Huang S - Search Results

1

Novel 3',6'-anhydro and N12,N13-bridged glycosylated fluoroindolo[2,3-a]carbazoles as topoisomerase I inhibitors. Fluorine as a leaving group from sp3 carbon.

Saulnier MG, Langley DR, Frennesson DB, Long BH, Huang S, Gao Q, Wu D, Fairchild CR, Ruediger E, Zimmermann K, St Laurent DR, Balasubramanian BN, Vyas DM. Saulnier MG, et al. Among authors: huang s. Org Lett. 2005 Mar 31;7(7):1271-4. doi: 10.1021/ol050013n. Org Lett. 2005. PMID: 15787484

2

Eupenifeldin, a novel cytotoxic bistropolone from Eupenicillium brefeldianum.

Mayerl F, Gao Q, Huang S, Klohr SE, Matson JA, Gustavson DR, Pirnik DM, Berry RL, Fairchild C, Rose WC. Mayerl F, et al. Among authors: huang s. J Antibiot (Tokyo). 1993 Jul;46(7):1082-8. doi: 10.7164/antibiotics.46.1082. J Antibiot (Tokyo). 1993. PMID: 8360103 Free article.

3

Synthesis of a novel C-10 spiro-epoxide of paclitaxel.

Walker MA, Johnson TD, Huang S, Vyas DM, Kadow JF. Walker MA, et al. Among authors: huang s. Bioorg Med Chem Lett. 2001 Jul 9;11(13):1683-5. doi: 10.1016/s0960-894x(01)00280-3. Bioorg Med Chem Lett. 2001. PMID: 11425537

4

An approach to the identification of potent inhibitors of influenza virus fusion using parallel synthesis methodology.

Deshpande MS, Wei J, Luo G, Cianci C, Danetz S, Torri A, Tiley L, Krystal M, Yu KL, Huang S, Gao Q, Meanwell NA. Deshpande MS, et al. Among authors: huang s. Bioorg Med Chem Lett. 2001 Sep 3;11(17):2393-6. doi: 10.1016/s0960-894x(01)00459-0. Bioorg Med Chem Lett. 2001. PMID: 11527739

5

Synthesis and structure-activity relationships of 3-aryloxindoles: a new class of calcium-dependent, large conductance potassium (maxi-K) channel openers with neuroprotective properties.

Hewawasam P, Erway M, Moon SL, Knipe J, Weiner H, Boissard CG, Post-Munson DJ, Gao Q, Huang S, Gribkoff VK, Meanwell NA. Hewawasam P, et al. Among authors: huang s. J Med Chem. 2002 Mar 28;45(7):1487-99. doi: 10.1021/jm0101850. J Med Chem. 2002. PMID: 11906290

6

Sordarin oxazepine derivatives as potent antifungal agents.

Serrano-Wu MH, St Laurent DR, Chen Y, Huang S, Lam KR, Matson JA, Mazzucco CE, Stickle TM, Tully TP, Wong HS, Vyas DM, Balasubramanian BN. Serrano-Wu MH, et al. Among authors: huang s. Bioorg Med Chem Lett. 2002 Oct 7;12(19):2757-60. doi: 10.1016/s0960-894x(02)00529-2. Bioorg Med Chem Lett. 2002. PMID: 12217370

7

Core-modified sordaricin derivatives: synthesis and antifungal activity.

Regueiro-Ren A, Carroll TM, Chen Y, Matson JA, Huang S, Mazzucco CE, Stickle TM, Vyas DM, Balasubramanian BN. Regueiro-Ren A, et al. Among authors: huang s. Bioorg Med Chem Lett. 2002 Dec 2;12(23):3403-5. doi: 10.1016/s0960-894x(02)00764-3. Bioorg Med Chem Lett. 2002. PMID: 12419371

8

Stephacidin A and B: two structurally novel, selective inhibitors of the testosterone-dependent prostate LNCaP cells.

Qian-Cutrone J, Huang S, Shu YZ, Vyas D, Fairchild C, Menendez A, Krampitz K, Dalterio R, Klohr SE, Gao Q. Qian-Cutrone J, et al. Among authors: huang s. J Am Chem Soc. 2002 Dec 11;124(49):14556-7. doi: 10.1021/ja028538n. J Am Chem Soc. 2002. PMID: 12465964

9

Phosphonooxymethyl prodrugs of the broad spectrum antifungal azole, ravuconazole: synthesis and biological properties.

Ueda Y, Matiskella JD, Golik J, Connolly TP, Hudyma TW, Venkatesh S, Dali M, Kang SH, Barbour N, Tejwani R, Varia S, Knipe J, Zheng M, Mathew M, Mosure K, Clark J, Lamb L, Medin I, Gao Q, Huang S, Chen CP, Bronson JJ. Ueda Y, et al. Among authors: huang s. Bioorg Med Chem Lett. 2003 Nov 3;13(21):3669-72. doi: 10.1016/j.bmcl.2003.08.029. Bioorg Med Chem Lett. 2003. PMID: 14552754

10

Cytotoxic xanthones from Psorospermum molluscum from the Madagascar rain forest.

Leet JE, Liu X, Drexler DM, Cantone JL, Huang S, Mamber SW, Fairchild CR, Hussain R, Newman DJ, Kingston DG. Leet JE, et al. Among authors: huang s. J Nat Prod. 2008 Mar;71(3):460-3. doi: 10.1021/np070523l. Epub 2008 Feb 5. J Nat Prod. 2008. PMID: 18247570 Free PMC article.

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