메뉴 건너뛰기




Volumn 48, Issue 21, 2005, Pages 6632-6642

Heteroaryl-substituted naphthalenes and structurally modified derivatives: Selective inhibitors of CYP11B2 for the treatment of congestive heart failure and myocardial fibrosis

Author keywords

[No Author keywords available]

Indexed keywords

1,5 DICHLORO 6 METHOXY 2 NAPHTHALEN 2 OL; 1,5 DICHLORO 6 METHOXY 2 NAPHTHYLTRIFLUOROMETHANESULFONATE; 3 (6 METHOXY 2 NAPHTHYL)PYRIDINE; 6 CYANO 2 NAPHTHYLTRIFLUOROMETHANESULFONATE; ALDOSTERONE SYNTHASE; ANDROSTENEDIONE; AROMATASE; CORTICOSTEROID; CYTOCHROME P450 11B1; CYTOCHROME P450 17; CYTOCHROME P450 3A4; CYTOCHROME P450 INHIBITOR; CYTOCHROME P450 ISOENZYME; DEOXYCORTICOSTERONE; DRUG METABOLITE; KETOCONAZOLE; NAPHTHALENE DERIVATIVE; PROGESTERONE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 27144472491     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm0503704     Document Type: Article
Times cited : (92)

References (54)
  • 2
    • 0033935122 scopus 로고    scopus 로고
    • Aldosterone and myocardial fibrosis in heart failure
    • Brilla, C. G. Aldosterone and myocardial fibrosis in heart failure. Herz 2000, 25, 299-306.
    • (2000) Herz , vol.25 , pp. 299-306
    • Brilla, C.G.1
  • 3
    • 0033840926 scopus 로고    scopus 로고
    • Induction of cardiac fibrosis by aldosterone
    • Lijnen, P.; Petrov, V. Induction of cardiac fibrosis by aldosterone. J. Mol. Cell. Cardiol. 2000, 32, 865-879.
    • (2000) J. Mol. Cell. Cardiol. , vol.32 , pp. 865-879
    • Lijnen, P.1    Petrov, V.2
  • 6
    • 3042616446 scopus 로고    scopus 로고
    • The role of aldosterone and aldosterone-receptor antagonists in heart failure
    • Khan, N. U. A.; Movahed, A. The role of aldosterone and aldosterone-receptor antagonists in heart failure. Rev. Cardiovasc. Med. 2004, 5, 71-81.
    • (2004) Rev. Cardiovasc. Med. , vol.5 , pp. 71-81
    • Khan, N.U.A.1    Movahed, A.2
  • 8
    • 0028026819 scopus 로고
    • Selective inhibition of steroidogenic P450 enzymes: Current status and future perspectives
    • Hartmann, R. W. Selective inhibition of steroidogenic P450 enzymes: current status and future perspectives. Eur. J. Pharm. Sci. 1994, 2, 15-16.
    • (1994) Eur. J. Pharm. Sci. , vol.2 , pp. 15-16
    • Hartmann, R.W.1
  • 9
    • 0036345081 scopus 로고    scopus 로고
    • Development of a test system for inhibitors of human aldosterone synthase (CYP11B2): Screening in fission yeast and evaluation of selectivity in V79 cells
    • Ehmer, P. B.; Bureik, M.; Bernhardt, R.; Müller, U.; Hartmann, R. W. Development of a test system for inhibitors of human aldosterone synthase (CYP11B2): Screening in fission yeast and evaluation of selectivity in V79 cells. J. Steroid Biochem. Mol. Biol. 2002, 81, 173-179.
    • (2002) J. Steroid Biochem. Mol. Biol. , vol.81 , pp. 173-179
    • Ehmer, P.B.1    Bureik, M.2    Bernhardt, R.3    Müller, U.4    Hartmann, R.W.5
  • 10
    • 0038054903 scopus 로고    scopus 로고
    • Discovery of selective CYP11B2 (aldosterone synthase) inhibitors for the therapy of congestive heart failure and myocardial fibrosis
    • Hartmann, R. W.; Müller, U.; Ehmer, P. B. Discovery of selective CYP11B2 (aldosterone synthase) inhibitors for the therapy of congestive heart failure and myocardial fibrosis. Eur. J. Med. Chem. 2003, 38, 363-366.
