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2'-Deoxy-5'-O-DMT-inosine 3'-CE phosphoramidite. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences.
Worldwide
2'-Deoxy-5'-O-MMT-inosine 3'-CE phosphoramidite
2'-Deoxy-5'-O-MMT-inosine 3'-CE phosphoramidite is a quintessential reagent for synthesizing modified nucleosides, amplifying the arsenal for research and diagnostic domains. Thanks to the unique properties of this product, it has been used extensively in constructing oligonucleotides, characterized by their formidable stability and selectivity in hybridization assays. Plus, its extravagant versatility and incomparable peculiarities make it prime for elucidating structure-activity relationships, thus, aiding in promptly fathoming out more efficacious drugs against multiple diseases. Synonyms: 2'-Deoxy-5'-O-MMT-D-inosine 3'-CE phosphoramidite; 5'-O-MMT-2'-deoxyinosine 3'-CE phosphoramidite. Molecular formula: C39H45N6O6P. Mole weight: 724.80.
2'-Deoxy-5'-O-tritylinosine 3'-CE phosphoramidite
2'-Deoxy-5'-O-tritylinosine 3'-CE phosphoramidite is a vital component in the synthesis of oligonucleotides used in biomedicine. It plays a crucial role in the development of drugs targeting specific diseases like cancer, genetic disorders, and viral infections. This highly pure and efficient phosphoramidite enables accurate and controlled incorporation of modified nucleotides during the oligonucleotide synthesis process, facilitating research and advancements in the biomedical industry. Synonyms: 2'-Deoxy-5'-O-trityl-D-inosine 3'-CE phosphoramidite; 5'-O-Trityl-2'-deoxyinosine 3'-CE phosphoramidite. Molecular formula: C38H43N6O5P. Mole weight: 694.78.
2'-Deoxyinosine 5'-monophosphate
2'-Deoxyinosine 5'-monophosphate, a vital biomolecule, intricately participates in the synthesis of DNA. With its involvement in the regulation of DNA replication and repair through the nucleotide dITP, this compound paves the way towards improved treatment processes. Notably, this biomolecule is also utilized in the management of autoimmune disorders inclusive of lupus and rheumatoid arthritis. Synonyms: Deoxyinosine monophosphate; 2''-Deoxyinosine-5''-monophosphoric acid; 2'-Deoxy-5'-inosinic acid; 2'-Deoxy-IMP; Hypoxanthine deoxyriboside; 9-(2-deoxy-5-O-phosphono-beta-D-erythro-pentofuranosyl)-9H-purin-6-ol. Grades: ≥98% by HPLC. CAS No. 3393-18-8. Molecular formula: C10H13N4O7P. Mole weight: 332.21.
2'-Deoxyinosine-5'-triphosphate sodium salt
2'-Deoxyinosine-5'-triphosphate sodium salt, renowned for its multifarious applications in enzymatic labeling, sequencing, and mutagenesis, is a popular nucleotide analogue adopted in the biomedical industry. Apart from its widespread usage in these areas, it has also shown promising outcomes in treating viral infections and cancer. Synonyms: dITP.3Na; Inosine 5'-(tetrahydrogen triphosphate), 2'-deoxy-, trisodium salt; 9H-Purin-6-ol, 9-[2-deoxy-5-O-[hydroxy[[hydroxy (phosphonooxy) phosphinyl]oxy]phosphinyl]-β -D-erythro-pentofuranosyl]-, sodium salt (1:3); sodium ((2R,3S,5R)-3-hydroxy-5-(6-hydroxy-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl hydrogen triphosphate. Grades: ≥99% by HPLC. CAS No. 95648-77-4. Molecular formula: C10H12N4Na3O13P3. Mole weight: 558.11.
5'-O-Benzoyl-2'-deoxyinosine 3'-CE phosphoramidite, an indispensable constituent in the synthesis of altered nucleosides, plays a pivotal role in the biomedical sector. Pertaining to its application, it finds frequent utilization in the formulation of pharmaceutical agents to combat distinctive ailments like cancer and viral infections. This particular compound assumes the status of a fundamental cornerstone in the production of tailored curative interventions, with the ultimate objective of enhancing patient prognosis and propelling the advancement of the biomedicine domain. Synonyms: 5'-O-Benzoyl-2'-deoxy-D-inosine 3'-CE phosphoramidite. Molecular formula: C26H33N6O6P. Mole weight: 556.56.
5'-O-Benzyl-2'-deoxyinosine 3'-CE phosphoramidite
5'-O-Benzyl-2'-deoxyinosine 3'-CE phosphoramidite is a crucial compound used in biomedicine for the synthesis of oligonucleotides. This phosphoramidite derivative facilitates the efficient incorporation of 5'-O-Benzyl-2'-deoxyinosine 3'-CE, which enables selective and controlled modification of DNA sequences. This modified oligonucleotide finds applications in the study and treatment of various diseases, including cancer and infectious diseases, due to its ability to enhance therapeutic efficacy and improve drug delivery systems. Synonyms: 5'-O-Benzyl-2'-deoxy-D-inosine 3'-CE phosphoramidite. Molecular formula: C26H35N6O5P. Mole weight: 542.58.
5'-O-DMT-2'-deoxyinosine 3'-CE phosphoramidite
5'-O-DMT-2'-deoxyinosine 3'-CE phosphoramidite is a key reagent used in the biomedical industry for the synthesis of modified nucleosides. It is commonly employed in the development of DNA and RNA molecules for research purposes, such as studying DNA-protein interactions or designing gene therapies. Its unique chemical structure enables specific targeting and modulation of gene expression related to certain diseases, providing insights into novel treatment strategies. Synonyms: Inosine (dI) phosphoramidite;2'-Deoxy-5'-O-DMT-inosine 3'-CE phosphoramidite; DMT-dI Phosphoramidite; 5'-O-[Bis(4-methoxyphenyl)phenylmethyl]-2'-deoxyinosine 3'-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite]. Grades: ≥98% by HPLC. CAS No. 141684-35-7. Molecular formula: C40H47N6O7P. Mole weight: 754.83.
