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Cat. No. Product Name Information
PC-38455

AT-56

L-PGDS inhibitor

AT-56 is an orally active, selective inhibitor of lipocalin-type prostaglandin D synthase (L-PGDS) with Ki of 75 uM, IC50 of 95 uM.
PC-36096

Pizuglanstat

H-PGDS inhibitor

TAS-205 (Pizuglanstat, TAS205) is a potent, specific hematopoietic prostaglandin D synthase (H-PGDS) inhibitor with IC50 of 55.8 nM, does not inhibit LPGDS at 100 uM.
PC-36090

Crisdesalazine

mPGES-1 inhibitor

Crisdesalazine (AAD-2004, AAD2004) is a derivative of aspirin that inhibits microsomal PGE(2) synthase-1 (mPGES-1) activity in response to both LPS-treated BV2 cell with IC50 of 230 nM and recombinant human mPGES-1 protein with IC50 of 249 nM in vitro.
PC-43462

MF63

mPGES-1 inhibitor

MF63 is a potent, selective, and orally active mPGES-1 inhibitor with IC50 of 1.3 nM for human mPGES-1 enzyme, >1000-fold selectivity over other prostanoid synthases.
PC-43211

hPGDS-IN-1

H-PGDS inhibitor

hPGDS-IN-1 is a potent, selective hematopoietic prostaglandin D synthase (H-PGDS) inhibitor inhibitor with IC50 of 12 nM in FP or EIA assays.
PC-62820

mPGES1-IN-16

mPGES-1 inhibitor

mPGES1-IN-16 is a potent and selective mPGES-1 inhibitor with IC50 of 1 nM.
PC-62797

mPGES1-IN-17d

mPGES-1 inhibitor

mPGES1-IN-17d is a potent, selective mPGES-1 inhibitor with enzyme IC50 of 8 nM, A549 cell IC50 of 16.24 nM, human whole blood IC50 of 249.9 nM.
PC-61665

PF-9184

mPGES-1 inhibitor

PF-9184 is a potent, selective mPGES-1 (microsomal prostaglandin E synthase-1) inhibitor with IC50 of 16.5 nM.
PC-61406

LY3031207

mPGES-1 inhibitor

LY3031207 is a novel potent (IC50=910 ng/mL), highly selective microsomal prostaglandin E synthase 1 inhibitor (mPGES-1) for treatment of undisclosed indications.
PC-42585

HPGDS inhibitor 1

H-PGDS inhibitor

HPGDS inhibitor 1 is a potent, selective, oral hematopoietic prostaglandin D synthase (H-PGDS) inhibitor with enzyme IC50 of 0.6 nM.
PC-45791

Benzydamine hydrochloride

Benzydamine hydrochloride is a locally-acting nonsteroidal anti-inflammatory drug (NSAID) with local anaesthetic and analgesic properties for pain relief and anti-inflammatory treatment of inflammatory conditions.
PC-49641

TAS-205 monohydrate

H-PGDS inhibitor

TAS-205 (Pizuglanstat, TAS205) is a potent, specific hematopoietic prostaglandin D synthase (H-PGDS) inhibitor with IC50 of 55.8 nM, does not inhibit LPGDS at 100 uM.

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