公开(公告)号：US4929267A

公开(公告)日：1990-05-29

申请号：US938872

申请日：1986-12-08

申请人： Akinori Suzuki ,  Suong B. Hyeon ,  Toshio Kajita ,  Masakazu Furushima ,  Shigeo Yoshinaka ,  Takashi Suzuki ,  Mitsunori Oda ,  Akinori Tanaka

发明人： Akinori Suzuki ,  Suong B. Hyeon ,  Toshio Kajita ,  Masakazu Furushima ,  Shigeo Yoshinaka ,  Takashi Suzuki ,  Mitsunori Oda ,  Akinori Tanaka

IPC分类号： A01N33/08 ,  A01N33/12 ,  A01N33/18 ,  A01N37/02 ,  A01N37/06 ,  A01N37/10 ,  A01N43/36 ,  A01N43/40 ,  A01N43/84 ,  A01N47/06 ,  A01N47/12 ,  A01N47/20 ,  C07D295/08

CPC分类号： A01N33/12 ,  A01N33/18 ,  A01N37/02 ,  A01N37/06 ,  A01N37/10 ,  A01N47/06 ,  A01N47/12 ,  A01N47/20

摘要： Use of agriculturally acceptable salts of compounds of the following formula for promoting the growth of plants. ##STR1## wherein Hal represents a chlorine, bromine or iodine atom, X.sub.1 represents a hydrogen or chlorine atom, or a methyl, trifluoromethyl, nitro, methoxy or t-butyl group, and X.sub.2 represents a hydrogen atom, or both X.sub.1 and X.sub.2 represent a chlorine atom or a methyl group; and Y represents a hydrogen atom, or a C.sub.2-6 alkylcarbonyl, benzoyl, N-phenylcarbamoyl, N-3,4-dichlorophenylcarbamoyl, chloropropylcarbonyl, methoxycarbonyl, carbamoyl or methacryloyl group.

公开(公告)号：US5244487A

公开(公告)日：1993-09-14

申请号：US653643

申请日：1991-02-11

申请人： Takashi Oritani ,  Mitsunori Oda ,  Taketo Maruyama ,  Takashi Suzuki ,  Akinori Tanaka ,  Toshio Kajita ,  Shigeo Yoshinaka ,  Masakazu Furushima

发明人： Takashi Oritani ,  Mitsunori Oda ,  Taketo Maruyama ,  Takashi Suzuki ,  Akinori Tanaka ,  Toshio Kajita ,  Shigeo Yoshinaka ,  Masakazu Furushima

IPC分类号： A01N43/90 ,  C07D473/34

CPC分类号： C07D473/34 ,  A01N43/90

摘要： Disclosed are novel adenine derivatives represented by the formula I and agriculturally acceptable acid addition salts thereof represented by the formula: ##STR1## wherein n is an integer of 2-4. Compositions for increasing yield of crops such as leguminous crops and gramineous crops which contain the above adenine derivatives or salts thereof as an active ingredient and methods for increasing yield of crops using these compositions are also disclosed.

摘要翻译： 公开了由式I表示的新型腺嘌呤衍生物及其农业上可接受的由下式表示的酸加成盐：其中n为2-4的整数。 还公开了增加含有上述腺嘌呤衍生物或其盐作为活性成分的豆科作物和禾本科作物的作物的产量的组合物和使用这些组合物提高作物产量的方法。

公开(公告)号：US5211738A

公开(公告)日：1993-05-18

申请号：US861771

申请日：1992-04-02

申请人： Yoshinori Sasaki ,  Takashi Oritani ,  Akinori Tanaka ,  Taketo Maruyama ,  Mitsunori Oda ,  Takashi Suzuki ,  Yoshiaki Suzuki ,  Masakazu Furushima

发明人： Yoshinori Sasaki ,  Takashi Oritani ,  Akinori Tanaka ,  Taketo Maruyama ,  Mitsunori Oda ,  Takashi Suzuki ,  Yoshiaki Suzuki ,  Masakazu Furushima

IPC分类号： A01N43/90 ,  C07D473/34

CPC分类号： C07D473/34 ,  A01N43/90

摘要： A denine derivatives represented by the following formula: ##STR1## (wherein n is 1 or 2 and R and R' represent hydrogen or a methyl, ethyl, allyl, or propargyl group) and agriculturally acceptable acid addition salts thereof, which have cytokinin activity and besides, excellent rooting action, is applied to as plant growth regulators.

