Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H14N4O.C2H4O2 |
| Molecular Weight | 290.3177 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(O)=O.O=C1NC(=NC2=C1C=CC=C2)N3CCNCC3
InChI
InChIKey=NGEOOZRNZHUVFZ-UHFFFAOYSA-N
InChI=1S/C12H14N4O.C2H4O2/c17-11-9-3-1-2-4-10(9)14-12(15-11)16-7-5-13-6-8-16;1-2(3)4/h1-4,13H,5-8H2,(H,14,15,17);1H3,(H,3,4)
| Molecular Formula | C12H14N4O |
| Molecular Weight | 230.2658 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C2H4O2 |
| Molecular Weight | 60.052 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: map04911 Sources: https://www.ncbi.nlm.nih.gov/pubmed/788428 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:27:10 GMT 2025
by
admin
on
Mon Mar 31 23:27:10 GMT 2025
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| Record UNII |
E62XS34V5I
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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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Common Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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CENTPIPERALONE
Created by
admin on Mon Mar 31 23:27:10 GMT 2025 , Edited by admin on Mon Mar 31 23:27:10 GMT 2025
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PRIMARY | 22587-29-7(centpiperalone) Product Description | ||
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135449338
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DTXSID90177114
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admin on Mon Mar 31 23:27:10 GMT 2025 , Edited by admin on Mon Mar 31 23:27:10 GMT 2025
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327690
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admin on Mon Mar 31 23:27:10 GMT 2025 , Edited by admin on Mon Mar 31 23:27:10 GMT 2025
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22587-29-7
Created by
admin on Mon Mar 31 23:27:10 GMT 2025 , Edited by admin on Mon Mar 31 23:27:10 GMT 2025
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PRIMARY | |||
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E62XS34V5I
Created by
admin on Mon Mar 31 23:27:10 GMT 2025 , Edited by admin on Mon Mar 31 23:27:10 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
The insulin releasing effect of Centpiperalone (CP) leading to blood sugar lowering has been established. Presently, CP-induced changes on insulin biosynthesis has been studied in isolated rat islets. CP at 1 hr incubation acts mainly on insulin liberation but after 3 hr, it partly stimulates (pro) insulin biosynthesis along with the induction of cathepsin-B enzyme. During simultaneous use of CP and D-glucose at optimum concentrations, decrease in 3H-leucine incorporation in insulin was seen in comparison to values obtained by use of CP alone. The results suggest that CP not only stimulates insulin release profoundly but also directly or indirectly enhances insulin biosynthesis.
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