-
1
-
-
84855990581
-
Angucyclines: Biosynthesis, mode-of-action, new natural products, and synthesis
-
Kharel, M. K. et al. Angucyclines: biosynthesis, mode-of-action, new natural products, and synthesis. Nat. Prod. Rep. 29, 264-325 (2012).
-
(2012)
Nat. Prod. Rep
, vol.29
, pp. 264-325
-
-
Kharel, M.K.1
-
2
-
-
35348924832
-
Marmycins A and B, cytotoxic pentacyclic C-glycosides from a marine sediment-derived actinomycete related to the genus Streptomyces
-
Martin, G. D. A. et al. Marmycins A and B, cytotoxic pentacyclic C-glycosides from a marine sediment-derived actinomycete related to the genus Streptomyces. J. Nat. Prod. 70, 1406-1409 (2007).
-
(2007)
J. Nat. Prod
, vol.70
, pp. 1406-1409
-
-
Martin, G.D.A.1
-
3
-
-
77949833524
-
Diverse DNA-cleaving capacities of the jadomycins through precursor-directed biosynthesis
-
Cottreau, K. M. et al. Diverse DNA-cleaving capacities of the jadomycins through precursor-directed biosynthesis. Org. Lett. 12, 1172-1175 (2010).
-
(2010)
Org. Lett
, vol.12
, pp. 1172-1175
-
-
Cottreau, K.M.1
-
4
-
-
0028944090
-
Molecular basis for the DNA sequence specificity of the pluramycins. A novel mechanism involving groove interactions transmitted through the helix via intercalation to achieve sequence selectivity at the covalent bonding step
-
Sun, D., Hansen, M. & Hurley, L. Molecular basis for the DNA sequence specificity of the pluramycins. A novel mechanism involving groove interactions transmitted through the helix via intercalation to achieve sequence selectivity at the covalent bonding step. J. Am. Chem. Soc. 117, 2430-2440 (1995).
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 2430-2440
-
-
Sun, D.1
Hansen, M.2
Hurley, L.3
-
5
-
-
0029278899
-
Hedamycin intercalates the DNA helix and, through carbohydrate-mediated recognition in the minor groove, directs N7- alkylation of guanine in the major groove in a sequence-specific manner
-
Hansen, M., Yun, S. & Hurley, L. Hedamycin intercalates the DNA helix and, through carbohydrate-mediated recognition in the minor groove, directs N7- alkylation of guanine in the major groove in a sequence-specific manner. Chem. Biol. 2, 229-240 (1995).
-
(1995)
Chem. Biol
, vol.2
, pp. 229-240
-
-
Hansen, M.1
Yun, S.2
Hurley, L.3
-
6
-
-
0032563825
-
Doxorubicin-induced cardiomyopathy
-
Singal, P. K. & Iliskovic, N. Doxorubicin-induced cardiomyopathy. N. Engl. J. Med. 339, 900-905 (1998).
-
(1998)
N. Engl. J. Med
, vol.339
, pp. 900-905
-
-
Singal, P.K.1
Iliskovic, N.2
-
7
-
-
84877585708
-
Doxorubicin enhances nucleosome turnover around promoters
-
Yang, F., Kemp, C. J. & Henikoff, S. Doxorubicin enhances nucleosome turnover around promoters. Curr. Biol. 23, 782-787 (2013).
-
(2013)
Curr. Biol
, vol.23
, pp. 782-787
-
-
Yang, F.1
Kemp, C.J.2
Henikoff, S.3
-
8
-
-
84878732407
-
Drug-induced histone eviction from open chromatin contributes to the chemotherapeutic effects of doxorubicin
-
Pang, B. et al. Drug-induced histone eviction from open chromatin contributes to the chemotherapeutic effects of doxorubicin. Nature Commun. 4, 1908 (2013).
