Skip to Content
MilliporeSigma

4060

Inosine

A metabolite of adenosine that acts as a potent coronary vasodilator. Exhibits a positive inotropic action on heart muscle and can antagonize the ouabain-induced arrhythmias.

Synonym(s):

Inosine, Hypoxanthine Riboside

Slide 1 of 1
Sign In to View Organizational & Contract Pricing

Select a Size

50 G

$191.00

$191.00

Check Cart for Availability
Request a Bulk Order

About This Item

Empirical Formula (Hill Notation):
C10H12N4O5
CAS Number:
58-63-9
Molecular Weight:
268.23
MDL number:
MFCD00066770
UNSPSC Code:
12352208
NACRES:
NA.51

Key Documents

View All Documentation

Skip To

Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

100

description

RTECS - NM7460000
Merck USA index - 14, 4975

assay

≥99% (by assay)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze

color

white

solubility

water: soluble

shipped in

ambient

storage temp.

15-25°C

SMILES string

[n]2(c3nc[nH][c](c3nc2)=O)C1OC(C(C1O)O)CO

InChI

1S/C10H12N4O5/c15-1-4-6(16)7(17)10(19-4)14-3-13-5-8(14)11-2-12-9(5)18/h2-4,6-7,10,15-17H,1H2,(H,11,12,18)

InChI key

UGQMRVRMYYASKQ-UHFFFAOYSA-N

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
PHR2412I4125119140
Inosine A metabolite of adenosine that acts as a potent coronary vasodilator. Exhibits a positive inotropic action on heart muscle and can antagonize the ouabain-induced arrhythmias.

Millipore

4060

Inosine

Adenosine Impurity G Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR2412

Adenosine Impurity G

Inosine ≥99% (HPLC)

Sigma-Aldrich

I4125

Inosine

Adenosine Receptor Agonist, NECA

Sigma-Aldrich

119140

Adenosine Receptor Agonist, NECA

Quality Level

100

Quality Level

300

Quality Level

200

Quality Level

100

manufacturer/tradename

Calbiochem®

manufacturer/tradename

-

manufacturer/tradename

-

manufacturer/tradename

Calbiochem®

assay

≥99% (by assay)

assay

-

assay

≥99% (HPLC)

assay

≥99% (HPLC)

form

solid

form

solid

form

-

form

solid

solubility

water: soluble

solubility

-

solubility

-

solubility

DMSO: 50 mM

color

white

color

-

color

-

color

white

General description

A metabolite of adenosine that acts as a potent coronary vasodilator. Exhibits a positive inotropic action on heart muscle and can antagonize the ouabain-induced arrhythmias.
Correlates well with myocardial contractile performance.

Other Notes

Aviado, D.M. 1983. J. Pharmacol. 14 (suppl. 3), 47.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Juan M Roldan-Romero et al.
International journal of cancer, 146(5), 1435-1444 (2019-07-25)
The mammalian target of rapamycin (mTOR) pathway inhibitors are key drugs for the treatment of many tumor types, however, there are no predictive biomarkers in clinical use. Here, we performed a molecular and immunohistochemical characterization of key mTOR pathway components
Heejung Yang et al.
Planta medica, 79(1), 78-82 (2012-11-17)
Bioassay-guided fractionation of an 80% methanolic extract of Salix pseudo-lasiogyne twigs has resulted in the isolation of two new compounds (1-2) along with ten known ones (3-12). The new compounds were determined to be 3'-O-acetylsalicin (1) and 2',6'-O-acetylsalicortin (2) by
Hsiao-Chun Chen et al.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 49(5), 1813-1824 (2018-09-20)
Acupuncture involves inserting a fine needle into a specific point, often called an acupoint, thereby initiating a therapeutic effect accompanied by phenomena such as soreness, heaviness, fullness, and numbness. Acupoints are characterized as points located in deep tissues with abundant
Laureline Février et al.
Journal of environmental radioactivity, 235-236, 106645-106645 (2021-05-22)
Actinide-based mineral phases occurring in contaminated soils can be solubilized by organic chelators excreted by plants, such as citrate. Herein, the efficiency of citrate towards U and Pu extraction is compared to that of siderophores, whose primary function is the
Aiqun Lin et al.
The Journal of antibiotics, 61(4), 245-249 (2008-05-27)
Two new compounds, 4-(hydroxymethyl)-5-hydroxy-2H-pyran-2-one (1) and (5-hydroxy-2-oxo-2H-pyran-4-yl) methyl acetate (2), have been isolated from a marine-derived fungus Aspergillus flavus. Their structures were determined by spectroscopic data. Compound 1 induced the production of cAMP on GPR12 transfected CHO and HEK293 cells
View All Related Papers

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service