-
1
-
-
84864578590
-
The bromodomain interaction module
-
Filippakopoulos, P.; Knapp, S. The bromodomain interaction module FEBS Lett. 2012, 586, 2692-2704 10.1016/j.febslet.2012.04.045
-
(2012)
FEBS Lett.
, vol.586
, pp. 2692-2704
-
-
Filippakopoulos, P.1
Knapp, S.2
-
2
-
-
84859181036
-
Histone recognition and large-scale structural analysis of the human bromodomain family
-
Filippakopoulos, P.; Picaud, S.; Mangos, M.; Keates, T.; Lambert, J.-P.; Barsyte-Lovejoy, D.; Felletar, I.; Volkmer, R.; Muller, S.; Pawson, T.; Gingras, A.-C.; Arrowsmith, C. H.; Knapp, S. Histone recognition and large-scale structural analysis of the human bromodomain family Cell 2012, 149, 214-231 10.1016/j.cell.2012.02.013
-
(2012)
Cell
, vol.149
, pp. 214-231
-
-
Filippakopoulos, P.1
Picaud, S.2
Mangos, M.3
Keates, T.4
Lambert, J.-P.5
Barsyte-Lovejoy, D.6
Felletar, I.7
Volkmer, R.8
Muller, S.9
Pawson, T.10
Gingras, A.-C.11
Arrowsmith, C.H.12
Knapp, S.13
-
3
-
-
84870013141
-
Progress in the development and application of small molecule inhibitors of bromodomain-acetyl-lysine interactions
-
Hewings, D. S.; Rooney, T. P.; Jennings, L. E.; Hay, D. A.; Schofield, C. J.; Brennan, P. E.; Knapp, S.; Conway, S. J. Progress in the development and application of small molecule inhibitors of bromodomain-acetyl-lysine interactions J. Med. Chem. 2012, 55, 9393-9413 10.1021/jm300915b
-
(2012)
J. Med. Chem.
, vol.55
, pp. 9393-9413
-
-
Hewings, D.S.1
Rooney, T.P.2
Jennings, L.E.3
Hay, D.A.4
Schofield, C.J.5
Brennan, P.E.6
Knapp, S.7
Conway, S.J.8
-
4
-
-
1642564551
-
Selective recognition of acetylated histones by bromodomain proteins visualized in living cells
-
Kanno, T.; Kanno, Y.; Siegel, R. M.; Jang, M. K.; Lenardo, M. J.; Ozato, K. Selective recognition of acetylated histones by bromodomain proteins visualized in living cells Mol. Cell 2004, 13, 33-43 10.1016/S1097-2765(03)00482-9
-
(2004)
Mol. Cell
, vol.13
, pp. 33-43
-
-
Kanno, T.1
Kanno, Y.2
Siegel, R.M.3
Jang, M.K.4
Lenardo, M.J.5
Ozato, K.6
-
5
-
-
35948981189
-
Solution structure of the second bromodomain of Brd2 and its specific interaction with acetylated histone tails
-
Huang, H.; Zhang, J.; Shen, W.; Wang, X.; Wu, J.; Wu, J.; Shi, Y. Solution structure of the second bromodomain of Brd2 and its specific interaction with acetylated histone tails BMC Struct. Biol. 2007, 7, 57 10.1186/1472-6807-7-57
-
(2007)
BMC Struct. Biol.