5'-O-DMT-2'-O-methylinosine 3'-CE phosphoramidite
5'-O-DMT-2'-O-methylinosine 3'-CE phosphoramidite is a vital component used in the research and development of RNA molecules for biomedical research. It functions as a phosphoramidite building block to introduce the modified nucleoside 5'-O-DMT-2'-O-methylinosine into RNA sequences. This modified nucleoside plays a crucial role in studying the structure, function and therapeutic potential of RNA molecules involved in various diseases, including cancer and genetic disorders. Synonyms: 2/'-O-METHYL-I CEP; 2'-O-METHYL-5'-O-DMT-INOSINE-3'-CE-PHOSPHORAMIDITE; 3-[[ (2R, 3R, 4R, 5R) -2-[[Bis (4-methoxyphenyl) -phenylmethoxy]methyl]-4-methoxy-5- (6-oxo-1H-purin-9-yl) oxolan-3-yl]oxy-[di (propan-2-yl) amino]phosphanyl]oxypropanenitrile; 2'-O-Methyl InosinePhosphoramidite; 5'-O-(4,4-Dimethoxytrityl)-2'-O-methyl inosine-3'-CED phosphoramidite; 5'-O-(4,4'-Dimethoxytrityl)-2'-O-methyl-inosine-3'-cyanoethyl phosphoramidite; Inosine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-methyl-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]. Grades: ≥ 98%. CAS No. 128219-85-2. Molecular formula: C41H49N6O8P. Mole weight: 784.83.
Antiviral and anticancer drug for cells infected with influenza A virus, herpes simplex virus type 2, and human lymphocytic leukemia cells. Synonyms: 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-inosine 3'-CE phosphoramidite; 2'-O-(tert-Butyldimethylsilyl)-3'-O-[(diisopropylamino)(2-cyanoethoxy)phosphino]-5'-O-(4,4'-dimethoxytrityl)inosine; Inosine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-, 3'-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite]; 5'-O-[Bis (4-methoxyphenyl) (phenyl)methyl]-3'-O-[ (2-cyanoethoxy) (diisopropylamino)phosphino]-2'-O-[dimethyl (2-methyl-2-propanyl)silyl]inosine. Grades: ≥97% by HPLC. CAS No. 261518-12-1. Molecular formula: C46H61N6O8PSi. Mole weight: 885.07.
5'-O-tert-Butyldimethylsilyl-2'-deoxyinosine 3'-CE phosphoramidite, one of the indispensable offerings in the realm of biomedical industries, plays a pivotal role in synthesizing oligonucleotides of paramount significance. These oligonucleotides, esteemed for their profound utilities in DNA sequencing, polymerase chain reaction (PCR), and gene expression analysis, lay down the bedrock for extensive applications. Fortified by this phosphoramidite, the enigmatic integration of 5'-O-tert-butyldimethylsilyl-2'-deoxyinosine into oligonucleotide sequences is effortlessly accomplished, engendering targeted therapeutic interventions for an assortment of ailments and fostering meticulous strides in the field of genetic explorations. Synonyms: 5'-O-tert-Butyldimethylsilyl-2'-deoxy-D-inosine 3'-CE phosphoramidite. Molecular formula: C25H43N6O5PSi. Mole weight: 566.72.
Inosine-3',5'-cyclic Monophosphate Sodium Salt
Inosine-3',5'-cyclic monophosphate is a cyclic nucleotide that stimulates steroidogenesis by adrenocortical cells in rats. Inosine-3',5'-cyclic monophosphate also stimulates insulin secretion in hamster pancreas cells. Synonyms: Inosine Cyclic 3',5'-(Hydrogen Phosphate) Sodium Salt; Inosine 3',5'-Phosphate (Cyclic) Sodium Salt; Inosine Cyclic 3',5'-(Hydrogen Phosphate) Monosodium Salt; 4H-Furo[3,2-d]-1,3,2-dioxaphosphorin Inosine Deriv.; 3',5'-cIMP Sodium Salt. Grades: 95%. CAS No. 41092-64-2. Molecular formula: C10H10N4NaO7P. Mole weight: 352.17.
Inosine-5'-diphosphate
Inosine-5-diphosphate is a nucleoside diphosphate that is indubitably vital to cellular energy metabolism. It serves as a crucial substrate for enzymes involved in purine salvage pathways and contributes to the biosynthesis of purine nucleotides. Additionally, IDP has been linked to an array of signal transduction pathways and has the ability to modulate the activity of ion channels. There is promising potential for IDP to become an effective therapy option for diseases characterized by purine metabolism imbalances. Synonyms: Inosine diphosphate; Riboxin; Inosine 5'-pyrophosphate; IDP; riboxine; Inosine pyrophosphate; Inosine 5'-(trihydrogen diphosphate); 9-{5-O-[Hydroxy(phosphonooxy)phosphoryl]-β-D-ribofuranosyl}-9H-purin-6-ol; 5'-IDP; Inosine 5'-diphosphoric acid. Grades: ≥98% by HPLC. CAS No. 86-04-4. Molecular formula: C10H14N4O11P2. Mole weight: 428.19.
