and N-[3-(6H-Dibenz[b, e]oxepin-11-ylidene)propyl]-N-methylamino-alkanoic Acid Derivatives and Rela
- Study on Zwitter-Ionization of Drugs. II. Synthesis and Pharmacological Activity of Some N-[3-(5H-Dibenzo[a, d]cyclohepten-5-ylidene)propyl]-N-methylamino- and N-[3-(6H-Dibenz[b, e]oxepin-11-ylidene)propyl]-N-methylamino-alkanoic Acid Derivatives and Rela
- Study on Zwitter-Ionization of Drugs. II. Synthesis and Pharmacological Activity of Some N-[3-(5H-Dibenzo[a, d]cyclohepten-5-ylidene)propyl]-N-methylamino- and N-[3-(6H-Dibenz[b, e]oxepin-11-ylidene)propyl]-N-methylamino-alkanoic Acid Derivatives and Rela
- Study on Zwitter-Ionization of Drugs. II. Synthesis and Pharmacological Activity of Some N-[3-(5H-Dibenzo[a, d]cyclohepten-5-ylidene)propyl]-N-methylamino- and N-[3-(6H-Dibenz[b, e]oxepin-11-ylidene)propyl]-N-methylamino-alkanoic Acid Derivatives and Rela
- Study on Zwitter-Ionization of Drugs. II. Synthesis and Pharmacological Activity of Some N-[3-(5H-Dibenzo[a, d]cyclohepten-5-ylidene)propyl]-N-methylamino- and N-[3-(6H-Dibenz[b, e]oxepin-11-ylidene)propyl]-N-methylamino-alkanoic Acid Derivatives and Rela
- Study on Zwitter-Ionization of Drugs. II. Synthesis and Pharmacological Activity of Some N-[3-(5H-Dibenzo[a, d]cyclohepten-5-ylidene)propyl]-N-methylamino- and N-[3-(6H-Dibenz[b, e]oxepin-11-ylidene)propyl]-N-methylamino-alkanoic Acid Derivatives and Rela
- Study on Zwitter-Ionization of Drugs. II. Synthesis and Pharmacological Activity of Some N-[3-(5H-Dibenzo[a, d]cyclohepten-5-ylidene)propyl]-N-methylamino- and N-[3-(6H-Dibenz[b, e]oxepin-11-ylidene)propyl]-N-methylamino-alkanoic Acid Derivatives and Rela
- Crystal Structures of Polymorphs of α-[(tert-Butylamino) methyl]-2-chloro-4-hydroxybenzyl Alcohol Hydrochloride (HOKU-81)
- 鎮痙剤の研究(第7報)N-Alkyl Diarylmethylenequinolizidinium Bromides, N-Alkyl Diarylmethyleneindolizidinium Bromidesおよび関連化合物の構造活性相関
- 鎮痙薬の薬理学的研究(第1報)Diarylmethylene-5-methyl-transquinolizidinium Bromide類の鎮痙作用への選択性
- Studies on Antispasmodics. VI. Synthesis of N-Alkyl 6- and 7-Diarylmethyleneindolizidinium Bromides
- Studies on Antispasmodics. V. Synthesis and Anticholinergic Activity of N-Alkyl 1- and 2-Diarylmethylene-indolizidinium Bromides
- 鎮痙剤の研究(第4報)Diarylhydroxymethylquinolizidine Methohalidesの合成と抗アセチルコリン作用
- 鎮痙剤の研究(第3報)2位置換Quinolizidine類の簡便な新合成法とそれらの立体構造について
- 鎮痙剤の研究(第2報)3位置換Quinolizidine類の簡便な新合成法とそれらの立体構造について
- Studies on Antispasmodics. I. Synthesis and Anticholinergic Activity of 1-, 2-, and 3-Diarylmethylenequinolizidine Quaternary Ammonium Salts
- o-Chloro-α-(tert-butylaminomethyl)benzylalcohol Hydrochloride(C-78)および関連化合物の合成と気管支拡張作用
- Studies on 1-Azabicyclo Compounds. XXVI. Synthesis of Ten-membered Ring Amines from 9a-Cyanomethyl-, 9a-Ethoxycarbonylmethyl-, and 1-Ethoxycarbonyl-octahydroquinolizine
- Studies on the Relationship between Physico-chemical Properties and Crystalline Forms of Tulobuterol Hydrochloride. II. Crystal Structure Analyses of the Four Crystalline Forms of Tulobuterol Hydrochloride
- 2-Methyl-3-pyrrolidinopropiophenone誘導体の中枢性筋弛緩作用
- Studies on the Metabolic Products of Aspergillus terreus. II. Structure and Biosynthesis of the Metabolites of the Strain ATCC12238
- Tulobuterolの生体内運命(第5報)ラット, イヌ, モルモットおよびウサギにおける代謝および排泄に関する種差
