Document Detail


Receptor binding of norgestimate--a new orally active synthetic progestational compound.
MedLine Citation:
PMID:  8384965     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Binding of the new progestagen, norgestimate (D-(-)-13 beta-ethyl-17 beta-acetoxy-17-ethinyl-4-gonen-3-one-oxime), and its metabolites (levonorgestrel-3-oxime, levonorgestrel-17-acetate and levonorgestrel) to the progesterone receptor was investigated by competition experiments using cytosol from human myometrial tissue. Compared to R5020, a highly potent synthetic ligand for progesterone receptor analysis, the L-isomer of norgestimate shows only a weak specific behaviour with regard to binding to the progesterone receptor from uterine cytosol with an RBA value of 0.8%, whereas the D-isomer of this compound is characterized by a lack of binding activity to the progesterone receptor. Levonorgestrel-3-oxime, one of the possible metabolites of norgestimate, binds to the progesterone receptor with an RBA value of 8%, whereas levonorgestrel-17-acetate, the other possible metabolite of norgestimate, binds with a binding affinity of 110% which is in the same order of magnitude as levonorgestrel itself. The competition experiments suggest that norgestimate is a prodrug and that the metabolites, levonorgestrel and levonorgestrel-17-acetate, which actively bind to the progesterone receptor, must first be formed from the parent drug via metabolic processes in vivo. These are the actual biologically active compounds which are responsible for the gestagenic potency.
Authors:
M Juchem; K Pollow; W Elger; G Hoffmann; V Möbus
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Publication Detail:
Type:  In Vitro; Journal Article    
Journal Detail:
Title:  Contraception     Volume:  47     ISSN:  0010-7824     ISO Abbreviation:  Contraception     Publication Date:  1993 Mar 
Date Detail:
Created Date:  1993-05-06     Completed Date:  1993-05-06     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0234361     Medline TA:  Contraception     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  283-94     Citation Subset:  IM    
Affiliation:
Abteilung für Experimentelle Endokrinologie, Johannes Gutenberg-Universität Mainz, F.R.G.
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MeSH Terms
Descriptor/Qualifier:
Animals
Binding, Competitive
Carrier Proteins / metabolism
Female
Humans
Kidney / metabolism
Liver / metabolism
Male
Norgestrel / analogs & derivatives*,  metabolism
Pregnancy / blood
Prostate / metabolism
Rats
Rats, Wistar
Receptors, Androgen / metabolism
Receptors, Estrogen / metabolism
Receptors, Glucocorticoid / metabolism
Receptors, Mineralocorticoid
Receptors, Progesterone / metabolism*
Receptors, Steroid / metabolism
Sex Hormone-Binding Globulin / metabolism
Uterus / metabolism
Chemical
Reg. No./Substance:
0/Carrier Proteins; 0/Receptors, Androgen; 0/Receptors, Estrogen; 0/Receptors, Glucocorticoid; 0/Receptors, Mineralocorticoid; 0/Receptors, Progesterone; 0/Receptors, Steroid; 0/Sex Hormone-Binding Globulin; 0/cortisol binding globulin; 35189-28-7/norgestimate; 6533-00-2/Norgestrel

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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