    • (2003) Eur. J. Med. Chem. , vol.38 , pp. 363-366
    • Hartmann, R.W.1    Müller, U.2    Ehmer, P.B.3
  • 11
    • 0029044427 scopus 로고
    • Pyridyl-substituted tetrahydrocyclopropa[α]naphthalenes: Highly active and selective inhibitors of P450 arom
    • (a) Hartmann, R. W.; Bayer, H.; Grün, G.; Sergejew, T.; Bartz, U.; Mitrenga, M. Pyridyl-substituted tetrahydrocyclopropa[α]naphthalenes: Highly active and selective inhibitors of P450 arom. J. Med. Chem. 1995, 38, 2103-2111.
    • (1995) J. Med. Chem. , vol.38 , pp. 2103-2111
    • Hartmann, R.W.1    Bayer, H.2    Grün, G.3    Sergejew, T.4    Bartz, U.5    Mitrenga, M.6
  • 13
    • 84872647271 scopus 로고    scopus 로고
    • A new class of nonsteroidal aromatase inhibitors: Design and synthesis of chromone and xanthone derivatives and inhibition of the P450 enzymes aromatase and 17α-hydroxylase/C17,20-lyase
    • (c) Recanatini, M.; Bisi, A.; Cavalli, A.; Belluti, F.; Gobbi, S.; Rampa, A.; Valenti, P.; Palzer, M.; Palusczak, A.; Hartmann, R. W. A new class of nonsteroidal aromatase inhibitors: Design and synthesis of chromone and xanthone derivatives and inhibition of the P450 enzymes aromatase and 17α-hydroxylase/C17,20-lyase. J. Med. Chem. 2001, 44, 672-680.
    • (2001) J. Med. Chem. , vol.44 , pp. 672-680
    • Recanatini, M.1    Bisi, A.2    Cavalli, A.3    Belluti, F.4    Gobbi, S.5    Rampa, A.6    Valenti, P.7    Palzer, M.8    Palusczak, A.9    Hartmann, R.W.10
  • 15
    • 0032835607 scopus 로고    scopus 로고
    • Imidazole substituted biphenyls: A new class of highly potent and in vivo active inhibitors of P450 17 as potential therapeutics for treatment of prostate cancer
    • (a) Wachall, B. G.; Hector, M.; Zhuang, Y.; Hartmann, R. W. Imidazole substituted biphenyls: A new class of highly potent and in vivo active inhibitors of P450 17 as potential therapeutics for treatment of prostate cancer. Bioorg. Med. Chem. 1999, 7, 1913-1924.
    • (1999) Bioorg. Med. Chem. , vol.7 , pp. 1913-1924
    • Wachall, B.G.1    Hector, M.2    Zhuang, Y.3    Hartmann, R.W.4
  • 16
    • 0034676307 scopus 로고    scopus 로고
    • Synthesis and evaluation of 17-aliphatic heterocycle-substituted steroidal inhibitors of 17α-hydroxylase/C17-20-lyase (P450 17)
    • (b) Hartmann, R. W.; Hector, M.; Wachall, B. G.; Palusczak, A.; Palzer, M.; Huch, V.; Veith, M. Synthesis and evaluation of 17-aliphatic heterocycle-substituted steroidal inhibitors of 17α-hydroxylase/C17-20- lyase (P450 17). J. Med. Chem. 2000, 43, 4437-4445.
    • (2000) J. Med. Chem. , vol.43 , pp. 4437-4445
    • Hartmann, R.W.1    Hector, M.2    Wachall, B.G.3    Palusczak, A.4    Palzer, M.5    Huch, V.6    Veith, M.7
  • 17
    • 0034088239 scopus 로고    scopus 로고
    • Novel imidazolyl and triazolyl substituted biphenyl compounds: Synthesis and evaluation as nonsteroidal inhibitors of human 17α-hydroxylase-C17,20- lyase (P450 17)
    • (c) Zhuang, Y.; Wachall, B. G.; Hartmann, R. W. Novel imidazolyl and triazolyl substituted biphenyl compounds: Synthesis and evaluation as nonsteroidal inhibitors of human 17α-hydroxylase-C17,20-lyase (P450 17). Bioorg. Med. Chem. 2000, 8, 1245-1252.
