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Volumn 3, Issue 3, 2011, Pages 367-390

Crystal structures of 11β-hydroxysteroid dehydrogenase type 1 and their use in drug discovery

Author keywords

[No Author keywords available]

Indexed keywords

11BETA HYDROXYSTEROID DEHYDROGENASE 1; 11BETA HYDROXYSTEROID DEHYDROGENASE 2; HYDROCORTISONE; INCB 13739; LIGAND; METFORMIN; OXIDOREDUCTASE INHIBITOR; PROTEIN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; UNCLASSIFIED DRUG;

EID: 79953235168     PISSN: 17568919     EISSN: None     Source Type: Journal    
DOI: 10.4155/fmc.10.282     Document Type: Review
Times cited : (26)

References (58)
  • 1
    • 72449133267 scopus 로고    scopus 로고
    • Obesity and corticosteroids: 11β-hydroxysteroid type 1 as a cause and therapeutic target in metabolic disease
    • Reviews the evidence that 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) is a good target for metabolic disease intervention
    • Morton NM. Obesity and corticosteroids: 11β-hydroxysteroid type 1 as a cause and therapeutic target in metabolic disease. Mol. Cell. Endocrinol. 316, 154-164 (2010). Reviews the evidence that 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) is a good target for metabolic disease intervention.
    • (2010) Mol. Cell. Endocrinol , vol.316 , pp. 154-164
    • Morton, N.M.1
  • 2
    • 2942675088 scopus 로고    scopus 로고
    • Obesity, metabolic syndrome, and cardiovascular disease
    • DOI 10.1210/jc.2004-0372
    • Grundy SM. Obesity, metabolic syndrome, and cardiovascular disease. J. Clin. Endocrinol. Metab. 89, 2595-2600 (2004). (Pubitemid 38766337)
    • (2004) Journal of Clinical Endocrinology and Metabolism , vol.89 , Issue.6 , pp. 2595-2600
    • Grundy, S.M.1
  • 4
    • 33751215200 scopus 로고    scopus 로고
    • Cortisol - Cause and cure for metabolic syndrome?
    • DOI 10.1111/j.1464-5491.2006.01998.x
    • Walker BR. Cortisol - cause and cure for metabolic syndrome? Diabet. Med. 23, 1281-1288 (2006). (Pubitemid 44787789)
    • (2006) Diabetic Medicine , vol.23 , Issue.12 , pp. 1281-1288
    • Walker, B.R.1
  • 5
    • 0027288233 scopus 로고
    • Glucocorticoids regulate the induction of phosphoenolpyruvate carboxykinase (GTP) gene transcription during diabetes
    • Friedman JE, Yun JS, Patel YM, McGrane MM, Hanson RW. Glucocorticoids regulate the induction of phosphoenolpyruvate carboxykinase (GTP) gene transcription during diabetes. J. Biol. Chem. 268, 12952-12957 (1993). (Pubitemid 23182469)
    • (1993) Journal of Biological Chemistry , vol.268 , Issue.17 , pp. 12952-12957
    • Friedman, J.E.1    Yun, J.S.2    Patel, Y.M.3    McGrane, M.M.4    Hanson, R.W.5
  • 6
    • 15444366462 scopus 로고    scopus 로고
    • The role of glucocorticoid action in the pathophysiology of the metabolic syndrome
    • Wang M. The role of glucocorticoid action in the pathophysiology of the metabolic syndrome. Nutr. Metab. 2, 3 (2005).
