Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C11H16N2O5 |
Molecular Weight | 256.2551 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC1=CN([C@H]2C[C@H](O)[C@@H](CO)O2)C(=O)NC1=O
InChI
InChIKey=XACKNLSZYYIACO-DJLDLDEBSA-N
InChI=1S/C11H16N2O5/c1-2-6-4-13(11(17)12-10(6)16)9-3-7(15)8(5-14)18-9/h4,7-9,14-15H,2-3,5H2,1H3,(H,12,16,17)/t7-,8+,9+/m0/s1
Approval Year
PubMed
Title | Date | PubMed |
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Relative potencies of different anti-herpes agents in the topical treatment of cutaneous herpes simplex virus infection of athymic nude mice. | 1979 Nov |
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Synthesis and antitumor and antiviral properties of 5-alkyl-2'-deoxyuridines, 3',5'-cyclic monophosphates, and neutral cyclic triesters. | 1986 Apr |
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Comparison of susceptibilities of varicella-zoster virus and herpes simplex viruses to nucleoside analogs. | 1986 Mar |
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Thymidine and thymidine-5'-O-monophosphate analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase. | 2003 Sep 15 |
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3D-QSAR studies on antitubercular thymidine monophosphate kinase inhibitors based on different alignment methods. | 2006 Feb 15 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1894930
topical edoxudine 3.0% cream
Route of Administration:
Topical
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WHO-VATC |
QD06BB09
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WHO-ATC |
D06BB09
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NCI_THESAURUS |
C29575
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NCI_THESAURUS |
C281
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15176-29-1
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100000080512
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CHEMBL318153
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SUB06460MIG
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m4833
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66377
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758405
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DTXSID4045890
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49428
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C87662
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15ZQM81Y3R
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C022811
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239-226-1
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DB13421
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3173
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EDOXUDINE
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U-62
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ACTIVE MOIETY