-
(1908)
Nature Commun
, vol.4
-
-
Pang, B.1
-
9
-
-
0015494420
-
Stereochemistry of intercalation: Interaction of daunomycin with DNA
-
Pigram, W. J., Fuller, W. & Hamilton, L. D. Stereochemistry of intercalation: interaction of daunomycin with DNA. Nature 235, 17-19 (1972).
-
(1972)
Nature
, vol.235
, pp. 17-19
-
-
Pigram, W.J.1
Fuller, W.2
Hamilton, L.D.3
-
10
-
-
64649090292
-
Targeting DNA topoisomerase II in cancer chemotherapy
-
Nitiss, J. L. Targeting DNA topoisomerase II in cancer chemotherapy. Nature Rev. Cancer 9, 338-350 (2009).
-
(2009)
Nature Rev. Cancer
, vol.9
, pp. 338-350
-
-
Nitiss, J.L.1
-
11
-
-
36049018701
-
Mechanisms underlying the anticancer activities of the angucycline landomycin e
-
Korynevska, A. et al. Mechanisms underlying the anticancer activities of the angucycline landomycin E. Biochem. Pharmacol. 74, 1713-1726 (2007).
-
(2007)
Biochem. Pharmacol
, vol.74
, pp. 1713-1726
-
-
Korynevska, A.1
-
12
-
-
78649511027
-
Small-moleculemediated G-quadruplex isolation from human cells
-
Müller, S., Kumari, S., Rodriguez, R. & Balasubramanian, S. Small-moleculemediated G-quadruplex isolation from human cells. Nature Chem. 2, 1095-1098 (2010).
-
(2010)
Nature Chem
, vol.2
, pp. 1095-1098
-
-
Müller, S.1
Kumari, S.2
Rodriguez, R.3
Balasubramanian, S.4
-
13
-
-
80053279143
-
A single-molecule platform for investigation of interactions between G-quadruplexes and small-molecule ligands
-
Koirala, D. et al. A single-molecule platform for investigation of interactions between G-quadruplexes and small-molecule ligands. Nature Chem. 3, 782-787 (2011).
-
(2011)
Nature Chem
, vol.3
, pp. 782-787
-
-
Koirala, D.1
-
14
-
-
84857163904
-
Small-molecule-induced DNA damage identifies alternative DNA structures in human genes
-
Rodriguez, R. et al. Small-molecule-induced DNA damage identifies alternative DNA structures in human genes. Nature Chem. Biol. 8, 301-310 (2012).
-
(2012)
Nature Chem. Biol
, vol.8
, pp. 301-310
-
-
Rodriguez, R.1
-
15
-
-
84939789743
-
Unravelling the genomic targets of small molecules using high-throughput sequencing
-
Rodriguez, R. & Miller, K. M. Unravelling the genomic targets of small molecules using high-throughput sequencing. Nature Rev. Genet. 77, 5439-5444 (2012).
-
(2012)
Nature Rev. Genet
, vol.77
, pp. 5439-5444
-
-
Rodriguez, R.1
Miller, K.M.2
-
16
-
-
0242467745
-
InBr3-catalyzed cyclization of glycals with aryl amines
-
Yadav, J. S. et al. InBr3-catalyzed cyclization of glycals with aryl amines. Angew. Chem. Int. Ed. 42, 5198-5201 (2003).
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 5198-5201
-
-
Yadav, J.S.1
-
17
-
-
70349119077
-
Synthesis study on marmycin A: Preparation of the C3'-desmethyl analogues
-
Ding, C. et al. Synthesis study on marmycin A: preparation of the C3'-desmethyl analogues. J. Org. Chem. 74, 6111-6119 (2009).
-
(2009)
J. Org. Chem
, vol.74
, pp. 6111-6119
-
-
Ding, C.1
-
18
-
-
70350623199
-
Efficient synthesis of the tetracyclic aminoquinone moiety of marmycin A
-
Maugel, N. & Snider, B. B. Efficient synthesis of the tetracyclic aminoquinone moiety of marmycin A. Org. Lett. 11, 4926-4929 (2009).
