-
1
-
-
34248357083
-
Nicotinamide adenine dinucleotide metabolism as an attractive target for drug discovery
-
Khan, J. A.; Forouhar, F.; Tao, X.; Tong, L. Nicotinamide adenine dinucleotide metabolism as an attractive target for drug discovery. Expert Opin. Ther. Targets 2007, 11, 695-705.
-
(2007)
Expert Opin. Ther. Targets
, vol.11
, pp. 695-705
-
-
Khan, J.A.1
Forouhar, F.2
Tao, X.3
Tong, L.4
-
2
-
-
25144496904
-
The Sir 2 family of protein deacetylases
-
Denu, J. M. The Sir 2 family of protein deacetylases. Curr. Opin. Chem. Biol. 2005, 9, 431-440.
-
(2005)
Curr. Opin. Chem. Biol
, vol.9
, pp. 431-440
-
-
Denu, J.M.1
-
3
-
-
33845921542
-
NAD+ metabolism in health and disease
-
Belenky, P.; Bogan, K. L.; Brenner, C.NAD+ metabolism in health and disease. Trends Biochem. Sci. 2007, 32, 12-19.
-
(2007)
Trends Biochem. Sci
, vol.32
, pp. 12-19
-
-
Belenky, P.1
Bogan, K.L.2
Brenner, C.3
-
4
-
-
1542346420
-
The new life of a centenarian: Signalling functions of NAD(P)
-
Berger, F.; Ramírez-Hernández, M. H.; Ziegler, M. The new life of a centenarian: signalling functions of NAD(P). Trends Biochem. Sci. 2004, 29, 111-118.
-
(2004)
Trends Biochem. Sci
, vol.29
, pp. 111-118
-
-
Berger, F.1
Ramírez-Hernández, M.H.2
Ziegler, M.3
-
6
-
-
50349083286
-
Evolution and function of the ADP ribosyl cyclase/CD38 gene family in physiology and pathology
-
Malavasi, F.; Deaglio, S.; Funaro, A.; Ferrero, E.; Horenstein, A. L.; Ortolan, E.; Vaisitti, T.; Aydin, S. Evolution and function of the ADP ribosyl cyclase/CD38 gene family in physiology and pathology. Physiol. Rev. 2008, 88, 841-886.
-
(2008)
Physiol. Rev
, vol.88
, pp. 841-886
-
-
Malavasi, F.1
Deaglio, S.2
Funaro, A.3
Ferrero, E.4
Horenstein, A.L.5
Ortolan, E.6
Vaisitti, T.7
Aydin, S.8
-
7
-
-
1642458398
-
+ homeostasis in man
-
+ homeostasis in man. Cell. Mol. Life Sci. 2004, 61, 19-34.
-
(2004)
Cell. Mol. Life Sci
, vol.61
, pp. 19-34
-
-
Magni, G.1
Amici, A.2
Emanuelli, M.3
Orsomando, G.4
Raffaelli, N.5
Ruggieri, S.6
-
9
-
-
0242526050
-
FK866, a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltransferase, represents a novel mechanism for induction of tumor cell apoptosis
-
Hasmann, M.; Schemainda, I. FK866, a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltransferase, represents a novel mechanism for induction of tumor cell apoptosis. Cancer Res. 2003, 63, 7436-7442.
-
(2003)
Cancer Res
, vol.63
, pp. 7436-7442
-
-
Hasmann, M.1
Schemainda, I.2
-
10
-
-
65149084441
-
The NAD biosynthesis inhibitor APO866 has potent antitumor activity against hematologic malignancies
-
Nahimana, A.; Attinger, A.; Aubry, D.; Greaney, P.; Ireson, C.; Thougaard, A. V.; Tjoernelund, J.; Dawson, K. M.; Dupuis, M.; Duchosal, M A. The NAD biosynthesis inhibitor APO866 has potent antitumor activity against hematologic malignancies. Blood 2009, 113, 3276-3286.
