-
1
-
-
0035793406
-
Protein design of an HIV-1 entry inhibitor
-
(a) Root MJ, Kay MS, Kim PS. Protein design of an HIV-1 entry inhibitor. Science 2001; 291: 884;
-
(2001)
Science
, vol.291
, pp. 884
-
-
Root, M.J.1
Kay, M.S.2
Kim, P.S.3
-
2
-
-
0032577550
-
HIV entry and its inhibition
-
(b) Chan DC, Kim PS. HIV entry and its inhibition. Cell 1998; 93: 681;
-
(1998)
Cell
, vol.93
, pp. 681
-
-
Chan, D.C.1
Kim, P.S.2
-
3
-
-
0343431526
-
Current evidence and future directions for targeting HIV entry: Therapeutic and prophylactic strategies
-
(c) D'Souza MP, Cairns JS, Plaeger SF. Current evidence and future directions for targeting HIV entry: therapeutic and prophylactic strategies. JAMA 2000; 284: 215;
-
(2000)
JAMA
, vol.284
, pp. 215
-
-
D'Souza, M.P.1
Cairns, J.S.2
Plaeger, S.F.3
-
4
-
-
0031240001
-
Enveloped viruses: A common mode of membrane fusion?
-
(d) Hughson FM. Enveloped viruses: a common mode of membrane fusion? Curr. Biol. 1997; 7: R565;
-
(1997)
Curr. Biol.
, vol.7
-
-
Hughson, F.M.1
-
5
-
-
0028788472
-
The role of human immunodeficiency virus type 1 envelope glycoproteins in virus infection
-
(e) Freed EO and Martin MA. The role of human immunodeficiency virus type 1 envelope glycoproteins in virus infection. J. Biol. Chem. 1995; 270: 23883-23886.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 23883-23886
-
-
Freed, E.O.1
Martin, M.A.2
-
7
-
-
0034687711
-
Structural characterization of the human respiratory syncytial virus fusion protein core
-
Zhao XB. Structural characterization of the human respiratory syncytial virus fusion protein core. Proc. Natl. Acad. Sci. U.S.A. 2000; 97: 14172.
-
(2000)
Proc. Natl. Acad. Sci. U.S.A.
, vol.97
, pp. 14172
-
-
Zhao, X.B.1
-
8
-
-
0027959493
-
Peptides corresponding to a predictive alpha-helical domain of human immunodeficiency virus type 1 gp41 are potent inhibitors of virus infection
-
(a) Wild CT, Shugars DC, Greenwell TK, McDanal CB, Matthews TJ. Peptides corresponding to a predictive alpha-helical domain of human immunodeficiency virus type 1 gp41 are potent inhibitors of virus infection. Proc. Natl. Acad. Sci. U.S.A. 1994; 91: 9770-9774;
-
(1994)
Proc. Natl. Acad. Sci. U.S.A.
, vol.91
, pp. 9770-9774
-
-
Wild, C.T.1
Shugars, D.C.2
Greenwell, T.K.3
McDanal, C.B.4
Matthews, T.J.5
-
9
-
-
0032433685
-
Evidence that a prominent cavity in the coiled coil of HIV type 1 gp41 is an attractive drug target
-
(b) Chan DC, Chutkowski CT, Kim PS. Evidence that a prominent cavity in the coiled coil of HIV type 1 gp41 is an attractive drug target. Proc. Natl. Acad. Sci. U.S.A. 1998; 95: 15613-15617;
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, pp. 15613-15617
-
-
Chan, D.C.1
Chutkowski, C.T.2
Kim, P.S.3
-
10
-
-
0033214895
-
Inhibiting HIV- 1 entry: Discovery of D-peptide inhibitors that target the gp41 coiled-coil pocket
-
(c) Eckert DM, Malashkevich VN, Hong LH, Carr PA, Kim PS. Inhibiting HIV- 1 entry: discovery of D-peptide inhibitors that target the gp41 coiled-coil pocket. Cell 1999; 99: 103-115.
