Approval Year
Substance Class |
Protein
Created
by
admin
on
Edited
Sat Dec 16 13:56:19 GMT 2023
by
admin
on
Sat Dec 16 13:56:19 GMT 2023
|
Protein Type | ENZYME |
Protein Sub Type | SERINE/THREONINE-PROTEIN KINASE |
Sequence Origin | HUMAN |
Sequence Type | COMPLETE |
Record UNII |
U7FKT8J0J3
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Record Status |
Validated (UNII)
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Record Version |
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-
Download
Name | Type | Language | ||
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Common Name | English | ||
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Common Name | English |
Code System | Code | Type | Description | ||
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P15056
Created by
admin on Sat Dec 16 13:56:20 GMT 2023 , Edited by admin on Sat Dec 16 13:56:20 GMT 2023
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PRIMARY | |||
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U7FKT8J0J3
Created by
admin on Sat Dec 16 13:56:20 GMT 2023 , Edited by admin on Sat Dec 16 13:56:20 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
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INHIBITOR -> TARGET |
In contrast to approved therapies targeting Class I V600E BRAF mutant tumors, KIN-2787 was active across all classes of BRAF-altered melanoma cells.
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INHIBITOR -> TARGET |
IC50
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INHIBITOR -> TARGET | |||
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INHIBITOR -> TARGET | |||
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INHIBITOR -> TARGET |
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||
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INHIBITOR -> TARGET | |||
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INHIBITOR -> TARGET |
IC50
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INHIBITOR -> TARGET |
IC50
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RADIOLIGAND->TARGET |
A serine/threonine kinase PET
imaging agent for the melanomas mainly in the specific expression of the BRAFV600E mutation.
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INHIBITOR -> TARGET | |||
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INHIBITOR -> TARGET |
An ATP competitive inhibitor. Binding assay
COMPETITIVE INHIBITOR
IC50
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WEAK INHIBITOR->TARGET |
IC50
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INHIBITOR -> TARGET | |||
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INHIBITOR -> TARGET |
PRECLINICAL
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Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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MOL_WEIGHT:NUMBER(CALCULATED) | CHEMICAL |
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