author_facet Debouck, Christine
Metcalf, Brian W.
Debouck, Christine
Metcalf, Brian W.
author Debouck, Christine
Metcalf, Brian W.
spellingShingle Debouck, Christine
Metcalf, Brian W.
Drug Development Research
Human immunodeficiency virus protease: A target for aids therapy
Drug Discovery
author_sort debouck, christine
spelling Debouck, Christine Metcalf, Brian W. 0272-4391 1098-2299 Wiley Drug Discovery http://dx.doi.org/10.1002/ddr.430210102 <jats:title>Abstract</jats:title><jats:p>Human immunodeficiency virus, also called HIV, is the etiologic agent of acquired immune deficiency syndrome (AIDS). This retrovirus produces a small, dimeric aspartyl protease which specifically cleaves the precursor forms of the structural proteins and enzymes of the virus. This proteolytic activity is absolutely required for the production of mature, infectious viral particles and is therefore an attractive target for therapeutic intervention. Peptide analogues containing transition‐state mimics were synthesized and shown to inhibit the activity of the purified HIV protease in vitro to various extents. Most interestingly, the most potent inhibitors were shown to effectively block the protease in HIV‐infected cells and to impair the viral life cycle. Other approaches to interfere with the viral protease activity or production are also discussed.</jats:p> Human immunodeficiency virus protease: A target for aids therapy Drug Development Research
doi_str_mv 10.1002/ddr.430210102
facet_avail Online
finc_class_facet Chemie und Pharmazie
format ElectronicArticle
fullrecord blob:ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9kZHIuNDMwMjEwMTAy
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9kZHIuNDMwMjEwMTAy
institution DE-Bn3
DE-Brt1
DE-D161
DE-Gla1
DE-Zi4
DE-15
DE-Pl11
DE-Rs1
DE-105
DE-14
DE-Ch1
DE-L229
DE-D275
imprint Wiley, 1990
imprint_str_mv Wiley, 1990
issn 1098-2299
0272-4391
issn_str_mv 1098-2299
0272-4391
language English
mega_collection Wiley (CrossRef)
match_str debouck1990humanimmunodeficiencyvirusproteaseatargetforaidstherapy
publishDateSort 1990
publisher Wiley
recordtype ai
record_format ai
series Drug Development Research
source_id 49
title Human immunodeficiency virus protease: A target for aids therapy
title_unstemmed Human immunodeficiency virus protease: A target for aids therapy
title_full Human immunodeficiency virus protease: A target for aids therapy
title_fullStr Human immunodeficiency virus protease: A target for aids therapy
title_full_unstemmed Human immunodeficiency virus protease: A target for aids therapy
title_short Human immunodeficiency virus protease: A target for aids therapy
title_sort human immunodeficiency virus protease: a target for aids therapy
topic Drug Discovery
url http://dx.doi.org/10.1002/ddr.430210102
publishDate 1990
physical 1-17
description <jats:title>Abstract</jats:title><jats:p>Human immunodeficiency virus, also called HIV, is the etiologic agent of acquired immune deficiency syndrome (AIDS). This retrovirus produces a small, dimeric aspartyl protease which specifically cleaves the precursor forms of the structural proteins and enzymes of the virus. This proteolytic activity is absolutely required for the production of mature, infectious viral particles and is therefore an attractive target for therapeutic intervention. Peptide analogues containing transition‐state mimics were synthesized and shown to inhibit the activity of the purified HIV protease in vitro to various extents. Most interestingly, the most potent inhibitors were shown to effectively block the protease in HIV‐infected cells and to impair the viral life cycle. Other approaches to interfere with the viral protease activity or production are also discussed.</jats:p>
container_issue 1
container_start_page 1
container_title Drug Development Research
container_volume 21
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
_version_ 1792342710228615177
geogr_code not assigned
last_indexed 2024-03-01T16:39:51.866Z
geogr_code_person not assigned
openURL url_ver=Z39.88-2004&ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fvufind.svn.sourceforge.net%3Agenerator&rft.title=Human+immunodeficiency+virus+protease%3A+A+target+for+aids+therapy&rft.date=1990-01-01&genre=article&issn=1098-2299&volume=21&issue=1&spage=1&epage=17&pages=1-17&jtitle=Drug+Development+Research&atitle=Human+immunodeficiency+virus+protease%3A+A+target+for+aids+therapy&aulast=Metcalf&aufirst=Brian+W.&rft_id=info%3Adoi%2F10.1002%2Fddr.430210102&rft.language%5B0%5D=eng
SOLR
_version_ 1792342710228615177
author Debouck, Christine, Metcalf, Brian W.
author_facet Debouck, Christine, Metcalf, Brian W., Debouck, Christine, Metcalf, Brian W.
author_sort debouck, christine
container_issue 1
container_start_page 1
container_title Drug Development Research
container_volume 21
description <jats:title>Abstract</jats:title><jats:p>Human immunodeficiency virus, also called HIV, is the etiologic agent of acquired immune deficiency syndrome (AIDS). This retrovirus produces a small, dimeric aspartyl protease which specifically cleaves the precursor forms of the structural proteins and enzymes of the virus. This proteolytic activity is absolutely required for the production of mature, infectious viral particles and is therefore an attractive target for therapeutic intervention. Peptide analogues containing transition‐state mimics were synthesized and shown to inhibit the activity of the purified HIV protease in vitro to various extents. Most interestingly, the most potent inhibitors were shown to effectively block the protease in HIV‐infected cells and to impair the viral life cycle. Other approaches to interfere with the viral protease activity or production are also discussed.</jats:p>
doi_str_mv 10.1002/ddr.430210102
facet_avail Online
finc_class_facet Chemie und Pharmazie
format ElectronicArticle
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
geogr_code not assigned
geogr_code_person not assigned
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9kZHIuNDMwMjEwMTAy
imprint Wiley, 1990
imprint_str_mv Wiley, 1990
institution DE-Bn3, DE-Brt1, DE-D161, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275
issn 1098-2299, 0272-4391
issn_str_mv 1098-2299, 0272-4391
language English
last_indexed 2024-03-01T16:39:51.866Z
match_str debouck1990humanimmunodeficiencyvirusproteaseatargetforaidstherapy
mega_collection Wiley (CrossRef)
physical 1-17
publishDate 1990
publishDateSort 1990
publisher Wiley
record_format ai
recordtype ai
series Drug Development Research
source_id 49
spelling Debouck, Christine Metcalf, Brian W. 0272-4391 1098-2299 Wiley Drug Discovery http://dx.doi.org/10.1002/ddr.430210102 <jats:title>Abstract</jats:title><jats:p>Human immunodeficiency virus, also called HIV, is the etiologic agent of acquired immune deficiency syndrome (AIDS). This retrovirus produces a small, dimeric aspartyl protease which specifically cleaves the precursor forms of the structural proteins and enzymes of the virus. This proteolytic activity is absolutely required for the production of mature, infectious viral particles and is therefore an attractive target for therapeutic intervention. Peptide analogues containing transition‐state mimics were synthesized and shown to inhibit the activity of the purified HIV protease in vitro to various extents. Most interestingly, the most potent inhibitors were shown to effectively block the protease in HIV‐infected cells and to impair the viral life cycle. Other approaches to interfere with the viral protease activity or production are also discussed.</jats:p> Human immunodeficiency virus protease: A target for aids therapy Drug Development Research
spellingShingle Debouck, Christine, Metcalf, Brian W., Drug Development Research, Human immunodeficiency virus protease: A target for aids therapy, Drug Discovery
title Human immunodeficiency virus protease: A target for aids therapy
title_full Human immunodeficiency virus protease: A target for aids therapy
title_fullStr Human immunodeficiency virus protease: A target for aids therapy
title_full_unstemmed Human immunodeficiency virus protease: A target for aids therapy
title_short Human immunodeficiency virus protease: A target for aids therapy
title_sort human immunodeficiency virus protease: a target for aids therapy
title_unstemmed Human immunodeficiency virus protease: A target for aids therapy
topic Drug Discovery
url http://dx.doi.org/10.1002/ddr.430210102