-
1
-
-
0343961765
-
"Ilotycin, " a new antibiotic
-
Mcguire, J. M.; Bunch, R. L.; Anderson, R. C.; Boaz, H. E.; Flynn, E. H.; Powell, H. M.; Smith, J. W. "Ilotycin, " a new antibiotic Antibiot. Chemother. 1952, 2, 281-283
-
(1952)
Antibiot. Chemother.
, vol.2
, pp. 281-283
-
-
McGuire, J.M.1
Bunch, R.L.2
Anderson, R.C.3
Boaz, H.E.4
Flynn, E.H.5
Powell, H.M.6
Smith, J.W.7
-
3
-
-
0021697495
-
Erythromycin mimics exogenous motilin in gastrointestinal contractile activity in the dog
-
Itoh, Z.; Nakaya, M.; Suzuki, H.; Arai, H.; Wakabayashi, K. Erythromycin mimics exogenous motilin in gastrointestinal contractile activity in the dog Am. J. Physiol. 1984, 247, G688-G694
-
(1984)
Am. J. Physiol.
, vol.247
, pp. 688-G694
-
-
Itoh, Z.1
Nakaya, M.2
Suzuki, H.3
Arai, H.4
Wakabayashi, K.5
-
4
-
-
0023358888
-
Clinical effects of low-dose long-term erythromycin chemotherapy on diffuse panbronchiolitis
-
(in Japanese with English abstract)
-
Kudoh, S.; Uetake, T.; Hagiwara, K.; Hirayama, M.; Hus, L. H.; Kimura, H.; Sugiyama, Y. Clinical effects of low-dose long-term erythromycin chemotherapy on diffuse panbronchiolitis Jpn. J. Thorac. Dis. 1987, 25, 632-642 (in Japanese with English abstract)
-
(1987)
Jpn. J. Thorac. Dis.
, vol.25
, pp. 632-642
-
-
Kudoh, S.1
Uetake, T.2
Hagiwara, K.3
Hirayama, M.4
Hus, L.H.5
Kimura, H.6
Sugiyama, Y.7
-
5
-
-
39549115019
-
Macrolide antibiotics as immunomodulatory medications: Proposed mechanisms of action
-
Shinkai, M.; Henke, M. O.; Rubin, B. K. Macrolide antibiotics as immunomodulatory medications: proposed mechanisms of action Pharmacol. Ther. 2008, 117, 393-405
-
(2008)
Pharmacol. Ther.
, vol.117
, pp. 393-405
-
-
Shinkai, M.1
Henke, M.O.2
Rubin, B.K.3
-
6
-
-
84878665825
-
Nonantibiotic macrolides prevent human neutrophil elastase-induced mucus stasis and airway surface liquid volume depletion
-
Tarran, R.; Sabater, J. R.; Clarke, T. C.; Tan, C. D.; Davies, C. M.; Liu, J.; Yeung, A.; Garland, A. L.; Stutts, M. J.; Abraham, W. M.; Phillips, G.; Baker, W. R.; Wright, C. D.; Wilbert, S. Nonantibiotic macrolides prevent human neutrophil elastase-induced mucus stasis and airway surface liquid volume depletion Am. J. Physiol.: Lung Cell. Mol. Physiol. 2013, 304, L746-L756
-
(2013)
Am. J. Physiol.: Lung Cell. Mol. Physiol.
, vol.304
, pp. 746-L756
-
-
Tarran, R.1
Sabater, J.R.2
Clarke, T.C.3
Tan, C.D.4
Davies, C.M.5
Liu, J.6
Yeung, A.7
Garland, A.L.8
Stutts, M.J.9
Abraham, W.M.10
Phillips, G.11
Baker, W.R.12
Wright, C.D.13
Wilbert, S.14
-
7
-
-
79958267558
-
Development of non-antibiotic macrolide that corrects inflammation-driven immune dysfunction in models of inflammatory bowel diseases and arthritis
-
Mencarelli, A.; Distrutti, E.; Renga, B.; Cipriani, S.; Palladino, G.; Booth, C.; Tudor, G.; Guse, J.-H.; Hahn, U.; Burnet, M.; Fiorucci, S. Development of non-antibiotic macrolide that corrects inflammation-driven immune dysfunction in models of inflammatory bowel diseases and arthritis Eur. J. Pharmacol. 2011, 665, 29-39
-
(2011)
Eur. J. Pharmacol.
, vol.665
, pp. 29-39
-
-
Mencarelli, A.1
Distrutti, E.2
Renga, B.3
Cipriani, S.4
Palladino, G.5
Booth, C.6
Tudor, G.7
Guse, J.-H.8
Hahn, U.9
Burnet, M.10
Fiorucci, S.11
-
8
-
-
0022354987
-
Gastrointestinal motor-stimulating activity of macrolide antibiotics and the structure-activity relationship
-
Omura, S.; Tsuzuki, K.; Sunazuka, T.; Toyoda, H.; Takahashi, I.; Itoh, Z. Gastrointestinal motor-stimulating activity of macrolide antibiotics and the structure-activity relationship J. Antibiot. 1985, 38, 1631-1632
-
(1985)
J. Antibiot.
, vol.38
, pp. 1631-1632
-
-
Omura, S.1
Tsuzuki, K.2
Sunazuka, T.3
Toyoda, H.4
Takahashi, I.5
Itoh, Z.6
-
9
-
-
0023552637
-
Macrolides with gastrointestinal motor stimulating activity
-
Omura, S.; Tsuzuki, K.; Sunazuka, T.; Marui, S.; Toyoda, H.; Inatomi, N.; Itoh, Z. Macrolides with gastrointestinal motor stimulating activity J. Med. Chem. 1987, 30, 1941-1943
-
(1987)
