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| Product | Description | |
|---|---|---|
| glyoxal | glyoxal. Group: Biochemicals. Grades: Highly Purified. CAS No. 107-22-2. Pack Sizes: 1kg, 2kg, 5kg, 10kg, 25kg. Molecular Formula: C2H2O2. US Biological Life Sciences. |  Worldwide |
| Glyoxal | Glyoxal. CAS No: 107-22-2 |  Sarchem Laboratories New Jersey NJ |
| Glyoxal 40% | Biocide and Algicide. Alternative Names: Glyoxylaldehyd. CAS No. 107-22-2. Molecular formula: C2H2O2. Mole weight: 58.04. Catalog: ACM107222-3. |  |
| Glyoxal (40% w/w in H2O) | Glyoxal is a crosslinking agent used in protein and carbohydrate chemistry when linking together monomer units. Group: Biochemicals. Alternative Names: 1,2-Ethanedione; Aurarez 136; Biformal; Biformyl; Cartabond GH; Cartabond GHF; Daicel GY 60; Diformyl; Earth Works Linkup Plus; Ethanedione; Freechem 40DL; GX; GX (aldehyde); Glyfix CS 50; Glyoxal 40L; Glyoxal T 40; Glyoxal aldehyde; Glyoxazal; Glyoxazal GX; Glyoxylaldehyde; Gohsezal P; Oxal; Oxalaldehyde; Permafresh 114; Protorez BLF-C; XH 536. Grades: Highly Purified. CAS No. 107-22-2. Pack Sizes: 50ml. US Biological Life Sciences. | Worldwide |
| Glyoxalase I | Glyoxalase I (Glo-I) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Glo-I. CAS No. 9033-12-9. Pack Sizes: 100 U. Product ID: HY-P2774. |  |
| Glyoxalase I from Human, Recombinant | Glyoxalase I is universally expressed and involved in the protection against cellular damage due to cytotoxic metabolites such as advanced glycation end products (AGEs). It is an integral component of the detoxification system, catalyzing the conversion of reactive, acyclic a-oxoaldehydes into the corresponding a-hydroxyacids in a glutathione-dependent manner. Group: Enzymes. Synonyms: lactoylglutathione lyase; EC 4.4.1.5; methylglyoxalase; aldoketomutase; ketone-aldehyde mutase; glyoxylase I; (R)-S-lactoylglutathione methylglyoxal-lyase (isomerizing); 9033-12-9. Enzyme Commission Number: EC 4.4.1.5. Purity: > 90% by SDS-PAGE. Glyoxalase I. Mole weight: 20.7 kDa. Activity: >0.4 units/mg. Storage: Glyoxalase-I Human Recombinant although stable at 4 °C for weeks, should be stored desiccated below -18 °C. Please prevent freeze/thaw cycles. Form: Glyoxalase-1 solution containing 20 mM Tris pH-8, 1mM DTT and 10% glycerol. Source: E. coli. Species: Human. lactoylglutathione lyase; EC 4.4.1.5; methylglyoxalase; aldoketomutase; ketone-aldehyde mutase; glyoxylase I; (R)-S-lactoylglutathione methylglyoxal-lyase (isomerizing); 9033-12-9. Cat No: NATE-1651. |  |
| Glyoxalase II from Human, Recombinant | The glyoxalase system consists of Glyoxalase I (Glx I) and Glyoxalase II (Glx II) which is responsible for detoxifying α-ketoaldehydes such as the potent and cytotoxic methylglyoxal (MG). Glx I converts MG to S-D-lactoyl-glutathione (SLG). SLG is then hydrolyzed to D-lactate and reduced glutathione by Glx II. Glx II desensitizes cells to p53-dependent DNA damage-induced apoptosis. It also plays a role during development and in the pathogenesis of cancer and neurodegenerative diseases. Glyoxalase II may also be important in the regulation of spermatogenesis. Glx ii amino acid 14-308 (295 amino acids) with a c-terminal 6x his-tag. Group: Enzymes. Synonyms: Hydroxyacylglutathione hydrolase; mitochondrial; HAGH1; GLO2. Enzyme Commission Number: EC 3.1.2.6. Purity: > 90% by SDS-PAGE. Mole weight: 32.4 kDa. Activity: >10 U/mg. Storage: Store at -20 ?C for at least two years. Avoid repeated freeze thaw cycles. Form: Liquid. Source: E. coli. Species: Human. Hydroxyacylglutathione hydrolase; mitochondrial; HAGH1; GLO2; Glyoxalase II; Glx II; Glyoxalase. Cat No: NATE-1650. | |
