- Signaling Pathways
- Immunology/Inflammation
- PGE synthase
PGE synthase
Prostaglandin E synthase
PGE synthase (Prostaglandin E synthase), which converts cyclooxygenase (COX)-derived prostaglandin H2 (PGH2) to PGE2, is known to comprise a group of at least three structurally and biologically distinct enzymes. There are membrane-associated PGES (mPGES)-1, mPGES-2, and cytosolic PGES (cPGES).
mPGES-1 is a perinuclear protein that is markedly induced by proinflammatory stimuli and downregulated by anti-inflammatory glucocorticoids as in the case of COX-2. It is functionally coupled with COX-2 in marked preference to COX-1. mPGES-2 is synthesized as a Golgi membrane-associated protein, and the proteolytic removal of the N-terminal hydrophobic domain leads to the formation of a mature cytosolic enzyme. This enzyme is rather constitutively expressed in various cells and tissues and is functionally coupled with both COX-1 and COX-2. cPGES is constitutively expressed in a wide variety of cells and is functionally linked to COX-1 to promote immediate PGE2 production.
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PGE synthase Related Products (127)
Related Products (127)
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Antibodies (2)
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1-(2,5-Dihydroxyphenyl)-3-hydroxybutan-1-one
0 ImagesCat. No.: HY-N19110CAS No.: 1083202-40-71-(2,5-Dihydroxyphenyl)-3-hydroxybutan-1-one is an inhibitor of iNOS and COX-2. 1-(2,5-Dihydroxyphenyl)-3-hydroxybutan-1-one inhibits LPS-induced excessive production of NO and PGE2, as well as the mRNA expression of pro-inflammatory cytokines TNF-α, IL-1β, IL-6 and IL-12. 1-(2,5-Dihydroxyphenyl)-3-hydroxybutan-1-one can be used in inflammation-related research. -
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- Ethyl Caffeate (Standard)
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Suprofen L-lysine
0 ImagesCat. No.: HY-137157CAS No.: 69317-48-2Synonyms: TN-762 L-lysineSuprofen L-lysine (TN-762) is a non-steroidal anti-inflammatory drug (NSAID). -
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Dehydroevodiamine (Standard)
0 ImagesCat. No.: HY-N2106RCAS No.: 67909-49-3Dehydroevodiamine is a major bioactive quinazoline alkaloid isolated from Evodiae Fructus, has an antiarrhythmic effect in guinea-pig ventricular myocytes. Dehydroevodiamine inhibits LPS-induced iNOS, COX-2, prostaglandin E2 (PGE2) and nuclear factor-kappa B (NF-κB) expression in murine macrophage cells. -
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HPGDS inhibitor 1 (Standard)
0 ImagesCat. No.: HY-10439RCAS No.: 1033836-12-2HPGDS inhibitor 1 (Standard) is the analytical standard of HPGDS inhibitor 1 (HY-10439). This product is intended for research and analytical applications. HPGDS inhibitor 1 is a potent, selective and orally active Hematopoietic Prostaglandin D Synthase (HPGDS) inhibitor with an IC50s of 0.6 nM and 32 nM in enzyme and cellular assays, respectively. HPGDS inhibitor 1 does not inhibit human L-PGDS, mPGES, COX-1, COX-2, or 5-LOX. -
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Indigoticoside A
0 ImagesCat. No.: HY-N17277CAS No.: 107110-16-7Indigoticoside A is a phenylpropanoid lignan natural product that can be found in the traditional Chinese medicine Banlangen (Isatis indigotica Fort.), with antioxidant and anti-inflammatory activities. Indigoticoside A scavenges DPPH free radicals, superoxide anions and hydroxyl radicals in a dose-dependent manner, exhibiting significant in vitro antioxidant effects. The blood-absorbed components of Banlangen containing Indigoticoside A inhibit LPS (HY-D1056)-induced inflammatory responses in macrophages and reduce the production of inflammatory mediators such as NO, PGE2 and TNF-α. -
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Dehydroevodiamine hydrochloride (Standard)
0 ImagesCat. No.: HY-N6029RCAS No.: 111664-82-5Dehydroevodiamine hydrochloride is isolated from the leaves of Evodia rutaecarpa. -
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α-Gracinoic acid
0 ImagesCat. No.: HY-164358CAS No.: 2180947-76-4α-Gracinoic acid is an mPGES-1 inhibitor with anti-inflammatory activity. -
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F092
0 ImagesF092 is an inhibitor of hematopoietic prostaglandin D synthase (H-PGDS) with a KD value of 0.14 nM. F092 can be used in the study of allergic and inflammatory responses. -
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FR20
0 ImagesCat. No.: HY-122064CAS No.: 570373-45-4FR20 acts as an inhibitor of human microsomal prostaglandin synthase 1 (mPGES 1). -
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Zomepirac sodium salt (Standard)
