161 |
(Haloalkyl) dibenzo tellurocarbonyl Fe salt, the production intermediates, and methods for their production |
JP28954292 |
1992-10-02 |
JP3250679B2 |
2002-01-28 |
照雄 梅本; 寿美 石原 |
|
162 |
The pharmaceutical for the preparation of cells for use in bone marrow cells |
JP31411889 |
1989-12-01 |
JP3067779B2 |
2000-07-24 |
ベンジャミン、スレドニ; マイケル、アルベック |
|
163 |
The liquid crystal compounds having a perfluoroether terminal portion |
JP51605096 |
1995-10-05 |
JPH10508845A |
1998-09-02 |
エム. サブ,パトリシア; ピー. ジャニュリス,ユージーン; シー. ジョンソン,ギルバート; シー. スナスタッド,ダニエル; ディー. スパウン,テレンス; ディー. ラドクリフ,マルク |
(57)【要約】 少なくとも1個のカテナリーエーテル酸素を有するフルオロカーボン末端部分及び炭化水素末端部分を含むフッ素含有液晶化合物であって、前記末端部分が中心核により連結されたフッ素含有液晶化合物。 該化合物はスメクチック又は潜在的スメクチック中間相を示す。 |
164 |
Novel radical Bamo Iruteru Lido compound |
JP10664392 |
1992-04-24 |
JP2709774B2 |
1998-02-04 |
博友 佐々木; 亨 藤森 |
|
165 |
Dry immunity analyzing element and analyzing method of immunologically reactive ligand |
JP14619396 |
1996-06-07 |
JPH0921807A |
1997-01-21 |
MAAGARETSUTO ERIZABESU ROOGAN; KIYARORU AN DEKAN; MAASHIYA DENISU BEIRU OONITSUK; GEIRII RUISU SUNOTSUDOGURASU; ROI OOJIIN SUNOOKU |
PROBLEM TO BE SOLVED: To reduce a fluctuation in coloring rate observed by the uppermost element when a common test fluid is reacted with an element in a cartridge by containing an immobilized receptor or the like to a ligand by the constant concentration.
SOLUTION: A dry analyzing element to analyze a ligand contains a band of an oxygen labeled ligand or an oxygen labeled receptor, a developing band, an immobilized receptor to a ligand and a labeling ligand by the constant concentration. In that case the receptor contains a support body to carry the receptor band bonded with covalent bond to polymer beads having a diameter of 0.1 to 5μm. This element contains a diaryl telluride compound, and plural hands may exist in the same layer, or may exist in separate layers. According to this element, a first slide bias (that is, coloring speed of the uppermost element in a cartridge is different from cloring rate of its other element in the same cartridge) can be reduced.
COPYRIGHT: (C)1997,JPO |
166 |
Method of manufacturing a dialkyl tellurium and selenium dialkyl |
JP50039089 |
1988-12-02 |
JP2568287B2 |
1996-12-25 |
MARURIN JON BURAIAN; KOORUUHAMIRUTON DEBITSUDO JON; SHENAIIHATSUKUHEITO DEODATSUTA BINAYATSUKU; UETSUBU HOORU |
|
167 |
Lymphokine production stimulant |
JP18605694 |
1994-08-08 |
JP2528268B2 |
1996-08-28 |
スレドニ ベンジャミン; アルベック マイケル |
|
168 |
Purification methods of tellurium and selenium alkyl |
JP50094589 |
1988-12-02 |
JPH0830056B2 |
1996-03-27 |
MARIN JON BURAIAN; KOORUUHAMIRUTON DEIBITSUDO JON; SHENEIIKATOKEITO DEIODATA BAINAYOKU; UEBU HOORU |
|
169 |
JPH07506368A - |
JP51944993 |
1993-04-26 |
JPH07506368A |
1995-07-13 |
|
|
170 |
Surface latent image-type silver halide photographic emulsion |
JP10371893 |
1993-04-07 |
JPH06295009A |
1994-10-21 |
MIFUNE HIROYUKI; SASAKI HIROTOMO |
PURPOSE:To provide a silver halide photographic emulsion in which sensitivity for exposure in a long time with low illuminance and for spectral sensitizing are improved. CONSTITUTION:This surface latent image-type silver halide photographic emulsion contains silver halide particles doped with tellurium ions. Tellurium ions are given by at least one unstable tellurium compd. selected from tellurium- contg. org. compd. directly bonded with a single bond with S, SO, SO,, Se, P=0 or P:S, cyclic org. compd. having two or more chalcogen atoms containing at least one tellurium in the ring, and tellurium anion-contg. org. compd. |
171 |
Method of solubilizing tellurium using an organic acid |
JP20337392 |
1992-07-30 |
JPH0676372B2 |
1994-09-28 |
HAABAATO JEE KAIZAA |
|
172 |
New dicarbamoyl ditelluride compound |
JP10664492 |
1992-04-24 |
JPH05306269A |
1993-11-19 |
SASAKI HIROTOMO; FUJIMORI TORU |
PURPOSE: To provide a new compound useful as a synthetic intermediate for pharmaceuticals, agricultural chemicals, photographic chemicals, etc.