公开(公告)号：US5331011A

公开(公告)日：1994-07-19

申请号：US43854

申请日：1993-04-07

申请人： Mitsunori Oda ,  Kazutoshi Kikkawa ,  Akinori Tanaka ,  Satoko Imaruoka ,  Shigeo Yoshinaka

发明人： Mitsunori Oda ,  Kazutoshi Kikkawa ,  Akinori Tanaka ,  Satoko Imaruoka ,  Shigeo Yoshinaka

IPC分类号： A01N39/00 ,  C07C217/20 ,  A01N37/30 ,  C07C63/08 ,  C07C217/08

CPC分类号： C07C217/20 ,  A01N39/00

摘要： Disclosed is an N-benzyl-N-phenoxyethylamine selected from the group consisting of the N-benzyl-N-phenoxyethylamine represented by the following formula (I): ##STR1## and an agriculturally acceptable acid addition salt represented by the following formula (II): ##STR2## wherein m represents a number of 1 or 2 with a proviso that when m is 1 and a chlorine atom in the ring A is present at para(4)-position of the ring A, two chlorine atoms in the ring B are present at 2,3-, 2,5-, 2,6-, 3,4- or 3,5-positions of the ring B, and HX represents an acid.

摘要翻译： 公开了N-苄基-N-苯氧基乙胺，其选自由下式（I）表示的N-苄基-N-苯氧基乙胺：由下式（I）表示的农业上可接受的酸加成盐 式（II）：其中m表示1或2的数，条件是当m为1且环A中的氯原子存在于环A的对位（4）位时， 环B中的两个氯原子存在于环B的2,3-，2,5-，2,6-，3,4-或3,5位，HX表示酸。

公开(公告)号：US5409957A

公开(公告)日：1995-04-25

申请号：US35903

申请日：1993-03-23

申请人： Mitsunori Oda ,  Kazutoshi Kikkawa ,  Akinori Tanaka ,  Satoko Imaruoka ,  Shigeo Yoshinaka

发明人： Mitsunori Oda ,  Kazutoshi Kikkawa ,  Akinori Tanaka ,  Satoko Imaruoka ,  Shigeo Yoshinaka

IPC分类号： A01N39/00 ,  C07C217/00 ,  C07C217/20 ,  A01N33/26

CPC分类号： A01N39/00 ,  C07C217/20

摘要： Disclosed are a phenoxyalkylamine represented by the following general formula I and a salt of said phenoxyalkylamine represented by the following general formula II: ##STR1## wherein R represents a linear saturated hydrocarbon having 7 to 12 carbon atoms, n is an integer of from 1 to 5, m is an integer of from 2 to 4, and HX represents a mineral acid.These compounds have strong bacteriostatic and bactericidal actions for plants with no phytotoxicity. Therefore, these compounds are effectively used as the active ingredient of an agricultural and horticultural bactericide.