, vol.7
, pp. 57
-
-
Huang, H.1
Zhang, J.2
Shen, W.3
Wang, X.4
Wu, J.5
Wu, J.6
Shi, Y.7
-
6
-
-
41549115095
-
The double bromodomain proteins Brd2 and Brd3 couple histone acetylation to transcription
-
LeRoy, G.; Rickards, B.; Flint, S. J. The double bromodomain proteins Brd2 and Brd3 couple histone acetylation to transcription Mol. Cell 2008, 30, 51-60 10.1016/j.molcel.2008.01.018
-
(2008)
Mol. Cell
, vol.30
, pp. 51-60
-
-
LeRoy, G.1
Rickards, B.2
Flint, S.J.3
-
7
-
-
84908638606
-
Chemical biology. A bump-and-hole approach to engineer controlled selectivity of BET bromodomain chemical probes
-
Baud, M. G.; Lin-Shiao, E.; Cardote, T.; Tallant, C.; Pschibul, A.; Chan, K. H.; Zengerle, M.; Garcia, J. R.; Kwan, T. T.; Ferguson, F. M.; Ciulli, A. Chemical biology. A bump-and-hole approach to engineer controlled selectivity of BET bromodomain chemical probes Science 2014, 346, 638-641 10.1126/science.1249830
-
(2014)
Science
, vol.346
, pp. 638-641
-
-
Baud, M.G.1
Lin-Shiao, E.2
Cardote, T.3
Tallant, C.4
Pschibul, A.5
Chan, K.H.6
Zengerle, M.7
Garcia, J.R.8
Kwan, T.T.9
Ferguson, F.M.10
Ciulli, A.11
-
8
-
-
84889663966
-
RVX-208, an inhibitor of BET transcriptional regulators with selectivity for the second bromodomain
-
Picaud, S.; Wells, C.; Felletar, I.; Brotherton, D.; Martin, S.; Savitsky, P.; Diez-Dacal, B.; Philpott, M.; Bountra, C.; Lingard, H.; Fedorov, O.; Müller, S.; Brennan, P. E.; Knapp, S.; Filippakopoulos, P. RVX-208, an inhibitor of BET transcriptional regulators with selectivity for the second bromodomain Proc. Natl. Acad. Sci. U. S. A. 2013, 110, 19754-19759 10.1073/pnas.1310658110
-
(2013)
Proc. Natl. Acad. Sci. U. S. A.
, vol.110
, pp. 19754-19759
-
-
Picaud, S.1
Wells, C.2
Felletar, I.3
Brotherton, D.4
Martin, S.5
Savitsky, P.6
Diez-Dacal, B.7
Philpott, M.8
Bountra, C.9
Lingard, H.10
Fedorov, O.11
Müller, S.12
Brennan, P.E.13
Knapp, S.14
Filippakopoulos, P.15
-
9
-
-
84862911038
-
Two-pronged binding with bromodomain-containing protein 4 liberates positive transcription elongation factor b from inactive ribonucleoprotein complexes
-
Schröder, S.; Cho, S.; Zeng, L.; Zhang, Q.; Kaehlcke, K.; Mak, L.; Lau, J.; Bisgrove, D.; Schnölzer, M.; Verdin, E.; Zhou, M.-M.; Ott, M. Two-pronged binding with bromodomain-containing protein 4 liberates positive transcription elongation factor b from inactive ribonucleoprotein complexes J. Biol. Chem. 2012, 287, 1090-1099 10.1074/jbc.M111.282855
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 1090-1099
-
-
Schröder, S.1
Cho, S.2
Zeng, L.3
Zhang, Q.4
Kaehlcke, K.5
Mak, L.6
Lau, J.7
Bisgrove, D.8
Schnölzer, M.9
Verdin, E.10
Zhou, M.-M.11
Ott, M.12
-
10
-
-
77951920690
-
C-Myc regulates transcriptional pause release
-
Rahl, P. B.; Lin, C. Y.; Seila, A. C.; Flynn, R. A.; McCuine, S.; Burge, C. B.; Sharp, P. A.; Young, R. A. c-Myc regulates transcriptional pause release Cell 2010, 141, 432-445 10.1016/j.cell.2010.03.030
-
(2010)
Cell
, vol.141
, pp. 432-445
-
-
Rahl, P.B.1
Lin, C.Y.2
Seila, A.C.3
Flynn, R.A.4
McCuine, S.5
Burge, C.B.6
Sharp, P.A.7
Young, R.A.8
-
11
-
-
84862738480
-
BET domain co-regulators in obesity, inflammation and cancer
-
Belkina, A. C.; Denis, G. V. BET domain co-regulators in obesity, inflammation and cancer Nat. Rev. Cancer 2012, 12, 465-477 10.1038/nrc3256
-
(2012)
Nat. Rev. Cancer
, vol.12
, pp. 465-477
-
-
Belkina, A.C.1
Denis, G.V.2
-
12
-
-
84876222028
-
Selective inhibition of tumor oncogenes by disruption of super-enhancers
-
Lovén, J.; Hoke, H. A.; Lin, C. Y.; Lau, A.; Orlando, D. A.; Vakoc, C. R.; Bradner, J. E.; Lee, T. I.; Young, R. A. Selective inhibition of tumor oncogenes by disruption of super-enhancers Cell 2013, 153, 320-334 10.1016/j.cell.2013.03.036
