Approval Year
Substance Class |
Protein
Created
by
admin
on
Edited
Sat Dec 16 12:27:38 GMT 2023
by
admin
on
Sat Dec 16 12:27:38 GMT 2023
|
Protein Type | RECEPTOR |
Protein Sub Type | CYTOKINE RECEPTOR |
Sequence Origin | HUMAN |
Sequence Type | COMPLETE |
Record UNII |
B5GGG91KI4
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Record Status |
Validated (UNII)
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Record Version |
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-
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Code System | Code | Type | Description | ||
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P61073
Created by
admin on Sat Dec 16 12:27:39 GMT 2023 , Edited by admin on Sat Dec 16 12:27:39 GMT 2023
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PRIMARY | |||
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P61073
Created by
admin on Sat Dec 16 12:27:39 GMT 2023 , Edited by admin on Sat Dec 16 12:27:39 GMT 2023
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PRIMARY | |||
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B5GGG91KI4
Created by
admin on Sat Dec 16 12:27:39 GMT 2023 , Edited by admin on Sat Dec 16 12:27:39 GMT 2023
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PRIMARY | |||
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CXCR4
Created by
admin on Sat Dec 16 12:27:39 GMT 2023 , Edited by admin on Sat Dec 16 12:27:39 GMT 2023
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PRIMARY |
From | To |
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1_28 | 1_274 |
1_109 | 1_186 |
Glycosylation Type | HUMAN |
Glycosylation Link Type | Site |
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N | 1_11 |
N | 1_176 |
O | 1_18 |
Related Record | Type | Details | ||
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INHIBITOR -> TARGET | |||
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INHIBITOR -> TARGET |
Binds to CXCR4, thereby preventing the binding of stromal cell-derived factor-1 (SDF-1 or CXCL12) to CXCR4 and inhibiting CXCR4 activation. This results in decreased proliferation and migration of CXCR4-expressing tumor cells. In addition, PF-06747143 promotes cell death through the induction of both complement-dependent cytotoxicity (CDC) and antibody-dependent cellular cytotoxicity (ADCC).
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AGONIST -> TARGET |
Dimeric form acts as a partial agonist of CXCR4.
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INHIBITOR -> TARGET |
AGONIST
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RADIOLIGAND->TARGET |
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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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LIGAND->TARGET |
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INHIBITOR -> TARGET |
Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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MOL_WEIGHT | CHEMICAL |
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Molecular Formula | CHEMICAL |
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