메뉴 건너뛰기




Volumn 236, Issue , 2017, Pages 17-32

Ligands at the free fatty acid receptors 2/3 (GPR43/GPR41)

Author keywords

Diabetes; Free fatty acids; Inflammation; Microbiota

Indexed keywords

3 (CYCLOPENTYLMETHYL) 4 [CYCLOPROPYL [4 (2,6 DICHLOROPHENYL)THIAZOL 2 YL]AMINO] 4 OXOBUTANOIC ACID; 3 BENZYL 4 [CYCLOPROPYL [4 (2,5 DICHLOROPHENYL)THIAZOL 2 YL]AMINO] 4 OXOBUTANOIC ACID; 3 [2 (3 CHLOROPHENYL)ACETAMIDO] 4 [4 (TRIFLUOROMETHYL)PHENYL]BUTANOIC ACID; 4 (FURAN 2 YL) 2 METHYL 5 OXO N (2 TOLYL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBOXAMIDE; 4 [4 (DIMETHYLAMINO)PHENYL] N (3,5 DIMETHYLPHENYL) 6 METHYL 2 OXO 1,2,3,4 TETRAHYDRO 5 PYRIMIDINECARBOXAMIDE; 4 [4 (DIMETHYLAMINO)PHENYL] N (4,5 DIMETHYLPHENYL) 6 METHYL 2 OXO 1,2,3,4 TETRAHYDRO 5 PYRIMIDINECARBOXAMIDE; 4 [[1 (BENZO[B]THIOPHENE 3 CARBONYL) 2 METHYLAZETIDINE 2 CARBONYL](3 CHLOROBENZYL)AMINO]BUTYRIC ACID; 5 (2 CHLOROPHENYL) 1 [2' METHOXY(1,1' BIPHENYL) 4 CARBONYL]PYRROLIDINE 2 CARBOXYLIC ACID; AR 420626; AZ 1729; CARBOXYLIC ACID DERIVATIVE; CMP 71; CYTOKINE RECEPTOR AGONIST; CYTOKINE RECEPTOR ANTAGONIST; FR 900359; G PROTEIN COUPLED RECEPTOR; G PROTEIN COUPLED RECEPTOR 41; G PROTEIN COUPLED RECEPTOR 43; MECMP 71; SHORT CHAIN FATTY ACID; UNCLASSIFIED DRUG; CELL SURFACE RECEPTOR; FFAR3 PROTEIN, HUMAN; G-PROTEIN COUPLED RECEPTOR 43, HUMAN; LIGAND;

EID: 85014070872     PISSN: 01712004     EISSN: 18650325     Source Type: Book Series    
DOI: 10.1007/164_2016_49     Document Type: Chapter
Times cited : (26)

References (55)
  • 2
    • 84975230323 scopus 로고    scopus 로고
    • GPR41 and GPR43 in obesity and inflammation - protective or causative?
    • Ang Z, Ding JL (2016) GPR41 and GPR43 in obesity and inflammation - protective or causative? Front Immunol 7:28
    • (2016) Front Immunol , vol.7 , pp. 28
    • Ang, Z.1    Ding, J.L.2
  • 3
    • 77957055780 scopus 로고
    • Integrated methods for modeling G-protein coupled receptors
    • Ballesteros JA, Weinstein H (1995) Integrated methods for modeling G-protein coupled receptors. Methods Neurosci 25:366-428
    • (1995) Methods Neurosci , vol.25 , pp. 366-428
    • Ballesteros, J.A.1    Weinstein, H.2
  • 4
    • 84961217329 scopus 로고    scopus 로고
    • The pharmacology and function of short chain fatty acid receptors
    • Bolognini D, Tobin AB, Milligan G, Moss CE (2016a) The pharmacology and function of short chain fatty acid receptors. Mol Pharmacol 89:388-398
    • (2016) Mol Pharmacol , vol.89 , pp. 388-398
    • Bolognini, D.1    Tobin, A.B.2    Milligan, G.3    Moss, C.E.4
  • 6
    • 84892589626 scopus 로고    scopus 로고
    • Novel amino acid derivatives and their use as gpr43 receptor modulators
    • Brantis C, Ooms F, Bernard J (2011) Novel amino acid derivatives and their use as gpr43 receptor modulators. PCT Int Appl WO2011092284
    • (2011) PCT Int Appl
    • Brantis, C.1    Ooms, F.2    Bernard, J.3
  • 10
    • 84952338130 scopus 로고    scopus 로고
    • Selective FFA2 agonism appears to act via intestinal PYY to reduce transit and food intake but does not improve glucose tolerance in mouse models
    • Forbes S, Stafford S, Coope G, Heffron H, Real K, Newman R, Davenport R, Barnes M, Grosse J, Cox H (2015) Selective FFA2 agonism appears to act via intestinal PYY to reduce transit and food intake but does not improve glucose tolerance in mouse models. Diabetes 64:3763-3771
    • (2015) Diabetes , vol.64 , pp. 3763-3771
    • Forbes, S.1    Stafford, S.2    Coope, G.3    Heffron, H.4    Real, K.5    Newman, R.6    Davenport, R.7    Barnes, M.8    Grosse, J.9    Cox, H.10
  • 12
    • 84874361271 scopus 로고    scopus 로고
    • Compounds, pharmaceutical composition and methods for use in treating metabolic disorders
    • WO2011076732
    • Hoveyda H, Brantis CE, Dutheuil G, Zoute L, Schils D, Bernard J (2010) Compounds, pharmaceutical composition and methods for use in treating metabolic disorders. PCT Int Appl WO2011076732
    • (2010) PCT Int Appl
    • Hoveyda, H.1    Brantis, C.E.2    Dutheuil, G.3    Zoute, L.4    Schils, D.5    Bernard, J.6
  • 13
    • 84874375020 scopus 로고    scopus 로고
    • Compounds, pharmaceutical composition and methods for use in treating inflammatory diseases
    • WO2011076734
    • Hoveyda H, Brantis CE, Dutheuil G, Zoute L, Schils D, Bernard J (2011a) Compounds, pharmaceutical composition and methods for use in treating inflammatory diseases. PCT Int Appl WO2011076734
    • (2011) PCT Int Appl
    • Hoveyda, H.1    Brantis, C.E.2    Dutheuil, G.3    Zoute, L.4    Schils, D.5    Bernard, J.6
  • 14
    • 84874375020 scopus 로고    scopus 로고
    • Compounds, pharmaceutical composition and methods for use in treating for use in the treatment of gastrointestinal disorders
    • WO2011076732
    • Hoveyda H, Brantis CE, Dutheuil G, Zoute L, Schils D, Fraser G (2011b) Compounds, pharmaceutical composition and methods for use in treating for use in the treatment of gastrointestinal disorders. PCT Int Appl WO2011076732
    • (2011) PCT Int Appl
    • Hoveyda, H.1    Brantis, C.E.2    Dutheuil, G.3    Zoute, L.4    Schils, D.5    Fraser, G.6
  • 15
    • 84890327356 scopus 로고    scopus 로고
    • Pyrrolidine or thiazolidine carboxylic acid derivatives, pharmaceutical compositions and methods for use as in treating metabolic disorders as agonists of G-protein coupled receptor 43 (GPR43)
    • WO2011073376
    • Hoveyda H, Schils D, Zoute L, Parcq J (2011c) Pyrrolidine or thiazolidine carboxylic acid derivatives, pharmaceutical compositions and methods for use as in treating metabolic disorders as agonists of G-protein coupled receptor 43 (GPR43). PCT Int Appl WO2011073376
