메뉴 건너뛰기




Volumn 8, Issue 15, 2003, Pages 701-709

Molecular diversity through sugar scaffolds

Author keywords

Carbohydrate; Drug discovery; Libraries; Scaffold; Structural diversity

Indexed keywords

CARBOHYDRATE DERIVATIVE; MELANOCORTIN RECEPTOR; N,N DIMETHYLFORMAMIDE; SOMATOSTATIN RECEPTOR; TETRABUTYLAMMONIUM;

EID: 0043123209     PISSN: 13596446     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1359-6446(03)02751-X     Document Type: Review
Times cited : (93)

References (65)
  • 1
    • 0028953765 scopus 로고
    • Measuring diversity: Experimental design of combinatorial libraries for drug discovery
    • Martin E.J., et al. Measuring diversity: experimental design of combinatorial libraries for drug discovery. J. Med. Chem. 38:1995;1431-1436.
    • (1995) J. Med. Chem. , vol.38 , pp. 1431-1436
    • Martin, E.J.1
  • 4
    • 0035950118 scopus 로고    scopus 로고
    • Measuring molecular similarity and diversity: Total pharmacophore diversity
    • Makara G.M. Measuring molecular similarity and diversity: total pharmacophore diversity. J. Med. Chem. 44:2001;3563-3571.
    • (2001) J. Med. Chem. , vol.44 , pp. 3563-3571
    • Makara, G.M.1
  • 5
    • 0001073278 scopus 로고    scopus 로고
    • The design of combinatorial libraries using properties and 3D pharmacophore fingerprints
    • Beno B.R., Mason J.S. The design of combinatorial libraries using properties and 3D pharmacophore fingerprints. Drug Discov. Today. 6:2001;251-258.
    • (2001) Drug Discov. Today , vol.6 , pp. 251-258
    • Beno, B.R.1    Mason, J.S.2
  • 6
    • 0033630852 scopus 로고    scopus 로고
    • Pharmacophore fingerprinting. 2. Application to primary library design
    • McGregor M.J., Muskal S.M. Pharmacophore fingerprinting. 2. Application to primary library design. J. Chem. Inf. Comput. Sci. 40:2000;117-125.
    • (2000) J. Chem. Inf. Comput. Sci. , vol.40 , pp. 117-125
    • McGregor, M.J.1    Muskal, S.M.2
  • 7
    • 0033606988 scopus 로고    scopus 로고
    • New 4-point pharmacophore method for molecular similarity and diversity applications: Overview of the method and applications, including a novel approach to the design of combinatorial libraries containing privileged substructures
    • Mason J.S., et al. New 4-point pharmacophore method for molecular similarity and diversity applications: overview of the method and applications, including a novel approach to the design of combinatorial libraries containing privileged substructures. J. Med. Chem. 42:1999;3251-3264.
    • (1999) J. Med. Chem. , vol.42 , pp. 3251-3264
    • Mason, J.S.1
  • 8
    • 15744363581 scopus 로고    scopus 로고
    • Metric validation and the receptor-relevant subspace concept
    • Pearlman R.S., Smith K.M. Metric validation and the receptor-relevant subspace concept. J. Chem. Inf. Comput. Sci. 39:1999;28-35.
    • (1999) J. Chem. Inf. Comput. Sci. , vol.39 , pp. 28-35
    • Pearlman, R.S.1    Smith, K.M.2
  • 9
    • 5244364312 scopus 로고    scopus 로고
    • The information content of 2d and 3d structural descriptors relevant to ligand-receptor binding
    • Brown R.D., Martin Y.C. The information content of 2d and 3d structural descriptors relevant to ligand-receptor binding. J. Chem. Inf. Comput. Sci. 37:1997;1-9.
    • (1997) J. Chem. Inf. Comput. Sci. , vol.37 , pp. 1-9
    • Brown, R.D.1    Martin, Y.C.2
  • 10
    • 0034074354 scopus 로고    scopus 로고
    • Functional diversity of compound libraries
    • Gorse D., Lahana R. Functional diversity of compound libraries. Curr. Opin. Chem. Biol. 4:2000;287-294.
    • (2000) Curr. Opin. Chem. Biol. , vol.4 , pp. 287-294
    • Gorse, D.1    Lahana, R.2
  • 11
    • 2342622593 scopus 로고    scopus 로고
    • B-turn nomenclature: A topographical classification system
    • P.T.P. Kaumaya, & R.S. Hodges. Mayflower Scientific
    • Bourne G.T., et al. b-turn nomenclature: a topographical classification system. Kaumaya P.T.P., Hodges R.S. Peptides: Chemistry, Structure and Biology. 1996;354-355 Mayflower Scientific.
    • (1996) Peptides: Chemistry, Structure and Biology , pp. 354-355
    • Bourne, G.T.1
  • 12
    • 0042842020 scopus 로고    scopus 로고
    • The side-chain classification of loops from high-resolution protein crystal structures
    • G.B. et al. Fields. Kluwer Academic Publishers
    • Tran T.T., et al. The side-chain classification of loops from high-resolution protein crystal structures. Fields G.B., et al. Peptides for the New Millenium. 2000;320-321 Kluwer Academic Publishers.
    • (2000) Peptides for the New Millenium , pp. 320-321
    • Tran, T.T.1
  • 13
    • 0000327897 scopus 로고
    • Ariens E.J. Academic New York
    • Farmer P.S. Ariens E.J. Drug Design. 10:1980;119 Academic New York.
    • (1980) Drug Design , vol.10 , pp. 119
    • Farmer, P.S.1
  • 14
    • 0026726041 scopus 로고
    • Peptoids: A modular approach to drug discovery
    • Zuckermann R.N., et al. Peptoids: a modular approach to drug discovery. Proc. Natl. Acad. Sci. U. S. A. 89:1992;9367-9371.
    • (1992) Proc. Natl. Acad. Sci. U. S. A. , vol.89 , pp. 9367-9371
    • Zuckermann, R.N.1
  • 15
    • 0036783393 scopus 로고    scopus 로고
    • Design, synthesis, and application of peptide secondary structure mimetics
    • Kahn M., et al. Design, synthesis, and application of peptide secondary structure mimetics. Mini. Rev. Med. Chem. 2:2002;447-462.
    • (2002) Mini. Rev. Med. Chem. , vol.2 , pp. 447-462
    • Kahn, M.1
  • 16
    • 0042341124 scopus 로고    scopus 로고
    • Peptidomimetics and peptide backbone modifications
    • Janda K.D., et al. Peptidomimetics and peptide backbone modifications. Mini. Rev. Med. Chem. 2:2002;447-462.
    • (2002) Mini. Rev. Med. Chem. , vol.2 , pp. 447-462
    • Janda, K.D.1
  • 17
    • 0037203973 scopus 로고    scopus 로고
    • Designing non-peptide peptidomimetics in the 21st century: Inhibitors targeting conformational ensembles
    • Rich D.H., et al. Designing non-peptide peptidomimetics in the 21st century: inhibitors targeting conformational ensembles. J. Med. Chem. 45:2002;541-558.
    • (2002) J. Med. Chem. , vol.45 , pp. 541-558
    • Rich, D.H.1
  • 18
    • 0033509033 scopus 로고    scopus 로고
    • New opioid peptides, peptidomimetics, and heterocyclic compounds from combinatorial libraries
    • Houghten R.A., et al. New opioid peptides, peptidomimetics, and heterocyclic compounds from combinatorial libraries. Biopolymers. 51:1999;379-390.
    • (1999) Biopolymers , vol.51 , pp. 379-390
    • Houghten, R.A.1
  • 19
    • 0001019227 scopus 로고
    • Preparation of exo-6-Benzyl- exo-2-(m-hydroxyphenyl)-1-dimethylaminomethylbicyclo[2.2.2]octane. A non-peptide mimetic of enkephalins
    • Bélanger P.C., Dufresne C. Preparation of exo-6-Benzyl- exo-2-(m-hydroxyphenyl)-1-dimethylaminomethylbicyclo[2.2.2]octane. A non-peptide mimetic of enkephalins. Can. J. Chem. 64:1986;1514-1520.