    • (2000) Bioorg. Med. Chem. , vol.8 , pp. 1245-1252
    • Zhuang, Y.1    Wachall, B.G.2    Hartmann, R.W.3
  • 18
    • 0038062686 scopus 로고    scopus 로고
    • Effects of novel 17α-hydroxylase/C17,20-lyase (P450 17, CYP 17) inhibitors on androgen biosynthesis in vitro and in vivo
    • (d) Haidar, S.; Ehmer, P. B.; Barassin, S.; Batzl-Hartmann, C.; Hartmann, R. W. Effects of novel 17α-hydroxylase/C17,20-lyase (P450 17, CYP 17) inhibitors on androgen biosynthesis in vitro and in vivo. J. Steroid Biochem. Mol. Biol. 2003, 84, 555-562.
    • (2003) J. Steroid Biochem. Mol. Biol. , vol.84 , pp. 555-562
    • Haidar, S.1    Ehmer, P.B.2    Barassin, S.3    Batzl-Hartmann, C.4    Hartmann, R.W.5
  • 20
    • 0024850612 scopus 로고
    • Evidence that corticosterone is not an obligatory intermediate in aldosterone biosynthesis in the rat adrenal
    • Häusler, A.; Monnet, G.; Borer, C.; Bhatnagar, A. S. Evidence that corticosterone is not an obligatory intermediate in aldosterone biosynthesis in the rat adrenal. J. Steroid Biochem. 1989, 34, 567-570.
    • (1989) J. Steroid Biochem. , vol.34 , pp. 567-570
    • Häusler, A.1    Monnet, G.2    Borer, C.3    Bhatnagar, A.S.4
  • 22
    • 2342632561 scopus 로고    scopus 로고
    • Development of test systems for the discovery of selective human aldosterone synthase (CYP11B2) and 11beta-hydroxylase (CYP11B1) inhibitors. Discovery of a new lead compound for the therapy of congestive heart failure, myocardial fibrosis and hypertension
    • Bureik, M.; Hubel, K.; Dragan, C. A.; Scher, J.; Becker, H.; Lenz, N.; Bernhardt, R. Development of test systems for the discovery of selective human aldosterone synthase (CYP11B2) and 11beta-hydroxylase (CYP11B1) inhibitors. Discovery of a new lead compound for the therapy of congestive heart failure, myocardial fibrosis and hypertension. Mol. Cell. Endocrinol. 2004, 217, 249-254.
    • (2004) Mol. Cell. Endocrinol. , vol.217 , pp. 249-254
    • Bureik, M.1    Hubel, K.2    Dragan, C.A.3    Scher, J.4    Becker, H.5    Lenz, N.6    Bernhardt, R.7
  • 24
    • 14944355617 scopus 로고    scopus 로고
    • Synthesis and evaluation of (pyridylmethylene)tetrahydronaphthalenes/- indanes and structurally modified derivatives: Potent and selective inhibitors of aldosterone synthase
    • Ulmschneider, S.; Müller-Vieira, U.; Klein, C. D.; Antes, I.; Lengauer, T.; Hartmann, R. W. Synthesis and evaluation of (pyridylmethylene) tetrahydronaphthalenes/-indanes and structurally modified derivatives: Potent and selective inhibitors of aldosterone synthase. J. Med. Chem. 2005, 48, 1563-1575.
    • (2005) J. Med. Chem. , vol.48 , pp. 1563-1575
    • Ulmschneider, S.1    Müller-Vieira, U.2    Klein, C.D.3    Antes, I.4    Lengauer, T.5    Hartmann, R.W.6
  • 25
    • 2042507954 scopus 로고
    • Palladium-catalyzed cross-coupling reactions of organoboron compounds
    • Miyaura, N.; Suzuki, N. Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem. Rev. 1995, 95, 2457-2483.
    • (1995) Chem. Rev. , vol.95 , pp. 2457-2483
    • Miyaura, N.1    Suzuki, N.2
  • 26
    • 84918727092 scopus 로고
    • Orientating phenomena in the substitution on aromatic bicyclic compounds. III. Radical substitutions in the naphthalene group
    • Huisgen, R.; Sorge, G. Orientating phenomena in the substitution on aromatic bicyclic compounds. III. Radical substitutions in the naphthalene group. Liebigs Ann. Chem. 1950, 566, 162-184.