    • (2005) Nutr. Metab. , vol.2 , pp. 3
    • Wang, M.1
  • 9
    • 34447105433 scopus 로고    scopus 로고
    • Inhibition of 11ß-hydroxysteroid dehydrogenase type 1 as a promising therapeutic target
    • DOI 10.1016/j.drudis.2007.06.001, PII S1359644607002280
    • Wamil M, Seckl JR. Inhibition of 11β-hydroxysteroid dehydrogenase type 1 as a promising therapeutic target. Drug Discov. Today 12, 504-520 (2007). (Pubitemid 47031664)
    • (2007) Drug Discovery Today , vol.12 , Issue.13-14 , pp. 504-520
    • Wamil, M.1    Seckl, J.R.2
  • 10
    • 0033018598 scopus 로고    scopus 로고
    • Cortisol effects on body mass, blood pressure, and cholesterol in the general population
    • Fraser R, Ingram MC, Anderson NH, Morrison C, Davies E, Connell JMC. Cortisol effects on body mass, blood pressure, and cholesterol in the general population. Hypertension 33, 1364-1368 (1999). (Pubitemid 29282655)
    • (1999) Hypertension , vol.33 , Issue.6 , pp. 1364-1368
    • Fraser, R.1    Ingram, M.C.2    Anderson, N.H.3    Morrison, C.4    Davies, E.5    Connell, J.M.C.6
  • 11
    • 0028324103 scopus 로고
    • 11β-Hydroxysteroid dehydrogenase activity and corticosteroid hormone action
    • DOI 10.1016/0039-128X(94)90082-5
    • Stewart PM, Whorwood CB. 11β-hydroxysteroid dehydrogenase activity and corticosteroid hormone action. Steroids 59, 90-95 (1994). (Pubitemid 24080364)
    • (1994) Steroids , vol.59 , Issue.2 , pp. 90-95
    • Stewart, P.M.1    Whorwood, C.B.2
  • 12
    • 0031572610 scopus 로고    scopus 로고
    • The 11β-hydroxysteroid dehydrogenase system, a determinant of glucocorticoid and mineralocorticoid action: Function, gene organization and protein structures of 11β-hydroxysteroid dehydrogenase isoforms
    • Oppermann UCT, Persson B, Jörnvall H.The 11β-hydroxysteroid dehydrogenase system, a determinant of glucocorticoid and mineralocorticoid action: Function, gene organization and protein structures of 11β-hydroxysteroid dehydrogenase isoforms. Eur. J. Biochem. 249, 355-360 (1997).
    • (1997) Eur. J. Biochem. , vol.249 , pp. 355-360
    • Oppermann, U.C.T.1    Persson, B.2    Jörnvall, H.3
  • 13
    • 85047683614 scopus 로고    scopus 로고
    • Minireview: 11β-hydroxysteroid dehydrogenase type 1 - A tissue-specific amplifier of glucocorticoid action
    • DOI 10.1210/en.142.4.1371
    • Seckl JR, Walker BR. 11β-hydroxysteroid dehydrogenase type 1 - a tissue-specific amplifier of glucocorticoid action. Endocrinology 142, 1371-1376 (2001). (Pubitemid 32299662)
    • (2001) Endocrinology , vol.142 , Issue.4 , pp. 1371-1376
    • Seckl, J.R.1    Walker, B.R.2
  • 14
    • 0023242981 scopus 로고
    • Mineralocorticoid activity of liquorice: 11β-hydroxysteroid dehydrogenase deficiency comes of age
    • Stewart PM, Valentino R, Wallace AM, Burt D, Shackleton CHL, Edwards CRW. Mineralocorticoid activity of liquorice: 11β-hydroxysteroid dehydrogenase deficiency comes of age. Lancet 330, 821-824 (1987).
    • (1987) Lancet , vol.330 , pp. 821-824
    • Stewart, P.M.1    Valentino, R.2    Wallace, A.M.3    Burt, D.4    Shackleton, C.H.L.5    Edwards, C.R.W.6
  • 15
    • 0028081325 scopus 로고
    • NAD+-dependent isoform of 11β-hydroxysteroid dehydrogenase
    • Agarwal AK, Mune T, Monder C, White PC. NAD+-dependent isoform of 11β-hydroxysteroid dehydrogenase. J. Biol. Chem. 269, 25959-25962 (1994).
    • (1994) J. Biol. Chem. , vol.269 , pp. 25959-25962
    • Agarwal, A.K.1    Mune, T.2    Monder, C.3    White, P.C.4
  • 16
    • 15944394711 scopus 로고    scopus 로고
    • Adipocyte-specific glucocorticoid inactivation protects against diet-induced obesity
    • DOI 10.2337/diabetes.54.4.1023
    • Kershaw EE, Morton NM, Dhillon H, Ramage L, Seckl JR, Flier JS. Adipocyte-specific glucocorticoid inactivation protects against diet-induced obesity. Diabetes 54, 1023-1031 (2005). (Pubitemid 40446315)
    • (2005) Diabetes , vol.54 , Issue.4 , pp. 1023-1031
    • Kershaw, E.E.1    Morton, N.M.2    Dhillon, H.3    Ramage, L.4    Seckl, J.R.5    Flier, J.S.6
  • 21
    • 77956489883 scopus 로고    scopus 로고
    • Targeting the prereceptor metabolism of cortisol as a novel therapy in obesity and diabetes
    • Reviews the role of cortisol in disease as well as the reports of in vivo pharmacological inhibition of 11β-HSD1
    • Gathercole LL, Stewart PM. Targeting the prereceptor metabolism of cortisol as a novel therapy in obesity and diabetes. J. Steroid Biochem. Molec. Biol. 122, 21-27 (2010). Reviews the role of cortisol in disease as well as the reports of in vivo pharmacological inhibition of 11β-HSD1.