-
(1999)
Cell
, vol.99
, pp. 103-115
-
-
Eckert, D.M.1
Malashkevich, V.N.2
Hong, L.H.3
Carr, P.A.4
Kim, P.S.5
-
12
-
-
0038065763
-
Dilation of the human immunodeficiency virus-1 envelope glycoprotein fusion pore revealed by the inhibitory action of a synthetic peptide from gp41
-
(b) Muñoz-Barroso I, Durell S, Sakaguchi K, Appella E, Blumenthal R. Dilation of the human immunodeficiency virus-1 envelope glycoprotein fusion pore revealed by the inhibitory action of a synthetic peptide from gp41. J. Cell. Biol. 1998; 140: 315-323;
-
(1998)
J. Cell. Biol.
, vol.140
, pp. 315-323
-
-
Muñoz-Barroso, I.1
Durell, S.2
Sakaguchi, K.3
Appella, E.4
Blumenthal, R.5
-
13
-
-
0037470227
-
The prefusogenic intermediate of HIV-1 gp41 contains exposed C-peptide regions
-
(c) Koshiba T., Chan DC. The prefusogenic intermediate of HIV-1 gp41 contains exposed C-peptide regions. J. Biol. Chem. 2003; 278: 7573-7579;
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 7573-7579
-
-
Koshiba, T.1
Chan, D.C.2
-
14
-
-
0035949493
-
Design of potent inhibitors of HIV-1 entry from the gp41 N-peptide region
-
(d) Eckert DM, Kim PK. Design of potent inhibitors of HIV-1 entry from the gp41 N-peptide region. Proc. Natl Acad. Sci. U.S.A. 2001; 98: 11187-11192.
-
(2001)
Proc. Natl Acad. Sci. U.S.A.
, vol.98
, pp. 11187-11192
-
-
Eckert, D.M.1
Kim, P.K.2
-
15
-
-
0035800816
-
Design and properties of N(CCG)-gp41, a chimeric gp41 molecule with nanomolar HIV fusion inhibitory activity
-
(a) Louis JM, Bewley CA, Clore GM. Design and properties of N(CCG)-gp41, a chimeric gp41 molecule with nanomolar HIV fusion inhibitory activity. J. Biol. Chem. 2001; 276: 29485-29489;
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 29485-29489
-
-
Louis, J.M.1
Bewley, C.A.2
Clore, G.M.3
-
16
-
-
0037490139
-
Covalent trimers of the internal N-terminal trimeric coiled-coil of gp41 and antibodies directed against them are potent inhibitors of HIV envelope-mediated cell fusion
-
(b) Louis JM, Nesheiwat I, Chang L, Clore GM, Bewley CA. Covalent trimers of the internal N-terminal trimeric coiled-coil of gp41 and antibodies directed against them are potent inhibitors of HIV envelope-mediated cell fusion. J. Biol. Chem. 2003; 278: 20278-20285;
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 20278-20285
-
-
Louis, J.M.1
Nesheiwat, I.2
Chang, L.3
Clore, G.M.4
Bewley, C.A.5
-
17
-
-
41649121143
-
Design of an engineered N-terminal HIV-1 gp41 trimer with enhanced stability and potency
-
DOI 10.1110/ps.073307608
-
(c) Dwyer JJ, Wilson KL, Martin K, Seedorff JE, Hasan A, Medinas RJ, Davison DK, Feese MD, Richter HT, Kim H, Matthews TJ, Delmedico MK. Design of an engineered N-terminal HIV-1 gp41 trimer with enhanced stability and potency. Protein Sci. 2008; 17: 633-643. (Pubitemid 351480857)
-
(2008)
Protein Science
, vol.17
, Issue.4
, pp. 633-643
-
-
Dwyer, J.J.1
Wilson, K.L.2
Martin, K.3
Seedorff, J.E.4
Hasan, A.5
Medinas, R.J.6
Davison, D.K.7
Feese, M.D.8
Richter, H.-T.9
Kim, H.10
Matthews, T.J.11
Delmedico, M.K.12
-
18
-
-
0034645796
-
Inhibition of HIV-1 entry before gp41 folds into its fusion-active conformation
-
Kliger Y, Shai Y. Inhibition of HIV-1 entry before gp41 folds into its fusion-active conformation. J.Mol. Biol. 2000; 295: 163-168.