Inosine 5'-monophosphate
Inosine 5'-monophosphate (IMP) is a profound molecular compound magnanimously entrusted with the profound responsibility of studying an extensive array of afflictions, encompassing neurologic dysfunctions, cardiac anomalies and immunological imperfections. Synonyms: Inosinic acid; IMP; 1-5'-P; inosinemonophosphate; [(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-1H-purin-9-yl)oxolan-2-yl]methyl dihydrogen phosphate. Grades: ≥ 98%. CAS No. 131-99-7. Molecular formula: C10H13N4O8P. Mole weight: 348.20.
Inosine 5'-monophosphate disodium salt
Disodium inosinate (E631) is the disodium salt of inosinic acid with the chemical formula C10H11N4Na2O8P. It is used as a food additive and often found in instant noodles, potato chips, and a variety of other snacks. This salt is used as a flavor enhancer made from microbial fermentation growth media that are all-vegetable, usually consisting mainly of tapioca starch. Synonyms: Disodium 5'-inosinate; Disodium inosinate; Sodium Inosine 5'-Phosphate (2:1); 5'-Inosinic Acid Disodium Salt; 5'-IMP Disodium Salt; Disodium 5'-IMP; Disodium 5'-Inosinate; Disodium IMP; Disodium Inosinate; Disodium Inosine 5'-Monophosphate; Disodium Inosine 5'-Phosphate; IMP Disodium Salt; Inosine 5'-Monophosphate Disodium Salt; Inosine 5'-Monophosphoric Acid Disodium Salt. Grades: ≥97% by HPLC. CAS No. 4691-65-0. Molecular formula: C10H11N4Na2O8P. Mole weight: 392.17.
Inosine 5'-triphosphate trisodium salt
Inosine-5'-triphosphate, an inosine nucleotide, is an intermediate in the purine metabolism pathway. Synonyms: Inosine 5'-(Tetrahydrogen Triphosphate) Trisodium Salt; NSC 20266; Trisodium Inosine-5'-triphosphate; ITP; 9H-Purin-6-ol, 9-[5-O-[hydroxy[[hydroxy (phosphonooxy) phosphinyl]oxy]phosphinyl]-β -D-ribofuranosyl]-, sodium salt (1:3); Trisodium 5'-O-[ ({[ (hydroxyphosphinato) oxy]phosphinato}oxy) phosphinato]inosine. Grades: ≥97% by HPLC. CAS No. 35908-31-7. Molecular formula: C10H12N4O14P3.3Na. Mole weight: 574.11.
(-)-Inosine Dehydroxy-N-(6-iminohexyl)-2,2,2-trifluoroacetamide Phosphate is an intermediate in synthesizing N6-(6-Aminohexyl)-FAD, a Flavine Adenine Dinucleotide (FAD) derivative. Attachment of a ligand to the 6-Aminohexyl side chain of this compound, can be used as a FAD-labelled conjugate to measure the concentration of the free ligand in a competitive binding immunoassay. Synonyms: ((2R,3S,4R,5R)-3,4-Dihydroxy-5-(6-((6-(2,2,2-trifluoroacetamido)hexyl)amino)-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl Dihydrogen Phosphate. Molecular formula: C18H26F3N6O8P. Mole weight: 542.4.
(-)-Inosine Dehydroxy-N-(6-iminohexyl)-2,2,2-trifluoroacetamide Phospho-morpholine is an intermediate in synthesizing N6-(6-Aminohexyl)-FAD, a derivative of Flavine Adenine Dinucleotide (FAD). Synonyms: ((2R,3S,4R,5R)-3,4-Dihydroxy-5-(6-((6-(2,2,2-trifluoroacetamido)hexyl)amino)-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl Morpholino Hydrogen Phosphate. Molecular formula: C22H33F3N7O9P. Mole weight: 627.51.
inosine diphosphate phosphatase
The human enzyme also hydrolyses GDP and dGDP, and to a lesser extent ITP, dITP and XTP. Group: Enzymes. Synonyms: (deoxy)inosine diphosphatase; NUDT16. Enzyme Commission Number: EC 3.6.1.64. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4637; inosine diphosphate phosphatase; EC 3.6.1.64; (deoxy)inosine diphosphatase; NUDT16. Cat No: EXWM-4637.
Inosine Monophosphate Dehydrogenase from Staphylococcus aureus, Recombinant
E.coli. Applications: Impdh is a recombinant protein of ca. 53kda cloned by pcr amplification of guab gene of staphylococcus aureus and expressed in e.coli. Group: Enzymes. Synonyms: inosine-5'-phosphate dehydrogenase; inosinic acid dehydrogenase; inosinate dehydrogenase; inosine 5'-monophosphate dehydrogenase; inosine monophosphate dehydrogenase; IMP oxidoreductase; inosine monophosphate oxidoreductase; IMP dehydrogenase; IMP:NAD+ oxidoreductase; EC 1.1.1.205; IMPDH. Enzyme Commission Number: EC 1.1.1.205. CAS No. 9028-93-7. IMPDH2. Mole weight: 53kDa. Activity: ≥ 0.3 unit/mg protein. Source: S. aureus. Species: IMPDH2. inosine-5'-phosphate dehydrogenase; inosinic acid dehydrogenase; inosinate dehydrogenase; inosine 5'-monophosphate dehydrogenase; inosine monophosphate dehydrogenase; IMP oxidoreductase; inosine monophosphate oxidoreductase; IMP dehydrogenase; IMP:NAD+ oxidoreductase; EC 1.1.1.205; IMPDH. Pack: stable lyophilized form. Cat No: NATE-1739.
