| Dokumentenart: | Artikel | ||||
|---|---|---|---|---|---|
| Titel eines Journals oder einer Zeitschrift: | Bioconjugate Chemistry | ||||
| Verlag: | AMER CHEMICAL SOC | ||||
| Ort der Veröffentlichung: | WASHINGTON | ||||
| Band: | 11 | ||||
| Nummer des Zeitschriftenheftes oder des Kapitels: | 2 | ||||
| Seitenbereich: | S. 239-252 | ||||
| Datum: | 2000 | ||||
| Institutionen: | Chemie und Pharmazie > Institut für Organische Chemie | ||||
| Identifikationsnummer: |
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| Stichwörter / Keywords: | CORTICOSTEROID-BINDING GLOBULIN; COMPETITIVE CHEMILUMINESCENCE IMMUNOASSAY; CHEMI-LUMINESCENCE IMMUNOASSAY; LINKED-IMMUNOSORBENT-ASSAY; ANDROGEN RECEPTOR; STEREOSELECTIVE SYNTHESIS; SANDWICH IMMUNOASSAY; ESTRADIOL CONJUGATE; STAUDINGER REACTION; ENZYME-IMMUNOASSAY; | ||||
| Dewey-Dezimal-Klassifikation: | 500 Naturwissenschaften und Mathematik > 540 Chemie | ||||
| Status: | Veröffentlicht | ||||
| Begutachtet: | Ja, diese Version wurde begutachtet | ||||
| An der Universität Regensburg entstanden: | Ja | ||||
| Dokumenten-ID: | 74386 |
Web of ScienceZusammenfassung
We describe synthetic strategies for the biotinylation of testosterone (T) at positions 3, 7 alpha, 17 alpha, and 19. These T probes are able to mimic ligand binding and may provide for a better understanding of the biospecific interaction with steroid-binding proteins such as the androgen receptor, anti-steroid antibodies, or steroid-binding serum globulins. For the 7 alpha- and 17 ...
Zusammenfassung
We describe synthetic strategies for the biotinylation of testosterone (T) at positions 3, 7 alpha, 17 alpha, and 19. These T probes are able to mimic ligand binding and may provide for a better understanding of the biospecific interaction with steroid-binding proteins such as the androgen receptor, anti-steroid antibodies, or steroid-binding serum globulins. For the 7 alpha- and 17 alpha-derivatives, biotinyl-N-hydroxy-succinimide esters with different types of spacer chains were used. The S-biotin hydrazone derivative was produced using N-(epsilon-biotinyl)-caproyl hydrazide, whereas for the 19-biotinylation, a biotinyl-1N-diamino-3,6-dioxaoctane-amide was applied. Key reaction for the biotinylation at position 3 is the oximation of the 3-oxo function. The 17 alpha-position is accessible by the reaction of the 3-protected 4-androsten-17-epoxide with oxygen in the beta-position, followed by nucleophilic ring opening with cyanide which provides the 17 alpha-cyanomethyl derivative. The key step is the regioselective ketal protection of the 3-oxo function of androst-4-ene-3,17-dione using a stannoxane catalyst. An alternative pathway for the insertion of biotin at the 19-position was established by the synthesis of 17 beta-hydroxy-androst-4-en-3-one-19-yl carboxymethyl ether. After activation by the carbodiimide method, the compound reacts with aminoterminal biotin derivatives. The copper(I)-catalyzed 1,6 Michael addition of 17-acetoxy-6,7-dehydro-T leads to 7 alpha-derivatives by use of omega-silyl protected hydroxylalkyl-modified Grignard reagents. A functional group interconversion using the Staudinger reaction transforms the azide function into a primary omega-amino group. The absolute configurations of the different biotinylated derivatives were investigated by H-1 NMR studies. For the 7 alpha-biotinylated T series, additionally, an X-ray analysis proved the axial position of the spacer group. This,results in a vertical orientation of the biotin moiety toward the alpha-face of the planar tetracyclic backbone. Thus, a negligible alteration of the original structure of the upper beta-face offers the feasibility of applying the 7 alpha-derivatives as optimal immunochemical tracers in competitive immunoassays. Biotinylated T derivatives should be also suitable for ligand-binding studies to the androgen receptor or to sex hormone-binding globulin.
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