摘要翻译： 公开了由以下通式I表示的苯氧基烷基胺和由以下通式II表示的所述苯氧基烷基胺的盐：其中R表示具有7至12个碳原子的直链饱和烃，n是 1〜5的整数，m为2〜4的整数，HX表示无机酸。 这些化合物对没有植物毒性的植物具有很强的抑菌和杀菌作用。 因此，这些化合物有效地用作农业和园艺杀菌剂的活性成分。

公开(公告)号：US5221694A

公开(公告)日：1993-06-22

申请号：US691798

申请日：1991-04-26

申请人： Mitsunori Oda ,  Kazutoshi Kikkawa ,  Akinori Tanaka ,  Satoko Imaruoka ,  Shigeo Yoshinaka

发明人： Mitsunori Oda ,  Kazutoshi Kikkawa ,  Akinori Tanaka ,  Satoko Imaruoka ,  Shigeo Yoshinaka

IPC分类号： A01N39/00 ,  C07C217/20

CPC分类号： C07C217/20 ,  A01N39/00

摘要： Disclosed is an N-benzyl-N-phenoxyethylamine selected from the group consisting of the N-benzyl-N-phenoxyethylamine represented by the following formula (I): ##STR1## and an agriculturally acceptable acid addition salt represented by the following formula (II): ##STR2## wherein m represents a number of 1 or 2 with a proviso that when m is 1 and a chlorine atom in the ring A is present at para(4)-position of the ring A, two chlorine atoms in the ring B are present at 2,3-, 2,5-, 2,6-, 3,4- or 3,5-positions of the ring B and HX represents an acid.

公开(公告)号：US5429940A

公开(公告)日：1995-07-04

申请号：US060240

申请日：1993-07-12

申请人： Teizi Urakami ,  Mitsunori Oda ,  Chieko Itoh ,  Hisao Kobayashi ,  Toshio Nagai ,  Kazuhiro Sugamura

发明人： Teizi Urakami ,  Mitsunori Oda ,  Chieko Itoh ,  Hisao Kobayashi ,  Toshio Nagai ,  Kazuhiro Sugamura

IPC分类号： C07D498/14 ,  C12P17/18 ,  A61K31/435 ,  C12P17/16

CPC分类号： C07D498/14 ,  C12P17/188 ,  Y10S435/822 ,  Y10S435/863

摘要： The present invention provides a process for producing oxazopyrroloquinolines which comprises culturing microorganisms to produce pyrroloquinolinequinone and adding .alpha.-amino acids or monomethylamine to the resulting culture broth which contains the pyrroloquinolinequinone and from which cells of microorganisms are not separated, thereby to convert the pyrroloquinolinequinone to the corresponding oxazopyrroloquinolines. The thus obtained oxazopyrroloquinolines include novel compounds. The present invention further provides aldose reductase inhibitors, diabetic combined disease curing agents, immunopotentiating agents and liver disease inhibiting agents which contain as active ingredient these oxazopyrroloquinolines having excellent physiological activity.

摘要翻译： 本发明提供一种生产恶唑并吡咯并喹啉的方法，其包括培养微生物以产生吡咯并喹啉醌，并向所得的含有吡咯并喹啉醌的培养液中加入α-氨基酸或一甲基胺，并且微生物细胞未分离，从而将吡咯并喹啉醌转化为 对应的恶唑并吡咯啉喹啉。 由此获得的恶唑并吡咯啉喹啉包括新化合物。 本发明还提供了具有优异生理活性的醛糖还原酶抑制剂，糖尿病合并疾病固化剂，免疫增强剂和肝病抑制剂，其含有作为活性成分的恶唑吡咯并喹啉。

公开(公告)号：US09016235B2

公开(公告)日：2015-04-28

申请号：US13256562

申请日：2010-03-12

申请人： Yoshinori Ikagawa ,  Mitsunori Oda ,  Minoru Yamamoto ,  Takashi Kawaguchi ,  Masaaki Tanabe ,  Hideo Hirata

发明人： Yoshinori Ikagawa ,  Mitsunori Oda ,  Minoru Yamamoto ,  Takashi Kawaguchi ,  Masaaki Tanabe ,  Hideo Hirata

