-
1
-
-
78651363548
-
Angiotensin II receptors and drug discovery in cardiovascular disease
-
Dasgupta C, Zhang L. Angiotensin II receptors and drug discovery in cardiovascular disease. Drug Discov Today 2011;16:22-34
-
(2011)
Drug Discov Today
, Issue.16
, pp. 22-34
-
-
Dasgupta, C.1
Zhang, L.2
-
2
-
-
84880159174
-
Targeting the renin Angiotensin Aldosterone system in heart failure
-
Lang CC, Struthers DA. Targeting the renin Angiotensin Aldosterone system in heart failure. Nat Rev Cardiol 2013;10:125-34
-
(2013)
Nat Rev Cardiol
, Issue.10
, pp. 125-134
-
-
Lang, C.C.1
Struthers, D.A.2
-
3
-
-
84871620989
-
Key developments in renin-Angiotensin aldosterone system
-
Pessôa BS, Van der Lubbe N, Verdonk K, et al. Key developments in renin-Angiotensin aldosterone system. Nat Rev Nephrol 2013;9:26-36
-
(2013)
Nat Rev Nephrol
, Issue.9
, pp. 26-36
-
-
Pessôa, B.S.1
Van Der Lubbe, N.2
Verdonk, K.3
-
4
-
-
78649449966
-
Angiotensin II receptor type 1 (AT1) selective nonpeptidic antagonists a perspective
-
Naik P, Murumkar P, Giridhar R, et al. Angiotensin II receptor type 1 (AT1) selective nonpeptidic antagonists - a perspective. Bioorg Med Chem 2010;18:8418-56
-
(2010)
Bioorg Med Chem
, Issue.18
, pp. 8418-8456
-
-
Naik, P.1
Murumkar, P.2
Giridhar, R.3
-
5
-
-
84878287822
-
It is time to reconsider the cardiovascular protection afforded by RAAS blockade-overview of RAAS systems
-
Tsukamoto O, Kitakaze M. It is time to reconsider the cardiovascular protection afforded by RAAS blockade-overview of RAAS systems. Cardiovasc Drugs Ther 2013;27:133-8
-
(2013)
Cardiovasc Drugs Ther
, Issue.27
, pp. 133-138
-
-
Tsukamoto, O.1
Kitakaze, M.2
-
7
-
-
84555190258
-
Emerging drugs which target rennin-Angiotensin-Aldosterone system
-
Steckelings UM, Paulis L, Unger T, et al. Emerging drugs which target rennin-Angiotensin-Aldosterone system. Expert Opin Emerg Drugs 2011;16:619-30
-
(2011)
Expert Opin Emerg Drugs
, Issue.16
, pp. 619-630
-
-
Steckelings, U.M.1
Paulis, L.2
Unger, T.3
-
24
-
-
33845538684
-
Angiotensin II and inflammation: The effect of angiotensin-converting enzyme inhibition and angiotensin II receptor blockade
-
Dandona P, Dhindsa S, Ghanim H, et al. Angiotensin II and inflammation: The effect of angiotensin-converting enzyme inhibition and angiotensin II receptor blockade. J Hum Hyp 2007;21:20-7
-
(2007)
J Hum Hyp
, vol.21
, pp. 20-27
-
-
Dandona, P.1
Dhindsa, S.2
Ghanim, H.3
-
34
-
-
84886920785
-
In silico identification of novel lead compounds with AT1 receptor antagonist activity: Successful application of chemical database screening protocol
-
Mahima P, Sarvesh P. In silico identification of novel lead compounds with AT1 receptor antagonist activity: Successful application of chemical database screening protocol. Org Med Chem Lett. 2012.2(1):7
-
(2012)
Org Med Chem Lett
, vol.2
, Issue.1
, pp. 7
-
-
Mahima, P.1
Sarvesh, P.2
-
36
-
-
84886930685
-
1, 3,5-substituted imidazoles and their use in the treatment of hypertension and methods for their preparation
-
Matsoukas J, Maragoudakis M, Vlachakos D, et al. 1,3,5-substituted imidazoles and their use in the treatment of hypertension and methods for their preparation. MX012755; 2009
-
(2009)
MX012755
-
-
Matsoukas, J.1
Maragoudakis, M.2
Vlachakos, D.3
-
37
-
-
84886920382
-
-
US0216854
-
Matsoukas J, Gavras C, Vlachakos D, et al. 1,3 and 1,3,5 substituted imidazoles as antihypertensives. US0216854; 2010
-
(2010)
1,3 and 1, 35 Substituted Imidazoles As Antihypertensives
-
-
Matsoukas, J.1
Gavras, C.2
Vlachakos, D.3
-
39
-
-
77955653002
-
