YKP1447, A Novel Potential Atypical Antipsychotic Agent
(S)-Carbamic acid 2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-1-phenyl-ethyl ester hydrochloride (YKP1447) is a novel "atypical" antipsychotic drug which selectively binds to serotonin (5-HT(2A), Ki=0.61 nM, 5-HT(2C), Ki=20.7 nM) and dopamine (D(2), Ki=45.9 nM, D(3), Ki=42.1 nM) receptors with...
Saved in:
Published in | The Korean journal of physiology & pharmacology Vol. 13; no. 2; pp. 71 - 78 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
The Korean Physiological Society and The Korean Society of Pharmacology
01.04.2009
대한약리학회 |
Subjects | |
Online Access | Get full text |
ISSN | 1226-4512 2093-3827 |
DOI | 10.4196/kjpp.2009.13.2.71 |
Cover
Abstract | (S)-Carbamic acid 2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-1-phenyl-ethyl ester hydrochloride (YKP1447) is a novel "atypical" antipsychotic drug which selectively binds to serotonin (5-HT(2A), Ki=0.61 nM, 5-HT(2C), Ki=20.7 nM) and dopamine (D(2), Ki=45.9 nM, D(3), Ki=42.1 nM) receptors with over 10~100-fold selectivity over the various receptors which exist in the brain. In the behavioral studies using mice, YKP1447 antagonized the apomorphine-induced cage climbing (ED(50)=0.93 mg/kg) and DOI-induced head twitch (ED(50)=0.18 mg/kg) behavior. In the dextroamphetamine-induced hyperactivity and conditioned avoidance response (CAR) paradigm in rats, YKP1447 inhibited the hyperactivity induced by amphetamine (ED(50)=0.54 mg/kg) and the avoidance response (ED(50)=0.48 mg/kg); however, unlike other antipsychotic drugs, catalepsy was observed only at much higher dose (ED(50)=68.6 mg/kg). Based on the CAR and catalepsy results, the therapeutic index (TI) value for YKP1447 is over 100 (i.p.). These results indicate that YKP1447 has an atypical profile and less undesirable side effects than currently available drugs. |
---|---|
AbstractList | (S)-Carbamic acid 2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-1-phenyl-ethyl ester hydrochloride (YKP1447) is a novel "atypical" antipsychotic drug which selectively binds to serotonin (5-HT(2A), Ki=0.61 nM, 5-HT(2C), Ki=20.7 nM) and dopamine (D(2), Ki=45.9 nM, D(3), Ki=42.1 nM) receptors with over 10~100-fold selectivity over the various receptors which exist in the brain. In the behavioral studies using mice, YKP1447 antagonized the apomorphine-induced cage climbing (ED(50)=0.93 mg/kg) and DOI-induced head twitch (ED(50)=0.18 mg/kg) behavior. In the dextroamphetamine-induced hyperactivity and conditioned avoidance response (CAR) paradigm in rats, YKP1447 inhibited the hyperactivity induced by amphetamine (ED(50)=0.54 mg/kg) and the avoidance response (ED(50)=0.48 mg/kg); however, unlike other antipsychotic drugs, catalepsy was observed only at much higher dose (ED(50)=68.6 mg/kg). Based on the CAR and catalepsy results, the therapeutic index (TI) value for YKP1447 is over 100 (i.p.). These results indicate that YKP1447 has an atypical profile and less undesirable side effects than currently available drugs. (S)-Carbamic acid 2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-1-phenyl-ethyl