About: Synthesis and angiotensin II receptor antagonistic activities of benzimidazole derivatives bearing acidic heterocycles as novel tetrazole bioisosteres

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About: Synthesis and angiotensin II receptor antagonistic activities of benzimidazole derivatives bearing acidic heterocycles as novel tetrazole bioisosteres Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 1996

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1996 (uk) article scientifique publié en 1996 (fr) im Dezember 1996 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 1996 (ast) scientific article published on 01 December 1996 (en)
publication date	wds:Q71935085-9F767ACE-1CBA-4748-8BDC-B77083B7E30B
publication date	1996-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q71935085-FF7C57BC-B383-438E-A8FE-F0BB1D32471C
language of work or name	English
author name string	wds:Q71935085-08DCD7CC-9CC4-49CC-A7FC-56E300444E6E wds:Q71935085-3BEDA5D5-A1E0-4948-A9F6-7C0D6043BF69 wds:Q71935085-4B444540-1602-4584-9536-17F4AD62C66A wds:Q71935085-B464DDAB-290F-44CE-A1DD-B95A87ABF213 wds:Q71935085-F290BED1-FA67-42B1-8C87-311637A6F7E9 wds:Q71935085-F7DB62F3-6B1C-48F9-8C28-D8B9DC5D53BF
author name string	Naka T Kohara Y Wada T Kubo K Inada Y Imamiya E
rdfs:label	Synthesis and angiotensin II receptor antagonistic activities of benzimidazole derivatives bearing acidic heterocycles as novel tetrazole bioisosteres (en) Synthesis and angiotensin II receptor antagonistic activities of benzimidazole derivatives bearing acidic heterocycles as novel tetrazole bioisosteres (nl)
skos:prefLabel	Synthesis and angiotensin II receptor antagonistic activities of benzimidazole derivatives bearing acidic heterocycles as novel tetrazole bioisosteres (en) Synthesis and angiotensin II receptor antagonistic activities of benzimidazole derivatives bearing acidic heterocycles as novel tetrazole bioisosteres (nl)
name	Synthesis and angiotensin II receptor antagonistic activities of benzimidazole derivatives bearing acidic heterocycles as novel tetrazole bioisosteres (en) Synthesis and angiotensin II receptor antagonistic activities of benzimidazole derivatives bearing acidic heterocycles as novel tetrazole bioisosteres (nl)
title	wds:Q71935085-848C9328-D16F-458E-8336-D8C6EFAE55AB
title	Synthesis and angiotensin II receptor antagonistic activities of benzimidazole derivatives bearing acidic heterocycles as novel tetrazole bioisosteres (en)
page(s)	wds:Q71935085-CFBAEAED-CC53-4A98-A84C-A82E89863CEB
page(s)	5228-5235
instance of	wds:Q71935085-95A6F9CB-64FF-4B7B-B111-205A7326BC63
instance of	scholarly article
PubMed ID	wds:Q71935085-7625960B-36ED-496C-ADB4-028F511BFB43
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8978851
PubMed ID	8978851
published in	wds:Q71935085-025781D7-D2C2-418C-BA5A-CDCD18EF9AFF
published in	Journal of Medicinal Chemistry
issue	wds:Q71935085-D132C30A-099B-45A1-B120-589C1BCA20AD
volume	wds:Q71935085-F785E2CA-679D-4358-AEB1-346990F089D0
issue	26
volume	39
DOI	wds:Q71935085-2FBDD0F9-351B-4288-95D8-F013930C00C2
DOI	http://dx.doi.org/10.1021/JM960547H
DOI	10.1021/JM960547H
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71935085
