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The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side...
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| Zeitschriftentitel: | Journal of Medicinal Chemistry |
|---|---|
| Personen und Körperschaften: | , , , , , , , , |
| In: | Journal of Medicinal Chemistry, 33, 1990, 10, S. 2828-2841 |
| Format: | E-Article |
| Sprache: | Englisch |
| veröffentlicht: |
American Chemical Society (ACS)
|
| Schlagwörter: |
| author_facet |
Galemmo, Robert A. Johnson, William H. Learn, Keith S. Lee, Thomas D. Y. Huang, Fu Chih Campbell, Henry F. Youssefyeh, Raymond O'Rourke, Susan V. Schuessler, Glenn Galemmo, Robert A. Johnson, William H. Learn, Keith S. Lee, Thomas D. Y. Huang, Fu Chih Campbell, Henry F. Youssefyeh, Raymond O'Rourke, Susan V. Schuessler, Glenn |
|---|---|
| author |
Galemmo, Robert A. Johnson, William H. Learn, Keith S. Lee, Thomas D. Y. Huang, Fu Chih Campbell, Henry F. Youssefyeh, Raymond O'Rourke, Susan V. Schuessler, Glenn |
| spellingShingle |
Galemmo, Robert A. Johnson, William H. Learn, Keith S. Lee, Thomas D. Y. Huang, Fu Chih Campbell, Henry F. Youssefyeh, Raymond O'Rourke, Susan V. Schuessler, Glenn Journal of Medicinal Chemistry The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency Drug Discovery Molecular Medicine |
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galemmo, robert a. |
| spelling |
Galemmo, Robert A. Johnson, William H. Learn, Keith S. Lee, Thomas D. Y. Huang, Fu Chih Campbell, Henry F. Youssefyeh, Raymond O'Rourke, Susan V. Schuessler, Glenn 0022-2623 1520-4804 American Chemical Society (ACS) Drug Discovery Molecular Medicine http://dx.doi.org/10.1021/jm00172a024 The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency Journal of Medicinal Chemistry |
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The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency |
| title_unstemmed |
The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency |
| title_full |
The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency |
| title_fullStr |
The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency |
| title_full_unstemmed |
The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency |
| title_short |
The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency |
| title_sort |
the development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. structural variation of the acidic side chain to give antagonists of enhanced potency |
| topic |
Drug Discovery Molecular Medicine |
| url |
http://dx.doi.org/10.1021/jm00172a024 |
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1990 |
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2828-2841 |
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| author | Galemmo, Robert A., Johnson, William H., Learn, Keith S., Lee, Thomas D. Y., Huang, Fu Chih, Campbell, Henry F., Youssefyeh, Raymond, O'Rourke, Susan V., Schuessler, Glenn |
| author_facet | Galemmo, Robert A., Johnson, William H., Learn, Keith S., Lee, Thomas D. Y., Huang, Fu Chih, Campbell, Henry F., Youssefyeh, Raymond, O'Rourke, Susan V., Schuessler, Glenn, Galemmo, Robert A., Johnson, William H., Learn, Keith S., Lee, Thomas D. Y., Huang, Fu Chih, Campbell, Henry F., Youssefyeh, Raymond, O'Rourke, Susan V., Schuessler, Glenn |
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| spelling | Galemmo, Robert A. Johnson, William H. Learn, Keith S. Lee, Thomas D. Y. Huang, Fu Chih Campbell, Henry F. Youssefyeh, Raymond O'Rourke, Susan V. Schuessler, Glenn 0022-2623 1520-4804 American Chemical Society (ACS) Drug Discovery Molecular Medicine http://dx.doi.org/10.1021/jm00172a024 The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency Journal of Medicinal Chemistry |
| spellingShingle | Galemmo, Robert A., Johnson, William H., Learn, Keith S., Lee, Thomas D. Y., Huang, Fu Chih, Campbell, Henry F., Youssefyeh, Raymond, O'Rourke, Susan V., Schuessler, Glenn, Journal of Medicinal Chemistry, The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency, Drug Discovery, Molecular Medicine |
| title | The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency |
| title_full | The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency |
| title_fullStr | The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency |
| title_full_unstemmed | The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency |
| title_short | The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency |
| title_sort | the development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. structural variation of the acidic side chain to give antagonists of enhanced potency |
| title_unstemmed | The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency |
| topic | Drug Discovery, Molecular Medicine |
| url | http://dx.doi.org/10.1021/jm00172a024 |