J. Med. Chem.
, vol.30
, pp. 1941-1943
-
-
Omura, S.1
Tsuzuki, K.2
Sunazuka, T.3
Marui, S.4
Toyoda, H.5
Inatomi, N.6
Itoh, Z.7
-
10
-
-
0024464368
-
Motilides, macrolides with gastrointestinal motor stimulating activity. I. O-Substituted and tertiary N-substituted derivatives of 8,9-anhydroerythromycin A 6,9-hemiacetal
-
Tsuzuki, K.; Sunazuka, T.; Marui, S.; Toyoda, H.; Omura, S. Motilides, macrolides with gastrointestinal motor stimulating activity. I. O-Substituted and tertiary N-substituted derivatives of 8,9-anhydroerythromycin A 6,9-hemiacetal Chem. Pharm. Bull. 1989, 37, 2687-2700
-
(1989)
Chem. Pharm. Bull.
, vol.37
, pp. 2687-2700
-
-
Tsuzuki, K.1
Sunazuka, T.2
Marui, S.3
Toyoda, H.4
Omura, S.5
-
11
-
-
0024436120
-
Motilides, macrolides with gastrointestinal motor stimulating activity. II. Quaternary N-substituted derivatives of 8,9-anhydroerythromycin A 6,9-hemiacetal and 9,9-dihydroerythromycin A 6,9-epoxide
-
Sunazuka, T.; Tsuzuki, K.; Marui, S.; Toyoda, H.; Omura, S.; Inatomi, N.; Itoh, Z. Motilides, macrolides with gastrointestinal motor stimulating activity. II. Quaternary N-substituted derivatives of 8,9-anhydroerythromycin A 6,9-hemiacetal and 9,9-dihydroerythromycin A 6,9-epoxide Chem. Pharm. Bull. 1989, 37, 2701-2709
-
(1989)
Chem. Pharm. Bull.
, vol.37
, pp. 2701-2709
-
-
Sunazuka, T.1
Tsuzuki, K.2
Marui, S.3
Toyoda, H.4
Omura, S.5
Inatomi, N.6
Itoh, Z.7
-
12
-
-
79956084563
-
Novel 12-membered non-antibiotic macrolides from erythromycin A; EM900 series as novel leads for anti-inflammatory and/or immunomodulatory agents
-
Sugawara, A.; Sueki, A.; Hirose, T.; Nagai, K.; Gouda, H.; Hirono, S.; Shima, H.; Akagawa, K. S.; Omura, S.; Sunazuka, T. Novel 12-membered non-antibiotic macrolides from erythromycin A; EM900 series as novel leads for anti-inflammatory and/or immunomodulatory agents Bioorg. Med. Chem. Lett. 2011, 21, 3373-3376
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 3373-3376
-
-
Sugawara, A.1
Sueki, A.2
Hirose, T.3
Nagai, K.4
Gouda, H.5
Hirono, S.6
Shima, H.7
Akagawa, K.S.8
Omura, S.9
Sunazuka, T.10
-
13
-
-
53549098210
-
Thalidomide as a multi-template for development of biologically active compounds
-
Hashimoto, Y. Thalidomide as a multi-template for development of biologically active compounds Arch. Pharm. Chem. Life Sci. 2008, 341, 536-547
-
(2008)
Arch. Pharm. Chem. Life Sci.
, vol.341
, pp. 536-547
-
-
Hashimoto, Y.1
-
14
-
-
0030787924
-
Regulation of chitin synthase activity in the dimorphic fungus Benjaminiella poitrasii by external osmotic pressure
-
Deshpande, M. V.; ODonnell, R.; Gooday, G. W. Regulation of chitin synthase activity in the dimorphic fungus Benjaminiella poitrasii by external osmotic pressure FEMS Microbiol. Lett. 1997, 152, 327-332
-
(1997)
FEMS Microbiol. Lett.
, vol.152
, pp. 327-332
-
-
Deshpande, M.V.1
Odonnell, R.2
Gooday, G.W.3
-
15
-
-
0026002418
-
Chitinase is required for cell separation during growth of Saccharomyces cerevisiae
-
Kuranda, M. J.; Robbins, P. W. Chitinase is required for cell separation during growth of Saccharomyces cerevisiae J. Biol. Chem. 1991, 266, 19758-19767
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 19758-19767
-
-
Kuranda, M.J.1
Robbins, P.W.2
-
16
-
-
0346399742
-
Chitin metabolism in insects: Structure, function and regulation of chitin synthases and chitinases
-
Merzendorfer, H.; Zimoch, L. Chitin metabolism in insects: structure, function and regulation of chitin synthases and chitinases J. Exp. Biol. 2003, 206, 4393-4412
-
(2003)
J. Exp. Biol.
, vol.206
, pp. 4393-4412
-
-
Merzendorfer, H.1
Zimoch, L.2
-
17
-
-
0027225980
-
New families in the classification of glycosyl hydrolases based on amino acid sequence similarities
-
Henrissat, B.; Bairoch, A. New families in the classification of glycosyl hydrolases based on amino acid sequence similarities Biochem. J. 1993, 293, 781-788
-
(1993)
Biochem. J.
, vol.293
, pp. 781-788
-
-
Henrissat, B.1
Bairoch, A.2
-
18
-
-
0030595119
-
The 1.8 Å resolution structure of hevamine, a plant chitinase/lysozyme, and analysis of the conserved sequence and structure motifs of glycosyl hydrolase family 18
-
Terwisscha van Scheltinga, A. C.; Hennig, M.; Dijikstra, B. W. The 1.8 Å resolution structure of hevamine, a plant chitinase/lysozyme, and analysis of the conserved sequence and structure motifs of glycosyl hydrolase family 18 J. Mol. Biol. 1996, 262, 243-257
-
(1996)
J. Mol. Biol.
, vol.262
, pp. 243-257
-
-
Terwisscha Van Scheltinga, A.C.1
Hennig, M.2
Dijikstra, B.W.3
-
19
-
-
26844441047
-
Natural product family 18 chitinase inhibitors
-
Andersen, O. A.; Dixon, M. J.; Eggleston, I. M.; van Aalten, D. M. F. Natural product family 18 chitinase inhibitors Nat. Prod. Rep. 2005, 22, 563-579
-
(2005)
Nat. Prod. Rep.