    • (2011) PCT Int Appl
    • Hoveyda, H.1    Schils, D.2    Zoute, L.3    Parcq, J.4
  • 16
    • 84892563863 scopus 로고    scopus 로고
    • Azepanes, azocanes and related compounds as GPR43 modulators and their preparation and use for the treatment of inflammatory, gastrointestinal and metabolic disorders
    • WO2011151436
    • Hoveyda H, Zoute L, Lenoir F (2011d) Azepanes, azocanes and related compounds as GPR43 modulators and their preparation and use for the treatment of inflammatory, gastrointestinal and metabolic disorders. PCT Int Appl WO2011151436
    • (2011) PCT Int Appl
    • Hoveyda, H.1    Zoute, L.2    Lenoir, F.3
  • 19
    • 84870361150 scopus 로고    scopus 로고
    • Extracellular ionic locks determine variation in constitutive activity and ligand potency between species orthologs of the free fatty acid receptors FFA2 and FFA3
    • Hudson BD, Tikhonova IG, Pandey SK, Ulven T, Milligan G (2012) Extracellular ionic locks determine variation in constitutive activity and ligand potency between species orthologs of the free fatty acid receptors FFA2 and FFA3. J Biol Chem 287:41195-41209
    • (2012) J Biol Chem , vol.287 , pp. 41195-41209
    • Hudson, B.D.1    Tikhonova, I.G.2    Pandey, S.K.3    Ulven, T.4    Milligan, G.5
  • 20
    • 84947500240 scopus 로고    scopus 로고
    • The effective application of biased signaling to new drug discovery
    • Kenakin T (2015) The effective application of biased signaling to new drug discovery. Mol Pharmacol 88:1055-1061
    • (2015) Mol Pharmacol , vol.88 , pp. 1055-1061
    • Kenakin, T.1
  • 23
    • 84871806221 scopus 로고    scopus 로고
    • Bridging the gap: Bitopic ligands of G-protein- coupled receptors
    • Lane JR, Sexton PM, Christopoulos A (2013) Bridging the gap: bitopic ligands of G-protein- coupled receptors. Trends Pharmacol Sci 34:59-66
    • (2013) Trends Pharmacol Sci , vol.34 , pp. 59-66
    • Lane, J.R.1    Sexton, P.M.2    Christopoulos, A.3
  • 26
    • 84874369632 scopus 로고    scopus 로고
    • GPR41 and modulators thereof for the treatment of insulin-related disorders
    • WO2006052566
    • Leonard JN, Chu ZL, Bruce MA, Boatman PD (2006) GPR41 and modulators thereof for the treatment of insulin-related disorders. PCT Int Appl WO2006052566
    • (2006) PCT Int Appl
    • Leonard, J.N.1    Chu, Z.L.2    Bruce, M.A.3    Boatman, P.D.4
  • 28
    • 0037453280 scopus 로고    scopus 로고
    • Identification of a free fatty acid receptor, FFA2R, expressed on leukocytes and activated by short-chain fatty acids
    • Nilsson NE, Kotarsky K, Owman C, Olde B (2003) Identification of a free fatty acid receptor, FFA2R, expressed on leukocytes and activated by short-chain fatty acids. Biochem Biophys Res Commun 303:1047-1052
    • (2003) Biochem Biophys Res Commun , vol.303 , pp. 1047-1052
    • Nilsson, N.E.1    Kotarsky, K.2    Owman, C.3    Olde, B.4
  • 30
    • 84973869309 scopus 로고    scopus 로고
    • Synthesis, activity and docking study of novel phenylthiazole-carboxamido acid derivatives as FFA2 agonists
    • Ma L, Wang T, Shi M, Fu P, Pei H, Ye H (2016) Synthesis, activity and docking study of novel phenylthiazole-carboxamido acid derivatives as FFA2 agonists. Chem Biol Drug Des 88:26-37
    • (2016) Chem Biol Drug Des , vol.88 , pp. 26-37
    • Ma, L.1    Wang, T.2    Shi, M.3    Fu, P.4    Pei, H.5    Ye, H.6
  • 32
    • 69249214021 scopus 로고    scopus 로고
    • Agonism and allosterism: The pharmacology of the free fatty acid receptors FFA2 and FFA3
    • Milligan G, Stoddart LA, Smith NJ (2009) Agonism and allosterism: the pharmacology of the free fatty acid receptors FFA2 and FFA3. Br J Pharmacol 158:146-153
    • (2009) Br J Pharmacol , vol.158 , pp. 146-153
    • Milligan, G.1    Stoddart, L.A.2    Smith, N.J.3
  • 33
    • 84871980480 scopus 로고    scopus 로고
    • Molecular alliance-from orthosteric and allosteric ligands to dualsteric/bitopic agonists at G protein coupled receptors
