About: Potent HIV-1 Protease Inhibitors: Stereoselective Synthesis of a Dipeptide Mimic

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scientific article published on 01 February 1993

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1993 (uk) artículu científicu espublizáu en febreru de 1993 (ast) artikull shkencor i botuar më 01 shkurt 1993 (sq) scientific article published on 01 February 1993 (en)
publication date	wds:Q92217515-A17A5C36-2CD5-4848-8EE5-EEBDFA970FCD
publication date	1993-02-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q92217515-20CC9514-5012-4783-AAD2-561BD45556C1 wds:Q92217515-3C5A78CD-9455-4E22-931C-7F42C25A97F0 wds:Q92217515-4FA63539-7BFB-4929-BB5F-FA580C5ECAD0 wds:Q92217515-5A217B9C-8BFA-4DA4-B7F0-4604EFE8EA3F wds:Q92217515-5AA344FF-0438-439A-A56F-4ED9B1C919D3 wds:Q92217515-810E92D7-B74C-4737-8DF4-4F6508C0E1FD wds:Q92217515-A77CA46A-38A5-4C76-ABC5-CF513D859F22 wds:Q92217515-B3544F8E-E5E0-451F-87EE-28473390B15C wds:Q92217515-BB23F94F-CBD7-4282-8C87-01AA0E0EFA78
cites work	Conserved folding in retroviral proteases: crystal structure of a synthetic HIV-1 protease Isolation of a T-Lymphotropic Retrovirus from a Patient at Risk for Acquired Immune Deficiency Syndrome (AIDS) Three-dimensional structure of aspartyl protease from human immunodeficiency virus HIV-1 Frequent Detection and Isolation of Cytopathic Retroviruses (HTLV-III) from Patients with AIDS and at Risk for AIDS Active human immunodeficiency virus protease is required for viral infectivity Design, activity, and 2.8 A crystal structure of a C2 symmetric inhibitor complexed to HIV-1 protease HIV protease: a novel chemotherapeutic target for AIDS. Structure-based, C2 symmetric inhibitors of HIV protease Affinity purification of the HIV-1 protease
author name string	wds:Q92217515-0AD1A589-F4C5-4073-BE64-03F7131C0757 wds:Q92217515-27AFD72D-457F-43FB-83E3-4964B7F4D619 wds:Q92217515-286187A2-0C28-4C6B-80BC-0AFD44F980A4 wds:Q92217515-6FB0AC35-DE5A-4C4B-A04F-3956F1AB29DE wds:Q92217515-CBF8732A-85D6-485E-A5A2-3A4E5EB281CE
author name string	Arun K Ghosh Paul L Darke Sean P McKee Wayne J Thompson Joan C Zugay
rdfs:label	Potent HIV-1 Protease Inhibitors: Stereoselective Synthesis of a Dipeptide Mimic (en) Potent HIV-1 Protease Inhibitors: Stereoselective Synthesis of a Dipeptide Mimic (nl) Potent HIV-1 Protease Inhibitors: Stereoselective Synthesis of a Dipeptide Mimic (sq)
skos:prefLabel	Potent HIV-1 Protease Inhibitors: Stereoselective Synthesis of a Dipeptide Mimic (en) Potent HIV-1 Protease Inhibitors: Stereoselective Synthesis of a Dipeptide Mimic (nl) Potent HIV-1 Protease Inhibitors: Stereoselective Synthesis of a Dipeptide Mimic (sq)
name	Potent HIV-1 Protease Inhibitors: Stereoselective Synthesis of a Dipeptide Mimic (en) Potent HIV-1 Protease Inhibitors: Stereoselective Synthesis of a Dipeptide Mimic (nl) Potent HIV-1 Protease Inhibitors: Stereoselective Synthesis of a Dipeptide Mimic (sq)
title	wds:Q92217515-EDB14994-AE4C-44A3-A5F9-F96C42667616
title	Potent HIV-1 Protease Inhibitors: Stereoselective Synthesis of a Dipeptide Mimic (en)
page(s)	wds:Q92217515-96CAF8F6-4816-4F5B-9699-0EE6C965685E
page(s)	1025-1029
instance of	wds:Q92217515-F9ECFDAF-9C41-43FE-BC4A-CCC43FFA7B0D
instance of	scholarly article
main subject	wds:Q92217515-CE6A52A2-AA13-4E08-9A52-D5BB79F29093
main subject	stereoselectivity
PubMed ID	wds:Q92217515-9C5002C3-456E-4B41-B4ED-AA34F26A8391
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30310240
PubMed ID	30310240
published in	wds:Q92217515-687EF0F5-0662-437E-85BD-BACE887FF09A
published in	Journal of Organic Chemistry
issue	wds:Q92217515-6520E187-67A4-4935-8D3F-48893F1E9C81
volume	wds:Q92217515-61B9A31C-D1DE-477F-B0C7-3F3FFC288A2B
issue	5
volume	58
DOI	wds:Q92217515-604FA4FB-86B9-411E-8F19-25F854F42796
DOI	http://dx.doi.org/10.1021/JO00057A011
DOI	10.1021/JO00057A011
PMCID	wds:Q92217515-0D37FABE-7319-42FF-9669-74325E2E313B
PMCID	6177225
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q92217515
is cites work of	Syntheses of FDA Approved HIV Protease Inhibitors RING-CLOSING METATHESIS STRATEGY TO UNSATURATED γ- AND δ-LACTONES: SYNTHESIS OF HYDROXYETHYLENE ISOSTERE FOR PROTEASE INHIBITORS. cis-1-Aminoindan-2-ol in Asymmetric Syntheses. Design of orally bioavailable, symmetry-based inhibitors of HIV protease Asymmetric alkylations and aldol reactions: (1S,2R)-2-aminocyclopentan-1-ol derived new chiral auxiliary The Curtius Rearrangement: Applications in Modern Drug Discovery and Medicinal Chemistry An enantioselective synthesis of the C1-C9 segment of antitumor macrolide peloruside A Asymmetric dihydroxylation route to a dipeptide isostere of a protease inhibitor: enantioselective synthesis of the core unit of ritonavir. Synthesis of novel inhibitors of the HIV-1 protease: difunctional enols of simple N-protected amino acids Synthesis of anti-1,3 Amino Alcohol Motifs via Pd(II)/SOX Catalysis with the Capacity for Stereodivergence
is cites work of	wds:Q92749499-949B5195-B9B7-43EE-A0A5-FF42A2030898 wds:Q92799051-64BAD451-82D9-4883-9E7A-856E16A5EAD2 wds:Q92799093-85DB93EF-2FE3-4D31-AC22-E10AC168F275 wds:Q64928511-C0B3238C-28F3-4F6A-B7B0-E1F9FFD62654 wds:Q64910502-6D5D2665-7E1E-4FF8-85C5-97D7C21EF73D wds:Q72145444-FF38010E-CB51-4EBA-8BA9-EC354D614785 wds:Q91311649-163A0B2F-915C-4A7B-91E7-CE469FB1E10D wds:Q64974257-6515CDD7-4153-45EE-917C-B594B538FE70 wds:Q72707303-58AAFB44-C7AB-4080-932A-D07927873013 wds:Q92369379-A8BEE860-3469-401E-99C8-D11F898AE04B

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