Zhu J - Search Results

1

Discovering potent small molecule inhibitors of cyclophilin A using de novo drug design approach.

Ni S, Yuan Y, Huang J, Mao X, Lv M, Zhu J, Shen X, Pei J, Lai L, Jiang H, Li J. Ni S, et al. Among authors: zhu j. J Med Chem. 2009 Sep 10;52(17):5295-8. doi: 10.1021/jm9008295. J Med Chem. 2009. PMID: 19691347

2

Discovery of a novel CCR5 antagonist lead compound through fragment assembly.

Liu Y, Zhou E, Yu K, Zhu J, Zhang Y, Xie X, Li J, Jiang H. Liu Y, et al. Among authors: zhu j. Molecules. 2008 Oct 1;13(10):2426-41. doi: 10.3390/molecules13102426. Molecules. 2008. PMID: 18830165 Free PMC article.

3

2-amido-3-(1H-indol-3-yl)-N-substituted-propanamides as a new class of falcipain-2 inhibitors. 1. Design, synthesis, biological evaluation and binding model studies.

Zhu J, Chen T, Chen L, Lu W, Che P, Huang J, Li H, Li J, Jiang H. Zhu J, et al. Molecules. 2009 Jan 21;14(1):494-508. doi: 10.3390/molecules14010494. Molecules. 2009. PMID: 19158658 Free PMC article.

4

2-(3,4-dihydro-4-oxothieno[2,3-d]pyrimidin-2-ylthio) acetamides as a new class of falcipain-2 inhibitors. 3. design, synthesis and biological evaluation.

Zhu J, Chen T, Liu J, Ma R, Lu W, Huang J, Li H, Li J, Jiang H. Zhu J, et al. Molecules. 2009 Feb 16;14(2):785-97. doi: 10.3390/molecules14020785. Molecules. 2009. PMID: 19223827 Free PMC article.

5

Identification of novel falcipain-2 inhibitors as potential antimalarial agents through structure-based virtual screening.

Li H, Huang J, Chen L, Liu X, Chen T, Zhu J, Lu W, Shen X, Li J, Hilgenfeld R, Jiang H. Li H, et al. Among authors: zhu j. J Med Chem. 2009 Aug 13;52(15):4936-40. doi: 10.1021/jm801622x. J Med Chem. 2009. PMID: 19586036

6

Direct oxidation of beta-aryl substituted aldehydes to alpha,beta-unsaturated aldehydes promoted by an o-anisidine-Pd(OAc)2 co-catalyst.

Liu J, Zhu J, Jiang H, Wang W, Li J. Liu J, et al. Among authors: zhu j. Chem Asian J. 2009 Nov 2;4(11):1712-6. doi: 10.1002/asia.200900238. Chem Asian J. 2009. PMID: 19746509

7

Pd-catalyzed cascade Heck-Saegusa: direct synthesis of enals from aryl iodides and allyl alcohol.

Liu J, Zhu J, Jiang H, Wang W, Li J. Liu J, et al. Among authors: zhu j. Chem Commun (Camb). 2010 Jan 21;46(3):415-7. doi: 10.1039/b922351g. Epub 2009 Dec 1. Chem Commun (Camb). 2010. PMID: 20066310

8

Microwave-assisted one-pot synthesis of pyrazolone derivatives under solvent-free conditions.

Ma R, Zhu J, Liu J, Chen L, Shen X, Jiang H, Li J. Ma R, et al. Among authors: zhu j. Molecules. 2010 May 17;15(5):3593-601. doi: 10.3390/molecules15053593. Molecules. 2010. PMID: 20657501 Free PMC article.

9

HL005--a new selective PPARγ antagonist specifically inhibits the proliferation of MCF-7.

Lu W, Che P, Zhang Y, Li H, Zou S, Zhu J, Deng J, Shen X, Jiang H, Li J, Huang J. Lu W, et al. Among authors: zhu j. J Steroid Biochem Mol Biol. 2011 Apr;124(3-5):112-20. doi: 10.1016/j.jsbmb.2011.01.019. Epub 2011 Feb 4. J Steroid Biochem Mol Biol. 2011. PMID: 21296151

10

Organocatalytic enantioselective β-functionalization of aldehydes by oxidation of enamines and their application in cascade reactions.

Zhang SL, Xie HX, Zhu J, Li H, Zhang XS, Li J, Wang W. Zhang SL, et al. Among authors: zhu j. Nat Commun. 2011;2:211. doi: 10.1038/ncomms1214. Nat Commun. 2011. PMID: 21364550 Free article.

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