Details
| Stereochemistry | UNKNOWN |
| Molecular Formula | C9H14N4O |
| Molecular Weight | 194.2337 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(N1CC1C#N)N2CC2C(N)=O
InChI
InChIKey=RPZOFMHRRHHDPZ-UHFFFAOYSA-N
InChI=1S/C9H14N4O/c1-9(2,12-4-6(12)3-10)13-5-7(13)8(11)14/h6-7H,4-5H2,1-2H3,(H2,11,14)
| Molecular Formula | C9H14N4O |
| Molecular Weight | 194.2337 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Azimexon, a synthetic derivative of the 2-cyanaziridines, possesses the immunorestorative properties that were shown for patients with acquired immunodeficiency syndrome. Besides, azimexon had a role in managing cancer-associated dysregulation of the immune response. It was studied in clinical trials phase I to determine the drug's tolerable dose, toxicity, and effects on immune and nonimmune host defense parameters.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Modulation in vitro of immune parameters in homosexual males with the preclinical complex of symptoms related to acquired immune deficiency syndrome by azimexon. | 1986-06 |
|
| Animal experiments on the compensation of the immunosuppressive action of cyclophosphamide by 2-[-2-cyanaziridinyl-(1)-]-2-[-2-carbamoylaziridinyl-(1)]-propane BM 12 531. | 1978 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2874196
Azimexon was given intravenously daily for 5 days to 19 cancer patients in a Phase I trial
Route of Administration:
Intravenous
| Substance Class |
Chemical
Created
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admin
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Wed Apr 02 08:52:04 GMT 2025
by
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| Record UNII |
4NJ842U6BZ
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| Record Status |
Validated (UNII)
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C797
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C2139
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C2080
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C1347
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264-679-7
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CHEMBL149579
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4NJ842U6BZ
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4546
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SUB05656MIG
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DTXSID60867055
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47294
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64118-86-1
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100000086084
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C016866
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |