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| Product | Description | |
|---|---|---|
| Glyoxylic acid | Glyoxylic acid. Group: Biochemicals. Alternative Names: 2-Oxoacetic acid. Grades: Highly Purified. CAS No. 298-12-4. Pack Sizes: 100g, 250g, 500g, 1kg, 2kg. Molecular Formula: C2H2O3. US Biological Life Sciences. |  Worldwide |
| Glyoxylic Acid-13C2 Monohydrate | Labeled Glyoxylic Acid. Occurs in unripe fruit and in young green leaves; has also been found in very young sugar beets. Group: Biochemicals. Alternative Names: 2-Oxoacetic Acid-13C2 Monohydrate; Glyoxalic Acid-13C2 Monohydrate; Formylformic Acid-13C2 Monohydrate; NSC 27785-13C2; Oxalaldehydic Acid-13C2 Monohydrate; Oxoacetic Acid-13C2 Monohydrate; Oxoethanoic Acid-13C2 Monohydrate; α-Ketoacetic Acid-13C2 Monohydrate. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Glyoxylic Acid (50% aqueous solution) | Glyoxylic Acid is used as a reagent in the synthesis of N-{[6-chloro-4- (2, 6-dimethoxyphenyl) quinazolin-2-yl]carbonyl}-L-leucine, a novel nonpeptide chemotype selective for neurotensin receptor 2. Also used as a reagent in the synthesis of elemonic acid derivatives as Pin1 inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 298-12-4. Pack Sizes: 1g, 10g. Molecular Formula: C2H2O3. US Biological Life Sciences. | Worldwide |
| Glyoxylic Acid Hydrate-13C2 | Glyoxylic Acid Hydrate-13C2 is the labelled hydrated analog of Glyoxylic Acid (G754995) which is used as a reagent in the synthesis of N-{[6-chloro-4- (2, 6-dimethoxyphenyl) quinazolin-2-yl]carbonyl}-L-leucine, a novel nonpeptide chemotype selective for neurotensin receptor 2. Also used as a reagent in the synthesis of elemonic acid derivatives as Pin1 inhibitors. Glyoxylic Acid-13C2 was used in the synthesis of carbon labelled 6-N-carboxymethyllysine (CML) which is the most used marker for advanced glycation endproducts in food analysis. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 5mg. Molecular Formula: 3C2H4O4, Molecular Weight: 94.04. US Biological Life Sciences. | Worldwide |
| Glyoxylic acid monohydrate | 100g Pack Size. Group: Building Blocks, Organics. Formula: C2H2O3 ·H2O. CAS No. 563-96-2. Prepack ID 31823498-100g. Molecular Weight 92.05. See USA prepack pricing. |  |
| Glyoxylic Acid Monohydrate | Occurs in unripe fruit and in young green leaves; has also been found in very young sugar beets. Group: Biochemicals. Grades: Highly Purified. CAS No. 563-96-2. Pack Sizes: 10g, 50g, 100g, 250g, 500g. Molecular Formula: C?H?O?, Molecular Weight: 92.05. US Biological Life Sciences. | Worldwide |
| 2-(2-Aminothiazol-4-yl) glyoxylic acid | 2-(2-Aminothiazol-4-yl) glyoxylic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 73150-67-1. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| 2-(2-Formamido-4-thiazolyl)glyoxylic Acid Hydrate | 2-(2-Formamido-4-thiazolyl)glyoxylic Acid is used as a reagent in the synthesis of cephalosporins which are a class of beta-lactam antibiotics which are active against gram-positive and potentially against gram-negative bacteria. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg, 100mg. Molecular Formula: C6H4N2O4S xH2O. US Biological Life Sciences. | Worldwide |
| 2-(2-Tritylamino-4-thiazolyl)glyoxylic Acid | 2-(2-Tritylamino-4-thiazolyl)glyoxylic Acid was used to prepare and stuyd the antibacterial activity of aceto hydroxamoyl ethyl iminoacetyl cephalosporins. Group: Biochemicals. Grades: Highly Purified. CAS No. 68363-44-0. Pack Sizes: 50mg, 100mg. Molecular Formula: C24H18N2O3S, Molecular Weight: 414.48. US Biological Life Sciences. | Worldwide |
| 2- (4-Chlorophenyl) indolizine 3-Glyoxylic Acid | 2- (4-Chlorophenyl) indolizine 3-Glyoxylic Acid is a derivative of 2- (4-Chlorophenyl) indolizine (C377760); a reagent in the synthesis of 2-Aryl -3- (4-dialkyl aminopropoxybenzoyl ) indolizines which are useful in the treatment of angina pectoris. Group: Biochemicals. Grades: Highly Purified. CAS No. 890091-80-2. Pack Sizes: 25mg, 250mg. Molecular Formula: C16H10ClNO3, Molecular Weight: 299.709999999999. US Biological Life Sciences. | Worldwide |
| 7-Ethylindole-3-glyoxylic acid ethyl ester | Heterocyclic Organic Compound. Alternative Names: 7-ETHYLINDOLE-3-GLYOXYLIC ACID ETHYL ESTER. CAS No. 111478-90-1. Molecular formula: C14H15NO3. Mole weight: 245.27. Catalog: ACM111478901. |  |
