About: Chloramphenicol (Chloromycetin).1IV.1aChemical Studies

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rdf:type	Item
description	article (en) ലേഖനം (ml) наукова стаття, опублікована в липні 1949 (uk) im Juli 1949 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q56028222-0999C1E3-9545-460B-9A24-7343D5480E39
publication date	1949-07-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56028222-0B8ABC98-6297-425B-ADFA-074E23BB34AD
language of work or name	English
author name string	wds:Q56028222-0B54707C-8735-4D3A-B277-D7FA693EA927 wds:Q56028222-9B54072B-E501-4EA5-9CF5-3D146A64CCF2 wds:Q56028222-BD786724-20A2-473B-A45D-87C96042B8B1 wds:Q56028222-F885A878-815C-49F3-8BC5-15AF515688A1
author name string	Quentin R. Bartz Harry M. Crooks John. Controulis Mildred C. Rebstock
rdfs:label	Chloramphenicol (Chloromycetin).1IV.1aChemical Studies (en)
skos:prefLabel	Chloramphenicol (Chloromycetin).1IV.1aChemical Studies (en)
name	Chloramphenicol (Chloromycetin).1IV.1aChemical Studies (en)
title	wds:Q56028222-71F29FB0-5B72-4C61-A469-D079DAB1904B
title	Chloramphenicol (Chloromycetin).1IV.1aChemical Studies (en)
page(s)	wds:Q56028222-D87F3064-725C-4D44-9E33-9302A30C2BA6
page(s)	2458-2462
instance of	wds:Q56028222-22261E1D-E13F-4798-94C2-C2A50DBD39F8
instance of	scholarly article
main subject	wds:Q56028222-4D2594F9-07BD-42CD-84D3-B070AD8DFC58 wds:Q56028222-AE08BC6A-84EB-4D31-B4F7-AD51684504C8 wds:Q56028222-EBBDF03F-0F98-4AEF-B87E-EF64D61E5019
main subject	BROMAMPHENICOL Streptomyces venezuelae 2,2-dichloro-N-[1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide
published in	wds:Q56028222-1A01C35D-216F-412A-8676-C646C9090C88
published in	Journal of the American Chemical Society
issue	wds:Q56028222-9A2BC350-763A-4919-9093-D52E4798FDF9
volume	wds:Q56028222-410E2A26-703E-426A-9EF8-1FFEB7CEA904
issue	7
volume	71
number of pages	wds:Q56028222-2D47F51D-0C0B-4D9B-9834-57E503CC6399
number of pages	5 (xsd:decimal)
DOI	wds:Q56028222-C46561DD-193D-4081-989A-DF0137035AB6
DOI	http://dx.doi.org/10.1021/JA01175A065
DOI	10.1021/JA01175A065
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56028222
is cites work of	Relationship between the structure of chloramphenicol and its action upon peptide synthetase New aromatic nitro compounds from Salegentibacter sp. T436, an Arctic Sea ice bacterium: taxonomy, fermentation, isolation and biological activities. Resistance Mechanism of Chloramphenicol inStreptococcus haemolyticus, Streptococcus pneumoniaeandStreptococcus faecalis Chloramphenicol Acetyltransferase: Enzymology and Molecular Biology Reconstitution and characterization of aminopyrrolnitrin oxygenase, a Rieske N-oxygenase that catalyzes unusual arylamine oxidation Studies on the oxidation of p-aminobenzoate to p-nitrobenzoate by Streptomyces thioluteus The Enzymatic Acetylation of Chloramphenicol by Extracts of R Factor-resistant Escherichia coli On the mechanism of action of chloramphenicol in protein synthesis Chemistry of antibiotics of clinical importance The Clinical