메뉴 건너뛰기




Volumn 57, Issue 23, 2014, Pages 9983-9994

SAR Studies on tetrahydroisoquinoline derivatives: The role of flexibility and bioisosterism to raise potency and selectivity toward P-glycoprotein

Author keywords

[No Author keywords available]

Indexed keywords

BIPHENYL DERIVATIVE; GLYCOPROTEIN; HYDROXYL GROUP; MULTIDRUG RESISTANCE PROTEIN; OXAZOLE DERIVATIVE; TETRAHYDROISOQUINOLINE; TETRAHYDROISOQUINOLINE DERIVATIVE; 6,7-DIMETHOXY-2-(4-METHOXYBIPHENYL-4-YL-METHYL)-1,2,3,4-TETRAHYDROISOQUINOLINE; BIPHENYL; CALCEIN AM; FLUORESCEIN DERIVATIVE; LIGAND; MULTIDRUG RESISTANCE-ASSOCIATED PROTEIN 1;

EID: 84918585092     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm501640e     Document Type: Article
Times cited : (29)

References (29)
  • 1
    • 84860688652 scopus 로고    scopus 로고
    • Overcoming multidrug resistance in cancer: 35 years after the discovery of ABCB1
    • Gillet, J. P.; Gottesman, M. M. Overcoming multidrug resistance in cancer: 35 years after the discovery of ABCB1 Drug Resist. Updat. 2012, 15, 2-4
    • (2012) Drug Resist. Updat. , vol.15 , pp. 2-4
    • Gillet, J.P.1    Gottesman, M.M.2
  • 3
    • 0036364467 scopus 로고    scopus 로고
    • Multidrug resistance in cancer: Role of ATP-dependent transporters
    • Gottesman, M. M.; Fojo, T.; Bates, S. E. Multidrug resistance in cancer: role of ATP-dependent transporters Nat. Rev. Cancer 2002, 2, 48-58
    • (2002) Nat. Rev. Cancer , vol.2 , pp. 48-58
    • Gottesman, M.M.1    Fojo, T.2    Bates, S.E.3
  • 4
    • 0033799839 scopus 로고    scopus 로고
    • Multidrug resistance (MDR) in cancer. Mechanisms, reversal using modulators of MDR and the role of MDR modulators in influencing the pharmacokinetics of anticancer drugs
    • Krishna, R.; Mayer, L. D. Multidrug resistance (MDR) in cancer. Mechanisms, reversal using modulators of MDR and the role of MDR modulators in influencing the pharmacokinetics of anticancer drugs Eur. J. Pharm. Sci. 2000, 11, 265-283
    • (2000) Eur. J. Pharm. Sci. , vol.11 , pp. 265-283
    • Krishna, R.1    Mayer, L.D.2
  • 5
    • 80053504148 scopus 로고    scopus 로고
    • Blood-brain barrier P-glycoprotein function in neurodegenerative disease
    • Bartels, A. L. Blood-brain barrier P-glycoprotein function in neurodegenerative disease Curr. Pharm. Des. 2011, 17, 2771-2777
    • (2011) Curr. Pharm. Des. , vol.17 , pp. 2771-2777
    • Bartels, A.L.1
  • 7
    • 84860535245 scopus 로고    scopus 로고
    • Three decades of P-gp inhibitors: Skimming through several generations and scaffolds
    • Palmeira, A.; Sousa, E.; Vasconcelos, M. H.; Pinto, M. M. Three decades of P-gp inhibitors: skimming through several generations and scaffolds Curr. Med. Chem. 2012, 19, 1946-2025
    • (2012) Curr. Med. Chem. , vol.19 , pp. 1946-2025
    • Palmeira, A.1    Sousa, E.2    Vasconcelos, M.H.3    Pinto, M.M.4
  • 14
    • 84873736052 scopus 로고    scopus 로고
    • 11C]methoxy-3,4-dihydro-2 H -naphthalen-(1 E)-ylidene] propyl}-1,2,3,4-tetrahydro-isoquinoline
    • NCBI: Bethesda, MD
    • 11C]methoxy-3,4-dihydro-2 H -naphthalen-(1 E)-ylidene] propyl}-1,2,3,4-tetrahydro-isoquinoline. Molecular Imaging and Contrast Agent Database (MICAD); NCBI: Bethesda, MD, 2010.
    • (2010) Molecular Imaging and Contrast Agent Database (MICAD)
    • Leung, K.1
  • 15
    • 84873735751 scopus 로고    scopus 로고
    • 11C]methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)- propyl]-1,2,3,4-tetrahydro-isoquinoline
    • NCBI: Bethesda, MD
    • 11C]methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)- propyl]-1,2,3,4-tetrahydro-isoquinoline. Molecular Imaging and Contrast Agent Database (MICAD); NCBI: Bethesda, MD, 2010.
    • (2010) Molecular Imaging and Contrast Agent Database (MICAD)
    • Leung, K.1
  • 19
    • 84918544296 scopus 로고    scopus 로고
    • 11C]Methyl Derivative of 6,7-Dimethoxy-2-(4-methoxybiphenyl-4-ylmethyl)-1,2,3,4-tetrahydro-isoquinoline
    • NCBI: Bethesda, MD
    • 11C]Methyl Derivative of 6,7-Dimethoxy-2-(4-methoxybiphenyl-4-ylmethyl)-1,2,3,4-tetrahydro-isoquinoline. Imaging and Contrast Agent Database (MICAD); NCBI: Bethesda, MD, 2013.
    • (2013) Imaging and Contrast Agent Database (MICAD)
    • Chopra, A.1
  • 20
    • 60849085184 scopus 로고    scopus 로고
    • Multi-drug-resistance-reverting agents: 2-aryloxazole and 2-arylthiazole derivatives as potent BCRP or MRP1 inhibitors
