메뉴 건너뛰기




Volumn 41, Issue S, 2014, Pages

Radioiodinated and astatinated NHC rhodium complexes: Synthesis

Author keywords

Astatine 211; Iodine 125; N heterocyclic carbene (NHC); Radioimmunotherapy; Rhodium

Indexed keywords

ASTATINE (1 BENZYL 3 NITROPHENYLIMIDAZOLIDENE)RHODIUM CHLORIDE COMPLEX AS 211; ASTATINE 211; IODINE (1 BENZYL 3 NITROPHENYLIMIDAZOLIDENE)RHODIUM CHLORIDE COMPLEX I 125; IODINE 125; RADIOISOTOPE; RHODIUM COMPLEX; UNCLASSIFIED DRUG; ASTATINE; HETEROCYCLIC COMPOUND; ORGANOMETALLIC COMPOUND; RADIOACTIVE IODINE; RHODIUM;

EID: 84899100628     PISSN: 09698051     EISSN: 18729614     Source Type: Journal    
DOI: 10.1016/j.nucmedbio.2013.12.004     Document Type: Article
Times cited : (10)

References (46)
  • 2
    • 84872176323 scopus 로고    scopus 로고
    • Production of [(211)At]-astatinated radiopharmaceuticals and applications in targeted a-particle therapy
    • Guérard F., Gestin J.F., Brechbiel M.W. Production of [(211)At]-astatinated radiopharmaceuticals and applications in targeted a-particle therapy. Cancer Biother Radiopharm 2013, 28:1-20.
    • (2013) Cancer Biother Radiopharm , vol.28 , pp. 1-20
    • Guérard, F.1    Gestin, J.F.2    Brechbiel, M.W.3
  • 4
    • 0035076265 scopus 로고    scopus 로고
    • Dry-distillation of astatine-211 from irradiated bismuth targets: a time-saving procedure with high recovery yields
    • Sture Lindegren S., Bäck T., Jensen H.J. Dry-distillation of astatine-211 from irradiated bismuth targets: a time-saving procedure with high recovery yields. Appl Radiat Isot 2001, 55:157-160.
    • (2001) Appl Radiat Isot , vol.55 , pp. 157-160
    • Sture, L.S.1    Bäck, T.2    Jensen, H.J.3
  • 5
    • 11144300321 scopus 로고    scopus 로고
    • Wet harvesting of no-carrier-added 211At from an irradiated 209Bi target for radiopharmaceutical applications
    • Yordanov A.T., Pozzi O., Carlin S., Akabani G., Wieland B., Zalutsky M.R. Wet harvesting of no-carrier-added 211At from an irradiated 209Bi target for radiopharmaceutical applications. J Radioanal Nucl Chem 2004, 262:593-599.
    • (2004) J Radioanal Nucl Chem , vol.262 , pp. 593-599
    • Yordanov, A.T.1    Pozzi, O.2    Carlin, S.3    Akabani, G.4    Wieland, B.5    Zalutsky, M.R.6
  • 6
    • 0010732883 scopus 로고
    • Inorganic astatine chemistry: formation of complexes of astatine
    • Visser G.W.M., Diemer E.L. Inorganic astatine chemistry: formation of complexes of astatine. Radiochim Acta 1983, 33:145-151.
    • (1983) Radiochim Acta , vol.33 , pp. 145-151
    • Visser, G.W.M.1    Diemer, E.L.2
  • 8
    • 0018232828 scopus 로고
    • The preparation of astatine labelled proteins using an electrophilic reaction
    • Vaughan A.T.M., Fremlin J.H. The preparation of astatine labelled proteins using an electrophilic reaction. Int J Nucl Med Biol 1978, 5:229-230.
    • (1978) Int J Nucl Med Biol , vol.5 , pp. 229-230
    • Vaughan, A.T.M.1    Fremlin, J.H.2
  • 11
    • 0038735123 scopus 로고    scopus 로고
    • N-succinimidyl 3-[211At]astato-4-guanidinomethylbenzoate: an acylation agent for labeling internalizing antibodies with α-particle emitting 211At
    • Vaidyanathan G., Affleck D.J., Bigner D.D., Zalutsky M.R. N-succinimidyl 3-[211At]astato-4-guanidinomethylbenzoate: an acylation agent for labeling internalizing antibodies with α-particle emitting 211At. Nucl Med Biol 2003, 30:351-359.
    • (2003) Nucl Med Biol , vol.30 , pp. 351-359
    • Vaidyanathan, G.1    Affleck, D.J.2    Bigner, D.D.3    Zalutsky, M.R.4
  • 13
    • 0021523467 scopus 로고
    • Preparation of a 211At-IgG conjugate which is stable in vivo
