Approval Year
Substance Class |
Protein
Created
by
admin
on
Edited
Sat Dec 16 12:11:01 GMT 2023
by
admin
on
Sat Dec 16 12:11:01 GMT 2023
|
Protein Sub Type | |
Sequence Type | COMPLETE |
Record UNII |
1AG1A6ENX6
|
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 |
Code System | Code | Type | Description | ||
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1AG1A6ENX6
Created by
admin on Sat Dec 16 12:11:02 GMT 2023 , Edited by admin on Sat Dec 16 12:11:02 GMT 2023
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PRIMARY |
From | To |
---|---|
1_155 | 1_231 |
Glycosylation Type | HUMAN |
Glycosylation Link Type | Site |
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N | 1_5 |
N | 1_66 |
Related Record | Type | Details | ||
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AGONIST -> TARGET | |||
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INHIBITOR -> TARGET | |||
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AGONIST -> TARGET |
Ki
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INHIBITOR -> TARGET |
Ki
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INHIBITOR -> TARGET |
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INHIBITOR -> TARGET |
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INHIBITOR -> TARGET |
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INHIBITOR -> TARGET |
INHIBITOR
Ki
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AGONIST -> TARGET |
In vitro binding assays revealed that RA-7 possessed higher 5-HT7 receptor affinity than LP-211 and a better selectivity profile over a panel of 5-HT receptor subtypes.
ANTAGONIST
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TARGET -> AGONIST |
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INHIBITOR -> TARGET |
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INHIBITOR -> TARGET |
INHIBITOR
Ki
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INHIBITOR -> TARGET |
Ki
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INHIBITOR -> TARGET | |||
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AGONIST -> TARGET |
Eletriptan binds with high affinity to 5-HT1B, 5-HT1D and 5-HT1F receptors, has modest affinity for 5-HT1A, 5-HT1E, 5-HT2B and 5-HT7 receptors
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INHIBITOR -> TARGET |
ANTAGONIST
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AGONIST -> TARGET | |||
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AGONIST -> TARGET | |||
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INHIBITOR -> TARGET |
Cell:SF9; ligand:3H-5-ct
BINDING
Ki
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AGONIST -> TARGET |
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AGONIST -> TARGET |
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INHIBITOR -> TARGET | |||
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AGONIST -> TARGET |
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Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
---|---|---|---|---|---|---|
MOL_WEIGHT | CHEMICAL |
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