Corrigendum to: Validating Eaton's Hypothesis: Cubane as a Benzene Bioisostere (Angewandte Chemie International Edition, (2016), 55, 11, (3580-3585), 10.1002/anie.201510675);Validating Eaton's Hypothesis: Cubane as a Benzene Bioisostere

Angewandte Chemie - International Edition

Volumn 55, Issue 11, 2016, Pages 3580-3585

  Chalmers, Benjamin A ^a   Xing, Hui ^a   Houston, Sevan ^a   Clark, Charlotte ^a   Ghassabian, Sussan ^b   Kuo, Andy ^b   Cao, Benjamin ^d   Reitsma, Andrea ^c,d   Murray, Cody Ellen P ^e   Stok, Jeanette E ^a   Boyle, Glen M ^d   Pierce, Carly J ^d   Littler, Stuart W ^c   Winkler, David A ^c,g   Bernhardt, Paul V ^a   Pasay, Cielo ^d   De Voss, James J ^a   McCarthy, James ^d,g   Parsons, Peter G ^d   Walter, Gimme H ^f   Smith, Maree T ^b   Cooper, Helen M ^a   Nilsson, Susan K ^c,d   Tsanaktsidis, John ^c   Savage, G Paul ^c   Williams, Craig M ^a   more..

^a UNIVERSITY OF QUEENSLAND   (Australia)

^b Ctr for Drug Design and Development   (Australia)

^c CSIRO   (Australia)

^d MONASH UNIVERSITY   (Australia)

^e UNSW   (Australia)

^f QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE   (Australia)

^g Australian Centre for International and Tropical Health   (Australia)

Author keywords

agrochemicals; bioisosteres; cubane; pharmaceuticals; structure activity relationships; structure activity relationships

Indexed keywords

AGRICULTURAL CHEMICALS; BIOACTIVITY; DRUG PRODUCTS; MOLECULES; SCAFFOLDS;

AGROCHEMICALS; BIOACTIVE MOLECULES; BIOISOSTERES; CANDIDATE IDENTIFICATIONS; CUBANE; GLOBAL DEMAND; PLATONIC SOLIDS; STRUCTURE ACTIVITY RELATIONSHIPS;

BENZENE;

BENZENE;

AGED; ANIMAL; CHEMISTRY; HUMAN; MOUSE; NONOBESE DIABETIC MOUSE; SCID MOUSE; VALIDATION STUDY;

AGED; ANIMALS; BENZENE; HUMANS; MICE; MICE, INBRED NOD; MICE, SCID;

EID: 84969394786     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201711161     Document Type: Erratum

References (38)

