-
1
-
-
46249134106
-
Thiol cofactors for selenoenzymes and their synthetic mimics
-
Sarma B.K., Mugesh G. (2008) Thiol cofactors for selenoenzymes and their synthetic mimics. Org Biomol Chem 6 : 965 974.
-
(2008)
Org Biomol Chem
, vol.6
, pp. 965-974
-
-
Sarma, B.K.1
Mugesh, G.2
-
2
-
-
36349019345
-
Chemosensitization of B-cell lymphomas by methylseleninic acid involves nuclear factor-kappaB inhibition and the rapid generation of other selenium species
-
Jueliger S., Goenaga-Infante H., Lister T.A., Fitzgibbon J., Joel S.P. (2007) Chemosensitization of B-cell lymphomas by methylseleninic acid involves nuclear factor-kappaB inhibition and the rapid generation of other selenium species. Cancer Res 67 : 10984 10992.
-
(2007)
Cancer Res
, vol.67
, pp. 10984-10992
-
-
Jueliger, S.1
Goenaga-Infante, H.2
Lister, T.A.3
Fitzgibbon, J.4
Joel, S.P.5
-
3
-
-
36649023534
-
Selenium methylselenocysteine protects human hepatoma HepG2 cells against oxidative stress induced by tert-butyl hydroperoxide
-
Cuello S., Ramos S., Mateao R., Martin M.A., Madrid Y., Camara C., Bravo L., Goya L. (2007) Selenium methylselenocysteine protects human hepatoma HepG2 cells against oxidative stress induced by tert-butyl hydroperoxide. Anal Bioanalyt Chem 389 : 2167 2178.
-
(2007)
Anal Bioanalyt Chem
, vol.389
, pp. 2167-2178
-
-
Cuello, S.1
Ramos, S.2
Mateao, R.3
Martin, M.A.4
Madrid, Y.5
Camara, C.6
Bravo, L.7
Goya, L.8
-
4
-
-
38649128166
-
Subchronic oral toxicity studies of Se-methylselenocysteine, an organoselenium compound for breast cancer prevention
-
Johnson W.D., Morrissey R.L., Kapetanovic I., Crowell J.A., McCormick D.L. (2008) Subchronic oral toxicity studies of Se-methylselenocysteine, an organoselenium compound for breast cancer prevention. Food Chem Toxicol 46 : 1068 1078.
-
(2008)
Food Chem Toxicol
, vol.46
, pp. 1068-1078
-
-
Johnson, W.D.1
Morrissey, R.L.2
Kapetanovic, I.3
Crowell, J.A.4
McCormick, D.L.5
-
6
-
-
0035670487
-
Se-methylselenocysteine: A new compound for chemoprevention of breast cancer
-
Medina D., Thompson H., Ganther H., Ip C. (2001) Se-methylselenocysteine: a new compound for chemoprevention of breast cancer. Nutr Cancer 40 : 12.
-
(2001)
Nutr Cancer
, vol.40
, pp. 12
-
-
Medina, D.1
Thompson, H.2
Ganther, H.3
Ip, C.4
-
7
-
-
0000653330
-
Concise syntheses of l-selenomethionine and of l-selenocystine using radical chain reactions
-
Barton D.H.R., Bridon D., Herve Y., Potier P., Thierry J., Zard S.Z. (1986) Concise syntheses of l-selenomethionine and of l-selenocystine using radical chain reactions. Tetrahedron 42 : 4983 4990.
-
(1986)
Tetrahedron
, vol.42
, pp. 4983-4990
-
-
Barton, D.H.R.1
Bridon, D.2
Herve, Y.3
Potier, P.4
Thierry, J.5
Zard, S.Z.6
-
8
-
-
22744448418
-
Internally stabilized selenocysteine derivatives: Syntheses, 77Se NMR and biomimetic studies
-
Phadnis P.P., Mugesh G. (2005) Internally stabilized selenocysteine derivatives: syntheses, 77Se NMR and biomimetic studies. Org Biomol Chem 3 : 2476 2481.