is cites work of	14,15-Epoxyeicosa-5,8,11-trienoic Acid (14,15-EET) surrogates: carboxylate modifications Synthesis and SAR of a novel positive allosteric modulator (PAM) of the metabotropic glutamate receptor 4 (mGluR4). Next generation multifunctional angiotensin receptor blockers Ethyl 1-sec-butyl-2-(4-methoxy-phen-yl)-1H-benzimidazole-5-carboxyl-ate EARLY Treatment with azilsartan compared to ACE-inhibitors in anti-hypertensive therapy--rationale and design of the EARLY hypertension registry Differential pharmacology and benefit/risk of azilsartan compared to other sartans Structure Property Relationships of Carboxylic Acid Isosteres International Union of Basic and Clinical Pharmacology. XCIX. Angiotensin Receptors: Interpreters of Pathophysiological Angiotensinergic Stimuli [corrected]. Unique binding behavior of the recently approved angiotensin II receptor blocker azilsartan compared with that of candesartan Preclinical research strategies for newly approved drugs as reflected in early publication patterns Carboxylic acid (bio)isosteres in drug design Synthesis and Antifungal Potential of Some Novel Benzimidazole-1,3,4-Oxadiazole Compounds Design and synthesis of N¹,N⁵-bis[4-(5-alkyl-1,2,4-oxadiazol-3-yl)phenyl]glutaramides as potential antifungal prodrugs Angiotensin II type 1 receptor antagonists in animal models of vascular, cardiac, metabolic and renal disease Improvement of Diurnal Blood Pressure Variation by Azilsartan. Synthesis, Antibacterial, and Anti HepG2 Cell Line Human Hepatocyte Carcinoma Activity of Some New Potentially Benzimidazole-5-(Aryldiazenyl)Thiazole Derivatives A general synthesis of ethyl 4-aminophenyl and ethyl 4-[amino(hydroxyimino)methyl]phenyl phosphonates Solubility of Azilsartan in Methanol, Ethanol, Acetonitrile, n-Propanol, Isopropanol, Tetrahydrofuran, and Binary Solvent Mixtures between 293.15 and 333.15 K Divergent Spatiotemporal Interaction of Angiotensin Receptor Blocking Drugs with Angiotensin Type 1 Receptor. Molecule-specific effects of angiotensin II-receptor blockers independent of the renin-angiotensin system Rational drug design and synthesis of molecules targeting the angiotensin II type 1 and type 2 receptors Crystal structure of azilsartan methyl ester ethyl acetate hemisolvate Highly efficient water-mediated approach to access benzazoles: metal catalyst and base-free synthesis of 2-substituted benzimidazoles, benzoxazoles, and benzothiazoles Facile and efficient syntheses of a series of N-benzyl and N-biphenylmethyl substituted imidazole derivatives based on (E)-urocanic acid, as angiotensin II AT1 receptor blockers. The use of sulfonylamido pyrimidines incorporating an unsaturated side chain as endothelin receptor antagonists Synthesis of biphenylyltetrazole derivatives of 1-aminopyrroles as angiotensin II antagonists
is cites work of	wds:Q38258427-77D17E3C-1FDF-45BD-9C20-B7378B82A691 wds:Q36241932-D3A64783-A315-4975-925D-E7A3F24D27DD wds:Q38411081-07990382-CC21-4AB6-9695-3EB1F76FCCE8 wds:Q85773304-0B0154C9-6E41-48FD-BC92-5854F0ED3931 wds:Q36808250-7B54A4DA-6B49-4B93-BBB6-DA3D4C0ED54B wds:Q47142567-4CEF2616-9EB3-4C45-A3FC-16B770398ED7 wds:Q60960519-3D5E1B0C-6354-4DD1-9769-681A4821806C wds:Q58216132-D888A600-244E-4067-9A87-52B1E58E2F9C wds:Q90748924-AAD30D7B-7249-4F21-9ABA-F2DFD62F6290 wds:Q47383912-67C06C5A-0482-4EAC-A558-42B18AFC39EF wds:Q42070301-97048EFD-ABF9-4019-B31A-C3A879C7B093 wds:Q34319220-F5A165CD-9121-47C6-A9EE-A3CF9F1F8ABC wds:Q43216042-539BBF0D-6A9F-4AF4-B7B9-E32E9869337C wds:Q86901568-99A5F96B-E962-4311-A1E8-C8D7B19A54A6 wds:Q26748814-DC809D48-619E-44BD-BB3B-E3DC23C3EEC9 wds:Q37184065-903C471C-43EA-4B56-9B9A-85CD0452AC96 wds:Q44808670-853D5743-2B82-4831-B04D-9107977BB25F wds:Q27023787-04F395FB-5369-4FB2-8891-9B6AF66C39A9 wds:Q35808748-C466A649-2815-4A1C-A2AB-81D90C5588D7 wds:Q37588484-105F6E33-F76D-42A0-9356-33CEEFD59126 wds:Q44345544-C7ECB6B4-3151-4836-AE42-50C8FCAC62CD wds:Q77732014-D7402AAE-7398-4EEE-9C2D-475F7E36D910 wds:Q34790309-6FB013CC-1C5E-49D9-B7F7-FC2950B864E8 wds:Q36803734-0426F61E-31A8-4F0A-8843-67E59949EAA4 wds:Q61450897-8AE77F44-24F5-4B3C-B92C-9B126D2805F0 wds:Q37364758-D4AA1256-57FF-4600-8124-AFFED2732686

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