-
(2009)
Blood
, vol.113
, pp. 3276-3286
-
-
Nahimana, A.1
Attinger, A.2
Aubry, D.3
Greaney, P.4
Ireson, C.5
Thougaard, A.V.6
Tjoernelund, J.7
Dawson, K.M.8
Dupuis, M.9
Duchosal, M.A.10
-
11
-
-
77249088730
-
-
accessed on May 25, 2009
-
http://www.clinicaltrials.gov/ct2/results?term=APO866; accessed on May 25, 2009.
-
-
-
-
12
-
-
77249166664
-
-
accessed on May 25, 2009
-
http://www.clinicaltrials.gov/ct2/results?term=GMX1777; accessed on May 25, 2009.
-
-
-
-
13
-
-
0031472361
-
Novel cyanoguanidines with potent oral antitumour activity
-
Schou, C.; Ottosen, E. R.; Petersen, H. J.; Björkling, F.; Latini, S.; Hjarnaa, P. V.; Bramm, E.; Binderup, L. Novel cyanoguanidines with potent oral antitumour activity. Bioorg. Med. Chem. 1997, 7, 3095-3100.
-
(1997)
Bioorg. Med. Chem
, vol.7
, pp. 3095-3100
-
-
Schou, C.1
Ottosen, E.R.2
Petersen, H.J.3
Björkling, F.4
Latini, S.5
Hjarnaa, P.V.6
Bramm, E.7
Binderup, L.8
-
14
-
-
38649096263
-
Anticancer agent CHS-828 inhibits cellular synthesis of NAD
-
Olesen, U. H.; Christensen, M. K.; Björkling, F.; Jäättelä, M.; Jensen, P. B.; Sehested, M.; Nielsen, S. J. Anticancer agent CHS-828 inhibits cellular synthesis of NAD. Biochem. Biophys. Res. Commun. 2008, 367, 799-804.
-
(2008)
Biochem. Biophys. Res. Commun
, vol.367
, pp. 799-804
-
-
Olesen, U.H.1
Christensen, M.K.2
Björkling, F.3
Jäättelä, M.4
Jensen, P.B.5
Sehested, M.6
Nielsen, S.J.7
-
15
-
-
47649094272
-
Synthesis and biological evaluation of isosteric analogues ofFK866, an inhibitor of NAD salvage
-
Galli, U.; Ercolano, E.; Carraro, L.; Blasi Roman, C. R.; Sorba, G.; Canonico, P. L.; Genazzani, A. A.; Tron, G. C.; Billington, R. A. Synthesis and biological evaluation of isosteric analogues ofFK866, an inhibitor of NAD salvage. ChemMedChem 2008, 3, 771-779.
-
(2008)
ChemMedChem
, vol.3
, pp. 771-779
-
-
Galli, U.1
Ercolano, E.2
Carraro, L.3
Blasi Roman, C.R.4
Sorba, G.5
Canonico, P.L.6
Genazzani, A.A.7
Tron, G.C.8
Billington, R.A.9
-
16
-
-
33745817828
-
Molecular basis for the inhibition of human NMPRTase, a novel target for anticancer agents
-
Khan, J. A.; Tao, X.; Tong, L. Molecular basis for the inhibition of human NMPRTase, a novel target for anticancer agents. Nat. Struct. Mol. Biol. 2006, 13, 582-588.
-
(2006)
Nat. Struct. Mol. Biol
, vol.13
, pp. 582-588
-
-
Khan, J.A.1
Tao, X.2
Tong, L.3
-
17
-
-
11644261806
-
Automated docking using a Lamarckian genetic algorithm and empirical binding free energy function
-
Morris, G. M.; Goodsell, D. S.; Halliday, R. S.; Huey, R.; Hart, W. E.; Belew, R. K.; Olson, A. J. Automated docking using a Lamarckian genetic algorithm and empirical binding free energy function. J. Comput. Chem. 1998, 19, 1639-1662.
