-
1
-
-
1642286980
-
Challenges in antimicrobial drug discovery and the potential of nucleoside antibiotics
-
Rachakonda, S.; Cartee, L. Challenges in antimicrobial drug discovery and the potential of nucleoside antibiotics. Curr. Med. Chem., 2004, 11, 775-793.
-
(2004)
Curr. Med. Chem.
, vol.11
, pp. 775-793
-
-
Rachakonda, S.1
Cartee, L.2
-
2
-
-
0038587681
-
Oxazolidinone structureactivity relationships leading to linezolid
-
Barbachyn, M. R.; Ford, C. W. Oxazolidinone structureactivity relationships leading to linezolid. Angew. Chem. Int. Ed., 2003, 42, 2010-2023.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 2010-2023
-
-
Barbachyn, M.R.1
Ford, C.W.2
-
3
-
-
0346958244
-
Daptomycin
-
Raja, A.; LaBonte, J.; Lebbos, J.; Kirkpatrick, P. Daptomycin. Nat. Rev. Drug Discov., 2003, 2, 943-944.
-
(2003)
Nat. Rev. Drug Discov
, vol.2
, pp. 943-944
-
-
Raja, A.1
LaBonte, J.2
Lebbos, J.3
Kirkpatrick, P.4
-
4
-
-
16244421046
-
Daptomycin: A new drug class for the treatment of Gram-positive infections
-
Alder, J. D. Daptomycin: A new drug class for the treatment of Gram-positive infections. Drugs Today, 2005, 41, 81-90.
-
(2005)
Drugs Today
, vol.41
, pp. 81-90
-
-
Alder, J.D.1
-
5
-
-
84887254933
-
Fidaxomicin: A review of its use in patients with Clostridium difficile infection
-
Scott, L. Fidaxomicin: A review of its use in patients with Clostridium difficile infection. Drugs, 2013, 15, 1733-1747.
-
(2013)
Drugs
, vol.15
, pp. 1733-1747
-
-
Scott, L.1
-
6
-
-
84977098261
-
A review of the evidence for using bedaquiline (TMC207) to treat multi-drug resistant tuberculosis
-
Fox, G. J.; Menzies, D. A review of the evidence for using bedaquiline (TMC207) to treat multi-drug resistant tuberculosis. Infect. Dis. Ther., 2013, 2, 123-144.
-
(2013)
Infect. Dis. Ther.
, vol.2
, pp. 123-144
-
-
Fox, G.J.1
Menzies, D.2
-
7
-
-
84858308226
-
Natural products as sources of new drugs over the 30 years from 1981 to 2010
-
a) Newman, D. J.; Cragg, G. M. Natural products as sources of new drugs over the 30 years from 1981 to 2010. J. Nat. Prod., 2012, 75, 311-335.
-
(2012)
J. Nat. Prod.
, vol.75
, pp. 311-335
-
-
Newman, D.J.1
Cragg, G.M.2
-
8
-
-
34247109045
-
Natural products as sources of new drugs over the last 25 years
-
b) Newman, D. J.; Cragg, G. M. Natural products as sources of new drugs over the last 25 years. J. Nat. Prod., 2007, 70, 461-477.
-
(2007)
J. Nat. Prod.
, vol.70
, pp. 461-477
-
-
Newman, D.J.1
Cragg, G.M.2
-
9
-
-
43949129098
-
Physicochemical properties of antibacterial compounds: Implications for drug discovery
-
c) O'Shea, R.; Moser, H. E. Physicochemical properties of antibacterial compounds: Implications for drug discovery. J. Med. Chem., 2008, 51, 2871-2878.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 2871-2878
-
-
O'Shea, R.1
Moser, H.E.2
-
10
-
-
33746001269
-
Antibacterial natural products in medicinal chemistry-exodus or revival?
-
von Nussbaum, F.; Brands, M.; Hinzen, B.; Weigand, S;. Habich, D. Antibacterial natural products in medicinal chemistry-exodus or revival? Angew. Chem. Int. Ed., 2006, 45, 5072-5129.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 5072-5129
-
-
Von Nussbaum, F.1
Brands, M.2
Hinzen, B.3
Weigand, S.4
Habich, D.5
-
11
-
-
43949129098
-
Physicochemical properties of antibacterial compounds: Implications for drug discovery
-
O'Shea, R.; Moser, H. E. Physicochemical properties of antibacterial compounds: Implications for drug discovery. J. Med. Chem., 2008, 51, 2871-2878.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 2871-2878
-
-
O'Shea, R.1
Moser, H.E.2
-
13
-
-
0002376649
-
The biochemistry of nucleoside antibiotics
-
Goodchild, J. The biochemistry of nucleoside antibiotics. Top. Antibiot. Chem., 1982, 6, 99-227.
-
(1982)
Top. Antibiot. Chem.
, vol.6
, pp. 99-227
-
-
Goodchild, J.1
-
15
-
-
0024209272
-
Nucleoside antibiotics: Structure, biological activity, and biosynthesis
-
Isono, K. Nucleoside antibiotics: Structure, biological activity, and biosynthesis. J. Antibiot., 1988, 41, 1711-1739.
-
(1988)
J. Antibiot
, vol.41
, pp. 1711-1739
-
-
Isono, K.1
-
16
-
-
0026387906
-
Current progress on nucleoside antibiotics
-
Isono, K. Current progress on nucleoside antibiotics. Pharmacol. Ther., 1991, 52, 296-286.
-
(1991)
Pharmacol. Ther.
, vol.52
, pp. 296-286
-
-
Isono, K.1
-
17
-
-
34248392226
-
Nucleoside natural products and related analogs
-
Ichikawa, S.; Matsuda, A. Nucleoside natural products and related analogs. Expert Opin. Ther. Pat., 2007, 17, 487-498.
-
(2007)
Expert Opin. Ther. Pat.
, vol.17
, pp. 487-498
-
-
Ichikawa, S.1
Matsuda, A.2
-
18
-
-
39149123173
-
The biosynthesis of peptidoglycan lipid-linked intermediates
-
Bouhss, A.; Trunkfield, A. E.; Bugg, T. D.; Mengin-Lecreulx, D. The biosynthesis of peptidoglycan lipid-linked intermediates. FEMS Microbiol. Rev., 2008, 32, 208-233.
-
(2008)
FEMS Microbiol. Rev.
, vol.32
, pp. 208-233
-
-
Bouhss, A.1
Trunkfield, A.E.2
Bugg, T.D.3
Mengin-Lecreulx, D.4
-
19
-
-
76249100888
-
Antimicrobial nucleoside antibiotics targeting cell wall assembly: Recent advances in structure-function studies and nucleoside biosynthesis
-
a) Winn, M.; Goss, R. J. M.; Kimura, K.; Bugg, T. D. H. Antimicrobial nucleoside antibiotics targeting cell wall assembly: Recent advances in structure-function studies and nucleoside biosynthesis. Nat. Prod. Rep., 2010, 27, 279-304.
-
(2010)
Nat. Prod. Rep.
, vol.27
, pp. 279-304
-
-
Winn, M.1
Goss, R.J.M.2
Kimura, K.3
Bugg, T.D.H.4
-
20
-
-
33745090237
-
Phospho-MurNAc-pentapeptide translocase (MraY) as a target for antibacterial agents and antibacterial proteins
-
b) Bugg, T. D. H.; Lloyd, A. J.; Roper, D. I. Phospho-MurNAc-pentapeptide translocase (MraY) as a target for antibacterial agents and antibacterial proteins. Infect. Dis. Drug Targets, 2006, 6, 85-106.
-
(2006)
Infect. Dis. Drug Targets
, vol.6
, pp. 85-106
-
-
Bugg, T.D.H.1
Lloyd, A.J.2
Roper, D.I.3
-
21
-
-
0037394583
-
Phospho-MurNAc-pentapeptide translocase (MraY) as a target for antibacterial agents and antibacterial proteins
-
c) Kimura, K.; Bugg, T. D. H. Phospho-MurNAc-pentapeptide translocase (MraY) as a target for antibacterial agents and antibacterial proteins. Nat. Prod. Rep., 2003, 20, 252-273.
-
(2003)
Nat. Prod. Rep.
, vol.20
, pp. 252-273
-
-
Kimura, K.1
Bugg, T.D.H.2
-
22
-
-
0001222924
-
Synthesis of complex nucleoside antibiotics
-
Knapp, S. Synthesis of complex nucleoside antibiotics. Chem. Rev., 1995, 95, 1859-1876.
-
(1995)
Chem. Rev.
, vol.95
, pp. 1859-1876
-
-
Knapp, S.1
-
23
-
-
0017188814
-
Tunicamycin inhibits the formation of lipid intermediate in cell-free peptidoglycan synthesis of bacteria
-
Tamura, G.; Sasaki, T.; Matsuhashi, M.; Takatsuki, A.; Yamasaki, M. Tunicamycin inhibits the formation of lipid intermediate in cell-free peptidoglycan synthesis of bacteria. Agric. Biol. Chem., 1976, 40, 447-449.
-
(1976)
Agric. Biol. Chem.
, vol.40
, pp. 447-449
-
-
Tamura, G.1
Sasaki, T.2
Matsuhashi, M.3
Takatsuki, A.4
Yamasaki, M.5
-
24
-
-
0013047363
-
-
Japan Scientific Press: Tokyo
-
Tamura, G. Tunicamycin; Japan Scientific Press: Tokyo, 1982.
-
(1982)
Tunicamycin
-
-
Tamura, G.1
-
25
-
-
0013871031
-
On the initial stage in peptidoglycan synthesis. Phospho-Nacetylmuramyl-peptapeptide translocase (uridine monophosphste)
-
Struve, W. G.; Sinha, R. K.; Neuhaus, F. C. On the initial stage in peptidoglycan synthesis. Phospho-Nacetylmuramyl-peptapeptide translocase (uridine monophosphste). Biochemistry, 1966, 5, 82-93.
-
(1966)
Biochemistry
, vol.5
, pp. 82-93
-
-
Struve, W.G.1
Sinha, R.K.2
Neuhaus, F.C.3
-
26
-
-
50149105188
-
Active site mapping of MraY, a member of the polyprenylphosphate N-acetylhexosamine 1-Phosphate transferase superfamily, catalyzing the first membrane step of peptidoglycan biosynthesis
-
Al-Dabbagh, B.; Henry, X.; El Ghachi, M.; Auger, G.; Blanot, D.; Parquet, C.; Mengin-Lecreulx, D.; Bouhss, A. Active site mapping of MraY, a member of the polyprenylphosphate N-acetylhexosamine 1-Phosphate transferase superfamily, catalyzing the first membrane step of peptidoglycan biosynthesis. Biochemistry, 2008, 47, 8919-8928.
-
(2008)
Biochemistry
, vol.47
, pp. 8919-8928
-
-
Al-Dabbagh, B.1
Henry, X.2
El Ghachi, M.3
Auger, G.4
Blanot, D.5
Parquet, C.6
Mengin-Lecreulx, D.7
Bouhss, A.8
-
27
-
-
0032746748
-
Topological analysis of the MraY protein catalyzing the first membrane step of peptidoglycan synthesis
-
Bouhss, A.; Mengin-Lecreulx, D.; Le Beller, D.; Van Heijenoort, J. Topological analysis of the MraY protein catalyzing the first membrane step of peptidoglycan synthesis. Mol. Microbiol., 1999, 34. 576-585.
