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oxindole/kanceri

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CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority based on Korean Patent Application No. 10-2017-0065385, filed on May 26, 2017, the contents of which is incorporated herein by reference in its entirety. FIELD OF THE INVENTION The present invention relates to a novel oxindole

C5, C6 substituted and/or fused oxindoles as anti-cancer agents and process for preparation thereof

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Identifikohuni Regjistrohu
RELATED APPLICATION This application claims the benefit of Indian Application No. 201611037409, filed Nov. 2, 2016. The entire content of that application is hereby incorporated by reference. FIELD OF THE INVENTION The present invention relates to C5, C6 substituted and/or fused oxindole compounds

4,5-azolo-oxindoles

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Identifikohuni Regjistrohu
FIELD OF THE INVENTION The present invention is directed to novel 4,5-azolo-oxindoles which inhibit cyclin-dependent kinases (CDKs), in particular CDK2. These compounds and their pharmaceutically acceptable salts, and prodrugs of said compounds, are anti-proliferative agents useful in the treatment

4,5-azolo-oxindoles

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Identifikohuni Regjistrohu
FIELD OF THE INVENTION The present invention is directed to novel 4,5-azolo-oxindoles which inhibit cyclin-dependent kinases (CDKs), in particular CDK2. These compounds and their pharmaceutically acceptable salts, and prodrugs of said compounds, are anti-proliferative agents useful in the treatment

Use of spiro-oxindole compounds as therapeutic agents

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FIELD OF THE INVENTION The present invention is directed to methods of using spiro-oxindole compounds as therapeutic agents. In particular, this invention is directed to the use of certain spiro-oxindole compounds in treating diseases or conditions such as hypercholesterolemia, benign prostatic

Substituted oxindole derivatives as tyrosine kinase inhibitors

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Identifikohuni Regjistrohu
BACKGROUND OF THE INVENTION The present invention is related to oxindole derivatives, compositions containing the same, and methods of use and manufacture of the same. Such compounds generally are useful pharmacologically as agents in those disease states alleviated by the alteration of mitogen

Substituted oxindole derivatives as tyrosine kinase inhibitors

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Identifikohuni Regjistrohu
BACKGROUND OF THE INVENTION The present invention is related to oxindole derivatives, compositions containing the same, and methods of use and manufacture of the same. Such compounds generally are useful pharmacologically as agents in those disease states alleviated by the alteration of mitogen

3-(anilinomethylene) oxindoles

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Identifikohuni Regjistrohu
This application claims priority to GB 9904933.0 filed Mar. 4, 1999. The present invention relates generally to novel amine substituted oxindole compounds and compositions having utility as pharmacological agents in treating diseases or conditions alleviated by the inhibition or antagonism of

Oxindole derivatives

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Identifikohuni Regjistrohu
BACKGROUND OF THE INVENTION The present invention is related to oxindole derivatives, compositions containing the same, and methods of use and manufacture of the same. Such compounds generally are useful pharmacologically as agents in those disease states alleviated by the alteration of mitogen

Spiro-oxindole MDM2 antagonists

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Identifikohuni Regjistrohu
BACKGROUND The aggressive cancer cell phenotype is the result of a variety of genetic and epigenetic alterations leading to deregulation of intracellular signaling pathways (Ponder, Nature 411:336 (2001)). Cancer cells typically fail to execute an apoptotic program, and lack of appropriate apoptosis

Spiro-oxindole MDM2 antagonists

Vetëm përdoruesit e regjistruar mund të përkthejnë artikuj
Identifikohuni Regjistrohu
BACKGROUND The aggressive cancer cell phenotype is the result of a variety of genetic and epigenetic alterations leading to deregulation of intracellular signaling pathways (Ponder, Nature 411:336 (2001)). Cancer cells typically fail to execute an apoptotic program, and lack of appropriate apoptosis

Spiro-oxindole MDM2 antagonists

Vetëm përdoruesit e regjistruar mund të përkthejnë artikuj
Identifikohuni Regjistrohu
BACKGROUND The aggressive cancer cell phenotype is the result of a variety of genetic and epigenetic alterations leading to deregulation of intracellular signaling pathways (Ponder, Nature 411:336 (2001)). Cancer cells typically fail to execute an apoptotic program, and lack of appropriate apoptosis

Spiro-oxindole MDM2 antagonists

Vetëm përdoruesit e regjistruar mund të përkthejnë artikuj
Identifikohuni Regjistrohu
BACKGROUND The aggressive cancer cell phenotype is the result of a variety of genetic and epigenetic alterations leading to deregulation of intracellular signaling pathways (Ponder, Nature 411:336 (2001)). Cancer cells typically fail to execute an apoptotic program, and lack of appropriate apoptosis

Spiro-oxindole MDM2 antagonists

Vetëm përdoruesit e regjistruar mund të përkthejnë artikuj
Identifikohuni Regjistrohu
BACKGROUND The aggressive cancer cell phenotype is the result of a variety of genetic and epigenetic alterations leading to deregulation of intracellular signaling pathways (Ponder, Nature 411:336 (2001)). Cancer cells typically fail to execute an apoptotic program, and lack of appropriate apoptosis

Spiro-oxindole MDM2 antagonists

Vetëm përdoruesit e regjistruar mund të përkthejnë artikuj
Identifikohuni Regjistrohu
BACKGROUND The aggressive cancer cell phenotype is the result of a variety of genetic and epigenetic alterations leading to deregulation of intracellular signaling pathways (Ponder, Nature 411:336 (2001)). Cancer cells typically fail to execute an apoptotic program, and lack of appropriate apoptosis
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