    • (2010) J. Steroid Biochem. Molec. Biol. , vol.122 , pp. 21-27
    • Gathercole, L.L.1    Stewart, P.M.2
  • 22
    • 0028839840 scopus 로고
    • Carbenoxolone increases hepatic insulin sensitivity in man: A novel role for 11-oxosteroid reductase in enhancing glucocorticoid receptor activation
    • Walker BR, Connacher AA, Lindsay RM, Webb DJ, Edwards CR. Carbenoxolone increases hepatic insulin sensitivity in man: A novel role for 11-oxosteroid reductase in enhancing glucocorticoid receptor activation. J. Clin. Endocrinol. Metab. 80, 3155-3159 (1995).
    • (1995) J. Clin. Endocrinol. Metab. , vol.80 , pp. 3155-3159
    • Walker, B.R.1    Connacher, A.A.2    Lindsay, R.M.3    Webb, D.J.4    Edwards, C.R.5
  • 23
    • 77955630861 scopus 로고    scopus 로고
    • The 11β-hydroxysteroid dehydrogenase type 1 inhibitor INCB13739 improves hyperglycemia in patients with Type 2 diabetes inadequately controlled by metformin monotherapy
    • Rosenstock J, Banarer S, Fonseca VA et al. The 11β-hydroxysteroid dehydrogenase type 1 inhibitor INCB13739 improves hyperglycemia in patients with Type 2 diabetes inadequately controlled by metformin monotherapy. Diabetes Care 33, 1516-1522 (2010).
    • (2010) Diabetes Care , vol.33 , pp. 1516-1522
    • Rosenstock, J.1    Banarer, S.2    Fonseca, V.A.3
  • 24
    • 38149133022 scopus 로고    scopus 로고
    • 11β-hydroxysteroid dehydrogenase type 1 inhibitors as therapeutic agents
    • Reviews the development of 11β-HSD1 inhibitors
    • Webster SP, Pallin TD. 11β-hydroxysteroid dehydrogenase type 1 inhibitors as therapeutic agents. Expert Opin. Ther. Patents 17, 1407-1422 (2007). Reviews the development of 11β-HSD1 inhibitors.
    • (2007) Expert Opin. Ther. Patents , vol.17 , pp. 1407-1422
    • Webster, S.P.1    Pallin, T.D.2
  • 25
    • 42149162795 scopus 로고    scopus 로고
    • 11-Beta-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitors in type 2 diabetes mellitus and obesity
    • DOI 10.1517/13543784.17.4.481
    • Hughes KA, Webster SP, Walker BR. 11-b-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitors in Type 2 diabetes mellitus and obesity. Expert Opin. Investig. Drugs 17, 481-496 (2008). Reviews the development of 11β-HSD1 inhibitors. (Pubitemid 351578167)
    • (2008) Expert Opinion on Investigational Drugs , vol.17 , Issue.4 , pp. 481-496
    • Hughes, K.A.1    Webster, S.P.2    Walker, B.R.3
  • 26
    • 41149085727 scopus 로고    scopus 로고
    • Inhibitors of 11β-hydroxysteroid dehydrogenase type 1
    • Reviews the development of 11β-HSD1 inhibitors
    • Su X, Vicker N, Potter BVL. Inhibitors of 11β-hydroxysteroid dehydrogenase type 1. Prog. Med. Chem. 46, 29-130 (2008). Reviews the development of 11β-HSD1 inhibitors.
    • (2008) Prog. Med. Chem. , vol.46 , pp. 29-130
    • Su, X.1    Vicker, N.2    Potter, B.V.L.3
  • 27
    • 67649362287 scopus 로고    scopus 로고
    • 11β-hydroxysteroid dehydrogenase type 1 inhibitors: A review of recent patents
    • Reviews the development of 11β-HSD1 inhibitors
    • Boyle CD, Kowalski TJ. 11β-hydroxysteroid dehydrogenase type 1 inhibitors: A review of recent patents. Expert Opin. Ther. Patents 19, 801-825 (2009). Reviews the development of 11β-HSD1 inhibitors.
    • (2009) Expert Opin. Ther. Patents , vol.19 , pp. 801-825
    • Boyle, C.D.1    Kowalski, T.J.2
  • 30
    • 66749093622 scopus 로고    scopus 로고
    • N-(Pyridin-2-yl) arylsulfonamide inhibitors of 11β-hydroxysteroid dehydrogenase type 1: Discovery of PF-915275
    • Siu M, Johnson TO, Wang Y et al. N-(Pyridin-2-yl) arylsulfonamide inhibitors of 11β-hydroxysteroid dehydrogenase type 1: Discovery of PF-915275. Bioorg. Med. Chem. Lett. 19, 3493-3497 (2009).
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 3493-3497
    • Siu, M.1    Johnson, T.O.2    Wang, Y.3
  • 31
    • 77953182919 scopus 로고    scopus 로고
    • Discovery of a potent, orally active 11β-hydroxysteroid dehydrogenase type 1 inhibitor for clinical study: Identification of (S)-2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol- 4(5H)-one (AMG 221)
    • Véniant MM, Hale C, Hungate RW et al. Discovery of a potent, orally active 11β-hydroxysteroid dehydrogenase type 1 inhibitor for clinical study: Identification of (S)-2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2- ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one (AMG 221). J. Med. Chem. 53, 4481-4487 (2010).
    • (2010) J. Med. Chem. , vol.53 , pp. 4481-4487
    • Véniant, M.M.1    Hale, C.2    Hungate, R.W.3
  • 32
    • 77954141448 scopus 로고    scopus 로고
    • Discovery of adamantyl ethanone derivatives as potent 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD-1) inhibitors
    • Su X, Pradaux-Caggiano F, Thomas MP et al. Discovery of adamantyl ethanone derivatives as potent 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD-1) inhibitors. ChemMedChem 5, 1577-1593 (2010).
    • (2010) ChemMedChem , vol.5 , pp. 1577-1593
    • Su, X.1    Pradaux-Caggiano, F.2    Thomas, M.P.3
  • 33
    • 77952625669 scopus 로고    scopus 로고
    • 11β-hydroxysteroid dehydrogenase type 1 expression is increased in the aged mouse hippocampus and parietal cortex and causes memory impairments
    • Holmes MC, Carter RN, Noble J et al. 11β-hydroxysteroid dehydrogenase type 1 expression is increased in the aged mouse hippocampus and parietal cortex and causes memory impairments. J. Neurosci. 30, 6916-6920 (2010).
    • (2010) J. Neurosci. , vol.30 , pp. 6916-6920
    • Holmes, M.C.1    Carter, R.N.2    Noble, J.3
  • 34
    • 77958067558 scopus 로고    scopus 로고
    • Partial deficiency or short-term inhibition of 11β-hydroxysteroid dehydrogenase type 1 improves cognitive function in aging mice
    • Sooy K, Webster SP, Noble J et al. Partial deficiency or short-term inhibition of 11β-hydroxysteroid dehydrogenase type 1 improves cognitive function in aging mice. J. Neurosci. 30, 13867-13872 (2010).
    • (2010) J. Neurosci. , vol.30 , pp. 13867-13872
    • Sooy, K.1    Webster, S.P.2    Noble, J.3
  • 35
    • 14244252559 scopus 로고    scopus 로고
    • Conformational flexibility in crystal structures of human 11β-hydroxysteroid dehydrogenase type I provide insights into glucocorticoid interconversion and enzyme regulation
    • DOI 10.1074/jbc.M411104200
    • Hosfield DJ, Wu Y, Skene RJ et al. Conformational flexibility in crystal structures of human 11β-hydroxysteroid dehydrogenase type 1 provide insights into glucocorticoid interconversion and enzyme regulation. J. Biol. Chem. 280, 4639-4648 (2005). References [35-52] describe the crystal structures that are the subject of this review. (Pubitemid 40288633)
    • (2005) Journal of Biological Chemistry , vol.280 , Issue.6 , pp. 4639-4648
    • Hosfield, D.J.1    Wu, Y.2    Skene, E.J.3    Hilgers, M.4    Jennings, A.5    Snell, G.P.6    Aertgeerts, K.7
  • 38
    • 35148832557 scopus 로고    scopus 로고
    • The discovery of 2-anilinothiazolones as 11β-HSD1 inhibitors
    • Yuan C, St. Jean DJ Jr, Liu Q et al. The discovery of 2-anilinothiazolones as 11β-HSD1 inhibitors. Bioorg. Med. Chem. Lett. 17, 6056-6061 (2007).
