Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C12H17N5O4 |
| Molecular Weight | 295.2945 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)C1=NC=NC2=C1N=CN2[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O
InChI
InChIKey=WVGPGNPCZPYCLK-WOUKDFQISA-N
InChI=1S/C12H17N5O4/c1-16(2)10-7-11(14-4-13-10)17(5-15-7)12-9(20)8(19)6(3-18)21-12/h4-6,8-9,12,18-20H,3H2,1-2H3/t6-,8-,9-,12-/m1/s1
| Molecular Formula | C12H17N5O4 |
| Molecular Weight | 295.2945 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis of pyrrolo[2,3-d]pyrimidine nucleoside derivatives as potential anti-HCV agents. | 2007-02 |
|
| Analogs of 3'-amino-3'-deoxyadenosine inhibit HIV-1 replication. | 1989-12 |
|
| Ribosome structure: localization of N6,N6-dimethyladenosine by electron microscopy of a ribosome-antibody complex. | 1977-04 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:56:43 GMT 2025
by
admin
on
Mon Mar 31 21:56:43 GMT 2025
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| Record UNII |
0L9766EW9W
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| Record Status |
Validated (UNII)
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| Record Version |
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2620-62-4
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28284
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627046
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DTXSID90949075
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220-057-7
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0L9766EW9W
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440004
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