2004
DOI: 10.1016/j.bmcl.2004.04.107
|View full text |Cite
|
Sign up to set email alerts
|

Non-peptide oxytocin agonists

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
21
0
1

Year Published

2004
2004
2024
2024

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 58 publications
(27 citation statements)
references
References 13 publications
1
21
0
1
Order By: Relevance
“…The benefit of non-peptide agonists lies in the potential for increased stability, central penetration and oral bioavailability, making the agonist more amenable to classical routes of pharmacotherapeutic administration (Ashworth et al, 2006; Pitt et al, 2004). In addition, the increased epitope specificity possible with small, non-peptide agonists potentially allows for increased selectivity for the OTR over the structurally similar vasopressin receptors (Hawtin et al, 2001).…”
Section: Therapeutic Strategies For Targeting the Ot Systemmentioning
confidence: 99%
See 1 more Smart Citation
“…The benefit of non-peptide agonists lies in the potential for increased stability, central penetration and oral bioavailability, making the agonist more amenable to classical routes of pharmacotherapeutic administration (Ashworth et al, 2006; Pitt et al, 2004). In addition, the increased epitope specificity possible with small, non-peptide agonists potentially allows for increased selectivity for the OTR over the structurally similar vasopressin receptors (Hawtin et al, 2001).…”
Section: Therapeutic Strategies For Targeting the Ot Systemmentioning
confidence: 99%
“…However, the effects of WAY-267464 have not yet been reported in paradigms assessing social cognition. Ferring Pharmaceuticals also developed a potent nonpeptide agonist, which maximally stimulates the OTR to the same degree as OT and is 25 times for selective for the OTR than any other receptors in the family (Pitt et al, 2004). Behavioral efficacy of the Ferring agonist, though, has yet to be demonstrated.…”
Section: Therapeutic Strategies For Targeting the Ot Systemmentioning
confidence: 99%
“…For example, oxytocin receptor agonists have been developed that can be delivered orally and stimulate the oxytocin receptor 137,138 , and there is evidence that melanocortin 4 receptor agonists stimulate the central release of oxytocin in rats 139 . Given the evidence presented here of the potentially broad and diverse impact of oxytocin across a range of neuropsychiatric disorders, drug development along these lines would presumably be advantageous for a wide number of patients.…”
Section: Clinical Implications and Limitationsmentioning
confidence: 99%
“…Further, in human neuropsychiatric disorders characterized by impaired sociability, the roles of Oxt and Avp are being elucidated and better pharmacological agents are being developed. 189192 …”
Section: Discussionmentioning
confidence: 99%