About: Synthesis and structure-activity relationships of bestatin analogues, inhibitors of aminopeptidase B

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scientific article published on 01 April 1977

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 1977 (uk) im April 1977 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'abril de 1977 (ast) scientific article published on 01 April 1977 (en)
publication date	wds:Q67560989-1F852ECC-6423-4C16-9A36-961170761A14
publication date	1977-04-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q67560989-16E58FA6-5FDB-4443-AAD2-F885CB63BC47
language of work or name	English
cites work	wds:Q67560989-147394D8-94D2-4B13-9EB3-1D81489D2D50
cites work	The structure of bestatin
author name string	wds:Q67560989-0DD6CDE6-F254-466C-828E-0B58DC65B80A wds:Q67560989-20074D6C-A0C3-4E2C-8726-5219D7EDEA73 wds:Q67560989-48DCAAE7-138B-452A-843A-E1B9ECB315A0 wds:Q67560989-6C5EAADC-5597-4BBA-8C71-099F229D9D69 wds:Q67560989-8566E1F9-016C-440E-8876-90A2BE988ECF
author name string	T Aoyagi H Suda T Saino T Takita R Nishizawa
rdfs:label	Synthesis and structure-activity relationships of bestatin analogues, inhibitors of aminopeptidase B (en) Synthesis and structure-activity relationships of bestatin analogues, inhibitors of aminopeptidase B (nl)
skos:prefLabel	Synthesis and structure-activity relationships of bestatin analogues, inhibitors of aminopeptidase B (en) Synthesis and structure-activity relationships of bestatin analogues, inhibitors of aminopeptidase B (nl)
name	Synthesis and structure-activity relationships of bestatin analogues, inhibitors of aminopeptidase B (en) Synthesis and structure-activity relationships of bestatin analogues, inhibitors of aminopeptidase B (nl)
title	wds:Q67560989-454DA433-6AC4-4572-9DCE-A9612D8401AD
title	Synthesis and structure-activity relationships of bestatin analogues, inhibitors of aminopeptidase B (en)
page(s)	wds:Q67560989-1C830574-4B06-4200-AD84-765CB85377A1
page(s)	510-515
instance of	wds:Q67560989-4EE92708-880C-46D7-9AF2-E93F94174880
instance of	scholarly article
PubMed ID	wds:Q67560989-75B0E09C-0B1C-483C-B1B8-DBD4F8E7B506
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/850237
PubMed ID	850237
published in	wds:Q67560989-30B7C552-F0FF-4947-8267-D5D95FBBE4CD
published in	Journal of Medicinal Chemistry
issue	wds:Q67560989-0BDFB2CC-C2EF-4ED1-A9E4-C4E716C9195B
volume	wds:Q67560989-9804971B-2F7F-456B-A259-A7118ABF726B
issue	4
volume	20
DOI	wds:Q67560989-6494EBE6-F36E-42CD-B71B-F66A0F032B9D
DOI	http://dx.doi.org/10.1021/JM00214A010
DOI	10.1021/JM00214A010
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q67560989
is cites work of	In vitro anti-human immunodeficiency virus (HIV) activities of transition state mimetic HIV protease inhibitors containing allophenylnorstatine BACE1- and BACE2-expressing human cells: characterization of beta-amyloid precursor protein-derived catabolites, design of a novel fluorimetric assay, and identification of new in vitro inhibitors Synthesis of New (−)-Bestatin-Based Inhibitor Libraries Reveals a Novel Binding Mode in the S1 Pocket of the Essential Malaria M1 Metalloaminopeptidase Bestatin-based chemical biology strategy reveals distinct roles for malaria M1- and M17-family aminopeptidases Aminopeptidase-N/CD13 (EC 3.4.11.2) inhibitors: chemistry, biological evaluations, and therapeutic prospects. 