-
(2000)
J.Mol. Biol.
, vol.295
, pp. 163-168
-
-
Kliger, Y.1
Shai, Y.2
-
19
-
-
0032876381
-
Selection of gp41- mediated HIV-1 cell entry inhibitors from biased combinatorial libraries of non-natural binding elements
-
Ferrer ME, Kapoor TM, Strassmaier TL, Weissenhorn W., Skehel JJ, Oprian DT, Schreiber SL, Wiley DC, Harrison SC. Selection of gp41- mediated HIV-1 cell entry inhibitors from biased combinatorial libraries of non-natural binding elements. Nat. Struct. Biol. 1999; 6: 953-960;
-
(1999)
Nat. Struct. Biol.
, vol.6
, pp. 953-960
-
-
Ferrer, M.E.1
Kapoor, T.M.2
Strassmaier, T.L.3
Weissenhorn, W.4
Skehel, J.J.5
Oprian, D.T.6
Schreiber, S.L.7
Wiley, D.C.8
Harrison, S.C.9
-
20
-
-
0028834461
-
A trimeric structural domain of the HIV-1 transmembrane glycoprotein
-
(b) Lu M, Blacklow SC, Kim PS. A trimeric structural domain of the HIV-1 transmembrane glycoprotein. Nat. Struct. Biol. 1995; 2: 1075-1082.
-
(1995)
Nat. Struct. Biol.
, vol.2
, pp. 1075-1082
-
-
Lu, M.1
Blacklow, S.C.2
Kim, P.S.3
-
21
-
-
0030962291
-
Atomic structure of the ectodomain from HIV-1 gp41
-
DOI 10.1038/387426a0
-
Weissenhorn W, Dessen A, Harrison SC, Skehel JJ, Wiley DC. Atomic structure of the ectodomain from HIV gp41. Nature 1997; 387: 426-430. (Pubitemid 27227210)
-
(1997)
Nature
, vol.387
, Issue.6631
, pp. 426-430
-
-
Weissenhorn, W.1
Dessen, A.2
Harrison, S.C.3
Skehel, J.J.4
Wiley, D.C.5
-
22
-
-
35148889908
-
A template-assembled model of the N-peptide helix bundle for HIV-1 gp41 with high affinity for C-peptide
-
(a) Xu W, Taylor JW. A template-assembled model of the N-peptide helix bundle for HIV-1 gp41 with high affinity for C-peptide. Chem. Biol. Drug Des. 2007; 70: 319-328;
-
(2007)
Chem. Biol. Drug Des.
, vol.70
, pp. 319-328
-
-
Xu, W.1
Taylor, J.W.2
-
23
-
-
24644449058
-
Covalent stabilization of coiled coils of the HIV gp41 N region yields extremely potent and broad inhibitors of viral infection
-
(b) Bianchi E, Finotto M, Ingallinella P, Hrin R, Carella AV, Hou XS, Schleif WA, Miller MD, Geleziunas R, Pessi A. Covalent stabilization of coiled coils of the HIV gp41 N region yields extremely potent and broad inhibitors of viral infection. Proc. Natl. Acad. Sci. U.S.A. 2005; 102: 12903-12908;
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 12903-12908
-
-
Bianchi, E.1
Finotto, M.2
Ingallinella, P.3
Hrin, R.4
Carella, A.V.5
Hou, X.S.6
Schleif, W.A.7
Miller, M.D.8
Geleziunas, R.9
Pessi, A.10
-
25
-
-
77951287748
-
Remodeling of dynamic structures of HIV-1 envelope proteins leads to synthetic antigen molecules inducing neutralizing antibodies
-
(d) Nakahara T, Nomura W, Ohba K, Ohya A, Tanaka T, Hashimoto C, Narumi T, Murakami T, Yamamoto N, Tamamura H. Remodeling of dynamic structures of HIV-1 envelope proteins leads to synthetic antigen molecules inducing neutralizing antibodies. Bioconjug. 2010; 21: 709-714.
