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Inosine 5′-monophosphate disodium salt hydrate_Molecular_structure_CAS_352195-40-5)
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Inosine 5′-monophosphate disodium salt hydrate

Catalog No. 57510 Name Sigma Aldrich
CAS Number 352195-40-5 Website http://www.sigmaaldrich.com
M. F. C10H13N4Na2O9P Telephone 1-800-521-8956
M. W. 410.184921 Fax
Purity ≥99.0% (HPLC) Email
Storage Chembase ID: 155967

SYNONYMS

IUPAC name
disodium hydrate [(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-6,9-dihydro-1H-purin-9-yl)oxolan-2-yl]methyl phosphate
IUPAC Traditional name
disodium hydrate inosine 5'-phosphate
Synonyms
5′-IMP-Na2
5′-Inosinic acid disodium salt hydrate
I-5′-P
IMP
Inosinic Acid

DATABASE IDS

CAS Number 352195-40-5
MDL Number MFCD00150372
PubChem SID 24880778

PROPERTIES

Empirical Formula (Hill Notation) C10H11N4O8PNa2 · xH2O
Impurities ~25% water
Purity ≥99.0% (HPLC)
Optical Rotation [α]20/D -32±2°, c = 1% in H2O
MSDS Link Download
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Inosine monophosphate, or inosinic acid, is the ribonucleotide of hypoxanthine and the first nucleotide formed during purine synthesis.
Application
Inosine-5′-monophosphate (5′-IMP) may be used as a substrate to study the activity, specificity and kinetics of inosine 5′-monophosphate dehydrogenase (IMPDH) EC 1.1.1.205, the rate limiting enzyme for the formation of GMP and the guanine nucleotide pool.
Description (简体中文)
Biochem/physiol Actions
Inosine monophosphate, or inosinic acid, is the ribonucleotide of hypoxanthine and the first nucleotide formed during purine synthesis.
Application
Inosine-5′-monophosphate (5′-IMP) may be used as a substrate to study the activity, specificity and kinetics of inosine 5′-monophosphate dehydrogenase (IMPDH) EC 1.1.1.205, the rate limiting enzyme for the formation of GMP and the guanine nucleotide pool.

REFERENCES