, vol.22
, pp. 563-579
-
-
Andersen, O.A.1
Dixon, M.J.2
Eggleston, I.M.3
Van Aalten, D.M.F.4
-
20
-
-
66749141911
-
Chitinases and chitinase-like proteins: Potential therapeutic targets for the treatment of T-helper type 2 allergies
-
Sutherland, T. E.; Maizels, R. M.; Allen, J. E. Chitinases and chitinase-like proteins: potential therapeutic targets for the treatment of T-helper type 2 allergies Clin. Exp. Allergy 2009, 39, 943-955
-
(2009)
Clin. Exp. Allergy
, vol.39
, pp. 943-955
-
-
Sutherland, T.E.1
Maizels, R.M.2
Allen, J.E.3
-
21
-
-
2942668626
-
Acidic mammalian chitinase in asthmatic Th2 inflammation and IL-13 pathway activation
-
Zhu, Z.; Zheng, T.; Homer, R. J.; Kim, Y.-K.; Chen, N. Y.; Cohn, L.; Hamid, Q.; Elias, J. A. Acidic mammalian chitinase in asthmatic Th2 inflammation and IL-13 pathway activation Science 2004, 304, 1678-1682
-
(2004)
Science
, vol.304
, pp. 1678-1682
-
-
Zhu, Z.1
Zheng, T.2
Homer, R.J.3
Kim, Y.-K.4
Chen, N.Y.5
Cohn, L.6
Hamid, Q.7
Elias, J.A.8
-
23
-
-
77649268555
-
Repositioning of an existing drug for the neglected tropical disease onchocerciasis
-
Gloeckner, C.; Garner, A. L.; Mersha, F.; Oksov, Y.; Tricoche, N.; Eubanks, L. M.; Lustigman, S.; Kaufmann, G. F.; Janda, K. D. Repositioning of an existing drug for the neglected tropical disease onchocerciasis Proc. Natl. Acad. Sci. U.S.A. 2010, 107, 3424-3429
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 3424-3429
-
-
Gloeckner, C.1
Garner, A.L.2
Mersha, F.3
Oksov, Y.4
Tricoche, N.5
Eubanks, L.M.6
Lustigman, S.7
Kaufmann, G.F.8
Janda, K.D.9
-
24
-
-
84904365342
-
Dual protonophore-chitinase inhibitors dramatically affect O. Volvulus molting
-
Gooyit, M.; Tricoche, N.; Lustigman, S.; Janda, K. D. Dual protonophore-chitinase inhibitors dramatically affect O. volvulus molting J. Med. Chem. 2014, 57, 5792-5799
-
(2014)
J. Med. Chem.
, vol.57
, pp. 5792-5799
-
-
Gooyit, M.1
Tricoche, N.2
Lustigman, S.3
Janda, K.D.4
-
25
-
-
0000602126
-
Structure of allosamisin, a novel insect chitinase inhibitor, produced by Streptomyces sp
-
Sakuda, S.; Isogai, A.; Matsumoto, S.; Suzuki, A.; Koseki, K. Structure of allosamisin, a novel insect chitinase inhibitor, produced by Streptomyces sp Tetrahedron Lett. 1986, 27, 2475-2478
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 2475-2478
-
-
Sakuda, S.1
Isogai, A.2
Matsumoto, S.3
Suzuki, A.4
Koseki, K.5
-
26
-
-
0008763295
-
Studies on the chitinase inhibitors, allosamidins
-
Muzzarelli, R. A. A. Atec Edizioni: Grottammare, Italy, Vol
-
Sakuda, S. Studies on the chitinase inhibitors, allosamidins. In Chitin Enzymology; Muzzarelli, R. A. A., Ed.; Atec Edizioni: Grottammare, Italy, 1996; Vol. 2, pp 203-212.
-
(1996)
Chitin Enzymology
, vol.2
, pp. 203-212
-
-
Sakuda, S.1
-
27
-
-
0028936559
-
Styloguanidines, new chitinase inhibitors from the marine sponge Stylotella aurantium
-
Kato, T.; Shizuri, Y.; Izumida, H.; Yokoyama, A.; Endo, M. Styloguanidines, new chitinase inhibitors from the marine sponge Stylotella aurantium Tetrahedron Lett. 1995, 36, 2133-2136
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 2133-2136
-
-
Kato, T.1
Shizuri, Y.2
Izumida, H.3
Yokoyama, A.4
Endo, M.5
-
28
-
-
0030050683
-
A novel chitinase inhibitor from a marine bacterium, Pseudomonas sp
-
Izumida, H.; Imamura, N.; Sano, H. A novel chitinase inhibitor from a marine bacterium, Pseudomonas sp J. Antibiot. 1996, 76, 76-80
-
(1996)
J. Antibiot.
, vol.76
, pp. 76-80
-
-
Izumida, H.1
Imamura, N.2
Sano, H.3
-
29
-
-
0029793429
-
The effect of chitinase inhibitors, cyclo(Arg-Pro) against cell separation of Saccharomyces cerevisiae and the morphological change of Candida albicans
-
Takadera, T.; Nomoto, A.; Izumida, H.; Nishijima, M.; Sano, H. The effect of chitinase inhibitors, cyclo(Arg-Pro) against cell separation of Saccharomyces cerevisiae and the morphological change of Candida albicans J. Antibiot. 1996, 49, 829-831
-
(1996)
