CAS 7387-57-7|2',3',5'-Tri-O-acetyladenosine

Introduction:Basic information about CAS 7387-57-7|2',3',5'-Tri-O-acetyladenosine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name2',3',5'-Tri-O-acetyladenosine
CAS Number7387-57-7Molecular Weight393.35
Density1.6±0.1 g/cm3Boiling Point594.1±60.0 °C at 760 mmHg
Molecular FormulaC16H19N5O7Melting Point168-170ºC
MSDSUSAFlash Point313.1±32.9 °C

Names

Name2',3',5'-Tri-O-acetyl-D-adenosine
SynonymMore Synonyms

2',3',5'-Tri-O-acetyladenosine BiologicalActivity

Description2’,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].
Related CatalogResearch Areas >>CancerSignaling Pathways >>Cell Cycle/DNA Damage >>Nucleoside Antimetabolite/Analog
References

[1]. Man S, et al. Potential and promising anticancer drugs from adenosine and its analogs. Drug Discov Today. 2021 Jun;26(6):1490-1500.  

Chemical & Physical Properties

Density1.6±0.1 g/cm3
Boiling Point594.1±60.0 °C at 760 mmHg
Melting Point168-170ºC
Molecular FormulaC16H19N5O7
Molecular Weight393.35
Flash Point313.1±32.9 °C
Exact Mass393.128448
PSA157.75000
LogP0.99
Vapour Pressure0.0±1.7 mmHg at 25°C
Index of Refraction1.680
InChIKeyGCVZNVTXNUTBFB-XNIJJKJLSA-N
SMILESCC(=O)OCC1OC(n2cnc3c(N)ncnc32)C(OC(C)=O)C1OC(C)=O
Storage condition−20°C

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard CodesXi
RIDADRNONH for all modes of transport
WGK Germany3

Articles2

More Articles
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...

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...

Synonyms

MFCD00057001
Tri-O-acetyladenosine
2',3',5'-Tri-O-acetyladenosine
Adenosine, 2',3',5'-triacetate
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