Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H26N4O2 |
| Molecular Weight | 318.4139 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1N=C(C)C(NCCNCC(O)COC2=CC=CC=C2)=C1C
InChI
InChIKey=CRKZWPJRHFAGCJ-UHFFFAOYSA-N
InChI=1S/C17H26N4O2/c1-13-17(14(2)21(3)20-13)19-10-9-18-11-15(22)12-23-16-7-5-4-6-8-16/h4-8,15,18-19,22H,9-12H2,1-3H3
| Molecular Formula | C17H26N4O2 |
| Molecular Weight | 318.4139 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:22:59 GMT 2025
by
admin
on
Mon Mar 31 18:22:59 GMT 2025
|
| Record UNII |
7GDN12Q42M
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Preferred Name | English | ||
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Official Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C29576
Created by
admin on Mon Mar 31 18:22:59 GMT 2025 , Edited by admin on Mon Mar 31 18:22:59 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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81528-80-5
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DTXSID50868617
Created by
admin on Mon Mar 31 18:22:59 GMT 2025 , Edited by admin on Mon Mar 31 18:22:59 GMT 2025
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100000083994
Created by
admin on Mon Mar 31 18:22:59 GMT 2025 , Edited by admin on Mon Mar 31 18:22:59 GMT 2025
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5992
Created by
admin on Mon Mar 31 18:22:59 GMT 2025 , Edited by admin on Mon Mar 31 18:22:59 GMT 2025
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SUB06889MIG
Created by
admin on Mon Mar 31 18:22:59 GMT 2025 , Edited by admin on Mon Mar 31 18:22:59 GMT 2025
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Dalbraminol
Created by
admin on Mon Mar 31 18:22:59 GMT 2025 , Edited by admin on Mon Mar 31 18:22:59 GMT 2025
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205958
Created by
admin on Mon Mar 31 18:22:59 GMT 2025 , Edited by admin on Mon Mar 31 18:22:59 GMT 2025
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PRIMARY | |||
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7GDN12Q42M
Created by
admin on Mon Mar 31 18:22:59 GMT 2025 , Edited by admin on Mon Mar 31 18:22:59 GMT 2025
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PRIMARY | |||
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C74200
Created by
admin on Mon Mar 31 18:22:59 GMT 2025 , Edited by admin on Mon Mar 31 18:22:59 GMT 2025
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CHEMBL2106134
Created by
admin on Mon Mar 31 18:22:59 GMT 2025 , Edited by admin on Mon Mar 31 18:22:59 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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|
ENANTIOMER -> RACEMATE | |||
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|
ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |