36 Results for "

EP2 agonist

" in MedChemExpress (MCE) Product Catalog:
Products (36)

36 Results for "EP2 agonist" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-14899
CAS No.: 752187-80-7
Purity:  98.79%
Synonyms: CP-544326
Research Areas:  

Endocrinology

Taprenepag (CP-544326) is a potent and selective prostaglandin EP(2) agonist with IC50s of 10 and 15 nM for human and rat EP2, respectively. Taprenepag shows selectivity for EP2 over other EP receptors (IC50s>3200 nM for EP1, EP3, and EP4) and a panel of 37 G protein-coupled receptors .
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3
3 Cited Publications
Cat. No.: HY-128686
CAS No.: 1215192-68-9
Purity:  98.62%
KAG-308 is a potent selective and orally active agonist of EP4 receptor (a prostaglandin E2 receptor subtype), suppresses colitis and promotes histological mucosal healing, potently inhibits TNF-α production. KAG-308 shows a Ki and an EC50 of 2.57 nM and 17 nM for human EP4 receptor, respectively, more selective over EP1, EP2, EP3 and IP receptor .
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2
2 Cited Publications
Cat. No.: HY-100441
CAS No.: 81846-19-7
Purity:  99.95%
Synonyms: UT-15
Treprostinil (UT-15) is a potent DP1 and EP2 agonist with EC50 values of 0.6±0.1 and 6.2±1.2 nM, respectively.
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2
2 Cited Publications
Cat. No.: HY-16504
CAS No.: 289480-64-4
Synonyms: UT-15 sodium
Treprostinil (UT-15) sodium is a potent DP1 and EP2 agonist with EC50 values of 0.6±0.1 and 6.2±1.2 nM, respectively.
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2
2 Cited Publications
Cat. No.: HY-100448A
CAS No.: 69685-22-9
Purity:  99.2%
Research Areas:  

Endocrinology

Butaprost is a selective prostaglandin E receptor (EP2) agonist with an EC50 of 33 nM and a Ki of 2.4 μM for murine EP2 receptor. Butaprost is less activity against murine EP1, EP3 and EP4 receptors. Butaprost attenuates fibrosis by hampering TGF-β/Smad2 signalling .
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2
2 Cited Publications
Cat. No.: HY-14839
CAS No.: 223488-57-1
Purity:  99.78%
Synonyms: CP-533536 free acid
Evatanepag (CP-533536) is a non-prostanoid, potent and selective EP2 receptor agonist. Evatanepag can induce local bone formation in vivo. Evatanepag can be used in the research of fractures, bone defects, asthma .
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2
2 Cited Publications
Cat. No.: HY-B0813
CAS No.: 830354-48-8
Synonyms: UT-15C
Research Areas:  

Endocrinology

Treprostinil (UT-15C) diethanolamine is a potent EP2, DP1 and IP agonist with Ki values of 3.6, 4.4, 32.1, 212, 826, 2505 and 4680 nM for EP2, DP1, IP, EP1, EP4, EP3 and FP, respectively. Treprostinil (UT-15C) diethanolamine increases upregulation of cAMP toward maintaining homeostasis within the vasculature. Treprostinil (UT-15C) diethanolamine can result in vasodilatation of human pulmonary arteries .
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1
1 Cited Publications
Cat. No.: HY-17642
CAS No.: 1187451-41-7
Synonyms: UR-7276
Research Areas:  