    • (1986) Can. J. Chem. , vol.64 , pp. 1514-1520
    • Bélanger, P.C.1    Dufresne, C.2
  • 20
    • 1242313153 scopus 로고
    • Concepts and progress in the design of peptide mimetics, beta turns and thyrotropin releasing hormone
    • Conference Management Association
    • Olsen, G.L. et al. (1989) Concepts and progress in the design of peptide mimetics, beta turns and thyrotropin releasing hormone. In Proc. Biotechnol. (U. S. A.), pp. 348-360, Conference Management Association.
    • (1989) Proc. Biotechnol. (U. S. A.) , pp. 348-360
    • Olsen, G.L.1
  • 21
    • 0032497355 scopus 로고    scopus 로고
    • Highly efficient and versatile synthesis of libraries of constrained beta-strand mimetics
    • Kahn M., et al. Highly efficient and versatile synthesis of libraries of constrained beta-strand mimetics. Bioorg. Med. Chem. Lett. 8:1998;2321-2326.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 2321-2326
    • Kahn, M.1
  • 22
    • 0027423502 scopus 로고
    • Concepts and progress in the development of peptide mimetics
    • Olsen G., et al. Concepts and progress in the development of peptide mimetics. J. Med. Chem. 36:1993;3039-3049.
    • (1993) J. Med. Chem. , vol.36 , pp. 3039-3049
    • Olsen, G.1
  • 23
    • 0028038601 scopus 로고
    • Peptidomimetics - tailored enzyme inhibitors
    • Gante J. Peptidomimetics - tailored enzyme inhibitors. Angew. Chem. Int. Ed. Engl. 33:1994;1699-1720.
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 1699-1720
    • Gante, J.1
  • 24
    • 0034703477 scopus 로고    scopus 로고
    • Tetrahydrofuran as a scaffold for peptidomimetics. Application to the design and synthesis of conformationally constrained metalloproteinase inhibitors
    • Hanessian S., et al. Tetrahydrofuran as a scaffold for peptidomimetics. Application to the design and synthesis of conformationally constrained metalloproteinase inhibitors. Tetrahedron. 56:2000;7643-7660.
    • (2000) Tetrahedron , vol.56 , pp. 7643-7660
    • Hanessian, S.1
  • 25
    • 0034549337 scopus 로고    scopus 로고
    • Efficient synthesis of a stereochemically defined carbohydrate scaffold: Carboxymethyl 2-acetamido-6-azido-4-o-benzyl-2-deoxy-β-D-glucopyranoside
    • Ghosh M., et al. Efficient synthesis of a stereochemically defined carbohydrate scaffold: carboxymethyl 2-acetamido-6-azido-4-o-benzyl-2-deoxy-β-D-glucopyranoside. J. Org. Chem. 65:2000;8387-8390.
    • (2000) J. Org. Chem. , vol.65 , pp. 8387-8390
    • Ghosh, M.1
  • 26
    • 0035887225 scopus 로고    scopus 로고
    • 1 integrin antagonists based on β-D-mannose as a rigid scaffold
    • 1 integrin antagonists based on β-D-mannose as a rigid scaffold. Angew. Chem. Int. Ed. Engl. 40:2001;3870-3873.
    • (2001) Angew. Chem. Int. Ed. Engl. , vol.40 , pp. 3870-3873
    • Boer, J.1
  • 27
    • 0036462603 scopus 로고    scopus 로고
    • Carbohydrate-based mimetics in drug design: Sugar amino acids and carbohydrate scaffolds
    • Gruner S., et al. Carbohydrate-based mimetics in drug design: sugar amino acids and carbohydrate scaffolds. Chem. Rev. 102:2002;491-514.
