About: Structure of FK506, a novel immunosuppressant isolated from Streptomyces

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scientific article published on 18 March 2005

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2005 (fr) наукова стаття, опублікована в березні 2005 (uk) im März 2005 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 18 March 2005 (en) artículu científicu espublizáu en marzu de 2005 (ast)
publication date	wds:Q78319647-E232ED4E-164D-4069-BB2C-8901B0F99CCE
publication date	2005-03-18 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q78319647-0544491E-B5FF-465A-A5E6-455D483FD770
language of work or name	English
author name string	wds:Q78319647-2196AA58-C6F7-4C99-9944-3B0D5FFAA19D wds:Q78319647-2A89DD0F-53A0-4A5F-82D3-C8EDE9161E7B wds:Q78319647-314A7BDF-7C3C-4171-92E2-C297958D423B wds:Q78319647-4FD3BF4C-9B0F-415D-A957-557ECB480780 wds:Q78319647-9803DA09-B2F5-49C0-A2BE-DFD9E0B03E30 wds:Q78319647-B9C423CC-BABC-4AC4-92D9-A7035CAC152E wds:Q78319647-C33F7D02-481C-4001-8F73-AD451BAF982A wds:Q78319647-C3C44C3F-818A-45DE-B44B-8F2BF7987845
author name string	Akio Kuroda Hiroshi Hatanaka Hirokazu Tanaka Toshio Goto Masashi Hashimoto Hiroshi Marusawa Toru Kino Toru Taga
rdfs:label	Structure of FK506, a novel immunosuppressant isolated from Streptomyces (en) Structure of FK506, a novel immunosuppressant isolated from Streptomyces (nl)
skos:prefLabel	Structure of FK506, a novel immunosuppressant isolated from Streptomyces (en) Structure of FK506, a novel immunosuppressant isolated from Streptomyces (nl)
name	Structure of FK506, a novel immunosuppressant isolated from Streptomyces (en) Structure of FK506, a novel immunosuppressant isolated from Streptomyces (nl)
title	wds:Q78319647-0A2E9F27-8C0A-438C-92D1-37FB84FE3920
title	Structure of FK506, a novel immunosuppressant isolated from Streptomyces (en)
page(s)	wds:Q78319647-F1E91B2C-822F-4017-89BA-435FCDBA7A2C
page(s)	5031-5033
instance of	wds:Q78319647-5982EE21-5A03-47E1-B2E8-8FB1B822050B
instance of	scholarly article
published in	wds:Q78319647-9C04C703-A856-42D3-848B-F166163558DF
published in	Journal of the American Chemical Society
issue	wds:Q78319647-13B6B692-A6D2-41D9-8EAB-CB7A464476E8
volume	wds:Q78319647-9774BA83-EA85-4AF9-8737-EA9D2243AA65
issue	16
volume	109
DOI	wds:Q78319647-6F2D6F0A-6347-4ED3-AD0D-11A88EBFC74A
DOI	http://dx.doi.org/10.1021/JA00250A050
DOI	10.1021/JA00250A050
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q78319647
is cites work of	Unprecedented immunosuppressive polyketides from Daldinia eschscholzii, a mantis-associated fungus The cytosolic-binding protein for the immunosuppressant FK-506 is both a ubiquitous and highly conserved peptidyl-prolyl cis-trans isomerase A receptor for the immunosuppressant FK506 is a cis-trans peptidyl-prolyl isomerase Probing Immunosuppressant Action with a Nonnatural Immunophilin Ligand Complete amino acid sequence of the FK506 and rapamycin binding protein, FKBP, isolated from calf thymus Toxicology of FK506 in the cynomolgus monkey: a clinical, biochemical, and histopathological study Molecular cloning and overexpression of the human FK506-binding protein FKBP A new family of ATP-dependent oligomerization-macrocyclization biocatalysts Potent immunosuppressive C32-O-arylethyl ether derivatives of ascomycin with reduced toxicity C32-O-imidazol-2-yl-methyl ether derivatives of the immunosuppressant ascomycin with improved therapeutic potential C32-O-phenalkyl ether derivatives of the