Matera, Carlo; Pucci, Luca; Fiorentini, Chiara; Fucile, Sergio; Missale, Cristina; Grazioso, Giovanni; Clementi, Francesco; Zoli, Michele et al. (2015-08-28). “Bifunctional compounds targeting both D2 and non-α7 nACh receptors: Design, synthesis and pharmacological characterization”. European Journal of Medicinal Chemistry101: 367–383. doi:10.1016/j.ejmech.2015.06.039. PMID26164842.
Matera, Carlo; Flammini, Lisa; Quadri, Marta; Vivo, Valentina; Ballabeni, Vigilio; Holzgrabe, Ulrike; Mohr, Klaus; De Amici, Marco et al. (2014-03-21). “Bis(ammonio)alkane-type agonists of muscarinic acetylcholine receptors: Synthesis, in vitro functional characterization, and in vivo evaluation of their analgesic activity”. European Journal of Medicinal Chemistry75: 222–232. doi:10.1016/j.ejmech.2014.01.032. PMID24534538.
Erez M, Takemori AE, Portoghese PS (July 1982). “Narcotic antagonistic potency of bivalent ligands which contain beta-naltrexamine. Evidence for bridging between proximal recognition sites”. Journal of Medicinal Chemistry25 (7): 847–9. doi:10.1021/jm00349a016. PMID7108900.
Portoghese PS, Ronsisvalle G, Larson DL, Yim CB, Sayre LM, Takemori AE (1982). “Opioid agonist and antagonist bivalent ligands as receptor probes”. Life Sciences31 (12–13): 1283–6. doi:10.1016/0024-3205(82)90362-9. PMID6292615.
Portoghese PS, Akgün E, Lunzer MM (January 2017). “Heteromer Induction: An Approach to Unique Pharmacology?”. ACS Chemical Neuroscience8 (3): 426–428. doi:10.1021/acschemneuro.7b00002. PMID28139906.
Conn PM, Rogers DC, Stewart JM, Niedel J, Sheffield T (April 1982). “Conversion of a gonadotropin-releasing hormone antagonist to an agonist”. Nature296 (5858): 653–5. Bibcode: 1982Natur.296..653C. doi:10.1038/296653a0. PMID6280058.
Nimczick M, Pemp D, Darras FH, Chen X, Heilmann J, Decker M (August 2014). “Synthesis and biological evaluation of bivalent cannabinoid receptor ligands based on hCB₂R selective benzimidazoles reveal unexpected intrinsic properties”. Bioorganic & Medicinal Chemistry22 (15): 3938–46. doi:10.1016/j.bmc.2014.06.008. PMID24984935.
Russo O, Berthouze M, Giner M, Soulier JL, Rivail L, Sicsic S, Lezoualc'h F, Jockers R, Berque-Bestel I (September 2007). “Synthesis of specific bivalent probes that functionally interact with 5-HT(4) receptor dimers”. Journal of Medicinal Chemistry50 (18): 4482–92. doi:10.1021/jm070552t. PMID17676726.
Soulier JL, Russo O, Giner M, Rivail L, Berthouze M, Ongeri S, Maigret B, Fischmeister R, Lezoualc'h F, Sicsic S, Berque-Bestel I (October 2005). “Design and synthesis of specific probes for human 5-HT4 receptor dimerization studies”. Journal of Medicinal Chemistry48 (20): 6220–8. doi:10.1021/jm050234z. PMID16190749.
Busnelli M, Kleinau G, Muttenthaler M, Stoev S, Manning M, Bibic L, Howell LA, McCormick PJ, Di Lascio S, Braida D, Sala M, Rovati GE, Bellini T, Chini B (August 2016). “Design and Characterization of Superpotent Bivalent Ligands Targeting Oxytocin Receptor Dimers via a Channel-Like Structure”. Journal of Medicinal Chemistry59 (15): 7152–66. doi:10.1021/acs.jmedchem.6b00564. PMID27420737.
Shonberg J, Scammells PJ, Capuano B (June 2011). “Design strategies for bivalent ligands targeting GPCRs”. ChemMedChem6 (6): 963–74. doi:10.1002/cmdc.201100101. PMID21520422.
Berque-Bestel I, Lezoualc'h F, Jockers R (December 2008). “Bivalent ligands as specific pharmacological tools for G protein-coupled receptor dimers”. Current Drug Discovery Technologies5 (4): 312–8. doi:10.2174/157016308786733591. PMID19075611.
Kombarov R, Altieri A, Genis D, Kirpichenok M, Kochubey V, Rakitina N, Titarenko Z (February 2010). “BioCores: identification of a drug/natural product-based privileged structural motif for small-molecule lead discovery”. Molecular Diversity14 (1): 193–200. doi:10.1007/s11030-009-9157-5. PMID19468851.
