Year |
Citation |
Score |
2009 |
Brahimi F, Malakhov A, Lee HB, Pattarawarapan M, Ivanisevic L, Burgess K, Saragovi HU. A peptidomimetic of NT-3 acts as a TrkC antagonist. Peptides. 30: 1833-9. PMID 19647025 DOI: 10.1016/J.Peptides.2009.07.015 |
0.539 |
|
2005 |
Zaccaro MC, Lee HB, Pattarawarapan M, Xia Z, Caron A, L'Heureux PJ, Bengio Y, Burgess K, Saragovi HU. Selective small molecule peptidomimetic ligands of TrkC and TrkA receptors afford discrete or complete neurotrophic activities. Chemistry & Biology. 12: 1015-28. PMID 16183026 DOI: 10.1016/J.Chembiol.2005.06.015 |
0.598 |
|
2004 |
Lee HB, Zaccaro MC, Pattarawarapan M, Roy S, Saragovi HU, Burgess K. Syntheses and activities of new C10 beta-turn peptidomimetics. The Journal of Organic Chemistry. 69: 701-13. PMID 14750794 DOI: 10.1021/Jo034167X |
0.569 |
|
2003 |
Pattarawarapan M, Burgess K. Molecular basis of neurotrophin-receptor interactions. Journal of Medicinal Chemistry. 46: 5277-91. PMID 14640536 DOI: 10.1021/Jm030221Q |
0.462 |
|
2003 |
Pattarawarapan M, Reyes S, Xia Z, Zaccaro MC, Saragovi HU, Burgess K. Selective formation of homo- and heterobivalent peptidomimetics. Journal of Medicinal Chemistry. 46: 3565-7. PMID 12904060 DOI: 10.1021/Jm034103E |
0.579 |
|
2003 |
Lee HB, Pattarawarapan M, Roy S, Burgess K. Syntheses of second generation, 14-membered ring beta-turn mimics. Chemical Communications (Cambridge, England). 1674-5. PMID 12877497 DOI: 10.1039/B304454H |
0.524 |
|
2002 |
Pattarawarapan M, Zaccaro MC, Saragovi UH, Burgess K. New templates for syntheses of ring-fused, C(10) beta-turn peptidomimetics leading to the first reported small-molecule mimic of neurotrophin-3. Journal of Medicinal Chemistry. 45: 4387-90. PMID 12238916 DOI: 10.1021/Jm0255421 |
0.565 |
|
2001 |
Pattarawarapan M, Chen J, Steffensen M, Burgess K. A rigid linker-scaffold for solid-phase synthesis of dimeric pharmacophores. Journal of Combinatorial Chemistry. 3: 102-16. PMID 11148071 DOI: 10.1021/Cc000081V |
0.579 |
|
2000 |
Pattarawarapan M, Burgess K. A Linker Scaffold to Present Dimers of Pharmacophores Prepared by Solid-Phase Syntheses. Angewandte Chemie (International Ed. in English). 39: 4299-4301. PMID 29711923 DOI: 10.1002/1521-3773(20001201)39:23<4299::Aid-Anie4299>3.0.Co;2-N |
0.521 |
|
2000 |
Chen J, Pattarawarapan M, Zhang AJ, Burgess K. Solution- and solid-phase syntheses of substituted guanidinocarboxylic acids. Journal of Combinatorial Chemistry. 2: 276-81. PMID 10827936 DOI: 10.1021/Cc990084B |
0.509 |
|
2000 |
Reyes S, Pattarawarapan M, Roy S, Burgess K. Preferred Secondary Structures as a Possible Driving Force for Macrocyclization Tetrahedron. 56: 9809-9818. DOI: 10.1016/S0040-4020(00)00888-7 |
0.517 |
|
2000 |
Pattarawarapan M, Burgess K. A linker scaffold to present dimers of pharmacophores prepared by solid-phase syntheses Angewandte Chemie - International Edition. 39: 4299-4301. DOI: 10.1002/1521-3773(20001201)39:23<4299::AID-ANIE4299>3.0.CO;2-N |
0.48 |
|
1999 |
Feng Y, Pattarawarapan M, Wang Z, Burgess K. Solid-phase SN2 macrocyclization reactions to form beta-turn mimics. Organic Letters. 1: 121-4. PMID 10822547 DOI: 10.1021/Ol990597R |
0.523 |
|
1999 |
Feng Y, Pattarawarapan M, Wang Z, Burgess K. Stereochemical implications on diversity in β-turn peptidomimetic libraries Journal of Organic Chemistry. 64: 9175-9177. DOI: 10.1021/Jo991150Z |
0.506 |
|
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