CAS 890-38-0|2'-Deoxyinosine

Introduction:Basic information about CAS 890-38-0|2'-Deoxyinosine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name2'-Deoxyinosine
CAS Number890-38-0Molecular Weight252.227
Density1.9±0.1 g/cm3Boiling Point620.6±65.0 °C at 760 mmHg
Molecular FormulaC10H12N4O4Melting Point250 °C
MSDSUSAFlash Point329.1±34.3 °C

Names

Name2ʼ-deoxyinosine
SynonymMore Synonyms

2'-Deoxyinosine BiologicalActivity

Description2’-deoxyadenosine inhibits the growth of human colon-carcinoma cell lines and is found to be associated with purine nucleoside phosphorylase (PNP) deficiency.
Related CatalogNatural Products >>Saccharides and GlycosidesResearch Areas >>CancerResearch Areas >>Metabolic Disease
Target

Human Endogenous Metabolite

In VitroIn the absence of deoxycoformycin, 2’-deoxyadenosine is primarily deaminated to 2’-deoxyinosine and then converted into hypoxanthine. In the presence of the inhibitor, the deoxynucleoside, in addition to a phosphorylation process, undergoes phosphorolytic cleavage giving rise to adenine. The conversion of 2’-deoxyadenosine to adenine might represent a protective device, emerging when the activity of adenosine deaminase is reduced or inhibited. There is much evidence to indicate that the enzyme catalyzing this processs may be distinct from methylthioadenosine phosphorylase and S-adenosyl homocysteine hydrolase, which are the enzymes reported to be responsible for the formation of adenine from 28-deoxyadenosine in mammals[1].
Cell AssayVarious amounts of cells, ranging from 1,000 to 900,000, suspended in 3 mL of standard medium, are plated in 35-mm dishes and incubated in the absence (control) and in the presence of both 1 μM dCF and 0.1 mM dAdo, as indicated in each experiment. dCf was added to the standard medium 30 min before 2’-deoxyadenosine (dAdo). Furthermore, an incubation is performed in which 0.1 mM 2’-deoxyadenosine alone is added to the standard medium. After 4 days of incubation, the standard medium is withdrawn, then 0.5 mL of 0.025% trypsin containing 0.02% EDTA is added and kept for few minutes at 37°C. The cells are collected, diluted in an appropriate volume of standard medium, and counted[1].
References

[1]. Bemi V, et al. Deoxyadenosine metabolism in a human colon-carcinoma cell line (LoVo) in relation to its cytotoxic effect in combination with deoxycoformycin. Int J Cancer. 1998 Mar 2;75(5):713-20.

Chemical & Physical Properties

Density1.9±0.1 g/cm3
Boiling Point620.6±65.0 °C at 760 mmHg
Melting Point250 °C
Molecular FormulaC10H12N4O4
Molecular Weight252.227
Flash Point329.1±34.3 °C
Exact Mass252.085861
PSA113.26000
LogP-1.43
Vapour Pressure0.0±1.9 mmHg at 25°C
Index of Refraction1.837
InChIKeyVGONTNSXDCQUGY-RRKCRQDMSA-N
SMILESO=c1[nH]cnc2c1ncn2C1CC(O)C(CO)O1
Storage condition-20°C

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard CodesXn,Xi
Risk PhrasesR20/21/22
Safety PhrasesS24/25
RIDADRNONH for all modes of transport
WGK Germany3
HS Code2934999090

Customs

HS Code2934999090
Summary2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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Synonyms

INOSINE, 2'-DEOXY-
Inosine,2'-deoxy
EINECS 212-964-1
9H-Purin-6-ol, 9-(2-deoxy-β-D-erythro-pentofuranosyl)-
2'-Deoxyinosine
9-(2-deoxy-b-D-erythro-pentofuranosyl)-Hypoxanthine
9-(2-deoxy-β-D-erythro-pentofuranosyl)-Hypoxanthine
9-(2-Deoxy-b-D-erythro-pentofuranosyl)-1,9-dihydro-6H-purin-6-one
9-((2R,4S,5R)-4-Hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-9H-purin-6-ol
Deoxyinosine
(-)-2'-Deoxyinosine
d-Ino
2'-DEOXYGUANOSINE-5'-TRIPHOSPHATE TRISODIUM SALT,DGTP
MFCD00005762
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