Inosine Monophosphate Dehydrogenase Type II from Human, Recombinant
Type II is the predominant IMPDH isoform and is specifically linked to a wide range of cancers and lymphocyte proliferation. Group: Enzymes. Synonyms: inosine-5'-phosphate dehydrogenase; inosinic acid dehydrogenase; inosinate dehydrogenase; inosine 5'-monophosphate dehydrogenase; inosine monophosphate dehydrogenase; IMP oxidoreductase; inosine monophosphate oxidoreductase; IMP dehydrogenase; IMP:NAD+ oxidoreductase; EC 1.1.1.205; IMPDH II; IMPDH2; IMPD 2. Enzyme Commission Number: EC 1.1.1.205. CAS No. 231-791-2. IMPDH2. Storage: -70°C. Form: Solution in 20 mM Tris-HCl, pH 8.0, containing 0.5 mM EDTA and 1 mM DTT. Source: E. coli. Species: Human. inosine-5'-phosphate dehydrogenase; inosinic acid dehydrogenase; inosinate dehydrogenase; inosine 5'-monophosphate dehydrogenase; inosine monophosphate dehydrogenase; IMP oxidoreductase; inosine monophosphate oxidoreductase; IMP dehydrogenase; IMP:NAD+ oxidoreductase; EC 1.1.1.205; IMPDH II; IMPDH2; IMPD 2. Pack: vial of > 0.002 unit. Cat No: NATE-0352.
2',3'-O-(1-Methylethylidene)-6-thio-5'-inosinic Acid Bis(1,1-Dimethylethyl) Ester is an intermediate in the synthesis of 6-ThioinosinePhosphate, a metabolite of 6-Mercaptopurine. CAS No. 1375103-71-1. Molecular formula: C21H33N4O7PS. Mole weight: 516.55.
2',3'-O-(1-Methylethylidene)-6-thio-5-inosinic Acid Bis(1,1-Dimethylethyl) Ester is an intermediate in the synthesis of 6-ThioinosinePhosphate (T344500), a metabolite of 6-Mercaptopurine (M225450). Group: Biochemicals. Grades: Highly Purified. CAS No. 1375103-71-1. Pack Sizes: 5mg, 25mg. Molecular Formula: C21H33N4O7PS, Molecular Weight: 516.549999999999. US Biological Life Sciences.
Worldwide
5'-acylphosphoadenosine hydrolase
Also acts on inosine and uridine compounds. Group: Enzymes. Synonyms: 5-phosphoadenosine hydrolase. Enzyme Commission Number: EC 3.6.1.20. CAS No. 37289-31-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4604; 5'-acylphosphoadenosine hydrolase; EC 3.6.1.20; 37289-31-9; 5-phosphoadenosine hydrolase. Cat No: EXWM-4604.
5'-O-Tritylinosine
KIN59 is a purine riboside derivative that suppresses thymidine phosphorylase (TPase). TPase is an enzyme catalyzing the reversible phosphorolysis of pyrimidine deoxynucleosides to 2-deoxy-d-ribose-1-phosphate and their respective pyrimidine bases. KIN59 noncompetitively inhibits TPase-induced angiogenesis in the chorioallantoic membrane assay. Synonyms: 5'-Trt-rI; (2R,3R,4S,5R)-9-(3,4-Dihydroxy-5-trityloxymethyl-tetrahydrofuran-2-yl)-1,9-dihydropurin-6-one; KIN-59; Inosine, 5'-O-(triphenylmethyl)-; 5'-O-(triphenylmethyl)-inosine. Grades: ≥98% by HPLC. CAS No. 4152-77-6. Molecular formula: C29H26N4O5. Mole weight: 510.55.
adenylosuccinate synthase
In molecular biology, Adenylosuccinate synthase (EC 6.3.4.4.) is an enzyme that plays an important role in purine biosynthesis, by catalysing the guanosine triphosphate (GTP)-dependent conversion of inosine monophosphate (IMP) and aspartic acid to guanosine diphosphate (GDP), phosphate and N(6)-(1,2-dicarboxyethyl)-AMP. Group: Enzymes. Synonyms: IMP-aspartate ligase; adenylosuccinate synthetase; succinoadenylic kinosynthetase; succino-AMP synthetase. Enzyme Commission Number: EC 6.3.4.4. CAS No. 9023-57-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5796; adenylosuccinate synthase; EC 6.3.4.4; 9023-57-8; IMP-aspartate ligase; adenylosuccinate synthetase; succinoadenylic kinosynthetase; succino-AMP synthetase. Cat No: EXWM-5796.
Diphosphoryl Chloride 90%
Diphosphoryl Chloride is used in the synthesis of potent and orally bioavailable tricyclic CGRP receptor antagonists. Also used in the synthesis of transition state analogue inhbitors of inosine monophosphate. Group: Biochemicals. Alternative Names: Pyrophosphoryl Chloride; Phosphorodichloridic Anhydride; Phosphorus Chloride Oxide; Pyrophosphoryl Tetrachloride; Tetra chloropyrophosphoric Acid. Grades: Highly Purified. CAS No. 13498-14-1. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
F13459
It is produced by the strain of Penicillum sp. F13459. F13459 had inhibitory activity against inosine 5'-phosphate dehydrogenase and it can inhibit the synthesis of Newcastle disease virus (NDV) hemagglutinin (HA) at 25 μg/mL. Molecular formula: C27H28O11. Mole weight: 528.50.