immunosuppressant ascomycin: a tether length study The role of 1,3-dithianes in natural product synthesis Neuroprotective effect of immunosuppressant FK506 in transient focal ischemia in rat: therapeutic time window for FK506 in transient focal ischemia Multifunctional organoboron compounds for scalable natural product synthesis Studies towards the total synthesis of rapamycin: Preparation of the cyclohexyl C33C42 fragment and further coupling to afford the C22C42 carbon unit Determination of heteronuclear long-range couplings to heteronuclei in natural abundance by two- and three-dimensional NMR spectroscopy The influence of FK-506 on the thymus and spleen in normal C3H/He mice: flow cytometric analysis of lymphocyte subpopulations Rapamycin-inspired macrocycles with new target specificity Identification of an 18-Methyl Derivative of Tacrolimus API in Streptomyces clavuligerus CKD-1119 Synthesis of β-hydroxy-propenamide derivatives and the inhibition of human dihydroorotate dehydrogenase Calcineurin inhibitors and the generalization of the presenting protein strategy Alpha-ketoamides and alpha-ketocarbonyls: conformational analysis and development of all-atom OPLS force field Phosphatases PP1 and PP2A act after the G0/G1 interface in lymphocyte activation Effect of donor-specific transfusion in combination with FK 506 in rat cardiac allotransplantation Analogous conformations of both binding and effector regions in cyclosporin A, FK506 and rapamycin. Solution conformational preferences of a peptidic analogue of a natural macrolide 1H-NMR determination of the solution structure and absolute configuration of FR134043, a novel inhibitor of human leukocyte elastase Discovery of fingolimod based on the chemical modification of a natural product from the fungus, Isaria sinclairii Application of coil centrifugal counter-current chromatography to the separation of macrolide antibiotic analogues III. Effects of flow-rate, mass load and rotation speed on the peak resolution Application of centrifugal counter-current chromatography to the separation of macrolide antibiotic analogues. I. Selection of solvent systems based on solubility and partition coefficient investigations. Diastereoselective esterification of (±)-N-trifluoroacetyl pipecolic acid using (S)-α-methyl pantolactone: synthesis of (S)-N-Boc pipecolic acid and (S)-N-Boc-2-piperidinemethanol Evaluation, synthesis and characterization of tacrolimus impurities
is cites work of	wds:Q24296311-2E107A7D-0470-4C43-8B20-8E086A7D01DD wds:Q31122003-FCEAC761-7BEE-4943-B426-4A20B573F30B wds:Q28370952-A4D373AD-8CE9-4FD3-B77E-9A10A99D590E wds:Q56832953-C31611FD-5A0E-4600-A2B4-4512875B6245 wds:Q52438679-83752390-571A-42A0-937A-0857FFEE0F0F wds:Q67702316-68380A9A-E67E-446B-9974-609AA1265B15 wds:Q77749256-055D41D4-929F-4E6E-A8ED-49A84B7AFDD2 wds:Q24302504-BE467828-D4AA-4BCA-9B8C-98A8126F8495 wds:Q44424740-5621AA3D-975F-4823-8B3D-437414B8EBDA wds:Q34236648-8A77E612-837B-4EAE-BBF0-C7075423C19F wds:Q46108118-D57F1A6D-9458-4312-B811-0721B1FCAB5D wds:Q44826202-79C7328E-0BD4-45B7-A8B4-52A77F1D3953 wds:Q73219538-8E81A684-6817-4042-9D07-258E498A0327 wds:Q78438400-A637BC35-30C8-4165-B343-B6112AE2A6E4 wds:Q43779453-4FBB8AA4-49DB-490D-8A28-8B29A44E9E98 wds:Q57099056-56A7EF62-EE21-43CE-94CA-AD18F11B7E12 wds:Q81514763-37513CFD-9216-4C5A-BCAE-7955A58ECC1E wds:Q34569267-AFCD99C1-B80A-4F09-A969-E780C3EB9DB0 wds:Q57599909-59B53583-0D40-42AC-ABDC-FA5A35DBEB7C

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