-
(2009)
Org. Lett
, vol.11
, pp. 4926-4929
-
-
Maugel, N.1
Snider, B.B.2
-
19
-
-
79954437854
-
Synthetic studies towards marmycins A and B: Development of the vinylogous aldol-aza-Michael domino reaction
-
Bourcet, E., Bröhmer, M. C., Nieger, M. & Bräse, S. Synthetic studies towards marmycins A and B: development of the vinylogous aldol-aza-Michael domino reaction. Org. Biomol. Chem. 9, 3136-3138 (2011).
-
(2011)
Org. Biomol. Chem
, vol.9
, pp. 3136-3138
-
-
Bourcet, E.1
Bröhmer, M.C.2
Nieger, M.3
Bräse, S.4
-
20
-
-
83655183058
-
Scalable enantioselective total synthesis of taxanes
-
Mendoza, A., Ishihara, Y. & Baran, P. S. Scalable enantioselective total synthesis of taxanes. Nature Chem. 4, 21-25 (2012).
-
(2012)
Nature Chem
, vol.4
, pp. 21-25
-
-
Mendoza, A.1
Ishihara, Y.2
Baran, P.S.3
-
21
-
-
67650538334
-
Stereoselective synthesis of CD-ring precursors of Vitamin D derivatives
-
Rodriguez, R., Chapelon, A.-S., Ollivier, C. & Santelli, M. Stereoselective synthesis of CD-ring precursors of vitamin D derivatives. Tetrahedron 65, 7001-7015 (2009).
-
(2009)
Tetrahedron
, vol.65
, pp. 7001-7015
-
-
Rodriguez, R.1
Chapelon, A.-S.2
Ollivier, C.3
Santelli, M.4
-
22
-
-
6444237050
-
A new and efficient method for o-quinone methide intermediate generation: Application to the biomimetic synthesis of (±)-alboatrin
-
Rodriguez, R., Adlington, R. M., Moses, J. E., Cowley, A. & Baldwin, J. E. A new and efficient method for o-quinone methide intermediate generation: application to the biomimetic synthesis of (±)-alboatrin. Org. Lett. 6, 3617-3619 (2004).
-
(2004)
Org. Lett
, vol.6
, pp. 3617-3619
-
-
Rodriguez, R.1
Adlington, R.M.2
Moses, J.E.3
Cowley, A.4
Baldwin, J.E.5
-
23
-
-
34247153954
-
Total synthesis of cyercene A and the biomimetic synthesis of (±)-9, 10-deoxytridachione and (±)-ocellapyrone A.
-
Rodriguez, R. et al. Total synthesis of cyercene A and the biomimetic synthesis of (±)-9, 10-deoxytridachione and (±)-ocellapyrone A. Tetrahedron 63, 4500-4509 (2007).
-
(2007)
Tetrahedron
, vol.63
, pp. 4500-4509
-
-
Rodriguez, R.1
-
24
-
-
46849120817
-
Biomimetic synthesis of pyrone-derived natural products: Exploring chemical pathways from a unique polyketide precursor
-
Eade, S. J. et al. Biomimetic synthesis of pyrone-derived natural products: exploring chemical pathways from a unique polyketide precursor. J. Org. Chem. 73, 4830-4839 (2008).
-
(2008)
J. Org. Chem
, vol.73
, pp. 4830-4839
-
-
Eade, S.J.1
-
25
-
-
0008848059
-
Regiospecific synthesis of bromojuglone derivatives
-
Heinzman, S. W. & Grunwell, J. R. Regiospecific synthesis of bromojuglone derivatives. Tetrahedron Lett. 21, 4305-4308 (1980).
-
(1980)
Tetrahedron Lett
, vol.21
, pp. 4305-4308
-
-
Heinzman, S.W.1
Grunwell, J.R.2
-
26
-
-
0034599077
-
Enantioselective Diels-Alder approach to C-3-oxygenated angucyclinones from (SS)-2-( p-tolylsulfinyl)- 1, 4-naphthoquinone
-
Carreño, M. C., Urbano, A. & Di Vitta, C. Enantioselective Diels-Alder approach to C-3-oxygenated angucyclinones from (SS)-2-( p-tolylsulfinyl)- 1, 4-naphthoquinone. Chem. Eur. J. 6, 906-913 (2000).