    • (1950) Liebigs Ann. Chem. , vol.566 , pp. 162-184
    • Huisgen, R.1    Sorge, G.2
  • 27
    • 0033390320 scopus 로고    scopus 로고
    • Preparation and pharmacological evaluation of novel glycoprotein (Gp) IIb/IIIa antagonists. 1. The selection of naphthalene derivatives
    • Ono, S.; Inoue, Y.; Yoshida, T.; Ashimori, A.; Kosaka, K.; Imada, T.; Fukaya, C.; Nakamura, N. Preparation and pharmacological evaluation of novel glycoprotein (Gp) IIb/IIIa antagonists. 1. The selection of naphthalene derivatives. Chem. Pharm. Bull. 1999, 49, 1685-1693.
    • (1999) Chem. Pharm. Bull. , vol.49 , pp. 1685-1693
    • Ono, S.1    Inoue, Y.2    Yoshida, T.3    Ashimori, A.4    Kosaka, K.5    Imada, T.6    Fukaya, C.7    Nakamura, N.8
  • 28
    • 27144556191 scopus 로고    scopus 로고
    • (Wyeth). Substituted phenyl naphthalenes as estrogenic agents. Patent WO03051805, 2003
    • Mewshaw, R. E.; Edsall, R. J.; Yang, C.; Harris, H. A.; Keith, J. C.; Albert, L. M. (Wyeth). Substituted phenyl naphthalenes as estrogenic agents. Patent WO03051805, 2003.
    • Mewshaw, R.E.1    Edsall, R.J.2    Yang, C.3    Harris, H.A.4    Keith, J.C.5    Albert, L.M.6
  • 29
    • 27144459656 scopus 로고
    • Halogen reactivities. Certain heterocyclic iminohalide systems
    • Young, T. E.; Amstutz, E. D. Halogen reactivities. Certain heterocyclic iminohalide systems. J. Am. Chem. Soc. 1951, 4773-4775.
    • (1951) J. Am. Chem. Soc. , pp. 4773-4775
    • Young, T.E.1    Amstutz, E.D.2
  • 30
    • 0001444643 scopus 로고
    • A mild efficient procedure for the conversion of carboxylic acid esters to primary amides using formamide/methanolic sodium methoxide
    • Jagdmann, G. E.; Munson, H. R.; Gero, T. W. A mild efficient procedure for the conversion of carboxylic acid esters to primary amides using formamide/methanolic sodium methoxide. Synth. Commun. 1990, 20, 1203-1208.
    • (1990) Synth. Commun. , vol.20 , pp. 1203-1208
    • Jagdmann, G.E.1    Munson, H.R.2    Gero, T.W.3
  • 31
    • 0032493017 scopus 로고    scopus 로고
    • New aryl/heteroaryl C-N bond cross-coupling reactions via arylboronic acid/cupric acetate arylation
    • Lam, P. Y. S.; Clark, C. G.; Saubern, S.; Adams, J.; Winters, M. P.; Chan, D. M. T.; Combs, A. New aryl/heteroaryl C-N bond cross-coupling reactions via arylboronic acid/cupric acetate arylation. Tetrahedron Lett. 1998, 39, 2941-2944.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2941-2944
    • Lam, P.Y.S.1    Clark, C.G.2    Saubern, S.3    Adams, J.4    Winters, M.P.5    Chan, D.M.T.6    Combs, A.7
  • 32
    • 1642480209 scopus 로고    scopus 로고
    • A simple copper salt catalysed the coupling of imidazole with arylboronic acids in protic solvent
    • Lan, J.; Chen, L.; Yu, X.; You, J.; Xie, R. A simple copper salt catalysed the coupling of imidazole with arylboronic acids in protic solvent. Chem. Commun. 2004, 2, 188-189.
    • (2004) Chem. Commun. , vol.2 , pp. 188-189
    • Lan, J.1    Chen, L.2    Yu, X.3    You, J.4    Xie, R.5
  • 33
    • 84979394958 scopus 로고
    • Imidazolsynthesen mit formamid
    • Bredereck, H.; Theilig, G. Imidazolsynthesen mit Formamid. Chem. Ber. 1953, 86, 88-96.
    • (1953) Chem. Ber. , vol.86 , pp. 88-96
    • Bredereck, H.1    Theilig, G.2
  • 34
    • 0029016986 scopus 로고
    • Cloning of CYP11B1 and CYP11B2 from normal human adrenal and their functional expression in COS-7 and V79 chinese hamster cells
    • Denner, K.; Doehmer, J.; Bernhardt, R. Cloning of CYP11B1 and CYP11B2 from normal human adrenal and their functional expression in COS-7 and V79 chinese hamster cells. Endocr. Res. 1995, 21, 443-448.
