Difference between revisions of "Transformation of PGI2 to 6-K-PGF1α"

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[[Welcome to the In-Silico Model of Cutaneous Lipids Wiki | Return to overview]]
 
[[Welcome to the In-Silico Model of Cutaneous Lipids Wiki | Return to overview]]
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Due to ring strain, PGI2 is rapidly hydrolysed to 6-keto-PGF1a. This is a non-enzymatic reaction and results in the formation of a hydroxyl group at C9 and a ketone at C6, by incorporating two hydrogens and one oxygen.
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== Reaction ==
 
== Reaction ==
 
[[File:R7_PGI2_-_K6PGF2A.jpg ‎|center|500px]]
 
[[File:R7_PGI2_-_K6PGF2A.jpg ‎|center|500px]]

Revision as of 17:16, 1 February 2019

Return to overview

Due to ring strain, PGI2 is rapidly hydrolysed to 6-keto-PGF1a. This is a non-enzymatic reaction and results in the formation of a hydroxyl group at C9 and a ketone at C6, by incorporating two hydrogens and one oxygen.

Reaction

R7 PGI2 - K6PGF2A.jpg

Chemical equation

 PGI2 \rightleftharpoons 6-K-PGF1α

Rate equation

R07.PNG

Parameters

Related Reactions