-
(2000)
Chem. Eur. J.
, vol.6
, pp. 906-913
-
-
Carreño, M.C.1
Urbano, A.2
Di Vitta, C.3
-
27
-
-
37049108468
-
Convenient syntheses of L-digitoxose, L-cymarose, and L-ristosamine
-
Brimacombe, J. S., Hanna, R., Saeed, M. S. & Tucker, L. C. N. Convenient syntheses of L-digitoxose, L-cymarose, and L-ristosamine. J. Chem. Soc. 2583-2587 (1982).
-
(1982)
J. Chem. Soc
, pp. 2583-2587
-
-
Brimacombe, J.S.1
Hanna, R.2
Saeed, M.S.3
Tucker, L.C.N.4
-
28
-
-
0027304545
-
A new stereoselective route to branchedchain nitro and amino sugars: Synthesis of both enantiomers of decilonitrose and avidinosamine
-
Greven, R., Jütten, P. & Scharf, H.-D. A new stereoselective route to branchedchain nitro and amino sugars: synthesis of both enantiomers of decilonitrose and avidinosamine. J. Org. Chem. 58, 3742-3747 (1993).
-
(1993)
J. Org. Chem
, vol.58
, pp. 3742-3747
-
-
Greven, R.1
Jütten, P.2
Scharf, H.-D.3
-
29
-
-
33947602410
-
Total synthesis of marine natural products without using protecting groups
-
Baran, P. S., Maimone, T. J. & Richter, J. M. Total synthesis of marine natural products without using protecting groups. Nature 446, 404-408 (2007).
-
(2007)
Nature
, vol.446
, pp. 404-408
-
-
Baran, P.S.1
Maimone, T.J.2
Richter, J.M.3
-
30
-
-
84982497955
-
Simple synthesis of methyl 4, 6-ortho-benzylidene- 2-desoxy-alpha-D-erythro-hexopyranosid-3-ulose
-
Klemer, A. & Rodemeyer, G. Simple synthesis of methyl 4, 6-ortho-benzylidene- 2-desoxy-alpha-D-erythro-hexopyranosid-3-ulose. Chem. Ber. 107, 2612-2614 (1974).
-
(1974)
Chem. Ber
, vol.107
, pp. 2612-2614
-
-
Klemer, A.1
Rodemeyer, G.2
-
31
-
-
0001038733
-
Rational development of practical catalysts for aromatic carbon-nitrogen bond formation
-
Wolfe, J. P., Wagaw, S., Marcoux, J.-F. & Buchwald, S. L. Rational development of practical catalysts for aromatic carbon-nitrogen bond formation. Acc. Chem. Res. 31, 805-818 (1998).
-
(1998)
Acc. Chem. Res
, vol.31
, pp. 805-818
-
-
Wolfe, J.P.1
Wagaw, S.2
Marcoux, J.-F.3
Buchwald, S.L.4
-
32
-
-
84899077420
-
Copper catalysed Ullmann type chemistry: From mechanistic aspects to modern development
-
Sambiagio, C., Marsden, S. P., Blacker, A. J. & McGowan, P. C. Copper catalysed Ullmann type chemistry: from mechanistic aspects to modern development. Chem. Soc. Rev. 43, 3525-3550 (2014).
-
(2014)
Chem. Soc. Rev
, vol.43
, pp. 3525-3550
-
-
Sambiagio, C.1
Marsden, S.P.2
Blacker, A.J.3
McGowan, P.C.4
-
33
-
-
84900330481
-
Chemical inhibition of NAT10 corrects defects of laminopathic cells
-
Larrieu, D., Britton, S., Demir, M., Rodriguez, R. & Jackson, S. P. Chemical inhibition of NAT10 corrects defects of laminopathic cells. Science 344, 527- 532 (2014).