ester hydrochloride (YKP1447) is a novel “atypical” antipsychotic drug which selectively binds to serotonin (5-HT2A, Ki=0.61 nM, 5-HT2C, Ki=20.7 nM) and dopamine (D2, Ki=45.9 nM, D3, Ki=42.1 nM) receptors with over 10∼100-fold selectivity over the various receptors which exist in the brain. In the behavioral studies using mice, YKP1447 antagonized the apomorphine-induced cage climbing (ED50=0.93 mg/kg) and DOI-induced head twitch (ED50=0.18 mg/kg) behavior. In the dextroamphetamine-induced hyperactivity and conditioned avoidance response (CAR) paradigm in rats, YKP1447 inhibited the hyperactivity induced by amphetamine (ED50=0.54 mg/kg) and the avoidance response (ED50=0.48 mg/kg); however, unlike other antipsychotic drugs, catalepsy was observed only at much higher dose (ED50=68.6 mg/kg). Based on the CAR and catalepsy results, the therapeutic index (TI) value for YKP1447 is over 100 (i.p.). These results indicate that YKP1447 has an atypical profile and less undesirable side effects than currently available drugs. (S)-Carbamic acid 2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-1-phenyl-ethyl ester hydrochloride (YKP1447) is a novel “atypical” antipsychotic drug which selectively binds to serotonin (5-HT2A, Ki=0.61 nM, 5-HT2C, Ki=20.7 nM) and dopamine (D2, Ki=45.9 nM, D3, Ki=42.1 nM) receptors with over 10∼100-fold selectivity over the various receptors which exist in the brain. In the behavioral studies using mice, YKP1447 antagonized the apomorphine-induced cage climbing (ED50=0.93 mg/kg) and DOI-induced head twitch (ED50=0.18 mg/kg) behavior. In the dextroamphetamine-induced hyperactivity and conditioned avoidance response (CAR) paradigm in rats, YKP1447 inhibited the hyperactivity induced by amphetamine (ED50=0.54 mg/kg) and the avoidance response (ED50=0.48 mg/kg); however, unlike other antipsychotic drugs, catalepsy was observed only at much higher dose (ED50=68.6 mg/kg). Based on the CAR and catalepsy results, the therapeutic index (TI) value for YKP1447 is over 100 (i.p.). These results indicate that YKP1447 has an atypical profile and less undesirable side effects than currently available drugs. KCI Citation Count: 9 (S)-Carbamic acid 2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-1-phenyl-ethyl ester hydrochloride (YKP1447) is a novel "atypical" antipsychotic drug which selectively binds to serotonin (5-HT 2A , Ki=0.61 nM, 5-HT 2C , Ki=20.7 nM) and dopamine (D 2 , Ki=45.9 nM, D 3 , Ki=42.1 nM) receptors with over 10~100-fold selectivity over the various receptors which exist in the brain. In the behavioral studies using mice, YKP1447 antagonized the apomorphine-induced cage climbing (ED 50 =0.93 mg/kg) and DOI-induced head twitch (ED 50 =0.18 mg/kg) behavior. In the dextroamphetamine-induced hyperactivity and conditioned avoidance response (CAR) paradigm in rats, YKP1447 inhibited the hyperactivity induced by amphetamine (ED 50 =0.54 mg/kg) and the avoidance response (ED 50 =0.48 mg/kg); however, unlike other antipsychotic drugs, catalepsy was observed only at much higher dose (ED 50 =68.6 mg/kg). Based on the CAR and catalepsy results, the therapeutic index (TI) value for YKP1447 is over 100 (i.p.). These results indicate that YKP1447 has an atypical profile and less undesirable side effects than currently available drugs. |