-
(2013)
Cell
, vol.153
, pp. 320-334
-
-
Lovén, J.1
Hoke, H.A.2
Lin, C.Y.3
Lau, A.4
Orlando, D.A.5
Vakoc, C.R.6
Bradner, J.E.7
Lee, T.I.8
Young, R.A.9
-
13
-
-
84886276286
-
The brd-Inhibitor OTX015 shows pre-clinical activity in anaplastic large T-cell lymphoma (ALCL)
-
Boi, M.; Bonetti, P.; Ponzoni, M.; Tibiletti, M. G.; Stathis, A.; Cvitkovic, E.; Inghirami, G.; Zucca, E.; Bertoni, F. The brd-Inhibitor OTX015 shows pre-clinical activity in anaplastic large T-cell lymphoma (ALCL) ASH Annu. Meet. Abstr., Blood 2012, 120, 4872
-
(2012)
ASH Annu. Meet. Abstr., Blood
, vol.120
, pp. 4872
-
-
Boi, M.1
Bonetti, P.2
Ponzoni, M.3
Tibiletti, M.G.4
Stathis, A.5
Cvitkovic, E.6
Inghirami, G.7
Zucca, E.8
Bertoni, F.9
-
14
-
-
84893160224
-
-
Bonetti, P.; Boi, M.; Ponzoni, M.; Tibiletti, M. G.; Stahis, A.; Inghirami, G.; Noel, K.; Zucca, E.; Bertoni, F. ASH Annu. Meet. Abstr., Blood 2012, 120, 1657
-
(2012)
ASH Annu. Meet. Abstr., Blood
, vol.120
, pp. 1657
-
-
Bonetti, P.1
Boi, M.2
Ponzoni, M.3
Tibiletti, M.G.4
Stahis, A.5
Inghirami, G.6
Noel, K.7
Zucca, E.8
Bertoni, F.9
-
15
-
-
84901054033
-
Preclinical study of the bromodomain inhibitor OTX015 in acute myeloid (AML) and lymphoid (ALL) leukemias
-
Braun, T.; Coude, M.; Berrou, J.; Bertrand, S.; Riveiro, E.; Herait, P.; Baruchel, A.; Dombret, H.; Gardin, C. Preclinical study of the bromodomain inhibitor OTX015 in acute myeloid (AML) and lymphoid (ALL) leukemias ASH Annu. Meet. Abstr., Blood 2013, 122, 4218
-
(2013)
ASH Annu. Meet. Abstr., Blood
, vol.122
, pp. 4218
-
-
Braun, T.1
Coude, M.2
Berrou, J.3
Bertrand, S.4
Riveiro, E.5
Herait, P.6
Baruchel, A.7
Dombret, H.8
Gardin, C.9
-
16
-
-
84927588026
-
Development of the BET bromodomain inhibitor OTX015
-
Noel, J. K.; Iwata, K.; Ooike, S.; Sugahara, K.; Nakamura, H.; Daibata, M. Development of the BET bromodomain inhibitor OTX015 Mol. Cancer Ther. 2013, 12, C244 10.1158/1535-7163.TARG-13-C244
-
(2013)
Mol. Cancer Ther.
, vol.12
, pp. C244
-
-
Noel, J.K.1
Iwata, K.2
Ooike, S.3
Sugahara, K.4
Nakamura, H.5
Daibata, M.6
-
17
-
-
84905842525
-
A novel BET bromodomain inhibitor, RVX-208, shows reduction of atherosclerosis in hyperlipidemic ApoE deficient mice
-
Jahagirdar, R.; Zhang, H.; Azhar, S.; Tobin, J.; Attwell, S.; Yu, R.; Wu, J.; McLure, K. G.; Hansen, H. C.; Wagner, G. S.; Young, P. R.; Srivastava, R. A. K.; Wong, N. C. W.; Johansson, J. A novel BET bromodomain inhibitor, RVX-208, shows reduction of atherosclerosis in hyperlipidemic ApoE deficient mice Atherosclerosis 2014, 236, 91-100 10.1016/j.atherosclerosis.2014.06.008
-
(2014)
Atherosclerosis
, vol.236
, pp. 91-100
-
-
Jahagirdar, R.1
Zhang, H.2
Azhar, S.3
Tobin, J.4
Attwell, S.5
Yu, R.6
Wu, J.7
McLure, K.G.8
Hansen, H.C.9
Wagner, G.S.10
Young, P.R.11
Srivastava, R.A.K.12
Wong, N.C.W.13
Johansson, J.14
-
18
-
-
77949743743
-
Atomic analysis of protein-protein interfaces with known inhibitors: the 2P2I database
-
Bourgeas, R.; Basse, M.-J.; Morelli, X.; Roche, P. Atomic analysis of protein-protein interfaces with known inhibitors: the 2P2I database PLoS One 2010, 5, e9598 10.1371/journal.pone.0009598
-
(2010)
PLoS One
, vol.5
-
-
Bourgeas, R.1
Basse, M.-J.2
Morelli, X.3
Roche, P.4
-
19
-
-
84876546810
-
2P2Idb: a structural database dedicated to orthosteric modulation of protein-protein interactions
-
Basse, M.-J.; Betzi, S.; Bourgeas, R.; Bouzidi, S.; Chetrit, B.; Hamon, V.; Morelli, X.; Roche, P. 2P2Idb: a structural database dedicated to orthosteric modulation of protein-protein interactions Nucleic Acids Res. 2013, 41, D824-327 http://2p2idb.cnrs-mrs.fr 10.1093/nar/gks1002
-
(2013)
Nucleic Acids Res.