    • (2002) Chem. Rev. , vol.102 , pp. 491-514
    • Gruner, S.1
  • 28
    • 0037126832 scopus 로고    scopus 로고
    • Glycosamino acids: Building blocks for combinatorial synthesis-implications for drug discovery
    • Schweizer F. Glycosamino acids: building blocks for combinatorial synthesis-implications for drug discovery. Angew. Chem. Int. Ed. Engl. 41:2002;231-253.
    • (2002) Angew. Chem. Int. Ed. Engl. , vol.41 , pp. 231-253
    • Schweizer, F.1
  • 29
    • 57249092621 scopus 로고    scopus 로고
    • Carbohydrate-based scaffolds for the generation of sortiments of bioactive compounds
    • Peri, F. et al. Carbohydrate-based scaffolds for the generation of sortiments of bioactive compounds, Monatshefte Chem.133, 369-382.
    • Monatshefte Chem. , vol.133 , pp. 369-382
    • Peri, F.1
  • 30
    • 0026470597 scopus 로고
    • Nonpeptidal peptidomimetics with a β-D-glucose scaffolding. A partial somatostatin agonist bearing a close structural relationship to a potent, selective substance P antagonist
    • Hirschmann R., et al. Nonpeptidal peptidomimetics with a β-D-glucose scaffolding. A partial somatostatin agonist bearing a close structural relationship to a potent, selective substance P antagonist. J. Am. Chem. Soc. 114:1992;9217-9218.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 9217-9218
    • Hirschmann, R.1
  • 31
    • 0027857964 scopus 로고
    • De novo design and synthesis of somatostatin non-peptide peptidomimetics utilizing β-D-glucose as a novel scaffolding
    • Hirschmann R., et al. De novo design and synthesis of somatostatin non-peptide peptidomimetics utilizing β-D-glucose as a novel scaffolding. J. Am. Chem. Soc. 115:1993;12550-12568.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 12550-12568
    • Hirschmann, R.1
  • 32
    • 15844372436 scopus 로고    scopus 로고
    • Synthesis of potent cyclic hexapeptide NK-1 antagonists: Use of a minilibrary in transforming a peptidal somatostatin receptor ligand into an NK-1 receptor ligand via a polyvalent peptidomimetic
    • Hirschmann R., et al. Synthesis of potent cyclic hexapeptide NK-1 antagonists: use of a minilibrary in transforming a peptidal somatostatin receptor ligand into an NK-1 receptor ligand via a polyvalent peptidomimetic. J. Med. Chem. 39:1996;2441-2448.
    • (1996) J. Med. Chem. , vol.39 , pp. 2441-2448
    • Hirschmann, R.1
  • 33
    • 15444347630 scopus 로고    scopus 로고
    • Modulation of receptor and receptor subtype affinities using diastereomeric and enantiomeric monosaccharide scaffolds as a means to structural and biological diversity. A new route to ether synthesis
    • Hirschmann R., et al. Modulation of receptor and receptor subtype affinities using diastereomeric and enantiomeric monosaccharide scaffolds as a means to structural and biological diversity. A new route to ether synthesis. J. Med. Chem. 41:1998;1382-1391.
    • (1998) J. Med. Chem. , vol.41 , pp. 1382-1391
    • Hirschmann, R.1
  • 34
    • 0037009207 scopus 로고    scopus 로고
    • Design, synthesis and biological activity of carbohydrate containing peptidomimeticis as new ligands for the human Tachykinin NK-2 receptor
    • Capozzi G., et al. Design, synthesis and biological activity of carbohydrate containing peptidomimeticis as new ligands for the human Tachykinin NK-2 receptor. Bioorg. Med. Chem. Lett. 12:2002;2263-2266.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 2263-2266
    • Capozzi, G.1
  • 36
    • 0030872516 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of carbohydrate-based mimetics of cRGDFV
    • Nicolaou K.C., et al. Design, synthesis and biological evaluation of carbohydrate-based mimetics of cRGDFV. Tetrahedron. 53:1997;8751-8778.
