Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C24H32N4O3 |
| Molecular Weight | 424.5359 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCOC1=CC=C(CC2=NC3=CC(=CC=C3N2CCN(CC)CC)[N+]([O-])=O)C=C1
InChI
InChIKey=UZZPOLCDCVWLAZ-UHFFFAOYSA-N
InChI=1S/C24H32N4O3/c1-4-7-16-31-21-11-8-19(9-12-21)17-24-25-22-18-20(28(29)30)10-13-23(22)27(24)15-14-26(5-2)6-3/h8-13,18H,4-7,14-17H2,1-3H3
| Molecular Formula | C24H32N4O3 |
| Molecular Weight | 424.5359 |
| 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 18:55:13 GMT 2023
by
admin
on
Sat Dec 16 18:55:13 GMT 2023
|
| Record UNII |
C4CE9FVR7N
|
| 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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Common Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Code | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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DEA NO. |
9751
Created by
admin on Sat Dec 16 18:55:13 GMT 2023 , Edited by admin on Sat Dec 16 18:55:13 GMT 2023
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WIKIPEDIA |
Designer-drugs-Butonitazene
Created by
admin on Sat Dec 16 18:55:13 GMT 2023 , Edited by admin on Sat Dec 16 18:55:13 GMT 2023
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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156588955
Created by
admin on Sat Dec 16 18:55:13 GMT 2023 , Edited by admin on Sat Dec 16 18:55:13 GMT 2023
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PRIMARY | |||
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95810-54-1
Created by
admin on Sat Dec 16 18:55:13 GMT 2023 , Edited by admin on Sat Dec 16 18:55:13 GMT 2023
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PRIMARY | |||
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C4CE9FVR7N
Created by
admin on Sat Dec 16 18:55:13 GMT 2023 , Edited by admin on Sat Dec 16 18:55:13 GMT 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
TARGET -> AGONIST |
Butonitazene is tens of times superior to morphine when administered intravenously, as was found in chemical studies in rodents. Emax=103% of Fentanyl. beta-Arrestin assay
EC50
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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