-
(1999)
Mol. Microbiol
, vol.34
, pp. 576-585
-
-
Bouhss, A.1
Mengin-Lecreulx, D.2
Le Beller, D.3
Van Heijenoort, J.4
-
28
-
-
0035173340
-
Conserved amino acid residues found in a predicted cytosolic domain of the lipopolysaccharide biosynthetic protein WecA are implicated in the recognition of UDP-N-acetylglucosamine
-
Amer, A. O; Valvano, M. A. Conserved amino acid residues found in a predicted cytosolic domain of the lipopolysaccharide biosynthetic protein WecA are implicated in the recognition of UDP-N-acetylglucosamine. Microbiology, 2001, 147, 3015-3025.
-
(2001)
Microbiology
, vol.147
, pp. 3015-3025
-
-
Amer, A.O.1
Valvano, M.A.2
-
29
-
-
0036175254
-
Conserved aspartic acids are essential for the enzymic activity of the WecA protein initiating the biosynthesis of O-specific lipopolysaccharide and enterobacterial common antigen in Escherichia coli
-
Amer, A. O.; Valvano, M. A. Conserved aspartic acids are essential for the enzymic activity of the WecA protein initiating the biosynthesis of O-specific lipopolysaccharide and enterobacterial common antigen in Escherichia coli. Microbiology, 2002, 148, 571-582.
-
(2002)
Microbiology
, vol.148
, pp. 571-582
-
-
Amer, A.O.1
Valvano, M.A.2
-
30
-
-
84883060074
-
Crystal structure of MraY, an essential membrane enzyme for bacterial cell wall synthesis
-
Chung, B. C.; Zhao, J.; Kwon, D.-Y.; Guan, Z.; Hong, J.; Zhou, P.; Lee, S.-Y. Crystal structure of MraY, an essential membrane enzyme for bacterial cell wall synthesis. Science, 2013, 341, 1012-1016.
-
(2013)
Science
, vol.341
, pp. 1012-1016
-
-
Chung, B.C.1
Zhao, J.2
Kwon, D.-Y.3
Guan, Z.4
Hong, J.5
Zhou, P.6
Lee, S.-Y.7
-
31
-
-
0022355806
-
Liposidomycins: Novel nucleoside antibiotics which inhibit bacterial peptidoglycan synthesis
-
Isono, K.; Uramoto, M.; Kusakabe, H.; Kimura, K.; Izaki, K.; Nelson, C. C.; McCloskey, J. A. Liposidomycins: Novel nucleoside antibiotics which inhibit bacterial peptidoglycan synthesis. J. Antibiot., 1985, 38, 1617-1621.
-
(1985)
J. Antibiot
, vol.38
, pp. 1617-1621
-
-
Isono, K.1
Uramoto, M.2
Kusakabe, H.3
Kimura, K.4
Izaki, K.5
Nelson, C.C.6
McCloskey, J.A.7
-
32
-
-
0027098096
-
Structure elucidation of liposidomycins, a class of complex lipid nucleoside antibiotics
-
Ubukata, M.; Kimura, K.; Isono, K.; Nelson, C. C.; Gregson, J. M.; McCloskey J. A. Structure elucidation of liposidomycins, a class of complex lipid nucleoside antibiotics. J. Org. Chem., 1992, 57, 6392-6403.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 6392-6403
-
-
Ubukata, M.1
Kimura, K.2
Isono, K.3
Nelson, C.C.4
Gregson, J.M.5
McCloskey, J.A.6
-
33
-
-
0023876925
-
The structure of liposidomycin B, an inhibitor of bacterial peptidoglycan synthesis
-
a) Ubukata, M.; Isono, K. The structure of liposidomycin B, an inhibitor of bacterial peptidoglycan synthesis. J. Am. Chem. Soc. 1988, 110, 4416-4417.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 4416-4417
-
-
Ubukata, M.1
Isono, K.2
-
34
-
-
0031054564
-
Liposidomycin B inhibits in vitro formation of polyprenyl (pyro)phosphate Nacetylglucosamine, an intermediate in glycoconjugate biosynthesis
-
b) Muroi, M.; Kimura, K.; Osada, H.; Inukai, M.; Takatsuki, A. Liposidomycin B inhibits in vitro formation of polyprenyl (pyro)phosphate Nacetylglucosamine, an intermediate in glycoconjugate biosynthesis. J. Antibiot., 1997, 50, 103-104.
-
(1997)
J. Antibiot
, vol.50
, pp. 103-104
-
-
Muroi, M.1
Kimura, K.2
Osada, H.3
Inukai, M.4
Takatsuki, A.5
-
35
-
-
0024431333
-
Liposidomycin C inhibits phospho-Nacetylmuramyl-pentapeptide transferase in peptidoglycan synthesis of Escherichia coli Y-10
-
Kimura, K.; Miyata, N.; Kawanishi, G.; Kamio, Y.; Izaki, K.; Isono, K. Liposidomycin C inhibits phospho-Nacetylmuramyl-pentapeptide transferase in peptidoglycan synthesis of Escherichia coli Y-10. Agric. Biol. Chem., 1989, 53, 1811-1815.
-
(1989)
Agric. Biol. Chem.
, vol.53
, pp. 1811-1815
-
-
Kimura, K.1
Miyata, N.2
Kawanishi, G.3
Kamio, Y.4
Izaki, K.5
Isono, K.6
-
36
-
-
0031690618
-
New types of liposidomycins that inhibit bacterial peptidoglycan synthesis and are produced by Streptomyces
-
a) Kimura, K.; Kagami, S.; Ikeda, Y.; Takahashi, H.; Yoshihama, M.; Kusakabe, H.; Osada, H.; Isono, K. New types of liposidomycins that inhibit bacterial peptidoglycan synthesis and are produced by Streptomyces. I. Producing organism and medium components. J. Antibiot. 1998, 51, 640-646.
-
(1998)
I. Producing Organism and Medium Components. J. Antibiot
, vol.51
, pp. 640-646
-
-
Kimura, K.1
Kagami, S.2
Ikeda, Y.3
Takahashi, H.4
Yoshihama, M.5
Kusakabe, H.6
Osada, H.7
Isono, K.8
-
37
-
-
0031661534
-
New types of liposidomycins that inhibit bacterial peptidoglycan synthesis and are produced by Streptomyces
-
b) Kimura, K.; Ikeda, Y.; Kagami, S.; Yoshihama, M.; Ubukata, M.; Esumi, Y.; Osada, H.; Isono, K. New types of liposidomycins that inhibit bacterial peptidoglycan synthesis and are produced by Streptomyces. II. Isolation and structure elucidation. J. Antibiot. 1998, 51, 647-654.
-
(1998)
II. Isolation and Structure Elucidation. J. Antibiot
, vol.51
, pp. 647-654
-
-
Kimura, K.1
Ikeda, Y.2
Kagami, S.3
Yoshihama, M.4
Ubukata, M.5
Esumi, Y.6
Osada, H.7
Isono, K.8
-
38
-
-
0032428375
-
Selective inhibition of the bacterial peptidoglycan biosynthesis by the new types of liposidomycins
-
c) Kimura, K.; Ikeda, Y.; Kagami, S.; Yoshihama, M.; Suzuki, K.; Osada, H.; Isono, K.; Selective inhibition of the bacterial peptidoglycan biosynthesis by the new types of liposidomycins. J. Antibiot., 1998, 51, 1099-1104.
-
(1998)
J. Antibiot
, vol.51
, pp. 1099-1104
-
-
Kimura, K.1
Ikeda, Y.2
Kagami, S.3
Yoshihama, M.4
Suzuki, K.5
Osada, H.6
Isono, K.7
-
39
-
-
0038264165
-
Caprazamycin B, a novel antituberculosis antibiotic, from Streptomyces sp
-
a) Igarashi, M.; Nakagawa, N.; Doi, N.; Hattori, S.; Naganawa, H.; Hamada, M. Caprazamycin B, a novel antituberculosis antibiotic, from Streptomyces sp. J. Antibiot., 2003, 56, 580-583.
-
(2003)
J. Antibiot
, vol.56
, pp. 580-583
-
-
Igarashi, M.1
Nakagawa, N.2
Doi, N.3
Hattori, S.4
Naganawa, H.5
Hamada, M.6
-
40
-
-
21044451034
-
Caprazamycins, novel lipo-nucleoside antibiotics, from Streptomyces sp
-
b) Igarashi, M.; Takahashi, Y.; Shitara, T.; Nakamura, H.; Naganawa, Miyake T, Akamatsu Y: Caprazamycins, novel lipo-nucleoside antibiotics, from Streptomyces sp. J. Antibiot., 2005, 58, 327-337.
-
(2005)
J. Antibiot
, vol.58
, pp. 327-337
-
-
Igarashi, M.1
Takahashi, Y.2
Shitara, T.3
Nakamura, H.4
Naganawa Miyake, T.5
Akamatsu, Y.6
-
41
-
-
84957565295
-
-
2004046368. Sankyo Co., Ltd; Patent WO
-
Muramatsu, Y.; Yoko, F.; Azusa, A.; Masaaki K, Toshio T, Shunichi M. 2004046368. Sankyo Co., Ltd; Patent WO. 2004.
-
(2004)
-
-
Muramatsu, Y.1
Yoko, F.2
Azusa, A.3
Masaaki, K.4
Toshio, T.5
Shunichi, M.6
-
43
-
-
79960966685
-
A-90289 A and B, new inhibitors of bacterial translocase I, produced by Streptomyces sp. SANK 60405
-
Fujita, Y.; Kizuka, M.; Funabashi, M.; Ogawa, Y.; Ishikawa, T.; Nonaka, K.; Takatsu, T. A-90289 A and B, new inhibitors of bacterial translocase I, produced by Streptomyces sp. SANK 60405. J. Antibiot., 2011, 64, 495-501.
-
(2011)
J. Antibiot
, vol.64
, pp. 495-501
-
-
Fujita, Y.1
Kizuka, M.2
Funabashi, M.3
Ogawa, Y.4
Ishikawa, T.5
Nonaka, K.6
Takatsu, T.7
-
44
-
-
0001035322
-
Stereospecific synthesis of a ribosyl-diazepanone derivative; A synthetic approach for elucidation of the stereochemistry of a lipid nucleoside antibiotic liposidomycin B
-
Spada, M. R.; Ubukata, M.; Isono, K. Stereospecific synthesis of a ribosyl-diazepanone derivative; a synthetic approach for elucidation of the stereochemistry of a lipid nucleoside antibiotic liposidomycin B. Heterocycles, 1992, 34, 1147-1167.
-
(1992)
Heterocycles
, vol.34
, pp. 1147-1167
-
-
Spada, M.R.1
Ubukata, M.2
Isono, K.3
-
45
-
-
0037149072
-
Synthesis of the liposidomycin diazepanone nucleoside
-
a) Knapp, S.; Morriello, G. J.; Doss, G. A. Synthesis of the liposidomycin diazepanone nucleoside. Org. Lett. 2002, 4, 603-606.