    • (1997) Tetrahedron , vol.53 , pp. 8751-8778
    • Nicolaou, K.C.1
  • 37
    • 0035086633 scopus 로고    scopus 로고
    • Design, synthesis and preliminary biological evaluation of a focused combinatorial library of stereodiverse carbohydrate-scaffold-based
    • Moitessier N., et al. Design, synthesis and preliminary biological evaluation of a focused combinatorial library of stereodiverse carbohydrate-scaffold-based. Bioorg. Med. Chem. Lett. 9:2001;511-523.
    • (2001) Bioorg. Med. Chem. Lett. , vol.9 , pp. 511-523
    • Moitessier, N.1
  • 38
    • 0034611089 scopus 로고    scopus 로고
    • Design and synthesis of functionalized glycomers as non-peptidic ligands for SH2 binding and as inhibitors of A-431 Human epidermoid and HT-29 colon carcinoma cell lines
    • Hanessian S., et al. Design and synthesis of functionalized glycomers as non-peptidic ligands for SH2 binding and as inhibitors of A-431 Human epidermoid and HT-29 colon carcinoma cell lines. Bioorg. Med. Chem. Lett. 10:1999;439-442.
    • (1999) Bioorg. Med. Chem. Lett. , vol.10 , pp. 439-442
    • Hanessian, S.1
  • 39
    • 2542509173 scopus 로고    scopus 로고
    • Multi-component reactions with isocyanides
    • Dömling A., Ugi I. Multi-component reactions with isocyanides. Angew. Chem. Int. Ed. Engl. 39:2000;3168-3210.
    • (2000) Angew. Chem. Int. Ed. Engl. , vol.39 , pp. 3168-3210
    • Dömling, A.1    Ugi, I.2
  • 40
    • 0029132234 scopus 로고
    • Beyond peptide and nucleic acid combinatorial libraries-applying unions of multicomponent reactions towards the generation of carbohydrate combinatorial libraries
    • Goebel M., Ugi I. Beyond peptide and nucleic acid combinatorial libraries-applying unions of multicomponent reactions towards the generation of carbohydrate combinatorial libraries. Tetrahedron Lett. 36:1995;6043-6046.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 6043-6046
    • Goebel, M.1    Ugi, I.2
  • 41
    • 0033521568 scopus 로고    scopus 로고
    • An access to glycoconjugate lLibraries through multicomponent reactions
    • Lockhoff O. An access to glycoconjugate lLibraries through multicomponent reactions. Angew. Chem. Int. Ed. Engl. 37:1998;3436-3439.
    • (1998) Angew. Chem. Int. Ed. Engl. , vol.37 , pp. 3436-3439
    • Lockhoff, O.1
  • 42
    • 0029905917 scopus 로고    scopus 로고
    • Rapid combinatorial synthesis of aminoglycoside aAntibiotic mimetics: Use of a polyethylene glycol-linked amine and a neamine-derived aldehyde in multiple component condensation as a strategy for the discovery of new inhibitors of the HIV RNA rev responsive element
    • Park W.K.C., et al. Rapid combinatorial synthesis of aminoglycoside aAntibiotic mimetics: use of a polyethylene glycol-linked amine and a neamine-derived aldehyde in multiple component condensation as a strategy for the discovery of new inhibitors of the HIV RNA rev responsive element. J. Am. Chem. Soc. 118:1996;10150-10155.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 10150-10155
    • Park, W.K.C.1
  • 43
    • 0029801847 scopus 로고    scopus 로고
    • Generation of C-glycoside peptide ligands for cell surface carbohydrate receptors using a four-component condensation on solid support
    • Sutherlin D., et al. Generation of C-glycoside peptide ligands for cell surface carbohydrate receptors using a four-component condensation on solid support. J. Org. Chem. 61:1996;8350-8354.
