Zink DL - Search Results

1

Chemistry and Biology of Cylindrols: Novel Inhibitors of Ras Farnesyl-Protein Transferase from Cylindrocarpon lucidum.

Singh SB, Ball RG, Bills GF, Cascales C, Gibbs JB, Goetz MA, Hoogsteen K, Jenkins RG, Liesch JM, Lingham RB, Silverman KC, Zink DL. Singh SB, et al. Among authors: zink dl. J Org Chem. 1996 Nov 1;61(22):7727-7737. doi: 10.1021/jo961074p. J Org Chem. 1996. PMID: 11667727

2

Fusidienol A: A Novel Ras Farnesyl-Protein Transferase Inhibitor from Phoma sp.

Singh SB, Ball RG, Zink DL, Monaghan RL, Polishook JD, Sanchez M, Pelaez F, Silverman KC, Lingham RB. Singh SB, et al. Among authors: zink dl. J Org Chem. 1997 Oct 17;62(21):7485-7488. doi: 10.1021/jo9708304. J Org Chem. 1997. PMID: 11671871 No abstract available.

3

Structure and chemistry of apicidins, a class of novel cyclic tetrapeptides without a terminal alpha-keto epoxide as inhibitors of histone deacetylase with potent antiprotozoal activities.

Singh SB, Zink DL, Liesch JM, Mosley RT, Dombrowski AW, Bills GF, Darkin-Rattray SJ, Schmatz DM, Goetz MA. Singh SB, et al. Among authors: zink dl. J Org Chem. 2002 Feb 8;67(3):815-25. doi: 10.1021/jo016088w. J Org Chem. 2002. PMID: 11856024

4

Kampanols: novel Ras farnesyl-protein transferase inhibitors from Stachybotrys kampalensis.

Singh SB, Zink DL, Williams M, Polishook JD, Sanchez M, Silverman KC, Lingham RB. Singh SB, et al. Among authors: zink dl. Bioorg Med Chem Lett. 1998 Aug 18;8(16):2071-6. doi: 10.1016/s0960-894x(98)00371-0. Bioorg Med Chem Lett. 1998. PMID: 9873488

5

Structure, stereochemistry, and biological activity of integramycin, a novel hexacyclic natural product produced by Actinoplanes sp. that inhibits HIV-1 integrase.

Singh SB, Zink DL, Heimbach B, Genilloud O, Teran A, Silverman KC, Lingham RB, Felock P, Hazuda DJ. Singh SB, et al. Among authors: zink dl. Org Lett. 2002 Apr 4;4(7):1123-6. doi: 10.1021/ol025539b. Org Lett. 2002. PMID: 11922798

6

Integramides A and B, two novel non-ribosomal linear peptides containing nine C(alpha)-methyl amino acids produced by fungal fermentations that are inhibitors of HIV-1 integrase.

Singh SB, Herath K, Guan Z, Zink DL, Dombrowski AW, Polishook JD, Silverman KC, Lingham RB, Felock PJ, Hazuda DJ. Singh SB, et al. Among authors: zink dl. Org Lett. 2002 May 2;4(9):1431-4. doi: 10.1021/ol025540a. Org Lett. 2002. PMID: 11975596

7

Four novel bis-(naphtho-gamma-pyrones) isolated from Fusarium species as inhibitors of HIV-1 integrase.

Singh SB, Zink DL, Bills GF, Teran A, Silverman KC, Lingham RB, Felock P, Hazuda DJ. Singh SB, et al. Among authors: zink dl. Bioorg Med Chem Lett. 2003 Feb 24;13(4):713-7. doi: 10.1016/s0960-894x(02)01057-0. Bioorg Med Chem Lett. 2003. PMID: 12639565

8

Identification of diverse microbial metabolites as potent inhibitors of HIV-1 Tat transactivation.

Jayasuriya H, Zink DL, Polishook JD, Bills GF, Dombrowski AW, Genilloud O, Pelaez FF, Herranz L, Quamina D, Lingham RB, Danzeizen R, Graham PL, Tomassini JE, Singh SB. Jayasuriya H, et al. Among authors: zink dl. Chem Biodivers. 2005 Jan;2(1):112-22. doi: 10.1002/cbdv.200490162. Chem Biodivers. 2005. PMID: 17191924

9

Barceloneic acid A, a new farnesyl-protein transferase inhibitor from a Phoma species.

Jayasuriya H, Ball RG, Zink DL, Smith JL, Goetz MA, Jenkins RG, Nallin-Omstead M, Silverman KC, Bills GF, Lingham RB, et al. Jayasuriya H, et al. Among authors: zink dl. J Nat Prod. 1995 Jul;58(7):986-91. doi: 10.1021/np50121a002. J Nat Prod. 1995. PMID: 7561907

10

Zaragozic acids D and D2: potent inhibitors of squalene synthase and of Ras farnesyl-protein transferase.

Dufresne C, Wilson KE, Singh SB, Zink DL, Bergstrom JD, Rew D, Polishook JD, Meinz M, Huang L, Silverman KC, et al. Dufresne C, et al. Among authors: zink dl. J Nat Prod. 1993 Nov;56(11):1923-9. doi: 10.1021/np50101a009. J Nat Prod. 1993. PMID: 8289063

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