Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H23N3O |
| Molecular Weight | 285.384 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC1=C(NN(C2CCN(C)CC2)C1=O)C3=CC=CC=C3
InChI
InChIKey=LBFGQUCAQWAFNN-UHFFFAOYSA-N
InChI=1S/C17H23N3O/c1-3-15-16(13-7-5-4-6-8-13)18-20(17(15)21)14-9-11-19(2)12-10-14/h4-8,14,18H,3,9-12H2,1-2H3
| Molecular Formula | C17H23N3O |
| Molecular Weight | 285.384 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
PubMed
| Title | Date | PubMed |
|---|---|---|
| A study of the inhibition of adrenaline-induced vasoconstriction in the isolated perfused liver of rabbit. | 1990-11 |
|
| [Separation of some compound drugs by the method of column chromatography. II. Separation of 1-N-methylpiperidyl-(4')-3-phenyl-4-ethylpyrazolone-(5) (piperylone) from sodium (4-methylamino-2,3-dimethyl-1-phenylpyrazolone-5) salt of methane sulfonic acid (pyralgin)]. | 1968 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:57:34 GMT 2025
by
admin
on
Mon Mar 31 17:57:34 GMT 2025
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| Record UNII |
XWH5VH1L2F
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Official Name | English | ||
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| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C29698
Created by
admin on Mon Mar 31 17:57:34 GMT 2025 , Edited by admin on Mon Mar 31 17:57:34 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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Piperylone
Created by
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2531-04-6
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SUB09873MIG
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PRIMARY | |||
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C66401
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XWH5VH1L2F
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100000082213
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CHEMBL2104576
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1028
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219-788-4
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17319
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DTXSID90179956
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m894
Created by
admin on Mon Mar 31 17:57:34 GMT 2025 , Edited by admin on Mon Mar 31 17:57:34 GMT 2025
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PRIMARY | Merck Index |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |