메뉴 건너뛰기




Volumn 92, Issue 4-6, 2004, Pages 297-303

[123/131I]Iodometomidate as a radioligand for functional diagnosis of adrenal disease: Synthesis, structural requirements and biodistribution

Author keywords

131I IMTO; Adrenal scintigraphy; Inhibitor of 11 hydroxylase; Metomidate; SPECT

Indexed keywords

CYTOCHROME P450 INHIBITOR; ESTER; ETOMIDATE; IODINE 123; IODINE 131; IODOMETOMIDATE I 123; IODOMETOMIDATE I 131; METOMIDATE; RADIOLIGAND; UNCLASSIFIED DRUG;

EID: 3142757820     PISSN: 00338230     EISSN: None     Source Type: Journal    
DOI: 10.1524/ract.92.4.297.35598     Document Type: Article
Times cited : (19)

References (37)
  • 2
    • 0012814423 scopus 로고    scopus 로고
    • Adrenal Incidentalomas
    • (Margois, A. N., Chrousos, G. P., eds.) Humana Press Inc., Totawa, New Jersey
    • Allolio, B.: Adrenal Incidentalomas. In: Contemporary Endocrinology: Adrenal Disorders. (Margois, A. N., Chrousos, G. P., eds.) Humana Press Inc., Totawa, New Jersey (2001) pp. 249-261.
    • (2001) Contemporary Endocrinology: Adrenal Disorders , pp. 249-261
    • Allolio, B.1
  • 6
    • 0017287413 scopus 로고
    • Selenium-75-19-selenocholesterol - A new adrenal scanning agent with high concentration in the adrenal cortex
    • Sakar, S. D., Ice, R. D., Beierwaltes, W. H., Gill, S. P., Balanchandran, S., Basmadjian, G. P.: Selenium-75-19-selenocholesterol - a new adrenal scanning agent with high concentration in the adrenal cortex. J. Nucl. Med. 17, 212 (1976).
    • (1976) J. Nucl. Med. , vol.17 , pp. 212
    • Sakar, S.D.1    Ice, R.D.2    Beierwaltes, W.H.3    Gill, S.P.4    Balanchandran, S.5    Basmadjian, G.P.6
  • 7
    • 0014722772 scopus 로고
    • Inhibitors of adrenal steroid biosynthesis
    • Temple, T. F., Liddle, G. W.: Inhibitors of adrenal steroid biosynthesis. Ann. Rev. Pharmacol. 10, 199 (1970).
    • (1970) Ann. Rev. Pharmacol. , vol.10 , pp. 199
    • Temple, T.F.1    Liddle, G.W.2
  • 8
    • 0016290422 scopus 로고
    • Modifiers of steroid-hormone metabolism: A review of their chemistry biochemistry and clinical application
    • Gower, D. B.: Modifiers of steroid-hormone metabolism: A review of their chemistry, biochemistry and clinical application. J. Steroid Biochem. 5, 501 (1974).
    • (1974) J. Steroid Biochem. , vol.5 , pp. 501
    • Gower, D.B.1
  • 9
    • 0014500683 scopus 로고
    • The interaction of metopirone with adrenal mitochondrial cytochrome P-450. A mechanism for the inhibition of adrenal steroid 11β-hydroxylation
    • Williamson, D. G., O'Donnell, V. J.: The interaction of metopirone with adrenal mitochondrial cytochrome P-450. A mechanism for the inhibition of adrenal steroid 11β-hydroxylation. Biochemistry 8, 1306 (1969).
    • (1969) Biochemistry , vol.8 , pp. 1306
    • Williamson, D.G.1    O'Donnell, V.J.2
  • 10
    • 0016136264 scopus 로고
    • 3H]metyrapol, an inhibitor for the 11β-hydroxylation reaction
    • 3H]metyrapol, an inhibitor for the 11β-hydroxylation reaction. Biochem. 13, 2201 (1974).
    • (1974) Biochem. , vol.13 , pp. 2201
    • Satre, M.1    Vignais, P.V.2
  • 11
    • 3142760920 scopus 로고