    • (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 6056-6061
    • Yuan, C.1    St. Jean Jr., D.J.2    Liu, Q.3
  • 40
    • 37849041637 scopus 로고    scopus 로고
    • Structural characterization and pharmacodynamic effects of an orally active 11β-hydroxysteroid dehydrogenase type 1 inhibitor
    • Hale C, Véniant M, Wang Z et al. Structural characterization and pharmacodynamic effects of an orally active 11β-hydroxysteroid dehydrogenase type 1 inhibitor. Chem. Biol. Drug Des. 71, 36-44 (2008).
    • (2008) Chem. Biol. Drug Des. , vol.71 , pp. 36-44
    • Hale, C.1    Véniant, M.2    Wang, Z.3
  • 44
    • 52949108814 scopus 로고    scopus 로고
    • Distinctive molecular inhibition mechanisms for selective inhibitors of human 11β-hydroxysteroid dehydrogenase type 1
    • Tu H, Powers JP, Liu J et al. Distinctive molecular inhibition mechanisms for selective inhibitors of human 11β-hydroxysteroid dehydrogenase type 1. Bioorg. Med. Chem. 16, 8922-8931 (2008).
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 8922-8931
    • Tu, H.1    Powers, J.P.2    Liu, J.3
  • 45
    • 58149087619 scopus 로고    scopus 로고
    • Further studies with the 2-amino-1,3-thiazol-4(5H)-one class of 11β-hydroxysteroid dehydrogenase type 1 inhibitors: Reducing pregnane X receptor activity and exploring activity in a monkey pharmacodynamic model
    • Fotsch C, Bartberger MD, Bercot EA et al. Further studies with the 2-amino-1,3-thiazol-4(5H)-one class of 11β-hydroxysteroid dehydrogenase type 1 inhibitors: Reducing pregnane X receptor activity and exploring activity in a monkey pharmacodynamic model. J. Med. Chem. 51, 7953-7967 (2008).
    • (2008) J. Med. Chem. , vol.51 , pp. 7953-7967
    • Fotsch, C.1    Bartberger, M.D.2    Bercot, E.A.3
  • 46
    • 60449117428 scopus 로고    scopus 로고
    • Optimization of novel di-substituted cyclohexylbenzamide derivatives as potent 11β-HSD1 inhibitors
    • McMinn DL, Rew Y, Sudom A et al. Optimization of novel di-substituted cyclohexylbenzamide derivatives as potent 11β-HSD1 inhibitors. Bioorg. Med. Chem. Lett. 19, 1446-1450 (2009).
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 1446-1450
    • McMinn, D.L.1    Rew, Y.2    Sudom, A.3
  • 47
    • 61349172663 scopus 로고    scopus 로고
    • Discovery and optimization of piperidyl benzamide derivatives as a novel class of 11β-HSD1 inhibitors
    • Rew Y, McMinn DL, Wang Z et al. Discovery and optimization of piperidyl benzamide derivatives as a novel class of 11β-HSD1 inhibitors. Bioorg. Med. Chem. Lett. 19, 1797-1801 (2009).
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 1797-1801
    • Rew, Y.1    McMinn, D.L.2    Wang, Z.3
  • 48
    • 69949107020 scopus 로고    scopus 로고
    • Efficacious 11β-hydroxysteroid dehydrogenase type 1 inhibitors in the diet-induced obesity mouse model
    • Wan Z-K, Chenail E, Xiang J et al. Efficacious 11β-hydroxysteroid dehydrogenase type 1 inhibitors in the diet-induced obesity mouse model. J. Med. Chem. 52, 5449-5461 (2009).