- ツロブテロールの生体内運命(第4報)ラット日齢と生体内動態について
- ο-Chloro-α-(tert-butylaminomethyl)-benzyl Alcohol Hydrochloride(C-78)の生体内運命(第3報^)ラット肝臓におけるin Vitro代謝
- 塩酸ツロブテールの性状と結晶形との相関に関する研究(第3報) : 塩酸ツロブテール多形の吸湿特性
- 塩酸ツロブテロールの性状と結晶形との相関に関する研究(第3報)塩酸ツロブテロール多形の吸湿特性
- Studies on the Relationship between Physico-chemical Properties and Crystalline Forms of Tulobuterol Hydrochloride. I. Polymorphism of Tulobuterol Hydrochloride
- 胃粘膜微小循環に及ぼす3-(Di-2-thienylmethylene)-5-methyl-trans-quinolizidinium Bromide(HSR-902)の影響
- PARTIAL DEACETYLATION OF ASTERRIQUINONE DIACETATE BY AQUEOUS SODIUM BICARBONATE IN PYRIDINE
- Trichothecium roseum LINKの代謝産物の研究Rosein IIIの構造
- Relationship between the Structure and Cytotoxic Activity of Asterriquinone, an Antitumor Metabolite of Aspergillus terreus, and Its Alkyl Ether Derivatives
- Preparation and Structure-Activity Relationships of Novel Asterriquinone Derivatives
- Studies on the Cytotoxicity of Asterriquinone Derivatives
- Polymorphism of α-[(tert-Butylamino) methyl]-2-chloro-4-hydroxybenzyl Alcohol Hydrochloride (HOKU-81)
- 1-Azabicyclo化合物の研究(第21報)1,2,3,10,11,11a-Hexahydro-5H-pyrrolo-[2,1-c][1,4]benzodiazepin-11-oneおよび5,6,6a, 7,8,9,10,12-Octahydropyrido[2,1-c][1,4]benzodiazepin-6-oneから中環状AminolactamおよびSpiroaminolactam体の合成
- Studies on 1-Azabicyclo Compounds. XVI. Synthesis of 1'-Methylindan-2-spiro-2'-piperazine and Related Compounds
- Studies on 1-Azabicyclo Compounds. XV. Oxidation of 1,3,4,6,11,11a-Hexahydro-2H-pyrazino [1,2-b] isoquinolin-1-one Derivatives with Mercuric Acetate, and Their Conversion into 1,2,3,4,5,6,7,8-Octahydro-2-methyl-2,5-benzodiazecine and Related Compounds
- 薄層クロマトグラフィーによるベンジルヒドロクロロチアジド製剤中の1-アミノ-5-クロロベンゼン-2,4-ジスルホンアミドの直接定量
- 錯体生成による医薬品の間接原子吸光分析の利用(その3)ライネッケ塩による製剤中のノスカピンの定量
- 1-Azabicyclo化合物の研究その5 : 4-Oxoquinolizidineの水素化リチウムアルミニウム還元およびQuinolizidineの酢酸第二水銀酸化により得られた二量体の化学構造
- Preparation and Route of Asterriquinone Monoalkyl Ether from Asterriquinone Diacetate by Treatment with a Mixture of Alcohol and Alkali, Followed by Acidification
- TRANSFORMATION OF ASTERRIQUINONE DIACETATE TO ASTERRIQUINONE MONOALKYL ETHER VIA ITS MONOACETAL
- Studies on the Metabolic Products of Aspergillus terreus. III. Metabolites of the Strain IFO 8835. (1)
- Studies on the Metabolic Products of Aspergillus terreus. I. Metabolites of the Strain IFO 6123
- Studies on the Metabolic Products of Aspergillus fumigatus (J-4). Chemical Structure of Metabolic Products
- Diazabicycloalkanesの研究(第2報)4-[β-(10-Phenothiazinyl)-ethyl]-1,4-diazabicyclo[4,4,0]-decaneおよび類似化合物の抗ヒスタミン作用ならびに向精神作用
- 臭化チキジウム
- 鎮痙薬の薬理学的研究(第5報) : 3-(Di-2-Thienylmethylene)-5-Methyl-trans-Quinolizidinium Bromide (HSR-902) の骨盤神経終末と膀胱壁筋との神経伝達に及ぼす作用
- 鎮痙薬の薬理学的研究(第3報) 3-(Di-2-Thienylmethylene)-5-Methyl-trans-QuinolizidiniumBromide(HSR-902)の鎮痙作用とその臓器特異性
- 3-(5-Nitro-2-furyl)-benzo-1,2,4-triazine誘導体の合成ならびに抗細菌作用について
- 原子吸光法による生体試料中の臭化正ブチルスコポラミンおよび正ブチルスコポラミンタンニン酸の定量 : トロパンアルカロイドの分析研究(第3報)
- 1-Azabicyclo化合物の研究(第20報)Hexahydroisoquino[3,2-c][1,4]benzodiazepineおよび関連化合物の合成ならびにHexahydroisoquino[3,2-c]-[1,4]benzodiazepin-13-one から6-Methyl-hexahydro-5H-dibenzo[b, g][1,5]diazacycloundecineの生成
- 1-Azabicyclo化合物の研究(第25報)Octahydropyrrolo[1,2-α]pyrazin-1-oneから9員環状Aminolactamおよび関連化合物の合成