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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
72 Results for "
Prostanoid
" in MedChemExpress (MCE) Product Catalog:
Products (72)
72 Results for "Prostanoid" in MCE Product Catalog:
Cat. No.: HY-175077
Target:
Research Areas:
CAY10449 is an I prostanoid receptor antagonist. CAY10449 can reverse iloprost-induced TEER reduction. CAY10449 can also reverse the effect of ONO-1301 in mouse model. CAY10449 can be studied in research on athsma and allergic airway inflammation .
Cat. No.: HY-10794R
CAS No.: 915191-42-3
Research Areas:
MF498 (Standard) is the analytical standard of MF498 (HY-10794). This product is intended for research and analytical applications. MF498 is a selective and orally active E prostanoid Receptor 4 (EP4) antagonist with a Ki value of 0.7 nM. MF498 can be used in the research of inflammation, such as rheumatoid and osteoarthritis .
Cat. No.: HY-16635R
CAS No.: 866460-33-5
Synonyms: ACT-129968 (Standard); KYTH-105 (Standard)
Research Areas:
Setipiprant (Standard) is the analytical standard of Setipiprant. This product is intended for research and analytical applications. Setipiprant (ACT-129968) is an orally active and selective CRTH2 antagonist. Setipiprant interacts with hCRTH2 receptor with an IC50 value of 6 nM. Setipiprant inhibits prostanoid receptors hDP1 and hEP2 with IC50 values of 1290 and 2600 nM, respectively. Setipiprant can be used for the research of asthma and rhinitis .
Cat. No.: HY-175986
CAS No.: 3029113-61-6
Target:
Research Areas:
IP receptor agonist 1 (compound 6c-14S) is an orally active I prostanoid receptor agonist, with an IC50 of 0.15 μM for inhibiting platelet aggregation induced by ADP (HY-W010918,300 μM) in rabbit platelet-rich plasma. IP receptor agonist 1 can be used for study of Pulmonary arterial hypertension .
Cat. No.: HY-108565R
CAS No.: 152575-66-1
Research Areas:
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 .
Cat. No.: HY-113756B
CAS No.: 2699713-95-4
Research Areas:
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 .
Cat. No.: HY-183037
CAS No.: 1354060-46-0
Research Areas:
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 .
Cat. No.: HY-P703181
Purity: ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: PTGER4; PGE2 Receptor EP4 Subtype; Prostaglandin E Receptor 4; PGE Receptor, EP4 Subtype; Prostaglandin E2 Receptor EP4 Subtype; PGE Receptor EP4 Subtype; Prostanoid EP4 Receptor; PTGER2; EP4; EP4R; Prostaglandin E Receptor 4 (Subtype EP4)
Species:
Human
Source:
Sf9 insect cells
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
Cat. No.: HY-183149
CAS No.: 3120759-70-5
Research Areas:
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 .
Cat. No.: HY-187539S
CAS No.: 3085716-86-2
Target:
Research Areas:
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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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
