Similar articles for PMID: 18571929

Year	Number of Results
2002	1
2003	2
2004	2
2005	3
2006	8
2007	5
2008	8
2009	5
2010	3
2011	7
2012	8
2013	8
2014	7
2015	3
2016	7
2017	11
2018	5
2019	7
2020	7
2021	7
2022	3
2023	1
2024	0

1

Discovery of aminoquinolines as a new class of potent inhibitors of heat shock protein 90 (Hsp90): Synthesis, biology, and molecular modeling.

Ganesh T, Min J, Thepchatri P, Du Y, Li L, Lewis I, Wilson L, Fu H, Chiosis G, Dingledine R, Liotta D, Snyder JP, Sun A. Ganesh T, et al. Bioorg Med Chem. 2008 Jul 15;16(14):6903-10. doi: 10.1016/j.bmc.2008.05.047. Epub 2008 May 27. Bioorg Med Chem. 2008. PMID: 18571929 Free PMC article.

2

Identification and optimization of novel 6-acylamino-2-aminoquinolines as potent Hsp90 C-terminal inhibitors.

Jiang F, Guo AP, Xu JC, Wang HJ, Mo XF, You QD, Xu XL. Jiang F, et al. Eur J Med Chem. 2017 Dec 1;141:1-14. doi: 10.1016/j.ejmech.2017.07.080. Epub 2017 Aug 2. Eur J Med Chem. 2017. PMID: 29028527

3

Fragment-based hit discovery and structure-based optimization of aminotriazoloquinazolines as novel Hsp90 inhibitors.

Casale E, Amboldi N, Brasca MG, Caronni D, Colombo N, Dalvit C, Felder ER, Fogliatto G, Galvani A, Isacchi A, Polucci P, Riceputi L, Sola F, Visco C, Zuccotto F, Casuscelli F. Casale E, et al. Bioorg Med Chem. 2014 Aug 1;22(15):4135-50. doi: 10.1016/j.bmc.2014.05.056. Epub 2014 Jun 14. Bioorg Med Chem. 2014. PMID: 24980703

4

Drug Design, Synthesis and In Vitro Evaluation of Substituted Benzofurans as Hsp90 Inhibitors.

Kadasi S, Costa TEMM, Arukala N, Toshakani M, Duggineti C, Thota S, Dutta Gupta S, Raj S, Penido C, Henriques MG, Raghavendra NM. Kadasi S, et al. Med Chem. 2018;14(1):44-52. doi: 10.2174/1573406413666170623085534. Med Chem. 2018. PMID: 28641528

5

Hsp90 inhibitors and drugs from fragment and virtual screening.

Roughley S, Wright L, Brough P, Massey A, Hubbard RE. Roughley S, et al. Top Curr Chem. 2012;317:61-82. doi: 10.1007/128_2011_181. Top Curr Chem. 2012. PMID: 21647838 Review.

6

Tricyclic series of heat shock protein 90 (Hsp90) inhibitors part I: discovery of tricyclic imidazo[4,5-c]pyridines as potent inhibitors of the Hsp90 molecular chaperone.

Vallée F, Carrez C, Pilorge F, Dupuy A, Parent A, Bertin L, Thompson F, Ferrari P, Fassy F, Lamberton A, Thomas A, Arrebola R, Guerif S, Rohaut A, Certal V, Ruxer JM, Gouyon T, Delorme C, Jouanen A, Dumas J, Grépin C, Combeau C, Goulaouic H, Dereu N, Mikol V, Mailliet P, Minoux H. Vallée F, et al. J Med Chem. 2011 Oct 27;54(20):7206-19. doi: 10.1021/jm200784m. Epub 2011 Oct 5. J Med Chem. 2011. PMID: 21972823

7

Identification and optimization of novel Hsp90 inhibitors with tetrahydropyrido[4,3-d]pyrimidines core through shape-based screening.

Sun HP, Jia JM, Jiang F, Xu XL, Liu F, Guo XK, Cherfaoui B, Huang HZ, Pan Y, You QD. Sun HP, et al. Eur J Med Chem. 2014 May 22;79:399-412. doi: 10.1016/j.ejmech.2014.03.061. Epub 2014 Mar 21. Eur J Med Chem. 2014. PMID: 24763261

8

Evaluation of 8-arylsulfanyl, 8-arylsulfoxyl, and 8-arylsulfonyl adenine derivatives as inhibitors of the heat shock protein 90.

Llauger L, He H, Kim J, Aguirre J, Rosen N, Peters U, Davies P, Chiosis G. Llauger L, et al. J Med Chem. 2005 Apr 21;48(8):2892-905. doi: 10.1021/jm049012b. J Med Chem. 2005. PMID: 15828828

9

Hsp90 molecular chaperone inhibitors: are we there yet?

Neckers L, Workman P. Neckers L, et al. Clin Cancer Res. 2012 Jan 1;18(1):64-76. doi: 10.1158/1078-0432.CCR-11-1000. Clin Cancer Res. 2012. PMID: 22215907 Free PMC article. Review.

10

Rationally designed high-affinity 2-amino-6-halopurine heat shock protein 90 inhibitors that exhibit potent antitumor activity.

Kasibhatla SR, Hong K, Biamonte MA, Busch DJ, Karjian PL, Sensintaffar JL, Kamal A, Lough RE, Brekken J, Lundgren K, Grecko R, Timony GA, Ran Y, Mansfield R, Fritz LC, Ulm E, Burrows FJ, Boehm MF. Kasibhatla SR, et al. J Med Chem. 2007 Jun 14;50(12):2767-78. doi: 10.1021/jm050752+. Epub 2007 May 8. J Med Chem. 2007. PMID: 17488003

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