    • (1996) J. Org. Chem. , vol.61 , pp. 8350-8354
    • Sutherlin, D.1
  • 44
    • 0034678615 scopus 로고    scopus 로고
    • Stereoselective combinatorial Ugi-multicomponent synthesis on solid phase
    • Oertel K., et al. Stereoselective combinatorial Ugi-multicomponent synthesis on solid phase. Angew. Chem. Int. Ed. Engl. 39:2000;1431-1433.
    • (2000) Angew. Chem. Int. Ed. Engl. , vol.39 , pp. 1431-1433
    • Oertel, K.1
  • 45
    • 0034674257 scopus 로고    scopus 로고
    • Preparation of bioconjugates through a Ugi reaction
    • Ziegler T., et al. Preparation of bioconjugates through a Ugi reaction. Angew. Chem. Int. Ed. Engl. 39:2000;2109-2112.
    • (2000) Angew. Chem. Int. Ed. Engl. , vol.39 , pp. 2109-2112
    • Ziegler, T.1
  • 46
    • 0030477258 scopus 로고    scopus 로고
    • Combinatorial synthesis of small organic molecules
    • Balkenhohl F., et al. Combinatorial synthesis of small organic molecules. Angew. Chem. Int. Ed. Engl. 35:1996;2288-2337.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 2288-2337
    • Balkenhohl, F.1
  • 47
    • 13044269653 scopus 로고    scopus 로고
    • Discovery of novel disaccharide antibacterial agents using a combinatorial library approach
    • Sofia M., et al. Discovery of novel disaccharide antibacterial agents using a combinatorial library approach. J. Med. Chem. 42:1999;3193-3198.
    • (1999) J. Med. Chem. , vol.42 , pp. 3193-3198
    • Sofia, M.1
  • 48
    • 0038032026 scopus 로고    scopus 로고
    • D-Glucose as a pentavalent chiral scaffold
    • Opatz T., et al. D-Glucose as a pentavalent chiral scaffold. Eur. J. Org. Chem. 8:2003;1527-1536.
    • (2003) Eur. J. Org. Chem. , vol.8 , pp. 1527-1536
    • Opatz, T.1
  • 49
    • 0033615762 scopus 로고    scopus 로고
    • Combinatorial solid-phase synthesis using dGalactose as a chiral five-dimension-diversity scaffold
    • Kallus C., et al. Combinatorial solid-phase synthesis using dGalactose as a chiral five-dimension-diversity scaffold. Tetrahedron Lett. 40:1999;7783-7786.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 7783-7786
    • Kallus, C.1
  • 50
    • 0037137248 scopus 로고    scopus 로고
    • D-Glucose as a multivalent chiral scaffold for combinatorial chemistry
    • Opatz T., et al. D-Glucose as a multivalent chiral scaffold for combinatorial chemistry. Carbohydr. Res. 337:2002;2089-2110.
    • (2002) Carbohydr. Res. , vol.337 , pp. 2089-2110
    • Opatz, T.1
  • 51
    • 0034555871 scopus 로고    scopus 로고
    • Development of an efficient regio- and stereoselective route to libraries based on the β-D-Glucose scaffold
    • Hirschmann R., et al. Development of an efficient regio- and stereoselective route to libraries based on the β-D-Glucose scaffold. J. Org. Chem. 65:2000;8307-8316.
    • (2000) J. Org. Chem. , vol.65 , pp. 8307-8316
    • Hirschmann, R.1
  • 52
    • 0000845917 scopus 로고    scopus 로고
    • Carbohydrate-based small-molecule scaffolds for the construction of universal pharmacophore mapping libraries
    • Sofia M.J., et al. Carbohydrate-based small-molecule scaffolds for the construction of universal pharmacophore mapping libraries. J. Org. Chem. 63:1998;2802-2803.
    • (1998) J. Org. Chem. , vol.63 , pp. 2802-2803
    • Sofia, M.J.1
  • 53
    • 0041839929 scopus 로고    scopus 로고
    • Protecting groups for carbohydrate synthesis, PCT WO-00/42057
    • Dekany, G. et al. (2000) Protecting groups for carbohydrate synthesis, PCT WO-00/42057.
