Skip to content
2000
Volume 10, Issue 3
  • ISSN: 0929-8665
  • E-ISSN: 1875-5305

Abstract

The neurohypophyseal nonapeptide hormone oxytocin (OT) is the strongest uterotonic substance known and is responsible for the initiation of labor. Conversely, oxytocin antagonists blocking uterine OT receptor can suppress uterus contraction. In this paper we describe a computer simulated docking pertinent to affinity of an oxytocin antagonist atosiban towards OT receptor, versus vasopressin V1a and V2 receptors.

Loading

Article metrics loading...

/content/journals/ppl/10.2174/0929866033478898
2003-06-01
2025-05-05
Loading full text...

Full text loading...

/content/journals/ppl/10.2174/0929866033478898
Loading

  • Article Type:
    Review Article
Keyword(s): atosiban; gpcr/bioligand interactions; molecular docking; simulated annealing
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test