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PYRROLIDINE DERIVATIVES AS OXYTOCIN/VASOPRESSIN V1a RECEPTORS ANTAGONISTS

a technology of pyrrolidine and vasopressin, which is applied in the direction of drug composition, cardiovascular disorder, metabolic disorder, etc., can solve the problems of high cost of neonatal intensive care of premature babies, expulsion of fetuses, undeired premature birth,

Inactive Publication Date: 2016-08-04
OBSEVA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Repeated, concerted and regular contraction of the uterus will cause the dilatation of the cervix, the rupture of fetal membranes and lead to expulsion of the fetus.
Premature labor leads to undesired premature birth, a serious health problem that remains the major cause of perinatal mortality and severe morbidity, especially respiratory distress syndrome, intraventricular haemorrhage, bronchopulmonary dysplasia and necrotising enterocolitis that are far more common in preterm than in term infants.
Nowadays, preterm birth remains the leading cause of infant mortality and morbidity in industrialized nations, where, despite the significant improvements in obstetrical medicine, it is causing high costs for neonatal intensive care of premature babies.
The actual costs are even higher to society when taking into consideration the healthcare provision of preterm childbirth-related ailments, such as respiratory distress syndrome, heart conditions, cerebral palsy, epilepsy, and severe learning disabilities.
The management of preterm labor represents a significant problem in the field of obstetrics.
They have shown very limited efficacy, if any, in prolonging gestation and without clear demonstration of improvement of neonate outcome.
Current tocolytics are very often associated with unwanted adverse effects on women, foetus or neonate.
Some of the side effects that may occur include facial flushing, headache, nausea, palpitations, and lightheadedness.
Maternal side effects include abdominal discomfort, nausea, vomiting, depression and dizzy spells for the mother.
For magnesium sulfate, meta-analyses have failed to support it as a tocolytic agent.

Method used

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  • PYRROLIDINE DERIVATIVES AS OXYTOCIN/VASOPRESSIN V1a RECEPTORS ANTAGONISTS
  • PYRROLIDINE DERIVATIVES AS OXYTOCIN/VASOPRESSIN V1a RECEPTORS ANTAGONISTS
  • PYRROLIDINE DERIVATIVES AS OXYTOCIN/VASOPRESSIN V1a RECEPTORS ANTAGONISTS

Examples

Experimental program
Comparison scheme
Effect test

example 1

Purification of (3Z,5S)-5-(hydroxymethyl)-1-[(2′-methyl-1,1′-biphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methyloxime

1.1 Synthesis of (3Z / E,5S)-5-(hydroxymethyl)-1-[(2′-methyl-1,1′-biphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methyloxime

[0074]The present invention relates to the synthesis and purification of (3Z,5S)-5-(hydroxymethyl)-1-[(2′-methyl-1,1′-biphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methyloxime obtained as a crude isomeric mixture comprising (3Z,5S)-5-(hydroxymethyl)-1-[(2′-methyl-1,1′-biphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methyloxime and (3E,5S)-5-(hydroxymethyl)-1-[(2′-methyl-1,1′-biphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methyloxime.

[0075]Synthetic pathways of compounds of the invention are for example those described in WO2004005249 and WO2005082848.

[0076]For example, compound of the invention (3Z / E,5S)-5-(hydroxymethyl)-1-[(2′-methyl-1,1′-biphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methyloxime can also be prepared following stages 1 to 7 as described below:

Stage 1: Prepa...

example 2

(3Z,5S)-5-(hydroxymethyl)-1-[(2′-methyl-1,1′-biphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methyloxime Binding to OT-R and Vasopressin V1a Receptor

Binding to the OT-R and Vasopressin V1a Receptor

[0115]Competition binding to the human oxytocin receptor was measured in vitro using a scintillation proximity assay.

[0116]This assay allows determining the affinity of the test compounds for OT-R. Membranes from HEK293EBNA (cells expressing OT-R) were suspended in buffer containing 50 mM Tris-HCl, pH 7.4, 5 mM MgCl2 and 0.1% BSA (w / v). The membranes (2-4 μg) were mixed with 0.1 mg SPA bead coated with wheat-germ aglutinin (WGA-PVT-Polyethylene Imine beads from Amersham) and 0.2 nM of the 125 radiolabelled [I]-OVTA (OVTA being Ornithin Vasoactive, an analogue of OT for competitive binding experiments). Non-specific binding was determined in the presence of 1 μM Oxytocin. The total assay volume was 100 μl. The plates (Corning 0 NBS plate) were incubated at room temperature for 30 min and counted ...

example 3

(3Z,5S)-5-(hydroxymethyl)-1-[(2′-methyl-1,1′-biphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methyloxime is a OT-R Antagonist

[0119]The inhibition of oxytocin-induced Ca2+ mobilization in OT-R transfected HEK293EBNA cells was measured by FLIPR (fluorimetric imaging plate reader).

[0120]This assay allows the measurement of the inhibition of OT / OT-R mediated calcium mobilization by the compound (3Z,5S)-5-(hydroxymethyl)-1-[(2′-methyl-1,1′-biphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methyloxime.

[0121]FLIPR® is a fluorimetric imaging device using a laser (Argon-ion laser) for simultaneous illumination and reading (cooled CCD camera) of each well of a 96-well-plate, thus enabling rapid measurements on a large number of samples.

[0122]Preparing the plates: FLIPR-plates were pre-coated with PLL (Poly-L-Lysine) 10 μg / ml+0.1%) gelatine to attach HEK293EBNA cells (Human Embryonic Kidney cells expressing OT-R) and incubated for 30 min up to 2 days at 37° C. The cells were plated out into 96-well-plates (...

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Abstract

The present invention relates to a compound of formula (3Z,5S)-5-(hydroxymethyl)-1-[(2′-methyl-1,1′-biphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methl9243yloxime, and / or an active metabolite thereof having antagonist action at the oxytocin receptor and / or vasopressin V1a receptor, to processes for their preparation, pharmaceutical compositions containing them and their use.

Description

TECHNICAL FIELD[0001]The present invention relates to a compound of formula (3Z,5S)-5-(hydroxymethyl)-1-[(2′-methyl-1,1′-biphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methyloxime, and / or an active metabolite thereof having antagonist action at the oxytocin receptor and / or vasopressin V1a receptor, to processes for their preparation, pharmaceutical compositions containing them and their use in medicine.BACKGROUND OF THE INVENTION[0002]Oxytocin (OT) is a cyclic nona-peptide that mediates its physiological actions through activation of the oxytocin receptor (OT-R), a cell membrane receptor belonging to the class of G protein-coupled receptors that is similar to arginine vasopressin receptors. One important action of Oxytocin (OT) is to cause the contraction of the uterus of mammals during labor. Repeated, concerted and regular contraction of the uterus will cause the dilatation of the cervix, the rupture of fetal membranes and lead to expulsion of the fetus. Premature labor is when these c...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07D207/22
CPCC07D207/22A61K31/4025A61P5/10C07D207/09A61K31/40A61P13/08A61P15/00A61P15/04A61P15/06A61P15/08A61P15/10A61P25/00A61P25/02A61P25/14A61P25/18A61P25/22A61P25/24A61P3/14A61P43/00A61P5/00A61P5/38A61P5/40A61P9/00A61P9/08A61K9/0019A61K9/0034A61K31/401A61K31/573A61K45/06A61K2300/00A61K9/0053
Inventor CHOLLET, ANDRE
Owner OBSEVA
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