| Allantoin EP Impurity A (Glyoxylic acid) | Allantoin EP Impurity A (Glyoxylic acid). Uses: For analytical and research use. Group: Impurity standards. CAS No. 298-12-4. Molecular Formula: C2H2O3. Mole Weight: 74.04. Catalog: APB298124. |  |
| Indole-3-glyoxylic acid | Indole-3-glyoxylic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 1477-49-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C10H7NO3. US Biological Life Sciences. | Worldwide |
| Indole-3-glyoxylic acid ≥96% (HPLC) | Indole-3-glyoxylic acid ≥96% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Thiophene-2-glyoxylic acid | Thiophene-2-glyoxylic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 4075-59-6. Pack Sizes: 2g, 5g, 10g, 25g, 50g. US Biological Life Sciences. | Worldwide |
| Acetic acid,2-chloro-2-[2-(4-methoxy-2-nitrophenyl)hydrazinylidene]-,ethyl ester | Heterocyclic Organic Compound. Alternative Names: 119750-09-3, Ethyl 2-chloro-2-[2-(4-methoxy-2-nitrophenyl)hydrazono]acetate, Acetic acid,2-chloro-2-[2-(4-methoxy-2-nitrophenyl)hydrazinylidene]-, ethyl ester, Ethyl 2-chloro-2-(2-(4-methoxy-2-nitrophenyl)hydrazono)acetate, AC1MC8JC, ACMC-1C0RK, CTK4B1477, ANW-55816, AG-D-42878, KB-201305, A804351, ethyl 2-chloro-2-[ (4-methoxy-2-nitrophenyl) hydrazinylidene]acetate, ethyl 2-chloranyl-2-[(4-methoxy-2-nitro-phenyl)hydrazinylidene]ethanoate, 2-chloro-2-[(4-methoxy-2-nitrophenyl)hydrazinylidene]acetic acid ethyl ester, Glyoxylicacid, chloro-, ethyl ester, (4-methoxy-2-nitrophenyl)hydrazone (6CI). CAS No. 119750-09-3. Molecular formula: C11H12ClN3O5. Mole weight: 301.68. Purity: 0.96. IUPACName: ethyl 2-chloro-2-[(4-methoxy-2-nitrophenyl)hydrazinylidene]acetate. Canonical SMILES: CCOC (=O)C (=NNC1=C (C=C (C=C1)OC)[N+] (=O)[O-])Cl. Catalog: ACM119750093. | |
| Allantoin | Vulnerary; debriding agent. Purine metabolite via the uric acid pathway. Group: Biochemicals. Alternative Names: 5-Ureidohydantoin; (2,5-Dioxo-4-imidazolidinyl)urea; Allantol; Cordianine; Glyoxyldiureid; Glyoxyldiureide; Glyoxylic Diureide; NSC 7606; Psoralon; Sebical; Septalan. Grades: Highly Purified. CAS No. 97-59-6. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Benzeneacetic acid,3-fluoro-a-oxo-,ethyl ester | Heterocyclic Organic Compound. Alternative Names: ETHYL 2-(3-FLUOROPHENYL)-2-OXOACETATE;ETHYL 3-FLUOROBENZOYLFORMATE;ETHYL (3-FLUOROPHENYL)-OXO-ACETATE;(3-FLUOROPHENYL)GLYOXYLIC ACID ETHYL ESTER;(3-Fluorophenyl)oxoacetic acid ethyl ester. CAS No. 110193-59-4. Molecular formula: C10H9FO3. Mole weight: 196.18. Purity: 0.96. IUPACName: ethyl 2-(3-fluorophenyl)-2-oxoacetate. Canonical SMILES: CCOC(=O)C(=O)C1=CC(=CC=C1)F. Density: 1.213g/cm³. Catalog: ACM110193594. | |
| Benzeneacetic acid,a-oxo-3-(trifluoromethyl)-,ethylester | Heterocyclic Organic Compound. Alternative Names: ETHYL (3-TRIFLUOROMETHYLPHENYL)GLYOXYLATE;(3-TRIFLUOROMETHYLPHENYL)GLYOXYLIC ACID ETHYL ESTER;3-OXO-3-(3-TRIFLUOROMETHYLPHENYL)PROPIONIC ACID ETHYL ESTER;ethyl 2-oxo-2-[3-(trifluoromethyl)phenyl]acetate. CAS No. 110193-60-7. Molecular formula: C11H9F3O3. Mole weight: 260.21. Appearance: Yellow oil. Purity: ≥95%. IUPACName: ethyl 2-oxo-2-[3-(trifluoromethyl)phenyl]acetate. Canonical SMILES: CCOC(=O)C(=O)C1=CC(=CC=C1)C(F)(F)F. Density: 1.267g/mLat25°C(lit.). Catalog: ACM110193607. | |
| Ethyl 2-chloro-2-[2-(4-chloro-2-nitrophenyl)hydrazono]acetate | Heterocyclic Organic Compound. Alternative Names: 112091-27-7, Ethyl 2-chloro-2-(2-(4-chloro-2-nitrophenyl)hydrazono)acetate, Acetic acid,2-chloro-2-[2-(4-chloro-2-nitrophenyl)hydrazinylidene]-, ethyl ester, Ethyl chloro[2-(4-chloro-2-nitrophenyl)hydrazono]acetate, ethyl 2-chloro-2-[2-(4-chloro-2-nitrophenyl)hydrazono]acetate, AC1MC8JE, ACMC-20a3s2, CTK4A7654, ANW-55824, AG-D-30973, KB-252603, ethyl 2-chloro-2-[ (4-chloro-2-nitrophenyl) hydrazinylidene]acetate, Aceticacid, chloro[(4-chloro-2-nitrophenyl)hydrazono]-, ethyl ester (9CI); Glyoxylicacid, chloro-, ethyl ester, (4-chloro-2-nitrophenyl)hydrazone (6CI). CAS No. 112091-27-7. Molecular formula: C10H9Cl2N3O4. Mole weight: 306.1041. Purity: 0.96. IUPACName: ethyl 2-chloro-2-[(4-chloro-2-nitrophenyl)hydrazinylidene]acetate. Canonical SMILES: CCOC (=O)C (=NNC1=C (C=C (C=C1)Cl)[N+] (=O)[O-])Cl. Density: 1.51g/cm³. Catalog: ACM112091277. | |
