Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H26N2OS.ClH |
| Molecular Weight | 354.938 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(C)(C)C1=CC(=CC(=C1O)C(C)(C)C)C2=CSC(CN)=N2
InChI
InChIKey=WPWBWGUPSJCKKF-UHFFFAOYSA-N
InChI=1S/C18H26N2OS.ClH/c1-17(2,3)12-7-11(14-10-22-15(9-19)20-14)8-13(16(12)21)18(4,5)6;/h7-8,10,21H,9,19H2,1-6H3;1H
| Molecular Formula | C18H26N2OS |
| Molecular Weight | 318.477 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:35:31 UTC 2023
by
admin
on
Sat Dec 16 08:35:31 UTC 2023
|
| Record UNII |
210NPF5E6J
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Common Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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918656-59-4
Created by
admin on Sat Dec 16 08:35:31 UTC 2023 , Edited by admin on Sat Dec 16 08:35:31 UTC 2023
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PRIMARY | |||
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300000024692
Created by
admin on Sat Dec 16 08:35:31 UTC 2023 , Edited by admin on Sat Dec 16 08:35:31 UTC 2023
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PRIMARY | |||
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72941952
Created by
admin on Sat Dec 16 08:35:31 UTC 2023 , Edited by admin on Sat Dec 16 08:35:31 UTC 2023
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PRIMARY | |||
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210NPF5E6J
Created by
admin on Sat Dec 16 08:35:31 UTC 2023 , Edited by admin on Sat Dec 16 08:35:31 UTC 2023
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PRIMARY | |||
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EU/3/15/1481(POSITIVE)
Created by
admin on Sat Dec 16 08:35:31 UTC 2023 , Edited by admin on Sat Dec 16 08:35:31 UTC 2023
|
PRIMARY | Treatment of Huntington’s disease 24/04/2015 Positive |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