J. Antibiot.
, vol.49
, pp. 829-831
-
-
Takadera, T.1
Nomoto, A.2
Izumida, H.3
Nishijima, M.4
Sano, H.5
-
30
-
-
0037113166
-
The cyclic dipeptide CI-4 [cyclo-(L-Arg-D-Pro)] inhibits family 18 chitinases by structural mimicry of a reaction intermediate
-
Houston, D. R.; Eggleston, I.; Synstad, B.; Eijsink, V. G. H.; van Aalten, D. M. F. The cyclic dipeptide CI-4 [cyclo-(L-Arg-D-Pro)] inhibits family 18 chitinases by structural mimicry of a reaction intermediate Biochem. J. 2002, 368, 23-27
-
(2002)
Biochem. J.
, vol.368
, pp. 23-27
-
-
Houston, D.R.1
Eggleston, I.2
Synstad, B.3
Eijsink, V.G.H.4
Van Aalten, D.M.F.5
-
31
-
-
0000055673
-
Phenolic constituent of Psammaplysilla
-
Quinoa, E.; Crews, P. Phenolic constituent of Psammaplysilla Tetrahedron Lett. 1987, 28, 3229-3232
-
(1987)
Tetrahedron Lett.
, vol.28
, pp. 3229-3232
-
-
Quinoa, E.1
Crews, P.2
-
32
-
-
0023236004
-
Brominated tyrosine metabolites from an unidentified sponge
-
Arabshahi, L.; Schmitz, F. J. Brominated tyrosine metabolites from an unidentified sponge J. Org. Chem. 1987, 52, 3584-3586
-
(1987)
J. Org. Chem.
, vol.52
, pp. 3584-3586
-
-
Arabshahi, L.1
Schmitz, F.J.2
-
33
-
-
0033920903
-
Argifin, a new chitinase inhibitor, produced by Gliocladium sp. FTD-0668. I. Taxonomy, fermentation, and biological activities
-
Omura, S.; Arai, N.; Yamaguchi, Y.; Masuma, R.; Iwai, Y.; Namikoshi, M.; Turberg, A.; Kölbl, H.; Shiomi, K. Argifin, a new chitinase inhibitor, produced by Gliocladium sp. FTD-0668. I. Taxonomy, fermentation, and biological activities J. Antibiot. 2000, 53, 603-608
-
(2000)
J. Antibiot.
, vol.53
, pp. 603-608
-
-
Omura, S.1
Arai, N.2
Yamaguchi, Y.3
Masuma, R.4
Iwai, Y.5
Namikoshi, M.6
Turberg, A.7
Kölbl, H.8
Shiomi, K.9
-
34
-
-
0033923739
-
Argifin, a new chitinase inhibitor, produced by Gliocladium sp. FTD-0668. II. Isolation, physico-chemical properties, and structure elucidation
-
Arai, N.; Shiomi, K.; Iwai, Y.; Omura, S. Argifin, a new chitinase inhibitor, produced by Gliocladium sp. FTD-0668. II. Isolation, physico-chemical properties, and structure elucidation J. Antibiot. 2000, 53, 609-614
-
(2000)
J. Antibiot.
, vol.53
, pp. 609-614
-
-
Arai, N.1
Shiomi, K.2
Iwai, Y.3
Omura, S.4
-
35
-
-
0034719795
-
Structure of argifin, a new chitinase inhibitor produced by Gliocladium sp
-
Shiomi, K.; Arai, N.; Iwai, Y.; Turberg, A.; Kölbl, H.; Omura, S. Structure of argifin, a new chitinase inhibitor produced by Gliocladium sp Tetrahedron Lett. 2000, 41, 2141-2143
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 2141-2143
-
-
Shiomi, K.1
Arai, N.2
Iwai, Y.3
Turberg, A.4
Kölbl, H.5
Omura, S.6
-
36
-
-
0033788236
-
Argadin, a new chitinase inhibitor, produced by Clonostachys sp. FO-7314
-
Arai, N.; Shiomi, K.; Yamaguchi, Y.; Masuma, R.; Iwai, Y.; Turberg, A.; Kölbl, H.; Omura, S. Argadin, a new chitinase inhibitor, produced by Clonostachys sp. FO-7314 Chem. Pharm. Bull. 2000, 48, 1442-1446
-
(2000)
Chem. Pharm. Bull.
, vol.48
, pp. 1442-1446
-
-
Arai, N.1
Shiomi, K.2
Yamaguchi, Y.3
Masuma, R.4
Iwai, Y.5
Turberg, A.6
Kölbl, H.7
Omura, S.8
-
37
-
-
67649986131
-
Chitinase inhibitors: Extraction of the active framework from natural argifin and use of in situ click chemistry
-
Hirose, T.; Sunazuka, T.; Sugawara, A.; Endo, A.; Iguchi, K.; Yamamoto, T.; Ui, H.; Shiomi, K.; Watanabe, T.; Sharpless, K. B.; Omura, S. Chitinase inhibitors: extraction of the active framework from natural argifin and use of in situ click chemistry J. Antibiot. 2009, 62, 277-282
-
(2009)