| Ethyl benzoylformate-d5 | Heterocyclic Organic Compound. Alternative Names: α-Oxo-benzeneacetic-d5 Acid Ethyl Ester; Phenyl-glyoxylic-d5 Acid Ethyl Ester; 2-Oxo-2-phenylacetic-d5 Acid Ethyl Ester; Ethyl 2-Oxo-2-phenylacetate-d5; Ethyl 2-Phenyl-2-oxoacetate-d5; NSC 6766-d5; Phenylglyoxylic-d5 Acid Ethyl Ester. CAS No. 1025892-26-5. Molecular formula: C10H5D5O3. Mole weight: 183.22. Purity: 0.96. IUPACName: ethyl 2-oxo-2-(2,3,4,5,6-pentadeuteriophenyl)acetate. Canonical SMILES: CCOC(=O)C(=O)C1=CC=CC=C1. Catalog: ACM1025892265. | |
| glyoxylate reductase | Reduces glyoxylate to glycolate or hydroxypyruvate to D-glycerate. Group: Enzymes. Synonyms: NADH-glyoxylate reductase; glyoxylic acid reductase; NADH-dependent glyoxylate reductase. Enzyme Commission Number: EC 1.1.1.26. CAS No. 9028-32-4. 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-0165; glyoxylate reductase; EC 1.1.1.26; 9028-32-4; NADH-glyoxylate reductase; glyoxylic acid reductase; NADH-dependent glyoxylate reductase. Cat No: EXWM-0165. |  |
| meso-tartrate dehydrogenase | This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-CH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is meso-tartrate:NAD+ oxidoreductase. This enzyme participates in glyoxylic acid and dicarboxylic acid metabolism. Group: Enzymes. Enzyme Commission Number: EC 1.3.1.7. CAS No. 37251-06-2. 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-1338; meso-tartrate dehydrogenase; EC 1.3.1.7; 37251-06-2. Cat No: EXWM-1338. | |
| Sodium glyoxylate | Use as dispersing agent. Group: Anionic surfactants. Alternative Names: Glyoxylic acid, sodium salt. CAS No. 2706-75-4. Molecular formula: C2HNaO3. Mole weight: 96.02. Catalog: ACM2706754. | |
| 2,3-Dimethyl-1-butene | 2,3-Dimethyl-1-butene is used in reactions to convert fatty acids to flavor compounds. It is also used in reactions with asymmetric glyoxylate to form α-hydroxy esters. Group: Biochemicals. Alternative Names: 1-Isopropyl-1-methylethylene; 2,3-Dimethyl-1-butene; 2,3-Dimethyl-1-butylene; 2-Isopropylpropene; NSC 73906. Grades: Highly Purified. CAS No. 563-78-0. Pack Sizes: 50g. US Biological Life Sciences. | Worldwide |
| 2-hydroxyglutarate synthase | This enzyme belongs to the family of transferases, specifically those acyltransferases that convert acyl groups into alkyl groups on transfer. This enzyme participates in c5-branched dibasic acid metabolism. Group: Enzymes. Synonyms: 2-hydroxyglutaratic synthetase; 2-hydroxyglutaric synthetase; α-hydroxyglutarate synthase; hydroxyglutarate synthase; 2-hydroxyglutarate glyoxylate-lyase (CoA-propanoylating). Enzyme Commission Number: EC 2.3.3.11. CAS No. 9024-2-6. 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-2312; 2-hydroxyglutarate synthase; EC 2.3.3.11; 9024-02-6; 2-hydroxyglutaratic synthetase; 2-hydroxyglutaric synthetase; α-hydroxyglutarate synthase; hydroxyglutarate synthase; 2-hydroxyglutarate glyoxylate-lyase (CoA-propanoylating). Cat No: EXWM-2312. | |
| 3,4-Dihydroxy-3-cyclobutene-1,2-dione | 3,4-dihydroxy-3-cyclobutene-1,2 dione, commonly known as squaric acid, is widely used in bioorganic and medicinal chemistry. It is an inhibitor of glyoxylase, semiqauric acid, pyruvate dehrogenase, and transketolase. It is used as a replacement for phosphate in a peptide-based ligand for an SH2 domain. Its derivatives are high-affinity ligands for excitatory amino acid receptors. These derivatives are also used as dyes for fluorescence detection of small biological molecules. Uses: 3,4-dihydroxy-3-cyclobutene-1,2-dione can be used: in fluorescence detection in immunoassays, hybridization assays, enzymatic reactions, and other analytical procedures. to form diffraction quality crystals. to synthesize a squarate dianion, which is used as a building block to create uncharged polymeric networks. these ordered structures are used in catalysis, nonlinear optics, electrical conductivity, molecular recognition, and molecular sieves. Group: Organic & printed electronics. Alternative Names: Squaric acid. CAS No. 2892-51-5. Molecular formula: (HO)2C4(=O)2. Mole weight: 114.06. Appearance: Gray crystalline solid. Purity: 95%+. IUPACName: 3,4-Dihydroxycyclobut-3-ene-1,2-dione. Canonical SMILES: C1(=C(C(=O)C1=O)O)O. Density: 1.82 g/cm³. ECNumber: 220-761-4. Catalog: ACM2892515-1. | |