GTP cyclohydrolase IIa
Requires Mg2+. This enzyme catalyses the hydrolysis of the imidazole ring of guanosine 5'-triphosphate, N7-methylguanosine 5'-triphosphate or inosine 5'-triphosphate. Xanthosine 5'-triphosphate and ATP are not substrates. It also catalyses the hydrolysis of diphosphate to form two equivalents of phosphate. Unlike GTP cyclohydrolase II (EC 3.5.4.25), this enzyme does not release formate, but does hydrolyse the diphosphate from GTP to phosphate. Group: Enzymes. Enzyme Commission Number: EC 3.5.4.29. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4556; GTP cyclohydrolase IIa; EC 3.5.4.29. Cat No: EXWM-4556.
hypoxanthine phosphoribosyltransferase
Guanine and 6-mercaptopurine can replace hypoxanthine. Group: Enzymes. Synonyms: IMP pyrophosphorylase; transphosphoribosidase; hypoxanthine-guanine phosphoribosyltransferase; guanine phosphoribosyltransferase; GPRT; HPRT; guanosine 5'-phosphate pyrophosphorylase; IMP-GMP pyrophosphorylase; HGPRTase; 6-hydroxypurine phosphoribosyltransferase; 6-mercaptopurine phosphoribosyltransferas. Enzyme Commission Number: EC 2.4.2.8. CAS No. 9016-12-0. HGPRT. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2691; hypoxanthine phosphoribosyltransferase; EC 2.4.2.8; 9016-12-0; IMP pyrophosphorylase; transphosphoribosidase; hypoxanthine-guanine phosphoribosyltransferase; guanine phosphoribosyltransferase; GPRT; HPRT; guanosine 5'-phosphate pyrophosphorylase; IMP-GMP pyrophosphorylase; HGPRTase; 6-hydroxypurine phosphoribosyltransferase; 6-mercaptopurine phosphoribosyltransferase; GMP pyrophosphorylase; guanine-hypoxanthine phosphoribosyltransferase; guanosine phosphoribosyltransferase; guanylate pyrophosphorylase; guanylic pyrophosphorylase; inosinate pyrophosphorylase; inosine 5'-phosphate pyrophosphorylase; inosinic acid pyrophosphorylase; inosinic pyrophosphorylase; 6-mercaptopurine phosphoribosyltransferase; purine-6-thiol phosphoribosyltransferase. Cat No: EXWM-2691.
IMP dehydrogenase
The enzyme acts on the hydroxy group of the hydrated derivative of the substrate. Group: Enzymes. Synonyms: inosine-5'-phosphate dehydrogenase; inosinic acid dehydrogenase; inosinate dehydrogenase; inosine 5'-monophosphate dehydrogenase; inosine monophosphate dehydrogenase; IMP oxidoreductase; inosine monophosphate oxidoreductase. Enzyme Commission Number: EC 1.1.1.205. CAS No. 9028-93-7. IMPDH2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0109; IMP dehydrogenase; EC 1.1.1.205; 9028-93-7; inosine-5'-phosphate dehydrogenase; inosinic acid dehydrogenase; inosinate dehydrogenase; inosine 5'-monophosphate dehydrogenase; inosine monophosphate dehydrogenase; IMP oxidoreductase; inosine monophosphate oxidoreductase. Cat No: EXWM-0109.
IMP-specific 5'-nucleotidase
The enzyme, isolated from the yeast Saccharomyces cerevisiae, is highly specific for inosine 5'-phosphate, and has no detectable activity with other purine and pyrimidine nucleotides. Requires divalent metals, such as Mg2+, Co2+ or Mn2+. Group: Enzymes. Synonyms: ISN1 (gene name). Enzyme Commission Number: EC 3.1.3.99. CAS No. 9027-73-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3706; IMP-specific 5'-nucleotidase; EC 3.1.3.99; 9027-73-0; ISN1 (gene name). Cat No: EXWM-3706.
inosine kinase
This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol group as acceptor. The systematic name of this enzyme class is ATP:inosine 5'-phosphotransferase. Other names in common use include inosine-guanosine kinase, and inosine kinase (phosphorylating). This enzyme participates in purine metabolism. Group: Enzymes. Synonyms: inosine-guanosine kinase; inosine kinase (phosphorylating). Enzyme Commission Number: EC 2.7.1.73. CAS No. 37237-46-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3103; inosine kinase; EC 2.7.1.73; 37237-46-0; inosine-guanosine kinase; inosine kinase (phosphorylating). Cat No: EXWM-3103.
Inosinic acid
Inosinic acid is an endogenous metabolite. Inosinic acid is used as umami tastant, or as the dietary supplement to improve the yield and meat quality of pigs [1]. Uses: Scientific research. Group: Natural products. Alternative Names: 5'-IMP; IMP; Inosine 5'-(dihydrogen phosphate). CAS No. 131-99-7. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-108213.
inositol-polyphosphate 5-phosphatase
One mammalian isoform is known. This enzyme is distinguished from the family of enzymes classified under EC 3.1.3.36, phosphoinositide 5-phosphatase, by its inability to dephosphorylate inositol lipids. Group: Enzymes. Synonyms: type I inositol-polyphosphate phosphatase; inositol trisphosphate phosphomonoesterase; InsP3/Ins(1,3,4,5)P4 5-phosphatase; inosine triphosphatase; D-myo-inositol 1,4,5-triphosphate 5-. Enzyme Commission Number: EC 3.1.3.56. CAS No. 106283-14-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3661; inositol-polyphosphate 5-phosphatase; EC 3.1.3.56; 106283-14-1; type I inositol-polyphosphate phosphatase; inositol trisphosphate phosphomonoesterase; InsP3/Ins(1,3,4,5)P4 5-phosphatase; inosine triphosphatase; D-myo-inositol 1,4,5-triphosphate 5-phosphatase; D-myo-inositol 1,4,5-trisphosphate 5-phosphatase; L-myo-inositol 1,4,5-trisphosphate-monoesterase; inositol phosphate 5-phosphomonoesterase; inositol-1,4,5-trisphosphate/1,3,4,5-tetrakisphosphate 5-phosphatase; Ins(1,4,5)P3 5-phosphatase; D-myo-inositol(1,4,5)/(1,3,4,5)-polyphosphate 5-phosphatase; inositol 1,4,5-trisphosphate phosphatase; inositol polyphosphate-5-phosphatase; myo-inositol-1,4,5-trisphosphate 5-phosphatase; inositol-1,4,5-trisphosphate 5-phosphatase. Cat No: EXWM-3661.