An efficient synthesis of a rationally design 1,5 disubstituted imidazole AT1 angiotensin receptor antagonist: Reorientation of imidazole pharmacophore groups in losartan reserves high receptor affinity and confirms docking studies
-
Roumelioti P, Resvani A, Durdagi S, et al. An efficient synthesis of a rationally design 1,5 disubstituted imidazole AT1 angiotensin receptor antagonist: Reorientation of imidazole pharmacophore groups in losartan reserves high receptor affinity and confirms docking studies. J Comput Aided Mol Des 2010;24:749-58
-
(2010)
J Comput Aided Mol Des
, Issue.24
, pp. 749-758
-
-
Roumelioti, P.1
Resvani, A.2
Durdagi, S.3
-
40
-
-
78751508595
-
Towards non-peptide Ang II AT1 receptor antagonists based on urocanic acid: Rational design, synthesis and biological evaluation
-
Agelis G, Resvani A, Matsoukas A, et al. Towards non-peptide Ang II AT1 receptor antagonists based on urocanic acid: Rational design, synthesis and biological evaluation. Aminoacids 2011;40:411-20
-
(2011)
Aminoacids
, Issue.40
, pp. 411-420
-
-
Agelis, G.1
Resvani, A.2
Matsoukas, A.3
-
41
-
-
84865802763
-
The discovery of new potent non-peptide Angiotensin II AT1 receptor blockers: A concise synthesis, molecular docking studies and biological evaluation of N-substituted 5-butylimidazole derivatives
-
Agelis G, Resvani A, Durdagi S, et al. The discovery of new potent non-peptide Angiotensin II AT1 receptor blockers: A concise synthesis, molecular docking studies and biological evaluation of N-substituted 5-butylimidazole derivatives. Eur J Med Chem 2012;55:358-74
-
(2012)
Eur J Med Chem
, Issue.55
, pp. 358-374
-
-
Agelis, G.1
Resvani, A.2
Durdagi, S.3
-
42
-
-
84873052698
-
Rational design, efficient syntheses and biological evaluation of N, N'-symmetrically bis-substituted butylimidazole analogs as a new class of potent angiotensin II receptor blockers
-
Agelis G, Resvani A, Koukoulitsa C, et al. Rational design, efficient syntheses and biological evaluation of N, N'-symmetrically bis-substituted butylimidazole analogs as a new class of potent angiotensin II receptor blockers. Eur J Med Chem 2013;62:352-70
-
(2013)
Eur J Med Chem
, Issue.62
, pp. 352-370
-
-
Agelis, G.1
Resvani, A.2
Koukoulitsa, C.3
-
43
-
-
84877080243
-
Interactions Of The Potent Synthetic AT1 Antagonist Analog BV6 With Membrane Bilayers And Mesoporous Silicate Matrices
-
Mavromoustakos T, Agelis G, Resvani A, et al. Interactions of the potent synthetic AT1 antagonist analog BV6 with membrane bilayers and mesoporous silicate matrices. Biochim Biophys Acta 2013;1828:1846-55
-
(2013)
Biochim Biophys Acta
, pp. 1828-1846
-
-
Mavromoustakos, T.1
Agelis, G.2
Resvani, A.3
-
52
-
-
80155165710
-
Novel paramagnetic AT1 receptor antagonists
-
Tan NP, Taylor MK, Bottle SE, et al. Novel paramagnetic AT1 receptor antagonists. Chem Commun 2011;47:12083-5
-
(2011)
Chem Commun
, Issue.47
, pp. 12083-12085
-
-
Tan, N.P.1
Taylor, M.K.2
Bottle, S.E.3
-
53
-
-
84860224428
-
Peroxisome proliferator-Activated receptor-g activation with angiotensin II type 1 receptor blockade is pivotal for the prevention of blood-brain barrier impairment and cognitive decline in type 2 diabetic mice
-
Min LJ, Mogi M, Shudou M, et al. Peroxisome proliferator-Activated receptor-g activation with angiotensin II type 1 receptor blockade is pivotal for the prevention of blood-brain barrier impairment and cognitive decline in type 2 diabetic mice. Hypertension 2012;59:1079-88
-
(2012)
Hypertension
, Issue.59
, pp. 1079-1088
-
-
Min, L.J.1
Mogi, M.2
Shudou, M.3
-
54
-
-
84880941726
