66 Results for "

Prostanoid Receptor

" in MedChemExpress (MCE) Product Catalog:
Products (66)

66 Results for "Prostanoid Receptor" in MCE Product Catalog:

Cat. No.: HY-P705619
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PTGER3; Prostaglandin Receptor (PGE-2); Prostaglandin E Receptor 3; PGE Receptor, EP3 Subtype; Prostaglandin E2 Receptor EP3 Subtype; PGE Receptor EP3 Subtype; Prostanoid EP3 Receptor; EP3-III; Lnc003875; EP3-II; EP3; EP3-IV; Prostaglandin E Receptor 3 (S
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-113756B
CAS No.: 2699713-95-4
rel-Latanoprost acid is a relative configuration of Latanoprost acid (HY-113756A). Latanoprost acid, an analog of prostaglandin (PG) F2α, is an selective prostanoid receptor (FP) agonist that specifically activates the FP-PG receptor . Latanoprost acid inhibits RANKL-induced osteoclastgenesis and function by inhibiting ERK, AKT, JNK, and p38 cascade, following by the c-fos/NFATc1 pathway. Latanoprost acid is a medication which works to lower pressure inside the eyes .
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Cat. No.: HY-108565R
CAS No.: 152575-66-1
BMY 45778 (Standard) is the analytical standard of BMY 45778 (HY-108565). This product is intended for research and analytical applications. BMY 45778 is a non-prostanoid prostacyclin mimetic. BMY 45778 inhibits human (IC50 = 35 nM), rabbit (IC50: 136 nM) and rat (IC50 : 1.3 μM) platelet aggregation. BMY 45778 also activates adenylyl cyclase. BMY 45778 is a partial agonist at the prostacyclin receptor .
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Cat. No.: HY-183037
CAS No.: 1354060-46-0
AGN 225660 is a multi-prostanoid receptor antagonist with human IC50 values of 70, 70, 5, 220 and 180 nM for EP1, EP4, TP, DP1, FP. AGN 225660 inhibits secretion of RANTES, IL-8, MCP-1, IL-12p70, and IL-23. AGN 225660 exhibits good ocular bioavailability and reduces ocular inflammation linked to phacoemulsification surgery and uveitis .
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Cat. No.: HY-183149
CAS No.: 3120759-70-5
BPN-37440 is a blood-brain barrier-permeable, selective, and orally active EP2 receptor inhibitor with an IC50 of 53-60 nM. BPN-37440 inhibits the expression of inflammatory mediators IL-1β and COX-2, with an IC50 of 21 nM for IL-1β and 42 nM for COX-2. BPN-37440 reduces microgliosis in key brain regions of mice with pilocarpine (HY-B0726A)-induced status epilepticus and reverses their working memory and recognition memory deficits. BPN-37440 can be used for research on status epilepticus .
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Cat. No.: HY-187539S
CAS No.: 3085716-86-2
Research Areas:  

Cardiovascular Disease

IPR agonist-1 is a prostaglandin-based IP receptor agonist. IPR agonist-1 binds to the IP receptor, forms hydrogen bonds with Tyr75-Ser168-Arg279, and undergoes π-π stacking with Tyr281, thereby triggering downstream signaling pathways. IPR agonist-1 inhibits ADP (Adenosine 5'-diphosphate) (HY-W010918)-induced platelet aggregation in rabbit platelet-rich plasma. IPR agonist-1 can be used in the research of pulmonary arterial hypertension .
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