    • (2000)
    • Dekany, G.1
  • 54
    • 0035289779 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • Lipinski C.A., et al. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 46:2001;3-26.
    • (2001) Adv. Drug Deliv. Rev. , vol.46 , pp. 3-26
    • Lipinski, C.A.1
  • 55
    • 0032780823 scopus 로고    scopus 로고
    • Somatostatin and its receptor family
    • Patel Y.C. Somatostatin and its receptor family. Front. Neuroendocrinol. 20:1999;157-198.
    • (1999) Front. Neuroendocrinol. , vol.20 , pp. 157-198
    • Patel, Y.C.1
  • 56
    • 0035037495 scopus 로고    scopus 로고
    • Cellular biology of somatostatin receptors
    • Csaba Z., Dournaud P. Cellular biology of somatostatin receptors. Neuropeptides. 35:2001;1-23.
    • (2001) Neuropeptides , vol.35 , pp. 1-23
    • Csaba, Z.1    Dournaud, P.2
  • 57
    • 0029186254 scopus 로고
    • Somatostatin receptors
    • Reisine T. Somatostatin receptors. Am. J. Physiol. 269:1995;G813-G820.
    • (1995) Am. J. Physiol. , vol.269 , pp. 813-G820
    • Reisine, T.1
  • 58
    • 0020363575 scopus 로고
    • SMS201-995: A very potent and selective octapeptide analogue of somatostatin with prolonged action
    • Bauer W., et al. SMS201-995: A very potent and selective octapeptide analogue of somatostatin with prolonged action. Life Sci. 31:1982;1133-1140.
    • (1982) Life Sci. , vol.31 , pp. 1133-1140
    • Bauer, W.1
  • 59
    • 0030054029 scopus 로고    scopus 로고
    • Drug therapy: Octreotide
    • Lamberts S.W.J., et al. Drug therapy: Octreotide. N. Engl. J. Med. 334:1996;246-254.
    • (1996) N. Engl. J. Med. , vol.334 , pp. 246-254
    • Lamberts, S.W.J.1
  • 61
    • 0029114410 scopus 로고
    • Molecular biology of somatostatin receptors
    • Reisine T., Bell G.I. Molecular biology of somatostatin receptors. Endocr. Rev. 16:1995;427-442.
    • (1995) Endocr. Rev. , vol.16 , pp. 427-442
    • Reisine, T.1    Bell, G.I.2
  • 62
    • 0032990469 scopus 로고    scopus 로고
    • Melanocortin-4 receptor: A novel signalling pathway involved in body weight regulation
    • Fisher S.L., et al. Melanocortin-4 receptor: a novel signalling pathway involved in body weight regulation. Int. J. Obes. 23:(Suppl. A):1999;54-58.
    • (1999) Int. J. Obes. , vol.23 , Issue.SUPPL. A , pp. 54-58
    • Fisher, S.L.1
  • 63
    • 0032577350 scopus 로고    scopus 로고
    • Strategies and potential molecular targets for obesity treatment
    • Campfield L.A., et al. Strategies and potential molecular targets for obesity treatment. Science. 280:1998;1383-1387.
    • (1998) Science , vol.280 , pp. 1383-1387
    • Campfield, L.A.1
  • 64
    • 0024551431 scopus 로고
    • Design of a new class of super potent cyclic α-melanotropins based on quenched dynamics solutions
    • Al-Obeidi F., et al. Design of a new class of super potent cyclic α-melanotropins based on quenched dynamics solutions. J. Am. Chem. Soc. 111:1989;3413-3416.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 3413-3416
    • Al-Obeidi, F.1
  • 65
    • 0029154516 scopus 로고
    • 2 with bulky aromatic amino acids at position 7 show high antagonist potency and selectivity at specific melanocortin receptors
    • 2 with bulky aromatic amino acids at position 7 show high antagonist potency and selectivity at specific melanocortin receptors. J. Med. Chem. 38:1995;3454-3461.
    • (1995) J. Med. Chem. , vol.38 , pp. 3454-3461
    • Hruby, V.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.