Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C20H25FN2O3S |
| Molecular Weight | 392.488 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC(=O)C1=CC=C(C=C1)C2=CC=C(C=C2)[C@](C)(F)CNS(=O)(=O)C(C)C
InChI
InChIKey=MFJKNXILEXBWNQ-HXUWFJFHSA-N
InChI=1S/C20H25FN2O3S/c1-14(2)27(25,26)23-13-20(3,21)18-11-9-16(10-12-18)15-5-7-17(8-6-15)19(24)22-4/h5-12,14,23H,13H2,1-4H3,(H,22,24)/t20-/m1/s1
| Molecular Formula | C20H25FN2O3S |
| Molecular Weight | 392.488 |
| 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
Mon Mar 31 21:44:42 GMT 2025
by
admin
on
Mon Mar 31 21:44:42 GMT 2025
|
| Record UNII |
3NKZ7DGF3R
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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Preferred Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
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305447-04-5
Created by
admin on Mon Mar 31 21:44:42 GMT 2025 , Edited by admin on Mon Mar 31 21:44:42 GMT 2025
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SUPERSEDED | |||
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625820-83-9
Created by
admin on Mon Mar 31 21:44:42 GMT 2025 , Edited by admin on Mon Mar 31 21:44:42 GMT 2025
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PRIMARY | |||
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LY-503430
Created by
admin on Mon Mar 31 21:44:42 GMT 2025 , Edited by admin on Mon Mar 31 21:44:42 GMT 2025
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PRIMARY | |||
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DTXSID601027439
Created by
admin on Mon Mar 31 21:44:42 GMT 2025 , Edited by admin on Mon Mar 31 21:44:42 GMT 2025
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PRIMARY | |||
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3NKZ7DGF3R
Created by
admin on Mon Mar 31 21:44:42 GMT 2025 , Edited by admin on Mon Mar 31 21:44:42 GMT 2025
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PRIMARY | |||
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122164792
Created by
admin on Mon Mar 31 21:44:42 GMT 2025 , Edited by admin on Mon Mar 31 21:44:42 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET->POSITIVE ALLOSTERIC MODULATOR (PAM) |
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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