    • (1995) Endocr. Res. , vol.21 , pp. 443-448
    • Denner, K.1    Doehmer, J.2    Bernhardt, R.3
  • 35
    • 0016293443 scopus 로고
    • Utilization of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placental microsomes during aromatization of androstenedione
    • Thompson, E. A.; Siiteri, P. K. Utilization of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placental microsomes during aromatization of androstenedione. J. Biol. Chem. 1974, 249, 5364-5372.
    • (1974) J. Biol. Chem. , vol.249 , pp. 5364-5372
    • Thompson, E.A.1    Siiteri, P.K.2
  • 36
    • 0022470925 scopus 로고
    • Aromatase inhibitors. Synthesis and evaluation of mammary tumor inhibiting activity of 3-alkylated 3-(4-aminophenyl)piperidine-2,6-diones
    • Hartmann, R. W.; Batzl, C. Aromatase inhibitors. Synthesis and evaluation of mammary tumor inhibiting activity of 3-alkylated 3-(4-aminophenyl) piperidine-2,6-diones. J. Med. Chem. 1986, 29, 1362-1369.
    • (1986) J. Med. Chem. , vol.29 , pp. 1362-1369
    • Hartmann, R.W.1    Batzl, C.2
  • 37
    • 0034484809 scopus 로고    scopus 로고
    • 17,20-lyase (P450c17) by coexpression of P450c17 with NADPH-cytochrome-P450-reductase in Escherichia coli
    • 17,20-lyase (P450c17) by coexpression of P450c17 with NADPH-cytochrome-P450-reductase in Escherichia coli. J. Steroid Biochem. Mol. Biol. 2000, 75, 57-63.
    • (2000) J. Steroid Biochem. Mol. Biol. , vol.75 , pp. 57-63
    • Ehmer, P.B.1    Jose, J.2    Hartmann, R.W.3
  • 38
    • 1242352932 scopus 로고    scopus 로고
    • Synthesis of hydroxy derivatives of highly potent nonsteroidal CYP17 inhibitors as potential metabolites and evaluation of their activity by a non cellular assay using recombinant enzyme
    • Hutschenreuter, T. U.; Ehmer, P. B.; Hartmann, R. W. Synthesis of hydroxy derivatives of highly potent nonsteroidal CYP17 inhibitors as potential metabolites and evaluation of their activity by a non cellular assay using recombinant enzyme. J. Enzyme Inhib. Med. Chem. 2004, 19, 17-32.
    • (2004) J. Enzyme Inhib. Med. Chem. , vol.19 , pp. 17-32
    • Hutschenreuter, T.U.1    Ehmer, P.B.2    Hartmann, R.W.3
  • 39
    • 0035524138 scopus 로고    scopus 로고
    • Assessing the absorption of new pharmaceuticals
    • Hidalgo, I. J. Assessing the absorption of new pharmaceuticals. Curr. Top. Med. Chem. 2001, 1, 385-401.
    • (2001) Curr. Top. Med. Chem. , vol.1 , pp. 385-401
    • Hidalgo, I.J.1
  • 40
    • 0030990079 scopus 로고    scopus 로고
    • In vitro permeability across Caco-2 cells (colonic) can predict in vivo (small intestinal) absorption in men - Fact or myth
    • Yee, S. In vitro permeability across Caco-2 cells (colonic) can predict in vivo (small intestinal) absorption in men - fact or myth. Pharm. Res. 1997, 14, 763-766.
    • (1997) Pharm. Res. , vol.14 , pp. 763-766
    • Yee, S.1
  • 41
    • 0035048583 scopus 로고    scopus 로고
    • Compound mixtures in Caco-2 cell permeability screens as a means to increase screening capacity
    • Tannergren, C.; Langguth, P.; Hoffmann, K. J. Compound mixtures in Caco-2 cell permeability screens as a means to increase screening capacity. Pharmazie 2001, 56, 337-342.
    • (2001) Pharmazie , vol.56 , pp. 337-342
    • Tannergren, C.1    Langguth, P.2    Hoffmann, K.J.3
  • 43
    • 0033844748 scopus 로고    scopus 로고
    • Carrier-mediated transport of macrolide antimicrobial agents across Caco-2 cell monolayers
    • Saito, H.; Fukasawa, Y.; Otsubo, Y.; Yamada, K.; Sezaki, H.; Yamashita, S. Carrier-mediated transport of macrolide antimicrobial agents across Caco-2 cell monolayers. Pharm. Res. 2000, 17, 761-765.