Conn PM, Rogers DC, Stewart JM, Niedel J, Sheffield T (April 1982). “Conversion of a gonadotropin-releasing hormone antagonist to an agonist”. Nature296 (5858): 653–5. Bibcode: 1982Natur.296..653C. doi:10.1038/296653a0. PMID6280058.
Matera, Carlo; Pucci, Luca; Fiorentini, Chiara; Fucile, Sergio; Missale, Cristina; Grazioso, Giovanni; Clementi, Francesco; Zoli, Michele et al. (2015-08-28). “Bifunctional compounds targeting both D2 and non-α7 nACh receptors: Design, synthesis and pharmacological characterization”. European Journal of Medicinal Chemistry101: 367–383. doi:10.1016/j.ejmech.2015.06.039. PMID26164842.
Matera, Carlo; Flammini, Lisa; Quadri, Marta; Vivo, Valentina; Ballabeni, Vigilio; Holzgrabe, Ulrike; Mohr, Klaus; De Amici, Marco et al. (2014-03-21). “Bis(ammonio)alkane-type agonists of muscarinic acetylcholine receptors: Synthesis, in vitro functional characterization, and in vivo evaluation of their analgesic activity”. European Journal of Medicinal Chemistry75: 222–232. doi:10.1016/j.ejmech.2014.01.032. PMID24534538.
Erez M, Takemori AE, Portoghese PS (July 1982). “Narcotic antagonistic potency of bivalent ligands which contain beta-naltrexamine. Evidence for bridging between proximal recognition sites”. Journal of Medicinal Chemistry25 (7): 847–9. doi:10.1021/jm00349a016. PMID7108900.
Portoghese PS, Ronsisvalle G, Larson DL, Yim CB, Sayre LM, Takemori AE (1982). “Opioid agonist and antagonist bivalent ligands as receptor probes”. Life Sciences31 (12–13): 1283–6. doi:10.1016/0024-3205(82)90362-9. PMID6292615.
Portoghese PS, Akgün E, Lunzer MM (January 2017). “Heteromer Induction: An Approach to Unique Pharmacology?”. ACS Chemical Neuroscience8 (3): 426–428. doi:10.1021/acschemneuro.7b00002. PMID28139906.
Conn PM, Rogers DC, Stewart JM, Niedel J, Sheffield T (April 1982). “Conversion of a gonadotropin-releasing hormone antagonist to an agonist”. Nature296 (5858): 653–5. Bibcode: 1982Natur.296..653C. doi:10.1038/296653a0. PMID6280058.
Nimczick M, Pemp D, Darras FH, Chen X, Heilmann J, Decker M (August 2014). “Synthesis and biological evaluation of bivalent cannabinoid receptor ligands based on hCB₂R selective benzimidazoles reveal unexpected intrinsic properties”. Bioorganic & Medicinal Chemistry22 (15): 3938–46. doi:10.1016/j.bmc.2014.06.008. PMID24984935.
Russo O, Berthouze M, Giner M, Soulier JL, Rivail L, Sicsic S, Lezoualc'h F, Jockers R, Berque-Bestel I (September 2007). “Synthesis of specific bivalent probes that functionally interact with 5-HT(4) receptor dimers”. Journal of Medicinal Chemistry50 (18): 4482–92. doi:10.1021/jm070552t. PMID17676726.
Soulier JL, Russo O, Giner M, Rivail L, Berthouze M, Ongeri S, Maigret B, Fischmeister R, Lezoualc'h F, Sicsic S, Berque-Bestel I (October 2005). “Design and synthesis of specific probes for human 5-HT4 receptor dimerization studies”. Journal of Medicinal Chemistry48 (20): 6220–8. doi:10.1021/jm050234z. PMID16190749.
Busnelli M, Kleinau G, Muttenthaler M, Stoev S, Manning M, Bibic L, Howell LA, McCormick PJ, Di Lascio S, Braida D, Sala M, Rovati GE, Bellini T, Chini B (August 2016). “Design and Characterization of Superpotent Bivalent Ligands Targeting Oxytocin Receptor Dimers via a Channel-Like Structure”. Journal of Medicinal Chemistry59 (15): 7152–66. doi:10.1021/acs.jmedchem.6b00564. PMID27420737.
Shonberg J, Scammells PJ, Capuano B (June 2011). “Design strategies for bivalent ligands targeting GPCRs”. ChemMedChem6 (6): 963–74. doi:10.1002/cmdc.201100101. PMID21520422.
Berque-Bestel I, Lezoualc'h F, Jockers R (December 2008). “Bivalent ligands as specific pharmacological tools for G protein-coupled receptor dimers”. Current Drug Discovery Technologies5 (4): 312–8. doi:10.2174/157016308786733591. PMID19075611.
Kombarov R, Altieri A, Genis D, Kirpichenok M, Kochubey V, Rakitina N, Titarenko Z (February 2010). “BioCores: identification of a drug/natural product-based privileged structural motif for small-molecule lead discovery”. Molecular Diversity14 (1): 193–200. doi:10.1007/s11030-009-9157-5. PMID19468851.