| Glyoxalase I inhibitor | Glyoxalase I inhibitor is a potent Glyoxalase I inhibitor, candidate for anticancer agents. Synonyms: Glycine, L-γ-glutamyl-S-[[(4-bromophenyl)hydroxyamino]carbonyl]-L-cysteinyl-, diethyl ester, monohydrochloride (9CI). Grades: >98%. CAS No. 221174-33-0. Molecular formula: C21H30BrClN4O8S. Mole weight: 613.91. |  |
| Glyoxalase I inhibitor 5 | Glyoxalase I inhibitor 5 (Compound 9h) is a glyoxalase I (Glo-I) inhibitor with an IC 50 of 1.28 μM. Glyoxalase I inhibitor 5 can be used as anticancer agent [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2455508-17-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-147647. | |
| Glyoxal dithiosemicarbazone | Heterocyclic Organic Compound. Alternative Names: GLYOXAL DITHIOSEMICARBAZONE;GLYOXAL BIS(THIOSEMICARBAZONE);1,2-Ethanedione bis (aminomercaptomethylenehydrazone); 1, 2-Ethanedione bis(thiosemicarbazone);1,2-Ethanedione bisthiosemicarbazone;3,3'-(1,4-Diaza-1,3-butadiene-1,4-diyl)bis(isothiourea);Nsc22181. CAS No. 1072-12-4. Molecular formula: C4H8N6S2. Mole weight: 204.28. Catalog: ACM1072124. | |
| Glyoxalic acid (50% in water) | Glyoxalic acid (NSC 27785) (50% in water) is an organic compound that is both an aldehyde and a carboxylic acid. Glyoxalic acid (50% in water) induces fluorescence. Glyoxalic acid (50% in water) is used to study neurons [1]. Uses: Scientific research. Group: Natural products. Alternative Names: NSC 27785; Formylformic acid; Oxalaldehydic acid. CAS No. 298-12-4. Pack Sizes: 500 mg (6.75 M * 1 mL in Water); 1 g (6.75 M * 2 mL in Water). Product ID: HY-79494. | |
| 2, 2-Bis (ethylthio) acetaldehyde (Glyoxal Monoethylmercaptal) | 2, 2-Bis (ethylthio) acetaldehyde (Glyoxal Monoethylmercaptal). Group: Biochemicals. Alternative Names: Glyoxal Monoethylmercaptal. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| (3-Fluorophenyl)glyoxal hydrate | Heterocyclic Organic Compound. CAS No. 101906-06-3. Molecular formula: C8H7FO3. Mole weight: 170.138. Purity: 0.96. IUPACName: -. Catalog: ACM101906063. | |
| 4-Chlorophenyl glyoxal hydrate | 4-Chlorophenyl glyoxal hydrate. Group: Biochemicals. Grades: Highly Purified. CAS No. 4996-21-8. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| 4-Dimethylaminophenylglyoxal hydrate | Heterocyclic Organic Compound. Alternative Names: 4-Dimethylaminophenylglyoxal hydrate, 115282-41-2, 2-(4-(Dimethylamino)phenyl)-2-oxoacetaldehyde hydrate, 4-(Dimethylamino)phenylglyoxal hydrate, 1171790-84-3, [4- (Dimethylamino)phenyl] (oxo)acetaldehyde hydrate, 2-[4-(dimethylamino)phenyl]-2-oxoacetaldehyde hydrate, PubChem12238, AGN-PC-0389G8, SCHEMBL10350093, CTK7H7654, MolPort-001-757-343, YOKMNOZLZXDGBI-UHFFFAOYSA-N, ANW-45016, OR1612, SBB091870, AKOS015999484, AB05269, AG-A-74756, (4-Dimethylaminophenyl)glyoxal monohydrate. CAS No. 1171790-84-3. Molecular formula: C10H13NO3. Mole weight: 195.215120 [g/mol]. Purity: 0.96. IUPACName: 2-[4-(dimethylamino)phenyl]-2-oxoacetaldehyde;hydrate. Canonical SMILES: CN(C)C1=CC=C(C=C1)C(=O)C=O.O. Catalog: ACM1171790843. | |