-
(2010)
Bioconjug.
, vol.21
, pp. 709-714
-
-
Nakahara, T.1
Nomura, W.2
Ohba, K.3
Ohya, A.4
Tanaka, T.5
Hashimoto, C.6
Narumi, T.7
Murakami, T.8
Yamamoto, N.9
Tamamura, H.10
-
26
-
-
0000266881
-
Template-assembled synthetic proteins designed to adopt a globular, four-helix bundle conformation form ionic channels in lipid bilayers
-
Grove A, Mutter M, Rivier JE, Montal M. Template-assembled synthetic proteins designed to adopt a globular, four-helix bundle conformation form ionic channels in lipid bilayers. J. Am. Chem. Soc. 1993; 115: 5919-5924.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 5919-5924
-
-
Grove, A.1
Mutter, M.2
Rivier, J.E.3
Montal, M.4
-
27
-
-
0025162353
-
De novo design of a Zn 2+binding protein
-
(a) Handel T, DeGrado WF. De novo design of a Zn 2+binding protein. J. Am. Chem. Soc. 1990; 112: 6710-6711;
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 6710-6711
-
-
Handel, T.1
DeGrado, W.F.2
-
28
-
-
0027177971
-
Metal ion-dependent modulation of the dynamics of a designed protein
-
(b) Handel TM, Williams SA, DeGrado WF. Metal ion-dependent modulation of the dynamics of a designed protein. Science 1993; 261: 879-885.
-
(1993)
Science
, vol.261
, pp. 879-885
-
-
Handel, T.M.1
Williams, S.A.2
DeGrado, W.F.3
-
29
-
-
84989506919
-
Design of an artificial fourhelix bundle metalloprotein via a novel ruthenium(II)-assisted self-assembly process
-
(a) Ghadiri MR, Soares C, Choi C. Design of an artificial fourhelix bundle metalloprotein via a novel ruthenium(II)-assisted self-assembly process. J. Am. Chem. Soc. 1992; 114: 4000-4002;
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 4000-4002
-
-
Ghadiri, M.R.1
Soares, C.2
Choi, C.3
-
30
-
-
33748244071
-
De novo design of a novel heterodinuclear three-helix bundle metalloprotein
-
(b) Ghadiri RM, Case MA. De novo design of a novel heterodinuclear three-helix bundle metalloprotein. Angew Chem. Int. Ed. Engl. 1993; 32: 1594-1597.
-
(1993)
Angew Chem. Int. Ed. Engl.
, vol.32
, pp. 1594-1597
-
-
Ghadiri, R.M.1
Case, M.A.2
-
31
-
-
15844379316
-
A template-induced incipient collagen-like triple-helical structure
-
(a) Goodman M, Feng Y, Melacini GA, Taulane JP. A template-induced incipient collagen-like triple-helical structure. J. Am.Chem. Soc. 1996; 118:5156-5157;
-
(1996)
J. Am.Chem. Soc.
, vol.118
, pp. 5156-5157
-
-
Goodman, M.1
Feng, Y.2
Melacini, G.A.3
Taulane, J.P.4
-
32
-
-
0037184412
-
TREN (tris(2-aminoethyl)amine): An effective scaffold for the assembly of triple helical collagen mimetic structures
-
(b) Kwak J, Capua AN, Locardi EE, Goodman M. TREN (tris(2-aminoethyl) amine): an effective scaffold for the assembly of triple helical collagen mimetic structures. J. Am. Chem. Soc. 2002; 124: 14085-14091.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 14085-14091
-
-
Kwak, J.1
Capua, A.N.2
Locardi, E.E.3
Goodman, M.4
-
33
-
-
0035938175
-
Control of functional group proximity and directionbyconformationalnetworks: Synthesisandstereodynamics of persubstituted arenes
-
Kilway KV, Siegel JS. Control of functional group proximity and directionbyconformationalnetworks: synthesisandstereodynamics of persubstituted arenes. Tetrahedron 2001; 57: 3615-3627.
-
(2001)
Tetrahedron
, vol.57
, pp. 3615-3627
-
-
Kilway, K.V.1
Siegel, J.S.2
-
35
-
-
0035766088
-
Metal triggered fluorescence sensing of citrate using a synthetic receptor
-
(b) Cabell LA, Best MD, Lavigne JJ, Schneider SE, Perreault DM, Monahan MK, Anslyn EV. Metal triggered fluorescence sensing of citrate using a synthetic receptor. J. Chem. Soc., Perkin Trans 2 2001; 3: 315-323.
-
(2001)
J. Chem. Soc., Perkin Trans 2
, vol.3
, pp. 315-323
-
-
Cabell, L.A.1
Best, M.D.2
Lavigne, J.J.3
Schneider, S.E.4
Perreault, D.M.5
Monahan, M.K.6
Anslyn, E.V.7
-
36
-
-
0034716346
-
Coupling rational design with libraries leads to the production of an ATP selective chemosensor
-
(a) Schneider SE, O'Neil SN, Anslyn EV. Coupling rational design with libraries leads to the production of an ATP selective chemosensor. J. Am. Chem. Soc. 2000; 122: 542-543;
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 542-543
-
-
Schneider, S.E.1
O'Neil, S.N.2
Anslyn, E.V.3
-
37
-
-
14944376608
-
A molecular flytrap for the selective binding of citrate and other tricarboxylates in water
-
(b) Schmuck C, Schwegmann M. A molecular flytrap for the selective binding of citrate and other tricarboxylates in water. J. Am. Chem. Soc. 2005; 127: 3373-3379.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 3373-3379
-
-
Schmuck, C.1
Schwegmann, M.2
-
39
-
-
0041305923
-
Controlling the oxygenation level of hemoglobin by using a synthetic receptor for 2,3-bisphosphoglycerate
-
Zhong Z, Anslyn EV. Controlling the oxygenation level of hemoglobin by using a synthetic receptor for 2,3-bisphosphoglycerate. Angew Chem. Int. Ed. Engl 2003; 46: 3005-3008.
-
(2003)
Angew Chem. Int. Ed. Engl
, vol.46
, pp. 3005-3008
-
-
Zhong, Z.1
Anslyn, E.V.2
-
40
-
-
0038671938
-
The hydrophobic pocket contributes to the structural stability of the N-terminal coiled coil of HIV gp41 but is not required for six-helix bundle formation
-
(a) Dwyer JJ, Hasan A, Wilson KL, White JM, Matthews TJ, Delmedico MK. The hydrophobic pocket contributes to the structural stability of the N-terminal coiled coil of HIV gp41 but is not required for six-helix bundle formation. Biochemistry 2003; 42: 4945-4953;
-
(2003)
Biochemistry
, vol.42
, pp. 4945-4953
-
-
Dwyer, J.J.1
Hasan, A.2
Wilson, K.L.3
White, J.M.4
Matthews, T.J.5
Delmedico, M.K.6
-
41
-
-
4444375658
-
Resistance to enfuvirtide, the first HIV fusion inhibitor
-
(b) Greenberg ML, Cammack N. Resistance to enfuvirtide, the first HIV fusion inhibitor. J. Antimicrob. Chemother. 2004; 54: 333-340;
-
(2004)
J. Antimicrob. Chemother.
, vol.54
, pp. 333-340
-
-
Greenberg, M.L.1
Cammack, N.2
-
42
-
-
25144489604
-
Impact of human immunodeficiency virus type 1 gp41 amino acid substitutions selected during enfuvirtide treatment on gp41 binding and antiviral potency of enfuvirtide in vitro
-
(c) Mink M, Mosier SM, Janumpalli S, Davison D, Jin L, Melby T, Sista P, Erickson J, Lambert D, Stanfield-Oakley SA, Salgo M, Cammack N, Matthews T, Greenberg ML. Impact of human immunodeficiency virus type 1 gp41 amino acid substitutions selected during enfuvirtide treatment on gp41 binding and antiviral potency of enfuvirtide in vitro. J. Virol. 2005; 79: 12447-12454.
-
(2005)
J. Virol.
, vol.79
, pp. 12447-12454
-
-
Mink, M.1
Mosier, S.M.2
Janumpalli, S.3
Davison, D.4
Jin, L.5
Melby, T.6
Sista, P.7
Erickson, J.8
Lambert, D.9
Stanfield-Oakley, S.A.10
Salgo, M.11
Cammack, N.12
Matthews, T.13
Greenberg, M.L.14
-
43
-
-
0033607028
-
Structure-based identification of small molecule antiviral compounds targeted to the gp41 core structure of the human immunodeficiency virus type 1
-
(a) Debnath AK, Radigan L, Jiang S. Structure-based identification of small molecule antiviral compounds targeted to the gp41 core structure of the human immunodeficiency virus type 1. J. Med. Chem. 1999; 42: 3203-3209;
-
(1999)
J. Med. Chem.
, vol.42
, pp. 3203-3209
-
-
Debnath, A.K.1
Radigan, L.2
Jiang, S.3
-
44
-
-
1342279557
-
Synthesis and anti-HIV-1 activity of 4-[4-(4,6-bisphenylamino-triazin-2- ylamino)-5-methoxy- 2-methylphenylazo]-5-hydroxynaphthalene-2,7-disulfonic acid and its derivatives
-
(b) Naicker KP. Synthesis and anti-HIV-1 activity of 4-[4-(4,6- bisphenylamino-triazin-2-ylamino)-5-methoxy- 2-methylphenylazo]-5- hydroxynaphthalene-2,7-disulfonic acid and its derivatives. Bioorg. Med. Chem. 2004; 12: 1215-1220;
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 1215-1220
-
-
Naicker, K.P.1
-
45
-
-
7044231888
-
Conserved residues in the coiled-coil pocket of human immunodeficiency virus type 1 gp41 are essential for viral replication and interhelical interaction
-
(c) Mo H, Konstantinidis AK, Stewart KD, Dekhtyar T, Ng T, Swift K, Matayoshi ED, Kati W, Kohlbrenner W, Molla A. Conserved residues in the coiled-coil pocket of human immunodeficiency virus type 1 gp41 are essential for viral replication and interhelical interaction. Virology 2004; 329: 319-327.
-
(2004)
Virology
, vol.329
, pp. 319-327
-
-
Mo, H.1
Konstantinidis, A.K.2
Stewart, K.D.3
Dekhtyar, T.4
Ng, T.5
Swift, K.6
Matayoshi, E.D.7
Kati, W.8
Kohlbrenner, W.9
Molla, A.10
-
46
-
-
23744500512
-
Preparation of 1,3,5-tris(aminomethyl)-2,4,6-triethylbenzene from two versatile 1,3,5-tri(halosubstituted) 2,4,6-triethylbenzenederivatives
-
Wallace KJ, Hanes R, Anslyn E, Morey J, Kilway KV, Siegel J. Preparation of 1,3,5-tris(aminomethyl)-2,4,6-triethylbenzene from two versatile 1,3,5-tri(halosubstituted) 2,4,6-triethylbenzenederivatives. Synthesis 2005; 2080-2083.
