Approval Year
| Substance Class |
Protein
Created
by
admin
on
Edited
Tue Apr 01 19:08:57 GMT 2025
by
admin
on
Tue Apr 01 19:08:57 GMT 2025
|
| Protein Sub Type | |
| Sequence Type | COMPLETE |
| Record UNII |
7J9Y28299R
|
| Record Status |
Validated (UNII)
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| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Common Name | English | ||
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Preferred Name | English | ||
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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 | ||
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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 | ||
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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 | ||
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Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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7J9Y28299R
Created by
admin on Tue Apr 01 19:08:57 GMT 2025 , Edited by admin on Tue Apr 01 19:08:57 GMT 2025
|
PRIMARY | |||
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HER2/neu
Created by
admin on Tue Apr 01 19:08:57 GMT 2025 , Edited by admin on Tue Apr 01 19:08:57 GMT 2025
|
PRIMARY | |||
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P04626
Created by
admin on Tue Apr 01 19:08:57 GMT 2025 , Edited by admin on Tue Apr 01 19:08:57 GMT 2025
|
PRIMARY |
| From | To |
|---|---|
| 1_4 | 1_31 |
| 1_140 | 1_170 |
| 1_173 | 1_182 |
| 1_177 | 1_190 |
| 1_198 | 1_205 |
| 1_202 | 1_213 |
| 1_214 | 1_222 |
| 1_218 | 1_230 |
| 1_233 | 1_242 |
| 1_246 | 1_273 |
| 1_277 | 1_289 |
| 1_293 | 1_309 |
| 1_312 | 1_316 |
| 1_320 | 1_345 |
| 1_453 | 1_482 |
| 1_489 | 1_498 |
| 1_493 | 1_506 |
| 1_509 | 1_518 |
| 1_522 | 1_538 |
| 1_541 | 1_554 |
| 1_545 | 1_562 |
| 1_565 | 1_574 |
| 1_578 | 1_601 |
| 1_604 | 1_612 |
| 1_608 | 1_620 |
| Glycosylation Type | HUMAN |
| Glycosylation Link Type | Site |
|---|---|
| N | 1_46 |
| N | 1_102 |
| N | 1_165 |
| N | 1_237 |
| N | 1_508 |
| N | 1_549 |
| N | 1_607 |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
INHIBITOR -> TARGET |
|
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|
WEAK INHIBITOR->TARGET |
IC50
|
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LIGAND->TARGET |
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WEAK 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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INHIBITOR -> TARGET |
IgG1 bispecific antibody with enhanced antibody-dependent cell-mediated cytotoxicity (ADCC) activity targeting HER2 and HER3 receptors.
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CONJUGATED TOXIN->TARGET |
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INHIBITOR -> TARGET |
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LIGAND->TARGET | |||
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CONJUGATED TOXIN->TARGET | |||
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INHIBITOR -> TARGET |
BINDING
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INHIBITOR -> TARGET | |||
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RADIOLIGAND->TARGET |
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INHIBITOR -> TARGET | |||
|
INHIBITOR -> TARGET |
IRREVERSIBLE INHIBITOR
IC50
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LIGAND->TARGET |
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CONJUGATED TOXIN->TARGET |
MRG002 potently inhibited proliferation of HER2 expressing cancer cells in vitro with IC50 ranged from 1.8±0.8 to 59.9±8.9 ng/mL,
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INHIBITOR -> TARGET | |||
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INHIBITOR -> TARGET |
IC50
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WEAK INHIBITOR->TARGET |
IC50
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LIGAND->TARGET |
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INHIBITOR -> TARGET |
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INHIBITOR -> TARGET |
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VACCINE ANTIGEN->TARGET |
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INHIBITOR -> TARGET |
IC50
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INHIBITOR -> TARGET | |||
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LIGAND->TARGET | |||
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CONJUGATED TOXIN->TARGET |
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INHIBITOR -> TARGET | |||
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CYTOTOXIC T-CELL->TARGET |
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INHIBITOR -> TARGET |
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CONJUGATED TOXIN->TARGET |
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LIGAND->TARGET |
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|
LIGAND->TARGET | |||
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INHIBITOR -> TARGET |
IC50
|
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INHIBITOR -> TARGET |
IRREVERSIBLE INHIBITOR
IC50
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||
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INHIBITOR -> TARGET | |||
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ANTIGEN->TARGET |
Identified as a definitive diagnostic marker, key driver and therapeutic target for chordoma, a malignant tumor that arises from remnant notochordal cells lodged in the vertebrae
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INHIBITOR -> TARGET |
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CONJUGATED TOXIN->TARGET |
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INHIBITOR -> TARGET |
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LIGAND->TARGET |
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LIGAND->TARGET |
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INHIBITOR -> TARGET | |||
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ANTIGEN->TARGET | |||
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INHIBITOR -> TARGET |
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INHIBITOR -> TARGET |
irreversible selective inhibitor
IRREVERSIBLE INHIBITOR
IC50
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INHIBITOR -> TARGET |
|
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RADIOLIGAND->TARGET |
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|
|
INHIBITOR -> TARGET | |||
|
|
CONJUGATED TOXIN->TARGET |
|
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|
ANTIGEN->TARGET |
|
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|
INHIBITOR -> TARGET |
|
||
|
CONJUGATED TOXIN->TARGET |
|
||
|
|
INHIBITOR -> TARGET | |||
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RADIOLIGAND->TARGET |
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INHIBITOR -> TARGET |
BMS-690514 metabolite M2 showed HER2 inhibition similar to that of BMS-690514.
IC50
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INHIBITOR -> TARGET | |||
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INHIBITOR -> TARGET | |||
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INHIBITOR->OFF-TARGET |
IC50
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INHIBITOR -> TARGET | |||
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INHIBITOR -> TARGET | |||
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VACCINE ANTIGEN->TARGET |
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LIGAND->TARGET |
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INHIBITOR -> TARGET | |||
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INHIBITOR -> TARGET |
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Structural Modifications
| Modification Type | Location Site | Location Type | Residue Modified | Extent | Fragment Name | Fragment Approval |
|---|---|---|---|---|---|---|
| AMINO ACID SUBSTITUTION | [1_1117] [1_1174] [1_1226] | TYROSINE | TYROSINE O-PHOSPHATE | 2R86C98KDX | ||
| AMINO ACID SUBSTITUTION | [1_1032] [1_1056] [1_1061] [1_1085] [1_1129] | SERINE | DEXFOSFOSERINE | VI4F0K069V |
| Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
|---|---|---|---|---|---|---|
| Molecular Formula | CHEMICAL |
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| MOL_WEIGHT | CHEMICAL |
|