    • Synthesis of radiolabeled enzyme inhibitors of the adrenal cortex
    • Wieland, D. M., Ice, R. D., Beierwaltes, W. H.: Synthesis of radiolabeled enzyme inhibitors of the adrenal cortex. J. Nucl. Med. 17, 525 (1976).
    • (1976) J. Nucl. Med. , vol.17 , pp. 525
    • Wieland, D.M.1    Ice, R.D.2    Beierwaltes, W.H.3
  • 13
    • 0017644602 scopus 로고
    • New inhibitors of steroid 11β-hydroxylase. Structure-activity relationship studies of metyrapone-like compounds
    • Napoli, J. L., Counsell, R. E.: New inhibitors of steroid 11β-hydroxylase. Structure-activity relationship studies of metyrapone-like compounds. J. Med. Chem., 20, 762 (1977).
    • (1977) J. Med. Chem. , vol.20 , pp. 762
    • Napoli, J.L.1    Counsell, R.E.2
  • 16
    • 0342418985 scopus 로고
    • 123(131)I-Metyrapone for imaging of the adrenal cortex
    • (Höfer, R., Bergmann, H., eds.) Verlag H. Egermann, Vienna
    • 123(131)I-Metyrapone for imaging of the adrenal cortex. In: Radioaktive Isotope in Klinik und Forschung. (Höfer, R., Bergmann, H., eds.) Verlag H. Egermann, Vienna (1982) Vol. 15(2), pp. 589-595.
    • (1982) Radioaktive Isotope in Klinik und Forschung , vol.15 , Issue.2 , pp. 589-595
    • Zolle, I.1    Robien, W.2    Bergmann, H.3    Höfer, R.4
  • 17
    • 0020766034 scopus 로고
    • Synthesis of radioiodinated metyrapone - A potential adrenal imaging agent
    • Robien, W., Zolle, I.: Synthesis of radioiodinated metyrapone - a potential adrenal imaging agent. Int. J. Appl. Radiot. Isot. 34, 907 (1983).
    • (1983) Int. J. Appl. Radiot. Isot. , vol.34 , pp. 907
    • Robien, W.1    Zolle, I.2
  • 18
    • 0021350019 scopus 로고
    • Structure-activity relationship study of the inhibition of adrenal cortical 11β-hydroxylase by new metyrapone analogues
    • Hays, S. J., Tobes, M. C., Gildersleeve, D. L., Wieland, D. M., and Beierwaltes, W. H.: Structure-activity relationship study of the inhibition of adrenal cortical 11β-hydroxylase by new metyrapone analogues. J. Med. Chem. 27, 15 (1984).
    • (1984) J. Med. Chem. , vol.27 , pp. 15
    • Hays, S.J.1    Tobes, M.C.2    Gildersleeve, D.L.3    Wieland, D.M.4    Beierwaltes, W.H.5
  • 20
    • 0028966796 scopus 로고
    • Synthesis of radio-2-iodophenylmetyrapone using Cu(I)-assisted nucleophilic exchange labelling: Study of the reaction kinetics
    • Yu, J., Mertens, J., Rakias, F., Zolle, I.: Synthesis of radio-2-iodophenylmetyrapone using Cu(I)-assisted nucleophilic exchange labelling: Study of the reaction kinetics. Nucl. Med. Biol. 22, 257 (1995).
    • (1995) Nucl. Med. Biol. , vol.22 , pp. 257
    • Yu, J.1    Mertens, J.2    Rakias, F.3    Zolle, I.4
  • 21
    • 0028880966 scopus 로고
    • Comparison of non-isotopic exchange methods for n.c.a. labelling of 2-iodophenyl-metyrapone
    • Schirbel, A., Coenen, H. H.; Comparison of non-isotopic exchange methods for n.c.a. labelling of 2-iodophenyl-metyrapone. Nucl. Med. Biol. 22, 1075 (1995).
    • (1995) Nucl. Med. Biol. , vol.22 , pp. 1075
    • Schirbel, A.1    Coenen, H.H.2
  • 22
    • 0027992087 scopus 로고
