About: Design, Molecular Modeling, Synthesis, and Anti-HIV-1 Activity of New Indolyl Aryl Sulfones. Novel Derivatives of the Indole-2-carboxamide

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About: Design, Molecular Modeling, Synthesis, and Anti-HIV-1 Activity of New Indolyl Aryl Sulfones. Novel Derivatives of the Indole-2-carboxamide Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) article scientifique publié en 2006 (fr) наукова стаття, опублікована в червні 2006 (uk) im Juni 2006 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57266181-84456F43-27AA-47F0-84FD-D7B6BB756B8A
publication date	2006-06-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57266181-9C31C5EA-3AE7-4A29-90D8-FE118C07B73B
language of work or name	English
author name string	wds:Q57266181-0A68FE5A-E0EA-4879-B6DB-13F3E747EE4A wds:Q57266181-2153FDFE-D2E2-4149-AC40-6DD1D6C3348E wds:Q57266181-AB785AE3-40C8-4766-BC28-E0A5BFA6CB6D
author name string	Alberto Bergamini Anna Sinistro Chiara Ciaprini
rdfs:label	Design, Molecular Modeling, Synthesis, and Anti-HIV-1 Activity of New Indolyl Aryl Sulfones. Novel Derivatives of the Indole-2-carboxamide (en) Design, Molecular Modeling, Synthesis, and Anti-HIV-1 Activity of New Indolyl Aryl Sulfones. Novel Derivatives of the Indole-2-carboxamide (nl)
skos:prefLabel	Design, Molecular Modeling, Synthesis, and Anti-HIV-1 Activity of New Indolyl Aryl Sulfones. Novel Derivatives of the Indole-2-carboxamide (en) Design, Molecular Modeling, Synthesis, and Anti-HIV-1 Activity of New Indolyl Aryl Sulfones. Novel Derivatives of the Indole-2-carboxamide (nl)
name	Design, Molecular Modeling, Synthesis, and Anti-HIV-1 Activity of New Indolyl Aryl Sulfones. Novel Derivatives of the Indole-2-carboxamide (en) Design, Molecular Modeling, Synthesis, and Anti-HIV-1 Activity of New Indolyl Aryl Sulfones. Novel Derivatives of the Indole-2-carboxamide (nl)
author	wds:Q57266181-11D689CB-AAF7-46A7-A6F6-72F6AD288402 wds:Q57266181-131C4D40-37B4-49AA-8F96-0DD6542B8D7B wds:Q57266181-24B239DB-E7FC-4DAD-BE71-ACEC84CFD0D8 wds:Q57266181-2FE1B218-E31C-4033-9092-D9862707178F wds:Q57266181-4FC318D5-420A-4B9F-9B8B-2E80C43469D2 wds:Q57266181-562C70AA-43F3-4C30-9D49-B17C9D13EFBF wds:Q57266181-6A75F6D6-15C1-4A74-9F7D-10641FBF33A6 wds:Q57266181-729731F2-8605-4B8C-BCB4-85CCB3E2F523 wds:Q57266181-7775B078-E176-4558-96FF-6215D4F499FE wds:Q57266181-A607D34C-CBB4-4119-BD86-86A165755CDF wds:Q57266181-BF68DDCF-F943-4BD6-A539-EAB4D347B01B
author	Gabriella Martino Emmanuele Crespan Giovanni Maga Romano Silvestri Ettore Novellino Rino Ragno Antonio Lavecchia Giuseppe La Regina wd:Q64785685 Marino Artico Francesco Piscitelli
title	wds:Q57266181-D193A5FC-BCFD-4380-9BB5-2CA5B0160382
title	Design, molecular modeling, synthesis, and anti-HIV-1 activity of new indolyl aryl sulfones. Novel derivatives of the indole-2-carboxamide (en)
page(s)	wds:Q57266181-7F86DC4F-A751-4A55-A214-BF13BD6C1FED
page(s)	3172-3184
instance of	wds:Q57266181-4E068D4B-B916-4BA7-9A98-3B0992E3F815
instance of	scholarly article
PubMed ID	wds:Q57266181-9FA732E9-4B7B-4AB8-A492-F5983DD00FA0
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16722636
PubMed ID	16722636
published in	wds:Q57266181-5AB44791-0AF8-4AFA-8ED0-E0E7D1EAA904
published in	Journal of Medicinal Chemistry
issue	wds:Q57266181-4568E598-CC17-4127-96C7-26CCBC6F0FDE
volume	wds:Q57266181-810BF72D-1DCA-4193-9C4E-BA4EF462623A
issue	11
volume	49
DOI	wds:Q57266181-E04BB40F-D275-455D-8B21-A12AC125F10F
