Novel modulators of cell cycle checkpoints and their use in
combination with checkpoint kinase inhibitors

P 2009

Novel modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors

GUZI, Timothy, David PARRY, Marc LABROLI, Michael DWYER, Kamil PARUCH et. al.

Basic information

Original name

Novel modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors

Name in Czech

Novel modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors

Authors

GUZI, Timothy, David PARRY, Marc LABROLI, Michael DWYER, Kamil PARUCH, Kristen ROSNER, Ruichao SHEN and Janeta POPOVICI-MULLER

Edition

Number: WO 2009/061781 A1, Publisher: World Intellectual Property Organization, Place of publication: USA, Owner's name: Schering-Plough, 2009

Other information

Language

English

Type of outcome

Patent

Field of Study

30200 3.2 Clinical medicine

Country of publisher

United States of America

Confidentiality degree

není předmětem státního či obchodního tajemství

Organization unit

Faculty of Science

Keywords (in Czech)

checkpoint kinase; inhibitor; cancer

Keywords in English

checkpoint kinase; inhibitor; cancer

Abstract

ORIG CZ

V originále

Pyrimidine nucleoside analogs I were prepd., wherein G is H, halo, alkyl; X and Y are independently H, F, OR2, alkyl;Z is O, NR2, S, CR2R3, SO2; R is alkyl, alkenyl, cycloalkyl, aryl, alkylaryl, heteroaryl, alkylheteroaryl, heterocyclyl, alkylheterocyclyl, alkyl-C(O)R2 and alkyl-C(O)NR2R3, wherein each of said alkyl, aryl, heteroaryl and heterocyclyl can be (un)substituted with one or more groups which can be the same or different, each substituent being independently selected from the group consisting of halo, cyano, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, aryloxy, alkylthio, arylthio, aryl, heteroaryl, heterocyclyl, cycloalkyl, cycloalkenyl, OR, NR2R3, C(O)R2, C(O)OR2 and C(O)NR2R3; R2 is H, alkyl, aryl, heteroaryl, wherein each of said alkyl, aryl and heteroaryl can be unsubstituted or optionally independently substituted with one or more groups which can be the same or different and are independently selected from the group consisting of halo, cyano, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, aryloxy, alkylthio, arylthio, aryl, heterocyclyl, cycloalkyl, cycloalkenyl -OR2, NR2R3, C(O)R2, C(O)NR2R3; R3 is alkyl, aryl, heteroaryl, heterocyclyl, cycloalkyl, cycloalkenyl, OR2, NR2R3, C(O)R2 and C(O)NR2R3 as targeted mechanism-based modulators of cell cycle checkpoints. Cancers and/or malignancies can be treated by administration of a cell cycle checkpoint modulator of the invention. Also discussed are suitable combinations of the cell cycle checkpoint modulator with a checkpoint kinase inhibitor to produce synergistic apoptosis in cancer cells. The invention includes methods of treating cancers by administering the combination of the cell cycle checkpoint modulator and the checkpoint kinase inhibitor, pharmaceutical compns. comprising the activator as well as the combination and pharmaceutical kits. Thus, nucleosides II was prepd. and tested as kinase inhibitor and anticancer agent, wherein the cancer is selected from the group consisting of: cancer of the bladder, breast, colon, kidney, liver, lung, small cell lung cancer, non-small cell lung cancer, head and neck esophagus, gall bladder, ovary, cervix thyroid, prostate, and skin, squamous cell carcinoma; leukemia, acute lymphocytic leukemia, chronic lymphocytic leukemia, acute lymphoblastic leukemia, B-cell lymphoma, T-cell Iymphoma, Hodgkins lymphoma, non-Hodgkins lymphoma, hairy cell lymphoma, mantle cell lymphoma, and Burketlt's lymphoma; acute and chronic myelogenous leukemia, myelodysplastic syndrome and promyelocytic leukemia; fibrosarcoma, rhabdomyosarcoma; astrocytoma, neuroblastoma, glioma and melanoma, teratocarcinoma, osteosarcoma, thyroid cancer and Kaposi's sarcoma.

In Czech

viz anotace

Citovat

GUZI, Timothy, David PARRY, Marc LABROLI, Michael DWYER, Kamil PARUCH, Kristen ROSNER, Ruichao SHEN and Janeta POPOVICI-MULLER. Novel modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors. 2009.

@misc{837948,
   author = {Guzi, Timothy and Parry, David and Labroli, Marc and Dwyer, Michael and Paruch, Kamil and Rosner, Kristen and Shen, Ruichao and PopoviciandMuller, Janeta},
   keywords = {checkpoint kinase; inhibitor; cancer},
   language = {eng},
   title = {Novel modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors},
   year = {2009}
}

TY  - PAT
ID  - 837948
AU  - Guzi, Timothy - Parry, David - Labroli, Marc - Dwyer, Michael - Paruch, Kamil - Rosner, Kristen - Shen, Ruichao - Popovici-Muller, Janeta
PY  - 2009
TI  - Novel modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors
KW  - checkpoint kinase
KW  - inhibitor
KW  - cancer
N2  - Pyrimidine nucleoside analogs I were prepd., wherein G is H, halo, alkyl; X and Y are independently H, F, OR2, alkyl;Z is O, NR2, S, CR2R3, SO2; R is alkyl, alkenyl, cycloalkyl, aryl, alkylaryl, heteroaryl, alkylheteroaryl, heterocyclyl, alkylheterocyclyl, alkyl-C(O)R2 and alkyl-C(O)NR2R3, wherein each of said alkyl, aryl, heteroaryl and heterocyclyl can be (un)substituted with one or more groups which can be the same or different, each substituent being independently selected from the group consisting of halo, cyano, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, aryloxy, alkylthio, arylthio, aryl, heteroaryl, heterocyclyl, cycloalkyl, cycloalkenyl, OR, NR2R3, C(O)R2, C(O)OR2 and C(O)NR2R3; R2 is H, alkyl, aryl, heteroaryl, wherein each of said alkyl, aryl and heteroaryl can be unsubstituted or optionally independently substituted with one or more groups which can be the same or different and are independently selected from the group consisting of halo, cyano, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, aryloxy, alkylthio, arylthio, aryl, heterocyclyl, cycloalkyl, cycloalkenyl -OR2, NR2R3, C(O)R2, C(O)NR2R3; R3 is alkyl, aryl, heteroaryl, heterocyclyl, cycloalkyl, cycloalkenyl, OR2, NR2R3, C(O)R2 and C(O)NR2R3 as targeted mechanism-based modulators of cell cycle checkpoints. Cancers and/or malignancies can be treated by administration of a cell cycle checkpoint modulator of the invention. Also discussed are suitable combinations of the cell cycle checkpoint modulator with a checkpoint kinase inhibitor to produce synergistic apoptosis in cancer cells. The invention includes methods of treating cancers by administering the combination of the cell cycle checkpoint modulator and the checkpoint kinase inhibitor, pharmaceutical compns. comprising the activator as well as the combination and pharmaceutical kits. Thus, nucleosides II was prepd. and tested as kinase inhibitor and anticancer agent, wherein the cancer is selected from the group consisting of: cancer of the bladder, breast, colon, kidney, liver, lung, small cell lung cancer, non-small cell lung cancer, head and neck esophagus, gall bladder, ovary, cervix thyroid, prostate, and skin, squamous cell carcinoma; leukemia, acute lymphocytic leukemia, chronic lymphocytic leukemia, acute lymphoblastic leukemia, B-cell lymphoma, T-cell Iymphoma, Hodgkins lymphoma, non-Hodgkins lymphoma, hairy cell lymphoma, mantle cell lymphoma, and Burketlt's lymphoma; acute and chronic myelogenous leukemia, myelodysplastic syndrome and promyelocytic leukemia; fibrosarcoma, rhabdomyosarcoma; astrocytoma, neuroblastoma, glioma and melanoma, teratocarcinoma, osteosarcoma, thyroid cancer and Kaposi's sarcoma.
ER  -

GUZI, Timothy, David PARRY, Marc LABROLI, Michael DWYER, Kamil PARUCH, Kristen ROSNER, Ruichao SHEN and Janeta POPOVICI-MULLER. \textit{Novel modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors}. 2009.

Detailed Information on Publication Record