| 4-Hydroxyphenyl glyoxal | 4-Hydroxyphenyl glyoxal. Group: Biochemicals. Alternative Names: ?-Hydroxyphenyl glyoxal. Grades: Highly Purified. CAS No. 24645-80-5. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. US Biological Life Sciences. | Worldwide |
| 4-Hydroxyphenyl glyoxal 99+% (NMR) | 4-Hydroxyphenyl glyoxal 99+% (NMR). Group: Biochemicals. Grades: Reagent Grade. CAS No. 24645-80-5. Pack Sizes: 25mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| 4-Hydroxyphenyl glyoxal hydrate 99+% | 4-Hydroxyphenyl glyoxal hydrate 99+%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 197447-05-5,24645-80-5. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Albuterol Glyoxal | Albuterol Glyoxal. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 2-hydroxy-2-(4-hydroxy-3-(hydroxymethyl)phenyl)acetic acid. CAS No. 72189-44-7. Molecular Formula: C9H10O5. Mole Weight: 198.17. Catalog: APB72189447. |  |
| Cefdinir glyoxalic analog | Cefdinir glyoxalic analog. Uses: For analytical and research use. Group: Impurity standards. CAS No. 79350-14-4. Molecular Formula: C14H12N4O5S2. Mole Weight: 380.39. Catalog: APB79350144. | |
| Cefdinir Glyoxalic Analog | (6R,7R)-7-(2-(2-Aminothiazol-4-yl)-2-oxoacetamido)-8-oxo-3-vinyl-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid is used in the preparation of Cephalosporin C , an antibiottic used to study the effect of transpeptidase expression, binding, and inhibition on bacterial cell wall mucopeptide synthesis. Synonyms: (6R,7R)-7-(2-(2-Aminothiazol-4-yl)-2-oxoacetamido)-8-oxo-3-vinyl-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid. Grades: > 95%. CAS No. 79350-14-4. Molecular formula: C14H12N4O5S2. Mole weight: 380.4. | |
| Cefdinir glyoxalic analogm | Cefdinir glyoxalic analogm. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (6R,7R)-7-(2-(2-aminothiazol-4-yl)-2-oxoacetamido)-8-oxo-3-vinyl-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. Molecular Formula: C14H12N4O5S2. Mole Weight: 380.4. Catalog: APB04777. | |
| (methyl)glyoxal oxidase | The enzyme, originally characterized from the white rot fungus Phanerochaete chrysosporium, utilizes a free radical-coupled copper complex for catalysis. Group: Enzymes. Synonyms: glx1 (gene name); glx2 (gene name). Enzyme Commission Number: EC 1.2.3.15. 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-1209; (methyl)glyoxal oxidase; EC 1.2.3.15; glx1 (gene name); glx2 (gene name). Cat No: EXWM-1209. | |
| Native Saccharomyces cerevisiae Glyoxalase I | Glyoxalase I is universally expressed and involved in the protection against cellular damage due to cytotoxic metabolites such as advanced glycation end products (AGEs). It is an integral component of the detoxification system, catalyzing the conversion of reactive, acyclic a-oxoaldehydes into the corresponding a-hydroxyacids in a glutathione-dependent manner. Glyoxalase detoxification system consists of glyoxalase (glo)-i and glo-ii. glo-i is a cytosolic, 42 kda, dimeric zn2+ metalloenzyme. Group: Enzymes. Synonyms: lactoylglutathione lyase; EC 4.4.1.5; methylglyoxalase; aldoketomutase; ketone-aldehyde mutase; glyoxylase I; (R)-S-lactoylglutathione methylglyoxal-lyase (isomerizing); 9033-12-9. Enzyme Commission Number: EC 4.4.1.5. CAS No. 9033-12-9. Glyoxalase I. Mole weight: 42 kDa. Activity: > 400 units/mg protein. Storage: 2-8°C. Form: buffered aqueous glycerol solution; Solution in 50% glycerol, 0.4 M (NH4)2SO4 and 0.002 M KH2PO4 pH 6.5. Source: Saccharomyces cerevisiae. lactoylglutathione lyase; EC 4.4.1.5; methylglyoxalase; aldoketomutase; ketone-aldehyde mutase; glyoxylase I; (R)-S-lactoylglutathione methylglyoxal-lyase (isomerizing); 9033-12-9. Cat No: NATE-0308. | |
| p-Azidophenyl Glyoxal.H2O | p-Azidophenyl Glyoxal.H2O. CAS No. 96602-46-9. Pack Sizes: Milligram Quantities: 100 mg. Order Number: PA108. |  www.prochemonline.com |
| p-Azidophenylglyoxal monohydrate 99+% (NMR) | Photoreactive; Arginine residue reactive. Group: Biochemicals. Alternative Names: p-Azidophenyl glyoxal H2O; APG. Grades: Highly Purified. CAS No. 1196151-49-1. Pack Sizes: 100mg. Molecular Formula: C8H5N3O2?H2O, Molecular Weight: 175.14. US Biological Life Sciences. | Worldwide |
| p-Hydroxyphenyl Glyoxal | p-Hydroxyphenyl Glyoxal. Pack Sizes: Milligram Quantities: 100 mg. Order Number: M104. | www.prochemonline.com |
| Salbutamol glyoxal | Salbutamol glyoxal. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C9H10O5. Mole Weight: 198.17. Catalog: APB09503. | |
| Salbutamol Glyoxal Impurity | An impurity of salbutamol.Salbutamol is a short-acting, selective beta2-adrenergic receptor agonist used in the treatment of asthma and COPD. It is 29 times more selective for beta2 receptors than beta1 receptors giving it higher specificity for pulmonary beta receptors versus beta1-adrenergic receptors located in the heart. Synonyms: 2,2-Dihydroxyl-1-(4-hydroxy-3-(hydroxymethyl)phenyl)ethanone. Grades: > 95%. Molecular formula: C9H10O5. Mole weight: 198.18. | |
| 1-?Butylurea | 1-?Butylurea is a compound used for developing cosmetic compositions for straightening hair fibers. It is also used as a reagent for the synthesis of chiral mono-?, di-?, tri-?, and tetraalkylglycolurils by cyclocondensation of ureas with di hydroxyimidazolidin ones or glyoxal. Group: Biochemicals. Grades: Highly Purified. CAS No. 689-11-2. Pack Sizes: 1g, 5g. Molecular Formula: C5H12N2O. US Biological Life Sciences. | Worldwide |
| 2, 2-Bis (ethylthio) acetaldehyde | 2, 2-Bis (ethylthio) acetaldehyde. Group: Biochemicals. Alternative Names: Glyoxal monoethylmercaptal; 2,2-Bis(ethylthio)ethanal. Grades: Highly Purified. CAS No. 42919-45-9. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C6H12OS2. US Biological Life Sciences. | Worldwide |
| 2,2'-(Ethane-1,2-diylidenebis(azanylylidene))diphenol | Nitrogen-Donor Ligands. Alternative Names: Glyoxalbis(2-hydroxyanil). CAS No. 1149-16-2. Molecular formula: C14H12N2O2. Mole weight: 240.26. Appearance: Light yellow solid. Purity: 0.98. IUPACName: 2-[2- (2-hydroxyphenyl) iminoethylideneamino]phenol. Catalog: ACM1149162. | |
