1ohr: Difference between revisions

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[[Image:1ohr.gif|left|200px]]
[[Image:1ohr.gif|left|200px]]


{{Structure
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The line below this paragraph, containing "STRUCTURE_1ohr", creates the "Structure Box" on the page.
|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)
|LIGAND= <scene name='pdbligand=1UN:2-[2-HYDROXY-3-(3-HYDROXY-2-METHYL-BENZOYLAMINO)-4-PHENYL+SULFANYL-BUTYL]-DECAHYDRO-ISOQUINOLINE-3-CARBOXYLIC+ACID+TERT-BUTYLAMIDE'>1UN</scene>
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|DOMAIN=
{{STRUCTURE_1ohr| PDB=1ohr  | SCENE= }}  
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1ohr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ohr OCA], [http://www.ebi.ac.uk/pdbsum/1ohr PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1ohr RCSB]</span>
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'''VIRACEPT (R) (NELFINAVIR MESYLATE, AG1343): A POTENT ORALLY BIOAVAILABLE INHIBITOR OF HIV-1 PROTEASE'''
'''VIRACEPT (R) (NELFINAVIR MESYLATE, AG1343): A POTENT ORALLY BIOAVAILABLE INHIBITOR OF HIV-1 PROTEASE'''
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: II, J F.Davies.]]
[[Category: II, J F.Davies.]]
[[Category: aspartyl protease]]
[[Category: Aspartyl protease]]
[[Category: hiv-i protease]]
[[Category: Hiv-i protease]]
[[Category: hydrolase]]
[[Category: Hydrolase]]
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 22:45:31 2008''

Revision as of 03:51, 3 May 2008

File:1ohr.gif

Template:STRUCTURE 1ohr

VIRACEPT (R) (NELFINAVIR MESYLATE, AG1343): A POTENT ORALLY BIOAVAILABLE INHIBITOR OF HIV-1 PROTEASE


OverviewOverview

Using a combination of iterative structure-based design and an analysis of oral pharmacokinetics and antiviral activity, AG1343 (Viracept, nelfinavir mesylate), a nonpeptidic inhibitor of HIV-1 protease, was identified. AG1343 is a potent enzyme inhibitor (Ki = 2 nM) and antiviral agent (HIV-1 ED50 = 14 nM). An X-ray cocrystal structure of the enzyme-AG1343 complex reveals how the novel thiophenyl ether and phenol-amide substituents of the inhibitor interact with the S1 and S2 subsites of HIV-1 protease, respectively. In vivo studies indicate that AG1343 is well absorbed orally in a variety of species and possesses favorable pharmacokinetic properties in humans. AG1343 (Viracept) has recently been approved for marketing for the treatment of AIDS.

About this StructureAbout this Structure

1OHR is a Single protein structure of sequence from Human immunodeficiency virus 1. The following page contains interesting information on the relation of 1OHR with [HIV-1 Protease]. Full crystallographic information is available from OCA.

ReferenceReference

Viracept (nelfinavir mesylate, AG1343): a potent, orally bioavailable inhibitor of HIV-1 protease., Kaldor SW, Kalish VJ, Davies JF 2nd, Shetty BV, Fritz JE, Appelt K, Burgess JA, Campanale KM, Chirgadze NY, Clawson DK, Dressman BA, Hatch SD, Khalil DA, Kosa MB, Lubbehusen PP, Muesing MA, Patick AK, Reich SH, Su KS, Tatlock JH, J Med Chem. 1997 Nov 21;40(24):3979-85. PMID:9397180 Page seeded by OCA on Sat May 3 03:51:49 2008

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