, vol.41
, pp. D824-D327
-
-
Basse, M.-J.1
Betzi, S.2
Bourgeas, R.3
Bouzidi, S.4
Chetrit, B.5
Hamon, V.6
Morelli, X.7
Roche, P.8
-
20
-
-
79960990847
-
Chemical and structural lessons from recent successes in protein-protein interaction inhibition (2P2I)
-
Morelli, X.; Bourgeas, R.; Roche, P. Chemical and structural lessons from recent successes in protein-protein interaction inhibition (2P2I) Curr. Opin. Chem. Biol. 2011, 15, 475-481 10.1016/j.cbpa.2011.05.024
-
(2011)
Curr. Opin. Chem. Biol.
, vol.15
, pp. 475-481
-
-
Morelli, X.1
Bourgeas, R.2
Roche, P.3
-
21
-
-
84889646329
-
2P2I HUNTER: a tool for filtering orthosteric protein-protein interac interaction modulators via a dedicated support vector machine
-
Hamon, V.; Bourgeas, R.; Ducrot, P.; Theret, I.; Xuereb, L.; Basse, M.-J.; Brunel, J.-M.; Combes, S.; Morelli, X.; Roche, P. 2P2I HUNTER: a tool for filtering orthosteric protein-protein interac interaction modulators via a dedicated support vector machine J. R. Soc., Interface 2014, 11, 20130860 10.1098/rsif.2013.0860
-
(2014)
J. R. Soc., Interface
, vol.11
, pp. 20130860
-
-
Hamon, V.1
Bourgeas, R.2
Ducrot, P.3
Theret, I.4
Xuereb, L.5
Basse, M.-J.6
Brunel, J.-M.7
Combes, S.8
Morelli, X.9
Roche, P.10
-
22
-
-
84877278593
-
2P2Ichem: focused chemical libraries dedicated to orthosteric modulation of protein-protein interactions
-
Hamon, V.; Brunel, J. M.; Combes, S.; Basse, J.-M.; Roche, P.; Morelli, X. 2P2Ichem: focused chemical libraries dedicated to orthosteric modulation of protein-protein interactions MedChemComm 2013, 4, 797-809 10.1039/c3md00018d
-
(2013)
MedChemComm
, vol.4
, pp. 797-809
-
-
Hamon, V.1
Brunel, J.M.2
Combes, S.3
Basse, J.-M.4
Roche, P.5
Morelli, X.6
-
23
-
-
84906727867
-
Focused chemical libraries - Design and enrichment: an example of protein-protein interaction chemical space
-
Zhang, X.; Betzi, S.; Morelli, X.; Roche, P. Focused chemical libraries - design and enrichment: an example of protein-protein interaction chemical space Future Med. Chem. 2014, 6, 1291-1307 10.4155/fmc.14.57
-
(2014)
Future Med. Chem.
