Novel analogues of degarelix incorporating hydroxy-, methoxy-, and pegylated-urea moieties at positions 3, 5, 6 and the N-terminus. Part III (Q36876861)

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scientific article published on June 2006

Language	Label	Description	Also known as
English	Novel analogues of degarelix incorporating hydroxy-, methoxy-, and pegylated-urea moieties at positions 3, 5, 6 and the N-terminus. Part III	scientific article published on June 2006

Statements

scholarly article

1 reference

Europe PubMed Central

16 August 2017

Novel analogues of degarelix incorporating hydroxy-, methoxy-, and pegylated-urea moieties at positions 3, 5, 6 and the N-terminus. Part III (English)

1 reference

Europe PubMed Central

16 August 2017

author name string

Manoj P Samant

1

1 reference

Europe PubMed Central

16 August 2017

Doley J Hong

2

1 reference

Europe PubMed Central

16 August 2017

Glenn Croston

3

1 reference

Europe PubMed Central

16 August 2017

Catherine Rivier

4

1 reference

Europe PubMed Central

16 August 2017

Jean Rivier

5

1 reference

Europe PubMed Central

16 August 2017

language of work or name

0 references

publication date

1 June 2006

1 reference

Europe PubMed Central

16 August 2017

Journal of Medicinal Chemistry

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Europe PubMed Central

16 August 2017

49

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Europe PubMed Central

16 August 2017

12

1 reference

Europe PubMed Central

16 August 2017

3536-3543

1 reference

Europe PubMed Central

16 August 2017

Iterative approach to the discovery of novel degarelix analogues: substitutions at positions 3, 7, and 8. Part II.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536684

29 September 2017

Novel gonadotropin-releasing hormone antagonists with substitutions at position 5.

1 reference

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Effective drug delivery by PEGylated drug conjugates

1 reference

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Discovery of a thieno[2,3-d]pyrimidine-2,4-dione bearing a p-methoxyureidophenyl moiety at the 6-position: a highly potent and orally bioavailable non-peptide antagonist for the human luteinizing hormone-releasing hormone receptor

1 reference

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Solid-phase synthesis of substituted imidazoline-tethered 2,3-diketopiperazines, cyclic ureas, and cyclic thioureas

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GnRH antagonists: a new generation of long acting analogues incorporating p-ureido-phenylalanines at positions 5 and 6.

1 reference

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Peptide chemistry: development of high performance liquid chromatography and capillary zone electrophoresis

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Albumin binding of insulins acylated with fatty acids: characterization of the ligand-protein interaction and correlation between binding affinity and timing of the insulin effect in vivo

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Structure of the porcine LH- and FSH-releasing hormone. I. The proposed amino acid sequence

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Synthetic luteinizing hormone releasing factor analogs. Series of short-chain amide LRF homologs converging to the amino terminus

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Novel gonadotropin-releasing hormone antagonists: peptides incorporating modified N omega-cyanoguanidino moieties.

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Gonadotropin-releasing hormone antagonists with N.omega.-triazolylornithine, -lysine, or -p-aminophenylalanine residues at positions 5 and 6

1 reference

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Luteinizing hormone-releasing hormone. Antiovulatory activity of analogs substituted in positions 2 and 6

1 reference

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A general method for the solid-phase synthesis of unsymmetrical tri- and tetrasubstituted ureas

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Future trends in infertility treatment: challenges ahead

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Approaches to Alkaline Earth Metal-Organic Chemical Vapor Deposition Precursors. Synthesis and Characterization of Barium Fluoro-beta-ketoiminate Complexes Having Appended Polyether "Lariats"

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Ac-D-NAL(2)1,4FD-Phe2,D-Trp3,D-Arg6-LHRH, a potent antagonist of LHRH, produces transient edema and behavioral changes in rats

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New effective gonadotropin releasing hormone antagonists with minimal potency for histamine release in vitro

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Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides

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A new general solid-phase method for the synthesis of backbone-to-backbone cyclized peptides

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Inhibition of the Pre-Ovulatory Proestrous Gonadotropin Surge, Ovulation and Pregnancy with a Peptide Analogue of Luteinizing Hormone Releasing Hormone

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The effect of NMeTyr5 substitution in luteinizing hormone-releasing hormone antagonists

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Identifiers

10.1021/JM060240A

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

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