-
(2005)
Org Biomol Chem
, vol.3
, pp. 2476-2481
-
-
Phadnis, P.P.1
Mugesh, G.2
-
10
-
-
30344479954
-
Stereoselective synthesis of Boc-protected l-seleno- and tellurolanthionine, l-seleno- and tellurocystine and derivatives
-
Schneider A., Rodrigues O.E., Paixao M.W., Appelt H.R., Braga A.L., Wessjohann L.A. (2006) Stereoselective synthesis of Boc-protected l-seleno- and tellurolanthionine, l-seleno- and tellurocystine and derivatives. Tetrahedron Lett 47 : 1019 1021.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 1019-1021
-
-
Schneider, A.1
Rodrigues, O.E.2
Paixao, M.W.3
Appelt, H.R.4
Braga, A.L.5
Wessjohann, L.A.6
-
11
-
-
33646900442
-
Chiral seleno-amines from indium selenolates. A straightforward synthesis of selenocysteine derivatives
-
Braga A.L., Schneider P.H., Paixao M.W., Deobald A.M., Peppe C., Bottega D.P. (2006) Chiral seleno-amines from indium selenolates. A straightforward synthesis of selenocysteine derivatives. J Org Chem 71 : 4305 4307.
-
(2006)
J Org Chem
, vol.71
, pp. 4305-4307
-
-
Braga, A.L.1
Schneider, P.H.2
Paixao, M.W.3
Deobald, A.M.4
Peppe, C.5
Bottega, D.P.6
-
12
-
-
33846377131
-
Novel selenium-containing non-natural diamino acids
-
Caputo R., Capone S., Della Greca M., Longobardo L., Pinto G. (2007) Novel selenium-containing non-natural diamino acids. Tetrahedron Lett 48 : 1425 1427.
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 1425-1427
-
-
Caputo, R.1
Capone, S.2
Della Greca, M.3
Longobardo, L.4
Pinto, G.5
-
13
-
-
33847123581
-
Studies on deprotection of cysteine and selenocysteine side-chain protecting groups
-
Harris K.M., Flemer S. Jr., Hondal R.J.J. (2007) Studies on deprotection of cysteine and selenocysteine side-chain protecting groups. J Pept Sci 13 : 81 93.
-
(2007)
J Pept Sci
, vol.13
, pp. 81-93
-
-
Harris, K.M.1
Flemer Jr., S.2
Hondal, R.J.J.3
-
14
-
-
45549094197
-
Synthesis of selenocysteine and selenomethionine derivatives from sulfur-containing amino acids
-
Iwaoka M., Ooka R., Nakazato T., Yoshida S., Oishi S. (2008) Synthesis of selenocysteine and selenomethionine derivatives from sulfur-containing amino acids. Chem Biodivers 5 : 359 374.
-
(2008)
Chem Biodivers
, vol.5
, pp. 359-374
-
-
Iwaoka, M.1
Ooka, R.2
Nakazato, T.3
Yoshida, S.4
Oishi, S.5
-
15
-
-
45549086618
-
Synthesis of selenocysteine and its derivatives with an emphasis on selenenylsulfide (-Se-S-) formation
-
Wessjohann L., Schneider A. (2008) Synthesis of selenocysteine and its derivatives with an emphasis on selenenylsulfide (-Se-S-) formation. Chem Biodivers 5 : 375 388.
-
(2008)
Chem Biodivers
, vol.5
, pp. 375-388
-
-
Wessjohann, L.1
Schneider, A.2
-
16
-
-
33744831760
-
Biological evaluation of tubulysin A: A potential anticancer and antiangiogenic natural product
-
Kaur G., Hollingshead M., Holbeck S., Schauer-Vukašinović V., Camalier R.F., Dömling A., Agarwal S. (2006) Biological evaluation of tubulysin A: a potential anticancer and antiangiogenic natural product. Biochem J 396 : 235 242.
-
(2006)
Biochem J
, vol.396
, pp. 235-242
-
-
Kaur, G.1
Hollingshead, M.2
Holbeck, S.3
Schauer-Vukašinović, V.4
Camalier, R.F.5
Dömling, A.6
Agarwal, S.7
-
17
-
-
32044464374
-
Design and modular parallel synthesis of a MCR derived α-helix mimetic protein-protein interaction inhibitor scaffold
-
Antuch W., Menon S., Chen Q.-Z., Lu Y., Sakamuri S., Beck B., Schauer-Vukašinović V., Agarwal S., Hess S., Dömling A. (2006) Design and modular parallel synthesis of a MCR derived α-helix mimetic protein-protein interaction inhibitor scaffold. Bioorg Med Chem Lett 6 : 1740 1743.
-
(2006)
Bioorg Med Chem Lett
, vol.6
, pp. 1740-1743
-
-
Antuch, W.1
Menon, S.2
Chen, Q.-Z.3
Lu, Y.4
Sakamuri, S.5
Beck, B.6
Schauer-Vukašinović, V.7
Agarwal, S.8
Hess, S.9
Dömling, A.10
-
18
-
-
33751003264
-
Total synthesis of tubulysin U and V
-
Dömling A., Beck B., Eichelberger U., Sakamuri S., Menon S., Lu Y., Chi Q.-Z., Wessjohann L. (2006) Total synthesis of tubulysin U and V. Angew Chem Int Ed Engl 43 : 7235 7239.