DOI	http://dx.doi.org/10.1021/JM0512490
DOI	10.1021/JM0512490
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57266181
is cites work of	Antioxidant, cytotoxic activities, and structure-activity relationship of gallic acid-based indole derivatives Synthesis and SARs of indole-based α-amino acids as potent HIV-1 non-nucleoside reverse transcriptase inhibitors. Indolyl aryl sulphones as HIV-1 reverse transcriptase inhibitors: docking and 3D QSAR studies A review on recent developments of indole-containing antiviral agents A novel synthetic route to 3-sulfenyl- and 3-selenylindoles by n-Bu4NI-induced electrophilic cyclization Synthesis of 3-sulfenyl- and 3-selenylindoles by the Pd/Cu-catalyzed coupling of N,N-dialkyl-2-iodoanilines and terminal alkynes, followed by n-Bu(4)NI-induced electrophilic cyclization A selenium-based ionic liquid as a recyclable solvent for the catalyst-free synthesis of 3-selenylindoles. Synthesis of quinolin-2-one alkaloid derivatives and their inhibitory activities against HIV-1 reverse transcriptase. I2-Catalyzed sulfenylation of indoles and pyrroles using triethylammonium thiolates as sulfenylating agents. Copper-catalysed regioselective sulfenylation of indoles with sodium sulfinates. A tetra-n-butylammonium iodide mediated reaction of indoles with Bunte salts: efficient 3-sulfenylation of indoles under metal-free and oxidant-free conditions. Synthesis and antiviral properties of novel indole-based thiosemicarbazides and 4-thiazolidinones Iodine-Catalyzed Synthesis of 3-Arylthioindoles Employing a 1-Aryltriazene/CS2 Combination as a New Sulfenylation Source Dual vicinal functionalisation of heterocycles via an interrupted Pummerer coupling/[3,3]-sigmatropic rearrangement cascade. Synthetic strategies, SAR studies, and computer modeling of indole 2 and 3-carboxamides as the strong enzyme inhibitors: a review Synthesis of 3-sulfenylated indoles by a simple NaOH promoted sulfenylation reaction Indolylarylsulfones, a fascinating story of highly potent human immunodeficiency virus type 1 non-nucleoside reverse transcriptase inhibitors. Targeting the entrance channel of NNIBP: Discovery of diarylnicotinamide 1,4-disubstituted 1,2,3-triazoles as novel HIV-1 NNRTIs with high potency against wild-type and E138K mutant virus. Recent advances in the design and development of NNRTI scaffolds Arylsulfone-based HIV-1 non-nucleoside reverse transcriptase inhibitors. Convenient synthesis of 2-amino-3-(arylthio)indoles via the Rh-catalyzed reaction of 3-diazoindol-2-imines with thioesters.
is cites work of	wds:Q38089836-CA166B83-BFF9-4B89-859D-65144E6E324B wds:Q38280904-D21F3F27-5570-4324-AE9B-2E3107F42470 wds:Q39466929-6409640A-95C5-47CD-890A-BB4E1941B8FD wds:Q43357154-6A7D6200-C32C-4FAB-B853-CFB673FB734F wds:Q42726980-B0D16CFE-1F1A-4DFC-AE19-8D175DBBC113 wds:Q55285419-DD525F14-5FB0-47F1-AE9F-050B11285FC0 wds:Q48987179-D53023F0-395E-4D2E-974F-A185DFC930EF wds:Q91845673-A20AB09B-EAB5-48F1-8E49-83061F1B8379 wds:Q37073644-81093BDD-253C-43B7-AB15-8E7F1312F351 wds:Q94565119-C5E2C0BF-B2CB-48E0-BF47-6937FBAF8FC6 wds:Q55058175-54A7D3DD-59ED-4D9C-94F3-A7B95A185581 wds:Q57671107-2F6CEBD7-F31D-4BA7-B955-344FAD56607B wds:Q59351314-A11B7A69-3EA1-472F-BF94-458F56817229 wds:Q41018689-578786A7-32D7-4E29-8B23-88D8F1D81939 wds:Q42190198-1C5C0938-7EB9-4252-BC14-CC917641C8BA wds:Q38164839-D7CE50DB-63F4-408E-99BD-BB76A4414E81

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