TY - JOUR
T1 - The hexacarbonyl(ethyne)dicobalt unit
T2 - An androgen tag
AU - Osella, Domenico
AU - Galeotti, Francesco
AU - Cavigiolio, Giorgio
AU - Nervi, Carlo
AU - Hardcastle, Kenneth I.
AU - Vessières, Anne
AU - Jaouen, Gerard
PY - 2002
Y1 - 2002
N2 - The interaction of estrogens and androgens with their corresponding receptors is known to play an important role in cancers of the breast and prostate. This paper reports the synthesis, characterization, and biochemical properties of a novel organometallic complex derived from 17α-ethynyltestosterone, namely hexacarbonyl{μ[(20,21-η:20,21-η])-(17α)-17- hydroxypregn-4-en-20-yn-3-one}dicobalt ([Co2(CO)6(17α-ethynyltestosterone)]). The crystal and molecular structure of this compound was determined by single-crystal X-ray diffraction: it crystallizes in the monoclinic space group with a = 24.6600(18) Å, b = 12.9188(10) Å, c = 26.3573(19) Å, β = 108.651(2)°, and Z = 12. A biochemical study showed that the compound is still recognized by the androgen receptor even when the relative binding affinity (RBA) is quite low (0.5%). This finding can be explained by the recently published 3D structure of the androgen receptor that shows that its binding site cannot accommodate a bulky substituent at the 17α position of the steroid.
AB - The interaction of estrogens and androgens with their corresponding receptors is known to play an important role in cancers of the breast and prostate. This paper reports the synthesis, characterization, and biochemical properties of a novel organometallic complex derived from 17α-ethynyltestosterone, namely hexacarbonyl{μ[(20,21-η:20,21-η])-(17α)-17- hydroxypregn-4-en-20-yn-3-one}dicobalt ([Co2(CO)6(17α-ethynyltestosterone)]). The crystal and molecular structure of this compound was determined by single-crystal X-ray diffraction: it crystallizes in the monoclinic space group with a = 24.6600(18) Å, b = 12.9188(10) Å, c = 26.3573(19) Å, β = 108.651(2)°, and Z = 12. A biochemical study showed that the compound is still recognized by the androgen receptor even when the relative binding affinity (RBA) is quite low (0.5%). This finding can be explained by the recently published 3D structure of the androgen receptor that shows that its binding site cannot accommodate a bulky substituent at the 17α position of the steroid.
UR - http://www.scopus.com/inward/record.url?scp=0036396256&partnerID=8YFLogxK
U2 - 10.1002/1522-2675(200209)85:9<2918::AID-HLCA2918>3.0.CO;2-W
DO - 10.1002/1522-2675(200209)85:9<2918::AID-HLCA2918>3.0.CO;2-W
M3 - Article
SN - 0018-019X
VL - 85
SP - 2918
EP - 2925
JO - Helvetica Chimica Acta
JF - Helvetica Chimica Acta
IS - 9
ER -