-
(2014)
Science
, vol.344
, pp. 527-532
-
-
Larrieu, D.1
Britton, S.2
Demir, M.3
Rodriguez, R.4
Jackson, S.P.5
-
34
-
-
0031888955
-
A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD
-
Enari, M. et al. A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD. Nature 391, 43-50 (1998).
-
(1998)
Nature
, vol.391
, pp. 43-50
-
-
Enari, M.1
-
35
-
-
0037334339
-
At the acidic edge: Emerging functions for lysosomal membrane proteins
-
Eskelinen, E.-L., Tanaka, Y. & Saftig, P. At the acidic edge: emerging functions for lysosomal membrane proteins. Trends Cell Biol. 13, 137-145 (2003).
-
(2003)
Trends Cell Biol
, vol.13
, pp. 137-145
-
-
Eskelinen, E.-L.1
Tanaka, Y.2
Saftig, P.3
-
36
-
-
33846471307
-
LAMP proteins are required for fusion of lysosomes with phagosomes
-
Huynh, K. K. et al. LAMP proteins are required for fusion of lysosomes with phagosomes. EMBO J. 26, 313-324 (2007).
-
(2007)
EMBO J.
, vol.26
, pp. 313-324
-
-
Huynh, K.K.1
-
37
-
-
84862295360
-
Guidelines for the use and interpretation of assays for monitoring autophagy
-
Klionsky, D. J. et al. Guidelines for the use and interpretation of assays for monitoring autophagy. Autophagy 8, 445-544 (2012).
-
(2012)
Autophagy
, vol.8
, pp. 445-544
-
-
Klionsky, D.J.1
-
38
-
-
0035887215
-
Sphingosine-induced apoptosis is dependent on lysosomal proteases
-
Kågedal, K., Zhao, M., Svensson, I. & Brunk, U. T. Sphingosine-induced apoptosis is dependent on lysosomal proteases. Biochem. J. 359, 335-343 (2001).
-
(2001)
Biochem. J.
, vol.359
, pp. 335-343
-
-
Kågedal, K.1
Zhao, M.2
Svensson, I.3
Brunk, U.T.4
-
39
-
-
54949137644
-
Lysosomal membrane permeabilization in cell death
-
Boya, P. & Kroemer, G. Lysosomal membrane permeabilization in cell death. Oncogene 27, 6434-6451 (2008).
-
(2008)
Oncogene
, vol.27
, pp. 6434-6451
-
-
Boya, P.1
Kroemer, G.2
-
40
-
-
84905456971
-
Organelle-specific initiation of cell death
-
Galluzzi, L., Bravo-San Pedro, J. M. & Kroemer, G. Organelle-specific initiation of cell death. Nature Cell Biol. 16, 728-736 (2014).
-
(2014)
Nature Cell Biol
, vol.16
, pp. 728-736
-
-
Galluzzi, L.1
Bravo-San Pedro, J.M.2
Kroemer, G.3
-
41
-
-
0032555697
-
Cleavage of BID by caspase 8 mediates the mitochondrial damage in the Fas pathway of apoptosis
-
Li, H., Zhu, H., Xu, C.-J. & Yuan, J. Cleavage of BID by caspase 8 mediates the mitochondrial damage in the Fas pathway of apoptosis. Cell 94, 491-501 (1998).
-
(1998)
Cell
, vol.94
, pp. 491-501
-
-
Li, H.1
Zhu, H.2
Xu, C.-J.3
Yuan, J.4
-
42
-
-
33745950626
-
Mitochondrial outer membrane permeabilization during apoptosis: The innocent bystander scenario
-
Chipuk, J. E., Bouchier-Hayes, L. & Green, D. R. Mitochondrial outer membrane permeabilization during apoptosis: the innocent bystander scenario. Cell Death Differ. 13, 1396-1402 (2006).