J. Antibiot.
, vol.62
, pp. 277-282
-
-
Hirose, T.1
Sunazuka, T.2
Sugawara, A.3
Endo, A.4
Iguchi, K.5
Yamamoto, T.6
Ui, H.7
Shiomi, K.8
Watanabe, T.9
Sharpless, K.B.10
Omura, S.11
-
38
-
-
0037047120
-
High-resolution structures of a chitinase complexed with natural product cyclopentapeptide inhibitors: Mimicry of carbohydrate substrate
-
Houston, D. R.; Shiomi, K.; Arai, N.; Omura, S.; Peter, M. G.; Turberg, A.; Synstad, B.; Eijsink, V. G. H.; van Aalten, D. M. F. High-resolution structures of a chitinase complexed with natural product cyclopentapeptide inhibitors: mimicry of carbohydrate substrate Proc. Natl. Acad. Sci. U.S.A. 2002, 99, 9127-9132
-
(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 9127-9132
-
-
Houston, D.R.1
Shiomi, K.2
Arai, N.3
Omura, S.4
Peter, M.G.5
Turberg, A.6
Synstad, B.7
Eijsink, V.G.H.8
Van Aalten, D.M.F.9
-
39
-
-
12344317078
-
Specificity and affinity of natural product cyclopentapeptide inhibitors against A. Fumigatus, human, and bacterial chitinases
-
Rao, F. V.; Houston, D. R.; Boot, R. G.; Aerts, J. M.; Hodkinson, M.; Adams, D. J.; Shiomi, K.; Omura, S.; van Aalten, D. M. F. Specificity and affinity of natural product cyclopentapeptide inhibitors against A. fumigatus, human, and bacterial chitinases Chem. Biol. 2005, 12, 65-76
-
(2005)
Chem. Biol.
, vol.12
, pp. 65-76
-
-
Rao, F.V.1
Houston, D.R.2
Boot, R.G.3
Aerts, J.M.4
Hodkinson, M.5
Adams, D.J.6
Shiomi, K.7
Omura, S.8
Van Aalten, D.M.F.9
-
40
-
-
40749152751
-
Structure-based dissection of the natural product cyclopentapeptide chitinase inhibitor argifin
-
Anderson, O. A.; Nathubhai, A.; Dixon, M. J.; Eggleston, I. M.; van Aalten, D. M. F. Structure-based dissection of the natural product cyclopentapeptide chitinase inhibitor argifin Chem. Biol. 2008, 15, 295-301
-
(2008)
Chem. Biol.
, vol.15
, pp. 295-301
-
-
Anderson, O.A.1
Nathubhai, A.2
Dixon, M.J.3
Eggleston, I.M.4
Van Aalten, D.M.F.5
-
41
-
-
25444507108
-
An efficient synthesis of argifin: A natural product chitinase inhibitor with chemotherapeutic potential
-
Dixon, M. J.; Anderson, O. A.; van Aalten, D. M. F.; Eggleston, I. M. An efficient synthesis of argifin: a natural product chitinase inhibitor with chemotherapeutic potential Bioorg. Med. Chem. Lett. 2005, 15, 4717-4721
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 4717-4721
-
-
Dixon, M.J.1
Anderson, O.A.2
Van Aalten, D.M.F.3
Eggleston, I.M.4
-
42
-
-
58049146174
-
Solid-phase synthesis of cyclic peptide chitinase inhibitors: SAR of the argifin scaffold
-
Dixon, M. J.; Nathubhai, A.; Anderson, O. A.; van Aalten, D. M. F.; Eggleston, I. M. Solid-phase synthesis of cyclic peptide chitinase inhibitors: SAR of the argifin scaffold Org. Biomol. Chem. 2009, 7, 259-268
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 259-268
-
-
Dixon, M.J.1
Nathubhai, A.2
Anderson, O.A.3
Van Aalten, D.M.F.4
Eggleston, I.M.5
-
43
-
-
41649117502
-
Computational analysis of the binding affinities of the natural-product cyclopentapeptides argifin and argadin to chitinase B from Serratia marcescens
-
Gouda, H.; Yanai, Y.; Sugawara, A.; Sunazuka, T.; Omura, S.; Hirono, S. Computational analysis of the binding affinities of the natural-product cyclopentapeptides argifin and argadin to chitinase B from Serratia marcescens Bioorg. Med. Chem. 2008, 16, 3565-3579
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 3565-3579
-
-
Gouda, H.1
Yanai, Y.2
Sugawara, A.3
Sunazuka, T.4
Omura, S.5
Hirono, S.6
-
44
-
-
65349194561
-
Computer-aided rational molecular design of argifin-derivatives with increased inhibitory activity against chitinase B from Serratia marcescens
-
Gouda, H.; Sunazuka, T.; Iguchi, K.; Sugawara, A.; Hirose, T.; Noguchi, Y.; Saito, Y.; Yanai, Y.; Yamamoto, T.; Watanabe, T.; Shiomi, K.; Omura, S.; Hirono, S. Computer-aided rational molecular design of argifin-derivatives with increased inhibitory activity against chitinase B from Serratia marcescens Bioorg. Med. Chem. Lett. 2009, 19, 2630-2633
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 2630-2633