-
(2002)
Org. Lett.
, vol.4
, pp. 603-606
-
-
Knapp, S.1
Morriello, G.J.2
Doss, G.A.3
-
46
-
-
0035943268
-
Assignment of the liposidomycin diazepanone stereochemistry
-
b) Knapp, S.; Morriello, G. J.; Nandan, S. R.; Emge, T. J.; Doss, G. A.; Mosley, R. T.; Chen, L. Assignment of the liposidomycin diazepanone stereochemistry. J. Org. Chem., 2001, 66, 5822-5831.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 5822-5831
-
-
Knapp, S.1
Morriello, G.J.2
Nandan, S.R.3
Emge, T.J.4
Doss, G.A.5
Mosley, R.T.6
Chen, L.7
-
47
-
-
0026671067
-
Synthesis of the liposidomycin diazepanone
-
c) Knapp, S.; Nandan, S.; Resnick, L. Synthesis of the liposidomycin diazepanone. Tetrahedron Lett., 1992, 33, 5485-5486.
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 5485-5486
-
-
Knapp, S.1
Nandan, S.2
Resnick, L.3
-
48
-
-
0037068118
-
A Stevens rearrangement thwarts glycosylation with liposidomycin diazepanone ribofuranosyl donors
-
d) Knapp, S.; Morriello, G. J.; Doss, G. A. A Stevens rearrangement thwarts glycosylation with liposidomycin diazepanone ribofuranosyl donors. Tetrahedron Lett., 2002, 43, 5797-5800.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 5797-5800
-
-
Knapp, S.1
Morriello, G.J.2
Doss, G.A.3
-
49
-
-
0037224373
-
Toward the assignment of liposidomycin stereochemistry: Synthesis of 1,4-diazepan-3-one analogues by reductive amination approach
-
Nakajima, N.; Isobe, T.; Irisa, S.; Ubukata, M. Toward the assignment of liposidomycin stereochemistry: Synthesis of 1,4-diazepan-3-one analogues by reductive amination approach. Heterocycles, 2003, 59, 107-113.
-
(2003)
Heterocycles
, vol.59
, pp. 107-113
-
-
Nakajima, N.1
Isobe, T.2
Irisa, S.3
Ubukata, M.4
-
50
-
-
0034873368
-
Liposidomycins: Synthetic studies towards the ribosyldiazepanone moiety
-
a) Gravier-Pelletier, C.; Milla, M.; Le Merrer, Y.; Depezay, J. Liposidomycins: Synthetic studies towards the ribosyldiazepanone moiety. Eur. J. Org. Chem. 2001, 3089-3096.
-
(2001)
Eur. J. Org. Chem.
, pp. 3089-3096
-
-
Gravier-Pelletier, C.1
Milla, M.2
Le Merrer, Y.3
Depezay, J.4
-
51
-
-
0000783052
-
A general way, from L-ascorbic and D-isoascorbic acid, to homochiral a-hydroxy, a,β-dihydroxy and a,β-epoxyaldehydes, useful building blocks for the synthesis of linear oxygenated fatty acids metabolites
-
b) Gravier-Pelletier, C.; Dumas, J.; Le Merrer, Y.; Depezay, J. C. A general way, from L-ascorbic and D-isoascorbic acid, to homochiral a-hydroxy, a,β-dihydroxy and a,β-epoxyaldehydes, useful building blocks for the synthesis of linear oxygenated fatty acids metabolites. J. Carbohydr. Chem. 1992, 11, 969-998.
-
(1992)
J. Carbohydr. Chem.
, vol.11
, pp. 969-998
-
-
Gravier-Pelletier, C.1
Dumas, J.2
Le Merrer, Y.3
Depezay, J.C.4
-
52
-
-
0032576799
-
Accesss to enatiopure ribosyl-diazepanone core of liposidomycins
-
c) Le Merrer, Y.; Gravier-Pelletier, C.; Gerrouache, M.; Depezay, J. C. Accesss to enatiopure ribosyl-diazepanone core of liposidomycins. Tetrahedron Lett., 1998, 39, 385-388.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 385-388
-
-
Le Merrer, Y.1
Gravier-Pelletier, C.2
Gerrouache, M.3
Depezay, J.C.4
-
53
-
-
0346334386
-
A versatile scaffold for a library of liposidomycins analogues: A crucial and potent glycosylation step
-
d) Gravier-Pelletier, C.; Ginisty, M.; Le Merrer, Y. A versatile scaffold for a library of liposidomycins analogues: A crucial and potent glycosylation step. Tetrahedron Asymmetry 2004, 15, 189-193.
-
(2004)
Tetrahedron Asymmetry
, vol.15
, pp. 189-193
-
-
Gravier-Pelletier, C.1
Ginisty, M.2
Le Merrer, Y.3
-
54
-
-
30944460677
-
Chemical investigations in the synthesis of O-serinyl aminoribosides
-
e) Ginisty, M.; Gravier-Pelletier, C.; Le Merrer, Y. Chemical investigations in the synthesis of O-serinyl aminoribosides. Tetrahedron Asymmetry, 2006, 17, 142-150.
-
(2006)
Tetrahedron Asymmetry
, vol.17
, pp. 142-150
-
-
Ginisty, M.1
Gravier-Pelletier, C.2
Le Merrer, Y.3
-
55
-
-
0037474614
-
Diastereoselective syntheses of a-amino-β-hydroxyesters precursors of ribosyl-diazepanone core of the liposidomycins
-
a) Drouillat, B.; Poupardin, O.; Bourdreux, Y.; Greck, C. Diastereoselective syntheses of a-amino-β-hydroxyesters precursors of ribosyl-diazepanone core of the liposidomycins. Tetrahedron Lett., 2003, 44, 2781-2783.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 2781-2783
-
-
Drouillat, B.1
Poupardin, O.2
Bourdreux, Y.3
Greck, C.4
-
56
-
-
33746165539
-
Convergent synthetic studies towards the ribosyl-diazepanone core of the liposidomycins
-
b) Bourdreux, Y.; Drouillat, B.; Greck, C. Convergent synthetic studies towards the ribosyl-diazepanone core of the liposidomycins. Lett. Org. Chem., 2006, 3, 368-370.
-
(2006)
Lett. Org. Chem.
, vol.3
, pp. 368-370
-
-
Bourdreux, Y.1
Drouillat, B.2
Greck, C.3
-
57
-
-
34548543864
-
Synthetic route towards (5R,2′S,5′S,6′S)-ribosyl-diazepanone, an analogue core of the liposidomycins
-
c) Drouillat, B.; Bourdreux, Y.; Perdon, D.; Greck, C. Synthetic route towards (5R,2′S,5′S,6′S)-ribosyl-diazepanone, an analogue core of the liposidomycins. Tetrahedron Asymmetry, 2007, 18, 1955-1963.
-
(2007)
Tetrahedron Asymmetry
, vol.18
, pp. 1955-1963
-
-
Drouillat, B.1
Bourdreux, Y.2
Perdon, D.3
Greck, C.4
-
58
-
-
0032561229
-
Synthesis of the diazepanonenucleoside portion of liposidomycins by aldol reaction of the enolate of diazepanone with a nucleoside 5′-aldehyde
-
a) Kim, K. S.; Ahn, Y. H. Synthesis of the diazepanonenucleoside portion of liposidomycins by aldol reaction of the enolate of diazepanone with a nucleoside 5′-aldehyde. Tetrahedron: Asymmetry, 1998, 9, 3601-3605.
-
(1998)
Tetrahedron: Asymmetry
, vol.9
, pp. 3601-3605
-
-
Kim, K.S.1
Ahn, Y.H.2
-
59
-
-
37049085468
-
Synthesis of the 1,4-diazepanone-2-one moiety of liposidomycins
-
b) Kim, K. S.; Cho, I. H.; Ahn, Y. H.; Park, J. I. Synthesis of the 1,4-diazepanone-2-one moiety of liposidomycins. J. Chem. Soc. Perkin Trans. 1 1995, 1783-1785.
-
(1995)
J. Chem. Soc. Perkin Trans. 1
, pp. 1783-1785
-
-
Kim, K.S.1
Cho, I.H.2
Ahn, Y.H.3
Park, J.I.4
-
60
-
-
0001131775
-
B Synthetic study on lipid part of liposidomycins
-
c) Kim, K. S.; Cheong, C. S.; Hahn, J. S.; Park, J. I. B Synthetic study on lipid part of liposidomycins. Bull. Korean Chem. Soc., 1997, 18, 465-467.
-
(1997)
Bull. Korean Chem. Soc.
, vol.18
, pp. 465-467
-
-
Kim, K.S.1
Cheong, C.S.2
Hahn, J.S.3
Park, J.I.4
-
61
-
-
10744221552
-
A convergent synthetic approach to the nucleoside-type liposidomycin antibiotics
-
(a) Sarbia, F.; Martin-Ortiz, L.; Lopez-Herrera, F. J. A convergent synthetic approach to the nucleoside-type liposidomycin antibiotics. Org. Lett. 2003, 21, 3927-3930.
-
(2003)
Org. Lett.
, vol.21
, pp. 3927-3930
-
-
Sarbia, F.1
Martin-Ortiz, L.2
Lopez-Herrera, F.J.3
-
62
-
-
84856637031
-
Exploring the chemistry of epoxy amides for the synthesis of the 2′′-epi-diazepanone core of liposidomycins and caprazamycins
-
(b) Sarabia, F.; Vivar-Garcia, C.; Garcia-Ruiz, C.; Martin-Ortiz, L.; Romero-Carrasco, A. Exploring the chemistry of epoxy amides for the synthesis of the 2′′-epi-diazepanone core of liposidomycins and caprazamycins. J. Org. Chem., 2012, 77, 1328-1339.
-
(2012)
J. Org. Chem.
, vol.77
, pp. 1328-1339
-
-
Sarabia, F.1
Vivar-Garcia, C.2
Garcia-Ruiz, C.3
Martin-Ortiz, L.4
Romero-Carrasco, A.5
-
63
-
-
77956487329
-
Efficient synthesis of the core structure of muraymycin and caprazamycin nucleoside antibiotics based on a stereochemically revised ylide reaction
-
Spork, A. P.; Koppermann, S.; Dittrich, B.; Herbst-Irmer, R.; Ducho, C. Efficient synthesis of the core structure of muraymycin and caprazamycin nucleoside antibiotics based on a stereochemically revised ylide reaction. Tetrahedron Asymmetry, 2010, 21, 763-766.
-
(2010)
Tetrahedron Asymmetry
, vol.21
, pp. 763-766
-
-
Spork, A.P.1
Koppermann, S.2
Dittrich, B.3
Herbst-Irmer, R.4
Ducho, C.5
-
64
-
-
0342936076
-
Intramolecular Oglycoside bond formation
-
Jung, K.; Muller, M.; Schmidt, R. R. Intramolecular Oglycoside bond formation. Chem. Rev., 2000, 100, 4423-4442.
-
(2000)
Chem. Rev.