| 2-(4-Methoxyphenyl)-2-oxoacetaldehyde | Heterocyclic Organic Compound. Alternative Names: 2-(4-methoxyphenyl)-2-oxoacetaldehyde; 4-methoxyphenylglyoxal; 1-(4-Methoxyphenyl)-1, 2-ethanedione; 1-(4-Methoxyphenyl)ethanedione; 1-(4-Methoxyphenyl)glyoxal; 2-Oxo-2-(4-methoxyphenyl)ethanal; 4-Methoxy-α -oxobenzeneacetaldehyde; α -Oxo-4-methoxybenzeneacetaldehyde. CAS No. 1076-95-5. Molecular formula: C9H8O3. Mole weight: 164.15802. Catalog: ACM1076955. | |
| 4-Fluoro-α-oxo-benzeneacetaldehyde | 4-Fluoro-α-oxo-benzeneacetaldehyde. Group: Biochemicals. Alternative Names: (4-Fluorophenyl)glyoxal; (p-Fluorophenyl)glyoxal; 2-(4-Fluorophenyl)-2-oxoacetaldehyde; NSC 402742. Grades: Highly Purified. CAS No. 403-32-7. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| 4-Fluoro-a-oxo-benzeneacetaldehyde | 4-Fluoro-a-oxo-benzeneacetaldehyde. Group: Biochemicals. Alternative Names: (4-Fluorophenyl)glyoxal; (p-Fluorophenyl)glyoxal; 2-(4-Fluorophenyl)-2-oxoacetaldehyde. Grades: Highly Purified. CAS No. 403-32-7. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C8H5FO2·H2O. US Biological Life Sciences. | Worldwide |
| (5E)-6-(4-Hydroxy-3-methoxyphenyl)-5-hexene-2,4-dione | Curcumin and gingerdione derivative. A possible human glyoxalase I inhibitor. Flavor modifier. Group: Biochemicals. Alternative Names: (E)-6-(4-Hydroxy-3-methoxyphenyl)hex-5-ene-2,4-dione. Grades: Highly Purified. CAS No. 189181-53-1. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Benzeneacetaldehyde, a-oxo- | Heterocyclic Organic Compound. Alternative Names: phenylglyoxal, phenylethanedione, benzoylformaldehyde, glyoxal, phenyl-, benzoylcarboxaldehyde, Phenyl glyoxal, Oxo(phenyl)acetaldehyde, alpha-oxobenzeneacetaldehyde, Oxo-phenyl-acetaldehyde, Phenylglyoxal treated BSA, CCRIS 966, 2-oxo-2-phenylacetaldehyde, Phenylglyoxal treated casein, Benzeneacetaldehyde. alpha.-oxo-, Benzeneacetaldehyde, alpha-oxo-, C8H6O2, EINECS 214-036-1, NSC 26909, NSC627436, AIDS132769. CAS No. 1074-12-0. Molecular formula: C8H6 O2. Mole weight: 152.14. Appearance: White to light yellow powder. Purity: N/A. IUPACName: 2-oxo-2-phenylacetaldehyde. Canonical SMILES: C1=CC=C(C=C1)C(=O)C=O. Density: 1.133 g/cm³. ECNumber: 214-036-1. Catalog: ACM1074120. | |
| cis-Decahydro-2a,4a,6a,8a-tetraazacyclopent[fg]acenaphthylene | 2a, 4a, 6a, 8a-Decahydrotetraazacyclopent [fg]acenaphthylene is an intermediate of Gadoteridol. Gadoterido is a gadolinium-based MRI contrast agent. It is sold under the brand name ProHance. Synonyms: Decahydro-cis-2a,4a,6a,8a-tetraazacyclopent[fg]acenaphthylene; cis-2a, 4a, 6a, 8a-Decahydrotetraazacyclopent [fg]acenaphthylene; cis-Glyoxal-cyclen; 2a,4a,6a,8a-Tetraazacyclopent[fg]acenaphthylene, decahydro-, cis-. Grades: 98%. CAS No. 79236-92-3. Molecular formula: C10H18N4. Mole weight: 194.28. | |
| Dichloro[(S)-(-)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]palladium(II), min. 98% | Catalyst precursor, with AgBF4 , for the enantioselective addition of silyl ethers, to imines to produce β-amino ketones, and to aldehydes to produce 3-hydroxy-1-propanone aldol addition products. Catalyst precursor, with AgSbF6, for the asymmetric carbonyl-ene reaction. Catalyst precursor for hetero Diels-Alder reaction of simple dienes with aldehydes and aryl glyoxals. Group: Palladium series catalysts. Alternative Names: ST24050377; 5353AA; DICHLORO[2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL]PALLADIUM(II); 