Zhu YF - Search Results

1

Synthesis and structure-activity relationships of 1-arylmethyl-5-aryl-6-methyluracils as potent gonadotropin-releasing hormone receptor antagonists.

Guo Z, Zhu YF, Gross TD, Tucci FC, Gao Y, Moorjani M, Connors PJ Jr, Rowbottom MW, Chen Y, Struthers RS, Xie Q, Saunders J, Reinhart G, Chen TK, Bonneville AL, Chen C. Guo Z, et al. Among authors: zhu yf. J Med Chem. 2004 Feb 26;47(5):1259-71. doi: 10.1021/jm030472z. J Med Chem. 2004. PMID: 14971906

2

An improved synthesis of selectively protected L-dopa derivatives from L-tyrosine.

Chen C, Zhu YF, Wilcoxen K. Chen C, et al. Among authors: zhu yf. J Org Chem. 2000 Apr 21;65(8):2574-6. doi: 10.1021/jo9913661. J Org Chem. 2000. PMID: 10789475 No abstract available.

3

Progress towards the development of non-peptide orally-active gonadotropin-releasing hormone (GnRH) antagonists: therapeutic implications.

Millar RP, Zhu YF, Chen C, Struthers RS. Millar RP, et al. Among authors: zhu yf. Br Med Bull. 2000;56(3):761-72. doi: 10.1258/0007142001903346. Br Med Bull. 2000. PMID: 11255560 Review.

4

Identification of a nonpeptide ligand that releases bioactive insulin-like growth factor-I from its binding protein complex.

Liu XJ, Xie Q, Zhu YF, Chen C, Ling N. Liu XJ, et al. Among authors: zhu yf. J Biol Chem. 2001 Aug 31;276(35):32419-22. doi: 10.1074/jbc.C100299200. Epub 2001 Jul 9. J Biol Chem. 2001. PMID: 11445558 Free article.

5

Coupling of 2-Substituted 1-Fluorovinylstannanes with Organic Halides Catalyzed by Palladium(0)/Copper(I) Iodide. A Mild and Stereospecific Method to Monofluoroolefins.

Chen C, Wilcoxen K, Zhu YF, Kim Ki KI, McCarthy JR. Chen C, et al. Among authors: zhu yf. J Org Chem. 1999 May 14;64(10):3476-3482. doi: 10.1021/jo982200n. J Org Chem. 1999. PMID: 11674468

6

Discovery of a series of nonpeptide small molecules that inhibit the binding of insulin-like growth factor (IGF) to IGF-binding proteins.

Chen C, Zhu YF, Liu XJ, Lu ZX, Xie Q, Ling N. Chen C, et al. Among authors: zhu yf. J Med Chem. 2001 Nov 8;44(23):4001-10. doi: 10.1021/jm010304b. J Med Chem. 2001. PMID: 11689087

7

Initial structure-activity relationship studies of a novel series of pyrrolo[1,2-a]pyrimid-7-ones as GnRH receptor antagonists.

Zhu YF, Struthers RS, Connors PJ Jr, Gao Y, Gross TD, Saunders J, Wilcoxen K, Reinhart GJ, Ling N, Chen C. Zhu YF, et al. Bioorg Med Chem Lett. 2002 Feb 11;12(3):399-402. doi: 10.1016/s0960-894x(01)00779-x. Bioorg Med Chem Lett. 2002. PMID: 11814806

8

A novel synthesis of 2-arylpyrrolo[1,2-a]pyrimid-7-ones and their structure-activity relationships as potent GnRH receptor antagonists.

Zhu YF, Wilcoxen K, Saunders J, Guo Z, Gao Y, Connors PJ Jr, Gross TD, Tucci FC, Struthers RS, Reinhart GJ, Xie Q, Chen C. Zhu YF, et al. Bioorg Med Chem Lett. 2002 Feb 11;12(3):403-6. doi: 10.1016/s0960-894x(01)00780-6. Bioorg Med Chem Lett. 2002. PMID: 11814807

9

Synthesis and initial structure-activity relationships of a novel series of imidazolo[1,2-a]pyrimid-5-ones as potent GnRH receptor antagonists.

Wilcoxen KM, Zhu YF, Connors PJ, Saunders J, Gross TD, Gao Y, Reinhart GJ, Struthers RS, Chen C. Wilcoxen KM, et al. Among authors: zhu yf. Bioorg Med Chem Lett. 2002 Aug 19;12(16):2179-83. doi: 10.1016/s0960-894x(02)00370-0. Bioorg Med Chem Lett. 2002. PMID: 12127532

10

Design, synthesis and structure-activity relationships of novel imidazolo[1,2-a]pyrimid-5-ones as potent GnRH receptor antagonists.

Gross TD, Zhu YF, Saunders J, Wilcoxen KM, Gao Y, Connors PJ Jr, Guo Z, Struthers RS, Reinhart GJ, Chen C. Gross TD, et al. Among authors: zhu yf. Bioorg Med Chem Lett. 2002 Aug 19;12(16):2185-7. doi: 10.1016/s0960-894x(02)00371-2. Bioorg Med Chem Lett. 2002. PMID: 12127533

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