Quinoline derivatives
Quinoline derivatives of the formula, wherein >A @ represents a group >N-(CH2)n-, >C=, >C=CH(CH2)n-, or >CH(CH2)n-, wherein n is an integer of 0-7; Y represents a group >C=O or >CHOH, R is a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, or an alkylthio group, R...
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| creator | SEKINE, KUMIKO HASEGAWA, HIROSHI TAIDO, NAOKATA KOTSUGAI, TAKESHI SHIOIRI, NORIAKI SATO, SUSUMU KURAISHI, TADAYUKI ISOMAE, KAZUO |
| description | Quinoline derivatives of the formula, wherein >A @ represents a group >N-(CH2)n-, >C=, >C=CH(CH2)n-, or >CH(CH2)n-, wherein n is an integer of 0-7; Y represents a group >C=O or >CHOH, R is a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, or an alkylthio group, R is a hydrogen atom, a halogen atom, an alkyl group, a hydroxy group, an alkoxy group, a phenyl group which may have a substituent, a phenoxy group, an alkanoyloxy group, or an amino group which may have a substituent, R is a hydrogen atom, a halogen atom, an alkyl group, or an alkoxy group, and m is an integer of 1-3. The compounds and their salts exhibit a superior anti-acetylcholinesterase activity with no side effects and are effective for the prevention or cure of senile dementia or memory disturbance. |
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The compounds and their salts exhibit a superior anti-acetylcholinesterase activity with no side effects and are effective for the prevention or cure of senile dementia or memory disturbance.</description><edition>7</edition><language>eng ; fre ; ger</language><subject>BEER ; BIOCHEMISTRY ; CHEMISTRY ; COMPOSITIONS THEREOF ; CULTURE MEDIA ; ENZYMOLOGY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; MICROBIOLOGY ; MICROORGANISMS OR ENZYMES ; MUTATION OR GENETIC ENGINEERING ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS ; SPIRITS ; VINEGAR ; WINE</subject><creationdate>2001</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=20010124&DB=EPODOC&CC=EP&NR=0481429B1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20010124&DB=EPODOC&CC=EP&NR=0481429B1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>SEKINE, KUMIKO</creatorcontrib><creatorcontrib>HASEGAWA, HIROSHI</creatorcontrib><creatorcontrib>TAIDO, NAOKATA</creatorcontrib><creatorcontrib>KOTSUGAI, TAKESHI</creatorcontrib><creatorcontrib>SHIOIRI, NORIAKI</creatorcontrib><creatorcontrib>SATO, SUSUMU</creatorcontrib><creatorcontrib>KURAISHI, TADAYUKI</creatorcontrib><creatorcontrib>ISOMAE, KAZUO</creatorcontrib><title>Quinoline derivatives</title><description>Quinoline derivatives of the formula, wherein >A @ represents a group >N-(CH2)n-, >C=, >C=CH(CH2)n-, or >CH(CH2)n-, wherein n is an integer of 0-7; Y represents a group >C=O or >CHOH, R is a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, or an alkylthio group, R is a hydrogen atom, a halogen atom, an alkyl group, a hydroxy group, an alkoxy group, a phenyl group which may have a substituent, a phenoxy group, an alkanoyloxy group, or an amino group which may have a substituent, R is a hydrogen atom, a halogen atom, an alkyl group, or an alkoxy group, and m is an integer of 1-3. 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The compounds and their salts exhibit a superior anti-acetylcholinesterase activity with no side effects and are effective for the prevention or cure of senile dementia or memory disturbance.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
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| subjects | BEER BIOCHEMISTRY CHEMISTRY COMPOSITIONS THEREOF CULTURE MEDIA ENZYMOLOGY HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY MICROBIOLOGY MICROORGANISMS OR ENZYMES MUTATION OR GENETIC ENGINEERING ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS SPIRITS VINEGAR WINE |
| title | Quinoline derivatives |
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