    • Steroid biosynthesis inhibitors in Cushing's syndrome
    • Engelhardt, D.: Steroid biosynthesis inhibitors in Cushing's syndrome. Clin Investig. 72, 481 (1994).
    • (1994) Clin Investig. , vol.72 , pp. 481
    • Engelhardt, D.1
  • 26
    • 0021710333 scopus 로고
    • Effects of etomidate on steroid biosynthesis in subcellular fractions of bovine adrenals
    • van den Bossche, H., Willemsens, G., Cools, W., Bellens, D.: Effects of etomidate on steroid biosynthesis in subcellular fractions of bovine adrenals. Biochem. Pharmacology 33, 3861 (1984).
    • (1984) Biochem. Pharmacology , vol.33 , pp. 3861
    • Van Den Bossche, H.1    Willemsens, G.2    Cools, W.3    Bellens, D.4
  • 27
    • 0031838388 scopus 로고    scopus 로고
    • In vitro and in vivo primate evaluation of carbon-11-etomidate and carbon-11-metomidate as potential tracers for PET imaging of the adrenal cortex and its tumors
    • Bergström, M., Bonasera, T. A., Lu, L., Bergström, E., Backlin, C., Juhlin, C., Långström, B.: In vitro and in vivo primate evaluation of carbon-11-etomidate and carbon-11-metomidate as potential tracers for PET imaging of the adrenal cortex and its tumors. J. Nucl. Med. 39, 982 (1998).
    • (1998) J. Nucl. Med. , vol.39 , pp. 982
    • Bergström, M.1    Bonasera, T.A.2    Lu, L.3    Bergström, E.4    Backlin, C.5    Juhlin, C.6    Långström, B.7
  • 32
    • 0006292058 scopus 로고
    • A highly selective ester hydrolase from Pseudomonas Sp. for the enzymatic preparation of enantiomerically pure secondary alcohols; Chiral auxiliaries in organic synthesis
    • Laumen, K., Schneider, M. P.: A highly selective ester hydrolase from Pseudomonas Sp. for the enzymatic preparation of enantiomerically pure secondary alcohols; Chiral auxiliaries in organic synthesis. J. Chem. Soc. Chem. Commun. 598 (1988).
    • (1988) J. Chem. Soc. Chem. Commun. , pp. 598
    • Laumen, K.1    Schneider, M.P.2
  • 33
    • 85077634689 scopus 로고
    • The use of diethyl azodicarboxylate and triphenylphosphine in synthesis and transformation of natural products
    • Mitsunobu, O.: The use of diethyl azodicarboxylate and triphenylphosphine in synthesis and transformation of natural products. Synthesis 1 (1981).
    • (1981) Synthesis , pp. 1
    • Mitsunobu, O.1
  • 36
    • 0003633755 scopus 로고
    • NIH publication No. 8, Government Printing Office, Washington, DC
    • Guide for the care and use of laboratory animals. NIH publication No. 8, Government Printing Office, Washington, DC (1985) pp. 5-23.
    • (1985) Guide for the Care and Use of Laboratory Animals , pp. 5-23
  • 37
    • 3142708019 scopus 로고    scopus 로고
    • In vivo evaluation of new labelled derivatives of etomidate for adrenal imaging
    • Schirbel, A., Kvaternik, H., Hammerschmidt, F., Berger, M. L., Zolle, I.: in vivo evaluation of new labelled derivatives of etomidate for adrenal imaging. J. Nucl. Med. 44(Suppl. 5), 154P (2003).
    • (2003) J. Nucl. Med. , vol.44 , Issue.SUPPL. 5 , pp. 154
    • Schirbel, A.1    Kvaternik, H.2    Hammerschmidt, F.3    Berger, M.L.4    Zolle, I.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.