, vol.100
, pp. 4423-4442
-
-
Jung, K.1
Muller, M.2
Schmidt, R.R.3
-
65
-
-
37549058458
-
Development of a highly β-selective ribosylation reaction without using neighboring group participation: Total synthesis of (+)-caprazol, a core structure of caprazamycins
-
a) Hirano, S.; Ichikawa, S.; Matsuda, A. Development of a highly β-selective ribosylation reaction without using neighboring group participation: Total synthesis of (+)-caprazol, a core structure of caprazamycins. J. Org. Chem., 2007, 72, 9936-9946.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 9936-9946
-
-
Hirano, S.1
Ichikawa, S.2
Matsuda, A.3
-
66
-
-
17044432700
-
Total synthesis of caprazol, a core structure of the caprazamycin antituberculosis antibiotics
-
b) Hirano, S.; Ichikawa, S.; Matsuda, A. Total synthesis of caprazol, a core structure of the caprazamycin antituberculosis antibiotics. Angew. Chem. Int. Ed., 2005, 44, 1854-1856.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 1854-1856
-
-
Hirano, S.1
Ichikawa, S.2
Matsuda, A.3
-
67
-
-
58149195372
-
Highly β-selective C-allylation of a ribofuranoside controlling steric hindrance in the transition state
-
Ichikawa, S.; Hayashi, R.; Hirano, S.; Matsuda, A. Highly β-selective C-allylation of a ribofuranoside controlling steric hindrance in the transition state. Org. Lett., 2008, 10, 5107-5110.
-
(2008)
Org. Lett.
, vol.10
, pp. 5107-5110
-
-
Ichikawa, S.1
Hayashi, R.2
Hirano, S.3
Matsuda, A.4
-
68
-
-
84903155195
-
Catalytic asymmetric total synthesis of (+)-caprazol
-
Gopinath, P.; Wang, L.; Abe, H.; Ravi, G.; Masuda, T.; Watanabe, T.; Shibasaki, M. Catalytic asymmetric total synthesis of (+)-caprazol. Org. Lett., 2014, 16, 3364-3367.
-
(2014)
Org. Lett.
, vol.16
, pp. 3364-3367
-
-
Gopinath, P.1
Wang, L.2
Abe, H.3
Ravi, G.4
Masuda, T.5
Watanabe, T.6
Shibasaki, M.7
-
69
-
-
84923381490
-
Total synthesis of (-)-caprazamycin A
-
Nakamura, H.; Tsukamoto, C.; Yasui, M.; Yokouchi, S.; Igarashi, M.; Takemoto, Y. Total synthesis of (-)-caprazamycin A. Angew. Chem. Int. Ed., 2015, 54, 3136-3139.
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 3136-3139
-
-
Nakamura, H.1
Tsukamoto, C.2
Yasui, M.3
Yokouchi, S.4
Igarashi, M.5
Takemoto, Y.6
-
70
-
-
84930503792
-
Synthesis of caprazamycin B
-
Abe, H.; Gopoinath, P.; Ravi, G.; Wang, L.; Watanabe, T.; Shibasaki, M. Synthesis of caprazamycin B. Tetrahedron Lett., 2015, 56, 3782-3785.
-
(2015)
Tetrahedron Lett.
, vol.56
, pp. 3782-3785
-
-
Abe, H.1
Gopoinath, P.2
Ravi, G.3
Wang, L.4
Watanabe, T.5
Shibasaki, M.6
-
71
-
-
0034698781
-
Synthesis of nucleoside moiety of liposidomycins: Elucidation of the pharmacophore of this family of MraY inhibitor
-
a) Dini, C.; Collette, P.; Drochon, N.; Guillot, J. C.; Lemoine, G.; Mauvais, P.; Aszodi, J. Synthesis of nucleoside moiety of liposidomycins: Elucidation of the pharmacophore of this family of MraY inhibitor. Bioorg. Med. Chem. Lett., 2000, 10, 1839-1843.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 1839-1843
-
-
Dini, C.1
Collette, P.2
Drochon, N.3
Guillot, J.C.4
Lemoine, G.5
Mauvais, P.6
Aszodi, J.7
-
72
-
-
0035952292
-
Synthesis of analogues of the O-β-D-ribofuranosyl nucleoside moiety of liposidomycins
-
b) Dini, C.; Drochon, N.; Guillot, J. C.; Mauvais, P.; Walter, P.; Aszodi, J. Synthesis of analogues of the O-β-D-ribofuranosyl nucleoside moiety of liposidomycins. Part 2: Role of the hydroxyl groups upon the inhibition of MraY. Bioorg. Med. Chem. Lett., 2001, 11, 533-536.
-
(2001)
Part 2: Role of the Hydroxyl Groups Upon the Inhibition of MraY. Bioorg. Med. Chem. Lett.
, vol.11
, pp. 533-536
-
-
Dini, C.1
Drochon, N.2
Guillot, J.C.3
Mauvais, P.4
Walter, P.5
Aszodi, J.6
-
73
-
-
0035952253
-
Synthesis of analogues of the O-β-D-ribofuranosyl nucleoside moiety of liposidomycins
-
c) Dini, C.; Drochon, N.; Feteanu, S.; Guillot, J. C.; Peixoto, C.; Aszodi, J. Synthesis of analogues of the O-β-D-ribofuranosyl nucleoside moiety of liposidomycins. Part 1: Contribution of the amino group and the uracil moiety upon the inhibition of MraY. Bioorg. Med. Chem. Lett., 2001, 11, 529-531.
-
(2001)
Part 1: Contribution of the Amino Group and the Uracil Moiety Upon the Inhibition of MraY. Bioorg. Med. Chem. Lett.
, vol.11
, pp. 529-531
-
-
Dini, C.1
Drochon, N.2
Feteanu, S.3
Guillot, J.C.4
Peixoto, C.5
Aszodi, J.6
-
74
-
-
0037156358
-
Synthesis of sub-micromolor inhibitors of MraY by exploring the region originally occupied by the diazepanone ring in the liposidomycin structure
-
Dini, C.; Didier-Laurent, S.; Drochon, N.; Fereanu, S.; Guillot, J. C.; Monti, F.; Uridat, E.; Zhang, J.; Aszodi, J. Synthesis of sub-micromolor inhibitors of MraY by exploring the region originally occupied by the diazepanone ring in the liposidomycin structure. Bioorg. Med. Chem. Lett., 2002, 12, 1209-1213.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1209-1213
-
-
Dini, C.1
Didier-Laurent, S.2
Drochon, N.3
Fereanu, S.4
Guillot, J.C.5
Monti, F.6
Uridat, E.7
Zhang, J.8
Aszodi, J.9
-
75
-
-
40949120496
-
Synthesis of caprazamycin analogs and their structure-activity relationship for antibacterial activity
-
Hirano, S.; Ichikawa, S.; Matsuda, A. Synthesis of caprazamycin analogs and their structure-activity relationship for antibacterial activity. J. Org. Chem., 2008, 73, 569-577.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 569-577
-
-
Hirano, S.1
Ichikawa, S.2
Matsuda, A.3
-
76
-
-
84969220190
-
Carbacaprazamycins: Chemically stable analogues of the caprazamycin nucleoside antibiotics
-
Ichikawa, S.; Yamaguchi, M.; Hsuan, L. S.; Kato, Y.; Matsuda, A. Carbacaprazamycins: chemically stable analogues of the caprazamycin nucleoside antibiotics. ACS Infect. Dis., 2015, 1, 151-156.
-
(2015)
ACS Infect. Dis.
, vol.1
, pp. 151-156
-
-
Ichikawa, S.1
Yamaguchi, M.2
Hsuan, L.S.3
Kato, Y.4
Matsuda, A.5
-
77
-
-
43049148337
-
Structure-activity relationship of truncated analogs of caprazamycins as potential anti-tuberculosis agents
-
a) Hirano, S.; Ichikawa, S.; Matsuda, A. Structure-activity relationship of truncated analogs of caprazamycins as potential anti-tuberculosis agents. Bioorg. Med. Chem., 2008, 16, 5123-5133.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 5123-5133
-
-
Hirano, S.1
Ichikawa, S.2
Matsuda, A.3
-
78
-
-
38049092920
-
Design and synthesis of diketopiperazine and acyclic analogs related to the caprazamycins and liposidomycins as potential antibacterial agents
-
b) Hirano, S.; Ichikawa, S.; Matsuda, A. Design and synthesis of diketopiperazine and acyclic analogs related to the caprazamycins and liposidomycins as potential antibacterial agents. Bioorg. Med. Chem., 2008, 16, 428-436.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 428-436
-
-
Hirano, S.1
Ichikawa, S.2
Matsuda, A.3
-
79
-
-
84875723294
-
Novel semisynthetic antibiotics from caprazamycins A-G: Caprazene derivatives and their antibacterial activity
-
a) Takahashi, Y.; Igarashi, M.; Miyake, T.; Soutome, H.; Ishikawa, K.; Komatsuki, Y.; Koyama, Y.; Nakagawa, N.; Hattori, S.; Inoue, K.; Doi, N.; Akamatsu, Y. Novel semisynthetic antibiotics from caprazamycins A-G: Caprazene derivatives and their antibacterial activity. J. Antibiot., 2013, 66, 171-178.
-
(2013)
J. Antibiot
, vol.66
, pp. 171-178
-
-
Takahashi, Y.1
Igarashi, M.2
Miyake, T.3
Soutome, H.4
Ishikawa, K.5
Komatsuki, Y.6
Koyama, Y.7
Nakagawa, N.8
Hattori, S.9
Inoue, K.10
Doi, N.11
Akamatsu, Y.12
-
80
-
-
84886920443
-
Inhibition of the first step in synthesis of the mycobacterial cell wall core, catalyzed by the GlcNAc-1-phosphate transferase WecA, by the novel caprazamycin derivative CPZEN-45
-
Ishizaki, Y.; Hayashi, C.; Inoue, K.; Igarashi, M.; Takahashi, Y.; Pujari, V.; Crick, D. C.; Brennan, P. J.; Nomoto, A. Inhibition of the first step in synthesis of the mycobacterial cell wall core, catalyzed by the GlcNAc-1-phosphate transferase WecA, by the novel caprazamycin derivative CPZEN-45. J. Biol. Chem., 2013, 228, 30309-30319.
-
(2013)
J. Biol. Chem.
, vol.228
, pp. 30309-30319
-
-
Ishizaki, Y.1
Hayashi, C.2
Inoue, K.3
Igarashi, M.4
Takahashi, Y.5
Pujari, V.6
Crick, D.C.7
Brennan, P.J.8
Nomoto, A.9
-
81
-
-
84889076146
-
An update on the chemistry and medicinal chemistry of novel antimycobacterial compounds
-
Branco, F. S. C.; Pinto, A. C.; Boechat, N. An update on the chemistry and medicinal chemistry of novel antimycobacterial compounds. Curr. Top. Med. Chem., 2013, 13, 2808-2849.
-
(2013)
Curr. Top. Med. Chem.
, vol.13
, pp. 2808-2849
-
-
Branco, F.S.C.1
Pinto, A.C.2
Boechat, N.3
-
82
-
-
84886469710
-
Liquid chromatographic determination of CPZEN-45, a novel antitubercular drug, in biological samples
-
Hanif, S. N. M.; Hickey, A. J.; Garcia-Contreras, L. Liquid chromatographic determination of CPZEN-45, a novel antitubercular drug, in biological samples. J. Pharm. Biomed. Anal., 2014, 88, 370-376.