    • Harrison A., Royle L. Preparation of a 211At-IgG conjugate which is stable in vivo. Int J Appl Radiat Isot 1984, 35:1005-1008.
    • (1984) Int J Appl Radiat Isot , vol.35 , pp. 1005-1008
    • Harrison, A.1    Royle, L.2
  • 15
    • 0026164047 scopus 로고
    • Astatine-211 labeling of an antimelanoma antibody and its fragment using N-succimimidyl p-(211At)astatobenzoate: comparisons in vivo with the p-(125I)iodobenzoyl conjugate
    • Hadley S.W., Wilbur D.S., Gray M.A., Atcher R.W. Astatine-211 labeling of an antimelanoma antibody and its fragment using N-succimimidyl p-(211At)astatobenzoate: comparisons in vivo with the p-(125I)iodobenzoyl conjugate. Bioconjug Chem 1991, 2:171-179.
    • (1991) Bioconjug Chem , vol.2 , pp. 171-179
    • Hadley, S.W.1    Wilbur, D.S.2    Gray, M.A.3    Atcher, R.W.4
  • 17
    • 34547379205 scopus 로고    scopus 로고
    • Reagents for astatination of biomolecules. 2. Conjugation of anionic boron cage pendant groups to a protein provides a method for direct labeling that is stable to in vivo deastatination
    • Wilbur D.S., Chyan M.K., Hamlin D.K., Vessella R.L., Wedge T.J., Hawthorne M.F. Reagents for astatination of biomolecules. 2. Conjugation of anionic boron cage pendant groups to a protein provides a method for direct labeling that is stable to in vivo deastatination. Bioconjug Chem 2007, 18:1226-1240.
    • (2007) Bioconjug Chem , vol.18 , pp. 1226-1240
    • Wilbur, D.S.1    Chyan, M.K.2    Hamlin, D.K.3    Vessella, R.L.4    Wedge, T.J.5    Hawthorne, M.F.6
  • 18
    • 84872201372 scopus 로고    scopus 로고
    • Radiolabelling of proteins with stabilised hypervalent astatine-211: feasibility and stability
    • Guerard F., Rajerison H., Faivre-Chauvet A., Barbet J., Meyer G., Da Silva I., et al. Radiolabelling of proteins with stabilised hypervalent astatine-211: feasibility and stability. J Nucl Med 2011, 52:1486.
    • (2011) J Nucl Med , vol.52 , pp. 1486
    • Guerard, F.1    Rajerison, H.2    Faivre-Chauvet, A.3    Barbet, J.4    Meyer, G.5    Da Silva, I.6
  • 20
    • 0018627785 scopus 로고
    • The preparation and stability of astatotyrosine and astato-iodotyrosine
    • Visser G.W.M., Diemer E.L., Kaspersen F.M. The preparation and stability of astatotyrosine and astato-iodotyrosine. Int J Appl Radiat Isot 1979, 30:749-752.
    • (1979) Int J Appl Radiat Isot , vol.30 , pp. 749-752
    • Visser, G.W.M.1    Diemer, E.L.2    Kaspersen, F.M.3
  • 21
    • 0012543618 scopus 로고
    • Reaction of aromatic diazonium salts with carrier-free radioiodine and astatine. Evidence of complex formation
    • Meyer G.J., Roessler K., Stoecklin G. Reaction of aromatic diazonium salts with carrier-free radioiodine and astatine. Evidence of complex formation. J Am Chem Soc 1979, 101:3121-3123.
    • (1979) J Am Chem Soc , vol.101 , pp. 3121-3123
    • Meyer, G.J.1    Roessler, K.2    Stoecklin, G.3
  • 23
    • 43149087101 scopus 로고    scopus 로고
    • Preparation of Rh[16aneS4-diol]211At and Ir[16aneS4-diol]211At Complexes as Potential Precursors for Astatine Radiopharmaceuticals. Part I: Synthesis
    • Pruszyski M., Bilewicz A., Zalutsky M.R. Preparation of Rh[16aneS4-diol]211At and Ir[16aneS4-diol]211At Complexes as Potential Precursors for Astatine Radiopharmaceuticals. Part I: Synthesis. Bioconjugate Chem 2008, 19:958-965.
    • (2008) Bioconjugate Chem , vol.19 , pp. 958-965
    • Pruszyski, M.1    Bilewicz, A.2    Zalutsky, M.R.3
  • 24
    • 84978362719 scopus 로고
    • Aspects of nucleophilic carbene chemistry
    • Wanzlick H.W. Aspects of nucleophilic carbene chemistry. Angew Chem 1962, 1:7-80.