Purine nucleoside phosphorylase (also known as PNPase) is an enzyme (EC 2.4.2.1) involved in purine metabolism. PNP metabolizes adenosine into adenine, inosine into hypoxanthine, and guanosine into guanine, in each case creating ribose phosphate. NP encodes the enzyme purine nucleoside phosphorylase that together with adenosine deaminase (ADA) serves a key role in purine catabolism, referred to as the salvage pathway. Mutations in either enzyme result in a severe combined immunodeficiency (SCID). Confusingly, the same abbreviation (PNPase), is also used for another, otherwise unrelated, enzyme, namely Polynucleotide Phosphorylase. Purine nucleoside phosphorylase produced in microorganism has a molecular mass of 32 kda. Applications: Useful for enzymatic determination of inorganic phosphate. Group: Enzymes. Synonyms: inos. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. PNPase. Activity: > 500U/mL. Appearance: Colourless to light brown solution. Storage: -20°C. Form: Liquid. Source: Bacillus sp. inosinephosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; purine-nucleoside: phosphate ribosyltransferase; EC 2.4.2.1. Cat No: DIA-164.
In enzymology, a purine-nucleoside phosphorylase (EC 2.4.2.1) is an enzyme that catalyzes the chemical reaction: purine nucleoside + phosphate <-> purine + alpha-D-ribose 1-phosphate. Thus, the two substrates of this enzyme are purine nucleoside and phosphate, whereas its two products are purine and alpha-D-ribose 1-phosphate. This enzyme belongs to the family of glycosyltransferases, specifically the pentosyltransferases. Applications: This enzyme is useful for enzymatic determination of inorganic phosphorus, 5'-nucleotidase and adenosine deaminase when coupled with xanthine oxidase and uricase. Group: Enzymes. Synonyms: EC 2.4.2.1; inosinephosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynuc. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. PNPase. Mole weight: approx. 120 kDa. Activity: Grade? 15U/mg-solid or more. Stability: Stable at-20°C for at least 12 months. Appearance: White amorphous powder, lyophilized. Source: Microorganism. EC 2.4.2.1; inosinephosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; purine-nucleoside: phosphate ribosyltransferase. Cat No: DIA-216.
Native Microorganisms Nucleoside Phosphorylase
In enzymology, a purine-nucleoside phosphorylase (EC 2.4.2.1) is an enzyme that catalyzes the chemical reaction:purine nucleoside + phosphate<-> purine + alpha-D-ribose 1-phosphate. Thus, the two substrates of this enzyme are purine nucleoside and phosphate, whereas its two products are purine and alpha-D-ribose 1-phosphate. This enzyme belongs to the family of glycosyltransferases, specifically the pentosyltransferases. This enzyme participates in 3 metabolic pathways:purine metabolism, pyrimidine metabolism, and nicotinate and nicotinamide metabolism. Applications: Nucleoside phosphorylase is used in coupled enzyme systems to measure protein dephosphorylation. this e...osphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; 9030-21-1; EC 2.4.2.1. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. PNPase. Mole weight: mol wt ~120 kDa. Activity: > 10 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing potassium gluconate, mannitol and EDTA. Source: Microorganisms. purine-nucleoside phosphorylase; inosinephosphorylase; PNP; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; pu
Native Rabbit Phosphorylase b
Phosphorylase b is a non-active form and is present in resting muscle. Phosphorylase b kinase activity increases significantly when the Mg2+:ATP ratio exceeds. The breakdown of ATP during muscle contraction is thought to trigger in vivo conversion of phosphorylase b into a. Phosphorylase b is activated by inosine monophosphate. Applications: Phosphorylase b is used to study the conversion mechanism of inactive phosphorylase b to active phosphorylase in muscle. phosphorylase b is used to study which factors influence the conversion of phosphorylase b to phosphorylase a such as temperature, amp, fluoride and detergents. it is used to study phosphorylase b deficiency mutations. t...α-glucan phosphorylase; 1,4-α-glucan phosphorylase; glucosan phosphorylase; granulose phosphorylase; maltodextrin phosphorylase; muscle phosphorylase; myophosphorylase; potato phosphorylase; starch phosphorylase; 1,4-α-D-glucan:phosphate α-D-glucosyltransferase; phosphorylase (ambiguous). Enzyme Commission Number: EC 2.4.1.1. CAS No. 9012-69-5. Purity: 2× crystallization. GPBB. Mole weight: mol wt 97.2 kDa by calculation. Activity: Type I, > 20 units/mg protein; Type II, > 7 units/mg. Storage: -20°C. Form: Type I, Lyophilized powder containing lactose, 5?-AMP, and Mg (OAc)2 (10 μmole per 100 mg protein); Type II, lyophilized powder, light yellow. Sour
nucleoside diphosphate phosphatase
The enzyme, which appears to be limited to metazoa, acts on multiple nucleoside diphosphates as well as on D-ribose 5-diphosphate. Specificity depends on species and isoform. Group: Enzymes. Synonyms: nucleoside-diphosphatase; thiaminpyrophosphatase; UDPase; inosine diphosphatase; adenosine diphosphatase; IDPase; ADPase; adenosinepyrophosphatase; guanosine diphosphatase; guanosine 5'-diphosphatase; inosine 5'-diphosphatase; uridine diphosphatase; uridine 5'-diphosphatase; type B nucleoside diphosphatase; GDPase; CDPase; nucleoside 5'-diphosphatase; type L nucleoside diphosphatase; NDPase; nucleoside diphosphate phosphohydrolase. Enzyme Commission Number: EC 3.6.1.6. CAS No. 9027-69-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4632; nucleoside diphosphate phosphatase; EC 3.6.1.6; 9027-69-4; nucleoside-diphosphatase; thiaminpyrophosphatase; UDPase; inosine diphosphatase; adenosine diphosphatase; IDPase; ADPase; adenosinepyrophosphatase; guanosine diphosphatase; guanosine 5'-diphosphatase; inosine 5'-diphosphatase; uridine diphosphatase; uridine 5'-diphosphatase; type B nucleoside diphosphatase; GDPase; CDPase; nucleoside 5'-diphosphatase; type L nucleoside diphosphatase; NDPase; nucleoside diphosphate phosphohydrolase. Cat No: EXWM-4632.