-
(2005)
Synthesis
, pp. 2080-2083
-
-
Wallace, K.J.1
Hanes, R.2
Anslyn, E.3
Morey, J.4
Kilway, K.V.5
Siegel, J.6
-
48
-
-
0037667047
-
Large-scale manufacture of peptide therapeutics by chemical synthesis
-
(a) Bray B. Large-scale manufacture of peptide therapeutics by chemical synthesis. Nat. Rev. Drug Discov. 2003; 2: 587-593;
-
(2003)
Nat. Rev. Drug Discov.
, vol.2
, pp. 587-593
-
-
Bray, B.1
-
49
-
-
28044444334
-
Development of HIV fusion inhibitors
-
(b) Schneider SE, Bray BL, Mader CJ, Friedrich PE, Anderson MW, Taylor TS, Boshernitzan N, Niemi TE, Fulcher BC, Whight SR, White JM, Greene RJ, Stoltenberg LE, Lichty M. Development of HIV fusion inhibitors. J. Pept. Sci. 2005; 11: 744-753.
-
(2005)
J. Pept. Sci.
, vol.11
, pp. 744-753
-
-
Schneider, S.E.1
Bray, B.L.2
Mader, C.J.3
Friedrich, P.E.4
Anderson, M.W.5
Taylor, T.S.6
Boshernitzan, N.7
Niemi, T.E.8
Fulcher, B.C.9
Whight, S.R.10
White, J.M.11
Greene, R.J.12
Stoltenberg, L.E.13
Lichty, M.14
-
50
-
-
0032546258
-
An appraisal of new variants of Dde amine protecting group for solid phase peptide synthesis
-
Chhabra SR, Hothi B, David J, Evans DJ, White PD, Bycroft BW, Chan WC. An appraisal of new variants of Dde amine protecting group for solid phase peptide synthesis. Tetrahedron Lett. 1998; 39: 1603.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 1603
-
-
Chhabra, S.R.1
Hothi, B.2
David, J.3
Evans, D.J.4
White, P.D.5
Bycroft, B.W.6
Chan, W.C.7
-
51
-
-
0025671995
-
[(9-Fluorenylmethyl)oxy]carbonyl (FMOC) amino acid fluorides. Convenient new peptide coupling reagents applicable to the FMOC/tert-butyl strategy for solution and solid-phase syntheses
-
(a) Carpino LA, Sadat-Aalaee D, Chao HG, DeSelms RH. [(9-Fluorenylmethyl) oxy]carbonyl (FMOC) amino acid fluorides. Convenient new peptide coupling reagents applicable to the FMOC/tert-butyl strategy for solution and solid-phase syntheses. J. Am. Chem. Soc. 1990; 112: 9651-9652;
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 9651-9652
-
-
Carpino, L.A.1
Sadat-Aalaee, D.2
Chao, H.G.3
DeSelms, R.H.4
-
53
-
-
0030605880
-
Fmoc amino acid fluorides in peptide synthesis - Extension of the method to extremely hindered amino acids
-
DOI 10.1016/0040-4039(96)01160-4
-
(c) Wenschuh H, Beyermann M, Winter R, Bienert M, Ionescu D, Carpino LA. Fmoc amino acid fluorides in peptide synthesis - Extension of themethod to extremely hindered amino acids. Tetrahedron Lett. 1996; 37: 5483-5486. (Pubitemid 26241066)
-
(1996)
Tetrahedron Letters
, vol.37
, Issue.31
, pp. 5483-5486
-
-
Wenschuh, H.1
Beyermann, M.2
Winter, R.3
Bienert, M.4
Ionescu, D.5
Carpino, L.A.6
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