CONSTITUTION: The compound of formula I (R
1 is aromatic group; R
2 is aliphatic or aromatic group), e.g. the compound of formula II. The compound of formula I can be produced e.g. by reacting a carbamoyl chloride (R
1R
2NCOCl) with a reagent (Na
2Te
2) produced by reducing tellurium with sodium hydride, etc.
COPYRIGHT: (C)1993,JPO&Japio |
173 |
New tellurocarboxylate compound |
JP41403590 |
1990-12-26 |
JPH04224595A |
1992-08-13 |
YAGIHARA MORIO; SASAKI HIROTOMO; KATO SHINJI |
PURPOSE: To provide a tellurium compound useful as a synthetic intermediate for a compound for photography, medicines and agricultural chemicals.
CONSTITUTION: A tellurium compound shown by the general formula (I) RC-O- Te
-Li
+ (R is alkyl group or aryl group).
COPYRIGHT: (C)1992,JPO&Japio |
174 |
JPH0422847B2 - |
JP13565583 |
1983-07-25 |
JPH0422847B2 |
1992-04-20 |
SANTOKU ESU BADESHA; TOOMASU DABURYU SUMISU |
|
175 |
JPH0422846B2 - |
JP13565683 |
1983-07-25 |
JPH0422846B2 |
1992-04-20 |
SANTOKU ESU BADESHA |
|
176 |
Polycyclic amines useful as cerebrovascular agents |
JP6993390 |
1990-03-22 |
JPH03184943A |
1991-08-12 |
KURISUTOFUAA FURANKURIN BITSUJ; SHIERIRU JIIN HEIZU; GUREIAMU JIYONSON; PERII MAIKURU NOOBAKU; DANIERU FURETSUDO OOTOWAIN |
PURPOSE: To provide a cerebrovascular agent for treatment of neurodegenerative disorders including cerebrovascular diseases, comprising a polycyclic amine such as aminomethylhexahydrophenanthrene.
CONSTITUTION: A compound of the formula [R
1 and R
2 are each H, an alkyl, alkenyl, arylalkyl or a pharmaceutically acceptable labile group, or R
1 and R
2 together form a heterocyclic ring; R
3 and R
4 are each H, an alkyl, OH, alkoxy, halogen, NH
2, mono or dialkylamino, etc.; ring A may be thiophene; R
5 and R
6 are each H, an alkyl, alkenyl, OH, aldehyde, alkylcarbonyl, etc.; X' is CH
2, O, S, etc.; X is CR
7R
8, CR
7R
8CH
2, CR
7=CR
8, CHR
7S, etc. (R
7 and R
8 are each H, an alkyl, OH, methoxy, etc.); n is 0 to 2], e.g. 1,3,4,10a- tetrahydro-N-2-propenyl-4a(2H)-phenanthreneamine, is incorporated as an active ingredient.
COPYRIGHT: (C)1991,JPO |
177 |
JPS6353985B2 - |
JP9883 |
1983-01-04 |
JPS6353985B2 |
1988-10-26 |
ENOMOTO SABURO; KAMYAMA TSUTOMU; KATO KUNIOKI |
|
178 |
Fluorine-containing chiral smectic liquid crystal |
JP16220587 |
1987-06-29 |
JPS6327451A |
1988-02-05 |
YUUJIN PIITAA YANURISU |
|
179 |
Cytokine production stimulating compound |
JP25097785 |
1985-11-11 |
JPS61215386A |
1986-09-25 |
MAIKERU ARUBETSUKU; BENJIYAMIN SUREDONI |
|
180 |
Z-3-trihalochalcogenpropenone compound, manufacture and electrophotographic layer |
JP21528484 |
1984-10-16 |
JPS60109560A |
1985-06-15 |
MAIKERU AARU DETEII; JIEROOMU EICHI PAARUSUTEIN |
|