| 3,4-Dihydroxy-3-cyclobutene-1,2-dione | 3,4-dihydroxy-3-cyclobutene-1,2 dione, commonly known as squaric acid, is widely used in bioorganic and medicinal chemistry. It is an inhibitor of glyoxylase, semiqauric acid, pyruvate dehrogenase, and transketolase. It is used as a replacement for phosphate in a peptide-based ligand for an SH2 domain. Its derivatives are high-affinity ligands for excitatory amino acid receptors. These derivatives are also used as dyes for fluorescence detection of small biological molecules. Uses: 3,4-dihydroxy-3-cyclobutene-1,2-dione can be used: in fluorescence detection in immunoassays, hybridization assays, enzymatic reactions, and other analytical procedures. to form diffraction quality crystals. to synthesize a squarate dianion, which is used as a building block to create uncharged polymeric networks. these ordered structures are used in catalysis, nonlinear optics, electrical conductivity, molecular recognition, and molecular sieves. Group: Synthetic tools and reagents. Alternative Names: Squaric acid. CAS No. 2892-51-5. Pack Sizes: Packaging 5 g in glass bottle 25, 100 g in poly bottle. Product ID: 3,4-Dihydroxycyclobut-3-ene-1,2-dione. Molecular formula: 114.06. Mole weight: (HO)2C4(=O)2. C1(=C(C(=O)C1=O)O)O. InChI=1S/C4H2O4/c5-1-2 (6)4 (8)3 (1)7/h5-6H. PWEBUXCTKOWPCW-UHFFFAOYSA-N. 95%+. |  |
| 4-aminobutyrate-pyruvate transaminase | Requires pyridoxal 5'-phosphate. The enzyme is found in plants that do not have the 2-oxoglutarate dependent enzyme (cf. EC 2.6.1.19). The reaction with pyruvate is reversible while the reaction with glyoxylate only takes place in the forward direction. Group: Enzymes. Synonyms: aminobutyrate aminotransferase (ambiguous); γ-aminobutyrate aminotransaminase (ambiguous); γ-aminobutyrate transaminase (ambiguous); γ-aminobutyric acid aminotransferase (ambiguous); γ-aminobutyric acid pyruvate transamin. Enzyme Commission Number: EC 2.6.1.96. 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-2937; 4-aminobutyrate-pyruvate transaminase; EC 2.6.1.96; aminobutyrate aminotransferase (ambiguous); γ-aminobutyrate aminotransaminase (ambiguous); γ-aminobutyrate transaminase (ambiguous); γ-aminobutyric acid aminotransferase (ambiguous); γ-aminobutyric acid pyruvate transaminase; γ-aminobutyric acid transaminase (ambiguous); γ-aminobutyric transaminase (ambiguous); 4-aminobutyrate aminotransferase (ambiguous); 4-aminobutyric acid aminotransferase (ambiguous); aminobutyrate transaminase (ambiguous); GABA aminotransferase (ambiguous); GABA transaminase (ambiguous); GABA transferase; POP2 (gene name). Cat No: EXWM-2937. | |
| 5-(Benzyloxy)indole-3-glyoxylamide | An intermediate in the preparation of hydroxyindolyl glyoxyl ic acid amides and Serotonin derivatives. Group: Biochemicals. Alternative Names: [5-(Benzyloxy)indol-3-yl]glyoxylamide; α-Oxo-5-(phenylmethoxy)-1H-indole-3-acetamide. Grades: Highly Purified. CAS No. 22424-62-0. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Allantoin-13C2,15N4 | Vulnerary; debriding agent. Purine metabolite via the uric acid pathway. Group: Biochemicals. Alternative Names: 5-Ureidohydantoin-13C2,15N4; (2,5-Dioxo-4-imidazolidinyl)urea-13C2,15N4; Allantol-13C2,15N4; Cordianine-13C2,15N4; Glyoxyldiureid-13C2,15N4; NSC 7606-13C2,15N4; Psoralon-13C2,15N4; Sebical-13C2,15N4; Septalan-13C2,15N4. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| aromatic-amino-acid-glyoxylate transaminase | Phenylalanine, kynurenine, tyrosine and histidine can act as amino donors; glyoxylate, pyruvate and hydroxypyruvate can act as amino acceptors. Group: Enzymes. Enzyme Commission Number: EC 2.6.1.60. CAS No. 67185-76-6. 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-2902; aromatic-amino-acid-glyoxylate transaminase; EC 2.6.1.60; 67185-76-6. Cat No: EXWM-2902. | |
| Boronic acid,b-(3-methoxy-6-phenyl-4-pyridazinyl)- | Heterocyclic Organic Compound. Alternative Names: Glyoxylonitrile,phenyl-,oxime,O,O-dimethyl phosphorothioate; 3-methoxy-6-phenyl-4-pyridazinylboronic acid; Phoxim-methyl [ISO]; Phoxim-methyl; BAY 7660; 3-methoxy-6-phenyl-2,4-dioxa-5-aza-3-phosphahept-5-ene-7-nitrile,3-sulfide; 2,4-Dioxa-5-aza-3-phophahe. CAS No. 1015480-94-0. Molecular formula: C11H11BN2O3. Mole weight: 230.02764;g/mol. Purity: 0.96. IUPACName: (3-methoxy-6-phenylpyridazin-4-yl)boronicacid. Canonical SMILES: B(C1=CC(=NN=C1OC)C2=CC=CC=C2)(O)O. Catalog: ACM1015480940. | |
