Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H11N3.H3O4P |
| Molecular Weight | 235.1775 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OP(O)(O)=O.CC(C)NC1=NC=CC=N1
InChI
InChIKey=CXEBHWXMQKIKPJ-UHFFFAOYSA-N
InChI=1S/C7H11N3.H3O4P/c1-6(2)10-7-8-4-3-5-9-7;1-5(2,3)4/h3-6H,1-2H3,(H,8,9,10);(H3,1,2,3,4)
| Molecular Formula | C7H11N3 |
| Molecular Weight | 137.1823 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | H3O4P |
| Molecular Weight | 97.9952 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Isaxonine (N-isopropyl-amino-2-pyrimidine orthophosphate) is able to accelerate nerve regeneration and functional recovery. Isaxonine has specific affinity for peripheral nerves. It acts directly on the neuron or indirectly by stimulating the production of a growth factor remains unknown. It demonstrates activity in the treatment of neuropathies of various etiology. Isaxonine treatment may be associated with hepatotoxicity.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:01:15 GMT 2023
by
admin
on
Sat Dec 16 10:01:15 GMT 2023
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| Record UNII |
S52Q6EHI7F
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| Record Status |
Validated (UNII)
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| Record Version |
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m249
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admin on Sat Dec 16 10:01:16 GMT 2023 , Edited by admin on Sat Dec 16 10:01:16 GMT 2023
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163093
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S52Q6EHI7F
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65606-21-5
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DTXSID70215861
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265-845-1
Created by
admin on Sat Dec 16 10:01:16 GMT 2023 , Edited by admin on Sat Dec 16 10:01:16 GMT 2023
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