    • (2009) J. Med. Chem. , vol.52 , pp. 5449-5461
    • Wan, Z-.K.1    Chenail, E.2    Xiang, J.3
  • 50
    • 13644269232 scopus 로고    scopus 로고
    • The crystal structure of guinea pig 11β-hydroxysteroid dehydrogenase type 1 provides a model for enzyme-lipid bilayer interactions
    • DOI 10.1074/jbc.M412463200
    • Ogg D, Elleby B, Norström C et al. The crystal structure of guinea pig 11β-hydroxysteroid dehydrogenase type 1 provides a model for enzyme-lipid bilayer interactions. J. Biol. Chem. 280, 3789-3794 (2005). (Pubitemid 40227484)
    • (2005) Journal of Biological Chemistry , vol.280 , Issue.5 , pp. 3789-3794
    • Ogg, D.1    Elleby, B.2    Norstrom, C.3    Stefansson, K.4    Abrahmsen, L.5    Oppermann, U.6    Svensson, S.7
  • 51
    • 67650047734 scopus 로고    scopus 로고
    • Mutations of key hydrophobic surface residues of 11β-hydroxysteroid dehydrogenase type 1 increase solubility and monodispersity in a bacterial expression system
    • Lawson AJ, Walker EA, White SA, Dafforn TR, Stewart PM, Ride JP. Mutations of key hydrophobic surface residues of 11β-hydroxysteroid dehydrogenase type 1 increase solubility and monodispersity in a bacterial expression system. Protein Sci. 18, 1552-1563 (2009).
    • (2009) Protein Sci. , vol.18 , pp. 1552-1563
    • Lawson, A.J.1    Walker, E.A.2    White, S.A.3    Dafforn, T.R.4    Stewart, P.M.5    Ride, J.P.6
  • 52
    • 77950862672 scopus 로고    scopus 로고
    • The development and SAR of pyrrolidine carboxamide 11β-HSD1 inhibitors
    • Cheng H, Hoffman J, Le P et al. The development and SAR of pyrrolidine carboxamide 11β-HSD1 inhibitors. Bioorg. Med. Chem. Lett. 20, 2897-2902 (2010).
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 2897-2902
    • Cheng, H.1    Hoffman J Le, P.2
  • 53
    • 68449101064 scopus 로고    scopus 로고
    • Structure and inhibitor binding mechanisms of 11β-hydroxysteroid dehydrogenase type 1
    • Reviews the structures of 11β-HSD1 using a different approach from that adopted in this article, with which it is usefully read in conjunction
    • Wang Z, Wang M. Structure and inhibitor binding mechanisms of 11β-hydroxysteroid dehydrogenase type 1. Curr. Chem. Biol. 3, 159-170 (2009) Reviews the structures of 11β-HSD1 using a different approach from that adopted in this article, with which it is usefully read in conjunction.
    • (2009) Curr. Chem. Biol. , vol.3 , pp. 159-170
    • Wang, Z.1    Wang, M.2
  • 54
    • 0015834475 scopus 로고
    • Comparison of super-secondary structures in proteins
    • Rao ST, Rossmann MG. Comparison of super-secondary structures in proteins. J. Mol. Biol. 76, 241-256 (1973).
    • (1973) J. Mol. Biol. , vol.76 , pp. 241-256
    • Rao, S.T.1    Rossmann, M.G.2
  • 55
    • 33644905533 scopus 로고    scopus 로고
    • Active site variability of type 1 11β-hydroxysteroid dehydrogenase revealed by selective inhibitors and cross-species comparisons
    • Hult M, Shafqat N, Elleby B et al. Active site variability of type 1 11β-hydroxysteroid dehydrogenase revealed by selective inhibitors and cross-species comparisons. Mol. Cell. Endocrinol. 248, 26-33 (2006).
    • (2006) Mol. Cell. Endocrinol. , vol.248 , pp. 26-33
    • Hult, M.1    Shafqat, N.2    Elleby, B.3
  • 57
    • 78650510107 scopus 로고    scopus 로고
    • Synthesis and optimization of novel 4,4-disubstituted cyclohexylbenzamide derivatives as potent 11β-HSD1 inhibitors
    • Sun D, Wang Z, Caille S et al. Synthesis and optimization of novel 4,4-disubstituted cyclohexylbenzamide derivatives as potent 11β-HSD1 inhibitors. Bioorg. Med. Chem. Lett. 21, 405-410 (2011).
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 405-410
    • Sun, D.1    Wang, Z.2    Caille, S.3
  • 58
    • 0020997912 scopus 로고
    • Dictionary of protein secondary structure: Pattern recognition of hydrogen-bonded and geometrical features
    • Kabsch W, Sander C. Dictionary of protein secondary structure: Pattern recognition of hydrogen-bonded and geometrical features. Biopolymers 22, 2577-2637 (1983).
    • (1983) Biopolymers , vol.22 , pp. 2577-2637
    • Kabsch, W.1    Sander, C.2


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