| Cefmenoxime | It is produced by the strain of Semisynthetic third generation cephalosporin for injection. Synonyms: Cefmenoximum; Cefmenoxima; (6R,7R)-(2-(2-Amino-4-thiazolyl)glyoxylamido)-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-2-carbonsaeure-7-(Z)-(O-methyloxim); AB 50912; SCE 1365; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[ (2Z)- (2-amino-4-thiazolyl) (methoxyimino)acetyl]amino]-3-[[ (1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, (6R, 7R)-. Grades: ≥ 97%. CAS No. 65085-01-0. Molecular formula: C16H17N9O5S3. Mole weight: 511.56. |  |
| Cefteram | It is produced by the strain of Semisynthetic third generation cephalosporin. Synonyms: Ceftetrame; Cefterame; Cefteramum; (+)-(6R,7R)-7-(2-(2-Amino-4-thiazolyl)glyoxylamido)-3-((5-methyl-2H-tetrazol-2-yl)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7(sup 2)-(Z)-(O-methyloxime). Grades: > 95%. CAS No. 82547-58-8. Molecular formula: C16H17N9O5S2. Mole weight: 479.49. | |
| Cefuroxime | It is produced by the strain of Semisynthetic second generation cephalosporin. Cefuroxime is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime has a broad spectrum activity against Gram-positive and Gram-negative bacteria. Synonyms: Cephuroxime; Cefuroxim; Cefuroximo; Cefuroximum; Sharox; Zinacef; Biofuroksym; Cefuril; (6R,7R)-7-(2-(2-Furyl)glyoxylamido)-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid 7(sup 2)-(Z)-(O-methyloxime) carbamate (ester). Grades: 98%. CAS No. 55268-75-2. Molecular formula: C16H16N4O8S. Mole weight: 424.39. | |
| D-lysopine dehydrogenase | In the reverse reaction, a number of L-amino acids can act instead of L-lysine, and 2-oxobutanoate and, to a lesser extent, glyoxylate can act instead of pyruvate. Group: Enzymes. Synonyms: D-lysopine synthase; lysopine dehydrogenase; D(+)-lysopine dehydrogenase; 2-N-(D-1-carboxyethyl)-L-lysine:NADP+ oxidoreductase (L-lysine-forming). Enzyme Commission Number: EC 1.5.1.16. CAS No. 65187-41-9. 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-1497; D-lysopine dehydrogenase; EC 1.5.1.16; 65187-41-9; D-lysopine synthase; lysopine dehydrogenase; D(+)-lysopine dehydrogenase; 2-N-(D-1-carboxyethyl)-L-lysine:NADP+ oxidoreductase (L-lysine-forming). Cat No: EXWM-1497. | |
| Ethyl 2-(2-Aminothiazol-4-yl)glyoxylate | Ethyl 2-(2-Aminothiazol-4-yl)glyoxylate is used in the synthesis of antibacterial compounds. Also used in the synthesis of antiallergic and antiinflammatory agents, as glycolic amide derivatives. Group: Biochemicals. Alternative Names: (2-Amino-1,3-thiazol-4-yl)(oxo)acetic Acid Ethyl Ester; Ethyl 2-(2-Aminothiazol-4-yl)-2-oxoacetate; Ethyl 2-aminothiazol-4-ylglyoxylate; [2-Amino(thiazol-4-yl)](oxo)acetic Acid Ethyl Ester. Grades: Highly Purified. CAS No. 64987-08-2. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| Ethyl 4-fluorophenylglyoxylate | Ethyl 4-fluorophenyl glyoxyl ate. Group: Biochemicals. Alternative Names: 4-Fluoro-a-oxobenzeneacetic acid. Grades: Highly Purified. CAS No. 1813-94-1. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C10H9FO3. US Biological Life Sciences. | Worldwide |
| Ethyl Thiophene-2-glyoxylate | Ethyl Thiophene-2-glyoxylate. Group: Biochemicals. Alternative Names: 2-Oxo-2-(thiophen-2-yl)acetic Acid Ethyl Ester; Ethyl 2-oxo-2-(2-Thienyl)acetate; Ethyl 2-oxo-2-(2-Thienyl)ethanoate; Ethyl 2-oxo-2-(2'-thienyl)acetate; Ethyl 2-oxo-2-(Thiophen-2-yl)acetate; Ethyl 2-oxo-2-Thienylacetate; Ethyl 2-Thienylglyoxylate; Ethyl 2-Thiopheneglyoxylate; Ethyl oxo(2-Thienyl)acetate; Ethyl α-oxo-2-Thiopheneacetate. Grades: Highly Purified. CAS No. 4075-58-5. Pack Sizes: 10g. Molecular Formula: C8H8O3S, Molecular Weight: 184.21. US Biological Life Sciences. | Worldwide |
| glutamine-pyruvate transaminase | A pyridoxal-phosphate protein. L-Methionine can act as donor; glyoxylate can act as acceptor. Group: Enzymes. Synonyms: glutaminase II; L-glutamine transaminase L; glutamine-oxo-acid transaminase. Enzyme Commission Number: EC 2.6.1.15. CAS No. 9030-44-8. 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-2855; glutamine-pyruvate transaminase; EC 2.6.1.15; 9030-44-8; glutaminase II; L-glutamine transaminase L; glutamine-oxo-acid transaminase. Cat No: EXWM-2855. | |
