Multi-receptor drug design: Haloperidol as a scaffold for the design and synthesis of atypical antipsychotic agents von Peprah, Kwakye, Zhu, Xue Y., Eyunni, Suresh V.K., Setola, Vincent, Roth, Bryan L., Ablordeppey, Seth Y.

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Structure–activity relationship studies of SYA 013, a homopiperazine analog of haloperidol von Peprah, Kwakye, Zhu, Xue Y., Eyunni, Suresh V.K., Etukala, Jagan R., Setola, Vincent, Roth, Bryan L., Ablordeppey, Seth Y.

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The Antiproliferative Effects of Flavonoid MAO Inhibitors on Prostate Cancer Cells von Zarmouh, Najla O., Messeha, Samia S., Mateeva, Nelly, Gangapuram, Madhavi, Flowers, Kacy, Eyunni, Suresh V. K., Zhang, Wang, Redda, Kinfe K., Soliman, Karam F. A.

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Identification of a butyrophenone analog as a potential atypical antipsychotic agent: 4-[4-(4-Chlorophenyl)-1,4-diazepan-1-yl]-1-(4-fluorophenyl)butan-1-one von Ablordeppey, Seth Y., Altundas, Ramazan, Bricker, Barbara, Zhu, Xue Y., Suresh Kumar, Eyunni V.K., Jackson, Tanise, Khan, Abdul, Roth, Bryan L.

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Identification of 7,8‐dihydroxy‐3‐phenylcoumarin as a reversible monoamine oxidase enzyme inhibitor von Musa, Musiliyu A., Badisa, Veera L. D., Aghimien, Monica O., Eyunni, Suresh V. K., Latinwo, Lekan M.

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Evaluation of the Inhibitory Effects of Bavachinin and Bavachin on Human Monoamine Oxidases A and B von Eyunni, Suresh, Messeha, Samia S., Elshami, Faisel, Mazzio, Elizabeth, Zarmouh, Najla O., Soliman, Karam F. A.

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Development of CNS multi-receptor ligands: Modification of known D2 pharmacophores von Etukala, Jagan R., Zhu, Xue Y., Eyunni, Suresh V.K., Onyameh, Edem K., Ofori, Edward, Bricker, Barbara A., Kang, Hye J., Huang, Xi-Ping, Roth, Bryan L., Ablordeppey, Seth Y.

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SUBSTITUTED TETRAHYDROISOQUINOLINE ETHYLBENZAMIDE ANTI-CANCER AGENTS von Redda, Kinfe Ken, Eyunni, Suresh Kumar V. K

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Bioactivity-Guided Isolation of Neuritogenic Factor from the Seeds of the Gac Plant (Momordica cochinchinensis) von George, B., Ablordeppey, S., Eyunni, Suresh, Badisa, R., Mazzio, E., Soliman, Karam F. A.

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1,2,3,4,6-Penta-O-galloylglucose within Galla Chinensis Inhibits Human LDH-A and Attenuates Cell Proliferation in MDA-MB-231 Breast Cancer Cells von Soliman, Karam F. A., Mateeva, Nelly, McTier, Oshlii, Eyunni, Suresh, Mazzio, Elizabeth, Deiab, Shihab, Elshami, Faisel

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Biological evaluation of synthetic chalcone and flavone derivatives as anti-inflammatory agents von Mateeva, Nelly, Gangapuram, Madhavi, Mazzio, Elizabeth, Eyunni, Suresh, Soliman, Karam F. A., Redda, Kinfe K.

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1,2,3,4,6-penta-0-galloylglucose within Galla Chinensis inhibits human LDH-A and attenuates cell proliferation in MDA-MB-231 breast cancer cells von Deiab, Shihab, Mazzio, Elizabeth, Eyunni, Suresh, McTier, Oshlii, Mateeva, Nelly, Elshami, Faisel, Soliman, Karam F.A

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Chalcone derived benzoheterodiazepines for medicinal applications: A Two‐pot and one‐pot synthetic approach von Farooq, Saba, Ngaini, Zainab

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Synthesis, In Silico and In Vitro Evaluation for Acetylcholinesterase and BACE-1 Inhibitory Activity of Some N -Substituted-4-Phenothiazine-Chalcones von Tran, Thai-Son, Le, Minh-Tri, Nguyen, Thi-Cam-Vi, Tran, The-Huan, Tran, Thanh-Dao, Thai, Khac-Minh

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