-
(1998)
J. Comput. Chem
, vol.19
, pp. 1639-1662
-
-
Morris, G.M.1
Goodsell, D.S.2
Halliday, R.S.3
Huey, R.4
Hart, W.E.5
Belew, R.K.6
Olson, A.J.7
-
18
-
-
0000096835
-
Click chemistry: Diverse chemical function from a few good reactions
-
(a) Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Click chemistry: diverse chemical function from a few good reactions. Angew. Chem., Int. Ed. Engl. 2001, 40, 2004-2021.
-
(2001)
Angew. Chem., Int. Ed. Engl
, vol.40
, pp. 2004-2021
-
-
Kolb, H.C.1
Finn, M.G.2
Sharpless, K.B.3
-
19
-
-
0037012920
-
-
Tornoee, C. W.; Christensen, C.; Meldal, M. Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. J. Org. Chem. 2002, 67, 3057-3064.
-
(b) Tornoee, C. W.; Christensen, C.; Meldal, M. Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. J. Org. Chem. 2002, 67, 3057-3064.
-
-
-
-
20
-
-
0037099395
-
A stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regio-selective "ligation" of azides and terminal alkynes
-
(c) Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regio-selective "ligation" of azides and terminal alkynes. Angew. Chem., Int. Ed. 2002, 41, 2596-2599.
-
(2002)
Angew. Chem., Int. Ed
, vol.41
, pp. 2596-2599
-
-
Rostovtsev, V.V.1
Green, L.G.2
Fokin, V.V.3
Sharpless, K.B.4
-
21
-
-
0348109450
-
The growing impact of click chemistry on drug discovery
-
For medicinal chemistry applications of click chemistry see: a
-
For medicinal chemistry applications of click chemistry see: (a) Kolb, H. C.; Sharpless, K. B. The growing impact of click chemistry on drug discovery. Drug Discovery Today 2003, 8, 1128-1137.
-
(2003)
Drug Discovery Today
, vol.8
, pp. 1128-1137
-
-
Kolb, H.C.1
Sharpless, K.B.2
-
22
-
-
39549111477
-
Click chemistry reactions in medicinal chemistry: Applications of the 1,3-dipolar cycloaddition between azides and alkynes
-
(b) Tron, G. C.; Pirali, T.; Billington, R. A.; Canonico, P. L.; Sorba, G.; Genazzani, A. A. Click chemistry reactions in medicinal chemistry: applications of the 1,3-dipolar cycloaddition between azides and alkynes. Med. Res. Rev. 2008, 28, 278-308.
-
(2008)
Med. Res. Rev
, vol.28
, pp. 278-308
-
-
Tron, G.C.1
Pirali, T.2
Billington, R.A.3
Canonico, P.L.4
Sorba, G.5
Genazzani, A.A.6
-
23
-
-
31544472391
-
Rapid synthesis of triazole-modified resveratrol analogues via click chemistry
-
Pagliai, F.; Pirali, T.; Del Grosso, E.; Di Brisco, R.; Tron, G. C.; Sorba, G.; Genazzani, A. A. Rapid synthesis of triazole-modified resveratrol analogues via click chemistry. J. Med. Chem. 2006, 49, 467-470.
-
(2006)
J. Med. Chem
, vol.49
, pp. 467-470
-
-
Pagliai, F.1
Pirali, T.2
Del Grosso, E.3
Di Brisco, R.4
Tron, G.C.5
Sorba, G.6
Genazzani, A.A.7
-
24
-
-
44649103893
-
Estrogenic analogues synthesized via click chemistry
-
Pirali, T.; Gatti, S.; Di Brisco, R.; Tacchi, S.; Zaninetti, R.; Brunelli, E.; Massarotti, A.; Sorba, G.; Canonico, P. L.; Moro, L.; Genazzani, A. A.; Tron, G. C.; Billington, R. A. Estrogenic analogues synthesized via click chemistry. ChemMedChem 2007, 2, 437-440.