| glycerate 3-kinase | This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol group as acceptor. This enzyme participates in 3 metabolic pathways: serine/glycine/threonine metabolism, glycerolipid metabolism, and glyoxylate-dicarboxylate metabolism. Group: Enzymes. Synonyms: glycerate kinase (phosphorylating) (ambiguous); D-glycerate 3-kinase; D-glycerate kinase (ambiguous); glycerate-kinase (ambiguous); GK (ambiguous); D-glyceric acid kinase (ambiguous); ATP:(R)-glycerate 3-phosphotransferase. Enzyme Commission Number: EC 2.7.1.31. CAS No. 9026-61-3. 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-3062; glycerate 3-kinase; EC 2.7.1.31; 9026-61-3; glycerate kinase (phosphorylating) (ambiguous); D-glycerate 3-kinase; D-glycerate kinase (ambiguous); glycerate-kinase (ambiguous); GK (ambiguous); D-glyceric acid kinase (ambiguous); ATP:(R)-glycerate 3-phosphotransferase. Cat No: EXWM-3062. | |
| Glyoxylurea sodium salt | Heterocyclic Organic Compound. Alternative Names: UREIDOGLYCOLIC ACID;UREIDOGLYCOLIC ACID SODIUM SALT;GLYOXYLUREA SODIUM SALT;GLYOXYLUREA SODIUM. CAS No. 103192-53-6. Molecular formula: C3H5N2NaO4. Mole weight: 156.07. Catalog: ACM103192536. | |
| Hexyl glyoxylate | Hexyl glyoxylate. Group: Biochemicals. Alternative Names: Glyoxylsaeure-n-hexylester; Oxo-acetic acid hexyl ester. Grades: Highly Purified. CAS No. 52709-43-0. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C8H14O3. US Biological Life Sciences. | Worldwide |
| Hydroxypyruvic acid | Hydroxypyruvic acid (β-Hydroxypyruvic acid) is an intermediate in the metabolism of glycine, serine and threonine. Hydroxypyruvic acid is a substrate for serine-pyruvate aminotransferase and glyoxylate reductase/hydroxypyruvate reductase. Hydroxypyruvic acid is involved in the metabolic disorder which is the dimethylglycine dehydrogenase deficiency pathway. Uses: Scientific research. Group: Natural products. Alternative Names: β-Hydroxypyruvic acid; 3-Hydroxypyruvic acid. CAS No. 1113-60-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-113013. |  |
| Itaconic acid | Inhibitor of isocitrate lyase, the key enzyme of the glyoxylate cycle, essential for bacterial growth. Antimicrobial. Antibacterial. Inhibits the growth of bacteria expressing isocitrate lyase. Phosphofructokinase (PFKII) inhibitor. Suppresses glycolysis by decreasing the level of fructose 2,6-bisphosphate, resulting in decreased visceral fat. Might be involved in the regulation of metabolism. Group: Biochemicals. Alternative Names: 2-Methylenebutanedioic Acid; Methylenesuccinic Acid; 2-Methylenebutanedioic Acid; 2-Methylenesuccinic Acid; 2-Propene-1,2-dicarboxylic Acid; 4-Hydroxy-2-methylene-4-oxobutanoic Acid; Methylenebutanedioic Acid; NSC 3357; Propylenedicarboxylic Acid. Grades: Highly Purified. CAS No. 97-65-4. Pack Sizes: 1g, 5g. Molecular Formula: C?H?O?. US Biological Life Sciences. | Worldwide |
| malate-CoA ligase | This enzyme belongs to the family of ligases, specifically those forming carbon-sulfur bonds as acid-thiol ligases. This enzyme participates in glyoxylate and dicarboxylate metabolism. Group: Enzymes. Synonyms: malyl-CoA synthetase; malyl coenzyme A synthetase; malate thiokinase. Enzyme Commission Number: EC 6.2.1.9. CAS No. 37318-58-4. 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-5711; malate-CoA ligase; EC 6.2.1.9; 37318-58-4; malyl-CoA synthetase; malyl coenzyme A synthetase; malate thiokinase. Cat No: EXWM-5711. | |
| Methyl 7-azaindole-3-glyoxylate | Methyl 7-azaindole-3-glyoxylate. Group: Biochemicals. Alternative Names: Methyl (7-azaindol-3-yl)oxoacetate; a-Oxo-1H-pyrrolo[2,3-b]pyridine-3-acetic acid methyl ester; (Oxo)(1H-pyrrolo[2,3-b]pyridin-3-yl)acetic acid methyl ester. Grades: Highly Purified. CAS No. 357263-49-1. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C10H8N2O3. US Biological Life Sciences. | Worldwide |
| Methyl indolyl-3-glyoxylate | Methyl indolyl-3-glyoxylate. Group: Biochemicals. Alternative Names: Methyl (indol-3-yl)oxoacetate; a-Oxo-1H-indole-3-acetic acid methyl ester. Grades: Highly Purified. CAS No. 18372-22-0. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C11H9NO3. US Biological Life Sciences. | Worldwide |
