Inotropic activities of imidazopyridines

A series of 2-substituted 1H-imidazo[4,5-b]pyridines and the isomeric 1H-imidazo[4,5-c]pyridine derivatives has been prepared and evaluated as inotropic agents. The 1H-imidazo-[4,5-b] derivatives were found to be consistently more potent than their isomers in the [4,5-c] series in isolated guinea pi...

Full description

Saved in:
Bibliographic Details
Published inArchiv der Pharmazie (Weinheim) Vol. 323; no. 8; p. 501
Main Authors Barraclough, P, Black, J W, Cambridge, D, Gerskowitch, V P, Hull, R A, Lyer, R, King, W R, Kneen, C O, Nobbs, M S, Shah, G P
Format Journal Article
LanguageEnglish
Published Germany 1990
Subjects
Online AccessGet more information

Cover

Loading…
Abstract A series of 2-substituted 1H-imidazo[4,5-b]pyridines and the isomeric 1H-imidazo[4,5-c]pyridine derivatives has been prepared and evaluated as inotropic agents. The 1H-imidazo-[4,5-b] derivatives were found to be consistently more potent than their isomers in the [4,5-c] series in isolated guinea pig papillary muscle preparations. Structure-activity relationships and the species-dependence of inotropic potencies are discussed.
AbstractList A series of 2-substituted 1H-imidazo[4,5-b]pyridines and the isomeric 1H-imidazo[4,5-c]pyridine derivatives has been prepared and evaluated as inotropic agents. The 1H-imidazo-[4,5-b] derivatives were found to be consistently more potent than their isomers in the [4,5-c] series in isolated guinea pig papillary muscle preparations. Structure-activity relationships and the species-dependence of inotropic potencies are discussed.
Author Nobbs, M S
Hull, R A
Lyer, R
Black, J W
Gerskowitch, V P
Cambridge, D
King, W R
Kneen, C O
Barraclough, P
Shah, G P
Author_xml – sequence: 1
  givenname: P
  surname: Barraclough
  fullname: Barraclough, P
  organization: Department of Medicinal Chemistry, Wellcome Research Laboratories, Beckenham, Kent, U.K
– sequence: 2
  givenname: J W
  surname: Black
  fullname: Black, J W
– sequence: 3
  givenname: D
  surname: Cambridge
  fullname: Cambridge, D
– sequence: 4
  givenname: V P
  surname: Gerskowitch
  fullname: Gerskowitch, V P
– sequence: 5
  givenname: R A
  surname: Hull
  fullname: Hull, R A
– sequence: 6
  givenname: R
  surname: Lyer
  fullname: Lyer, R
– sequence: 7
  givenname: W R
  surname: King
  fullname: King, W R
– sequence: 8
  givenname: C O
  surname: Kneen
  fullname: Kneen, C O
– sequence: 9
  givenname: M S
  surname: Nobbs
  fullname: Nobbs, M S
– sequence: 10
  givenname: G P
  surname: Shah
  fullname: Shah, G P
BackLink https://www.ncbi.nlm.nih.gov/pubmed/2278516$$D View this record in MEDLINE/PubMed
BookMark eNotzj9LAzEcgOEMldpWdxfhRpervz9JLhmlaC0UXHQuySWBiHcX7k6hfnoHO73bw7sWi37ooxB3CFsEoEc3hrJFa4GJwSAuxApYq1oT87VYT9MnADCQWoolUWMU6pV4OPTDPA4lt5Vr5_yT5xynakhV7nJwv0M5jznkPk434iq5ryneXroRHy_P77vX-vi2P-yejnUrUWNt2LfkWmIrI2tMKnljTHDWGyuZSVEjKTUGMKFKIQA0TkptbWOTI-9pI-7_3fLtuxhOZcydG8-nyzH9AYyMQhQ
CitedBy_id crossref_primary_10_1002_chin_199052203
crossref_primary_10_1007_BF00772931
crossref_primary_10_1016_j_ejmech_2014_03_019
crossref_primary_10_1002_ardp_19923250918
crossref_primary_10_1016_0223_5234_92_90004_K
crossref_primary_10_1016_S0960_894X_01_81217_8
crossref_primary_10_1002_ardp_19923250407
ContentType Journal Article
DBID CGR
CUY
CVF
ECM
EIF
NPM
DOI 10.1002/ardp.19903230811
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
DatabaseTitleList MEDLINE
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
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod no_fulltext_linktorsrc
Discipline Pharmacy, Therapeutics, & Pharmacology
ExternalDocumentID 2278516
Genre Journal Article
GroupedDBID ---
.3N
.GA
.Y3
05W
0R~
10A
1L6
1OB
1OC
1ZS
23M
31~
33P
3SF
3WU
4.4
50Y
50Z
51W
51X
52M
52N
52O
52P
52S
52T
52U
52W
52X
53G
5GY
5VS
66C
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A03
