Basic Information | Post buying leads | Suppliers | Cas Database |
Phosphoric acid (3aR,4R,6R,6aR)-2,2-dimethyl-6-(6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester bis-(2,2,2-tribromo-ethyl) ester
5'-inosine monophosphate
Conditions | Yield |
---|---|
With Nafion 125; lithium perchlorate In N,N-dimethyl-formamide; acetonitrile electrolysis; | 89% |
5'-adenosine monophosphate
A
5'-inosine monophosphate
B
adenosine 5'-diphosphate
C
ATP
Conditions | Yield |
---|---|
With zinc(II) chloride In methanol at 25℃; Product distribution; biosynthesis; various typ-, and conc. of reagent; | |
In methanol at 25℃; biosynthesis by Candida boidnii No. 2201; pH = 6.5; | A 14.8 mmol B 36.8 mmol C 24.0 mmol |
With zinc(II) chloride In methanol at 25℃; biosynthesis by Candida boidnii No. 2201; pH = 6.5; | A 2.0 mmol B n/a C 36.8 mmol |
In methanol at 25℃; biosynthesis by Candida boidnii No. 2201; pH = 6.5; | A 14.8 mmol B 1.1 mmol C 24.0 mmol |
Conditions | Yield |
---|---|
With triethyl phosphate; trichlorophosphate In water at 0℃; for 2h; Rate constant; Product distribution; var. reaction conditions; | 91 % Chromat. |
With potassium dihydrogenphosphate; D-glucose; guanosine-inosine kinase from Exiguobacterium acetylicum In various solvent(s) at 32℃; pH=7.2; Enzymatic reaction; | |
With DL-dithiothreitol; recombinant cytosolic 5'-nucleotidase II; ATP In various solvent(s) at 37℃; pH=7.4; Enzyme kinetics; Further Variations:; Reagents; | |
With sodium pyrophosphate; sodium acetate buffer; Escherichia blattae wild type phosphotransferase at 30℃; pH=5.0; Enzyme kinetics; Further Variations:; Reagents; | |
With trimethyl phosphite; trichlorophosphate at 0℃; |
5-phosphoribosyl-1-pyrophosphate
hypoxanthine
5'-inosine monophosphate
Conditions | Yield |
---|---|
With Toxoplasma gondii phosphoribosyltransferase In alkaline aq. solution at 37℃; pH=7.4; Enzyme kinetics; |
Conditions | Yield |
---|---|
With disodium pyrophoshate; Shigella flexneri acid phosphatase In various solvent(s) at 30℃; pH=5.0; Enzyme kinetics; Further Variations:; Reagents; |
Conditions | Yield |
---|---|
With hypoxanthine phosphoribosyltransferase Enzyme kinetics; Further Variations:; Reagents; |
Conditions | Yield |
---|---|
With diothiothreitol; water at 37℃; pH=6.8; Enzyme kinetics; |
5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-CATGTACCGATAAGCGTATTATGGAAGGAGGCGTTATGAGGGGTCCA-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/bis(adenosine 5'-monophosphate) complex
A
5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-CATGTACCGATAAGCGTATTATGGAAGGAGGCGTTATGAGGGGTCCA-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/5'-CTCCTTCCATACGGTGCACCTTCCTC-3'5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-CATGTACCGATAAGCGTATTATGGAAGGAGGCGTTATGAGGGGTCCA-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/5'-CTCCTTCCATACGGTGCACCTTCCTC-3'
B
5'-inosine monophosphate
Conditions | Yield |
---|---|
With 4-(2-hydroxyethyl)piperazine-1-ethanesulfonic acid sodium salt; sodium chloride; adenosine deaminase In water at 25 - 70℃; for 1.33333h; pH=7.4; Enzymatic reaction; |
5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-AGGTGCACGTGGTCCAGTGCTGCAGTG-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/adenosine 5'-monophosphate complex
A
5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-AGGTGCACGTGGTCCAGTGCTGCAGTG-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/5'-CTCCTTCCATACGGTGCACCTTCCTC-3'5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-AGGTGCACGTGGTCCAGTGCTGCAGTG-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/5'-CTCCTTCCATACGGTGCACCTTCCTC-3'
B
5'-inosine monophosphate
Conditions | Yield |
---|---|
With adenosine deaminase aq. buffer; Enzymatic reaction; |
5'-inosine monophosphate
Conditions | Yield |
---|---|
Stage #1: C24H24N6O9PPol With ammonium hydroxide In water at 55℃; for 15h; solid phase reaction; Stage #2: With trifluoroacetic acid In dichloromethane at 20℃; for 0.333333h; solid phase reaction; |
Product Name: Inosinic acid (131-99-7)
Molecular Formula: C10H13N4O8P
Molecular Weight: 348.206g/mol
Mol File: 131-99-7.mol
Einecs:205-045-1
Storage Temperature: -20°C
Ynonyms of Ethyl Inosinic acid viki (131-99-7) : 5’-inosinicacid ; inosine5’-phosphate ; inosinemonophosphate ; imp ; inosinic acid ; inosine 5'-monophosphate ; inosine-5'-monophosphoric acid ; 1-5'-p .
Inosinic acid (131-99-7) and its salts such as disodium inosinate are used as flavour enhancers in the food industry,.
1. | orl-rat LD50:16 g/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
2. | ipr-rat LD50:4850 mg/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
3. | scu-rat LD50:3900 mg/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
4. | ivn-rat LD50:2730 mg/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
5. | orl-mus LD50:12 g/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
6. | ipr-mus LD50:5400 mg/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
7. | scu-mus LD50:5480 mg/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
8. | ivn-mus LD50:3300 mg/kg | ARTODN Archives of Toxicology. 47 (1981),77. |
Reported in EPA TSCA Inventory.
Moderately toxic by subcutaneous and intravenous routes. When heated to decomposition it emits toxic fumes of POx and NOx.
Inosinic acid (131-99-7) is a nucleoside monophosphate. Inosinic acid is important in metabolism. It is the ribonucleotide of hypoxanthine and the first nucleotide formed during the synthesis of purine. It is formed by the deamination of adenosine monophosphate, and is hydrolysed to form inosine.Important derivatives of inosinic acid include purine nucleotides found in nucleic acids and adenosine triphosphate, which is used to store chemical energy in muscle and other tissues.