| opine dehydrogenase | In the forward direction, the enzyme from Arthrobacter sp. acts also on secondary amine dicarboxylates such as N-(1-carboxyethyl)methionine and N-(1-carboxyethyl)phenylalanine. Dehydrogenation forms an imine, which dissociates to the amino acid and pyruvate. In the reverse direction, the enzyme acts also on neutral amino acids as an amino donor. They include L-amino acids such as 2-aminopentanoic acid, 2-aminobutyric acid, 2-aminohexanoic acid, 3-chloroalanine, O-acetylserine, methionine, isoleucine, valine, phenylalanine, leucine and alanine. The amino acceptors include 2-oxoacids such as pyruvate, oxaloacetate, glyoxylate and 2-oxobutyrate. Group: Enzymes. Synonyms: (2S)-2-{[1-(R)-carboxyethyl]amino}pentanoate dehydrogenase (NAD+, L-aminopentanoate-forming). Enzyme Commission Number: EC 1.5.1.28. CAS No. 108281-02-3. 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-1510; opine dehydrogenase; EC 1.5.1.28; 108281-02-3; (2S)-2-{[1-(R)-carboxyethyl]amino}pentanoate dehydrogenase (NAD+, L-aminopentanoate-forming). Cat No: EXWM-1510. | |
| Oxalacetic Acid (Oxaloacetic acid) | A four carbon dicarboxylic acid that is an intermediate in the citric acid cycle and glucogenesis. It has been shown to inhibit succinate dehydrogenase. Oxaloacetic acid, in the form of its conjugate base oxaloacetate, is a metabolic intermediate in many processes that occur in animals. It takes part in the: gluconeogenesis, urea cycle, glyoxylate cycle, amino acid synthesis, fatty acid synthesis and citric acid cycle. Gluconeogenesis[1] is a metabolic pathway consisting of a series of eleven enzyme-catalyzed reactions, resulting in the generation of glucose from non-carbohydrates substrates. The beginning of this process takes place in the mitochondrial matrix, where pyruvate molecules are found. A pyruvate molecule is carboxylated by a pyruvate carboxylase enzyme, activated by a molecule each of ATP and water. This reaction results in the formation of oxaloacetate. NADH reduces oxaloacetate to malate. This transformation is needed to transport the molecule out of the mitochondria. On Group: Biochemicals. Alternative Names: Oxobutanedioic Acid; Oxalacetic Acid; 2-Ketosuccinic acid; 2-Oxobutanedioic acid; 2-Oxosuccinic Acid; Ketosuccinic Acid; NSC 284205; NSC 77688; OAA; Oxaloacetic Acid; Oxaloethanoic Acid; Oxosuccinic Acid; α-Ketosuccinic Acid. Grades: Reagent Grade. CAS No. 328-42-7. Pack Sizes: 25g, 50g, 100g, 250g. Molecular Formula: C?H?O?, Molecular Weight: 132.07. US Biological Life Sciences. | Worldwide |
| oxalate-CoA ligase | This enzyme belongs to the family of ligases, specifically those forming carbon-sulfur bonds as acid-thiol ligases. This enzyme participates in glyoxylate and dicarboxylate metabolism. Group: Enzymes. Synonyms: oxalyl-CoA synthetase; oxalyl coenzyme A synthetase. Enzyme Commission Number: EC 6.2.1.8. CAS No. 37318-57-3. 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-5710; oxalate-CoA ligase; EC 6.2.1.8; 37318-57-3; oxalyl-CoA synthetase; oxalyl coenzyme A synthetase. Cat No: EXWM-5710. | |
| Oxalate Decarboxylase from Bacillus subtilis, recombinant | Oxalate decarboxylase (OxdC, EC4.1.1.2) is a manganese-containing enzyme, which decomposes oxalic acid and oxalate. With OxdC catalysis, oxalate is split into formate and CO2. This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. The systematic name of this enzyme class is oxalate carboxy-lyase (formate-forming). This enzyme is also called oxalate carboxy-lyase. The enzyme is composed of two cupin domains, each of which contains a Mn (II) ion. This enzyme participates in glyoxylate and dicarboxylate metabolism. This enzyme has been recognized for diagnostics in diverse biotechnological applications such as...ndustry, and agriculture to lower oxalate levels in foods and the environment. The recombinant protein made from the Bacillus Subtilis sequence includes OxdC with N-terminal His-tag. Group: Enzymes. Synonyms: Oxalate carboxy-lyase; EC 4.1.1.2; Oxalate decarboxylase; OxdC. Enzyme Commission Number: EC 4.1.1.2. CAS No. 9024-97-9. Purity: > 98% by SDS-PAGE. Mole weight: 45.9 kDa. Activity: 150U/mg. Storage: Stable for 1 year at -20°C. For long term storage, aliquot and store at -70°C. Avoid repeated freezing and thawing cycles. Form: Liquid. Source: E. coli. Species: Bacillus subtilis. Oxalate carboxy-lyase; EC 4.1.1.2; Oxalate decarboxylase; OxdC. Cat No: NATE-1688. | |