    • (1962) Angew Chem , vol.1 , pp. 7-80
    • Wanzlick, H.W.1
  • 25
    • 53049091364 scopus 로고    scopus 로고
    • Heterocyclic carbenes; synthesis and coordination chemistry
    • Hahn F.E., Jahnke M.C. Heterocyclic carbenes; synthesis and coordination chemistry. Angew Chem Int Ed 2008, 47:3122-3172.
    • (2008) Angew Chem Int Ed , vol.47 , pp. 3122-3172
    • Hahn, F.E.1    Jahnke, M.C.2
  • 27
    • 27744573100 scopus 로고    scopus 로고
    • Steric and electronic effects in the bonding of N-heterocyclic ligands to transition metals
    • Cavallo L., Correa A., Costabile C., Jacobsen H. Steric and electronic effects in the bonding of N-heterocyclic ligands to transition metals. J Organomet Chem 2005, 690:5407-5413.
    • (2005) J Organomet Chem , vol.690 , pp. 5407-5413
    • Cavallo, L.1    Correa, A.2    Costabile, C.3    Jacobsen, H.4
  • 28
    • 33846797894 scopus 로고    scopus 로고
    • Stereoelectronic parameters associated with N-heterocyclic carbene (NHC) ligands: a quest for understanding
    • Diez-Gonzälez S., Nolan S.P. Stereoelectronic parameters associated with N-heterocyclic carbene (NHC) ligands: a quest for understanding. Coord Chem Rev 2007, 251:874-883.
    • (2007) Coord Chem Rev , vol.251 , pp. 874-883
    • Diez-Gonzälez, S.1    Nolan, S.P.2
  • 29
    • 34548323830 scopus 로고    scopus 로고
    • Tuning the electronic properties of N-heterocyclic carbenes
    • Leuthäuer S., Schwarz D., Plenio H. Tuning the electronic properties of N-heterocyclic carbenes. Chem Eur J 2007, 13:7195-7203.
    • (2007) Chem Eur J , vol.13 , pp. 7195-7203
    • Leuthäuer, S.1    Schwarz, D.2    Plenio, H.3
  • 30
    • 33750069405 scopus 로고    scopus 로고
    • Routes to N-heterocyclic carbenes complexes
    • Peris E. Routes to N-heterocyclic carbenes complexes. Top Organomet Chem 2007, 21:83-116.
    • (2007) Top Organomet Chem , vol.21 , pp. 83-116
    • Peris, E.1
  • 31
    • 55049101760 scopus 로고    scopus 로고
    • Green catalysts: solid-phase peptide carbene ligands in aqueous transition-metal catalysis
    • Worm-Leonhard K., Meldal M. Green catalysts: solid-phase peptide carbene ligands in aqueous transition-metal catalysis. Eur J Org Chem 2008, 31:5244-5253.
    • (2008) Eur J Org Chem , vol.31 , pp. 5244-5253
    • Worm-Leonhard, K.1    Meldal, M.2
  • 32
    • 53349099421 scopus 로고    scopus 로고
    • The synthesis of ruthenium and rhodium complexes with functionalized N-heterocyclic carbenes and their use in solid phase peptide synthesis
    • Lemke J., Metzler-Nolte N. The synthesis of ruthenium and rhodium complexes with functionalized N-heterocyclic carbenes and their use in solid phase peptide synthesis. Eur J Inorg Chem 2008, 21:3359-3366.
    • (2008) Eur J Inorg Chem , vol.21 , pp. 3359-3366
    • Lemke, J.1    Metzler-Nolte, N.2
  • 33
    • 41149152953 scopus 로고    scopus 로고
    • Synthesis, stability, and antimicrobial studies of electronically tuned silver acetate N-heterocyclic carbenes
    • Hindi K.M., Siciliano T.J., Durmus S., Panzner M.J., Medvetz D.A., Reddy D., et al. Synthesis, stability, and antimicrobial studies of electronically tuned silver acetate N-heterocyclic carbenes. J Med Chem 2008, 51:1577-1583.
    • (2008) J Med Chem , vol.51 , pp. 1577-1583
    • Hindi, K.M.1    Siciliano, T.J.2    Durmus, S.3    Panzner, M.J.4    Medvetz, D.A.5    Reddy, D.6
  • 36
    • 77950266144 scopus 로고    scopus 로고
    • [(NHC)(NHCewg)RuCl2(CHPh)] complexes with modified NHCewg ligands for efficient ring-closing metathesis leading to tetrasubstituted olefins
