Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C11H14N4O4S.2H2O |
| Molecular Weight | 334.349 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.O.CSC1=NC=NC2=C1N=CN2[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O
InChI
InChIKey=CYFMOODRDYATGZ-LYYWGVPGSA-N
InChI=1S/C11H14N4O4S.2H2O/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;2*1H2/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 |
|
| Synthesis and antiviral activity of certain carbamoylpyrrolopyrimidine and pyrazolopyrimidine nucleosides. | 1982-11 |
|
| Purine analogs as potential anticytomegalovirus agents. | 1969-09 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
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Preferred Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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7143-67-1
Created by
admin on Mon Mar 31 22:44:04 GMT 2025 , Edited by admin on Mon Mar 31 22:44:04 GMT 2025
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PRIMARY | |||
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23616818
Created by
admin on Mon Mar 31 22:44:04 GMT 2025 , Edited by admin on Mon Mar 31 22:44:04 GMT 2025
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PRIMARY | |||
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LG7L4NU85R
Created by
admin on Mon Mar 31 22:44:04 GMT 2025 , Edited by admin on Mon Mar 31 22:44:04 GMT 2025
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PRIMARY | |||
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DTXSID10991798
Created by
admin on Mon Mar 31 22:44:04 GMT 2025 , Edited by admin on Mon Mar 31 22:44:04 GMT 2025
|
PRIMARY |
PARENT (SALT/SOLVATE)
SUBSTANCE RECORD
