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

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
Structure of 5-VINYLDEOXYURIDINE

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

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
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

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 08:32:58 GMT 2023
Edited
by admin
on Sat Dec 16 08:32:58 GMT 2023
Record UNII
87V72AT994
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5-VINYLDEOXYURIDINE
Systematic Name English
5-VINYL-2'-DEOXYURIDINE
Systematic Name English
Code System Code Type Description
PUBCHEM
148744
Created by admin on Sat Dec 16 08:32:58 GMT 2023 , Edited by admin on Sat Dec 16 08:32:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID10970866
Created by admin on Sat Dec 16 08:32:58 GMT 2023 , Edited by admin on Sat Dec 16 08:32:58 GMT 2023
PRIMARY
FDA UNII
87V72AT994
Created by admin on Sat Dec 16 08:32:58 GMT 2023 , Edited by admin on Sat Dec 16 08:32:58 GMT 2023
PRIMARY
CAS
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
PRIMARY
Related Record Type Details
ACTIVE MOIETY