Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H16N2O4 |
| Molecular Weight | 276.2878 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCOCN1C=C(CC2=CC=CC=C2)C(=O)NC1=O
InChI
InChIKey=SPJAGILXQBHHSZ-UHFFFAOYSA-N
InChI=1S/C14H16N2O4/c17-6-7-20-10-16-9-12(13(18)15-14(16)19)8-11-4-2-1-3-5-11/h1-5,9,17H,6-8,10H2,(H,15,18,19)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 5-benzylacyclouridine and 5-benzyloxybenzylacyclouridine, potent inhibitors of uridine phosphorylase. | 1982 May 15 |
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| Different effect of benzylacyclouridine on the toxic and therapeutic effects of azidothymidine in mice. | 1990 Dec 1 |
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| Benzylacyclouridine reverses azidothymidine-induced marrow suppression without impairment of anti-human immunodeficiency virus activity. | 1990 Dec 1 |
|
| Modulation of uridine phosphorylase gene expression by tumor necrosis factor-alpha enhances the antiproliferative activity of the capecitabine intermediate 5'-deoxy-5-fluorouridine in breast cancer cells. | 2006 Apr |
Patents
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| Code System | Code | Type | Description | ||
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DB07437
Created by
admin on Mon Mar 31 17:59:01 GMT 2025 , Edited by admin on Mon Mar 31 17:59:01 GMT 2025
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82857-69-0
Created by
admin on Mon Mar 31 17:59:01 GMT 2025 , Edited by admin on Mon Mar 31 17:59:01 GMT 2025
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41037
Created by
admin on Mon Mar 31 17:59:01 GMT 2025 , Edited by admin on Mon Mar 31 17:59:01 GMT 2025
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0H851I3O9D
Created by
admin on Mon Mar 31 17:59:01 GMT 2025 , Edited by admin on Mon Mar 31 17:59:01 GMT 2025
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DTXSID30232034
Created by
admin on Mon Mar 31 17:59:01 GMT 2025 , Edited by admin on Mon Mar 31 17:59:01 GMT 2025
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54929
Created by
admin on Mon Mar 31 17:59:01 GMT 2025 , Edited by admin on Mon Mar 31 17:59:01 GMT 2025
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ACTIVE MOIETY
