Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C6H14N2O |
| Molecular Weight | 130.1882 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C[C@H](N)C(N)=O
InChI
InChIKey=FORGMRSGVSYZQR-YFKPBYRVSA-N
InChI=1S/C6H14N2O/c1-4(2)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H2,8,9)/t5-/m0/s1
| Molecular Formula | C6H14N2O |
| Molecular Weight | 130.1882 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Chiral inversion of (R)-(-)-fenoprofen in guinea-pigs pretreated with clofibrate. | 2002 Jun |
|
| Identification of cytosolic leucyl aminopeptidase (EC 3.4.11.1) as the major cysteinylglycine-hydrolysing activity in rat liver. | 2003 Feb |
|
| First total synthesis of leucamide A. | 2003 Feb 21 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:01:04 GMT 2025
by
admin
on
Mon Mar 31 22:01:04 GMT 2025
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| Record UNII |
RP28A6538M
|
| Record Status |
Validated (UNII)
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| Record Version |
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21349
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69640
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RP28A6538M
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687-51-4
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DTXSID80883555
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211-696-2
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