Author | Cho, Jeong Woo Dong, Seon Min Kim, Yong Gil Ji, Mi Kyung Heo, Joon Kwak, Byong Sung |
AuthorAffiliation | Life Science Division, SK Holdings Co., Ltd., Daejeon 305-712, Korea |
AuthorAffiliation_xml | – name: Life Science Division, SK Holdings Co., Ltd., Daejeon 305-712, Korea |
Author_xml | – sequence: 1 givenname: Seon Min surname: Dong fullname: Dong, Seon Min organization: Life Science Division, SK Holdings Co., Ltd., Daejeon 305-712, Korea – sequence: 2 givenname: Yong Gil surname: Kim fullname: Kim, Yong Gil organization: Life Science Division, SK Holdings Co., Ltd., Daejeon 305-712, Korea – sequence: 3 givenname: Joon surname: Heo fullname: Heo, Joon organization: Life Science Division, SK Holdings Co., Ltd., Daejeon 305-712, Korea – sequence: 4 givenname: Mi Kyung surname: Ji fullname: Ji, Mi Kyung organization: Life Science Division, SK Holdings Co., Ltd., Daejeon 305-712, Korea – sequence: 5 givenname: Jeong Woo surname: Cho fullname: Cho, Jeong Woo organization: Life Science Division, SK Holdings Co., Ltd., Daejeon 305-712, Korea – sequence: 6 givenname: Byong Sung surname: Kwak fullname: Kwak, Byong Sung organization: Life Science Division, SK Holdings Co., Ltd., Daejeon 305-712, Korea |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/19885000$$D View this record in MEDLINE/PubMed https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001339370$$DAccess content in National Research Foundation of Korea (NRF) |
BookMark | eNp9kctOwzAQRS0Eghb4ADYoSxYkeGzHiTdIUcVLVIBQWbCyXMcubtMkSkKl_j0O5b1gNTOac69Gc4dou6xKg9AR4IiB4GeLeV1HBGMRAY1IlMAWGhAsaEhTkmyjARDCQxYD2UPDtp1jzBnjbBftgUjTGGM8QMnz7QMwlpwGWXBXrUwRPFSdKTuniiDr1rXTfePnul3rl6pzOshmfn-AdqwqWnP4UffR0-XFZHQdju-vbkbZONSMQhcKFeeYE8OpYlOrGDBrNBWQQhwLzlIbGxozEROKLbHWj1YTlgua5zrNjaX76GTjWzZWLrSTlXLvdVbJRSOzx8mNpBgAM4-eb9D6dbo0ufZXNqqQdeOWqlm_C39vSvfibVaSJJxzkXqD458GX8rPb3kANoBuqrZtjP1GsOwTkX0isk9EApVEJuA1yR-Ndp3qXNXf4Ip_lG_WeJDC |
CitedBy_id | crossref_primary_10_1155_2013_686304 crossref_primary_10_1097_FBP_0000000000000235 crossref_primary_10_1097_FBP_0000000000000669 crossref_primary_10_1097_MAJ_0000000000000531 crossref_primary_10_1007_s00213_022_06253_y crossref_primary_10_1007_s11011_014_9630_4 crossref_primary_10_1016_j_yebeh_2021_108521 crossref_primary_10_1038_npp_2013_346 crossref_primary_10_1016_j_jss_2013_08_001 crossref_primary_10_1016_j_kjms_2014_05_007 |
Cites_doi | 10.1038/257405a0 10.1016/S0074-7742(08)60573-5 10.1007/BF02245453 10.1016/S1043-6618(03)00242-1 10.1038/sj.bjp.0702350 10.1016/S0014-2999(03)01992-7 10.1016/0165-6147(94)90323-9 10.1007/BF00634146 10.1126/science.184.4143.1243 10.1002/jps.3030460322 10.1038/sj.npp.1300027 10.1007/s00213-003-1611-y 10.1016/S0165-6147(00)89044-6 10.1007/s002130000466 10.1016/S0091-3057(01)00745-6 10.1111/j.1600-0773.1990.tb01600.x 10.1111/j.1600-0773.1963.tb01730.x 10.1016/0024-3205(76)90205-8 10.1016/0014-2999(84)90567-3 10.1038/347146a0 10.1016/S0149-7634(99)00037-8 10.1111/j.1600-0773.1982.tb01032.x 10.1176/ajp.137.12.1518 10.1016/0091-3057(90)90098-3 10.1016/j.pnpbp.2003.09.010 |
ContentType | Journal Article |
Copyright | Copyright © 2009 The Korean Physiological Society and The Korean Society of Pharmacology 2009 |
Copyright_xml | – notice: Copyright © 2009 The Korean Physiological Society and The Korean Society of Pharmacology 2009 |
DBID | AAYXX CITATION NPM 5PM ACYCR |
DOI | 10.4196/kjpp.2009.13.2.71 |
DatabaseName | CrossRef PubMed PubMed Central (Full Participant titles) Korean Citation Index |
DatabaseTitle | CrossRef PubMed |
DatabaseTitleList | PubMed |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Anatomy & Physiology |
DocumentTitleAlternate | YKP1447, A Novel Potential Atypical Antipsychotic Agent |
EISSN | 2093-3827 |
EndPage | 78 |
ExternalDocumentID | oai_kci_go_kr_ARTI_301104 PMC2766698 19885000 10_4196_kjpp_2009_13_2_71 |
Genre | Journal Article |
GroupedDBID | --- 5-W 53G 5GY 8JR 8XY 9ZL AAYXX ABDBF ACUHS ADBBV AENEX ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL CITATION DIK E3Z EBD EF. ESX F5P GX1 HYE KVFHK MK0 OK1 P2P P5Y P6G RPM TR2 TUS NPM 5PM .UV ABPTK ACYCR |
ID | FETCH-LOGICAL-c431t-9a5d062e63a4bfa414fec39181559648f5e35495230f2fff5efc24d93ddc8def3 |
ISSN | 1226-4512 |
IngestDate | Tue Nov 21 21:05:18 EST 2023 Thu Aug 21 18:23:25 EDT 2025 Sun Jan 05 02:00:36 EST 2025 Tue Jul 01 02:33:13 EDT 2025 Thu Apr 24 22:51:23 EDT 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2 |
Keywords | YKP1447 Schizophrenia Atypical antipsychotics CAR Serotonin and dopamine receptors Catalepsy |
Language | English |
License | http://creativecommons.org/licenses/by-nc/3.0 |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c431t-9a5d062e63a4bfa414fec39181559648f5e35495230f2fff5efc24d93ddc8def3 |
Notes | G704-000764.2009.13.2.004 http://kmbase.medric.or.kr/Main.aspx?d=KMBASE&m=VIEW&i=0811720090130020071 |
OpenAccessLink | https://synapse.koreamed.org/upload/SynapseData/PDFData/0067kjpp/kjpp-13-71.pdf |
PMID | 19885000 |
PageCount | 8 |
ParticipantIDs | nrf_kci_oai_kci_go_kr_ARTI_301104 pubmedcentral_primary_oai_pubmedcentral_nih_gov_2766698 pubmed_primary_19885000 crossref_primary_10_4196_kjpp_2009_13_2_71 crossref_citationtrail_10_4196_kjpp_2009_13_2_71 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2009-04-01 |
PublicationDateYYYYMMDD | 2009-04-01 |
PublicationDate_xml | – month: 04 year: 2009 text: 2009-04-01 day: 01 |
PublicationDecade | 2000 |
PublicationPlace | Korea (South) |
PublicationPlace_xml | – name: Korea (South) |
PublicationTitle | The Korean journal of physiology & pharmacology |
PublicationTitleAlternate | Korean J Physiol Pharmacol |
PublicationYear | 2009 |
Publisher | The Korean Physiological Society and The Korean Society of Pharmacology 대한약리학회 |
Publisher_xml | – name: The Korean Physiological Society and The Korean Society of Pharmacology – name: 대한약리학회 |
