(R,S)-Ivosidenib((R,S)-AG-120)

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Reagent Code: #61675
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CAS Number 2070009-31-1

science Other reagents with same CAS 2070009-31-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 582.96 g/mol
Formula C₂₈H₂₂ClF₃N₆O₃
inventory_2 Storage & Handling
Storage -20°C, airtight, dry

description Product Description

(R,S)-Ivosidenib ((R,S)-AG-120) is the racemic form of an inhibitor targeting the mutant isocitrate dehydrogenase 1 (IDH1) enzyme. It is structurally related to Ivosidenib, which is investigated in research for treating cancers associated with IDH1 mutations, particularly acute myeloid leukemia (AML). The compound works by inhibiting the mutated IDH1 enzyme, thereby reducing the production of the oncometabolite 2-hydroxyglutarate (2-HG). This action helps to restore normal cellular differentiation and may promote cancer cell death. It is commonly used in laboratory and preclinical studies to explore IDH1-related pathways and develop targeted therapies, including potential combinations with other agents. Ongoing research also examines its application in other IDH1-mutated cancers.

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inventory 5mg
10-20 days ฿14,877.00

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(R,S)-Ivosidenib((R,S)-AG-120)
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(R,S)-Ivosidenib ((R,S)-AG-120) is the racemic form of an inhibitor targeting the mutant isocitrate dehydrogenase 1 (IDH1) enzyme. It is structurally related to Ivosidenib, which is investigated in research for treating cancers associated with IDH1 mutations, particularly acute myeloid leukemia (AML). The compound works by inhibiting the mutated IDH1 enzyme, thereby reducing the production of the oncometabolite 2-hydroxyglutarate (2-HG). This action helps to restore normal cellular differentiation and ma

(R,S)-Ivosidenib ((R,S)-AG-120) is the racemic form of an inhibitor targeting the mutant isocitrate dehydrogenase 1 (IDH1) enzyme. It is structurally related to Ivosidenib, which is investigated in research for treating cancers associated with IDH1 mutations, particularly acute myeloid leukemia (AML). The compound works by inhibiting the mutated IDH1 enzyme, thereby reducing the production of the oncometabolite 2-hydroxyglutarate (2-HG). This action helps to restore normal cellular differentiation and may promote cancer cell death. It is commonly used in laboratory and preclinical studies to explore IDH1-related pathways and develop targeted therapies, including potential combinations with other agents. Ongoing research also examines its application in other IDH1-mutated cancers.

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