AAESR
AAEVG
AAHHS
AANLZ
AAONW
AASGY
AAXRX
AAZKR
ABCQN
ABCUV
ABEML
ABIJN
ABOCM
ABPVW
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACGFS
ACPOU
ACSCC
ACXBN
ACXQS
ADBBV
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEIGN
AEIMD
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFFPM
AFGKR
AFPWT
AFZJQ
AHBTC
AHMBA
AITYG
AIURR
AIWBW
AJBDE
AJXKR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMBMR
AMYDB
ASPBG
ATUGU
AUFTA
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMNLL
BMXJE
BNHUX
BROTX
BRXPI
BY8
CGR
CS3
CUY
CVF
D-E
D-F
DCZOG
DPXWK
DR2
DRFUL
DRSTM
EBS
ECM
EIF
EJD
EMOBN
F00
F01
F04
F5P
FEDTE
G-S
G.N
GNP
GODZA
GWYGA
H.T
H.X
HF~
HGLYW
HHY
HHZ
HVGLF
HZ~
IX1
J0M
JPC
KQQ
LATKE
LAW
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
M6Q
MEWTI
MK4
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
N04
N05
N9A
NF~
NPM
O66
O9-
OIG
P2P
P2W
P2X
P4D
PALCI
PQQKQ
Q.N
Q11
QB0
QRW
R.K
RIWAO
RJQFR
ROL
RWI
RX1
RYL
SAMSI
SUPJJ
SV3
UB1
V2E
W8V
W99
WBFHL
WBKPD
WIH
WIK
WJL
WOHZO
WQJ
WRC
WUP
WWP
WXSBR
WYISQ
XG1
XV2
Y6R
YCJ
ZCG
ZZTAW
~IA
~WT
ID FETCH-LOGICAL-c4161-83bc2ac2394e361f5fb888da9b89433252742f7801f15fdd007a4469979fa2bb2
ISSN 0365-6233
IngestDate Sat Sep 28 08:38:28 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 8
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c4161-83bc2ac2394e361f5fb888da9b89433252742f7801f15fdd007a4469979fa2bb2
PMID 2278516
ParticipantIDs pubmed_primary_2278516
PublicationCentury 1900
PublicationDate 1990
PublicationDateYYYYMMDD 1990-01-01
PublicationDate_xml – year: 1990
  text: 1990
PublicationDecade 1990
PublicationPlace Germany
PublicationPlace_xml – name: Germany
PublicationTitle Archiv der Pharmazie (Weinheim)
PublicationTitleAlternate Arch Pharm (Weinheim)
PublicationYear 1990
SSID ssj0003025
Score 1.3850487
Snippet A series of 2-substituted 1H-imidazo[4,5-b]pyridines and the isomeric 1H-imidazo[4,5-c]pyridine derivatives has been prepared and evaluated as inotropic...
SourceID pubmed
SourceType Index Database
StartPage 501
SubjectTerms Anesthesia
Animals
Cardiotonic Agents - chemical synthesis
Dogs
Female
Guinea Pigs
Imidazoles - chemical synthesis
Imidazoles - pharmacology
In Vitro Techniques
Male
Papillary Muscles - drug effects
Pyridines - chemical synthesis
Pyridines - pharmacology
Structure-Activity Relationship
Title Inotropic activities of imidazopyridines
URI https://www.ncbi.nlm.nih.gov/pubmed/2278516
Volume 323
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3JTsMwELVYhMQFsVXsygFVSBBI47pxjoBYD1UPLXCrvMQiApKoVELt1zNeaNqyCLhEUZw4id_YmXH83iC0z7iKpCLUx1IFPhgF9qlQkc8J5VgGgYq5WSDbbFx36rcP5KEUVDDskj4_FsMveSX_QRWOAa6aJfsHZEeVwgHYB3xhCwjD9lcY32R5v5cXWnJVmCwQqZOQfUklG-bFoJdKvax93AO1UrOHWkKiZWSrh6lxM--TNHtMdG7l0dTAGev1mHjWeXwmmGBm0s_Af1iq9X5wvyZWEV-Bc_mUv6V9m3DqztUhHe0uGJtl-GBXER9cJTw-cmJLFXYmQsfGQWKv_TQ-W71XsP1C0yQDqABckolToYWLF4OXJukSS8T8sXBKL9uVzKLZiOqBr6mnb9ynGQcmC-_oZdx_a3iqk-lnWkQLrqapgMM4Hu1ltOQiBu_Uwr-CZpJsFVUtdmJw5LVLBt3rkVf1WqUY-WANHYxsxCttxMuVN20j66hzedE-v_Zddgxf6KDUp5iLkAmd2j7BjZoiilNKJYu5ltTHIdE_4VUEHoiqESWh30UMYv84jmLFQs7DCprL8izZQF6jIbhkOALnT9QhgqAM4oY63ICoEDos2UQV2wLdwkqgdF3TbH1XsI0WSyvaQfMKelyyC-5bn-8ZSN4BxflAjw
link.rule.ids 783
linkProvider National Library of Medicine
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=Inotropic+activities+of+imidazopyridines&rft.jtitle=Archiv+der+Pharmazie+%28Weinheim%29&rft.au=Barraclough%2C+P&rft.au=Black%2C+J+W&rft.au=Cambridge%2C+D&rft.au=Gerskowitch%2C+V+P&rft.date=1990-01-01&rft.issn=0365-6233&rft.volume=323&rft.issue=8&rft.spage=501&rft_id=info:doi/10.1002%2Fardp.19903230811&rft_id=info%3Apmid%2F2278516&rft_id=info%3Apmid%2F2278516&rft.externalDocID=2278516
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0365-6233&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0365-6233&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0365-6233&client=summon