Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C11H14N4O4S |
| Molecular Weight | 298.318 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CSC1=NC=NC2=C1N=CN2[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O
InChI
InChIKey=ZDRFDHHANOYUTE-IOSLPCCCSA-N
InChI=1S/C11H14N4O4S/c1-20-10-6-9(12-3-13-10)15(4-14-6)11-8(18)7(17)5(2-16)19-11/h3-5,7-8,11,16-18H,2H2,1H3/t5-,7-,8-,11-/m1/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Molecular mechanisms underlying the enhanced sensitivity of thiopurine-resistant T-lymphoblastic cell lines to methyl mercaptopurineriboside. | 2006-09-28 |
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| Synthesis and antiviral activity of certain carbamoylpyrrolopyrimidine and pyrazolopyrimidine nucleosides. | 1982-11 |
|
| Purine analogs as potential anticytomegalovirus agents. | 1969-09 |
Patents
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SUB179122
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44081
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Y5G39SHR0V
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206-442-2
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DTXSID5030454
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C2352
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342-69-8
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100000164627
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DB02896
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49555
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40774
Created by
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SALT/SOLVATE (PARENT)
SUBSTANCE RECORD