-
-
Gouda, H.1
Sunazuka, T.2
Iguchi, K.3
Sugawara, A.4
Hirose, T.5
Noguchi, Y.6
Saito, Y.7
Yanai, Y.8
Yamamoto, T.9
Watanabe, T.10
Shiomi, K.11
Omura, S.12
Hirono, S.13
-
45
-
-
68649118594
-
Molecular modeling of human acidic mammalian chitinase in complex with the natural-product cyclopentapeptide chitinase inhibitor argifin
-
Gouda, H.; Terashima, S.; Iguchi, K.; Sugawara, A.; Saito, Y.; Yamamoto, T.; Hirose, T.; Shiomi, K.; Sunazuka, T.; Omura, S.; Hirono, S. Molecular modeling of human acidic mammalian chitinase in complex with the natural-product cyclopentapeptide chitinase inhibitor argifin Bioorg. Med. Chem. 2009, 17, 6270-6278
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 6270-6278
-
-
Gouda, H.1
Terashima, S.2
Iguchi, K.3
Sugawara, A.4
Saito, Y.5
Yamamoto, T.6
Hirose, T.7
Shiomi, K.8
Sunazuka, T.9
Omura, S.10
Hirono, S.11
-
46
-
-
62949225622
-
Argifin; Efficient solid phase total synthesis and evaluation of analogues of acyclic peptide
-
Sunazuka, T.; Sugawara, A.; Iguchi, K.; Hirose, T.; Nagai, K.; Noguchi, Y.; Saito, Y.; Yamamoto, T.; Ui, H.; Gouda, H.; Shiomi, K.; Watanabe, T.; Omura, S. Argifin; efficient solid phase total synthesis and evaluation of analogues of acyclic peptide Bioorg. Med. Chem. 2009, 17, 2751-2758
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 2751-2758
-
-
Sunazuka, T.1
Sugawara, A.2
Iguchi, K.3
Hirose, T.4
Nagai, K.5
Noguchi, Y.6
Saito, Y.7
Yamamoto, T.8
Ui, H.9
Gouda, H.10
Shiomi, K.11
Watanabe, T.12
Omura, S.13
-
47
-
-
77955467025
-
NMR spectroscopy and computational analysis of interaction between Serratia marcescens chitinase B and a dipeptide derived from natural-product cyclopentapeptide chitinase inhibitor argifin
-
Gouda, H.; Sunazuka, T.; Hirose, T.; Iguchi, K.; Yamaotsu, N.; Sugawara, A.; Noguchi, Y.; Saito, Y.; Yamamoto, T.; Watanabe, T.; Shiomi, K.; Omura, S.; Hirono, S. NMR spectroscopy and computational analysis of interaction between Serratia marcescens chitinase B and a dipeptide derived from natural-product cyclopentapeptide chitinase inhibitor argifin Bioorg. Med. Chem. 2010, 18, 5835-5844
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 5835-5844
-
-
Gouda, H.1
Sunazuka, T.2
Hirose, T.3
Iguchi, K.4
Yamaotsu, N.5
Sugawara, A.6
Noguchi, Y.7
Saito, Y.8
Yamamoto, T.9
Watanabe, T.10
Shiomi, K.11
Omura, S.12
Hirono, S.13
-
48
-
-
79960951713
-
Solution-phase total synthesis of the hydrophilic natural product argifin using 3,4,5-tris(octadecyloxy)benzyl tag
-
Hirose, T.; Kasai, T.; Akimoto, T.; Endo, A.; Sugawara, A.; Nagasawa, K.; Shiomi, K.; Omura, S.; Sunazuka, T. Solution-phase total synthesis of the hydrophilic natural product argifin using 3,4,5-tris(octadecyloxy)benzyl tag Tetrahedron 2011, 67, 6633-6643
-
(2011)
Tetrahedron
, vol.67
, pp. 6633-6643
-
-
Hirose, T.1
Kasai, T.2
Akimoto, T.3
Endo, A.4
Sugawara, A.5
Nagasawa, K.6
Shiomi, K.7
Omura, S.8
Sunazuka, T.9
-
49
-
-
84877816554
-
Human acidic mammalian chitinase as a novel target for anti-asthma drug design using in silico screening
-
Wakasugi, M.; Gouda, H.; Hirose, T.; Sugawara, A.; Yamamoto, T.; Shiomi, K.; Sunazuka, T.; Omura, S.; Hirono, S. Human acidic mammalian chitinase as a novel target for anti-asthma drug design using in silico screening Bioorg. Med. Chem. 2013, 21, 3214-3220
-
(2013)
Bioorg. Med. Chem.
, vol.21
, pp. 3214-3220
-
-
Wakasugi, M.1
Gouda, H.2
Hirose, T.3
Sugawara, A.4
Yamamoto, T.5
Shiomi, K.6
Sunazuka, T.7
Omura, S.8
Hirono, S.9
-
50
-
-
84885052005
-
Observation of the controlled assembly of preclick components in the in situ click chemistry generation of a chitinase inhibitor
-
Hirose, T.; Maita, N.; Gouda, H.; Koseki, J.; Yamamoto, T.; Sugawara, A.; Nakano, H.; Hirono, S.; Shiomi, K.; Watanabe, T.; Taniguchi, H.; Sharpless, K. B.; Omura, S.; Sunazuka, T. Observation of the controlled assembly of preclick components in the in situ click chemistry generation of a chitinase inhibitor Proc. Natl. Acad. Sci. U.S.A. 2013, 110, 15892-15897
-
(2013)
Proc. Natl. Acad. Sci. U.S.A.
