Multiple cationic amphiphiles induce a Niemann-Pick C phenotype and inhibit Ebola virus entry and infection von Shoemaker, Charles J, Schornberg, Kathryn L, Delos, Sue E, Scully, Corinne, Pajouhesh, Hassan, Olinger, Gene G, Johansen, Lisa M, White, Judith M

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A novel slow-inactivation-specific ion channel modulator attenuates neuropathic pain von Hildebrand, Michael E., Smith, Paula L., Bladen, Chris, Eduljee, Cyrus, Xie, Jennifer Y., Chen, Lina, Fee-Maki, Molly, Doering, Clint J., Mezeyova, Janette, Zhu, Yongbao, Belardetti, Francesco, Pajouhesh, Hassan, Parker, David, Arneric, Stephen P., Parmar, Manjeet, Porreca, Frank, Tringham, Elizabeth, Zamponi, Gerald W., Snutch, Terrance P.

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Structure–activity relationships of diphenylpiperazine N-type calcium channel inhibitors von Pajouhesh, Hassan, Feng, Zhong-Ping, Ding, Yanbing, Zhang, Lingyun, Pajouhesh, Hossein, Morrison, Jerrie-Lynn, Belardetti, Francesco, Tringham, Elizabeth, Simonson, Eric, Vanderah, Todd W., Porreca, Frank, Zamponi, Gerald W., Mitscher, Lester A., Snutch, Terrance P.

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Medicinal Chemical Properties of Successful Central Nervous System Drugs von Pajouhesh, Hassan, Lenz, George R.

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Correction: Multiple Cationic Amphiphiles Induce a Niemann-Pick C Phenotype and Inhibit Ebola Virus Entry and Infection von Shoemaker, Charles J., Schornberg, Kathryn L., Delos, Sue E., Scully, Corinne, Pajouhesh, Hassan, Olinger, Gene G., Johansen, Lisa M., White, Judith M.

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Challenges and Opportunities for Therapeutics Targeting the Voltage-Gated Sodium Channel Isoform NaV1.7 von Mulcahy, John V, Pajouhesh, Hassan, Beckley, Jacob T, Delwig, Anton, Du Bois, J, Hunter, John C

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ST-2560, a selective inhibitor of the Na V 1.7 sodium channel, affects nocifensive and cardiovascular reflexes in non-human primates von Mulcahy, John V, Beckley, Jacob T, Klas, Sheri D, Odink, Debra A, Delwig, Anton, Pajouhesh, Hassan, Monteleone, Dennis, Zhou, Xiang, Du Bois, Justin, Yeomans, David C, Luu, George, Hunter, John C

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ST‐2560, a selective inhibitor of the NaV1.7 sodium channel, affects nocifensive and cardiovascular reflexes in non‐human primates von Mulcahy, John V., Beckley, Jacob T., Klas, Sheri D., Odink, Debra A., Delwig, Anton, Pajouhesh, Hassan, Monteleone, Dennis, Zhou, Xiang, Du Bois, Justin, Yeomans, David C., Luu, George, Hunter, John C.

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Challenges and Opportunities for Therapeutics Targeting the Voltage-Gated Sodium Channel Isoform Na V 1.7 von Mulcahy, John V, Pajouhesh, Hassan, Beckley, Jacob T, Delwig, Anton, Du Bois, J, Hunter, John C

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Discovery of Selective Inhibitors of Na V 1.7 Templated on Saxitoxin as Therapeutics for Pain von Pajouhesh, Hassan, Delwig, Anton, Beckley, Jacob T., Klas, Sheri, Monteleone, Dennis, Zhou, Xiang, Luu, George, Du Bois, J., Hunter, John C., Mulcahy, John V.

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Discovery of Selective Inhibitors of NaV1.7 Templated on Saxitoxin as Therapeutics for Pain von Pajouhesh, Hassan, Delwig, Anton, Beckley, Jacob T., Klas, Sheri, Monteleone, Dennis, Zhou, Xiang, Luu, George, Du Bois, J., Hunter, John C., Mulcahy, John V.

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Antinociceptive properties of an isoform-selective inhibitor of Nav1.7 derived from saxitoxin in mouse models of pain von Beckley, Jacob T., Pajouhesh, Hassan, Luu, George, Klas, Sheri, Delwig, Anton, Monteleone, Dennis, Zhou, Xiang, Giuvelis, Denise, Meng, Ian D., Yeomans, David C., Hunter, John C., Mulcahy, John V.

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Scaffold-based design and synthesis of potent N-type calcium channel blockers von Zamponi, Gerald W., Feng, Zhong-Ping, Zhang, Lingyun, Pajouhesh, Hossein, Ding, Yanbing, Belardetti, Francesco, Pajouhesh, Hassan, Dolphin, David, Mitscher, Lester A., Snutch, Terrance P.

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Enantioselective synthesis of both enantiomers of the neuroexcitant 2-amino-3-(3-hydroxy-5- tert -butylisoxazol-4-yl) propanoic acid (ATPA) von Pajouhesh, Hassan, Hosseini-Meresht, Mahmonir, Pajouhesh, Seyed Hossein, Curry, Ken

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Modular, efficient synthesis of asymmetrically substituted piperazine scaffolds as potent calcium channel blockers von Borzenko, Andrey, Pajouhesh, Hassan, Morrison, Jerrie-Lynn, Tringham, Elizabeth, Snutch, Terrance P., Schafer, Laurel L.

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Structure–activity relationships of trimethoxybenzyl piperazine N-type calcium channel inhibitors von Pajouhesh, Hassan, Feng, Zhong-Ping, Zhang, Lingyun, Pajouhesh, Hossein, Jiang, Xinpo, Hendricson, Adam, Dong, Haiheng, Tringham, Elizabeth, Ding, Yanbing, Vanderah, Todd W., Porreca, Frank, Belardetti, Francesco, Zamponi, Gerald W., Mitscher, Lester A., Snutch, Terrance P.

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11,13-modified saxitoxins for the treatment of pain von Zhou, Xiang, Pajouhesh, Hassan, Mulcahy, John

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A fluorescence-based high-throughput screening assay for the identification of T-type calcium channel blockers von Belardetti, Francesco, Tringham, Elizabeth, Eduljee, Cyrus, Jiang, Xinpo, Dong, Haiheng, Hendricson, Adam, Shimizu, Yoko, Janke, Diana L, Parker, David, Mezeyova, Janette, Khawaja, Afsheen, Pajouhesh, Hassan, Fraser, Robert A, Arneric, Stephen P, Snutch, Terrance P

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11,13-MODIFIED SAXITOXINS FOR THE TREATMENT OF PAIN von PAJOUHESH, Hassan, ZHOU, Xiang, MULCAHY, John

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NON-HYDRATED KETONE INHIBITORS OF NAV1.7 FOR THE TREATMENT OF PAIN von PAJOUHESH, Hassan, ZHOU, Xiang, MONTELEONE, Dennis, MULCAHY, John

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