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 |
---|---|---|
Ribosome structure: localization of N6,N6-dimethyladenosine by electron microscopy of a ribosome-antibody complex. | 1977 Apr |
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Analogs of 3'-amino-3'-deoxyadenosine inhibit HIV-1 replication. | 1989 Dec |
|
Synthesis of pyrrolo[2,3-d]pyrimidine nucleoside derivatives as potential anti-HCV agents. | 2007 Feb |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:13:28 GMT 2023
by
admin
on
Sat Dec 16 08:13:28 GMT 2023
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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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