IPC分类号： B05C11/00 ,  B05C5/00 ,  B05C11/10 ,  B05C5/02 ,  B05D1/30 ,  B05D1/02 ,  B05B12/08

CPC分类号： B05C11/1007 ,  B05B12/082 ,  B05C5/0258 ,  B05C11/1005

摘要： The substrate coating device (10) includes a slit nozzle (1), a first camera (3), a second camera (4), a control section (5), a pump (8), and a pressure control chamber (9). The control section (5) controls the supply of the coating liquid from the pump (8) to the slit nozzle (1) in accordance with the result of comparison between a bead shape imaged by the first camera (3) and a reference shape. The control section (5) also controls the air pressure on the upstream side of the slit nozzle (1) by the pressure control chamber (9) in accordance with the result of comparison between a distance measured from an image taken by the second camera (4) and a reference distance.

摘要翻译： 基板涂布装置（10）包括狭缝喷嘴（1），第一相机（3），第二相机（4），控制部分（5），泵（8）和压力控制室（9） 。 控制部（5）根据由第一照相机（3）成像的珠粒形状与基准形状的比较结果，控制从泵（8）到狭缝喷嘴（1）的涂布液的供给。 控制部（5）还根据从由第二照相机拍摄的图像测得的距离的比较来控制压力控制室（9）在狭缝喷嘴（1）的上游侧的空气压力 4）和参考距离。

公开(公告)号：US5236930A

公开(公告)日：1993-08-17

申请号：US826220

申请日：1992-01-23

申请人： Teizi Urakami ,  Mitsunori Oda ,  Chieko Itoh ,  Hisao Kobayashi ,  Toshio Nagai ,  Kazuhiro Sugamura

发明人： Teizi Urakami ,  Mitsunori Oda ,  Chieko Itoh ,  Hisao Kobayashi ,  Toshio Nagai ,  Kazuhiro Sugamura

IPC分类号： C07D498/14 ,  C12P17/18

CPC分类号： C07D498/14 ,  C12P17/188 ,  Y10S435/822 ,  Y10S435/863

摘要： The present invention provides a process for producing oxazopyrroloquinolines which comprises culturing microorganisms to produce pyrroloquinolinequinone and adding .alpha.-amino acids or monomethylamine to the resulting culture broth which contains the pyrroloquinolinequinone and from which cells of microorganisms are not separated, thereby to convert the pyrroloquinolinequinone to the corresponding oxazopyrroloquinolines.The thus obtained oxazopyrroloquinolines include novel compounds.The present invention further provides aldose reductase inhibitors, diabetic combined disease curing agents, immunopotentiating agents and liver disease inhibiting agents which contain as active ingredient these oxazopyrroloquinolines having excellent physiological activity.

摘要翻译： 本发明提供一种生产恶唑并吡咯并喹啉的方法，其包括培养微生物以产生吡咯并喹啉醌，并向所得的含有吡咯并喹啉醌的培养液中加入α-氨基酸或一甲基胺，并且微生物细胞未分离，从而将吡咯并喹啉醌转化为 对应的恶唑并吡咯啉喹啉。 由此获得的恶唑并吡咯啉喹啉包括新化合物。 本发明还提供了具有优异生理活性的醛糖还原酶抑制剂，糖尿病合并疾病固化剂，免疫增强剂和肝病抑制剂，其含有作为活性成分的恶唑吡咯并喹啉。

公开(公告)号：US5061711A

公开(公告)日：1991-10-29

申请号：US592266

申请日：1990-10-03

申请人： Teizi Urakami ,  Mitsunori Oda ,  Chieko Itoh

发明人： Teizi Urakami ,  Mitsunori Oda ,  Chieko Itoh

IPC分类号： A61K31/47

CPC分类号： A61K31/47

摘要： Disclosed is a method of curing liver diseases by administration of pyrrolo quinoline quinon triesters (PQQ triesters). The PQQ triesters include PQQ triallyl ester and PQQ tribenzyl ester which are novel. The PQQ triesters being ester form, they have no toxicity and can be orally adminstered.