, vol.6
, pp. 1291-1307
-
-
Zhang, X.1
Betzi, S.2
Morelli, X.3
Roche, P.4
-
24
-
-
78650847770
-
Selective inhibition of BET bromodomains
-
Filippakopoulos, P.; Qi, J.; Picaud, S.; Shen, Y.; Smith, W. B.; Fedorov, O.; Morse, E. M.; Keates, T.; Hickman, T. T.; Felletar, I.; Philpott, M.; Munro, S.; McKeown, M. R.; Wang, Y.; Christie, A. L.; West, N.; Cameron, M. J.; Schwartz, B.; Heightman, T. D.; La Thangue, N.; French, C. A.; Wiest, O.; Kung, A. L.; Knapp, S.; Bradner, J. E. Selective inhibition of BET bromodomains Nature 2010, 468, 1067-1073 10.1038/nature09504
-
(2010)
Nature
, vol.468
, pp. 1067-1073
-
-
Filippakopoulos, P.1
Qi, J.2
Picaud, S.3
Shen, Y.4
Smith, W.B.5
Fedorov, O.6
Morse, E.M.7
Keates, T.8
Hickman, T.T.9
Felletar, I.10
Philpott, M.11
Munro, S.12
McKeown, M.R.13
Wang, Y.14
Christie, A.L.15
West, N.16
Cameron, M.J.17
Schwartz, B.18
Heightman, T.D.19
La Thangue, N.20
French, C.A.21
Wiest, O.22
Kung, A.L.23
Knapp, S.24
Bradner, J.E.25
more..
-
25
-
-
73649124584
-
Structures of the dual bromodomains of the P-TEFb-activating protein Brd4 at atomic resolution
-
Vollmuth, F.; Blankenfeldt, W.; Geyer, M. Structures of the dual bromodomains of the P-TEFb-activating protein Brd4 at atomic resolution J. Biol. Chem. 2009, 284, 36547-36556 10.1074/jbc.M109.033712
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 36547-36556
-
-
Vollmuth, F.1
Blankenfeldt, W.2
Geyer, M.3
-
26
-
-
84924674529
-
Structure enabled design of BAZ2-ICR, a chemical probe targeting the bromodomains of BAZ2A and BAZ2B
-
Drouin, L.; McGrath, S.; Vidler, L. R.; Chaikuad, A.; Monteiro, O.; Tallant, C.; Philpott, M.; Rogers, C.; Fedorov, O.; Liu, M.; Akhtar, W.; Hayes, A.; Raynaud, F.; Müller, S.; Knapp, S.; Hoelder, S. Structure enabled design of BAZ2-ICR, a chemical probe targeting the bromodomains of BAZ2A and BAZ2B J. Med. Chem. 2015, 58, 2553-2559 10.1021/jm501963e
-
(2015)
J. Med. Chem.
, vol.58
, pp. 2553-2559
-
-
Drouin, L.1
McGrath, S.2
Vidler, L.R.3
Chaikuad, A.4
Monteiro, O.5
Tallant, C.6
Philpott, M.7
Rogers, C.8
Fedorov, O.9
Liu, M.10
Akhtar, W.11
Hayes, A.12
Raynaud, F.13
Müller, S.14
Knapp, S.15
Hoelder, S.16
-
27
-
-
84959421867
-
Discovery of a chemical tool inhibitor targeting the bromodomains of TRIM24 and BRPF
-
Bennett, J.; Fedorov, O.; Tallant, C.; Monteiro, O.; Meier, J.; Gamble, V.; Savitsky, P.; Nunez-Alonso, G. A.; Haendler, B.; Rogers, C.; Brennan, P. E.; Müller, S.; Knapp, S. Discovery of a chemical tool inhibitor targeting the bromodomains of TRIM24 and BRPF J. Med. Chem. 2015, 10.1021/acs.jmedchem.5b00458
-
(2015)
J. Med. Chem.
-
-
Bennett, J.1
Fedorov, O.2
Tallant, C.3
Monteiro, O.4
Meier, J.5
Gamble, V.6
Savitsky, P.7
Nunez-Alonso, G.A.8
Haendler, B.9
Rogers, C.10
Brennan, P.E.11
Müller, S.12
Knapp, S.13
-
28
-
-
84959366723
-
Structure-guided design of IACS-9571, a selective high-affinity dual TRIM24-BRPF1 bromodomain inhibitor
-
Palmer, W. S.; Poncet-Montange, G.; Liu, G.; Petrocchi, A.; Reyna, N.; Subramanian, G.; Theroff, J.; Yau, A.; Kost-Alimova, M.; Bardenhagen, J. P.; Leo, E.; Shepard, H. E.; Tieu, T. N.; Shi, X.; Zhan, Y.; Zhao, S.; Barton, M. C.; Draetta, G.; Toniatti, C.; Jones, P.; Geck Do, M.; Andersen, J. N. Structure-guided design of IACS-9571, a selective high-affinity dual TRIM24-BRPF1 bromodomain inhibitor J. Med. Chem. 2015, 10.1021/acs.jmedchem.5b00405
-
(2015)