    • Mohr K, Schmitz J, Schrage R, Tränkle C, Holzgrabe U (2013) Molecular alliance-from orthosteric and allosteric ligands to dualsteric/bitopic agonists at G protein coupled receptors. Angew Chem Int Ed Engl 52:508-516
    • (2013) Angew Chem Int Ed Engl , vol.52 , pp. 508-516
    • Mohr, K.1    Schmitz, J.2    Schrage, R.3    Tränkle, C.4    Holzgrabe, U.5
  • 42
    • 84952941040 scopus 로고    scopus 로고
    • Non-equivalence of key positively charged residues of the free fatty acid 2 receptor in the recognition and function of agonist versus antagonist ligands
    • Sergeev E, Hansen H, Pandey SK, MacKenzie AE, Hudson BD, Ulven T, Milligan G (2016) Non-equivalence of key positively charged residues of the free fatty acid 2 receptor in the recognition and function of agonist versus antagonist ligands. J Biol Chem 291:303-317
    • (2016) J Biol Chem , vol.291 , pp. 303-317
    • Sergeev, E.1    Hansen, H.2    Pandey, S.K.3    Mackenzie, A.E.4    Hudson, B.D.5    Ulven, T.6    Milligan, G.7
  • 43
    • 67650533801 scopus 로고    scopus 로고
    • The action and mode of binding of thiazolidinedione ligands at free fatty acid receptor 1
    • Smith NJ, Stoddart LA, Devine NM, Jenkins L, Milligan G (2009) The action and mode of binding of thiazolidinedione ligands at free fatty acid receptor 1. J Biol Chem 284:17527-31759
    • (2009) J Biol Chem , vol.284 , pp. 17527-31759
    • Smith, N.J.1    Stoddart, L.A.2    Devine, N.M.3    Jenkins, L.4    Milligan, G.5
  • 46
    • 58149095589 scopus 로고    scopus 로고
    • International Union of Pharmacology. LXXI. Free fatty acid receptors FFA1, -2, and -3: Pharmacology and pathophysiological functions
    • Stoddart L, Smith NJ, Milligan G (2008a) International Union of Pharmacology. LXXI. Free fatty acid receptors FFA1, -2, and -3: pharmacology and pathophysiological functions. Pharmacol Rev 60:405-417
    • (2008) Pharmacol Rev , vol.60 , pp. 405-417
    • Stoddart, L.1    Smith, N.J.2    Milligan, G.3
  • 47
    • 57749112018 scopus 로고    scopus 로고
    • Conserved polar residues in transmembrane domains V, VI, and VII of free fatty acid receptor 2 and free fatty acid receptor 3 are required for the binding and function of short chain fatty acids
    • Stoddart LA, Smith NJ, Jenkins L, Brown AJ, Milligan G (2008b) Conserved polar residues in transmembrane domains V, VI, and VII of free fatty acid receptor 2 and free fatty acid receptor 3 are required for the binding and function of short chain fatty acids. J Biol Chem 283:32913-32924
    • (2008) J Biol Chem , vol.283 , pp. 32913-32924
    • Stoddart, L.A.1    Smith, N.J.2    Jenkins, L.3    Brown, A.J.4    Milligan, G.5
  • 50
    • 84922620529 scopus 로고    scopus 로고
    • Loss of FFA2 and FFA3 increases insulin secretion and improves glucose tolerance in type 2 diabetes
    • Tang C, Ahmed K, Gille A, Lu S, Grone HJ, Tunaru S, Offermanns S (2015) Loss of FFA2 and FFA3 increases insulin secretion and improves glucose tolerance in type 2 diabetes. Nat Med 21:173-177
    • (2015) Nat Med , vol.21 , pp. 173-177
    • Tang, C.1    Ahmed, K.2    Gille, A.3    Lu, S.4    Grone, H.J.5    Tunaru, S.6    Offermanns, S.7
  • 51
    • 84874395887 scopus 로고    scopus 로고
    • Short-chain free fatty acid receptors FFA2/GPR43 and FFA3/GPR41 as new potential therapeutic targets
    • Ulven T (2012) Short-chain free fatty acid receptors FFA2/GPR43 and FFA3/GPR41 as new potential therapeutic targets. Front Endocrinol (Lausanne) 3:111
    • (2012) Front Endocrinol (Lausanne) , vol.3 , pp. 111
    • Ulven, T.1
  • 54
    • 84889078129 scopus 로고    scopus 로고
    • Beta-hydroxybutyrate modulates N-type calcium channels in rat sympathetic neurons by acting as an agonist for the G-protein-coupled receptor FFA3
    • Won YJ, Lu VB, Puhl HL 3rd, Ikeda SR (2013) Beta-hydroxybutyrate modulates N-type calcium channels in rat sympathetic neurons by acting as an agonist for the G-protein-coupled receptor FFA3. J Neurosci 33:19314-19325
    • (2013) J Neurosci , vol.33 , pp. 19314-19325
    • Won, Y.J.1    Lu, V.B.2    Puhl, H.L.3    Ikeda, S.R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.