, vol.110
, pp. 15892-15897
-
-
Hirose, T.1
Maita, N.2
Gouda, H.3
Koseki, J.4
Yamamoto, T.5
Sugawara, A.6
Nakano, H.7
Hirono, S.8
Shiomi, K.9
Watanabe, T.10
Taniguchi, H.11
Sharpless, K.B.12
Omura, S.13
Sunazuka, T.14
-
51
-
-
77951926872
-
Recent development of two chitinase inhibitors, argifin and argadin, produced by soil microorganisms
-
Hirose, T.; Sunazuka, T.; Omura, S. Recent development of two chitinase inhibitors, argifin and argadin, produced by soil microorganisms Proc. Jpn. Acad., Ser. B 2010, 86, 85-102
-
(2010)
Proc. Jpn. Acad., Ser. B
, vol.86
, pp. 85-102
-
-
Hirose, T.1
Sunazuka, T.2
Omura, S.3
-
52
-
-
33644974199
-
Three-dimensional solution structure of EM703 with potent promoting activity of monocyte-to-macrophage differentiation
-
Gouda, H.; Sunazuka, T.; Yoshida, K.; Sugawara, A.; Sakoh, Y.; Omura, S.; Hirono, S. Three-dimensional solution structure of EM703 with potent promoting activity of monocyte-to-macrophage differentiation Bioorg. Med. Chem. Lett. 2006, 16, 2496-2499
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 2496-2499
-
-
Gouda, H.1
Sunazuka, T.2
Yoshida, K.3
Sugawara, A.4
Sakoh, Y.5
Omura, S.6
Hirono, S.7
-
53
-
-
0026470597
-
Nonpeptidal peptidomimetics with β-D-glucose scaffolding. A partial somatostatin agonist bearing a close structural relationship to a potent, selective substance P antagonist
-
Hirschmann, R.; Nicolaou, K. C.; Pietranico, S.; Salvino, J.; Leahy, E. M.; Sprengeler, P. A.; Furst, G.; Smith, A. B., III; Strader, C. D.; Cascieri, M. A.; Candelore, M. R.; Donaldson, C.; Vale, W.; Maechler, L. Nonpeptidal peptidomimetics with β-D-glucose scaffolding. A partial somatostatin agonist bearing a close structural relationship to a potent, selective substance P antagonist J. Am. Chem. Soc. 1992, 114, 9217-9218
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 9217-9218
-
-
Hirschmann, R.1
Nicolaou, K.C.2
Pietranico, S.3
Salvino, J.4
Leahy, E.M.5
Sprengeler, P.A.6
Furst, G.7
Smith, A.B.8
Strader, C.D.9
Cascieri, M.A.10
Candelore, M.R.11
Donaldson, C.12
Vale, W.13
Maechler, L.14
-
54
-
-
0027857964
-
De novo design and synthesis of somatostatin non-peptide peptidomimetics utilizing and D-glucose as a novel scaffolding
-
Hirschmann, R.; Nicolaou, K. C.; Pietranico, S.; Leahy, E. M.; Salvino, J.; Arison, B.; Cichy, M. A.; Spoors, P. G.; Shakespeare, W. C.; Sprengeler, P. A.; Hamley, P.; Smith, A. B., III; Reisine, T.; Raynor, K.; Maechler, L.; Donaldson, C.; Vale, W.; Freidinger, R. M.; Cascieri, M. R.; Strader, C. D. De novo design and synthesis of somatostatin non-peptide peptidomimetics utilizing and D-glucose as a novel scaffolding J. Am. Chem. Soc. 1993, 115, 12550-12568
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 12550-12568
-
-
Hirschmann, R.1
Nicolaou, K.C.2
Pietranico, S.3
Leahy, E.M.4
Salvino, J.5
Arison, B.6
Cichy, M.A.7
Spoors, P.G.8
Shakespeare, W.C.9
Sprengeler, P.A.10
Hamley, P.11
Smith, A.B.12
Reisine, T.13
Raynor, K.14
Maechler, L.15
Donaldson, C.16
Vale, W.17
Freidinger, R.M.18
Cascieri, M.R.19
Strader, C.D.20
more..
-
55
-
-
10744224398
-
Nonpeptide luteinizing hormone-releasing hormone antagonists derived from erythromycin A: Design, synthesis, and biological activity of cladinose replacement analogues
-
Randolph, J. T.; Waid, P.; Nichols, C.; Sauer, D.; Haviv, F.; Diaz, G.; Bammert, G.; Besecke, L. M.; Segreti, J. A.; Mohning, K. M.; Bush, E. N.; Wegner, C. D.; Greer, J. Nonpeptide luteinizing hormone-releasing hormone antagonists derived from erythromycin A: design, synthesis, and biological activity of cladinose replacement analogues J. Med. Chem. 2004, 47, 1085-1097
-
(2004)
J. Med. Chem.
, vol.47
, pp. 1085-1097
-
-
Randolph, J.T.1
Waid, P.2
Nichols, C.3
Sauer, D.4
Haviv, F.5
Diaz, G.6
Bammert, G.7
Besecke, L.M.8
Segreti, J.A.9
Mohning, K.M.10
Bush, E.N.11
Wegner, C.D.12
Greer, J.13
-
56
-
-
60549102514
-
Non-peptide macrocyclic histone deacetylase inhibitors
-
Oyelere, A. K.; Chen, P. C.; Guerrant, W.; Mwakwari, S. C.; Hood, R.; Zhang, Y.; Fan, Y. Non-peptide macrocyclic histone deacetylase inhibitors J. Med. Chem. 2009, 52, 456-468
-
(2009)
J. Med. Chem.
, vol.52
, pp. 456-468
-
-
Oyelere, A.K.1
Chen, P.C.2
Guerrant, W.3
Mwakwari, S.C.4
Hood, R.5
Zhang, Y.6
Fan, Y.7
-
57
-
-
77955866855
-
Non-peptide macrocyclic histone deacetylase inhibitors derived from tricyclic ketolide skeleton
-
Mwakwari, S. C.; Guerrant, W.; Patil, V.; Khan, S. I.; Tekwani, B. L.; Gurard-Levin, Z. A.; Mrksich, M.; Oyelere, A. K. Non-peptide macrocyclic histone deacetylase inhibitors derived from tricyclic ketolide skeleton J. Med. Chem. 2010, 53, 6100-6111
-
(2010)
J. Med. Chem.
, vol.53
, pp. 6100-6111
-
-
Mwakwari, S.C.1
Guerrant, W.2
Patil, V.3
Khan, S.I.4
Tekwani, B.L.5
Gurard-Levin, Z.A.6
Mrksich, M.7
Oyelere, A.K.8
-
58
-
-
0016829297
-
A facile preparation of erythronolide A oxime
-
LeMahieu, R. A.; Carson, M.; Kierstead, R. W. A facile preparation of erythronolide A oxime J. Antibiot. 1975, 28, 704
-
(1975)
J. Antibiot.
, vol.28
, pp. 704
-
-
Lemahieu, R.A.1
Carson, M.2
Kierstead, R.W.3
-
59
-
-
0028936022
-
Application of highly stereocontrolled glycosidations employing 2,6-anhydro-2-thio sugars to the syntheses of erythromycin A and olivomycin A trisaccharide
-
Toshima, K.; Nozaki, Y.; Mukaiyama, S.; Tamai, T.; Nakata, M.; Tatsuta, K.; Kinoshita, M. Application of highly stereocontrolled glycosidations employing 2,6-anhydro-2-thio sugars to the syntheses of erythromycin A and olivomycin A trisaccharide J. Am. Chem. Soc. 1995, 117, 3717-3727
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 3717-3727
-
-
Toshima, K.1
Nozaki, Y.2
Mukaiyama, S.3
Tamai, T.4
Nakata, M.5
Tatsuta, K.6
Kinoshita, M.7
-
60
-
-
0000050333
-
High-throughput synthesis of Boc-substituted amidinoureas by liquid-phase approach
-
Sun, C.-M.; Shey, J.-Y. High-throughput synthesis of Boc-substituted amidinoureas by liquid-phase approach J. Comb. Chem. 1999, 1, 361-363
-
(1999)
J. Comb. Chem.
, vol.1
, pp. 361-363
-
-
Sun, C.-M.1
Shey, J.-Y.2
-
61
-
-
0037012920
-
Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides
-
Tornøe, 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
-
(2002)
J. Org. Chem.
, vol.67
, pp. 3057-3064
-
-
Tornøe, C.W.1
Christensen, C.2
Meldal, M.3
-
62
-
-
0037099395
-
A stepwise huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
-
Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "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
-
64
-
-
0035979240
-
Structural insights into the catalytic mechanism of a family 18 exo-chitinase
-
van Aalten, D. M. F.; Komander, D.; Synstad, B.; Gaseidnes, S.; Peter, M. G.; Eijsink, V. G. H. Structural insights into the catalytic mechanism of a family 18 exo-chitinase Proc. Natl. Acad. Sci. U.S.A. 2001, 98, 8979-8984
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 8979-8984
-
-
Van Aalten, D.M.F.1
Komander, D.2
Synstad, B.3
Gaseidnes, S.4
Peter, M.G.5
Eijsink, V.G.H.6
-
65
-
-
0029011701
-
A second generation force field for the simulation of proteins, nucleic acids, and organic molecules
-
Cornell, W. D.; Cieplak, P.; Bayly, C. I.; Gould, I. R.; Merz, K. M., Jr.; Ferguson, D. M.; Spellmeyer, D. C.; Fox, T.; Caldwell, J. W.; Kollman, P. A. A second generation force field for the simulation of proteins, nucleic acids, and organic molecules J. Am. Chem. Soc. 1995, 117, 5179-5197
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 5179-5197
-
-
Cornell, W.D.1
Cieplak, P.2
Bayly, C.I.3
Gould, I.R.4
Merz, K.M.5
Ferguson, D.M.6
Spellmeyer, D.C.7
Fox, T.8
Caldwell, J.W.9
Kollman, P.A.10
-
66
-
-
79953737180
-
Overview of the CCP4 suite and current developments
-
Winn, M. D.; Ballard, C. C.; Cowtan, K. D.; Dodson, E. J.; Emsley, P.; Evans, P. R.; Keegan, R. M.; Krissinel, E. B.; Leslie, A. G. W.; McCoy, A.; McNicholas, S. J.; Murshudov, G. N.; Pannu, N. S.; Potterton, E. A.; Powell, H. R.; Read, R. J.; Vagin, A.; Wilson, K. S. Overview of the CCP4 suite and current developments Acta Crystallogr., Sect. D: Biol. Crystallogr. 2011, 67, 235-242
-
(2011)
Acta Crystallogr., Sect. D: Biol. Crystallogr.
, vol.67
, pp. 235-242
-
-
Winn, M.D.1
Ballard, C.C.2
Cowtan, K.D.3
Dodson, E.J.4
Emsley, P.5
Evans, P.R.6
Keegan, R.M.7
Krissinel, E.B.8
Leslie, A.G.W.9
McCoy, A.10
McNicholas, S.J.11
Murshudov, G.N.12
Pannu, N.S.13
Potterton, E.A.14
Powell, H.R.15
Read, R.J.16
Vagin, A.17
Wilson, K.S.18
-
67
-
-
77949535720
-
Features and development of Coot
-
Emsley, P.; Lohkamp, B.; Scott, W. G.; Cowtan, K. Features and development of Coot Acta Crystallogr., Sect. D: Biol. Crystallogr. 2010, 66, 486-501
-
(2010)
Acta Crystallogr., Sect. D: Biol. Crystallogr.
, vol.66
, pp. 486-501
-
-
Emsley, P.1
Lohkamp, B.2
Scott, W.G.3
Cowtan, K.4
-
68
-
-
84860290638
-
JLigand: A graphical tool for the CCP4 template-restraint library
-
Lebedev, A. A.; Young, P.; Isupov, M. N.; Moroz, O. V.; Vagin, A. A.; Murshudov, G. N. JLigand: a graphical tool for the CCP4 template-restraint library Acta Crystallogr., Sect. D: Biol. Crystallogr. 2012, 68, 431-440
-
(2012)
Acta Crystallogr., Sect. D: Biol. Crystallogr.
, vol.68
, pp. 431-440
-
-
Lebedev, A.A.1
Young, P.2
Isupov, M.N.3
Moroz, O.V.4
Vagin, A.A.5
Murshudov, G.N.6
|