子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 141 | JPS59501982A - | JP50301083 | 1983-09-23 | JPS59501982A | 1984-11-29 | |
| 142 | Plant growth regulator | JP2968884 | 1984-02-21 | JPS59157067A | 1984-09-06 | HANSU GEORUKU SHIYUMITSUTO; KURAUSU RIYURUSEN; KARURUFURIITO BEDEMAIYAA |
| 143 | Diffusion transfer photographic film unit | JP25247083 | 1983-12-28 | JPS59136732A | 1984-08-06 | ABINATSUSHIYU SHII META |
| 144 | Propionic acid derivative and manufacture | JP24235483 | 1983-12-23 | JPS59130236A | 1984-07-26 | SEIKE KOUICHI; UBE PURIISUNITSUTSU; HANSUUYOTSUHEMU RIIBERU; RUUTOUITSUHI OIE; ROBERUTO AARU SHIYUMITSUTO |
| 145 | Enantiomer of propionic acid derivative and manufacture | JP24235383 | 1983-12-23 | JPS59130235A | 1984-07-26 | SEIKE KOUICHI; UBE PURIISUNITSUTSU; HANSUUYOTSUHEMU RIIBERU; RUUTOUITSUHI OIE; ROBERUTO AARU SHIYUMITSUTO |
| 146 | Leucotriene antagonist | JP18099883 | 1983-09-30 | JPS5993043A | 1984-05-29 | PATORISU SHII BERANJIYAA; REJIYAN FUOOTEIN; IBUAN GIYUINDON; JIYOSHIYUA ROKATSUCHI; KURISUCHIYAN YOAKIMU |
| 147 | Benzhydrylsulfinylacetamide derivative, manufacture and central nervous system therapy | JP9879883 | 1983-06-04 | JPS591459A | 1984-01-06 | RUI RAFUON |
| 148 | Polyanionic compound, manufacture and composition | JP1728983 | 1983-02-04 | JPS58145795A | 1983-08-30 | GIYUI BANRERUBERUGE; ANRI SEBATSUGU |
| 149 | Manufacture of alpha,alpha-difluoroalkoxy or alpha,alpha-difluoroalkylthiophenylsulfone | JP11088082 | 1982-06-29 | JPS58124760A | 1983-07-25 | MISHIERU DEBOWA |
| 150 | Aminophenol derivative, its preparation and remedy containing the same | JP20974081 | 1981-12-28 | JPS58113152A | 1983-07-05 | WAKATSUKA HIROHISA; MOURI TETSUYA; HASHIMOTO SHINSUKE |
| NEW MATERIAL:A compound of formulaI[R is formula II(Z is thio, sulfinyl; n is 1, 2, 3; R 1 is H, alkyl, halogen, hydroxyl), formula III (R 2 is H, alkyl, halogen; m is 1, 2), formula IV and formula V]. EXAMPLE: 2-Amino-4-phenylthiophenol. USE: A preventive of or remedy for allergic tracheitis, bronchitis, pneumonopathy, a variety of inflammations and a variety of inflammation caused by prostaglandins. PREPARATION: The selective reduction of the nitro group in the 2-position of the compound of formulaIis conducted with a hydrogen gas in the presence of a catalyst such as Ni, Pt or Pd on carbon or by using Fe, Zn, Sn or SnCl 2 and hydrochloric acid to give the compound of formulaIwith NH 2 group. COPYRIGHT: (C)1983,JPO&Japio | ||||||
| 151 | JPS5757015B2 - | JP13975878 | 1978-11-13 | JPS5757015B2 | 1982-12-02 | TOOMASU HENRII ORUZAISU; CHAARUZU AAMON HAABAATO; MAIKERU ROSU JONSON; ROORENSU SHAAMAN MERUBIN JUNIAA |
| Compounds of the formula <IMAGE> <IMAGE> wherein R1 is hydrogen, benzyl, benzoyl, alkanoyl of 1 to 5 carbon atoms or -CO-(CH2)p-NR'R'' wherein p is 0 or an integer from 1 to 4; each of R' and R'' when taken individually is hydrogen or alkyl of 1 to 4 carbon atoms; R' and R'' when taken together with the nitrogen to which they are attached form a 5- or 6-membered heterocyclic ring selected from piperidino, pyrollo, pyrrolidino, morpholino and N-alkylpiperazino having from 1 to 4 carbon atoms in the alkyl group; R2 is selected from hydrogen, alkanoyl of 1 to 6 carbon atoms and benzoyl; R3 is selected from hydrogen, methyl and ethyl; R4 is selected from hydrogen, alkyl of 1 to 6 carbon atoms and benzyl; Z is selected from: (a) alkylene having from one to nine carbon atoms; (b) -(alk1)m-X-(alk2)n- wherein each of (alk1) and (alk2) is alkylene having from 1 to 9 carbon atoms, with the proviso that the summation of carbon atoms in (alk1) plus (alk2) is not greater than 9; m and n are each 0 or 1; X is selected from O, S, SO, and SO2; and W is selected from hydrogen, methyl, pyridyl, piperidyl, phenyl, monochlorophenyl, monofluorophenyl and <IMAGE> wherein W1 is selected from hydrogen, phenyl, monochlorophenyl and monofluorophenyl; a is an integer from 1 to 5 and b is 0 or an integer from 1 to 4, with the proviso that the sum of a and b is not greater than 5. Compounds I and II are useful as analgesics. Compound III is useful as an intermediate for the preparation of Compounds I and II. Intermediates for the preparation of I, II and III are disclosed. A process for the use of compounds I and II to produce analgesia is also described. | ||||||
| 152 | Salt of 5-fluoro-2-methyl-1-(p- (methylsulfinyl)benzylidene)indene-3-acetic acid | JP4703282 | 1982-03-23 | JPS57167958A | 1982-10-16 | KARURO MIRANI; JIOBANNI MARIA KARUMINAACHI; ATSUCHIRIO SOBEERA |
| 153 | JPS5736899B2 - | JP1823977 | 1977-02-23 | JPS5736899B2 | 1982-08-06 | |
| 154 | JPS5727107B1 - | JP10151170 | 1970-11-19 | JPS5727107B1 | 1982-06-08 | |
| 155 | 4-substituted 3,3-dimethyl-butane-2-ones and manufacture | JP8583581 | 1981-06-05 | JPS5726636A | 1982-02-12 | BUORUFUGANGU KUREEMAA; HANSUURUUTOUITSUHI ERUBE |
| 156 | JPS5640152B2 - | JP14229777 | 1977-11-29 | JPS5640152B2 | 1981-09-18 | |
| 157 | JPS5640151B1 - | JP769372 | 1972-01-21 | JPS5640151B1 | 1981-09-18 | |
| 158 | JPS5639281B2 - | JP11037475 | 1975-09-11 | JPS5639281B2 | 1981-09-11 | |
| 159 | JPS5638587B1 - | JP630078 | 1978-01-25 | JPS5638587B1 | 1981-09-08 | |
| 160 | JPS5636163B2 - | JP9076074 | 1974-08-09 | JPS5636163B2 | 1981-08-22 | |
QQ群二维码
意见反馈
意见反馈