0 ImagesSynonyms: McN-2783-21-98 (Standard)Zomepirac sodium salt (Standard) is the analytical standard of Zomepirac sodium salt (HY-B0890). This product is intended for research and analytical applications. Zomepirac sodium salt (McN-2783-21-98) is an orally active prostaglandin synthetase inhibitor. Zomepirac sodium salt blocks prostaglandin synthesis and inhibits Collagen (HY-P72147)- or Epinephrine (HY-B0447)-induced platelet aggregation. Zomepirac sodium salt can be used for the research of postoperative pain and osteoarthritis. -
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AF3485
0 ImagesCat. No.: HY-118184CAS No.: 1195786-61-8AF3485 is a human mPGES-1 inhibitor that exhibits antitumor activity in vitro and in vivo. AF3485 inhibits tumor-associated angiogenesis by reducing PGE2 production, inhibiting EGFR signaling, and decreasing VEGF and FGF-2 expression. AF3485 reduced tumor growth in mice bearing human A431 xenograft tumors by subchronic administration. -
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Hydralazine hydrochloride (Standard)
0 ImagesHydralazine (hydrochloride) (Standard) is the analytical standard of Hydralazine (hydrochloride). This product is intended for research and analytical applications. Hydralazine hydrochloride is an orally active, blood-brain barrier-permeable DNA methyltransferase inhibitor with vasodilatory, arterial smooth muscle relaxant and hypotensive activities. Hydralazine hydrochloride reactivates silenced tumor suppressor genes via mediating DNA demethylation, while exerting neuroprotective and anti-inflammatory properties. Hydralazine hydrochloride inhibits NOS-2 (iNOS) and COX-2, and reduces the production of NO and PGEE2; meanwhile, Hydralazine hydrochloride scavenges reactive oxygen species and inhibits macrophage activation. Hydralazine hydrochloride alleviates motor dysfunction, neuropathic inflammatory pain, and formalin-induced somatic and emotional pain responses. In addition, Hydralazine hydrochloride directly induces DNA strand breaks and sister chromatid exchange, exhibiting certain mutagenic characteristics. Hydralazine hydrochloride has been widely used in studies on hypertension, various cancers (such as cervical cancer, leukemia), spinal cord injury and the mechanisms of inflammatory pain. -
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Furprofen (Standard)
0 ImagesCat. No.: HY-106907RCAS No.: 66318-17-0Furprofen (Standard) is the analytical standard of Furprofen (HY-106907). This product is intended for research and analytical applications. Furprofen is an non-steroidal anti-inflammatory drug (NSAID) with analgesic properties. Furprofen acts via the inhibition of prostaglandin (PGE) synthesis. Furprofen can be treated orally for the relief of pain. -
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Patrinoside aglucone
0 ImagesCat. No.: HY-160121CAS No.: 76319-15-8Synonyms: Patrinoside aglyconePatrinoside aglucone (Compound 8) is an iridoid glucoside that can be isolated from the Valeriana tuberosa. Patrinoside aglucone has potent anticancer activity with G2/M phase tumor cell cycle arrest and apoptosis induction. Patrinoside aglucone also significantly inhibits the proliferation of cancer stem cells (such as MDA-MB-231 and U-251MG cells). Patrinoside aglucone has great anti-inflammatory activity by inhibiting NO release (IC50: 43.44 μM) and significantly reduces the level of TNF-α, IL-1β, IL-6, PGE2 and COX-2. -
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mPGES1-IN-8
0 ImagesCat. No.: HY-13475CAS No.: 1381846-21-4mPGES1-IN-8, is a novel microsomal prostaglandin E synthase 1 (mPGES1) inhibitor. -
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Gingerdione
0 ImagesCat. No.: HY-N12643CAS No.: 61871-71-4Synonyms: [6]-Gingerdione[6]-Gingerdione is a prostaglandin synthesis inhibitor that can be isolated from ginger rhizomes. -
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ML388
0 ImagesCat. No.: HY-120581CAS No.: 1537192-31-6ML388 is a potent and selective hydroxyprostaglandin dehydrogenase (HPGD) inhibitor with an IC50 of 34 nM. ML388 induces PGE2 production in A549 cells and LNCaP prostate cancer cells. -
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HQL-79 (Standard)
0 ImagesCat. No.: HY-108259RCAS No.: 162641-16-9HQL-79 (Standard) is the analytical standard of HQL-79 (HY-108259). This product is intended for research and analytical applications. HQL-79, a potent, selective and orally active human hematopoietic prostaglandin D synthase (H-PGDS) inhibitor, highly selectively inhibits the synthesis of PGD2, and acts as an anti-allergic agent, with a Kd of 0.8 μM and an IC50 of 6 μM. Shows no obvious effect on COX-1, COX-2, m-PGES, or L-PGDS. -
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Suprofen (Standard)
0 ImagesCat. No.: HY-B0270RCAS No.: 40828-46-4Synonyms: TN-762 (Standard)Suprofen (Standard) is the analytical standard of Suprofen. This product is intended for research and analytical applications. Suprofen (TN-762) is a non-steroidal anti-inflammatory drug (NSAID). -
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