| Oxalate oxidase from B. subtilis, Recombinant | In enzymology, an oxalate oxidase (EC 1.2.3.4) is an enzyme that catalyzes the chemical reaction: oxalate + O2 + 2 H+ <-> 2 CO2 + H2O2.The 3 substrates of this enzyme are oxalate, O2, and H+, whereas its two products are CO2 and H2O2. This enzyme belongs to the family of oxidoreductases, specifically those acting on the aldehyde or oxo group of donor with oxygen as acceptor. The systematic name of this enzyme class is oxalate:oxygen oxidoreductase. This enzyme participates in glyoxylate and dicarboxylate metabolism. It has 2 cofactors: FAD, and Manganese. Group: Enzymes. Synonyms: OxO; OxOx; OxO_r; aero-oxalo dehydrogenase; oxalic acid oxidase. Enzyme Commission Number: EC 1.2.3.4. Mole weight: 43.6 kDa, His-tagged. Activity: > 230 mU/mg. Stability: Stable for at least 2 years as supplied. Storage: Store at -20°C. Form: Freeze dried. Source: E. coli. Species: B. subtilis. OxO; OxOx; OxO_r; aero-oxalo dehydrogenase; oxalic acid oxidase; oxalate oxidase; OxOx. Cat No: NATE-1642. | |
| Oxaloacetic acid | Oxaloacetic acid (2-Oxosuccinic acid) is a metabolic intermediate involved in several ways, such as citric acid cycle, gluconeogenesis, the urea cycle, the glyoxylate cycle, amino acid synthesis, and fatty acid synthesis, whereby Oxaloacetic acid facilitates the clearance of reactive oxygen species ( ROS ) and improves mitochondrial function [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: 2-Oxosuccinic acid. CAS No. 328-42-7. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-W010382. | |
| Oxaloacetic acid-13C4 | Oxaloacetic acid- 13 C 4 is the 13 C-labeled Oxaloacetic acid. Oxaloacetic acid (2-Oxosuccinic acid) is a metabolic intermediate involved in several ways, such as citric acid cycle, gluconeogenesis, the urea cycle, the glyoxylate cycle, amino acid synthesis, and fatty acid synthesis[1][2][3]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: 2-Oxosuccinic acid- 13 C4. CAS No. 161096-82-8. Pack Sizes: 1 mg. Product ID: HY-W010382S. | |
| oxalomalate lyase | This enzyme belongs to the family of lyases, specifically the oxo-acid-lyases, which cleave carbon-carbon bonds. This enzyme is also called 3-oxalomalate glyoxylate-lyase. This enzyme participates in glyoxylate and dicarboxylate metabolism. Group: Enzymes. Synonyms: 3-oxalomalate glyoxylate-lyase. Enzyme Commission Number: EC 4.1.3.13. CAS No. 37290-63-4. 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-4899; oxalomalate lyase; EC 4.1.3.13; 37290-63-4; 3-oxalomalate glyoxylate-lyase. Cat No: EXWM-4899. | |
| peptidylglycine monooxygenase | A copper protein. Peptidylglycines with a neutral amino acid residue in the penultimate position are the best substrates for the enzyme. The product is unstable and dismutates to glyoxylate and the corresponding desglycine peptide amide, a reaction catalysed by EC 4.3.2.5 peptidylamidoglycolate lyase. Involved in the final step of biosynthesis of α-melanotropin and related biologically active peptides. Group: Enzymes. Synonyms: peptidylglycine 2-hydroxylase; peptidyl α-amidating enzyme; peptide-α-amide synthetase; synthase, peptide α-amide; peptide α-amidating enzyme; peptide α-amide synthase; peptidylglycine α-hydroxylase; peptidylglycine α-amidating monooxygenase; PAM-A; PAM-B; PAM. Enzyme Commission Number: EC 1.14.17.3. CAS No. 90597-47-0. 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-0961; peptidylglycine monooxygenase; EC 1.14.17.3; 90597-47-0; peptidylglycine 2-hydroxylase; peptidyl α-amidating enzyme; peptide-α-amide synthetase; synthase, peptide α-amide; peptide α-amidating enzyme; peptide α-amide synthase; peptidylglycine α-hydroxylase; peptidylglycine α-amidating monooxygenase; PAM-A; PAM-B; PAM. Cat No: EXWM-0961. | |
| tartrate epimerase | This enzyme belongs to the family of isomerases, specifically those racemases and epimerases acting on hydroxy acids and derivatives. This enzyme participates in glyoxylate and dicarboxylate metabolism. Group: Enzymes. Synonyms: tartaric racemase. Enzyme Commission Number: EC 5.1.2.5. CAS No. 37318-33-5. 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-5392; tartrate epimerase; EC 5.1.2.5; 37318-33-5; tartaric racemase. Cat No: EXWM-5392. | |
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