Search Results - Hernandez, Delmis E

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  1. 1
    Quorum Sensing Autoinducer‑3 Finally Yields to Structural Elucidation

    Quorum Sensing Autoinducer‑3 Finally Yields to Structural Elucidation by Hernandez, Delmis E, Sintim, Herman O

    Published in ACS central science
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  2. 2
    Orally bioavailable STING antagonist synthesized via multi-component Povarov-Doebner type reaction

    Orally bioavailable STING antagonist synthesized via multi-component Povarov-Doebner type reaction by Owusu, Kofi B, Samal, Jyotrimayee, Hernandez, Delmis E, Sintim, Herman O

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  3. 3
    Tetrahydro-3H-pyrazolo[4,3-a]phenanthridine-based CDK inhibitor

    Tetrahydro-3H-pyrazolo[4,3-a]phenanthridine-based CDK inhibitor by Opoku-Temeng, Clement, Dayal, Neetu, Hernandez, Delmis E, Naganna, N, Sintim, Herman O

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  4. 4
    3H‑Pyrazolo[4,3‑f]quinoline-Based Kinase Inhibitors Inhibit the Proliferation of Acute Myeloid Leukemia Cells In Vivo

    3H‑Pyrazolo[4,3‑f]quinoline-Based Kinase Inhibitors Inhibit the Proliferation of Acute Myeloid Leukemia Cells In Vivo by Dayal, Neetu, Řezníčková, Eva, Hernandez, Delmis E, Peřina, Miroslav, Torregrosa-Allen, Sandra, Elzey, Bennett D, Škerlová, Jana, Ajani, Haresh, Djukic, Stefan, Vojáčková, Veronika, Lepšík, Martin, Řezáčová, Pavlína, Kryštof, Vladimír, Jorda, Radek, Sintim, Herman O

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  5. 5
    Dual FLT3/TOPK inhibitor with activity against FLT3-ITD secondary mutations potently inhibits acute myeloid leukemia cell lines

    Dual FLT3/TOPK inhibitor with activity against FLT3-ITD secondary mutations potently inhibits acute myeloid leukemia cell lines by Dayal, Neetu, Opoku-Temeng, Clement, Hernandez, Delmis E, Sooreshjani, Moloud Aflaki, Carter-Cooper, Brandon A, Lapidus, Rena G, Sintim, Herman O

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  6. 6
    Orally bioavailable STING antagonist synthesized multi-component Povarov-Doebner type reaction

    Orally bioavailable STING antagonist synthesized multi-component Povarov-Doebner type reaction by Owusu, Kofi B, Samal, Jyotrimayee, Hernandez, Delmis E, Sintim, Herman O

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  7. 7
    Tetrahydro-3 H -pyrazolo[4,3- a ]phenanthridine-based CDK inhibitor

    Tetrahydro-3 H -pyrazolo[4,3- a ]phenanthridine-based CDK inhibitor by Opoku-Temeng, Clement, Dayal, Neetu, Hernandez, Delmis E., Naganna, N., Sintim, Herman O.

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  8. 8
    3 H -Pyrazolo[4,3- f ]quinoline-Based Kinase Inhibitors Inhibit the Proliferation of Acute Myeloid Leukemia Cells In Vivo

    3 H -Pyrazolo[4,3- f ]quinoline-Based Kinase Inhibitors Inhibit the Proliferation of Acute Myeloid Leukemia Cells In Vivo by Dayal, Neetu, Řezníčková, Eva, Hernandez, Delmis E., Peřina, Miroslav, Torregrosa-Allen, Sandra, Elzey, Bennett D., Škerlová, Jana, Ajani, Haresh, Djukic, Stefan, Vojáčková, Veronika, Lepšík, Martin, Řezáčová, Pavlína, Kryštof, Vladimír, Jorda, Radek, Sintim, Herman O.

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  9. 9
    Tetrahydro-3-pyrazolo[4,3-]phenanthridine-based CDK inhibitor

    Tetrahydro-3-pyrazolo[4,3-]phenanthridine-based CDK inhibitor by Opoku-Temeng, Clement, Dayal, Neetu, Hernandez, Delmis E, Naganna, N, Sintim, Herman O

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