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Oxytocin Receptor

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Oxytocin Receptor

Chemical Structure Cat. No. Product Name CAS No.
LIT-001 TFA Chemical Structure
BCP32617 LIT-001 TFA 2245072-21-1
LIT-001 is the First Nonpeptide Oxytocin Receptor Agonist that Improves Social Interaction in a Mouse Model of Autism.
LIT-001 Chemical Structure
BCP31983 LIT-001 2245072-20-0
LIT-001 is the first potent nonpeptide agonist of oxytocin receptor (OT-R).
Alisertib Chemical Structure
BCP28930 Alisertib 1477482-19-1
Alisertib, also known as OBE001 or Erlosiban, is a novel, orally active nonpeptide oxytocin receptor antagonist under development for the treatment of preterm labor and improvement in embryo implantation and pregnancy rate in assisted reproductive technology (ART).
PF-3274167 Chemical Structure
BCP08878 PF-3274167 900510-03-4
PF-3274167 is a high-affinity nonpeptide oxytocin receptor (OTR) antagonist, with Ki of 9.5 nM.
Atosiban Chemical Structure
BCP02053 Atosiban 90779-69-4
Atosiban, a nonapeptide, desamino-oxytocin analogue, is a competitive inhibitor of the hormones oxytocin and vasopressinv.
Oxytocin Acetate Chemical Structure
BCP02057 Oxytocin Acetate 50-56-6
Oxytocin(Syntocinon) is a nine amino acid peptide that is synthesized in hypothalamic neurons and transported down axons of the posterior pituitary for secretion into blood.
Carbetocin Chemical Structure
BCP11964 Carbetocin 37025-55-1
Carbetocin is an obstetric drug used to control postpartum hemorrhage and bleeding after giving birth; an agonist at peripheral oxytocin receptors.
Oxytocin C-terminal tripeptide Chemical Structure
BCP13982 Oxytocin C-terminal tripeptide 2002-44-0
Oxytocin C-terminal tripeptide is shown to be effective in treating human depression with greater efficacy and faster onset of action than traditional anti-depressants. Also, it is used in the synthesis of novel analogs to be tested for their ability to enhance the binding of [3H]-N-propylnorapomorphine to short isoform of human dopamine D2 receptors.
OT-R antagonist 1 Chemical Structure
BCP30788 OT-R antagonist 1 364071-17-0
OT-R antagonist 1 is a new potent and selective nonpeptide low molecular weight OT-R antagonist.
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