+ |
prostaglandin E2(1-) | up-regulates quantity
precursor of
|
prostaglandin H2(1-) |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269767 |
|
|
in vitro |
|
pmid |
sentence |
10922363 |
Importantly, this enzyme is capable of converting COX-1-, but not COX-2-, derived PGH2 to PGE2 efficiently. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
PTGS2 | up-regulates quantity
chemical modification
|
prostaglandin H2(1-) |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269776 |
|
|
in vitro |
|
pmid |
sentence |
7592599 |
[14C]Arachidonate metabolism by oPGHS-1 and hPGHS-2 was examined in reactions with a series of GSP/Cox ratios (Fig. 3). The principal metabolite for both isoforms was the endoperoxide PGH2, with lesser amounts of PGF2a, PGE2, PGD2, |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
prostaglandin G2(1-) | up-regulates quantity
precursor of
|
prostaglandin H2(1-) |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269777 |
|
|
in vitro |
|
pmid |
sentence |
7592599 |
[14C]Arachidonate metabolism by oPGHS-1 and hPGHS-2 was examined in reactions with a series of GSP/Cox ratios (Fig. 3). The principal metabolite for both isoforms was the endoperoxide PGH2, with lesser amounts of PGF2a, PGE2, PGD2, |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
prostaglandin H2(1-) | up-regulates quantity
precursor of
|
prostaglandin G2(1-) |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269769 |
|
|
in vitro |
|
pmid |
sentence |
7592599 |
[14C]Arachidonate metabolism by oPGHS-1 and hPGHS-2 was examined in reactions with a series of GSP/Cox ratios (Fig. 3). The principal metabolite for both isoforms was the endoperoxide PGH2, with lesser amounts of PGF2a, PGE2, PGD2, |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
PTGS1 | up-regulates quantity
chemical modification
|
prostaglandin H2(1-) |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269778 |
|
|
in vitro |
|
pmid |
sentence |
7592599 |
[14C]Arachidonate metabolism by oPGHS-1 and hPGHS-2 was examined in reactions with a series of GSP/Cox ratios (Fig. 3). The principal metabolite for both isoforms was the endoperoxide PGH2, with lesser amounts of PGF2a, PGE2, PGD2, |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
prostaglandin H2(1-) | up-regulates quantity
precursor of
|
prostaglandin E2(1-) |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269765 |
|
|
in vitro |
|
pmid |
sentence |
10922363 |
Importantly, this enzyme is capable of converting COX-1-, but not COX-2-, derived PGH2 to PGE2 efficiently. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
PTGES2 | up-regulates quantity
chemical modification
|
prostaglandin H2(1-) |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269768 |
|
|
in vitro |
|
pmid |
sentence |
10922363 |
Importantly, this enzyme is capable of converting COX-1-, but not COX-2-, derived PGH2 to PGE2 efficiently. |
|
Publications: |
1 |
Organism: |
In Vitro |