2',3',5'-Tri-O-acetyladenosine
Modify Date: 2024-01-03 19:27:41
2',3',5'-Tri-O-acetyladenosine structure
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Common Name | 2',3',5'-Tri-O-acetyladenosine | ||
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| CAS Number | 7387-57-7 | Molecular Weight | 393.35 | |
| Density | 1.6±0.1 g/cm3 | Boiling Point | 594.1±60.0 °C at 760 mmHg | |
| Molecular Formula | C16H19N5O7 | Melting Point | 168-170ºC | |
| MSDS | USA | Flash Point | 313.1±32.9 °C | |
Use of 2',3',5'-Tri-O-acetyladenosine2’,3’,5’-Tri-O-acetyl adenosine is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277)[1]. |
| Name | 2',3',5'-Tri-O-acetyl-D-adenosine |
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| Synonym | More Synonyms |
| Description | 2’,3’,5’-Tri-O-acetyl adenosine is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277)[1]. |
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| Related Catalog | |
| References |
| Density | 1.6±0.1 g/cm3 |
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| Boiling Point | 594.1±60.0 °C at 760 mmHg |
| Melting Point | 168-170ºC |
| Molecular Formula | C16H19N5O7 |
| Molecular Weight | 393.35 |
| Flash Point | 313.1±32.9 °C |
| Exact Mass | 393.128448 |
| PSA | 157.75000 |
| LogP | 0.99 |
| Vapour Pressure | 0.0±1.7 mmHg at 25°C |
| Index of Refraction | 1.680 |
| Storage condition | −20°C |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| Hazard Codes | Xi |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
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Detection of proton-acceptor sites of hydrogen bonding in adenine X uracil base pairs by the use of 15N magnetic resonance.
Eur. J. Biochem. 117(3) , 553-8, (1981) 2',3',5'-Tri-O-acetyl[1,3,7,9,amino-15N]adenosine(ac3Ado) and its 8-2H and 8-bromo derivatives (ac3[8-2H]Ado and ac3br8Ado) were synthesized from 95% 15N-enriched adenosine which was obtained by micro... |
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An 15N NMR study of adenine-uracil base pair in a non-aqueous solvent.
Nucleic Acids Symp. Ser. (6) , s79-82, (1979) [1,3,7,9,10-15N]-2',3',5'-Tri-O-acetyl adenosine (A) and its 8-D and 8-Br derivatives (AD and ABr) were prepared from 95% 15N enriched adenosine obtained from microbial fermentation. The chemical shif... |
| MFCD00057001 |
| Tri-O-acetyladenosine |
| 2',3',5'-Tri-O-acetyladenosine |
| Adenosine, 2',3',5'-triacetate |