-
(2006)
Angew Chem Int Ed Engl
, vol.43
, pp. 7235-7239
-
-
Dömling, A.1
Beck, B.2
Eichelberger, U.3
Sakamuri, S.4
Menon, S.5
Lu, Y.6
Chi, Q.-Z.7
Wessjohann, L.8
-
19
-
-
15444370602
-
Myxobacterial epothilones and tubulysins as promising anticancer agents
-
Dömling A., Richter W. (2005) Myxobacterial epothilones and tubulysins as promising anticancer agents. Mol Divers 9 : 141 147.
-
(2005)
Mol Divers
, vol.9
, pp. 141-147
-
-
Dömling, A.1
Richter, W.2
-
20
-
-
47149111580
-
Isosteric exchange of the acylsulfonamide moiety in Abbott's Bcl-XL protein interaction antagonist
-
Dömling A., Antuch W., Beck B., Schauer-Vukašinović V. (2008) Isosteric exchange of the acylsulfonamide moiety in Abbott's Bcl-XL protein interaction antagonist. Bioorg Med Chem Lett 18 : 4115 4117.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 4115-4117
-
-
Dömling, A.1
Antuch, W.2
Beck, B.3
Schauer-Vukašinović, V.4
-
21
-
-
31544434530
-
Recent developments in isocyanide based multicomponent reactions in applied chemistry
-
Doemling A. (2006) Recent developments in isocyanide based multicomponent reactions in applied chemistry. Chem Rev 126 : 17 89.
-
(2006)
Chem Rev
, vol.126
, pp. 17-89
-
-
Doemling, A.1
-
22
-
-
84995181383
-
The α-addition of immonium ions and anions to isonitriles accompanied by secondary reactions
-
Ugi I. (1962) The α-addition of immonium ions and anions to isonitriles accompanied by secondary reactions. Angew Chem Int Ed Engl 1 : 8 21.
-
(1962)
Angew Chem Int Ed Engl
, vol.1
, pp. 8-21
-
-
Ugi, I.1
-
23
-
-
84986679840
-
Studies on isocyanides and related compounds. A facile synthesis of imidazo[1,5-a]imidazoles
-
Bossio R., Marcaccini S., Pepino R. (1993) Studies on isocyanides and related compounds. A facile synthesis of imidazo[1,5-a]imidazoles. Liebigs Ann Chem 11 : 1229 1231.
-
(1993)
Liebigs Ann Chem
, vol.11
, pp. 1229-1231
-
-
Bossio, R.1
Marcaccini, S.2
Pepino, R.3
-
24
-
-
33645456713
-
One pot synthesis of selenocysteine containing peptoid libraries by Ugi multi-component reactions in water
-
Abbas M., Bethke J., Wessjohann L.A. (2006) One pot synthesis of selenocysteine containing peptoid libraries by Ugi multi-component reactions in water. Chem Commun 5 : 541 543.
-
(2006)
Chem Commun
, vol.5
, pp. 541-543
-
-
Abbas, M.1
Bethke, J.2
Wessjohann, L.A.3
-
26
-
-
0347915136
-
Synthesis of chiral 1,l′-iminodicarboxylic acid derivatives from α-amino acids, aldehydes, isocyanides, and alcohols by the diastereoselective five-center-four-component reaction
-
Demharter A., Hörl W., Herdtweck E., Ugi I. (1996) Synthesis of chiral 1,l′-iminodicarboxylic acid derivatives from α-amino acids, aldehydes, isocyanides, and alcohols by the diastereoselective five-center-four-component reaction. Angew Chem Intl Ed Engl 35 : 173 175.
-
(1996)
Angew Chem Intl Ed Engl
, vol.35
, pp. 173-175
-
-
Demharter, A.1
Hörl, W.2
Herdtweck, E.3
Ugi, I.4
-
27
-
-
0030603133
-
Ugi reactions with trifunctional α-amino acids, aldehydes, isocyanides and alcohols
-
Ugi I., Demharter A., Hörl W., Schmid T. (1996) Ugi reactions with trifunctional α-amino acids, aldehydes, isocyanides and alcohols. Tetrahedron 52 : 11657 11664.
-
(1996)
Tetrahedron
, vol.52
, pp. 11657-11664
-
-
Ugi, I.1
Demharter, A.2
Hörl, W.3
Schmid, T.4
-
28
-
-
0037145162
-
An efficient synthesis of α-amino-β-valerolactones by the Ugi five-center three-component reaction
-
Kim Y.-B., Park S.-J., Keum G., Jang M.-S., Kang S.-B., Lee D.-H., Kim Y. (2002) An efficient synthesis of α-amino-β-valerolactones by the Ugi five-center three-component reaction. Bull Korean Chem Soc 23 : 1277 1284.