-
A systematic comparison of the properties of clinically used angiotensin II type 1 receptor antagonists
-
Martin MC, Foster MC, Brunner HR, et al. A systematic comparison of the properties of clinically used angiotensin II type 1 receptor antagonists. Pharmacol Rev 2013;65:809-48
-
(2013)
Pharmacol Rev
, Issue.65
, pp. 809-848
-
-
Martin, M.C.1
Foster, M.C.2
Brunner, H.R.3
-
55
-
-
1542547460
-
Identification of telmisartan as a unique angiotensin II receptor antagonist with selective PPARg-modulating activity
-
Benson CS, Pershadsingh HA, Ho CI, et al. Identification of telmisartan as a unique angiotensin II receptor antagonist with selective PPARg-modulating activity. Hypertension 2004;43:993-1002
-
(2004)
Hypertension
, vol.43
, pp. 993-1002
-
-
Benson, C.S.1
Pershadsingh, H.A.2
Ho, C.I.3
-
56
-
-
2442451618
-
Angiotensin type 1 receptor blockers induce peroxisome proliferator activated receptor-g activity
-
Schupp M, Janke J, Clasen R. Angiotensin type 1 receptor blockers induce peroxisome proliferator activated receptor-g activity. Circulation 2004;109:2054-7
-
(2004)
Circulation
, vol.109
, pp. 2054-2057
-
-
Schupp, M.1
Janke, J.2
Clasen, R.3
-
61
-
-
84864912078
-
Fimasartan, a novel angiotensin II receptor antagonist
-
Kim JH, Lee JH, Paik SH, et al. Fimasartan, a novel angiotensin II receptor antagonist. Arch Pharm Res 2012;35:1123-6
-
(2012)
Arch Pharm Res
, Issue.35
, pp. 1123-1126
-
-
Kim, J.H.1
Lee, J.H.2
Paik, S.H.3
-
62
-
-
0035852724
-
Angiotensin II type 1 receptor blockers
-
Burnier M. Angiotensin II type 1 receptor blockers. Circulation 2001;103:904-12
-
(2001)
Circulation
, vol.103
, pp. 904-912
-
-
Burnier, M.1
-
63
-
-
33646482724
-
Improvement of solubility and stability of valsartan by hydroxypropyl-b-cyclodextrin
-
Cappelo B, Di Maio C, Iervolino M, Miro A. Improvement of solubility and stability of valsartan by hydroxypropyl-b-cyclodextrin. J Incl Phenom Macro 2006;54:289-94
-
(2006)
J Incl Phenom Macro
, vol.54
, pp. 289-294
-
-
Cappelo, B.1
Di Maio, C.2
Iervolino, M.3
Miro, A.4
-
64
-
-
84863107521
-
Dual inhibitors for aspartic proteases HIV-1 PR and renin: Advancements in AIDS-hypertension-diabetes linkage via molecular dynamics, inhibition assays, and binding free energy calculations
-
Tzoupis H, Leonis G, Megariotis G, et al. Dual inhibitors for aspartic proteases HIV-1 PR and renin: Advancements in AIDS-hypertension-diabetes linkage via molecular dynamics, inhibition assays, and binding free energy calculations. J Med Chem 2012;55:5784-96
-
(2012)
J Med Chem
, Issue.55
, pp. 5784-5796
-
-
Tzoupis, H.1
Leonis, G.2
Megariotis, G.3
-
65
-
-
84865589426
-
Comparative study of the at1 receptor prodrug antagonist candesartan cilexetil with other sartans on the interactions with membrane bilayers
-
Fotakis C, Megariotis G, Christodouleas D, et al. Comparative study of the AT1 receptor prodrug antagonist candesartan cilexetil with other sartans on the interactions with membrane bilayers. Biochim Biophys Acta 2012;1818:3107-20
-
(2012)
Biochim Biophys Acta
, vol.1818
, pp. 3107-3120
-
-
Fotakis, C.1
Megariotis, G.2
Christodouleas, D.3
-
66
-
-
84860390562
-
Thermal, dynamic and structural properties of drug AT1 antagonist olmesartan in lipid bilayers
-
Ntountaniotis D, Mali G, Grdadolnik SG, et al. Thermal, dynamic and structural properties of drug AT1 antagonist olmesartan in lipid bilayers. Biochim Biophys Acta 2011;808:2995-3006
-
(2011)
Biochim Biophys Acta
, Issue.808
, pp. 2995-3006
-
-
Ntountaniotis, D.1
Mali, G.2
Grdadolnik, S.G.3
-
67
-
-
79956091106
-
