Search Results - Defex, Henry

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  1. 1
    Discovery of 2-amino-heteroaryl-benzothiazole-6-anilides as potent p56(lck) inhibitors

    Discovery of 2-amino-heteroaryl-benzothiazole-6-anilides as potent p56(lck) inhibitors by Das, Jagabandhu, Moquin, Robert V, Lin, James, Liu, Chunjian, Doweyko, Arthur M, DeFex, Henry F, Fang, Qiong, Pang, Suhong, Pitt, Sidney, Shen, Ding Ren, Schieven, Gary L, Barrish, Joel C, Wityak, John

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  2. 2
    Molecular design, synthesis, and structure-Activity relationships leading to the potent and selective p56(lck) inhibitor BMS-243117

    Molecular design, synthesis, and structure-Activity relationships leading to the potent and selective p56(lck) inhibitor BMS-243117 by Das, Jagabandhu, Lin, James, Moquin, Robert V, Shen, Zhongqi, Spergel, Steven H, Wityak, John, Doweyko, Arthur M, DeFex, Henry F, Fang, Qiong, Pang, Suhong, Pitt, Sidney, Shen, Ding Ren, Schieven, Gary L, Barrish, Joel C

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  3. 3
    The mGluR2 positive allosteric modulator, SAR218645, improves memory and attention deficits in translational models of cognitive symptoms associated with schizophrenia

    The mGluR2 positive allosteric modulator, SAR218645, improves memory and attention deficits in translational models of cognitive symptoms associated with schizophrenia by Griebel, Guy, Pichat, Philippe, Boulay, Denis, Naimoli, Vanessa, Potestio, Lisa, Featherstone, Robert, Sahni, Sukhveen, Defex, Henry, Desvignes, Christophe, Slowinski, Franck, Vigé, Xavier, Bergis, Olivier E., Sher, Rosy, Kosley, Raymond, Kongsamut, Sathapana, Black, Mark D., Varty, Geoffrey B.

    Published in Scientific reports
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  4. 4
    Molecular design, synthesis, and structure-activity relationships leading to the potent and selective p56lck inhibitor BMS-243117

    Molecular design, synthesis, and structure-activity relationships leading to the potent and selective p56lck inhibitor BMS-243117 by DAS, Jagabandhu, LIN, James, PITT, Sidney, DING REN SHEN, SCHIEVEN, Gary L, BARRISH, Joel C, MOQUIN, Robert V, ZHONGQI SHEN, SPERGEL, Steven H, WITYAK, John, DOWEYKO, Arthur M, DEFEX, Henry F, QIONG FANG, SUHONG PANG

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  5. 5
    Discovery of 2-amino-heteroaryl-benzothiazole-6-anilides as potent p56lck inhibitors

    Discovery of 2-amino-heteroaryl-benzothiazole-6-anilides as potent p56lck inhibitors by DAS, Jagabandhu, MOQUIN, Robert V, SCHIEVEN, Gary L, BARRISH, Joel C, WITYAK, John, LIN, James, LIU, Chunjian, DOWEYKO, Arthur M, DEFEX, Henry F, FANG, Qiong, PANG, Suhong, PITT, Sidney, DING REN SHEN

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  6. 6
    Molecular design, synthesis, and structure–Activity relationships leading to the potent and selective p56 lck inhibitor BMS-243117

    Molecular design, synthesis, and structure–Activity relationships leading to the potent and selective p56 lck inhibitor BMS-243117 by Das, Jagabandhu, Lin, James, Moquin, Robert V., Shen, Zhongqi, Spergel, Steven H., Wityak, John, Doweyko, Arthur M., DeFex, Henry F., Fang, Qiong, Pang, Suhong, Pitt, Sidney, Shen, Ding Ren, Schieven, Gary L., Barrish, Joel C.

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  7. 7
    Discovery of 2-amino-heteroaryl-benzothiazole-6-anilides as potent p56 lck inhibitors

    Discovery of 2-amino-heteroaryl-benzothiazole-6-anilides as potent p56 lck inhibitors by Das, Jagabandhu, Moquin, Robert V., Lin, James, Liu, Chunjian, Doweyko, Arthur M., DeFex, Henry F., Fang, Qiong, Pang, Suhong, Pitt, Sidney, Shen, Ding Ren, Schieven, Gary L., Barrish, Joel C., Wityak, John

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