5 Results for "

uterine contraction agent

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "uterine contraction agent" in MCE Product Catalog:

Cat. No.: HY-P4160
CAS No.: 634586-40-6
Synonyms: THG113.31; ILGHXDYK
Research Areas:  

Endocrinology

PDC31 (THG113.31; ILGHXDYK) is an allosteric and non-competitive inhibitor of FP Prostaglandin Receptor. PDC31 is the D-amino acid-based oligopeptide, is used for smooth muscle contractile agent. PDC31 decreases the strength and duration of uterine contractions in vivo, which can be used for research of preterm labor and primary dysmenorrhea (PD). PDC31 also enhances Ca 2+-dependent large-conductance K +-channel in human myometrial cells .
loading...
    loading...
Cat. No.: HY-135447
CAS No.: 284464-46-6
BM-531 is a dual-acting agent for thromboxane receptor (TXA2) antagonism and thromboxane synthase inhibition. BM-531 exerts anti-aggregatory effects on human citrated platelet-rich plasma (PRP), inhibiting Arachidonic acid (HY-109590A)-induced aggregation with an ED100 of 0.125 μM and U-46619 (HY-108566)-induced aggregation with an ED50 of 0.482 μM. BM-531 inhibits high-K +-induced contraction of porcine uterine smooth muscle .
loading...
    loading...
Cat. No.: HY-P2034
CAS No.: 33605-67-3
Target:  

Oxytocin Receptor

Research Areas:  

Endocrinology

Cargutocin, an oxytocin analogue, targets the oxytocin receptor and acts as a uterine contraction agent .
loading...
    loading...
Cat. No.: HY-15018A
CAS No.: 785048-28-4
Target:  

Oxytocin Receptor

Research Areas:  

Endocrinology

SSR126768A free base is an orally active antagonist for oxytocin receptor, with Ki of 0.44 nM. SSR126768A free base is a tocolytic agent, that antagonizes the Oxytocin (HY-17571)-induced intracellular Ca 2+ increase and prostaglandin release in human uterine smooth muscle cells, inhibits thus the Oxytocin (HY-17571)-induced uterine contraction and delays parturition in pregnant rats in labor .
loading...
    loading...
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 .
loading...
    loading...