115826-95-4; [(S)-(-)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL]PALLADIUM (II) CHLORIDE; FT-0696081; MFCD00075254; C44H32Cl2P2Pd; EBD2199625; PALLADIUM, [1, 1'-(1R)-[1, 1'-BINAPHTHALENE]-2, 2'-DIYLBIS[1, 1-DIPHENYLPHOSPHINE-KAPPAP]]DICHLORO-, (SP-4-2)-. CAS No. 127593-28-6. Molecular formula: C44H32Cl2P2Pd. Mole weight: 800.008g/mol. IUPACName: dichloropalladium;[1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Canonical SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=C (C4=CC=CC=C4C=C3)C5=C (C=CC6=CC=CC=C65)P (C7=CC=CC=C7)C8=CC=CC=C8. Cl[Pd]Cl. Catalog: ACM127593286. | |
| D/L-glyceraldehyde reductase | The enzyme takes part in a D-galacturonate degradation pathway in the fungi Aspergillus niger and Trichoderma reesei (Hypocrea jecorina). It has equal activity with D- and L-glyceraldehyde, and can also reduce glyoxal and methylglyoxal. The reaction is only observed in the direction of glyceraldehyde reduction. Group: Enzymes. Synonyms: gld1 (gene name); gaaD (gene name). Enzyme Commission Number: EC 1.1.1.372. 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-0290; D/L-glyceraldehyde reductase; EC 1.1.1.372; gld1 (gene name); gaaD (gene name). Cat No: EXWM-0290. | |
| Ethanone,1-[1,1'-biphenyl]-4-yl-2,2-dihydroxy- | Heterocyclic Organic Compound. Alternative Names: 4-BIPHENYLGLYOXAL HYDRATE;1-((1,1'-biphenyl)-4-yl)-2,2-dihydroxyethanone;2,2-dihydroxy-4'-phenyl-acetophenon;2,2-dihydroxy-4'-phenylacetophenone;4-diphenylglyoxalmonohydrate;Biphenyl-4-glyoxal hydrate;Biphenyl-4-glyoxal hydrate 95%;4-BIPHENYLGLYOXAL HYDR. CAS No. 1145-04-6. Molecular formula: C14H12O3. Mole weight: 228.24. Catalog: ACM1145046. | |
| Gloxazone | Gloxazone is an effective anaplasmacide. Group: Inhibitors. Alternative Names: Contrapar, Gloxazon, GLOXAZONE, KTS, pharmaceutical, Kethoxal bis(thiosemicarbazone), NSC82116, AIDS125723, AIDS-125723, BW 356C61, CID9571200, KC 1331, WR 9838, (1-Ethoxyethyl)glyoxal bis(thiosemicarbazone). alpha.-Ethoxyethylglyoxal dithiosemicarbazone, 3-Ethoxy-2-oxobutyraldehyde bis(thiosemicarbazone), Butyraldehyde, 3-ethoxy-2-oxo-, bis(thiosemicarbazone), 2-((Aminocarbothioyl)hydrazono)-3-ethoxybutanal thiosemicarbazone, Butyraldehyde, 3-ethoxy-2-oxo-, bis(thiosemicarbazone, hemihydrate, 2507-91-7, Hydrazinecarbothioamide, 2, {2-[1-(1-ethoxyethyl)-1,2-ethanediylidene]bis-}. CAS No. 2507-91-7. Molecular formula: C8H16N6OS2. Mole weight: 276.38. Appearance: Solid. Purity: 0.96. IUPACName: [(E)-[(1E)-1-(carbamothioylhydrazinylidene)-3-ethoxybutan-2-ylidene]amino]thiourea. Canonical SMILES: CC(C(/C=N/NC(N)=S)=N\NC(N)=S)OCC. Density: 1.41g/cm³. Catalog: ACM2507917. | |
| 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 |
| hydroxyacylglutathione hydrolase | Also hydrolyses S-acetoacetylglutathione, but more slowly. Group: Enzymes. Synonyms: glyoxalase II; S-2-hydroxylacylglutathione hydrolase; hydroxyacylglutathione hydrolase; acetoacetylglutathione hydrolase. Enzyme Commission Number: EC 3.1.2.6. CAS No. 9025-90-5. 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-3569; hydroxyacylglutathione hydrolase; EC 3.1.2.6; 9025-90-5; glyoxalase II; S-2-hydroxylacylglutathione hydrolase; hydroxyacylglutathione hydrolase; acetoacetylglutathione hydrolase. Cat No: EXWM-3569. | |
