Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H15NO2 |
| Molecular Weight | 157.2102 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC[C@H]1CC[C@H](CC1)C(O)=O
InChI
InChIKey=GYDJEQRTZSCIOI-KNVOCYPGSA-N
InChI=1S/C8H15NO2/c9-5-6-1-3-7(4-2-6)8(10)11/h6-7H,1-5,9H2,(H,10,11)/t6-,7+
| Molecular Formula | C8H15NO2 |
| Molecular Weight | 157.2102 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
Sample Use Guides
When human plasma was mixed with 50 units of urokinase and clotted with thrombin in the presence of S-2251, the hydrolysis of S-2251 in the clot was higher than that in the plasma. The addition of 6-aminohexanoic acid or cis-AMCHA (cis-Tranexamic Acid) showed changes in the rate of plasminogen activation similar to that shown in the presence of tranexamic acid. 1 mM of cis-AMCHA and 6-aminohexanoic acid totally inhibited clot lysis. The presence of 1 mM of these ω-aminoacids remarkably increased the activation of plasminogen by urokinase, but no clot lysis was observed.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:16:33 GMT 2023
by
admin
on
Sat Dec 16 09:16:33 GMT 2023
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| Record UNII |
37YD696II6
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| Record Status |
Validated (UNII)
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| Record Version |
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m11000
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1197-17-7
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37YD696II6
Created by
admin on Sat Dec 16 09:16:33 GMT 2023 , Edited by admin on Sat Dec 16 09:16:33 GMT 2023
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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