Approval Year
Substance Class |
Protein
Created
by
admin
on
Edited
Sat Dec 16 12:03:31 GMT 2023
by
admin
on
Sat Dec 16 12:03:31 GMT 2023
|
Protein Type | RECEPTOR |
Protein Sub Type | |
Sequence Origin | HUMAN |
Sequence Type | COMPLETE |
Record UNII |
7H1P16DG5J
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English |
Code System | Code | Type | Description | ||
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7H1P16DG5J
Created by
admin on Sat Dec 16 12:03:33 GMT 2023 , Edited by admin on Sat Dec 16 12:03:33 GMT 2023
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PRIMARY | |||
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Q13639
Created by
admin on Sat Dec 16 12:03:33 GMT 2023 , Edited by admin on Sat Dec 16 12:03:33 GMT 2023
|
PRIMARY |
From | To |
---|---|
1_93 | 1_184 |
Glycosylation Type | HUMAN |
Glycosylation Link Type | Site |
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N | 1_7 |
Related Record | Type | Details | ||
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PARTIAL AGONIST->TARGET |
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INHIBITOR -> TARGET |
Kb listed
Kd
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INHIBITOR -> TARGET |
Ki
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AGONIST -> TARGET | |||
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AGONIST -> TARGET |
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AGONIST -> TARGET |
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INHIBITOR -> TARGET |
INHIBITOR
Ki
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INHIBITOR -> TARGET |
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AGONIST -> TARGET |
Interaction with the 5-HT4 receptor leads to the elevation of cyclic adenosine monophosphate (cAMP) levels in HEK293 cells
EC50
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NON-INHIBITOR -> TRANSPORTER |
Ki
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AGONIST -> TARGET |
BINDING
Ki
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RADIOLIGAND->TARGET |
Kd
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PARTIAL AGONIST->TARGET |
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AGONIST -> TARGET |
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WEAK INHIBITOR->TARGET |
INHIBITOR
Ki
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RADIOLIGAND->TARGET |
Kd
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INHIBITOR -> TARGET |
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AGONIST -> TARGET |
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AGONIST -> TARGET |
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AGONIST -> TARGET |
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AGONIST -> TARGET |
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AGONIST -> TARGET |
BINDING
Ki
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AGONIST -> TARGET |
PARTIAL AGONIST
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AGONIST -> TARGET |
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RADIOLIGAND->TARGET |
IMAGING AGENT
Ki
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AGONIST -> TARGET |
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Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
---|---|---|---|---|---|---|
MOL_WEIGHT | CHEMICAL |
|