-
12
-
-
33745263964
-
-
B. Wu J. Chen J. D. Warren G. Chen Z. Hua S. J. Danishefsky Angew. Chem., Int. Ed. 2006 45 4116
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 4116
-
-
Wu, B.1
Chen, J.2
Warren, J.D.3
Chen, G.4
Hua, Z.5
Danishefsky, S.J.6
-
15
-
-
61849123611
-
-
C. Piontek D. V. Silva C. Heinlein C. Pöhner S. Mezzato P. Ring A. Martin F. X. Schmid C. Unverzagt Angew. Chem., Int. Ed. 2009 48 1941
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 1941
-
-
Piontek, C.1
Silva, D.V.2
Heinlein, C.3
Pöhner, C.4
Mezzato, S.5
Ring, P.6
Martin, A.7
Schmid, F.X.8
Unverzagt, C.9
-
16
-
-
61849161082
-
-
C. Piontek P. Ring O. Harjes C. Heinlein S. Mezzato N. Lombana C. Pöhner M. Püttner D. V. Silva A. Martin F. X. Schmid C. Unverzagt Angew. Chem., Int. Ed. 2009 48 1936
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 1936
-
-
Piontek, C.1
Ring, P.2
Harjes, O.3
Heinlein, C.4
Mezzato, S.5
Lombana, N.6
Pöhner, C.7
Püttner, M.8
Silva, D.V.9
Martin, A.10
Schmid, F.X.11
Unverzagt, C.12
-
22
-
-
20144371341
-
-
S.-Y. Chen S. Cressman F. Mao H. Shao D. W. Low H. S. Beilan E. N. Cagle M. Carnevali V. Gueriguian P. J. Keogh H. Porter S. M. Stratton M. C. Wiedeke L. Savatski J. W. Adamson C. E. Bozzini A. Kung S. B. H. Kent J. A. Bradburne G. G. Kochendoerfer Chem. Biol. 2005 12 371
-
(2005)
Chem. Biol.
, vol.12
, pp. 371
-
-
Chen, S.-Y.1
Cressman, S.2
Mao, F.3
Shao, H.4
Low, D.W.5
Beilan, H.S.6
Cagle, E.N.7
Carnevali, M.8
Gueriguian, V.9
Keogh, P.J.10
Porter, H.11
Stratton, S.M.12
Wiedeke, M.C.13
Savatski, L.14
Adamson, J.W.15
Bozzini, C.E.16
Kung, A.17
Kent, S.B.H.18
Bradburne, J.A.19
Kochendoerfer, G.G.20
more..
-
23
-
-
34247622775
-
-
S. I. van Kasteren H. B. Kramer H. H. Jensen S. J. Campbell J. Kirkpatrick N. J. Oldham D. C. Anthony B. G. Davis Nature 2007 446 1105
-
(2007)
Nature
, vol.446
, pp. 1105
-
-
Van Kasteren, S.I.1
Kramer, H.B.2
Jensen, H.H.3
Campbell, S.J.4
Kirkpatrick, J.5
Oldham, N.J.6
Anthony, D.C.7
Davis, B.G.8
-
38
-
-
0037423148
-
-
G. G. Kochendoerfer S.-Y. Chen F. Mao S. Cressman S. Traviglia H. Shao C. L. Hunter D. W. Low E. N. Cagle M. Carnevali V. Gueriguian P. J. Keogh H. Porter S. M. Stratton M. C. Wiedeke J. Wilken J. Tang J. J. Levy L. P. Miranda M. M. Crnogorac S. Kalbag P. Botti J. Schindler-Horvat L. Savatski J. W. Adamson A. Kung S. B. H. Kent J. A. Bradburne Science 2003 299 884
-
(2003)
Science
, vol.299
, pp. 884
-
-
Kochendoerfer, G.G.1
Chen, S.-Y.2
Mao, F.3
Cressman, S.4
Traviglia, S.5
Shao, H.6
Hunter, C.L.7
Low, D.W.8
Cagle, E.N.9
Carnevali, M.10
Gueriguian, V.11
Keogh, P.J.12
Porter, H.13
Stratton, S.M.14
Wiedeke, M.C.15
Wilken, J.16
Tang, J.17
Levy, J.J.18
Miranda, L.P.19
Crnogorac, M.M.20
Kalbag, S.21
Botti, P.22
Schindler-Horvat, J.23
Savatski, L.24
Adamson, J.W.25
Kung, A.26
Kent, S.B.H.27
Bradburne, J.A.28
more..
-
49
-
-
77749253827
-
-
See supporting information for further details
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See supporting information for further details.
-
-
-
-
50
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77749297238
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-
Note
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Note that 7 (Fig. 1) is not a thioester though conversion is plotted on the same graph for comparison.
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-
-
-
51
-
-
68849086984
-
-
Z. Du P. T. Shemella Y. Liu S. A. McCallum B. Pereira S. K. Nayak G. Belfort M. Belfort C. Wang J. Am. Chem. Soc. 2009 131 11581
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 11581
-
-
Du, Z.1
Shemella, P.T.2
Liu, Y.3
McCallum, S.A.4
Pereira, B.5
Nayak, S.K.6
Belfort, G.7
Belfort, M.8
Wang, C.9
-
53
-
-
69949151708
-
-
N. Suree C. K. Liew V. A. Villareal W. Thieu E. A. Fadeev J. J. Clemens M. E. Jung R. T. Clubb J. Biol. Chem. 2009 284 24465
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 24465
-
-
Suree, N.1
Liew, C.K.2
Villareal, V.A.3
Thieu, W.4
Fadeev, E.A.5
Clemens, J.J.6
Jung, M.E.7
Clubb, R.T.8
-
54
-
-
77749253825
-
-
Note
-
Coupling of cysteine to hydroxy-functionalised resins employing HBTU/HOBt may well lead to racemisation of the C-terminal cysteine though this should be of little consequence since the cysteine is excised. Cysteine racemisation can also be minimised by using a trityl resin, e.g. NovaSYN TGT
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56
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77749278716
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Note
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The D8E mutation is non-essential as hydrolysis at Asp is slow relative to thioesterification but the conservative mutation is unlikely to affect bioactivity as this region does not bind the EPO receptor.
-
-
-
-
61
-
-
77749253824
-
-
D. Macmillan, J. Blanc, J. PCT, Int. Appl., 2008, WO2008001109
-
(2008)
-
-
MacMillan, D.1
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