Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H20N2O.ClH |
| Molecular Weight | 268.782 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCC(=O)N(C1CCNCC1)C2=CC=CC=C2
InChI
InChIKey=KQGAIRYUMBGZQC-UHFFFAOYSA-N
InChI=1S/C14H20N2O.ClH/c1-2-14(17)16(12-6-4-3-5-7-12)13-8-10-15-11-9-13;/h3-7,13,15H,2,8-11H2,1H3;1H
| 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 |
| Molecular Formula | C14H20N2O |
| Molecular Weight | 232.3214 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Development of an enzyme-linked immunosorbent assay for fentanyl and applications of fentanyl antibody-coated nanoparticles for sample preparation. | 2006 Jun 16 |
|
| Development of novel enkephalin analogues that have enhanced opioid activities at both mu and delta opioid receptors. | 2007 Nov 1 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 19:11:49 GMT 2023
by
admin
on
Sat Dec 16 19:11:49 GMT 2023
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| Record UNII |
QZN69FF3RF
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| Record Status |
Validated (UNII)
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| Record Version |
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68720038
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22352-81-4
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admin on Sat Dec 16 19:11:50 GMT 2023 , Edited by admin on Sat Dec 16 19:11:50 GMT 2023
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DTXSID10858216
Created by
admin on Sat Dec 16 19:11:50 GMT 2023 , Edited by admin on Sat Dec 16 19:11:50 GMT 2023
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QZN69FF3RF
Created by
admin on Sat Dec 16 19:11:50 GMT 2023 , Edited by admin on Sat Dec 16 19:11:50 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
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