-
(2014)
J. Pharm. Biomed. Anal.
, vol.88
, pp. 370-376
-
-
Hanif, S.N.M.1
Hickey, A.J.2
Garcia-Contreras, L.3
-
83
-
-
84868704828
-
Antimycobacterial drugs currently in Phase II clinical trials and preclinical phase for tuberculosis treatment
-
Engohang-Ndong, J. Antimycobacterial drugs currently in Phase II clinical trials and preclinical phase for tuberculosis treatment. Expert. Opin. Investig. Drugs, 2012, 21, 1789-1800.
-
(2012)
Expert. Opin. Investig. Drugs
, vol.21
, pp. 1789-1800
-
-
Engohang-Ndong, J.1
-
84
-
-
84934948523
-
5′-Methylenetriazole-substituted-aminoribosyl uridines as MraY inhibitors: Synthesis, biological evaluation and molecular modeling
-
a) Fer, M. J.; Bouhss, A.; Patrao, M.; Le Corre, L.; Pietrancosta, N.; Amoroso, A.; Joris, B.; Mengin-Lecreulx, D.; Calvet-Vitale, S.; Gravier-Pelletier, C. 5′-Methylenetriazole-substituted-aminoribosyl uridines as MraY inhibitors: Synthesis, biological evaluation and molecular modeling. Org. Biomol. Chem., 2015, 13, 7193-7222.
-
(2015)
Org. Biomol. Chem.
, vol.13
, pp. 7193-7222
-
-
Fer, M.J.1
Bouhss, A.2
Patrao, M.3
Le Corre, L.4
Pietrancosta, N.5
Amoroso, A.6
Joris, B.7
Mengin-Lecreulx, D.8
Calvet-Vitale, S.9
Gravier-Pelletier, C.10
-
85
-
-
84886430232
-
Toward analogues of mray natural inhibitors: Synthesis of 5′-triazole-substituted-aminoribosyl uridines through a Cu-catalyzed azide-alkyne cycloaddition
-
b) Fer, M. J.; Olatunji, S.; Bouhss, A.; Calvet-Vitale, S.; Gravier-Pelletier, C. Toward analogues of mray natural inhibitors: Synthesis of 5′-triazole-substituted-aminoribosyl uridines through a Cu-catalyzed azide-alkyne cycloaddition. J. Org. Chem., 2013, 78, 10088-10105.
-
(2013)
J. Org. Chem.
, vol.78
, pp. 10088-10105
-
-
Fer, M.J.1
Olatunji, S.2
Bouhss, A.3
Calvet-Vitale, S.4
Gravier-Pelletier, C.5
-
86
-
-
35348865461
-
Efficient synthesis of polyfunctionalised enantiopure diazepanone scaffolds
-
a) Monasson, O.; Ginisty, M.; Bertho, G.; Gravier-Pelletier, C.; Le Merrer, Y. Efficient synthesis of polyfunctionalised enantiopure diazepanone scaffolds. Tetrahedron Lett., 2007, 48, 8149-8152.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 8149-8152
-
-
Monasson, O.1
Ginisty, M.2
Bertho, G.3
Gravier-Pelletier, C.4
Le Merrer, Y.5
-
87
-
-
79953217671
-
Synthesis and biological evaluation of a diazepanone-based library of liposidomycins analogs as MraY inhibitors
-
b) Mravljak, J.; Monasson, O.; Al-Dabbagh, B.; Crouvoisier, M.; Bouhss, A.; Gravier-Pelletier, C.; Le Merrer, Y. Synthesis and biological evaluation of a diazepanone-based library of liposidomycins analogs as MraY inhibitors. Eur. J. Med. Chem., 2011, 46, 1582-1592.
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 1582-1592
-
-
Mravljak, J.1
Monasson, O.2
Al-Dabbagh, B.3
Crouvoisier, M.4
Bouhss, A.5
Gravier-Pelletier, C.6
Le Merrer, Y.7
-
88
-
-
0037019522
-
Structure of the muraymycins, novel peptidoglycan biosynthesis inhibitors
-
Mcdonald, L. A.; Barbieri, L. R.; Carter, G. T.; Lenoy, E.; Lotvin, J.; Petersen, P. J.; Siegel, M. M.; Singh, G.; Williamson, R. T. Structure of the muraymycins, novel peptidoglycan biosynthesis inhibitors. J. Am. Chem. Soc., 2002, 124, 10260-10261.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 10260-10261
-
-
Mcdonald, L.A.1
Barbieri, L.R.2
Carter, G.T.3
Lenoy, E.4
Lotvin, J.5
Petersen, P.J.6
Siegel, M.M.7
Singh, G.8
Williamson, R.T.9
-
89
-
-
77949276693
-
Total synthesis of (-)-muraymycin D2 and its epimer
-
Tanino, T.; Ichikawa, S.; Shiro, M.; Matsuda, A. Total synthesis of (-)-muraymycin D2 and its epimer. J. Org. Chem., 2010, 75, 1366-1377.
-
(2010)
J. Org. Chem.
, vol.75
, pp. 1366-1377
-
-
Tanino, T.1
Ichikawa, S.2
Shiro, M.3
Matsuda, A.4
-
90
-
-
79961069233
-
Synthesis of L-epicapreomycidine derivatives via C-H amination
-
Tanino, T.; Ichikawa, S.; Matsuda, A. Synthesis of L-epicapreomycidine derivatives via C-H amination. Org. Lett., 2011, 13, 4028-4031.
-
(2011)
Org. Lett.
, vol.13
, pp. 4028-4031
-
-
Tanino, T.1
Ichikawa, S.2
Matsuda, A.3
-
91
-
-
70449348776
-
Improved convergent synthesis of 5′-epi-analogues of muraymycin nucleoside antibiotics
-
a) Spork, A. P.; Koppermann, S.; Ducho, C. Improved convergent synthesis of 5′-epi-analogues of muraymycin nucleoside antibiotics, Synlett, 2009, 2503-2507.
-
(2009)
Synlett
, pp. 2503-2507
-
-
Spork, A.P.1
Koppermann, S.2
Ducho, C.3
-
92
-
-
77952389694
-
Novel 5′-deoxy nucleosyl amino acid scaffolds for the synthesis of muraymycin analogues
-
b) Spork, A. P.; Ducho, C. Novel 5′-deoxy nucleosyl amino acid scaffolds for the synthesis of muraymycin analogues. Org. Biomol. Chem., 2010, 8, 2323-2326.
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 2323-2326
-
-
Spork, A.P.1
Ducho, C.2
-
93
-
-
84055193833
-
Stereoselective synthesis of uridine-derived nucleosyl amino acids
-
c) Spork, A. P.; Wiegmann, D.; Granitzka, M.; Stalke, D.; Ducho, C. Stereoselective synthesis of uridine-derived nucleosyl amino acids. J. Org. Chem. 2011, 76, 10083-10098.
-
(2011)
J. Org. Chem.
, vol.76
, pp. 10083-10098
-
-
Spork, A.P.1
Wiegmann, D.2
Granitzka, M.3
Stalke, D.4
Ducho, C.5
-
94
-
-
84872679752
-
Stereocontrolled synthesis of 5′-and 6′-epimeric analogues of muraymycin nucleoside antibiotics
-
d) Spork, A. P.; Ducho, C. Stereocontrolled synthesis of 5′-and 6′-epimeric analogues of muraymycin nucleoside antibiotics. Syn. Lett., 2013, 343-346.
-
(2013)
Syn. Lett.
, pp. 343-346
-
-
Spork, A.P.1
Ducho, C.2
-
95
-
-
84860160240
-
Synthesis of ureidomuraymycidine derivatives for structure-activity relationship studies of muraymydins
-
Aleiwi, B. A.; Schmeider, C. M.; Kurosu, M. Synthesis of ureidomuraymycidine derivatives for structure-activity relationship studies of muraymydins. J. Org. Chem., 2012, 77, 3859-3867.
-
(2012)
J. Org. Chem.
, vol.77
, pp. 3859-3867
-
-
Aleiwi, B.A.1
Schmeider, C.M.2
Kurosu, M.3
-
96
-
-
0037009244
-
Muraymycins, novel peptidoglycan biosynthesis inhibitors: Semisynthesis and SAR of their derivatives
-
Lin, Y. I.; Li, Z.; Francisco, G. D.; McDonald, L. A.; Davis, R. A.; Singh, G.; Yang, Y.; Mansour, T. S. Muraymycins, novel peptidoglycan biosynthesis inhibitors: Semisynthesis and SAR of their derivatives. Bioorg. Med. Chem. Lett., 2002, 12, 2341-2344.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 2341-2344
-
-
Lin, Y.I.1
Li, Z.2
Francisco, G.D.3
McDonald, L.A.4
Davis, R.A.5
Singh, G.6
Yang, Y.7
Mansour, T.S.8
-
97
-
-
0041330368
-
Muraymycins, novel peptidoglycan biosynthesis inhibitors: Synthesis and SAR of their analogues
-
Yamashita, A.; Norton, E.; Peterson, P. J.; Rasmussen, B. A.; Singh, G.; Yang, Y.; Mansour, T. S.; Ho, D. M. Muraymycins, novel peptidoglycan biosynthesis inhibitors: Synthesis and SAR of their analogues. Bioorg. Med. Chem. Lett., 2003, 13, 3345-3350.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3345-3350
-
-
Yamashita, A.1
Norton, E.2
Peterson, P.J.3
Rasmussen, B.A.4
Singh, G.5
Yang, Y.6
Mansour, T.S.7
Ho, D.M.8
-
98
-
-
84941037136
-
Lead structure for new antibacterials: Stereocontrolled synthesis of a bioactive muraymycin analogue
-
Spork, A. P.; Bueschleb, M.; Ries, O.; Wiegmann, D.; Boettcher, S.; Mihalyi, A.; Bugg, T. D. H.; Ducho, C. Lead structure for new antibacterials: Stereocontrolled synthesis of a bioactive muraymycin analogue. Chem. Eur. J., 2014, 20, 15292-15297.
-
(2014)
Chem. Eur. J
, vol.20
, pp. 15292-15297
-
-
Spork, A.P.1
Bueschleb, M.2
Ries, O.3
Wiegmann, D.4
Boettcher, S.5
Mihalyi, A.6
Bugg, T.D.H.7
Ducho, C.8
-
99
-
-
77956534326
-
Synthesis and biological evaluation of muraymycin analogues as potential anti-drug-resistant bacterial
-
Tanino, T.; Ichikawa, S.; Al-Dabbagh, B.; Bouhss, A.; Matsuda, A. Synthesis and biological evaluation of muraymycin analogues as potential anti-drug-resistant bacterial. ACS Med. Chem. Lett., 2010, 1, 258-262.
-
(2010)
ACS Med. Chem. Lett.
, vol.1
, pp. 258-262
-
-
Tanino, T.1
Ichikawa, S.2
Al-Dabbagh, B.3
Bouhss, A.4
Matsuda, A.5
-
100
-
-
84055217607
-
Mechanistic analysis of muraymycin analogues: A guide to the design of MraY inhibitors
-
Tanino, T.; Al-Dabbagh, B.; Mengin-Lecreulx, D.; Bouhss, A.; Oyama, H.; Ichikawa, S.; Matsuda, A. Mechanistic analysis of muraymycin analogues: A guide to the design of MraY inhibitors. J. Med. Chem., 2011, 54, 8421-8439.
-
(2011)
J. Med. Chem.
, vol.54
, pp. 8421-8439
-
-
Tanino, T.1
Al-Dabbagh, B.2
Mengin-Lecreulx, D.3
Bouhss, A.4
Oyama, H.5
Ichikawa, S.6
Matsuda, A.7
-
101
-
-
0022531920
-
Capuramycin, A new nucleoside antibiotic. Taxonomy, fermentation, isolation and characterization
-
a) Yamaguchi, H.; Sato, S.; Yoshida, S.; Takada, K.; Itoh, M.; Seto, H.; Otake, N. Capuramycin, A new nucleoside antibiotic. Taxonomy, fermentation, isolation and characterization. J. Antibiot., 1986, 39, 1047-1053.
-
(1986)
J. Antibiot
, vol.39
, pp. 1047-1053
-
-
Yamaguchi, H.1
Sato, S.2
Yoshida, S.3
Takada, K.4
Itoh, M.5
Seto, H.6
Otake, N.7
-
102
-
-
0023938632
-
The structure of a new nucleoside antibiotic, capuramycin
-
b) Seto, H.; Otake, N.; Sato, S.; Hamaguchi, H.; Takada, K.; Itoh, M.; Lu, H. S. M.; Clardy, J. The structure of a new nucleoside antibiotic, capuramycin. Tetrahedron Lett., 1988, 29, 2343-2346.
-
(1988)
Tetrahedron Lett.
, vol.29
, pp. 2343-2346
-
-
Seto, H.1
Otake, N.2
Sato, S.3
Hamaguchi, H.4
Takada, K.5
Itoh, M.6
Lu, H.S.M.7
Clardy, J.8
-
103
-
-
40949131933
-
A-102395, a novel inhibitor of bacterial translocase I, produced by Amycolatopsis sp. SANK 60206
-
c) Murakami, R.; Fujita, Y.; Kizuka, M.; Kagawa, T.; Muramatsu, Y.; Miyakoshi, S.; Takatsu, T.; Inukai, M. A-102395, a novel inhibitor of bacterial translocase I, produced by Amycolatopsis sp. SANK 60206. J. Antibiot., 2007, 60, 690-695.
-
(2007)
J. Antibiot
, vol.60
, pp. 690-695
-
-
Murakami, R.1
Fujita, Y.2
Kizuka, M.3
Kagawa, T.4
Muramatsu, Y.5
Miyakoshi, S.6
Takatsu, T.7
Inukai, M.8
-
104
-
-
0344404062
-
Studies on novel bacterial translocase i inhibitors, A-500359S. Taxonomy, fermentation, isolation, physico-chemical properties and structure elucidation of a-500359a, C, D and G
-
a) Muramatsu, Y.; Muramatsu, A.; Ohnuki, T.; Ishii, M. M.; Kizuka, M.; Enokita, R.; Tsutsumi, S.; Arai, M.; Ogawa, Y.; Suzuki, T.; Takatsu, T.; Inukai, M. Studies on novel bacterial translocase I inhibitors, A-500359S. Taxonomy, fermentation, isolation, physico-chemical properties and structure elucidation of A-500359A, C, D and G. J. Antibiot., 2003, 56, 243-252.
-
(2003)
J. Antibiot
, vol.56
, pp. 243-252
-
-
Muramatsu, Y.1
Muramatsu, A.2
Ohnuki, T.3
Ishii, M.M.4
Kizuka, M.5
Enokita, R.6
Tsutsumi, S.7
Arai, M.8
Ogawa, Y.9
Suzuki, T.10
Takatsu, T.11
Inukai, M.12
-
105
-
-
33751234202
-
Studies on novel bacterial translocase i inhibitors, A-500359S
-
b) Muramatsu, Y.; Arai, M.; Sakaida, Y.; Takamatsu, Y.; Miyakoshi, S.; Inukai, M. Studies on novel bacterial translocase I inhibitors, A-500359S. J. Antibiot., 2006, 59, 601-606.
-
(2006)
J. Antibiot
, vol.59
, pp. 601-606
-
-
Muramatsu, Y.1
Arai, M.2
Sakaida, Y.3
Takamatsu, Y.4
Miyakoshi, S.5
Inukai, M.6
-
106
-
-
0028327031
-
Synthesis of capuramycin
-
Knapp, S.; Nanda, S. R. Synthesis of capuramycin. J. Org. Chem., 1994, 59, 281-283.
-
(1994)
J. Org. Chem.
, vol.59
, pp. 281-283
-
-
Knapp, S.1
Nanda, S.R.2
-
107
-
-
66149190559
-
Concise synthesis of capuramycin
-
a) Kurosu, M.; Li, K.; Crick, D. C. Concise synthesis of capuramycin. Org. Lett., 2009, 11, 2393-2396.
-
(2009)
Org. Lett.
, vol.11
, pp. 2393-2396
-
-
Kurosu, M.1
Li, K.2
Crick, D.C.3
-
108
-
-
84885383708
-
Improved synthesis of capuramycin and its analogues
-
b) Wang, Y.; Siricilla, S.; Aleiwi, B. A.; Kurosu, M. Improved synthesis of capuramycin and its analogues. Chem. Eur. J., 2013, 19, 13847-13858.
-
(2013)
Chem. Eur. J
, vol.19
, pp. 13847-13858
-
-
Wang, Y.1
Siricilla, S.2
Aleiwi, B.A.3
Kurosu, M.4
-
109
-
-
10744222686
-
Synthesis and antimycobacterial activity of capuramycin analogues. Part 1: Substitution of the azepan-2-one moiety of capuramycin
-
a) Hotoda, H.; Furukawa, M.; Daigo, M.; Murayama, K.; Kaneko, M.; Muramatsu. Y.; Ishi, M. M.; Miyakoshi, S.; Takatsu, T.; Inukai, M.; Kakuta, M.; Abe, T.; Harasaki, T.; Fukuoka, T.; Utsui, Y.; Ohya, S. Synthesis and antimycobacterial activity of capuramycin analogues. Part 1: Substitution of the azepan-2-one moiety of capuramycin. Bioorg. Med. Chem. Lett., 2003, 13, 2829-2832.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 2829-2832
-
-
Hotoda, H.1
Furukawa, M.2
Daigo, M.3
Murayama, K.4
Kaneko, M.5
Muramatsu, Y.6
Ishi, M.M.7
Miyakoshi, S.8
Takatsu, T.9
Inukai, M.10
Kakuta, M.11
Abe, T.12
Harasaki, T.13
Fukuoka, T.14
Utsui, Y.15
Ohya, S.16
-
110
-
-
10744223630
-
Synthesis and antimycobacterial activity of capuramycin analogues. Part 2: Acylated derivatives of capuramycin-related compounds
-
b) Hotoda, H.; Daigo, M.; Furukawa, M.; Murayama, K.; Hasegawa, C. A.; Kaneko, M.; Muramatsu, Y.; Ishi, M. M.; Miyakoshi, S.; Takatsu, T.; Inukai, M.; Kakuta, M.; Abe, T.; Fukuoka, T.; Utsui, Y.; Ohya, S. Synthesis and antimycobacterial activity of capuramycin analogues. Part 2: Acylated derivatives of capuramycin-related compounds. Bioorg. Med. Chem. Lett., 2003, 13, 2833-2836.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 2833-2836
-
-
Hotoda, H.1
Daigo, M.2
Furukawa, M.3
Murayama, K.4
Hasegawa, C.A.5
Kaneko, M.6
Muramatsu, Y.7
Ishi, M.M.8
Miyakoshi, S.9
Takatsu, T.10
Inukai, M.11
Kakuta, M.12
Abe, T.13
Fukuoka, T.14
Utsui, Y.15
Ohya, S.16
-
111
-
-
6344255049
-
Activity of capuramycin analogues against Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium intracellulare in vitro and in vivo
-
c) Koga, T.; Fukuoka, T.; Doi, N.; Harasaki, T.; Inoue, H.; Hotoda, H.; Kakuta, M.; Muramatsu, Y.; Yamamura, N.; Hoshi, M.; Hirota, T. Activity of capuramycin analogues against Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium intracellulare in vitro and in vivo. J. Antibicrob. Chemother., 2004, 54, 755-760.
-
(2004)
J. Antibicrob. Chemother
, vol.54
, pp. 755-760
-
-
Koga, T.1
Fukuoka, T.2
Doi, N.3
Harasaki, T.4
Inoue, H.5
Hotoda, H.6
Kakuta, M.7
Muramatsu, Y.8
Yamamura, N.9
Hoshi, M.10
Hirota, T.11
-
112
-
-
84891526259
-
Threrapeutic efficacy of SQ641-NE against Mycobacterium tuberculosis
-
a) Nikonenko, B.; Reddy, V. M.; Bogatcheva, E.; Protopopova, M.; Einck, L.; Nancy, C. A. Threrapeutic efficacy of SQ641-NE against Mycobacterium tuberculosis. Antimicrob. Agents Chemother., 2014, 58, 587-589.
-
(2014)
Antimicrob. Agents Chemother
, vol.58
, pp. 587-589
-
-
Nikonenko, B.1
Reddy, V.M.2
Bogatcheva, E.3
Protopopova, M.4
Einck, L.5
Nancy, C.A.6
-
113
-
-
67649950670
-
Activity of SQ641, a capuramycin analog, in a murine model of tuberculosis
-
b) Nikonenko, B.; Reddy, V. M.; Protopopova, M.; Bogatcheva, E.; Einck, L.; Nancy, C. A. Activity of SQ641, a capuramycin analog, in a murine model of tuberculosis. Antimicrob. Agents Chemother., 2009, 53, 3138-3139.
-
(2009)
Antimicrob. Agents Chemother
, vol.53
, pp. 3138-3139
-
-
Nikonenko, B.1
Reddy, V.M.2
Protopopova, M.3
Bogatcheva, E.4
Einck, L.5
Nancy, C.A.6
-
114
-
-
79951534255
-
Chemical modification of capuramycins to enhance antibacterial activity
-
c) Bogatcheva, E.; Dubuisson, T.; Protopopova, M.; Einck, L.; Nancy, C. A.; Reddy, V. M. Chemical modification of capuramycins to enhance antibacterial activity. J. Antimicrob. Chemother., 2011, 66, 578-587.
-
(2011)
J. Antimicrob. Chemother
, vol.66
, pp. 578-587
-
-
Bogatcheva, E.1
Dubuisson, T.2
Protopopova, M.3
Einck, L.4
Nancy, C.A.5
Reddy, V.M.6
-
115
-
-
67649950670
-
Activity of SQ641, a capuramycin analogue, in a murine model of tuberculosis
-
d) Nikonenko, B. V.; Reddy, V. M.; Protopopova, M.; Bogatcheva, E.; Einck, L.; Nacy, C. A. Activity of SQ641, a capuramycin analogue, in a murine model of tuberculosis. Antimicrob. Agents Chemother., 2009, 53, 3138-3139.
