Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H7N5O |
| Molecular Weight | 165.1527 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1C(=O)C2=C(N=CN2)N=C1N
InChI
InChIKey=RFLVMTUMFYRZCB-UHFFFAOYSA-N
InChI=1S/C6H7N5O/c1-11-5(12)3-4(9-2-8-3)10-6(11)7/h2H,1H3,(H2,7,10)(H,8,9)
| Molecular Formula | C6H7N5O |
| Molecular Weight | 165.1527 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Urinary excretion of modified purines and nucleosides in immunodeficient children. | 1985 Aug |
|
| Structure-activity relationships for the binding of ligands to xanthine or guanine phosphoribosyl-transferase from Toxoplasma gondii. | 1995 Nov 9 |
|
| Fast-atom bombardment mass spectrometry for mapping of endogenous methylated purine bases in urine extracts. | 1997 |
|
| Determination of urinary methylated purine pattern by high-performance liquid chromatography. | 2001 Feb 10 |
|
| Locked nucleoside analogues expand the potential of DNAzymes to cleave structured RNA targets. | 2006 Jun 5 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:08:29 GMT 2023
by
admin
on
Sat Dec 16 02:08:29 GMT 2023
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| Record UNII |
1ATY0M8242
|
| Record Status |
Validated (UNII)
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| Record Version |
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213-348-5
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938-85-2
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70315
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DTXSID4049377
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1ATY0M8242
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50718
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21803
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