| Name | 5,6-Dihydro-5-azacytidine |
|---|---|
| Synonyms |
1,3,5-triazin-2(1H)-one, 4-amino-5,6-dihydro-1-β-D-ribofuranosyl-
4-Amino-1-(β-D-ribofuranosyl)-5,6-dihydro-1,3,5-triazin-2(1H)-one 5,6 dihydro-5-azacytidine 1,3,5-Triazin-2(1H)-one, 4-amino-3,6-dihydro-1-β-D-ribofuranosyl- 6-Amino-3-(β-D-ribofuranosyl)-3,4-dihydro-1,3,5-triazin-2(1H)-one |
| Description | Dihydro-5-azacytidine (DHAC), the nucleoside analog, is incorporated into DNA and inhibits DNA methylation. Dihydro-5-azacytidine has an antitumor activity[1][2]. |
|---|---|
| Related Catalog | |
| In Vitro | Methylation studies show that an LD10 dose of [3H]DHAC results in a 25.06% hypomethylation of DNA in L1210/0 cells and a 46.32% hypomethylation in a deoxycytidine kinase mutant cell line L1210/dCK(-), compared with their respective controls[2]. Dihydro-5-azacytidine (DHAC) competes with cytidine triphosphate for incorporation into RNA, leading to ribosomal degradation and defective protein synthesis[1]. |
| In Vivo | In tumor-bearing mice (injected with L1210/0 cells), after an LD10 dose of Dihydro-5-azacytidine (DHAC; 1500 mg/kg), the plasma peak concentration achieved is 317 μM and is eliminated biexponentially, with a t1/2 α of 1.03 h and a t1/2 β of 5 h[2]. |
| References |
| Density | 2.1±0.1 g/cm3 |
|---|---|
| Boiling Point | 529.1ºC at 760 mmHg |
| Molecular Formula | C8H14N4O5 |
| Molecular Weight | 246.221 |
| Flash Point | 273.8ºC |
| Exact Mass | 246.096420 |
| PSA | 140.64000 |
| LogP | -2.20 |
| Index of Refraction | 1.823 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATAMUTATION DATA
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