U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Structure of EDOXUDINE

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

HIDE SMILES / InChI
Edoxudine (5-ethyl-2'-deoxyuridine), an antiviral drug, has been clinically studied against the recurrent genital herpes.

Approval Year

PubMed

PubMed

TitleDatePubMed
Antiviral activity of 2,3'-anhydro and related pyrimidine nucleosides against hepatitis B virus.
2010-11-15
3D-QSAR studies on antitubercular thymidine monophosphate kinase inhibitors based on different alignment methods.
2006-02-15
Synthesis and in vitro anti-mycobacterial activity of 5-substituted pyrimidine nucleosides.
2005-12-15
Design of Mycobacterium tuberculosis thymidine monophosphate kinase inhibitors.
2003-10-21
Thymidine and thymidine-5'-O-monophosphate analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase.
2003-09-15
Comparative study of purine and pyrimidine nucleoside analogues acting on the thymidylate kinases of Mycobacterium tuberculosis and of humans.
2003-08-04
Synthesis and antiviral activity of novel 5-(1-cyanamido-2-haloethyl) and 5-(1-hydroxy(or methoxy)-2-azidoethyl) analogues of uracil nucleosides.
2001-10-11
Vaccinia virus inhibitors as a paradigm for the chemotherapy of poxvirus infections.
2001-04
Anti-(herpes simplex virus) activity of 4'-thio-2'-deoxyuridines: a biochemical investigation for viral and cellular target enzymes.
2000-10-15
Structure-activity relationship of the affinity of 5-substituted uracil nucleoside analogues for varicella-zoster virus thymidine kinase and their activity against varicella-zoster virus.
1997-08
Synthesis of new acyclic pyrimidine nucleoside analogs as potential antiviral drugs.
1994-09-16
Synthesis and antiviral activity of novel 5-(1-azido-2-haloethyl) and 5-(1-azido-, amino-, or methoxyethyl) analogs of 2'-deoxyuridine.
1993-08-20
Synthesis and antiviral activity of phosphonoacetic and phosphonoformic acid esters of 5-bromo-2'-deoxyuridine and related pyrimidine nucleosides and acyclonucleosides.
1989-02
Incorporation and metabolism of 2'-fluoro-5-substituted arabinosyl pyrimidines and their selective inhibition of viral DNA synthesis in herpes simplex virus type 1 (HSV-1)-infected and mock-infected Vero cells.
1988-12-01
Synthesis and antitumor and antiviral properties of 5-alkyl-2'-deoxyuridines, 3',5'-cyclic monophosphates, and neutral cyclic triesters.
1986-04
Comparison of susceptibilities of varicella-zoster virus and herpes simplex viruses to nucleoside analogs.
1986-03
Activities of 1-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-iodocytosine and its metabolites against herpes simplex virus types 1 and 2 in cell culture and in mice infected intracerebrally with herpes simplex virus type 2.
1986-01
Synthesis and antiviral activity of the carbocyclic analogues of 5-ethyl-2'-deoxyuridine and of 5-ethynyl-2'-deoxyuridine.
1986-01
Selective in vitro and in vivo activities of 5-(2-haloalkyl)pyrimidine nucleoside analogs, particularly 5-(2-chloroethyl)-2'-deoxyuridine, against herpes simplex virus.
1985-08
5-substituted deoxyuridines--structural requirements for antiviral activity against herpes simplex virus types 1 and 2 and possible biochemical basis for relative potency.
1984-06
Antiherpes activity of (E)-5-(2-bromovinyl)- and 5-vinyl-1-beta-D-arabinofuranosyluracil and some other 5-substituted uracil arabinosyl nucleosides in two different cell lines.
1983-09
Susceptibility of recent clinical isolates of herpes simplex virus to 5-ethyl-2'-deoxyuridine: preferential inhibition of herpes simplex virus type 2.
1983-05
In vitro susceptibility of varicella-zoster virus to E-5-(2-bromovinyl)-2'-deoxyuridine and related compounds.
1982-01
The 5'-monophosphates of 5-propyl- and 5-ethyl-2'-deoxyuridine do not inhibit the replication of deoxythymidine kinase deficient (TK-) mutants of herpes simplex virus.
1980-10-15
Combination chemotherapy: interaction of 5-methoxymethyldeoxyuridine with adenine arabinoside, 5-ethyldeoxyuridine, 5-iododeoxyuridine, and phosphonoacetic acid against herpes simplex virus types 1 and 2.
1980-04
Relative potencies of different anti-herpes agents in the topical treatment of cutaneous herpes simplex virus infection of athymic nude mice.
1979-11
In vitro antiherpesviral activity of 5-alkyl derivatives of 1-beta-D-arabinofuranosyluracil.
1979-08
(E)-5-(2-Bromovinyl)-2'-deoxyuridine: a potent and selective anti-herpes agent.
1979-06
Effect of treatment with 5-ethyl-2'-deoxyuridine on herpes simplex virus encephalitis in normal and immunosuppressed mice.
1978-11
5-Propyl-2'-deoxyuridine: a specific anti-herpes agent.
1978-03
Antiviral action and cellular toxicity of four thymidine analogues: 5-ethyl-,5-vinyl-, 5-propyl-, and 5-allyl-2'- deoxyuridine.
1976-07
Effect of cytosine, arabinoside, iododeoxyuridine, ethyldeoxyuridine, thiocyanatodeoxyuridine, and ribavirin on tail lesion formation in mice infected with vaccinia virus.
1976-03
13-Alkylpyrimidine nucleosides. Preparation and properties of 5-ethyl-2'-deoxycytidine and related nucleosides.
1974-03
Patents

Sample Use Guides

topical edoxudine 3.0% cream
Route of Administration: Topical
Name Type Language
EDOXUDINE
INN   MART.   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
NSC-758405
Preferred Name English
EDU
Common Name English
URIDINE, 2'-DEOXY-5-ETHYL-
Systematic Name English
2'-DEOXY-5-ETHYLURIDINE
Systematic Name English
ORF-15817
Code English
EDOXUDINE [USAN]
Common Name English
EUDR
Common Name English
Edoxudine [WHO-DD]
Common Name English
5-ETHYL-3-(2'-DEOXYRIBOSYL)URACIL
Common Name English
EDOXUDINE [MI]
Common Name English
ORF 15817
Code English
RWJ-15817
Code English
RWJ 15817
Code English
5-ETHYL-2'-DEOXYURIDINE
Systematic Name English
edoxudine [INN]
Common Name English
EDOXUDINE [MART.]
Common Name English
Classification Tree Code System Code
WHO-VATC QD06BB09
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
WHO-ATC D06BB09
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
NCI_THESAURUS C29575
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
NCI_THESAURUS C281
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
Code System Code Type Description
CAS
15176-29-1
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
SMS_ID
100000080512
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
ChEMBL
CHEMBL318153
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
EVMPD
SUB06460MIG
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
MERCK INDEX
m4833
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY Merck Index
PUBCHEM
66377
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
NSC
758405
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
EPA CompTox
DTXSID4045890
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
RXCUI
49428
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY RxNorm
NCI_THESAURUS
C87662
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
FDA UNII
15ZQM81Y3R
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
MESH
C022811
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
ECHA (EC/EINECS)
239-226-1
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
DRUG BANK
DB13421
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
INN
5512
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
DRUG CENTRAL
3173
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
WIKIPEDIA
EDOXUDINE
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY
USAN
U-62
Created by admin on Mon Mar 31 17:56:02 GMT 2025 , Edited by admin on Mon Mar 31 17:56:02 GMT 2025
PRIMARY