References | Arnt (10.4196/kjpp.2009.13.2.71_ref1) 1982; 51 Cook (10.4196/kjpp.2009.13.2.71_ref4) 1955; 113 Willins (10.4196/kjpp.2009.13.2.71_ref34) 1997; 282 Ogren (10.4196/kjpp.2009.13.2.71_ref18) 1984; 102 Van Rossum (10.4196/kjpp.2009.13.2.71_ref31) 1966; 160 Wadenberg (10.4196/kjpp.2009.13.2.71_ref32) 1999; 23 Peroutka (10.4196/kjpp.2009.13.2.71_ref20) 1980; 137 Snyder (10.4196/kjpp.2009.13.2.71_ref27) 1974; 184 Costentin (10.4196/kjpp.2009.13.2.71_ref5) 1975; 257 Seeman (10.4196/kjpp.2009.13.2.71_ref25) 1994; 15 Sibley (10.4196/kjpp.2009.13.2.71_ref26) 1993; 35 Wadenberg (10.4196/kjpp.2009.13.2.71_ref33) 2000; 150 Meltzer (10.4196/kjpp.2009.13.2.71_ref15) 2003; 27 Park (10.4196/kjpp.2009.13.2.71_ref19) 2003; 48 Moore (10.4196/kjpp.2009.13.2.71_ref17) 1994; 114 Matthysse (10.4196/kjpp.2009.13.2.71_ref14) 1973; 32 Darmani (10.4196/kjpp.2009.13.2.71_ref6) 1990; 36 Protais (10.4196/kjpp.2009.13.2.71_ref22) 1976; 50 Sokoloff (10.4196/kjpp.2009.13.2.71_ref29) 1995; 16 Kroeze (10.4196/kjpp.2009.13.2.71_ref11) 2003; 28 Stahl (10.4196/kjpp.2009.13.2.71_ref30) 1997 Sokoloff (10.4196/kjpp.2009.13.2.71_ref28) 1990; 347 Protais (10.4196/kjpp.2009.13.2.71_ref21) 1976; 50 Carlsson (10.4196/kjpp.2009.13.2.71_ref3) 1963; 20 Davidson (10.4196/kjpp.2009.13.2.71_ref7) 1976; 18 Gustafsson (10.4196/kjpp.2009.13.2.71_ref10) 1990; 66 Yoon (10.4196/kjpp.2009.13.2.71_ref35) 2008; 19 Jones (10.4196/kjpp.2009.13.2.71_ref13) 2002; 71 Moore (10.4196/kjpp.2009.13.2.71_ref16) 1992; 262 Dunham (10.4196/kjpp.2009.13.2.71_ref8) 1957; 46 Egashira (10.4196/kjpp.2009.13.2.71_ref9) 2004; 171 Reavill (10.4196/kjpp.2009.13.2.71_ref23) 1999; 126 Schreiber (10.4196/kjpp.2009.13.2.71_ref24) 1995; 273 Janssen (10.4196/kjpp.2009.13.2.71_ref12) 1965; 15 Bartoszyk (10.4196/kjpp.2009.13.2.71_ref2) 2003; 473 |
References_xml | – volume: 257 start-page: 405 year: 1975 ident: 10.4196/kjpp.2009.13.2.71_ref5 publication-title: Nature doi: 10.1038/257405a0 – volume: 35 start-page: 391 year: 1993 ident: 10.4196/kjpp.2009.13.2.71_ref26 publication-title: Int Rev Neurobiol doi: 10.1016/S0074-7742(08)60573-5 – volume: 114 start-page: 123 year: 1994 ident: 10.4196/kjpp.2009.13.2.71_ref17 publication-title: Psychopharmacology doi: 10.1007/BF02245453 – volume: 48 start-page: 615 year: 2003 ident: 10.4196/kjpp.2009.13.2.71_ref19 publication-title: Pharmacological Research doi: 10.1016/S1043-6618(03)00242-1 – volume: 126 start-page: 572 year: 1999 ident: 10.4196/kjpp.2009.13.2.71_ref23 publication-title: Br J Pharmacol doi: 10.1038/sj.bjp.0702350 – volume: 15 start-page: 56 year: 1965 ident: 10.4196/kjpp.2009.13.2.71_ref12 publication-title: Drug Res – volume: 473 start-page: 229 year: 2003 ident: 10.4196/kjpp.2009.13.2.71_ref2 publication-title: Eur J Pharmacol doi: 10.1016/S0014-2999(03)01992-7 – start-page: 31 volume-title: Psychopharmacology of antidepressants year: 1997 ident: 10.4196/kjpp.2009.13.2.71_ref30 – volume: 19 start-page: 38 year: 2008 ident: 10.4196/kjpp.2009.13.2.71_ref35 publication-title: Korean J Psychopharmacol – volume: 15 start-page: 264 year: 1994 ident: 10.4196/kjpp.2009.13.2.71_ref25 publication-title: Trends Pharmacol Sci doi: 10.1016/0165-6147(94)90323-9 – volume: 262 start-page: 545 year: 1992 ident: 10.4196/kjpp.2009.13.2.71_ref16 publication-title: J Pharmacol Exp Ther – volume: 50 start-page: 1 year: 1976 ident: 10.4196/kjpp.2009.13.2.71_ref21 publication-title: Psychopharmacology doi: 10.1007/BF00634146 – volume: 32 start-page: 200 year: 1973 ident: 10.4196/kjpp.2009.13.2.71_ref14 publication-title: Fed Proc – volume: 184 start-page: 1243 year: 1974 ident: 10.4196/kjpp.2009.13.2.71_ref27 publication-title: Science doi: 10.1126/science.184.4143.1243 – volume: 46 start-page: 208 year: 1957 ident: 10.4196/kjpp.2009.13.2.71_ref8 publication-title: J Am Pharm Assoc Am Pharm Assoc (Baltim) doi: 10.1002/jps.3030460322 – volume: 273 start-page: 101 year: 1995 ident: 10.4196/kjpp.2009.13.2.71_ref24 publication-title: J Pharmacol Exp Ther – volume: 28 start-page: 519 year: 2003 ident: 10.4196/kjpp.2009.13.2.71_ref11 publication-title: Neuropsychopharmacology doi: 10.1038/sj.npp.1300027 – volume: 171 start-page: 382 year: 2004 ident: 10.4196/kjpp.2009.13.2.71_ref9 publication-title: Psychopharmacology doi: 10.1007/s00213-003-1611-y – volume: 16 start-page: 270 year: 1995 ident: 10.4196/kjpp.2009.13.2.71_ref29 publication-title: Trends Pharmacol Sci doi: 10.1016/S0165-6147(00)89044-6 – volume: 150 start-page: 422 year: 2000 ident: 10.4196/kjpp.2009.13.2.71_ref33 publication-title: Psychopharmacology doi: 10.1007/s002130000466 – volume: 113 start-page: 11 year: 1955 ident: 10.4196/kjpp.2009.13.2.71_ref4 publication-title: J Pharmacol Exp Ther – volume: 71 start-page: 555 year: 2002 ident: 10.4196/kjpp.2009.13.2.71_ref13 publication-title: Pharmacol Biochem Behav doi: 10.1016/S0091-3057(01)00745-6 – volume: 66 start-page: 12 issue: Suppl 1 year: 1990 ident: 10.4196/kjpp.2009.13.2.71_ref10 publication-title: Pharmacol Toxicol doi: 10.1111/j.1600-0773.1990.tb01600.x – volume: 160 start-page: 492 year: 1966 ident: 10.4196/kjpp.2009.13.2.71_ref31 publication-title: Arch Int Pharmacodyn Ther – volume: 20 start-page: 140 year: 1963 ident: 10.4196/kjpp.2009.13.2.71_ref3 publication-title: Acta Pharmacol Toxicol (Copenh) doi: 10.1111/j.1600-0773.1963.tb01730.x – volume: 18 start-page: 1279 year: 1976 ident: 10.4196/kjpp.2009.13.2.71_ref7 publication-title: Life Sci doi: 10.1016/0024-3205(76)90205-8 – volume: 102 start-page: 459 year: 1984 ident: 10.4196/kjpp.2009.13.2.71_ref18 publication-title: Eur J Pharmacol doi: 10.1016/0014-2999(84)90567-3 – volume: 347 start-page: 146 year: 1990 ident: 10.4196/kjpp.2009.13.2.71_ref28 publication-title: Nature doi: 10.1038/347146a0 – volume: 23 start-page: 851 year: 1999 ident: 10.4196/kjpp.2009.13.2.71_ref32 publication-title: Neurosci Biobehav Rev doi: 10.1016/S0149-7634(99)00037-8 – volume: 50 start-page: 1 year: 1976 ident: 10.4196/kjpp.2009.13.2.71_ref22 publication-title: Psychopharmacology (Berlin) doi: 10.1007/BF00634146 – volume: 51 start-page: 321 year: 1982 ident: 10.4196/kjpp.2009.13.2.71_ref1 publication-title: Acta Pharmacol Toxicol (Copenh) doi: 10.1111/j.1600-0773.1982.tb01032.x – volume: 137 start-page: 1518 year: 1980 ident: 10.4196/kjpp.2009.13.2.71_ref20 publication-title: Am J Psychiatry doi: 10.1176/ajp.137.12.1518 – volume: 36 start-page: 901 year: 1990 ident: 10.4196/kjpp.2009.13.2.71_ref6 publication-title: Pharmacol Biochem Behav doi: 10.1016/0091-3057(90)90098-3 – volume: 27 start-page: 1159 year: 2003 ident: 10.4196/kjpp.2009.13.2.71_ref15 publication-title: Prog Neuropsychopharmacol Biol Psychiatry doi: 10.1016/j.pnpbp.2003.09.010 – volume: 282 start-page: 699 year: 1997 ident: 10.4196/kjpp.2009.13.2.71_ref34 publication-title: J Pharmacol Exp Ther |