    • (2000) Pharm. Res. , vol.17 , pp. 761-765
    • Saito, H.1    Fukasawa, Y.2    Otsubo, Y.3    Yamada, K.4    Sezaki, H.5    Yamashita, S.6
  • 44
    • 0035893679 scopus 로고    scopus 로고
    • Modelling of three-dimensional structures of cytochromes P450 11B2 and 11B1
    • Belkina, N. V.; Lisurek, M.; Ivanov, A. S.; Bernhardt, R. Modelling of three-dimensional structures of cytochromes P450 11B2 and 11B1. J. Inorg. Biochem. 2001, 87, 197-207.
    • (2001) J. Inorg. Biochem. , vol.87 , pp. 197-207
    • Belkina, N.V.1    Lisurek, M.2    Ivanov, A.S.3    Bernhardt, R.4
  • 45
    • 0033595869 scopus 로고    scopus 로고
    • Palladium catalyzed cross-coupling between phenyl- Or naphthylboronic acids and benzylic bromides
    • Chowdhury, S.; Georghiou, P. E. Palladium catalyzed cross-coupling between phenyl- or naphthylboronic acids and benzylic bromides. Tetrahedron Lett. 1999, 40, 7599-7603.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 7599-7603
    • Chowdhury, S.1    Georghiou, P.E.2
  • 47
    • 84984207285 scopus 로고
    • Kondensation von 3-(1-Imidazolyl)- und -(1-benzimidazolyl)-chinolin zu heterocyclotetraaromaten
    • Kauffmann, T.; Tigler, D.; Woltermann, A. Kondensation von 3-(1-Imidazolyl)- und -(1-Benzimidazolyl)-chinolin zu Heterocyclotetraaromaten. Chem. Ber. 1982, 115, 452-458.
    • (1982) Chem. Ber. , vol.115 , pp. 452-458
    • Kauffmann, T.1    Tigler, D.2    Woltermann, A.3
  • 48
    • 0000213449 scopus 로고
    • Synthesis of bromoacetyl derivatives by use of tetrabutylammonium tribromide
    • Kajigaeshi, S.; Kakinami, T.; Okamoto, T.; Fujisaki, S. Synthesis of bromoacetyl derivatives by use of tetrabutylammonium tribromide. Bull. Chem. Soc. Jpn. 1987, 60, 1159-1160.
    • (1987) Bull. Chem. Soc. Jpn. , vol.60 , pp. 1159-1160
    • Kajigaeshi, S.1    Kakinami, T.2    Okamoto, T.3    Fujisaki, S.4
  • 49
    • 84981838580 scopus 로고
    • Über die katalytische hydrogenolyse von derivaten des p-phenylbenzylamins
    • Dahn, H.; Zoller, P. Über die katalytische Hydrogenolyse von Derivaten des p-Phenylbenzylamins. Helv. Chim. Acta 1952, 35, 1348-1351.
    • (1952) Helv. Chim. Acta , vol.35 , pp. 1348-1351
    • Dahn, H.1    Zoller, P.2
  • 53
    • 0035789518 scopus 로고    scopus 로고
    • GROMACS 3.0: A package for molecular simulation and trajectory analysis
    • Lindahl, E.; Hess, B.; van der Spoel, D. GROMACS 3.0: a package for molecular simulation and trajectory analysis. J. Mol. Mod. 2001, 7, 306-317.
    • (2001) J. Mol. Mod. , vol.7 , pp. 306-317
    • Lindahl, E.1    Hess, B.2    Van Der Spoel, D.3
  • 54
    • 0002775934 scopus 로고
    • Interaction models for water in relation to protein hydration
    • Pullman, B., Ed.; Reidel Publishing Co.: Dordrecht
    • Berendsen, H. J. C.; Postma, J. P. M.; van Gunsteren, W. F.; Hermans, J. Interaction models for water in relation to protein hydration. In Intermolecular Forces; Pullman, B., Ed.; Reidel Publishing Co.: Dordrecht, 1981; pp 331-342.
    • (1981) Intermolecular Forces , pp. 331-342
    • Berendsen, H.J.C.1    Postma, J.P.M.2    Van Gunsteren, W.F.3    Hermans, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.