Endocrinology

Omidenepag (UR-7276), a pharmacologically active form of Omidenepag Isopropyl, is a selective, non-prostanoid EP2 receptor agonist, with an EC50 of 1.1 nM. Omidenepag shows binding affinities (IC50) 10 nM for h-EP2. Omidenepag is used in research on diseases related to intraocular pressure .
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1
1 Cited Publications
Cat. No.: HY-19998
CAS No.: 1005549-94-9
Synonyms: PF-04217329
Taprenepag isopropyl is a highly selective EP2 receptor agonist.
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Cat. No.: HY-111406
CAS No.: 1187451-19-9
Purity:  99.20%
Synonyms: DE-117
Omidenepag isopropyl is a selective EP2 receptor agonist. Omidenepag isopropyl is converted to the active product Omidenepag during corneal penetration, and Omidenepag is a highly selective EP2 receptor agonist. Omidenepag isopropyl shows only weak affinity for EP1, EP2, and FP receptors. Omidenepag isopropyl is under development for the treatment of glaucoma as an intraocular pressure (IOP)-lowering agent.
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Cat. No.: HY-145684
CAS No.: 848920-08-1
Purity:  99.45%
Research Areas:  

Inflammation/Immunology

EP2 receptor antagonist-1 (compound 1) is a potent, reversible, and agonist dependent allosteric prostaglandin EP2 receptor antagonist. EP2 receptor antagonist-1 shows anti-inflammatory effects .
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Cat. No.: HY-100441S2
CAS No.: 2747918-14-3
Purity:  99.79%
Synonyms: UT-15-d9
Treprostinil-d9 (UT-15-d9) is the deuterium-labeled Treprostinil (HY-100441) . Treprostinil (UT-15) is a potent DP1 and EP2 agonist with EC50 values of 0.6±0.1 and 6.2±1.2 nM, respectively.
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Cat. No.: HY-118609
CAS No.: 493035-81-7
Purity:  ≥99.0%
Research Areas:  

Inflammation/Immunology

EP4 receptor agonist 2 (compound 31) a potent EP4 receptor agonist with an EC50 value of 0.8 nM; Ki values of >100000, 38000, 3.1 nM for EP2, EP3, EP4 respectively .
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Cat. No.: HY-121091
CAS No.: 212310-16-2
Research Areas:  

Others

EP2 receptor agonist 4 is a selective agonist for EP2 receptor with an EC50 of 43 nM .
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Cat. No.: HY-120973
CAS No.: 215168-33-5
Butaprost free acid is a selective prostaglandin E receptor (EP2) agonist with an EC50 of 33 nM and a Ki of 2.4 μM for murine EP2 receptor. Butaprost free acid is less activity against murine EP1, EP3 and EP4 receptors. Butaprost free acid attenuates fibrosis by hampering TGF-β/Smad2 signalling .
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Cat. No.: HY-19923
CAS No.: 910562-20-8
Synonyms: AGN-210961
Research Areas:  

Endocrinology

Aganepag isopropyl (AGN-210961) is an EP2 agonist .
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Cat. No.: HY-115462
CAS No.: 863704-91-0
Purity:  98.90%
Research Areas:  

Inflammation/Immunology

PGN-9856 is a selective and high affinity (pKi ≥ 8.3) ligand at EP2 receptor. PGN-9856 is a potetn and non-prostanoid EP2 receptor agonist (pEC50 ≥ 8.5). PGN-9856 shows anti-inflammatory and anti-glaucoma activities .
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Cat. No.: HY-128496
CAS No.: 1807780-00-2
Research Areas:  

Neurological Disease Cancer

EP2 receptor agonist 2 (compound 18a) is a potent and selective G protein-biased EP2 receptor agonist (hEP2G protein EC50 = 13 nM, hEP2β arrestin EC50 > 10000 nM). EP2 receptor agonist 2 exhibits excellent selectivity over hEP1/3/4, hIP and hFP (EC50s > 10000 nM) .
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Cat. No.: HY-120973A
CAS No.: 433219-55-7
Research Areas:  

Endocrinology

(S)-Butaprost (free acid) is a potent and highly selective agonist of EP2 receptor .
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Cat. No.: HY-19864
CAS No.: 910562-18-4
Synonyms: AGN 210937
Research Areas:  

Inflammation/Immunology

Aganepag is a potent Prostanoid EP2 receptor agonist, with an EC50 of 0.19 nM, and shows no activity at EP4 receptor. Aganepag can be used in the research of wound healing, scar reduction, scar prevention and wrinkle treatment and prevention.
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