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Steven W Elmore

Explore the profile of Steven W Elmore including associated specialties, affiliations and a list of published articles. Areas
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Articles 38
Citations 6077
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Recent Articles
21.
Ackler S, Xiao Y, Mitten M, Foster K, Oleksijew A, Refici M, et al.
Mol Cancer Ther . 2008 Oct; 7(10):3265-74. PMID: 18852130
ABT-263 is a potent, orally bioavailable inhibitor of the antiapoptotic Bcl-2 family members Bcl-2, Bcl-x(L), and Bcl-w, which is currently in phase I clinical trials. Previous work has shown that...
22.
Park C, Bruncko M, Adickes J, Bauch J, Ding H, Kunzer A, et al.
J Med Chem . 2008 Oct; 51(21):6902-15. PMID: 18841882
Overexpression of prosurvival proteins such as Bcl-2 and Bcl-X L has been correlated with tumorigenesis and resistance to chemotherapy, and thus, the development of antagonists of these proteins may provide...
23.
Shoemaker A, Mitten M, Adickes J, Ackler S, Refici M, Ferguson D, et al.
Clin Cancer Res . 2008 Jun; 14(11):3268-77. PMID: 18519752
Purpose: The purpose of this study was to characterize the activity of the Bcl-2 protein family inhibitor ABT-263 in a panel of small cell lung cancer (SCLC) xenograft models. Experimental...
24.
Tse C, Shoemaker A, Adickes J, Anderson M, Chen J, Jin S, et al.
Cancer Res . 2008 May; 68(9):3421-8. PMID: 18451170
Overexpression of the prosurvival Bcl-2 family members (Bcl-2, Bcl-xL, and Mcl-1) is commonly associated with tumor maintenance, progression, and chemoresistance. We previously reported the discovery of ABT-737, a potent, small-molecule...
25.
Huth J, Park C, Petros A, Kunzer A, Wendt M, Wang X, et al.
Chem Biol Drug Des . 2007 Jul; 70(1):1-12. PMID: 17630989
The molecular chaperone HSP90 has been shown to facilitate cancer cell survival by stabilizing key proteins responsible for a malignant phenotype. We report here the results of parallel fragment-based drug...
26.
Wendt M, Sun C, Kunzer A, Sauer D, Sarris K, Hoff E, et al.
Bioorg Med Chem Lett . 2007 Mar; 17(11):3122-9. PMID: 17391963
Survivin is one of the most tumor-specific genes in the human genome and is an attractive target for cancer therapy. However, small-molecule ligands for survivin have not yet been described....
27.
Bruncko M, Oost T, Belli B, Ding H, Joseph M, Kunzer A, et al.
J Med Chem . 2007 Jan; 50(4):641-62. PMID: 17256834
Overexpression of the antiapototic proteins Bcl-2 and Bcl-xL provides a common mechanism through which cancer cells gain a survival advantage and become resistant to conventional chemotherapy. Inhibition of these prosurvival...
28.
Park C, Oie T, Petros A, Zhang H, Nimmer P, Henry R, et al.
J Am Chem Soc . 2006 Dec; 128(50):16206-12. PMID: 17165773
One of the primary objectives in the design of protein inhibitors is to shape the three-dimensional structures of small molecules to be complementary to the binding site of a target...
29.
Shoemaker A, Oleksijew A, Bauch J, Belli B, Borre T, Bruncko M, et al.
Cancer Res . 2006 Sep; 66(17):8731-9. PMID: 16951189
Inhibition of the prosurvival members of the Bcl-2 family of proteins represents an attractive strategy for the treatment of cancer. We have previously reported the activity of ABT-737, a potent...
30.
Wendt M, Shen W, Kunzer A, McClellan W, Bruncko M, Oost T, et al.
J Med Chem . 2006 Feb; 49(3):1165-81. PMID: 16451081
Development of a rationally designed potentiator of cancer chemotherapy, via inhibition of Bcl-X(L) function, is described. Lead compounds generated by NMR screening and directed parallel synthesis displayed sub-microM binding but...