Cyclooxygenase

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
{{Seed}}
+
==Structure==
-
[[Image:6cox.png|left|200px]]
+
<Structure load='5cox' size='400' frame='true' align='right' caption='Unhibited mouse cyclooxygenase-2' scene='Insert optional scene name here' />
-
 
+
-
<!--
+
-
The line below this paragraph, containing "STRUCTURE_2i37", creates the "Structure Box" on the page.
+
-
You may change the PDB parameter (which sets the PDB file loaded into the applet)
+
-
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
+
-
or leave the SCENE parameter empty for the default display.
+
-
-->
+
-
{{STRUCTURE_6cox| PDB=6cox | SCENE= }}
+
-
 
+
-
===Crystal structure of COX-2===
+
-
 
+
-
 
+
-
==About this Structure==
+
-
2I37 is a 3 chains structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2I37 OCA].
+
-
 
+
==NSAIDs==
==NSAIDs==
{| border="1" style="margin: 1em auto 1em auto;"
{| border="1" style="margin: 1em auto 1em auto;"

Revision as of 09:48, 7 December 2010

Structure

Unhibited mouse cyclooxygenase-2

Drag the structure with the mouse to rotate

NSAIDs

Drug Coefficient of selectivity (IC50Cox-1/IC50Cox-2)
Ketorolac
100-1000
Naproxen
1-10
Ibuprofen
1-10
Indometacin
1-10
Acetylsalicylic acid
1
Diclofenac
1-0.1
Valdecoxib
0.01-0.001
Etoricoxib
0.01-0.001
Table X: Selectivity of some NSAIDs
Pharmacologic group Drug
Salicylates Acetylsalicylic acid
Propionic Naproxen
Ibuprofen
Para-aminophenols Paracetamol
Indolacetic Indometacin
Pirrolacetic Ketorolac
Phenilacetic Diclofenac
Piranoidacetic Etodolac
Anthranilic Mefenamic acid
Nicotinic Clonixin
Sulfonanilides Nimesulide
Table X: Chemical variety of NSAIDs

Reference

  • Salom D, Lodowski DT, Stenkamp RE, Le Trong I, Golczak M, Jastrzebska B, Harris T, Ballesteros JA, Palczewski K. Crystal structure of a photoactivated deprotonated intermediate of rhodopsin. Proc Natl Acad Sci U S A. 2006 Oct 31;103(44):16123-8. Epub 2006 Oct 23. PMID:17060607

Page seeded by OCA on Tue Feb 17 02:59:53 2009

  • Ghosh N, Chaki R, Mandal V, Mandal SC. COX-2 as a target for cancer chemotherapy. Pharmacol Rep. 2010 Mar-Apr;62(2):233-44. PMID:20508278
  • Rang HP, Dale MM, Ritter JM, Flower RJ. 2008. Pharmacology. Elsevier. 6th edition. 844 p.
  • Smith WL, Langenbach R. Why there are two cyclooxygenase isozymes. J Clin Invest. 2001 Jun;107(12):1491-5. PMID:11413152 doi:10.1172/JCI13271
  • Chandrasekharan NV, Dai H, Roos KL, Evanson NK, Tomsik J, Elton TS, Simmons DL. COX-3, a cyclooxygenase-1 variant inhibited by acetaminophen and other analgesic/antipyretic drugs: cloning, structure, and expression. Proc Natl Acad Sci U S A. 2002 Oct 15;99(21):13926-31. Epub 2002 Sep 19. PMID:12242329 doi:10.1073/pnas.162468699
Personal tools