Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C11H14N2O5 |
Molecular Weight | 254.2393 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC[C@H]1O[C@H](C[C@@H]1O)N2C=C(C=C)C(=O)NC2=O
InChI
InChIKey=YAAQOXBNCODRSI-DJLDLDEBSA-N
InChI=1S/C11H14N2O5/c1-2-6-4-13(11(17)12-10(6)16)9-3-7(15)8(5-14)18-9/h2,4,7-9,14-15H,1,3,5H2,(H,12,16,17)/t7-,8+,9+/m0/s1
Molecular Formula | C11H14N2O5 |
Molecular Weight | 254.2393 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Antiviral action and cellular toxicity of four thymidine analogues: 5-ethyl-,5-vinyl-, 5-propyl-, and 5-allyl-2'- deoxyuridine. | 1976 Jul |
|
(E)-5-(2-Bromovinyl)-2'-deoxyuridine: a potent and selective anti-herpes agent. | 1979 Jun |
|
Synthesis and antiviral activity of phosphonoacetic and phosphonoformic acid esters of 5-bromo-2'-deoxyuridine and related pyrimidine nucleosides and acyclonucleosides. | 1989 Feb |
|
Vaccinia virus inhibitors as a paradigm for the chemotherapy of poxvirus infections. | 2001 Apr |
|
Synthesis and biological investigations of 5-substituted pyrimidine nucleosides coupled to a dihydropyridine/pyridinium salt redox chemical delivery system. | 2001 Nov |
|
Synthesis and in vitro anti-mycobacterial activity of 5-substituted pyrimidine nucleosides. | 2005 Dec 15 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:32:58 GMT 2023
by
admin
on
Sat Dec 16 08:32:58 GMT 2023
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Record UNII |
87V72AT994
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Record Status |
Validated (UNII)
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Record Version |
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DTXSID10970866
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87V72AT994
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55520-67-7
Created by
admin on Sat Dec 16 08:32:58 GMT 2023 , Edited by admin on Sat Dec 16 08:32:58 GMT 2023
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