-
(2007)
ChemMedChem
, vol.2
, pp. 437-440
-
-
Pirali, T.1
Gatti, S.2
Di Brisco, R.3
Tacchi, S.4
Zaninetti, R.5
Brunelli, E.6
Massarotti, A.7
Sorba, G.8
Canonico, P.L.9
Moro, L.10
Genazzani, A.A.11
Tron, G.C.12
Billington, R.A.13
-
25
-
-
53049101458
-
Triazole-modified histone deacetylase inhibitors as a rapid route to drug discovery
-
(a) Pirali, T.; Pagliai, F.; Mercurio, C.; Boggio, R.; Canonico, P. L.; Sorba, G.; Tron, G. C.; Genazzani, A. A. Triazole-modified histone deacetylase inhibitors as a rapid route to drug discovery. J. Comb. Chem. 2008, 10, 624-627.
-
(2008)
J. Comb. Chem
, vol.10
, pp. 624-627
-
-
Pirali, T.1
Pagliai, F.2
Mercurio, C.3
Boggio, R.4
Canonico, P.L.5
Sorba, G.6
Tron, G.C.7
Genazzani, A.A.8
-
26
-
-
0345306644
-
Rapid diversity-oriented synthesis in microtiter plates for in situ screening of HIV protease inhibitors
-
(b) Brik, A.; Muldoon, J.; Lin, Y.; Elder, J. H.; Goodsell, D. S.; Olson, A. J.; Fokin,V. V.; Sharpless, K. B.; Wong, C. Rapid diversity-oriented synthesis in microtiter plates for in situ screening of HIV protease inhibitors. ChemBioChem 2003, 4, 1246-1248.
-
(2003)
ChemBioChem
, vol.4
, pp. 1246-1248
-
-
Brik, A.1
Muldoon, J.2
Lin, Y.3
Elder, J.H.4
Goodsell, D.S.5
Olson, A.J.6
Fokin, V.V.7
Sharpless, K.B.8
Wong, C.9
-
27
-
-
0042125393
-
A Potent and high selective inhibitor of human α-1,3- fucosyltransferase via click chemistry
-
(c) Lee, L. V.; Mitchell, M. L.; Huang, S.; Fokin, V. V.; Sharpless, K. B.; Wong, C. A Potent and high selective inhibitor of human α-1,3- fucosyltransferase via click chemistry. J. Am. Chem. Soc. 2003, 125, 9588-9589.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 9588-9589
-
-
Lee, L.V.1
Mitchell, M.L.2
Huang, S.3
Fokin, V.V.4
Sharpless, K.B.5
Wong, C.6
-
28
-
-
0003103675
-
Influence of electron-withdrawing N-1 substituents on the thermal behavior of 5-azido-1,2,3-triazoles
-
L'Abbè, G.; Beenaerts, L. Influence of electron-withdrawing N-1 substituents on the thermal behavior of 5-azido-1,2,3-triazoles. Tetrahedron 1989, 45, 749-756.
-
(1989)
Tetrahedron
, vol.45
, pp. 749-756
-
-
L'Abbè, G.1
Beenaerts, L.2
-
29
-
-
37049097409
-
Reactions of 2-azidopyridine and 1-pyridinio ylides with transition-metal complexes
-
Pizzotti, M.; Cenini, S.; Porta, F. Reactions of 2-azidopyridine and 1-pyridinio ylides with transition-metal complexes. J. Chem. Soc., Dalton Trans. 1978, 1155-1160.
-
(1978)
J. Chem. Soc., Dalton Trans
, pp. 1155-1160
-
-
Pizzotti, M.1
Cenini, S.2
Porta, F.3
-
30
-
-
84949695566
-
Methanolysis of dimethyl(1-diazo-2-oxopropyl)phosphonate. Generation of (diazomethyl) phosphonate and reaction with carbonyl compounds
-
Ohira, S. Methanolysis of dimethyl(1-diazo-2-oxopropyl)phosphonate. Generation of (diazomethyl) phosphonate and reaction with carbonyl compounds. Synth. Commun. 1989, 19, 561-564.
-
(1989)
Synth. Commun
, vol.19
, pp. 561-564
-
-
Ohira, S.1
-
31
-
-
1542504084
-
An improved one-pot procedure for the synthesis of alkynes from aldehydes
-
Müller, S.; Liepold, B.; Roth, G. J.; Bestmann, H. J. An improved one-pot procedure for the synthesis of alkynes from aldehydes. Synlett 1996, 521-522.
-
(1996)
Synlett
, pp. 521-522
-
-
Müller, S.1
Liepold, B.2
Roth, G.J.3
Bestmann, H.J.4
-
32
-
-
44449171041
-
Characterization of NAD uptake in mammalian cells
-
Billington, R. A.; Travelli, C.; Ercolano, E.; Galli, U.; Roman, C. B.; Grolla, A. A.; Canonico, P. L.; Condorelli, F.; Genazzani, A. A. Characterization of NAD uptake in mammalian cells. J. Biol. Chem. 2008, 283, 6367-6374.
-
(2008)
J. Biol. Chem
, vol.283
, pp. 6367-6374
-
-
Billington, R.A.1
Travelli, C.2
Ercolano, E.3
Galli, U.4
Roman, C.B.5
Grolla, A.A.6
Canonico, P.L.7
Condorelli, F.8
Genazzani, A.A.9
-
33
-
-
41449118098
-
NAD depletion by FK866 induces autophagy
-
Billington, R. A.; Genazzani, A. A.; Travelli, C.; Condorelli, F. NAD depletion by FK866 induces autophagy. Autophagy 2008, 4, 385-387.
-
(2008)
Autophagy
, vol.4
, pp. 385-387
-
-
Billington, R.A.1
Genazzani, A.A.2
Travelli, C.3
Condorelli, F.4
-
34
-
-
35448981935
-
Autophagy: From phenomenology to molecular understanding in less than a decade
-
Klionsky, D. J. Autophagy: from phenomenology to molecular understanding in less than a decade. Nat. Rev. Mol. Cell. Biol. 2007, 8, 931-937.
-
(2007)
Nat. Rev. Mol. Cell. Biol
, vol.8
, pp. 931-937
-
-
Klionsky, D.J.1
-
35
-
-
38949108670
-
Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes
-
Klionsky, D. J.; Abeliovich, H.; Agostinis, P.; Agrawal, D. K.; Aliev, G.; Askew, D. S.; Baba, M.; Baehrecke, E. H.; Bahr, B. A.; Ballabio, A.; et al. Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes. Autophagy 2008, 4, 151-175.
-
(2008)
Autophagy
, vol.4
, pp. 151-175
-
-
Klionsky, D.J.1
Abeliovich, H.2
Agostinis, P.3
Agrawal, D.K.4
Aliev, G.5
Askew, D.S.6
Baba, M.7
Baehrecke, E.H.8
Bahr, B.A.9
Ballabio, A.10
-
36
-
-
67650318141
-
Preclinical development of the nicotinamide phosphoribosyl transferase inhibitor prodrug GMX1777
-
Beauparlant, P.; Bédard, D.; Bernier, C.; Chan, H.; Gilbert, K.; Goulet, D.; Gratton, M. O.; Lavoie, M.; Roulston, A.; Turcotte, E.; Watson, M. Preclinical development of the nicotinamide phosphoribosyl transferase inhibitor prodrug GMX1777. Anti-Cancer Drugs 2009, 20, 346-354.
-
(2009)
Anti-Cancer Drugs
, vol.20
, pp. 346-354
-
-
Beauparlant, P.1
Bédard, D.2
Bernier, C.3
Chan, H.4
Gilbert, K.5
Goulet, D.6
Gratton, M.O.7
Lavoie, M.8
Roulston, A.9
Turcotte, E.10
Watson, M.11
|