    • Colabufo, N. A.; Berardi, F.; Perrone, M. G.; Cantore, M.; Contino, M.; Inglese, C.; Niso, M.; Perrone, R. Multi-drug-resistance-reverting agents: 2-aryloxazole and 2-arylthiazole derivatives as potent BCRP or MRP1 inhibitors Chem. Med. Chem. 2009, 4, 188-195
    • (2009) Chem. Med. Chem. , vol.4 , pp. 188-195
    • Colabufo, N.A.1    Berardi, F.2    Perrone, M.G.3    Cantore, M.4    Contino, M.5    Inglese, C.6    Niso, M.7    Perrone, R.8
  • 21
    • 0034601776 scopus 로고    scopus 로고
    • Drug binding sites on P-glycoprotein are altered by ATP binding prior to nucleotide hydrolysis
    • Martin, C.; Berridge, G.; Mistry, P.; Higgins, C.; Charlton, P.; Callaghan, R. Drug binding sites on P-glycoprotein are altered by ATP binding prior to nucleotide hydrolysis Biochemistry 2000, 39, 11901-11906
    • (2000) Biochemistry , vol.39 , pp. 11901-11906
    • Martin, C.1    Berridge, G.2    Mistry, P.3    Higgins, C.4    Charlton, P.5    Callaghan, R.6
  • 22
    • 84891747485 scopus 로고    scopus 로고
    • PET radiotracers for imaging P-glycoprotein: The challenge for early diagnosis in AD
    • Leopoldo, M.; Contino, M.; Berardi, F.; Perrone, R.; Colabufo, N. A. PET radiotracers for imaging P-glycoprotein: the challenge for early diagnosis in AD Chem. Med. Chem. 2014, 9, 38-42
    • (2014) Chem. Med. Chem. , vol.9 , pp. 38-42
    • Leopoldo, M.1    Contino, M.2    Berardi, F.3    Perrone, R.4    Colabufo, N.A.5
  • 23
    • 84876532065 scopus 로고    scopus 로고
    • Radioligands targeting P-glycoprotein and other drug efflux proteins at the blood-brain barrier
    • Wanek, T.; Mairinger, S.; Langer, O. Radioligands targeting P-glycoprotein and other drug efflux proteins at the blood-brain barrier J. Labelled Compd. Radiopharm. 2013, 56, 68-77
    • (2013) J. Labelled Compd. Radiopharm. , vol.56 , pp. 68-77
    • Wanek, T.1    Mairinger, S.2    Langer, O.3
  • 24
    • 80053499640 scopus 로고    scopus 로고
    • PET and SPECT radiotracers to assess function and expression of ABC transporters in vivo
    • Mairinger, S.; Erker, T.; Muller, M.; Langer, O. PET and SPECT radiotracers to assess function and expression of ABC transporters in vivo Curr. Drug Metab. 2011, 12, 774-792
    • (2011) Curr. Drug Metab. , vol.12 , pp. 774-792
    • Mairinger, S.1    Erker, T.2    Muller, M.3    Langer, O.4
  • 25
    • 38749087222 scopus 로고    scopus 로고
    • In vitro P-glycoprotein assays to predict the in vivo interactions of P-glycoprotein with drugs in the central nervous system
    • Feng, B.; Mills, J. B.; Davidson, R. E.; Mireles, R. J.; Janiszewski, J. S.; Troutman, M. D.; de Morais, S. M. In vitro P-glycoprotein assays to predict the in vivo interactions of P-glycoprotein with drugs in the central nervous system Drug Metab. Dispos. 2008, 36, 268-275
    • (2008) Drug Metab. Dispos. , vol.36 , pp. 268-275
    • Feng, B.1    Mills, J.B.2    Davidson, R.E.3    Mireles, R.J.4    Janiszewski, J.S.5    Troutman, M.D.6    De Morais, S.M.7
  • 26
    • 33746256441 scopus 로고    scopus 로고
    • A highly active catalyst for Suzuki-Miyaura cross-coupling reactions of heteroaryl compounds
    • Billingsley, K. L.; Anderson, K. W.; Buchwald, S. L. A highly active catalyst for Suzuki-Miyaura cross-coupling reactions of heteroaryl compounds Angew. Chem., Int. Ed. 2006, 45, 3484-3488
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 3484-3488
    • Billingsley, K.L.1    Anderson, K.W.2    Buchwald, S.L.3
  • 27
    • 33645805657 scopus 로고    scopus 로고
    • In vitro P-glycoprotein inhibition assays for assessment of clinical drug interaction potential of new drug candidates: A recommendation for probe substrates
    • Rautio, J.; Humphreys, J. E.; Webster, L. O.; Balakrishnan, A.; Keogh, J. P.; Kunta, J. R.; Serabjit-Singh, C. J.; Polli, J. W. In vitro P-glycoprotein inhibition assays for assessment of clinical drug interaction potential of new drug candidates: a recommendation for probe substrates Drug Metab. Dispos. 2006, 34, 786-792
    • (2006) Drug Metab. Dispos. , vol.34 , pp. 786-792
    • Rautio, J.1    Humphreys, J.E.2    Webster, L.O.3    Balakrishnan, A.4    Keogh, J.P.5    Kunta, J.R.6    Serabjit-Singh, C.J.7    Polli, J.W.8
  • 29


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.