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A potent immunomodulatory compound, (S,R)-3-Phenyl-4,5-dihydro-5-isoxazole acetic acid, prevents spontaneous and accelerated forms of autoimmune diabetes in NOD mice and inhibits the immunoinflammatory diabetes induced by multiple low doses of streptozotocin in CBA/H mice (✓) [2007]

Stošić-Grujičić, Stanislava ; Stojanović, Ivana D. ; Mangano, Katia; Fresta, Massimo; Maksimović-Ivanić, Danijela ; Harhaji Trajković, Ljubica ; Popadić, Dušan; Momčilović, Miljana ; Miljković, Đorđe ; Kim, Joseph;

Al-Abed, Yousef; Nicoletti, Ferdinando;

Vimocin and Vidapin, cyclic KTS peptides, dual antagonists of α1β1/α2β1 integrins with antiangiogenic activity [2014]

Momić, Tatjana ; Katzehendler, Jehoshua; Benny, Ofra; Lahiani, Adi; Cohen, Gadi; Noy, Efrat; Senderowitz, Hanoch; Eble, Johannes A.; Marcinkiewicz, Cezary; Lazarovici, Philip

Structural Analogs of the GABAkine KRM-II-81 Are Orally Bioavailable Anticonvulsants without Sedation (✓) [2023]

Pandey, Kamal P; Divović, Branka ; ...; Savić, Miroslav ; (broj, koautora 18)

A potent immunomodulatory compound, (S,R)-3-Phenyl-4,5-dihydro-5-isoxazole acetic acid, prevents spontaneous and accelerated forms of autoimmune diabetes in NOD mice and inhibits the immunoinflammatory diabetes induced by multiple low doses of streptozotocin in CBA/H mice (✓) [2007]

Vimocin and Vidapin, cyclic KTS peptides, dual antagonists of α1β1/α2β1 integrins with antiangiogenic activity [2014]

Structural Analogs of the GABAkine KRM-II-81 Are Orally Bioavailable Anticonvulsants without Sedation (✓) [2023]

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