Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C10H12N4O4 |
Molecular Weight | 252.2267 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC[C@@H]1C[C@@H](O)[C@@H](O1)N2C=NC3=C2N=CNC3=O
InChI
InChIKey=RPZDLTVHZJHPAW-BAJZRUMYSA-N
InChI=1S/C10H12N4O4/c15-2-5-1-6(16)10(18-5)14-4-13-7-8(14)11-3-12-9(7)17/h3-6,10,15-16H,1-2H2,(H,11,12,17)/t5-,6+,10+/m0/s1
Approval Year
PubMed
Title | Date | PubMed |
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Anti-parasite activity of nucleoside analogues in Leishmania tropica promastigotes. | 1984 |
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3'-Deoxyinosine as an anti-leishmanial agent: the metabolism and cytotoxic effects of 3'-deoxyinosine in Leishmania tropica promastigotes. | 1984 Sep 17 |
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Studies on the mechanism of cytotoxicity of 3'-deoxyadenosine N1-oxide in different strains of Ehrlich ascites tumor cells. | 1987 |
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Synergistic effect of 3'-deoxyadenosine N1-oxide and adenosine deaminase inhibitors on growth of Ehrlich ascites tumor cells in vivo. | 1988 |
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Antileukemic activity and mechanism of action of cordycepin against terminal deoxynucleotidyl transferase-positive (TdT+) leukemic cells. | 2000 Feb 1 |
Patents
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DTXSID70927210
Created by
admin on Sat Dec 16 03:27:50 GMT 2023 , Edited by admin on Sat Dec 16 03:27:50 GMT 2023
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13146-72-0
Created by
admin on Sat Dec 16 03:27:50 GMT 2023 , Edited by admin on Sat Dec 16 03:27:50 GMT 2023
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135513783
Created by
admin on Sat Dec 16 03:27:50 GMT 2023 , Edited by admin on Sat Dec 16 03:27:50 GMT 2023
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J71U8QAU3Q
Created by
admin on Sat Dec 16 03:27:50 GMT 2023 , Edited by admin on Sat Dec 16 03:27:50 GMT 2023
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PRIMARY |
PARENT (METABOLITE INACTIVE)
SUBSTANCE RECORD