N,N-SUBSTITUTED 3-AMINOPYRROLIDINE COMPOUNDS USEFUL AS MONOAMINES REUPTAKE INHIBITORS
or a salt thereof, wherein R101 and R102 are each independently a phenyl group or a pyridyl group, the phenyl group or the pyridyl group may have one or more substituents selected from halogen atoms and lower alkyl groups optionally substituted with one or more halogen atoms, etc. The pyrrolidine co...
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| creator | ITO Nobuaki MATSUZAKI Takayuki AKAZAWA Kohei AMADA Naoki SASAKI Hirofumi TAKEMURA Noriaki MASUMOTO Takumi MIYAMURA Shin SAKURAI Yohji WATANABE Akihito NAKAJIMA Satoko KURIMURA Muneaki OHASHI Satoshi TAI Kuninori SHINOHARA Tomoichi TAIRA Shinichi MENJO Yasuhiro MORITA Chisako TOMOYASU Takahiro SAKATA Yasuyo SUGINO Haruhiko YAMASHITA Junko |
| description | or a salt thereof, wherein R101 and R102 are each independently a phenyl group or a pyridyl group, the phenyl group or the pyridyl group may have one or more substituents selected from halogen atoms and lower alkyl groups optionally substituted with one or more halogen atoms, etc. The pyrrolidine compound or a salt thereof of the present invention is usable to produce a pharmaceutical preparation having a wider therapeutic spectrum and being capable of exhibiting sufficient therapeutic effects after short-term administration. |
| format | Patent |
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TAI Kuninori ; SHINOHARA Tomoichi ; TAIRA Shinichi ; MENJO Yasuhiro ; MORITA Chisako ; TOMOYASU Takahiro ; SAKATA Yasuyo ; SUGINO Haruhiko ; YAMASHITA Junko</creator><creatorcontrib>ITO Nobuaki ; MATSUZAKI Takayuki ; AKAZAWA Kohei ; AMADA Naoki ; SASAKI Hirofumi ; TAKEMURA Noriaki ; MASUMOTO Takumi ; MIYAMURA Shin ; SAKURAI Yohji ; WATANABE Akihito ; NAKAJIMA Satoko ; KURIMURA Muneaki ; OHASHI Satoshi ; TAI Kuninori ; SHINOHARA Tomoichi ; TAIRA Shinichi ; MENJO Yasuhiro ; MORITA Chisako ; TOMOYASU Takahiro ; SAKATA Yasuyo ; SUGINO Haruhiko ; YAMASHITA Junko</creatorcontrib><description>or a salt thereof, wherein R101 and R102 are each independently a phenyl group or a pyridyl group, the phenyl group or the pyridyl group may have one or more substituents selected from halogen atoms and lower alkyl groups optionally substituted with one or more halogen atoms, etc. The pyrrolidine compound or a salt thereof of the present invention is usable to produce a pharmaceutical preparation having a wider therapeutic spectrum and being capable of exhibiting sufficient therapeutic effects after short-term administration.</description><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2017</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20170615&DB=EPODOC&CC=US&NR=2017166524A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76418</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20170615&DB=EPODOC&CC=US&NR=2017166524A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>ITO Nobuaki</creatorcontrib><creatorcontrib>MATSUZAKI Takayuki</creatorcontrib><creatorcontrib>AKAZAWA Kohei</creatorcontrib><creatorcontrib>AMADA Naoki</creatorcontrib><creatorcontrib>SASAKI Hirofumi</creatorcontrib><creatorcontrib>TAKEMURA Noriaki</creatorcontrib><creatorcontrib>MASUMOTO Takumi</creatorcontrib><creatorcontrib>MIYAMURA Shin</creatorcontrib><creatorcontrib>SAKURAI Yohji</creatorcontrib><creatorcontrib>WATANABE Akihito</creatorcontrib><creatorcontrib>NAKAJIMA Satoko</creatorcontrib><creatorcontrib>KURIMURA Muneaki</creatorcontrib><creatorcontrib>OHASHI Satoshi</creatorcontrib><creatorcontrib>TAI Kuninori</creatorcontrib><creatorcontrib>SHINOHARA Tomoichi</creatorcontrib><creatorcontrib>TAIRA Shinichi</creatorcontrib><creatorcontrib>MENJO Yasuhiro</creatorcontrib><creatorcontrib>MORITA Chisako</creatorcontrib><creatorcontrib>TOMOYASU Takahiro</creatorcontrib><creatorcontrib>SAKATA Yasuyo</creatorcontrib><creatorcontrib>SUGINO Haruhiko</creatorcontrib><creatorcontrib>YAMASHITA Junko</creatorcontrib><title>N,N-SUBSTITUTED 3-AMINOPYRROLIDINE COMPOUNDS USEFUL AS MONOAMINES REUPTAKE INHIBITORS</title><description>or a salt thereof, wherein R101 and R102 are each independently a phenyl group or a pyridyl group, the phenyl group or the pyridyl group may have one or more substituents selected from halogen atoms and lower alkyl groups optionally substituted with one or more halogen atoms, etc. The pyrrolidine compound or a salt thereof of the present invention is usable to produce a pharmaceutical preparation having a wider therapeutic spectrum and being capable of exhibiting sufficient therapeutic effects after short-term administration.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2017</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNysEKgkAQAFAvHaL6h4WuCalp51VHHNIZ2dk5dBKJ7RQl2P8TQR_Q6V3eOlI6UCxaikevHmqTxbZH4uHqHHdYI4GpuB9YqRajAo12xorpmfgbQYwDHby9gEFqsUTPTrbR6j49lrD7uYn2DfiqjcP8GsMyT7fwDO9RJT0m56Qo8vRkk-y_9QF0XTIA</recordid><startdate>20170615</startdate><enddate>20170615</enddate><creator>ITO Nobuaki</creator><creator>MATSUZAKI Takayuki</creator><creator>AKAZAWA Kohei</creator><creator>AMADA Naoki</creator><creator>SASAKI Hirofumi</creator><creator>TAKEMURA Noriaki</creator><creator>MASUMOTO Takumi</creator><creator>MIYAMURA Shin</creator><creator>SAKURAI Yohji</creator><creator>WATANABE Akihito</creator><creator>NAKAJIMA Satoko</creator><creator>KURIMURA Muneaki</creator><creator>OHASHI Satoshi</creator><creator>TAI Kuninori</creator><creator>SHINOHARA Tomoichi</creator><creator>TAIRA Shinichi</creator><creator>MENJO Yasuhiro</creator><creator>MORITA Chisako</creator><creator>TOMOYASU Takahiro</creator><creator>SAKATA Yasuyo</creator><creator>SUGINO Haruhiko</creator><creator>YAMASHITA Junko</creator><scope>EVB</scope></search><sort><creationdate>20170615</creationdate><title>N,N-SUBSTITUTED 3-AMINOPYRROLIDINE COMPOUNDS USEFUL AS MONOAMINES REUPTAKE INHIBITORS</title><author>ITO Nobuaki ; MATSUZAKI Takayuki ; AKAZAWA Kohei ; AMADA Naoki ; SASAKI Hirofumi ; TAKEMURA Noriaki ; MASUMOTO Takumi ; MIYAMURA Shin ; SAKURAI Yohji ; WATANABE Akihito ; NAKAJIMA Satoko ; KURIMURA Muneaki ; OHASHI Satoshi ; TAI Kuninori ; SHINOHARA Tomoichi ; TAIRA Shinichi ; MENJO Yasuhiro ; MORITA Chisako ; TOMOYASU Takahiro ; SAKATA Yasuyo ; SUGINO Haruhiko ; YAMASHITA Junko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US2017166524A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2017</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>ITO Nobuaki</creatorcontrib><creatorcontrib>MATSUZAKI Takayuki</creatorcontrib><creatorcontrib>AKAZAWA Kohei</creatorcontrib><creatorcontrib>AMADA Naoki</creatorcontrib><creatorcontrib>SASAKI Hirofumi</creatorcontrib><creatorcontrib>TAKEMURA Noriaki</creatorcontrib><creatorcontrib>MASUMOTO Takumi</creatorcontrib><creatorcontrib>MIYAMURA Shin</creatorcontrib><creatorcontrib>SAKURAI Yohji</creatorcontrib><creatorcontrib>WATANABE Akihito</creatorcontrib><creatorcontrib>NAKAJIMA Satoko</creatorcontrib><creatorcontrib>KURIMURA Muneaki</creatorcontrib><creatorcontrib>OHASHI Satoshi</creatorcontrib><creatorcontrib>TAI Kuninori</creatorcontrib><creatorcontrib>SHINOHARA Tomoichi</creatorcontrib><creatorcontrib>TAIRA Shinichi</creatorcontrib><creatorcontrib>MENJO Yasuhiro</creatorcontrib><creatorcontrib>MORITA Chisako</creatorcontrib><creatorcontrib>TOMOYASU Takahiro</creatorcontrib><creatorcontrib>SAKATA Yasuyo</creatorcontrib><creatorcontrib>SUGINO Haruhiko</creatorcontrib><creatorcontrib>YAMASHITA Junko</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>ITO Nobuaki</au><au>MATSUZAKI Takayuki</au><au>AKAZAWA Kohei</au><au>AMADA Naoki</au><au>SASAKI Hirofumi</au><au>TAKEMURA Noriaki</au><au>MASUMOTO Takumi</au><au>MIYAMURA Shin</au><au>SAKURAI Yohji</au><au>WATANABE Akihito</au><au>NAKAJIMA Satoko</au><au>KURIMURA Muneaki</au><au>OHASHI Satoshi</au><au>TAI Kuninori</au><au>SHINOHARA Tomoichi</au><au>TAIRA Shinichi</au><au>MENJO Yasuhiro</au><au>MORITA Chisako</au><au>TOMOYASU Takahiro</au><au>SAKATA Yasuyo</au><au>SUGINO Haruhiko</au><au>YAMASHITA Junko</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>N,N-SUBSTITUTED 3-AMINOPYRROLIDINE COMPOUNDS USEFUL AS MONOAMINES REUPTAKE INHIBITORS</title><date>2017-06-15</date><risdate>2017</risdate><abstract>or a salt thereof, wherein R101 and R102 are each independently a phenyl group or a pyridyl group, the phenyl group or the pyridyl group may have one or more substituents selected from halogen atoms and lower alkyl groups optionally substituted with one or more halogen atoms, etc. The pyrrolidine compound or a salt thereof of the present invention is usable to produce a pharmaceutical preparation having a wider therapeutic spectrum and being capable of exhibiting sufficient therapeutic effects after short-term administration.</abstract><oa>free_for_read</oa></addata></record> |
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| title | N,N-SUBSTITUTED 3-AMINOPYRROLIDINE COMPOUNDS USEFUL AS MONOAMINES REUPTAKE INHIBITORS |
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