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Details

Stereochemistry ABSOLUTE
Molecular Formula C11H13IN2O5
Molecular Weight 380.1358
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of 5-(2-IODOVINYL)-2'-DEOXYURIDINE

SMILES

OC[C@H]1O[C@H](C[C@@H]1O)N2C=C(\C=C\I)C(=O)NC2=O

InChI

InChIKey=LOLNFJHUEIDGNH-PIXDULNESA-N
InChI=1S/C11H13IN2O5/c12-2-1-6-4-14(11(18)13-10(6)17)9-3-7(16)8(5-15)19-9/h1-2,4,7-9,15-16H,3,5H2,(H,13,17,18)/b2-1+/t7-,8+,9+/m0/s1

HIDE SMILES / InChI

Molecular Formula C11H13IN2O5
Molecular Weight 380.1358
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 1
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and in vitro anti-mycobacterial activity of 5-substituted pyrimidine nucleosides.
2005-12-15
Synthesis and biological investigations of 5-substituted pyrimidine nucleosides coupled to a dihydropyridine/pyridinium salt redox chemical delivery system.
2001-11
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 and cytotoxic activity of iodohydrin and iodomethoxy derivatives of 5-vinyl-2'-deoxyuridines, 2'-fluoro-2'-deoxyuridine, and uridine.
1990-02
Synthesis and antiviral activity of the carbocyclic analogues of (E)-5-(2-halovinyl)-2'-deoxyuridines and (E)-5-(2-halovinyl)-2'-deoxycytidines.
1985-05
In vitro susceptibility of varicella-zoster virus to E-5-(2-bromovinyl)-2'-deoxyuridine and related compounds.
1982-01
(E)-5-(2-Bromovinyl)-2'-deoxyuridine: a potent and selective anti-herpes agent.
1979-06
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:44:44 GMT 2025
Edited
by admin
on Mon Mar 31 23:44:44 GMT 2025
Record UNII
4WLK8JC9AR
Record Status Validated (UNII)
Record Version
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Name Type Language
5-(2-IODOVINYL)-2'-DEOXYURIDINE
Systematic Name English
IVDU
Preferred Name English
E-5-(2-IODOVINYL)-2'-DEOXYURIDINE
Systematic Name English
URIDINE, 2'-DEOXY-5-(2-IODOETHENYL)-, (E)-
Common Name English
Code System Code Type Description
PUBCHEM
6440124
Created by admin on Mon Mar 31 23:44:44 GMT 2025 , Edited by admin on Mon Mar 31 23:44:44 GMT 2025
PRIMARY
CAS
69304-48-9
Created by admin on Mon Mar 31 23:44:44 GMT 2025 , Edited by admin on Mon Mar 31 23:44:44 GMT 2025
PRIMARY
CAS
87727-68-2
Created by admin on Mon Mar 31 23:44:44 GMT 2025 , Edited by admin on Mon Mar 31 23:44:44 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
MESH
C030360
Created by admin on Mon Mar 31 23:44:44 GMT 2025 , Edited by admin on Mon Mar 31 23:44:44 GMT 2025
PRIMARY
EPA CompTox
DTXSID70219364
Created by admin on Mon Mar 31 23:44:44 GMT 2025 , Edited by admin on Mon Mar 31 23:44:44 GMT 2025
PRIMARY
FDA UNII
4WLK8JC9AR
Created by admin on Mon Mar 31 23:44:44 GMT 2025 , Edited by admin on Mon Mar 31 23:44:44 GMT 2025
PRIMARY