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
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
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
In vitro susceptibility of varicella-zoster virus to E-5-(2-bromovinyl)-2'-deoxyuridine and related compounds. | 1982 Jan |
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Synthesis and antiviral activity of the carbocyclic analogues of (E)-5-(2-halovinyl)-2'-deoxyuridines and (E)-5-(2-halovinyl)-2'-deoxycytidines. | 1985 May |
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Synthesis and antiviral activity of novel 5-(1-azido-2-haloethyl) and 5-(1-azido-, amino-, or methoxyethyl) analogs of 2'-deoxyuridine. | 1993 Aug 20 |
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Code System | Code | Type | Description | ||
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6440124
Created by
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PRIMARY | |||
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69304-48-9
Created by
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87727-68-2
Created by
admin on Sat Dec 16 11:17:24 GMT 2023 , Edited by admin on Sat Dec 16 11:17:24 GMT 2023
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NON-SPECIFIC STEREOCHEMISTRY | |||
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C030360
Created by
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DTXSID70219364
Created by
admin on Sat Dec 16 11:17:24 GMT 2023 , Edited by admin on Sat Dec 16 11:17:24 GMT 2023
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4WLK8JC9AR
Created by
admin on Sat Dec 16 11:17:24 GMT 2023 , Edited by admin on Sat Dec 16 11:17:24 GMT 2023
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PRIMARY |
SUBSTANCE RECORD