Tian F - Search Results

1

The synthesis of substituted bipiperidine amide compounds as CCR3 ligands: antagonists versus agonists.

Ting PC, Umland SP, Aslanian R, Cao J, Garlisi CG, Huang Y, Jakway J, Liu Z, Shah H, Tian F, Wan Y, Shih NY. Ting PC, et al. Among authors: tian f. Bioorg Med Chem Lett. 2005 Jun 15;15(12):3020-3. doi: 10.1016/j.bmcl.2005.04.054. Bioorg Med Chem Lett. 2005. PMID: 15908209

2

Identification of full, partial and inverse CC chemokine receptor 3 agonists using [35S]GTPgammaS binding.

Wan Y, Jakway JP, Qiu H, Shah H, Garlisi CG, Tian F, Ting P, Hesk D, Egan RW, Billah MM, Umland SP. Wan Y, et al. Among authors: tian f. Eur J Pharmacol. 2002 Dec 5;456(1-3):1-10. doi: 10.1016/s0014-2999(02)02621-3. Eur J Pharmacol. 2002. PMID: 12450563

3

The synthesis of substituted bipiperidine amide compounds as CCR3 antagonists.

Ting PC, Lee JF, Wu J, Umland SP, Aslanian R, Cao J, Dong Y, Garlisi CG, Gilbert EJ, Huang Y, Jakway J, Kelly J, Liu Z, McCombie S, Shah H, Tian F, Wan Y, Shih NY. Ting PC, et al. Among authors: tian f. Bioorg Med Chem Lett. 2005 Mar 1;15(5):1375-8. doi: 10.1016/j.bmcl.2005.01.016. Bioorg Med Chem Lett. 2005. PMID: 15713390

4

Receptor reserve analysis of the human CCR3 receptor in eosinophils and CCR3-transfected cells.

Umland SP, Wan Y, Shortall J, Shah H, Jakway J, Garlisi CG, Tian F, Egan RW, Billah MM. Umland SP, et al. Among authors: tian f. J Leukoc Biol. 2000 Mar;67(3):441-7. doi: 10.1002/jlb.67.3.441. J Leukoc Biol. 2000. PMID: 10733106

5

A three-step protocol for lead optimization: quick identification of key conformational features and functional groups in the SAR studies of non-ATP competitive MK2 (MAPKAPK2) inhibitors.

Huang X, Zhu X, Chen X, Zhou W, Xiao D, Degrado S, Aslanian R, Fossetta J, Lundell D, Tian F, Trivedi P, Palani A. Huang X, et al. Among authors: tian f. Bioorg Med Chem Lett. 2012 Jan 1;22(1):65-70. doi: 10.1016/j.bmcl.2011.11.074. Epub 2011 Nov 23. Bioorg Med Chem Lett. 2012. PMID: 22169260

6

Facile synthesis of tetracyclic azepine and oxazocine derivatives and their potential as MAPKAP-K2 (MK2) inhibitors.

Rao AU, Xiao D, Huang X, Zhou W, Fossetta J, Lundell D, Tian F, Trivedi P, Aslanian R, Palani A. Rao AU, et al. Among authors: tian f. Bioorg Med Chem Lett. 2012 Jan 15;22(2):1068-72. doi: 10.1016/j.bmcl.2011.11.113. Epub 2011 Dec 6. Bioorg Med Chem Lett. 2012. PMID: 22182499

7

Conformation constraint of anilides enabling the discovery of tricyclic lactams as potent MK2 non-ATP competitive inhibitors.

Xiao D, Palani A, Huang X, Sofolarides M, Zhou W, Chen X, Aslanian R, Guo Z, Fossetta J, Tian F, Trivedi P, Spacciapoli P, Whitehurst CE, Lundell D. Xiao D, et al. Among authors: tian f. Bioorg Med Chem Lett. 2013 Jun 1;23(11):3262-6. doi: 10.1016/j.bmcl.2013.03.109. Epub 2013 Apr 4. Bioorg Med Chem Lett. 2013. PMID: 23602398

8

Discovery of a novel series of potent MK2 non-ATP competitive inhibitors using 1,2-substituted azoles as cis-amide isosteres.

Xiao D, Zhu X, Sofolarides M, Degrado S, Shao N, Rao A, Chen X, Aslanian R, Fossetta J, Tian F, Trivedi P, Lundell D, Palani A. Xiao D, et al. Among authors: tian f. Bioorg Med Chem Lett. 2014 Aug 1;24(15):3609-13. doi: 10.1016/j.bmcl.2014.05.024. Epub 2014 May 16. Bioorg Med Chem Lett. 2014. PMID: 24913714

9

The assignment of chemokine-chemokine receptor pairs: TARC and MIP-1 beta are not ligands for human CC-chemokine receptor 8.

Garlisi CG, Xiao H, Tian F, Hedrick JA, Billah MM, Egan RW, Umland SP. Garlisi CG, et al. Among authors: tian f. Eur J Immunol. 1999 Oct;29(10):3210-5. doi: 10.1002/(SICI)1521-4141(199910)29:10<3210::AID-IMMU3210>3.0.CO;2-W. Eur J Immunol. 1999. PMID: 10540332 Free article.

10

Human ADAM33: protein maturation and localization.

Garlisi CG, Zou J, Devito KE, Tian F, Zhu FX, Liu J, Shah H, Wan Y, Motasim Billah M, Egan RW, Umland SP. Garlisi CG, et al. Among authors: tian f. Biochem Biophys Res Commun. 2003 Jan 31;301(1):35-43. doi: 10.1016/s0006-291x(02)02976-5. Biochem Biophys Res Commun. 2003. PMID: 12535637

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