Nucleoside Phosphorylase from bacterial, Recombinant
In enzymology, a purine-nucleoside phosphorylase (EC 2.4.2.1) is an enzyme that catalyzes the chemical reaction:purine nucleoside + phosphate<-> purine + alpha-D-ribose 1-phosphate. Thus, the two substrates of this enzyme are purine nucleoside and phosphate, whereas its two products are purine and alpha-D-ribose 1-phosphate. This enzyme belongs to the family of glycosyltransferases, specifically the pentosyltransferases. This enzyme participates in 3 metabolic pathways:purine metabolism, pyrimidine metabolism, and nicotinate and nicotinamide metabolism. Applications: Nucleoside phosphorylase is used in coupled enzyme systems to measure protein dephosphorylation. bac...eoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; 9030-21-1; EC 2.4.2.1. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. PNPase. Activity: > 10 units/mg protein. Storage: -20°C. Form: lyophilized powder. Source: E. coli. Species: Bacterial. purine-nucleoside phosphorylase; inosinephosphorylase; PNP; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; 9030-21-1; EC 2.4.2.1. Cat No: NATE-0607.
In decreasing order of activity, guanosine, inosine and adenosine diphosphate hexoses are substrates in the reverse reaction, with either glucose or mannose as the sugar. Group: Enzymes. Synonyms: NDP hexose pyrophosphorylase; hexose 1-phosphate nucleotidyltransferase; hexose nucleotidylating enzyme; nucleoside diphosphohexose pyrophosphorylase; hexose-1-phosphate guanylyltransferase; GTP:α-D-hexose-1-phosphate guanylyltransferase; GDP hexose pyrophosphorylase; guanosine diphosphohexose pyrophosphorylase; nucleoside-triphosphate-hexose-1-phosphate nucleotidyltransferase; NTP:he. Enzyme Commission Number: EC 2.7.7.28. CAS No. 37278-26-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3239; nucleoside-triphosphate-aldose-1-phosphate nucleotidyltransferase; EC 2.7.7.28; 37278-26-5; NDP hexose pyrophosphorylase; hexose 1-phosphate nucleotidyltransferase; hexose nucleotidylating enzyme; nucleoside diphosphohexose pyrophosphorylase; hexose-1-phosphate guanylyltransferase; GTP:α-D-hexose-1-phosphate guanylyltransferase; GDP hexose pyrophosphorylase; guanosine diphosphohexose pyrophosphorylase; nucleoside-triphosphate-hexose-1-phosphate nucleotidyltransferase; NTP:hexose-1-phosphate nucleotidyltransferase. Cat No: EXWM-3239.
phosphoribosylglycinamide formyltransferase
This THF dependent enzyme catalyzes a nucleophilic acyl substitution of the formyl group from 10-formyltetrahydrofolate (fTHF) to N1-(5-phospho-D-ribosyl)glycinamide (GAR) to form N2-formyl-N1-(5-phospho-D-ribosyl)glycinamide (fGAR) as shown above. This reaction plays an important role in the formation of purine through the de novo purine biosynthesis pathway. This pathway creates inosine monophosphate (IMP), a precursor to adenosine monophosphate (AMP) and guanosine monophosphate (GMP). Group: Enzymes. Synonyms: 2-amino-N-ribosylacetamide 5'-phosphate transformylase; GAR formyltransferase; GAR transformylase; glycinamide ribonucleotide transformylase; GAR TFase; 5,10-methenyltetrahydrofolate:2-amino-N-ribosylacetamide ribonucleotide transformylase. Enzyme Commission Number: EC 2.1.2.2. CAS No. 9032-2-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2004; phosphoribosylglycinamide formyltransferase; EC 2.1.2.2; 9032-02-4; 2-amino-N-ribosylacetamide 5'-phosphate transformylase; GAR formyltransferase; GAR transformylase; glycinamide ribonucleotide transformylase; GAR TFase; 5,10-methenyltetrahydrofolate:2-amino-N-ribosylacetamide ribonucleotide transformylase. Cat No: EXWM-2004.
purine-nucleoside phosphorylase
Specificity not completely determined. Can also catalyse ribosyltransferase reactions of the type catalysed by EC 2.4.2.5, nucleoside ribosyltransferase. Group: Enzymes. Synonyms: inosinephosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. PNPase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2638; purine-nucleoside phosphorylase; EC 2.4.2.1; 9030-21-1; inosinephosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase. Cat No: EXWM-2638.