-
(2009)
Antimicrob. Agents Chemother
, vol.53
, pp. 3138-3139
-
-
Nikonenko, B.V.1
Reddy, V.M.2
Protopopova, M.3
Bogatcheva, E.4
Einck, L.5
Nacy, C.A.6
-
116
-
-
38649100344
-
In vitro antimycobacterial activities of capuramycin analogues
-
e) Reddy, V. M.; Einck, L.; Nacy, C. A. In vitro antimycobacterial activities of capuramycin analogues. Antimicrob. Agents Chemother., 2008, 52, 719-721.
-
(2008)
Antimicrob. Agents Chemother
, vol.52
, pp. 719-721
-
-
Reddy, V.M.1
Einck, L.2
Nacy, C.A.3
-
117
-
-
84969389559
-
Discovery of a cauramycin analog that kill nonreplicating Mycobacterium tuberculosis and its synergistic effects with translocase i inhibitors
-
a) Siricilla, S.; Mitachi, K.; Wan, B.; Franzblau, S. G.; Kurosu, M. Discovery of a cauramycin analog that kill nonreplicating Mycobacterium tuberculosis and its synergistic effects with translocase I inhibitors. J. Antibiot., 2014, 67, 1-8.
-
(2014)
J. Antibiot
, vol.67
, pp. 1-8
-
-
Siricilla, S.1
Mitachi, K.2
Wan, B.3
Franzblau, S.G.4
Kurosu, M.5
-
118
-
-
84862179666
-
A reliable Pd-mediated hydrogenolytic deprotection of BOM group of uridine ureido nitrogen
-
b) Aleiwi, B. A.; Kurosu, M. A reliable Pd-mediated hydrogenolytic deprotection of BOM group of uridine ureido nitrogen. Tetrahedron Lett., 2012, 53, 3758-3762.
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 3758-3762
-
-
Aleiwi, B.A.1
Kurosu, M.2
-
119
-
-
58049217566
-
Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf
-
c) Kurosu, M.; Li, K. Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf. J. Org. Chem., 2008, 73, 9767-9770.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 9767-9770
-
-
Kurosu, M.1
Li, K.2
-
120
-
-
0024354147
-
Mureidomycins AD, novel peptidyl nucleoside antibiotics with speroplast forming activity. I. Taxonomy, fermentation, isolation and physicochemical properties
-
a) Inukai, M.; Isono, F.; Takahashi, S.; Enokita, R.; Sakaida, Y.; Haneishi, T. Mureidomycins AD, novel peptidyl nucleoside antibiotics with speroplast forming activity. I. taxonomy, fermentation, isolation and physicochemical properties. J. Antibiot., 1989, 42, 662-666.
-
(1989)
J. Antibiot
, vol.42
, pp. 662-666
-
-
Inukai, M.1
Isono, F.2
Takahashi, S.3
Enokita, R.4
Sakaida, Y.5
Haneishi, T.6
-
121
-
-
0026081814
-
Mureidomycin A, a new inhibitor of bacterial peptidoglycan synthesis
-
b) Isono, F.; Inukai, M. Mureidomycin A, a new inhibitor of bacterial peptidoglycan synthesis. Antimicrob. Agents Chemother. 1991, 35, 234-236.
-
(1991)
Antimicrob. Agents Chemother
, vol.35
, pp. 234-236
-
-
Isono, F.1
Inukai, M.2
-
122
-
-
0027233035
-
Selective inhibition of the bacterial translocase reaction in peptidoglycan synthesis by mureidomycins
-
c) Inukai, M.; Isono, F.; Takatsuki, A. Selective inhibition of the bacterial translocase reaction in peptidoglycan synthesis by mureidomycins. Antimicrob. Agents Chemother., 1993, 37, 980-983.
-
(1993)
Antimicrob. Agents Chemother
, vol.37
, pp. 980-983
-
-
Inukai, M.1
Isono, F.2
Takatsuki, A.3
-
123
-
-
0024309666
-
Mureidomycins A-D, novel peptidylnucleoside antibiotics with spheroplast forming activity. III. Biological properties
-
d) Isono, F.; Katayama, T.; Inukai, M.; Haneishi, T. Mureidomycins A-D, novel peptidylnucleoside antibiotics with spheroplast forming activity. III. biological properties. J. Antibiot., 1989, 42, 674-679.
-
(1989)
J. Antibiot
, vol.42
, pp. 674-679
-
-
Isono, F.1
Katayama, T.2
Inukai, M.3
Haneishi, T.4
-
124
-
-
0024315077
-
Mureidomycins A-D, novel peptidylnucleoside antibiotics with spheroplast forming activity. II. Structural elucidation
-
e) Isono, F.; Inukai, M.; Takahashi, S.; Haneishi, T.; Kinoshita, T.; Kuwano, H. Mureidomycins A-D, novel peptidylnucleoside antibiotics with spheroplast forming activity. II. Structural elucidation. J. Antibiot., 1989, 42, 667-673.
-
(1989)
J. Antibiot
, vol.42
, pp. 667-673
-
-
Isono, F.1
Inukai, M.2
Takahashi, S.3
Haneishi, T.4
Kinoshita, T.5
Kuwano, H.6
-
125
-
-
0027201010
-
Mureidomycins e and F, minor components of mureidomycins
-
f) Isono, F.; Sakaida, Y.; Takahashi, S.; Kinoshita, T.; Nakamura, T.; Inukai, M. Mureidomycins E and F, minor components of mureidomycins. J. Antibiot., 1993, 46, 1203-1207.
-
(1993)
J. Antibiot
, vol.46
, pp. 1203-1207
-
-
Isono, F.1
Sakaida, Y.2
Takahashi, S.3
Kinoshita, T.4
Nakamura, T.5
Inukai, M.6
-
126
-
-
0028238932
-
Napsamycins, new pseudomonas active antibiotics of the mureidomycin family from Streptomyces sp Hily-82, 11372
-
Chatterjee, S.; Nadkarni, S. R.; Vijayakumar, E. K. S.; Patel, M. V.; Ganguli, B. N.; Fehlhaber, H. W.; Vertesy, L. Napsamycins, new pseudomonas active antibiotics of the mureidomycin family from Streptomyces sp. Hily-82, 11372. J. Antibiot., 1994, 47, 595-598.
-
(1994)
J. Antibiot
, vol.47
, pp. 595-598
-
-
Chatterjee, S.1
Nadkarni, S.R.2
Vijayakumar, E.K.S.3
Patel, M.V.4
Ganguli, B.N.5
Fehlhaber, H.W.6
Vertesy, L.7
-
127
-
-
0024518180
-
Pacidamycins, a novel series of antibiotics with antl-Pseudomonas aeruginosa activity. I. Taxonomy of the producing organism and fermentation
-
a) Karwowski, J. P.; Jackson, M.; Theriault, R. J.; Chen, R. H.; Barlow. G. J.; Maus, M. L. Pacidamycins, a novel series of antibiotics with antl-Pseudomonas aeruginosa activity. I. taxonomy of the producing organism and fermentation. J. Antibiot., 1989, 42, 506-511.
-
(1989)
J. Antibiot
, vol.42
, pp. 506-511
-
-
Karwowski, J.P.1
Jackson, M.2
Theriault, R.J.3
Chen, R.H.4
Barlow, G.J.5
Maus, M.L.6
-
128
-
-
0024593455
-
Pacidamycins, a novel series of antibiotics with anti-Pseudomonas aeruginosa activity. II. Isolation and structural elucidation
-
b) Chen, R. H.; Buko, A. M.; Whittern, D. N.; Mcalpin, J. Pacidamycins, a novel series of antibiotics with anti-Pseudomonas aeruginosa activity. II. isolation and structural elucidation. J. Antibiot., 1989, 42, 512-520.
-
(1989)
J. Antibiot
, vol.42
, pp. 512-520
-
-
Chen, R.H.1
Buko, A.M.2
Whittern, D.N.3
Mcalpin, J.4
-
129
-
-
0024509967
-
Pacidamycins, a novel series of antibiotics with anti-Pseudomonas aeruginosa activity. III. Microbiologic profile
-
c) Fernandes, P. B.; Swanson, R. N.; Hardy, D. J.; Hanson, C. W.; Coen, L.; Rasmussen, R. R.; Chen, R. H. Pacidamycins, a novel series of antibiotics with anti-Pseudomonas aeruginosa activity. III. microbiologic profile. J. Antibiot., 1989, 42, 521-526.
-
(1989)
J. Antibiot
, vol.42
, pp. 521-526
-
-
Fernandes, P.B.1
Swanson, R.N.2
Hardy, D.J.3
Hanson, C.W.4
Coen, L.5
Rasmussen, R.R.6
Chen, R.H.7
-
130
-
-
0034521120
-
New pacidamycins produced by Streptomyces coeruleorubidus, NRRL 18370
-
Fronko, R. M.; Lee, J. C.; Galazzo, J. G.; Chamberland, S.; Malouin, F.; Lee, M. D. New pacidamycins produced by Streptomyces coeruleorubidus, NRRL 18370. J. Antibiot., 2000, 53, 1405-1410.
-
(2000)
J. Antibiot
, vol.53
, pp. 1405-1410
-
-
Fronko, R.M.1
Lee, J.C.2
Galazzo, J.G.3
Chamberland, S.4
Malouin, F.5
Lee, M.D.6
-
131
-
-
34249739056
-
A new nucleosidyl-peptide antibiotic, Sansanmycin
-
a) Xie, Y.; Chen, R.; Si, S.; Sun, C.; Xu, H. A new nucleosidyl-peptide antibiotic, Sansanmycin. J. Antibiot., 2007, 60, 158-161.
-
(2007)
J. Antibiot
, vol.60
, pp. 158-161
-
-
Xie, Y.1
Chen, R.2
Si, S.3
Sun, C.4
Xu, H.5
-
132
-
-
49649103142
-
Sansanmycins B and C, new components of sansanmycins
-
b) Xie, Y.; Xu, H.; Si, S.; Sun, C.; Chen, R. Sansanmycins B and C, new components of sansanmycins. J. Antibiot., 2008, 61, 237-240.
-
(2008)
J. Antibiot
, vol.61
, pp. 237-240
-
-
Xie, Y.1
Xu, H.2
Si, S.3
Sun, C.4
Chen, R.5
-
133
-
-
0002862508
-
Role of the enamide linkage of nucleoside antibiotic mureidomycin A: Synthesis and reactivity of enamide-containing analogues
-
Gentl, C. A.; Bugg, T. D. H. Role of the enamide linkage of nucleoside antibiotic mureidomycin A: Synthesis and reactivity of enamide-containing analogues. J. Chem. Soc. Perkin Trans., 1999, 1, 1279-1286.
-
(1999)
J. Chem. Soc. Perkin Trans
, vol.1
, pp. 1279-1286
-
-
Gentl, C.A.1
Bugg, T.D.H.2
-
134
-
-
84856660619
-
Total synthesis and biological evaluation of pacidamycin D and its 3′-hydroxy analogue
-
a) Okamoto, K.; Sakagami, M.; Feng, F.; Togame, H.; Takemoto, H.; Ichikawa, S.; Matsuda A. Total synthesis and biological evaluation of pacidamycin D and its 3′-hydroxy analogue. J. Org. Chem., 2012, 77, 1367-1377.