Use of Chloramphenicol Colorimetric Determination of 1-(4′-Nitrophenyl)-2-aminopropane-1, 3-diol with 2,4,6-Trinitrobenzenesulfonic Acid in the Presence of Chloramphenicol The structure of aureothin, a nitro compound obtained from Streptomyces thioluteus Photodegradation Products of Chloramphenicol in Aqueous Solution A brief history of antibiotics and select advances in their synthesis Mass spectrometric measurement of 15N enrichment in nitrogen obtained by Dumas combustion Study of the mechanism of metabolic activation of chloramphenicol by rat liver microsomes Chloramphenicol; applied pharmacology Chemoprophylaxis with chloramphenicol in scrub typhus Synthetic multispecies microbial communities reveals shifts in secondary metabolism and facilitates cryptic natural product discovery Metabolism of chloramphenicol: a story of nearly 50 years N-Benzoyl-L-phenylalaninol from Catharanthus pusillus (Murr.) G. Don = Vinca pusilla Murr Catalytic diastereoselective sulfimidation of diaryl sulfides and application of chiral sulfimides to asymmetric allylic alkylation Chloramphenicol. Transesterification Synthesis of Chloramphenicol Esters with the Lipase from Bacillus amyloliquefaciens. Configurational Correlation of Chloramphenicol and of nor-pseudo-Ephedrine Enantioselective synthesis of (-)-chloramphenicol via silver-catalysed asymmetric isocyanoacetate aldol reaction. Metabolic oxidation of aralkyl oximes to nitro compounds by fortified 9000g liver supernatants from various species Chloramphenicol
is cites work of	wds:Q39297619-272274AB-59DF-4C92-9976-EB725A1B13ED wds:Q71208967-2C324D08-3C9F-4448-8CF2-107F82052E83 wds:Q74267090-AC40310B-2EB0-44C1-9517-220972AA441B wds:Q80374662-94854026-A72E-4DE9-A77B-567FE7432581 wds:Q73819792-7FEFF935-FF18-4A1F-8FB9-177C65C95898 wds:Q39414195-070D4E04-DD7A-4655-9036-4B1E71052B92 wds:Q38676251-4CD2D365-4E8A-41BA-9BD1-5AA8C7E1DFED wds:Q40603819-38AE79A4-44B1-4C14-920B-8FE97C9B320C wds:Q72694600-9EFC8E37-03CE-42E0-B402-AF8270C4B267 wds:Q38527873-BE9239AF-E279-4480-A79A-55C25ABE7394 wds:Q40147707-F4146EC2-DF07-4DE2-B53A-A581573942BD wds:Q34990831-318C6CA2-E4E9-4724-B995-0F99DAAC3561 wds:Q78614196-4233364F-0984-43B7-AF2F-53561E4DAE7E wds:Q104104000-C9CC6B5E-A506-49DD-8987-1E0DBBE50619 wds:Q39145757-52566B3B-EF19-4482-88E8-728169246FAE wds:Q70709546-1FA63F3C-C9DD-441F-B6F0-A4CB5F7C73B9 wds:Q72621375-A3A5B880-1200-49AF-9293-02606A0AB022 wds:Q47806813-A7B5D9A6-A28B-4779-B654-317746DD9C63 wds:Q54702258-7650B52C-F734-475D-A545-524A2A541926 wds:Q59053664-35C417F3-C44D-44D6-83DF-EEAFD22041B9 wds:Q69835302-DFBCCCD4-9A89-483A-83B9-CF28AB729382 wds:Q67247922-913FBC92-2811-495A-86B8-6859F889C744 wds:Q39993119-BB3EFCD0-9B43-4FB2-B3CE-00BCDA6A3E4D wds:Q40123475-C6F02393-FC5C-40D2-B6B8-789238521AD2 wds:Q47660095-1F697346-D8A3-4A9C-AC08-BE29C31199A5 wds:Q46693381-34E001C4-6672-486C-B36C-65952E5F7C59 wds:Q54008584-77BD492F-4215-408B-8D0F-E5E28BCCFC51 wds:Q72381227-5747FB8E-C6D5-4F0B-961D-964CD5ABBB44

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