CAS 2004-04-8|Decoyinine

Introduction:Basic information about CAS 2004-04-8|Decoyinine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameDecoyinine
CAS Number2004-04-8Molecular Weight279.25
Density1.9±0.1 g/cm3Boiling Point580.3±60.0 °C at 760 mmHg
Molecular FormulaC11H13N5O4Melting Point/
MSDSUSAFlash Point304.7±32.9 °C
Symbol
GHS07
Signal WordWarning

Names

Name(2R,3R,4S)-2-(6-aminopurin-9-yl)-2-(hydroxymethyl)-5-methylideneoxolane-3,4-diol
SynonymMore Synonyms

Decoyinine BiologicalActivity

DescriptionDecoyinine is a selective inhibitor of GMP synthetase (GMPS).
Related CatalogSignaling Pathways >>Others >>OthersResearch Areas >>Cancer
Target

GMPS[1].

In VitroDecoyinine is an analog of adenosine which causes a decrease in intracellular GTP levels by inhibition of GMP synthetase. Decoyinine exerts a stimulatory effect on oaamylase synthesis only in the strain in which the catabolite repression component of a-amylase regulation has been rendered inoperable by the gra-10 mutation. The apparent stimnulation of a-amylase activity in WLN-11 by Decoyinine is not an artifactual effect exerted at the level of enzyme activity itself. It is observed that purine nucleotides, most notably GMP, exhibits a dramatic inhibitory effect on the activity of Bacillus circulans F-2 amylase and a less-pronounced inhibitory effect on B. subtilis aamylase. At the concentration used in the experiments (1.07 mM), Decoyinine has no effect in vitro on B. subtilis WLN-11 oaamylase activity. At the same concentration, GMP exerts a slight inhibitory effect on aamylase activity[2].
In VivoIt is showed that Decoyinine (Angustmycin A) treatment hinders tumor growth in xenograft mouse model. Moreover, like GMPS activity, the effect of Decoyinine does not appear to be subtype specific as it impairs growth of xenografts from cells harboring NRASQ61R (SK-Mel-103) or BRAFV600E (SK-Mel-28) mutations[1].
Cell AssayThe isogenic strains WLN-4 (sacA321 amyRJ-amyE+) and WLN-11 (sacA321 gra-10-amyE+) are inoculated into minimal S7 medium, containing 2% (wt/vol) glucose, from washed exponential-phase seed cultures grown in the same medium. At mid-logarithmic growth phase, each culture is evenly subdivided into two flasks containing either 1/10 the culture volume of fresh S7 medium or a 1/10 volume of filter-sterilized S7 medium to which 2.5 mg of Decoyinine per ml has previously been dissolved (final Decoyinine concentration, 250 μg/mL). At regular intervals before and after the decoyinine addition, samples are removed from the cultures and the culture supernatants are assayed for a-amylase as described previously. At 16 h after the Decoyinine addition, the frequency of heatresistant spores in each culture is determined[2].
Animal AdminMice[1] SK-Mel-103 and SK-Mel-28 cells are inoculated subcutaneously in both flanks of SCID mice (18 mice/cell line). Once tumors volume reach approximately 100 mm3, mice are randomly assigned to one of four groups and treated with daily i.p. injections of Decoyinine (120 mg/kg), MMF (30 mg/kg), or with respective vehicles. Tumor size is measured every other day with a caliper and mice are killed once tumor volume reach 1000 mm3 or the animals show signs of morbidity[1].
References

[1]. A Bianchi-Smiraglia, et al. Pharmacological targeting of guanosine monophosphate synthase suppresses melanoma cell invasion and tumorigenicity. Cell Death Differ. 2015 Nov; 22(11): 1858–1864.

[2]. W L Nicholson, et al. Effect of Decoyinine on the regulation of alpha-amylase synthesis in Bacillus subtilis. J Bacteriol. 1987 Dec; 169(12): 5867–5869.

Chemical & Physical Properties

Density1.9±0.1 g/cm3
Boiling Point580.3±60.0 °C at 760 mmHg
Molecular FormulaC11H13N5O4
Molecular Weight279.25
Flash Point304.7±32.9 °C
PSA128.54000
LogP-1.25
Vapour Pressure0.0±1.7 mmHg at 25°C
Index of Refraction1.837
InChIKeyUZSSGAOAYPICBZ-SOCHQFKDSA-N
SMILESC=C1OC(CO)(n2cnc3c(N)ncnc32)C(O)C1O
Storage condition2-8℃

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
AU6256000
CHEMICAL NAME :
Adenine, 9-(6-deoxy-beta-D-erythro-hex-5-enulofuranosyl)-
CAS REGISTRY NUMBER :
2004-04-8
LAST UPDATED :
199106
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C11-H13-N5-O4
MOLECULAR WEIGHT :
279.29

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>2500 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
UPJOH* "Compounds Available for Fundamental Research, Volume II-6, Antibiotics, A Program of Upjohn Company Research Laboratory." (Kalamazoo, MI 49001) Volume(issue)/page/year: 2(6),-,1971
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>1 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
UPJOH* "Compounds Available for Fundamental Research, Volume II-6, Antibiotics, A Program of Upjohn Company Research Laboratory." (Kalamazoo, MI 49001) Volume(issue)/page/year: 2(6),-,1971
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
2500 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
85GDA2 "CRC Handbook of Antibiotic Compounds," Vols.1- , Berdy, J., Boca Raton, FL, CRC Press, 1980- Volume(issue)/page/year: 5,294,1981

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH315-H319-H335
Precautionary StatementsP261-P305 + P351 + P338
RIDADRNONH for all modes of transport

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Synonyms

6-Amino-9H-purin-9-yl 5-deoxy-β-D-erythro-pent-4-enofuranoside
decoyinine
Decoyinin
Antibiotic A 14
U-7984
β-D-erythro-Pent-4-enofuranoside, 6-amino-9H-purin-9-yl 5-deoxy-
Angustmycin A
A 14
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