Drug Information
Drug (ID: DG01888) and It's Reported Resistant Information
Name |
Non-allosteric AKT inhibitors
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Synonyms |
Non-allosteric AKT inhibitors
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Target | . | NOUNIPROTAC | [1] |
Type(s) of Resistant Mechanism of This Drug
ADTT: Aberration of the Drug's Therapeutic Target
Drug Resistance Data Categorized by Their Corresponding Diseases
ICD-02: Benign/in-situ/malignant neoplasm
Solid tumour/cancer [ICD-11: 2A00-2F9Z]
Drug Sensitivity Data Categorized by Their Corresponding Mechanisms | ||||
Aberration of the Drug's Therapeutic Target (ADTT) | ||||
Key Molecule: RAC-alpha serine/threonine-protein kinase (AKT1) | [1] | |||
Molecule Alteration | Missense mutation | p.E17K (c.49G>A) |
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Sensitive Disease | Solid tumour/cancer [ICD-11: 2A00-2F9Z] | |||
Experimental Note | Identified from the Human Clinical Data | |||
Mechanism Description | The missense mutation p.E17K (c.49G>A) in gene AKT1 cause the sensitivity of non-allosteric AKT inhibitors by aberration of the drug's therapeutic target | |||
Key Molecule: RAC-alpha serine/threonine-protein kinase (AKT1) | [1] | |||
Molecule Alteration | Missense mutation | p.E17K (c.49G>A) |
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Sensitive Disease | Solid tumour/cancer [ICD-11: 2A00-2F9Z] | |||
Experimental Note | Identified from the Human Clinical Data | |||
Key Molecule: RAC-alpha serine/threonine-protein kinase (AKT1) | [1] | |||
Molecule Alteration | Missense mutation | p.E17K (c.49G>A) |
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Sensitive Disease | Solid tumour/cancer [ICD-11: 2A00-2F9Z] | |||
Experimental Note | Identified from the Human Clinical Data |
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