Comparative biophysical studies of sartan class drug molecules losartan and candesartan (CV- 11974) with membrane bilayers
-
Fotakis C, Christodouleas D, Zoumpoulakis P, et al. Comparative biophysical studies of sartan class drug molecules losartan and candesartan (CV- 11974) with membrane bilayers. J Phys Chem B 2011;115:6180-92
-
(2011)
J Phys Chem B
, Issue.115
, pp. 6180-6192
-
-
Fotakis, C.1
Christodouleas, D.2
Zoumpoulakis, P.3
-
69
-
-
79954794881
-
Interactions Of The AT1 Antagonist Valsartan With Dipalmitoyl- phosphatidylcholine Bilayers
-
Potamitis C, Chatzigeorgiou P, Siapi E, et al. Interactions of the AT1 antagonist valsartan with dipalmitoyl-phosphatidylcholine bilayers. Biochim Biophys Acta 2011;1808:1753-63
-
(2011)
Biochim Biophys Acta
, vol.1808
, pp. 1753-1763
-
-
Potamitis, C.1
Chatzigeorgiou, P.2
Siapi, E.3
-
70
-
-
65349139121
-
Antihypertensive drug valsartan in solution and at the AT1 receptor: Conformational analysis, dynamic NMR spectroscopy, in silico docking and molecular dynamics simulations
-
Potamitis C, Zervou M, Katsiaras V, et al. Antihypertensive drug valsartan in solution and at the AT1 receptor: Conformational analysis, dynamic NMR spectroscopy, in silico docking and molecular dynamics simulations. J Chem Inf Model 2009;49:726-39
-
(2009)
J Chem Inf Model
, vol.49
, pp. 726-739
-
-
Potamitis, C.1
Zervou, M.2
Katsiaras, V.3
-
71
-
-
84865802763
-
The discovery of new potent non-peptide Angiotensin II AT1 receptor blockers: A concise synthesis, molecular docking studies and biological evaluation of N-substituted 5-butylimidazole derivatives
-
Agelis D, Resvani A, Durdagi S, et al. The discovery of new potent non-peptide Angiotensin II AT1 receptor blockers: A concise synthesis, molecular docking studies and biological evaluation of N-substituted 5-butylimidazole derivatives. Eur J Med Chem 2012;55:358-74
-
(2012)
Eur J Med Chem
, vol.55
, pp. 358-374
-
-
Agelis, D.1
Resvani, A.2
Durdagi, S.3
-
72
-
-
78649526211
-
Development of accurate binding affinity predictions of novel renin inhibitors through molecular docking studies
-
Politi A, Durdagi S, Moutevelis- Minakaki P, et al. Development of accurate binding affinity predictions of novel renin inhibitors through molecular docking studies. J Mole Graph & Model 2010;29:425-35
-
(2010)
J Mole Graph & Model
, Issue.29
, pp. 425-435
-
-
Politi, A.1
Durdagi, S.2
Moutevelis-Minakaki, P.3
-
73
-
-
67650395306
-
Application of 3D QSAR CoMFA/CoMSIA and in silico docking studies on novel renin inhibitors against cardiovascular diseases
-
Politi A, Durdagi S, Moutevelis- Minakaki P, et al. Application of 3D QSAR CoMFA/CoMSIA and in silico docking studies on novel renin inhibitors against cardiovascular diseases. Euro J Med Chem 2009;44:3703-11
-
(2009)
Euro J Med Chem
, vol.44
, pp. 3703-3711
-
-
Politi, A.1
Durdagi, S.2
Moutevelis- Minakaki, P.3
-
74
-
-
77955653002
-
An efficient synthesis of a rationally designed 1,5 disubstituted imidazole AT (1) Angiotensin II receptor antagonist: Reorientation of imidazole pharmacophore groups in losartan reserves high receptor affinity and confirms docking studies
-
Agelis G, Roumelioti P, Resvani A, et al. An efficient synthesis of a rationally designed 1,5 disubstituted imidazole AT (1) Angiotensin II receptor antagonist: Reorientation of imidazole pharmacophore groups in losartan reserves high receptor affinity and confirms docking studies. J Comput Aided Mole Des 2010;49:726-39
-
(2010)
J Comput Aided Mole Des
, Issue.49
, pp. 726-739
-
-
Agelis, G.1
Roumelioti, P.2
Resvani, A.3
|