-
(2002)
Bull Korean Chem Soc
, vol.23
, pp. 1277-1284
-
-
Kim, Y.-B.1
Park, S.-J.2
Keum, G.3
Jang, M.-S.4
Kang, S.-B.5
Lee, D.-H.6
Kim, Y.7
-
29
-
-
0032563923
-
A facile synthesis of N-carbamoylmethyl-a-aminobutyrolactones by the Ugi multicomponent condensation reaction
-
Park S.-J., Keum G., Kang S.-B., Koh H.-Y., Kim Y., Lee D.-H. (1998) A facile synthesis of N-carbamoylmethyl-a-aminobutyrolactones by the Ugi multicomponent condensation reaction. Tetrahedron Lett 39 : 7019 7112.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 7019-7112
-
-
Park, S.-J.1
Keum, G.2
Kang, S.-B.3
Koh, H.-Y.4
Kim, Y.5
Lee, D.-H.6
-
30
-
-
0346501858
-
Application of MCR: Facile one-pot diastereoselective syntheses of novel chiral a,a′-iminodiacetic acid analogues
-
Sung K., Chen F.-L., Chung M.-J. (2003) Application of MCR: facile one-pot diastereoselective syntheses of novel chiral a,a′-iminodiacetic acid analogues. Mol Divers 6 : 213 221.
-
(2003)
Mol Divers
, vol.6
, pp. 213-221
-
-
Sung, K.1
Chen, F.-L.2
Chung, M.-J.3
-
31
-
-
0001220302
-
An efficient synthesis of morpholin-2-one derivatives using glycolaldehyde dimer by the Ugi multicomponent reaction
-
Kim Y.-B., Choi E.-H., Keum G., Kang S.-B., Lee D.-H., Koh H.-Y., Kim Y. (2001) An efficient synthesis of morpholin-2-one derivatives using glycolaldehyde dimer by the Ugi multicomponent reaction. Org Lett 3 : 4149 4152.
-
(2001)
Org Lett
, vol.3
, pp. 4149-4152
-
-
Kim, Y.-B.1
Choi, E.-H.2
Keum, G.3
Kang, S.-B.4
Lee, D.-H.5
Koh, H.-Y.6
Kim, Y.7
-
32
-
-
33747330904
-
2+ channel blockers
-
2+ channel blockers. Bioorg Med Chem Lett 16 : 5244 5248.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 5244-5248
-
-
Ku, I.-W.1
Cho, S.2
Doddareddy, M.-R.3
Jang, M.-S.4
Keum, G.5
Lee, J.-H.6
Chung, B.-Y.7
Kim, Y.8
Rhim, H.-K.9
Soon, B.10
-
33
-
-
0035796515
-
Repetitive Ugi reactions
-
Constabel F., Ugi I. (2001) Repetitive Ugi reactions. Tetrahedron 57 : 5785 5789.
-
(2001)
Tetrahedron
, vol.57
, pp. 5785-5789
-
-
Constabel, F.1
Ugi, I.2
-
34
-
-
45149100138
-
New end-on thiolactone scaffold by an isocyanide-based multicomponent reaction
-
Beck B., Srivastava S., Dömling A. (2007) New end-on thiolactone scaffold by an isocyanide-based multicomponent reaction. Heterocycles 73 : 177 182.
-
(2007)
Heterocycles
, vol.73
, pp. 177-182
-
-
Beck, B.1
Srivastava, S.2
Dömling, A.3
-
36
-
-
34250848349
-
Nucleophilicity parameters for alkyl and aryl isocyanides
-
Tumanov V.V., Tishkov A.A., Mayr H. (2007) Nucleophilicity parameters for alkyl and aryl isocyanides. Angew Chem Intl Ed Engl 46 : 3563 3566.
-
(2007)
Angew Chem Intl Ed Engl
, vol.46
, pp. 3563-3566
-
-
Tumanov, V.V.1
Tishkov, A.A.2
Mayr, H.3
-
37
-
-
46849091335
-
Catalysis of oxidative protein folding by small-molecule diselenides
-
Beld J., Woycechowsky K.J., Hilvert D. (2008) Catalysis of oxidative protein folding by small-molecule diselenides. Biochemistry 47 : 6985 6987.
-
(2008)
Biochemistry
, vol.47
, pp. 6985-6987
-
-
Beld, J.1
Woycechowsky, K.J.2
Hilvert, D.3
|