Purine nucleoside phosphorylase, Recombinant
Purine nucleoside phosphorylase is an enzyme involved in purine metabolism. PNP metabolizes adenosine into adenine, inosine into hypoxanthine, and guanosine into guanine. Mutations in the PNP gene are responsible for purine nucleoside phosphorylase deficiency. Applications: Purine nucleoside phosphorylase is used to study nucleotide salvage pathways and purine metabolism. it is used to study purine nucleoside phosphorylase deficiency and responsible pnp genetic mutations. this product is recombinant and expressed in e. coli. Group: Enzymes. Synonyms: purine-nucleoside phosphorylase; inosinephosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosp. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. PNPase. Activity: > 120 U/mL. Storage: -20°C. Form: buffered aqueous solution (100 mM phosphate buffer with 1 mM MgCl2. Source: E. coli. purine-nucleoside phosphorylase; inosinephosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; EC 2.4.2.1; 9030-21-1. Cat No: NATE-0644.
Recombinant mutant (Met62Val) purine nucleoside phosphorylase from E. coli
Purine nucleoside phosphorylase is an enzyme involved in purine metabolism. PNP metabolizes adenosine into adenine, inosine into hypoxanthine, and guanosine into guanine. Mutations in the PNP gene are responsible for purine nucleoside phosphorylase deficiency. Applications: These enzymes are widely used for the synthesis of modified nucleotides (virasol, cladribine, fludarabine) which are efficient antiviral and antitumor drugs. Group: Enzymes. Synonyms: purine-nucleoside phosphorylase; inosinephosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase;. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. Purity: > 95 %. PNPase. Mole weight: 156 kDa. Activity: 27 U/mg. Appearance: Colourless clear liquid. Storage: Store at -20 degree C, for extended storage, conserve at -20 degree C or -80 degree C. Source: E. coli. Species: E. coli. purine-nucleoside phosphorylase; inosinephosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; EC 2.4.2.1; 9030-21-1. Cat No: NATE-1000.
Ribavirin
Ribavirin is a nucleoside analog that inhibits the replication of both DNA and RNA viruses, including influenza type A and type B. Ribavirin, as ribavirin 5-phosphate, affects virus-infected cells primarily by inhibiting the enzyme inosine 5-monophosphate (IMP) dehydrogenase. It potently suppresses eIF4E-mediated oncogenic transformation of murine cells in vitro, of tumor growth of a mouse model of eIF4E-dependent human squamous cell carcinoma in vivo, and of colony formation of eIF4E-dependent acute myelogenous leukemia cells derived from human patients. Group: Biochemicals. Alternative Names: 1-ß-D-Ribofuranosyl-1H-1,2,4-triazole-3-carboxamide, ICN-1229, Rebetol, Viramid, Virazid, Virazole. Grades: Highly Purified. CAS No. 36791-04-5. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: C8H12N4O5, Molecular Weight: 244.2. US Biological Life Sciences.
Worldwide
Ribavirin 5'-monophosphate lithium salt
Ribavirin 5'-monophosphate is a metabolite of ribavirin, displaying broad-spectrum antiviral activity. It inhibits viral DNA and RNA replication in vitro via suppression of inosine monophosphate dehydrogenase (IMPDH), resulting in inhibition of guanosine triphosphate synthesis. Synonyms: Dilithium [5-(3-carbamoyl-1,2,4-triazol-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate. Grades: ≥95%. CAS No. 66983-94-6. Molecular formula: C8H11N4O8P·2Li. Mole weight: 336.1.
Ribavirin Monophosphate
Ribavirin-5'-monophosphate is a potent competitive inhibitor of inosine 5'-phosphate dehydrogenase. In addition, Ribavirin 5'-monophosphate inhibits viral DNA and RNA replication in vitro via the strong competitive inhibition of inosine monophosphate dehydrogenase (IMPDH) (Ki= 270 nM). Uses: Antiviral agents. Synonyms: Sodium salt. Grades: ≥ 95 % by HPLC. CAS No. 40925-28-8. Molecular formula: C8H13N4O8P (free acid). Mole weight: 324.18 (free acid).
Guanosine 5'-monophosphate disodium salt
Disodium guanylate, also known as sodium 5'-guanylate and disodium 5'-guanylate, is a natural sodium salt of the flavor enhancing nucleotide guanosine monophosphate (GMP). Disodium guanylate is a food additive with the E number E627. It is commonly used in conjunction with glutamic acid (monosodium glutamate, MSG). As it is a fairly expensive additive, it is not used independently of glutamic acid; if disodium guanylate is present in a list of ingredients but MSG does not appear to be, it is likely that glutamic acid is provided as part of another ingredient such as a processed soy protein complex. It is often added to foods in conjunction with disodium inosinate; the combination is known as disodium 5'-ribonucleotides. Disodium guanylate is produced from dried seaweed and is often added to instant noodles, potato chips and other snacks, savory rice, tinned vegetables, cured meats, and packaged soup. Synonyms: Disodium guanylate; Disodium GMP; Disodium 5'-gmp; GMP disodium salt; 5'-Gmp disodium salt; Disodium guanosine-5'-monophosphate; 5'-Guanylic acid disodium salt; Sodium 5'-guanylate; Guanosine 5'-phosphate disodium salt. Grades: 98%. CAS No. 5550-12-9. Molecular formula: C10H12N5O8P·2Na. Mole weight: 407.18.
inosinate nucleosidase
This enzyme belongs to the family of hydrolases, specifically those glycosylases that hydrolyse N-glycosyl compounds. The systematic name of this enzyme class is 5'-inosinate phosphoribohydrolase. This enzyme participates in purine metabolism. Group: Enzymes. Synonyms: 5'-inosinate phosphoribohydrolase. Enzyme Commission Number: EC 3.2.2.12. CAS No. 37288-61-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3966; inosinate nucleosidase; EC 3.2.2.12; 37288-61-2; 5'-inosinate phosphoribohydrolase. Cat No: EXWM-3966.
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