Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C19H20N4O2 |
Molecular Weight | 336.3877 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCOC1=CC=C(C=C1)[C@H]2CNC(=O)N2C3=CC4=C(NC=N4)C=C3
InChI
InChIKey=XHIKZWOEFZENIX-GOSISDBHSA-N
InChI=1S/C19H20N4O2/c1-2-9-25-15-6-3-13(4-7-15)18-11-20-19(24)23(18)14-5-8-16-17(10-14)22-12-21-16/h3-8,10,12,18H,2,9,11H2,1H3,(H,20,24)(H,21,22)/t18-/m1/s1
Molecular Formula | C19H20N4O2 |
Molecular Weight | 336.3877 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 16:54:29 GMT 2023
by
admin
on
Sat Dec 16 16:54:29 GMT 2023
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Record UNII |
E3DSH8LL4L
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Record Status |
Validated (UNII)
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Record Version |
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-
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Official Name | English | ||
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Code | English | ||
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Code | English | ||
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Code System | Code | Type | Description | ||
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51030870
Created by
admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
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E3DSH8LL4L
Created by
admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
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C179133
Created by
admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
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300000006000
Created by
admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
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1276021-65-8
Created by
admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
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NCT03919162
Created by
admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
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11664
Created by
admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
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PRIMARY | INN |
Related Record | Type | Details | ||
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TARGET->INHIBITOR OF EXPRESSION |
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TARGET->INHIBITOR OF EXPRESSION |
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SALT/SOLVATE -> PARENT |
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TARGET -> INHIBITOR |
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TARGET->INHIBITOR OF EXPRESSION |
Inhibit conversion of N-terminal Q to pE. formation of pE was prevented by inhibiting isoQC, CCL2 was more prone to N-terminal degradation, which resulted in less functional CCL2 activity. This had the net effect of decreasing monocyte infiltration in vivo, resulting in decreased lung inflammation,
IN-VIVO
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RACEMATE -> ENANTIOMER |
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TARGET -> INHIBITOR |
Inhibit conversion of N-terminal Q to pE. formation of pE was prevented by inhibiting isoQC, CCL2 was more prone to N-terminal degradation, which resulted in less functional CCL2 activity. This had the net effect of decreasing monocyte infiltration in vivo, resulting in decreased lung inflammation.
IN-VITRO
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
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