1. M. Hay, D. W. Thomas, J. L. Craighead, C. Economides, J. Rosenthal, Nat. Biotechnol. 2014, 32, 40-51;
2. C. Lamberth, S. Jeanmart, T. Luksch, A. Plant, Science 2013, 341, 742-746.
3. W. Krämer, Modern crop protection compounds, 2nd revised and enlarged ed., Wiley-VCH, Weinheim, 2012;
4. L. Wanka, K. Iqbal, P. R. Schreiner, Chem. Rev. 2013, 113, 3516-3604;
5. T. P. Stockdale, C. M. Williams, Chem. Soc. Rev. 2015, 44, 7737-7763.
6. P. E. Eaton, T. W. Cole, Jr., J. Am. Chem. Soc. 1964, 86, 3157-3158.
7. P. E. Eaton, Angew. Chem. Int. Ed. Engl. 1992, 31, 1421-1436;
8. Angew. Chem. 1992, 104, 1447-1462.
9. T. Yildirim, P. M. Gehring, D. A. Neumann, P. E. Eaton, T. Emrick, Carbon 1998, 36, 809-815.
10. L. T. Eremenko, L. B. Romanova, M. E. Ivanova, D. A. Nesterenko, V. S. Malygina, A. B. Ermeev, G. V. Lagodzinskaya, V. P. Lodygina, Russ. Chem. Bull. 1998, 47, 1137-1140;
11. H. Gunosewoyo, J. L. Guo, M. R. Bennett, M. J. Coster, M. Kassiou, Bioorg. Med. Chem. Lett. 2008, 18, 3720-3723;
12. R. Pellicciari, G. Costantino, E. Giovagnoni, L. Mattoli, I. Brabet, J.-P. Pin, Bioorg. Med. Chem. Lett. 1998, 8, 1569-1574;
13. A. S. Sklyarova, V. N. Rodionov, C. G. Parsons, G. Quack, P. R. Schreiner, A. A. Fokin, Med. Chem. Res. 2013, 22, 360-366;
14. S. M. Wilkinson, H. Gunosewoyo, M. L. Barron, A. Boucher, M. McDonnell, P. Turner, D. E. Morrison, M. R. Bennett, I. S. McGregor, L. M. Rendina, M. Kassiou, ACS Chem. Neurosci. 2014, 5, 335-339.
15. N. A. Meanwell, J. Med. Chem. 2011, 54, 2529-2591.
16. V. M. Richon, Br. J. Cancer 2006, 95, S 2 -S 6.
17. S. Grant, C. Easley, P. Kirkpatrick, Nat. Rev. Drug Discov. 2007, 6, 21-22.
18. P. J. Middlemiss, A. J. Glasky, M. P. Rathbone, E. Werstuik, S. Hindley, J. Gysbers, Neurosci. Lett. 1995, 199, 131-134.
19. M. P. Rathbone, P. J. Middlemiss, C. E. Crocker, M. S. Glasky, B. H. J. Juurlink, J. J. Ramirez, R. Ciccarelli, P. Di Iorio, F. Caciagli, Expert Opin. Investig. Drugs 1999, 8, 1255-1262.
20. D. Borsook, R. Hargreaves, C. Bountra, F. Porreca, Sci. Transl. Med. 2014, 6, 249sr 3.
21. M. J. O'Neil, The Merck index: an encyclopedia of chemicals, drugs, and biologicals, Vol. 15, Royal Society of Chemistry, Cambridge, 2013.
22. B. J. Currie, J. S. McCarthy, New Engl. J. Med. 2010, 362, 717-725.
23. R. J. Hay, A. C. Steer, D. Engelman, S. Walton, Clin. Microbiol. Infec. 2012, 18, 313-323.
24. H. Merzendorfer, H. S. Kim, S. S. Chaudhari, M. Kumari, C. A. Specht, S. Butcher, S. J. Brown, J. R. Manak, R. W. Beeman, K. J. Kramer, S. Muthukrishnan, Insect Biochem. Mol. Biol. 2012, 42, 264-276.
25. C. A. Lipinski, F. Lombardo, B. W. Dominy, P. J. Feeney, Adv. Drug Deliv. Rev. 1997, 23, 3-25.
26. Y. Hu, I. Doudevski, D. Wood, M. Moscarello, C. Husted, C. Genain, J. A. Zasadzinski, J. Israelachvili, Proc. Natl. Acad. Sci. USA 2004, 101, 13466-13471.
27. J. Hodgson, Nat. Biotechnol. 2001, 19, 722-726.
28. P. R. Ortiz de Montellano, Chem. Rev. 2010, 110, 932-948.
29. W. Adcock, M. J. Brunger, I. E. McCarthy, M. T. Michalewicz, W. von Niessen, F. Wang, E. Weigold, D. A. Winkler, J. Am. Chem. Soc. 2000, 122, 3892-3900.
30. O. Sibbesen, Z. Zhang, P. R. Ortiz de Montellano, Arch. Biochem. Biophys. 1998, 353, 285-296.
31. M. Newcomb, R. Shen, S.-Y. Choi, P. H. Toy, P. F. Hollenberg, A. D. N. Vaz, M. J. Coon, J. Am. Chem. Soc. 2000, 122, 2677-2686.
32. V. K. Jenkins, R. R. Perry, A. E. Ahmed, K. Ives, Invest. New Drugs 1986, 4, 325-335.
33. K. F. Biegasiewicz, J. R. Griffiths, G. P. Savage, J. Tsanaktsidis, R. Priefer, Chem. Rev. 2015, 115, 6719-6745.
34. M. J. Falkiner, S. W. Littler, K. J. McRae, G. P. Savage, J. Tsanaktsidis, Org. Process Res. Dev. 2013, 17, 1503-1509.
35. J. Wlochal, R. D. M. Davies, J. Burton, Org. Lett. 2014, 16, 4094-4097;
36. S. Plunkett, K. J. Flanagan, B. Twamley, M. O. Senge, Organometallics 2015, 34, 1408-1414;
37. R. Gianatassio, S. Kawamura, C. L. Eprile, K. Foo, J. Ge, A. C. Burns, M. R. Collins, P. S. Baran, Angew. Chem. Int. Ed. 2014, 53, 9851-9855;
38. Angew. Chem. 2014, 126, 10009-100013.