    • Sashuk V., Peeck L.H., Plenio H. [(NHC)(NHCewg)RuCl2(CHPh)] complexes with modified NHCewg ligands for efficient ring-closing metathesis leading to tetrasubstituted olefins. Chem Eur J 2010, 16:3983-3993.
    • (2010) Chem Eur J , vol.16 , pp. 3983-3993
    • Sashuk, V.1    Peeck, L.H.2    Plenio, H.3
  • 37
    • 53849139133 scopus 로고    scopus 로고
    • π-Face Donor Properties of N-Heterocyclic Carbenes in Grubbs II Complexes
    • Leuthäusser S., Schmidts V., Thiele C.M., Plenio H. π-Face Donor Properties of N-Heterocyclic Carbenes in Grubbs II Complexes. Chem Eur J 2008, 14:5465-5481.
    • (2008) Chem Eur J , vol.14 , pp. 5465-5481
    • Leuthäusser, S.1    Schmidts, V.2    Thiele, C.M.3    Plenio, H.4
  • 38
    • 70349304331 scopus 로고    scopus 로고
    • Electronically tunable N-heterocyclic carbene ligands: 1,3-diaryl vs. 4,5-diaryl substitution
    • Ogle J.W., Miller S.A. Electronically tunable N-heterocyclic carbene ligands: 1,3-diaryl vs. 4,5-diaryl substitution. Chem Comm 2009, 38:5728-5730.
    • (2009) Chem Comm , vol.38 , pp. 5728-5730
    • Ogle, J.W.1    Miller, S.A.2
  • 39
    • 41549147669 scopus 로고    scopus 로고
    • Synthesis and characterization of asymmetric NHC complexes
    • Zinner S.C., Hermann W.A., Kühn F.E. Synthesis and characterization of asymmetric NHC complexes. J Organomet Chem 2008, 693:1543-1546.
    • (2008) J Organomet Chem , vol.693 , pp. 1543-1546
    • Zinner, S.C.1    Hermann, W.A.2    Kühn, F.E.3
  • 40
    • 84857600410 scopus 로고
    • The iodometric titration of cysteine and allied substances
    • Lucas C.C., King E.J. The iodometric titration of cysteine and allied substances. Biochem J 1932, 26:2076-2089.
    • (1932) Biochem J , vol.26 , pp. 2076-2089
    • Lucas, C.C.1    King, E.J.2
  • 41
    • 84899060256 scopus 로고
    • The oxidation of cysteine with iodine: formation of a sulfinic acid
    • Simonsen D.G. The oxidation of cysteine with iodine: formation of a sulfinic acid. J Biol Chem 1933, 101:35-42.
    • (1933) J Biol Chem , vol.101 , pp. 35-42
    • Simonsen, D.G.1
  • 42
    • 0001952602 scopus 로고
    • Inorganic astatine chemistry: Part II. The chameleon behavior and electrophilicity of At-species
    • Visser G.M. Inorganic astatine chemistry: Part II. The chameleon behavior and electrophilicity of At-species. Radiochim Acta 1989, 47:97-103.
    • (1989) Radiochim Acta , vol.47 , pp. 97-103
    • Visser, G.M.1
  • 43
    • 34447330420 scopus 로고    scopus 로고
    • Radiopharmaceutical chemistry of targeted radiotherapeutics, part 3: α-particle-induced radiolytic effects on the chemical behavior of 211At
    • Pozzi O.R., Zalutsky M.R. Radiopharmaceutical chemistry of targeted radiotherapeutics, part 3: α-particle-induced radiolytic effects on the chemical behavior of 211At. J Nucl Med 2007, 48:1190-1196.
    • (2007) J Nucl Med , vol.48 , pp. 1190-1196
    • Pozzi, O.R.1    Zalutsky, M.R.2
  • 44
    • 1842428799 scopus 로고    scopus 로고
    • Nitric acid mediated oxidative transformation of thiols to disulfides
    • Misra A.K., Agnihotri G. Nitric acid mediated oxidative transformation of thiols to disulfides. Synth Commun 2004, 34:1079-1085.
    • (2004) Synth Commun , vol.34 , pp. 1079-1085
    • Misra, A.K.1    Agnihotri, G.2
  • 46
    • 14644414278 scopus 로고    scopus 로고
    • Radiohalogens for imaging and therapy
    • Adam M.J., Wilbur D.S. Radiohalogens for imaging and therapy. Chem Soc Rev 2005, 34:153-163.
    • (2005) Chem Soc Rev , vol.34 , pp. 153-163
    • Adam, M.J.1    Wilbur, D.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.