Chemical Formula: C20H33O5-

Chemical Formula C20H33O5-

Found 18 metabolite its formula value is C20H33O5-

Enzaprost F

Enzaprost F

C20H33O5- (353.2328)


D012102 - Reproductive Control Agents > D000019 - Abortifacient Agents D012102 - Reproductive Control Agents > D010120 - Oxytocics

   

prostaglandin E1(1-)

prostaglandin E1(1-)

C20H33O5- (353.2328)


Conjugate base of prostaglandin E1.

   

(5Z,9E,14Z)-(8xi,11xi,12S)-8,11,12-Trihydroxyicosa-5,9,14-trienoate

(5Z,9E,14Z)-(8xi,11xi,12S)-8,11,12-Trihydroxyicosa-5,9,14-trienoate

C20H33O5- (353.2328)


   

11-epi-prostaglandin F2alpha(1-)

11-epi-prostaglandin F2alpha(1-)

C20H33O5- (353.2328)


A prostaglandin carboxylic acid anion that is the conjugate base of 11-epi-prostaglandin F2alpha, obtained by deprotonation of the carboxy group; major species at pH 7.3.

   

prostaglandin H1(1-)

prostaglandin H1(1-)

C20H33O5- (353.2328)


A prostaglandin carboxylic acid anion that is the conjugate base of prostaglandin H1, obtained by deprotonation of the carboxy group; major species at pH 7.3.

   

prostaglandin D1(1-)

prostaglandin D1(1-)

C20H33O5- (353.2328)


A prostaglandin carboxylic acid anion that is the conjugate base of prostaglandin D1, obtained by deprotonation of the carboxy group; major species at pH 7.3.

   

(5Z,9E,12S,14Z)-8,11,12-Trihydroxyicosa-5,9,14-trienoate

(5Z,9E,12S,14Z)-8,11,12-Trihydroxyicosa-5,9,14-trienoate

C20H33O5- (353.2328)


Conjugate base of (5Z,9E,12S,14Z)-8,11,12-trihydroxyicosa-5,9,14-trienoic acid arising from deprotonation of the carboxylic acid function.

   

trioxilin A3(1-)

trioxilin A3(1-)

C20H33O5- (353.2328)


The trioxilin anion that is the anion formed from trioxilin A3 by deprotonation of its carboxylic acid moiety; major microspecies present at pH 7.3.

   

trioxilin B3(1-)

trioxilin B3(1-)

C20H33O5- (353.2328)


The trioxilin anion that is the anion formed from trioxilin B3 by deprotonation of its carboxylic acid moiety; major microspecies present at pH 7.3.

   

13,14-dihydrolipoxin A4(1-)

13,14-dihydrolipoxin A4(1-)

C20H33O5- (353.2328)


A hydroxy fatty acid anion obtained by deprotonation of the carboxy function of 13,14-dihydrolipoxin A4; major species at pH 7.3.

   

15-ketoprostaglandin F1alpha(1-)

15-ketoprostaglandin F1alpha(1-)

C20H33O5- (353.2328)


A prostaglandin carboxylic acid anion that is the conjugate base of 15-ketoprostaglandin F1alpha, obtained by deprotonation of the carboxy group; major species at pH 7.3.

   

(5Z,9alpha,11alpha)-9,11-dihydroxy-15-oxoprost-5-en-1-oate

(5Z,9alpha,11alpha)-9,11-dihydroxy-15-oxoprost-5-en-1-oate

C20H33O5- (353.2328)


   

11alpha-Hydroxy-9,15-dioxoprostan-1-oate

11alpha-Hydroxy-9,15-dioxoprostan-1-oate

C20H33O5- (353.2328)


   

prostaglandin F2beta(1-)

prostaglandin F2beta(1-)

C20H33O5- (353.2328)


A prostaglandin carboxylic acid anion that is the conjugate base of prostaglandin F2beta, obtained by deprotonation of the carboxy group; major species at pH 7.3.

   

8-epi-prostaglandin F2alpha(1-)

8-epi-prostaglandin F2alpha(1-)

C20H33O5- (353.2328)


A prostaglandin carboxylic acid anion that is the conjugate base of 8-epi-prostaglandin F2alpha, obtained by deprotonation of the carboxy group. Major structure at pH 7.3.

   

(5Z,8Z,12E)-11,14,15-Trihydroxyicosa-5,8,12-trienoate

(5Z,8Z,12E)-11,14,15-Trihydroxyicosa-5,8,12-trienoate

C20H33O5- (353.2328)


   

11,12,15-trihydroxyeicosa-(5Z,8Z,13E)-trienoate

11,12,15-trihydroxyeicosa-(5Z,8Z,13E)-trienoate

C20H33O5- (353.2328)


   

13,14,15-trihydroxyeicosa-(5Z,8Z,11Z)-trienoate

13,14,15-trihydroxyeicosa-(5Z,8Z,11Z)-trienoate

C20H33O5- (353.2328)