SSID | ssj0064464 ssib008505809 |
Score | 1.8227794 |
Snippet | (S)-Carbamic acid 2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-1-phenyl-ethyl ester hydrochloride (YKP1447) is a novel "atypical" antipsychotic drug which... (S)-Carbamic acid 2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-1-phenyl-ethyl ester hydrochloride (YKP1447) is a novel “atypical” antipsychotic drug which... |
SourceID | nrf pubmedcentral pubmed crossref |
SourceType | Open Website Open Access Repository Index Database Enrichment Source |
StartPage | 71 |
SubjectTerms | Original 약리학 |
Title | YKP1447, A Novel Potential Atypical Antipsychotic Agent |
URI | https://www.ncbi.nlm.nih.gov/pubmed/19885000 https://pubmed.ncbi.nlm.nih.gov/PMC2766698 https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001339370 |
Volume | 13 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
ispartofPNX | The Korean Journal of Physiology & Pharmacology, 2009, 13(2), , pp.71-78 |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELaWcuGCgPJYXgoS5kBJSWInto_ZdJdC1dUeWmk5RXk4ZbslWa1SpPIX-VOMnXd5qCCtrMSecbyeif2NMx4j9NrxkoxZMjYjZicm9aLYFE4MNk_iRpJJwlLtjHk89w5P6aeluxyNfvS8li7LeD_5_tt9Jf8jVcgDuapdsv8g2bZSyIBrkC-kIGFIbyTjz0cLsFRY9X7Pi2_yYm9RlMr_R3V8ebWpJAD39WarVbLnnzWuLuedohwV22ZFvkanesWjis-klGPTRbhu1-DxdIL5DAuBpwHmFPuWyvFneBJ0JD6eCOVNASTCx77QORx-HckBFgxzrkh8QLZWVwIZTDNX1XLN7ODJwWCtQvRcXJR26XYFmg-qdrEI9NNd4NM1edgPmiKhL3yg743OgBVN6tZ-11LnOZYgJuFVgIF6FK4Odann8-qEoOszBYWRB8S7Pt_UQUttsu_sN4z9qNzXZstBXO51sgrPinC9DcH6-BiqwVLFpr3tMKZ9Bj4su8GTA9bUsdIqmAA4VMc2a_9T9cldtev9L60agKZb-Tbr4aWhL28PHJ3cQ3drq8bwKxW9j0Yyf4B2_Twqi69Xxhtj0WrTLmK11r4zfEPrrNHqrNHorDHQWUPr7EN0OpueBIdmfXyHmQAqLU0RuanlOdIjEY2ziNo0kwkRACnBivUoz1xJXLDPwQjOnCyD2yxxaCpImiY8lRl5hHbyIpdPkJFRQM1unKYisqlrJTxT85BNCKGWFLE3RlbTP2FSx7ZXR6xchGDjqi4NVZeqI1dFaJPQCZk9Rm9blk0V2OVvxK-g07W4_yj2MXpcSaKrTnCuzhsZIzaQUUug6hqW5KsvOsS7wzzPE_zpDZ77DN3pXrXnaKfcXsoXAJTL-KVWQEjni-Of3iWo4w |
linkProvider | Geneva Foundation for Medical Education and Research |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=YKP1447%2C+A+Novel+Potential+Atypical+Antipsychotic+Agent&rft.jtitle=The+Korean+journal+of+physiology+%26+pharmacology&rft.au=%EB%8F%99%EC%84%A0%EB%AF%BC&rft.au=%EA%B9%80%EC%9A%A9%EA%B8%B8&rft.au=%ED%97%88%EC%A4%80&rft.au=%EC%A7%80%EB%AF%B8%EA%B2%BD&rft.date=2009-04-01&rft.pub=%EB%8C%80%ED%95%9C%EC%95%BD%EB%A6%AC%ED%95%99%ED%9A%8C&rft.issn=1226-4512&rft.eissn=2093-3827&rft.spage=71&rft.epage=78&rft_id=info:doi/10.4196%2Fkjpp.2009.13.2.71&rft.externalDBID=n%2Fa&rft.externalDocID=oai_kci_go_kr_ARTI_301104 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1226-4512&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1226-4512&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1226-4512&client=summon |