4 Results for "

TP receptor antagonist 1

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "TP receptor antagonist 1" in MCE Product Catalog:

Cat. No.: HY-160615
CAS No.: 1448452-21-8
TP receptor antagonist-1 (compound 7m) is a thromboxane A2 receptor (TP receptor) antagonist, with IC50 values of 9.46 μM for TPa and 8.49 μM for TPb, respectively. TP receptor antagonist-1 can be used for the research of cardiovascular disease .
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Cat. No.: HY-108972
CAS No.: 98672-91-4
Purity:  ≥99.0%
Research Areas:  

Metabolic Disease

SQ 29548 is a selective thromboxane-prostanoid (TP) receptor antagonist .
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Cat. No.: HY-186042
CAS No.: 899789-84-5
Research Areas:  

Cardiovascular Disease

TPα/β antagonist-1 is a TXA2 receptor α (TPα) and TPβ antagonist with IC50s of 1.52 nM and 0.79 nM, respectively. TPα/β antagonist-1 inhibits U-46619 (HY-108566)-induced intracellular calcium mobilization, and imhibits platelet aggregation. TPα/β antagonist-1 can be used for the research of cardiovascular disease .
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Cat. No.: HY-15007
CAS No.: 138382-23-7
Target:  

Oxytocin Receptor

Research Areas:  

Endocrinology

L 366509 is a spiroindenylpiperidine camphorsulfonamide oxytocin (OT) antagonist. Modifications led to a new series of o-tolylpiperazine (TP) camphorsulfonamides, exhibiting high affinity for OT receptors and selectivity over arginine vasopressin receptors. Notably, compound 7 (L-368,899) showed excellent OT receptor affinity, potency in inhibiting OT-stimulated uterine contractions, good aqueous solubility, and oral bioavailability in multiple species. Compound 7 has entered clinical testing as an oral and intravenous tocolytic agent. Molecular modeling suggests the TP camphorsulfonamide structure mimics the D-AA2-Ile3 dipeptide, crucial in potent OT antagonists .
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