-
(2006)
Cell Death Differ
, vol.13
, pp. 1396-1402
-
-
Chipuk, J.E.1
Bouchier-Hayes, L.2
Green, D.R.3
-
43
-
-
79953194472
-
Artesunate activates mitochondrial apoptosis in breast cancer cells via iron-catalyzed lysosomal reactive oxygen species production
-
Hamacher-Brady, A. et al. Artesunate activates mitochondrial apoptosis in breast cancer cells via iron-catalyzed lysosomal reactive oxygen species production. J. Biol. Chem. 286, 6587-6601 (2011).
-
(2011)
J. Biol. Chem
, vol.286
, pp. 6587-6601
-
-
Hamacher-Brady, A.1
-
44
-
-
84874630073
-
Target identification for small bioactive molecules: Finding the needle in the haystack
-
Ziegler, S., Pries, V., Hedberg, C. &Waldmann, H. Target identification for small bioactive molecules: finding the needle in the haystack. Angew. Chem. Int. Ed. 52, 2744-2792 (2013).
-
(2013)
Angew. Chem. Int. Ed
, vol.52
, pp. 2744-2792
-
-
Ziegler, S.1
Pries, V.2
Hedberg, C.3
Waldmann, H.4
-
45
-
-
76349095348
-
Amplification of LAPTM4B and YWHAZ contributes to chemotherapy resistance and recurrence of breast cancer
-
Li, Y. et al. Amplification of LAPTM4B and YWHAZ contributes to chemotherapy resistance and recurrence of breast cancer. Nature Med. 16, 214-218 (2010).
-
(2010)
Nature Med
, vol.16
, pp. 214-218
-
-
Li, Y.1
-
46
-
-
84861532088
-
Killing a cancer: What are the alternatives? Nature Rev
-
Kreuzaler, P. & Watson, C. J. Killing a cancer: what are the alternatives? Nature Rev. Cancer 12, 411-424 (2012).
-
(2012)
Cancer
, vol.12
, pp. 411-424
-
-
Kreuzaler, P.1
Watson, C.J.2
-
47
-
-
0022612462
-
Lysosomotropic agents reverse multiple drug resistance in human cancer cells
-
Shiraishi, N., Akiyama, S.-I., Kobayashi, M. & Kuwano, M. Lysosomotropic agents reverse multiple drug resistance in human cancer cells. Cancer Lett. 30, 251-259 (1986).
-
(1986)
Cancer Lett
, vol.30
, pp. 251-259
-
-
Shiraishi, N.1
Akiyama, S.-I.2
Kobayashi, M.3
Kuwano, M.4
-
48
-
-
0022971454
-
Chloroquine enhancement of anticancer drug cytotoxicity in multiple drug resistant human leukemic cells
-
Zamora, J. M. & Beck, W. T. Chloroquine enhancement of anticancer drug cytotoxicity in multiple drug resistant human leukemic cells. Biochem. Pharmacol. 35, 4303-4310 (1986).
-
(1986)
Biochem. Pharmacol
, vol.35
, pp. 4303-4310
-
-
Zamora, J.M.1
Beck, W.T.2
-
49
-
-
0034658440
-
Reversal of MRP-mediated doxorubicin resistance with quinoline-based drugs
-
Vezmar, M. & Georges, E. Reversal of MRP-mediated doxorubicin resistance with quinoline-based drugs. Biochem. Pharmacol. 59, 1245-1252 (2000).
-
(2000)
Biochem. Pharmacol
, vol.59
, pp. 1245-1252
-
-
Vezmar, M.1
Georges, E.2
-
50
-
-
33749054651
-
Risks and benefits of chloroquine use in anticancer strategies
-
Savarino, A., Lucia, M. B., Giordano, F. & Cauda, R. Risks and benefits of chloroquine use in anticancer strategies. Lancet Oncol. 7, 792-793 (2006).
-
(2006)
Lancet Oncol
, vol.7
, pp. 792-793
-
-
Savarino, A.1
Lucia, M.B.2
Giordano, F.3
Cauda, R.4
|