-
(2012)
J. Org. Chem.
, vol.77
, pp. 1367-1377
-
-
Okamoto, K.1
Sakagami, M.2
Feng, F.3
Togame, H.4
Takemoto, H.5
Ichikawa, S.6
Matsuda, A.7
-
135
-
-
80054716538
-
Total synthesis of pacidamycin D by Cu(I)-catalyzed oxy enamide formation
-
b) Okamoto, K.; Sakagami, M.; Feng, F.; Togame, H.; Takemoto, H.; Ichikawa, S.; Matsuda A. Total synthesis of pacidamycin D by Cu(I)-catalyzed oxy enamide formation. Org. Lett., 2011, 13, 5240-5243.
-
(2011)
Org. Lett.
, vol.13
, pp. 5240-5243
-
-
Okamoto, K.1
Sakagami, M.2
Feng, F.3
Togame, H.4
Takemoto, H.5
Ichikawa, S.6
Matsuda, A.7
-
136
-
-
84863452841
-
Synthesis of pacidamycin analogues via an Ugi-multicomponent reaction
-
c) Okamoto, K.; Sakagami, M.; Feng, F.; Takahashi, F.; Uotani, K.; Togame, H.; Takemoto, H.; Ichikawa, S.; Matsuda, A. Synthesis of pacidamycin analogues via an Ugi-multicomponent reaction. Bioorg. Med. Chem. Lett., 2012, 22, 4810-4815.
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 4810-4815
-
-
Okamoto, K.1
Sakagami, M.2
Feng, F.3
Takahashi, F.4
Uotani, K.5
Togame, H.6
Takemoto, H.7
Ichikawa, S.8
Matsuda, A.9
-
137
-
-
0002818190
-
Structure-function studies on nucleoside antibiotic mureidomycin A: Synthesis of 5′-functionalised uridine models
-
a) Gentle, C. A.; Harrison, S. A.; Inukai, M.; Bugg, T. D. H. Structure-function studies on nucleoside antibiotic mureidomycin A: Synthesis of 5′-functionalised uridine models. J. Chem. Soc. Perkin Trans.,1999, 1, 1287-1294.
-
(1999)
J. Chem. Soc. Perkin Trans
, vol.1
, pp. 1287-1294
-
-
Gentle, C.A.1
Harrison, S.A.2
Inukai, M.3
Bugg, T.D.H.4
-
138
-
-
0038462275
-
Synthesis and activity of 5′-Uridinyl dipeptide analogues mimicking the amino terminal peptide chain of nucleoside antibiotic mureidomycin A
-
b) Howard, N. I.; Bugg, T. D. H. Synthesis and activity of 5′-Uridinyl dipeptide analogues mimicking the amino terminal peptide chain of nucleoside antibiotic mureidomycin A. Bioorg. Med. Chem., 2003, 11, 3083-3099.
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 3083-3099
-
-
Howard, N.I.1
Bugg, T.D.H.2
-
139
-
-
0042832955
-
Synthetic dihydropacidamycin antibiotics: A modified spectrum of activity for the pacidamycin class
-
Boojamra, C. G.; Lemoine, R. C.; Nlais, J.; Vernier, N. G.; Stein, K. A.; Magon, A.; Chamberland, S.; Hecker, S. J.; Lee V. J. Synthetic dihydropacidamycin antibiotics: A modified spectrum of activity for the pacidamycin class. Bioorg. Med. Chem. Lett., 2003, 13, 3305-3309.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3305-3309
-
-
Boojamra, C.G.1
Lemoine, R.C.2
Nlais, J.3
Vernier, N.G.4
Stein, K.A.5
Magon, A.6
Chamberland, S.7
Hecker, S.J.8
Lee, V.J.9
-
140
-
-
0037041252
-
Synthesis of basemodified dihydropacidamycins
-
Lemoine, R. C.; Magon, A.; Hecker, S. Synthesis of basemodified dihydropacidamycins. Bioorg. Med. Chem. Lett., 2002, 12, 1121-1123.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1121-1123
-
-
Lemoine, R.C.1
Magon, A.2
Hecker, S.3
-
141
-
-
35848954049
-
Solid-phase synthesis and biological evaluation of a uridinyl branched peptide urea library
-
Sun, D.; Jones, V.; Carson, E. I.; Lee, R. E. B.; Scherman, M. S.; McNeil, M. R.; Lee, R. E. Solid-phase synthesis and biological evaluation of a uridinyl branched peptide urea library. Bioorg. Med. Chem. Lett., 2007, 17, 6899-6904.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 6899-6904
-
-
Sun, D.1
Jones, V.2
Carson, E.I.3
Lee, R.E.B.4
Scherman, M.S.5
McNeil, M.R.6
Lee, R.E.7
-
142
-
-
0034684764
-
A solid-phase approach to analogues of the antibiotic mureidomycin
-
Bozzoli, A.; Kazmierski, W.; Kennedy, G.; Pasquarello, A.; Pecunioso, A. A solid-phase approach to analogues of the antibiotic mureidomycin. Bioorg. Med. Chem. Lett., 2000, 10, 2759-2763.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2759-2763
-
-
Bozzoli, A.1
Kazmierski, W.2
Kennedy, G.3
Pasquarello, A.4
Pecunioso, A.5
-
143
-
-
60349121247
-
New pacidamycin antibiotics through precursor-directed biosynthesis
-
a) Gruschow, S.; Rackham, E. J.; Elkins, B.; Newill, P. L. A.; Hill, L. M.; Goss, R. J. M. New Pacidamycin Antibiotics Through Precursor-Directed Biosynthesis. Chem. Bio. Chem., 2009, 10, 355-360.
-
(2009)
Chem. Bio. Chem.
, vol.10
, pp. 355-360
-
-
Gruschow, S.1
Rackham, E.J.2
Elkins, B.3
Newill, P.L.A.4
Hill, L.M.5
Goss, R.J.M.6
-
144
-
-
77956261456
-
New Gene express enabling synthetic diversification of natural products: Chemogenetic generation of pacidamycin analogs
-
b) Deb Roy, A.; Gruschow, S.; Cairns, N.; Goss, R. J. M. New Gene express enabling synthetic diversification of natural products: Chemogenetic generation of pacidamycin analogs. J. Am. Chem., Soc., 2010, 132, 12243-12245.
-
(2010)
J. Am. Chem., Soc.
, vol.132
, pp. 12243-12245
-
-
Deb Roy, A.1
Gruschow, S.2
Cairns, N.3
Goss, R.J.M.4
-
145
-
-
77954578876
-
New pacidamycins biosynthetically: Probing N-and C-terminal substrate specificity
-
c) Ragab, A. E.; Gruschow, S.; Rackham, E. J.; Goss, R. J. M. New pacidamycins biosynthetically: Probing N-and C-terminal substrate specificity. Org. Biomol. Chem. 2010, 8, 3128-3129.
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 3128-3129
-
-
Ragab, A.E.1
Gruschow, S.2
Rackham, E.J.3
Goss, R.J.M.4
-
146
-
-
81355141991
-
Diversity in natural product families is governed by more than enzyme promiscuity alone: Establishing control of the pacidamycin portfolio
-
d) Gruschow, S.; Rackham, E. J.; Goss, R. J. M. Diversity in natural product families is governed by more than enzyme promiscuity alone: Establishing control of the pacidamycin portfolio. Chem. Sci., 2011, 2, 2182-2186.
-
(2011)
Chem. Sci.
, vol.2
, pp. 2182-2186
-
-
Gruschow, S.1
Rackham, E.J.2
Goss, R.J.M.3
-
147
-
-
80055021577
-
Chemical logic and enzymatic machinery for biological assembly of peptidyl nucleoside antibiotics
-
e) Walsh, C. T.; Zhang, W. Chemical logic and enzymatic machinery for biological assembly of peptidyl nucleoside antibiotics. ACS Chem. Biol., 2011, 6, 1000-1007.
-
(2011)
ACS Chem. Biol.
, vol.6
, pp. 1000-1007
-
-
Walsh, C.T.1
Zhang, W.2
-
148
-
-
79953727021
-
Nine enzymes are required for assembly of the pacidamycin group of peptidyl nucleoside antibiotics
-
f) Zhang, W.; Ntai, I.; Bolla, M. L.; Malcolmson, S. J.; Kahne, D.; Kelleher, N. L.; Walsh, C. T. Nine enzymes are required for assembly of the pacidamycin group of peptidyl nucleoside antibiotics. J. Am. Chem. Soc., 2011, 133, 5240-5243.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 5240-5243
-
-
Zhang, W.1
Ntai, I.2
Bolla, M.L.3
Malcolmson, S.J.4
Kahne, D.5
Kelleher, N.L.6
Walsh, C.T.7
-
149
-
-
84907734947
-
Mechanism of action of the uridyl peptide antibiotics: An unexpected link to a protein-protein interaction site in translocase MraY
-
g) Rodis, M. T.; Mihalyi, A.; Ducho, C.; Eitei, K.; Gust, B.; Goss, R. J.; Bugg, T. D. Mechanism of action of the uridyl peptide antibiotics: An unexpected link to a protein-protein interaction site in translocase MraY. Chem. Commun., 2014, 50, 13023-13025.
-
(2014)
Chem. Commun
, vol.50
, pp. 13023-13025
-
-
Rodis, M.T.1
Mihalyi, A.2
Ducho, C.3
Eitei, K.4
Gust, B.5
Goss, R.J.6
Bugg, T.D.7
-
150
-
-
84886070500
-
Structure-based gene targeting discovery of sphaerimicin, a bacterial translocase i inhibitor
-
Funabashi, M.; Baba. S.; Takatsu, T.; Kizuka, M.; Ohata, Y.; Tanaka, M.; Nonaka, K.; Spork, A. P.; Ducho, C.; Chen, W. L.; Van Lanen, S. G. Structure-based gene targeting discovery of sphaerimicin, a bacterial translocase I inhibitor. Angew. Chem. Int. Ed., 2013, 52, 11607-11611.
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 11607-11611
-
-
Funabashi, M.1
Baba, S.2
Takatsu, T.3
Kizuka, M.4
Ohata, Y.5
Tanaka, M.6
Nonaka, K.7
Spork, A.P.8
Ducho, C.9
Chen, W.L.10
Van Lanen, S.G.11
-
151
-
-
57849092815
-
A-94964, a novel inhibitor of bacterial translocase I, produced by Streptomyces sp. SANK 60404. I. Taxonomy, isolation and biological activity
-
Murakami, R.; Fujita, Y.; Kizuka, M.; Kagawa, T.; Muramatsu, Y.; Miyakoshi, S.; Takatsu, T.; Inukai, M. A-94964, a novel inhibitor of bacterial translocase I, produced by Streptomyces sp. SANK 60404. I. Taxonomy, isolation and biological activity. J. Antibiot., 2008, 61, 537-534.
-
(2008)
J. Antibiot
, vol.61
, pp. 537-534
-
-
Murakami, R.1
Fujita, Y.2
Kizuka, M.3
Kagawa, T.4
Muramatsu, Y.5
Miyakoshi, S.6
Takatsu, T.7
Inukai, M.8
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