J. Med. Chem.
-
-
Palmer, W.S.1
Poncet-Montange, G.2
Liu, G.3
Petrocchi, A.4
Reyna, N.5
Subramanian, G.6
Theroff, J.7
Yau, A.8
Kost-Alimova, M.9
Bardenhagen, J.P.10
Leo, E.11
Shepard, H.E.12
Tieu, T.N.13
Shi, X.14
Zhan, Y.15
Zhao, S.16
Barton, M.C.17
Draetta, G.18
Toniatti, C.19
Jones, P.20
Geck Do, M.21
Andersen, J.N.22
more..
-
29
-
-
5444265269
-
Improved synthesis of 7-(alkyl/aryl)guanine
-
Vidal, A.; Giraud, I.; Madelmont, J.-C. Improved synthesis of 7-(alkyl/aryl)guanine Synth. Commun. 2004, 34, 3359-3365 10.1081/SCC-200030585
-
(2004)
Synth. Commun.
, vol.34
, pp. 3359-3365
-
-
Vidal, A.1
Giraud, I.2
Madelmont, J.-C.3
-
30
-
-
38949111028
-
Selective, high affinity A2B adenosine receptor antagonists: N-1 monosubstituted 8-(pyrazol-4-yl)xanthines
-
Kalla, R. V.; Elzein, E.; Perry, T.; Li, X.; Gimbel, A.; Yang, M.; Zeng, D.; Zablocki, J. Selective, high affinity A2B adenosine receptor antagonists: N-1 monosubstituted 8-(pyrazol-4-yl)xanthines Bioorg. Med. Chem. Lett. 2008, 18, 1397-1401 10.1016/j.bmcl.2008.01.008
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 1397-1401
-
-
Kalla, R.V.1
Elzein, E.2
Perry, T.3
Li, X.4
Gimbel, A.5
Yang, M.6
Zeng, D.7
Zablocki, J.8
-
31
-
-
84942532115
-
Binding Kinetics versus Affinities in BRD4 Inhibition
-
Kuang, M.; Zhou, J.; Wang, L.; Liu, Z.; Guo, J.; Wu, R. Binding Kinetics versus Affinities in BRD4 Inhibition J. Chem. Inf. Model. 2015, 55, 1926-1935 10.1021/acs.jcim.5b00265
-
(2015)
J. Chem. Inf. Model.
, vol.55
, pp. 1926-1935
-
-
Kuang, M.1
Zhou, J.2
Wang, L.3
Liu, Z.4
Guo, J.5
Wu, R.6
-
32
-
-
84928162427
-
Insight into the key interactions of bromodomain inhibitors based on molecular docking, interaction fingerprinting, molecular dynamics and binding free energy calculation
-
Ran, T.; Zhang, Z.; Liu, K.; Lu, Y.; Li, H.; Xu, J.; Xiong, X.; Zhang, Y.; Xu, A.; Lu, S.; Liu, H.; Lu, T.; Chen, Y. Insight into the key interactions of bromodomain inhibitors based on molecular docking, interaction fingerprinting, molecular dynamics and binding free energy calculation Mol. BioSyst. 2015, 11, 1295-1304 10.1039/C4MB00723A
-
(2015)
Mol. BioSyst.
, vol.11
, pp. 1295-1304
-
-
Ran, T.1
Zhang, Z.2
Liu, K.3
Lu, Y.4
Li, H.5
Xu, J.6
Xiong, X.7
Zhang, Y.8
Xu, A.9
Lu, S.10
Liu, H.11
Lu, T.12
Chen, Y.13
-
33
-
-
80054911951
-
LigPlot+: multiple ligand-protein interaction diagrams for drug discovery
-
Laskowski, R. A.; Swindells, M. B. LigPlot+: multiple ligand-protein interaction diagrams for drug discovery J. Chem. Inf. Model. 2011, 51, 2778-2786 10.1021/ci200227u
-
(2011)
J. Chem. Inf. Model.
, vol.51
, pp. 2778-2786
-
-
Laskowski, R.A.1
Swindells, M.B.2
|