3'-RACE Amplification of Aminopeptidase N Gene from Anopheles stephensi Applicable in Transmission Blocking Vaccines Increased angiotensin-converting enzyme in peripheral blood monocytes from patients with sarcoidosis Bestatin analogue from Streptomyces neyagawaensis SL-387 Acyl sulfonamides as potent protease inhibitors of the hepatitis C virus full-Length NS3 (protease-helicase/NTPase): a comparative study of different C-terminals Leucine aminopeptidase: bestatin inhibition and a model for enzyme-catalyzed peptide hydrolysis Inhibitors of enkephalin-degrading enzymes as potential therapeutic agents. Inhibition of enkephalin-degrading aminopeptidase activity by certain peptides Synthesis of N-protected α-amino aldehydes from their morpholine amide derivatives Microginins, Zinc Metalloproteases Inhibitors from the Cyanobacterium Microcystis aeruginosa The potential of P1 site alterations in peptidomimetic protease inhibitors as suggested by virtual screening and explored by the use of C-C-coupling reagents Substrate analog inhibitors of HIV-1 protease containing phenylnorstatine as a transition state element Activation of DNA metabolism in T-cells by bestatin Structure-activity relationships among derivatives of arphamenines, inhibitors of aminopeptidase B New water-soluble prodrugs of HIV protease inhibitors based on O-->N intramolecular acyl migration Inhibitors of a Rat Brain Enkephalin Aminopeptidase Structure-activity relationships of HIV-1 PR inhibitors containing AHPBA. Purification and characterization of leukotriene A4 hydrolase from human epidermis Stereoselective cyanation of chiral α-amino aldehydes by reaction with Nagata's reagent: a route to enantiopure β-amino-α-hydroxy acids Synthesis of 1-deoxysphingosine derivatives with conformationally restricted pyrrolidinediol head groups. Peptide immunomodulators versus infection; an analysis Met5-enkephalin-Arg6-Phe7 inhibition of noradrenaline and acetylcholine release from peripheral organs
is cites work of	wds:Q36571471-CF9B4079-4D8D-43AF-87A4-15E0BD12014B wds:Q103812501-DA4EDFEA-CE08-41E9-BAC3-8D8EA40B173C wds:Q34536228-3A3138A6-E06D-4A7A-B126-AF27523450DD wds:Q44203282-D0A0D8DE-ECB0-4D1F-B0B1-D61CAE754432 wds:Q58104003-0245419C-1E23-4E6A-8C87-81E27252170A wds:Q27667128-E00ED519-C184-47E0-AB50-9B5A333AFA17 wds:Q40649318-17FB32DE-9308-4194-818B-B94C83E60D75 wds:Q60357340-E2DA0503-58D9-49BC-87C3-4D0CDC2B2697 wds:Q72443195-D3598305-EA1F-4AF7-AC02-A5CA1B401049 wds:Q24563697-E7425CD3-98BC-4E7A-A98E-E9619C941EF7 wds:Q27671783-A547EB87-694D-4112-A464-3EF4DC001EFA wds:Q42281368-AC173E4D-6503-4FBA-A101-20CC04B1CAD4 wds:Q70913765-6F584CD7-8CD3-4510-970F-957765FBF54C wds:Q72509323-61433580-FF6A-493A-A6DE-F28CF9EB8A94 wds:Q71249757-74B80CD6-FB1A-4D64-A57C-8C9421AB8A07 wds:Q28378709-F6546032-F94C-42B3-A3E8-A49A3DD2A4F0 wds:Q28333702-EEC7FA6E-4124-496A-B916-282E7A081E1A wds:Q40811955-275C5841-2E07-4348-8E9A-36A3948FEE7B wds:Q30935094-E8588F82-1BB7-4849-887A-D9D17D7B0154 wds:Q34719597-49E84BC7-CE32-4DB9-B03C-05CF8ACBD57D wds:Q40731083-ECFCCC87-EEE8-4581-AFA3-14EDB98ABD6F wds:Q46791848-20824DC2-BB92-4393-96A4-5AAF8138F916 wds:Q70755766-F4C769C3-DF66-4CDF-9439-514ACF66CCDD wds:Q36158616-0A743832-1014-430C-BAFE-4E1DAB99C857 wds:Q33990607-9D47DF70-6296-479E-9AD7-27F635F52E31 wds:Q33253061-7B614E25-86C9-4768-806C-8898DCDCECF3

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