Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H18N2O2 |
| Molecular Weight | 198.2621 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@H](N)CN1CC[C@@H]2OC(C)=O
InChI
InChIKey=YYIUHLPAZILPSG-GUBZILKMSA-N
InChI=1S/C10H18N2O2/c1-7(13)14-10-4-5-12-6-8(11)2-3-9(10)12/h8-10H,2-6,11H2,1H3/t8-,9-,10-/m0/s1
| Molecular Formula | C10H18N2O2 |
| Molecular Weight | 198.2621 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Biosynthesis of slaframine, (1S,6S,8aS)-1-acetoxy-6-aminooctahydroindolizine, a parasympathomimetic alkaloid of fungal origin. II. The origin of pipecolic acid. | 1973 Oct 9 |
|
| Biosynthesis of slaframine, (1S,6S,8aS)-1-acetoxy-6-aminooctahydroindolizine, a parasympathomimetic alkaloid of fungal origin. I. Pipecolic acid and slaframine biogenesis. | 1973 Oct 9 |
|
| Biosynthesis of slaframine, (1S,6S,8aS)-1-acetoxy-6-aminooctahydroindolizine, a parasympathomimetic alkaloid of fungal origin. 4. Metabolic fate of ethyl pipecolylacetate, 1,3-dioxooctahydroindolizine, and 1-hydroxyoctahydroindolizine in Rhizoctonia leguminicola. | 1979 Aug 21 |
|
| Biosynthesis of slaframine, (1S,6S,8aS)-1-acetoxy-6-aminooctahydroindolizine, a parasympathomimetic alkaloid of fungal origin. 3. Origin of the pyrrolidine ring. | 1979 Aug 21 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:29:28 GMT 2023
by
admin
on
Fri Dec 15 18:29:28 GMT 2023
|
| Record UNII |
51H2386GWI
|
| Record Status |
Validated (UNII)
|
| Record Version |
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-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Common Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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SLAFRAMINE
Created by
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DTXSID50942108
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51H2386GWI
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C009275
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88363
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20084-93-9
Created by
admin on Fri Dec 15 18:29:28 GMT 2023 , Edited by admin on Fri Dec 15 18:29:28 GMT 2023
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PRIMARY |