| Imidazo[1,2-a]pyridine | Imidazo[1,2-a]pyridine is one of four imidazopyridine isomers. Imidazopyridine derivatives possess activity as inhibitors of target enzymes and have medicinal and pharmaceutical applications and are used as herbicides and fungicides. Group: Biochemicals. Alternative Names: 1,3a-Diazaindene; 1-Azaindolizine; Pyridino[1', 2':1, 2]glyoxaline; Pyrimidazole. Grades: Highly Purified. CAS No. 274-76-0. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Imidazole | Imidazole (Glyoxaline; 1,3-Diaza-2,4-cyclopentadiene) is a heterocyclic aromatic compound. Imidazole bearing molecules have been used as corrosion, acetylcholinesterase (AChEI) and xanthine oxidase (XO) inhibitors, performing biological activities such as antifungal, antituberculosis, anti-inflammatory, antioxidant, and analgesic, amongst many others. Imidazole inhibits the enzymatic conversion of the endoperoxides (PGG 2 and PGH 2 ) to thromboxane A2 by platelet microsomes. Imidazole derivatives exhibits inhibition on SARS-CoV-2 3CL Pro enzyme, which is promising for research in the field of Alzheimers disease, gout, COVID-19 and thrombo-embolic disease [1] [2] [3]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Glyoxaline; 1,3-Diaza-2,4-cyclopentadiene. CAS No. 288-32-4. Pack Sizes: 10 mM * 1 mL; 5 g. Product ID: HY-D0837. | |
| Imidazole | Imidazole is a biocompatible molecule that is used as a scaffold for biomimetic applications. It is used as a bioreagent with an ability to hydrogen bond with drugs and proteins. It can be also be used as an additive for the formation of an electrolyte for fuel cell applications. Uses: Metal plating, electropolishing, metal reprocessing, phase transfer media, batteries fuel cells, nanomaterials, industrial solvents, nuclear fuel red waste, enzymatic catalysis, lubricants heat transfer and solar energy conversion. Group: Heterocyclic organic compound. Alternative Names: Glyoxaline. CAS No. 288-32-4. Molecular formula: C3H4N2. Mole weight: 68.08. Appearance: Crystalline. Purity: 99%+. IUPACName: 1H-imidazole. Canonical SMILES: C1=CN=CN1. Density: Relative density (water = 1): 1.03. ECNumber: 206-019-2. Catalog: ACM288324-3. | |
| Imidazole | Imidazole is a biocompatible molecule that is used as a scaffold for biomimetic applications. It is used as a bioreagent with an ability to hydrogen bond with drugs and proteins. It can be also be used as an additive for the formation of an electrolyte for fuel cell applications. Uses: Metal plating, electropolishing, metal reprocessing, phase transfer media, batteries fuel cells, nanomaterials, industrial solvents, nuclear fuel red waste, enzymatic catalysis, lubricants heat transfer and solar energy conversion. Group: Hydrogen storage materials metal organic frameworks (mofs). Alternative Names: Glyoxaline. CAS No. 288-32-4. Product ID: 1H-imidazole. Molecular formula: 68.08. Mole weight: C3H4N2. C1=CN=CN1. InChI=1S/C3H4N2/c1-2-5-3-4-1/h1-3H, (H, 4, 5). RAXXELZNTBOGNW-UHFFFAOYSA-N. 99%+. |  |
| Imidazole | Synonyms: Glyoxaline; 1,3-Diaza-2,4-cyclopentadiene; 1,3-Diazole; 3-Azapyrrole; Curezol SIZ; Glyoxalin; Imidazol; Imutex; Methanimidamide, N,N'-1,2-ethenediyl-; Miazole; NSC 60522. Grades: ≥95%. CAS No. 288-32-4. Molecular formula: C3H4N2. Mole weight: 68.08. | |
| Ketomycin | It is produced by the strain of Str. sp. Tu99, Ketomycin is resistant to subtilis on the synthetic medium. Synonyms: Antibiotic R-3; Antibiotic T 86A; Cyclohexenyl-1-glyoxalic acid; (R)-alpha-Oxo-3-cyclohexene-1-acetic acid; BRN 2964900. Grades: ≥98%. CAS No. 23364-22-9. Molecular formula: C8H10O3. Mole weight: 154.16. | |
| lactoylglutathione lyase | Also acts on 3-phosphoglycerol-glutathione. Group: Enzymes. Synonyms: methylglyoxalase; aldoketomutase; ketone-aldehyde mutase; glyoxylase I; (R)-S-lactoylglutathione methylglyoxal-lyase (isomerizing). Enzyme Commission Number: EC 4.4.1.5. CAS No. 9033-12-9. Glyoxalase I. 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-5339; lactoylglutathione lyase; EC 4.4.1.5; 9033-12-9; methylglyoxalase; aldoketomutase; ketone-aldehyde mutase; glyoxylase I; (R)-S-lactoylglutathione methylglyoxal-lyase (isomerizing). Cat No: EXWM-5339. | |
| L-glycol dehydrogenase | The 2-hydroxycarbonyl compound formed can be further oxidized to a vicinal dicarbonyl compound. In the reverse direction, vicinal diketones, glyceraldehyde, glyoxal, methylglyoxal, 2-oxo-hydroxyketones and 2-ketoacid esters can be reduced. Group: Enzymes. Synonyms: glycol (nicotinamide adenine dinucleotide (phosphate)) dehydrogenase; L-(+)-glycol:NAD(P) oxidoreductase; L-glycol:NAD(P) dehydrogenase. Enzyme Commission Number: EC 1.1.1.185. CAS No. 77967-75-0. 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-0087; L-glycol dehydrogenase; EC 1.1.1.185; 77967-75-0; glycol (nicotinamide adenine dinucleotide (phosphate)) dehydrogenase; L-(+)-glycol:NAD(P) oxidoreductase; L-glycol:NAD(P) dehydrogenase. Cat No: EXWM-0087. | |
| L-Histidine | L-Histidine is an essential amino acid and one of the 22 proteinogenic amino acids. L-Histidine plays a role in the production of histamine and blood cell. It exhibits anti-oxidant, anti-inflammatory and anti-secretory properties. Protein supplement in health care products. Uses: Ingredient of health care products. Synonyms: Histidine, L-; Histidine; H-His-OH; Glyoxaline-5-alanine; Anti-rheuma; (2S)-2-Amino-3-(1H-imidazol-4-yl)propanoic acid; (2S)-2-Azaniumyl-3-(1H-imidazol-5-yl)propanoate; (S)-2-Amino-3-(1H-imidazol-4-yl)propanoic acid; (S)-4-(2-Amino-2-carboxyethyl)imidazole; (S)-Histidine; (S)-α-Amino-1H-imidazole-4-propanoic acid; 1H-Imidazole-4-alanine, (S)-; 1H-Imidazole-4-propanoic acid, α-amino-, (S)-; L-(-)-Histidine; L-Alanine, 3-(1H-imidazol-4-yl)-; NSC 137773. Grades: 98%. CAS No. 71-00-1. Molecular formula: C6H9N3O2. Mole weight: 155.20. | |
| L-Histidine | Supplement. CAS No. 71-00-1. Categories: histidine, h-his-oh, glyoxaline-5-alanine, l-(-)-histidine. |  US, Austria, Lithuania |
| L-Histidine (L-His-OH) | L-Histidine is an essential amino acid for human development which the body cannot produce on its own. L-Histidine is one of the 22 proteinogenic amino acids. L-Histidine precursor to histamine and a component of carnosine. Group: Biochemicals. Alternative Names: L-His-OH; (2S)-2-Amino-3-(1H-imidazol-4-yl)propanoic Acid; (S)-Histidine; L-(-)-Histidine; (S) -4- (2-Amino-2-carboxyethyl) imidazole; (S)-α-Amino-1H-imidazole-4-propanoic Acid; 1448: PN: EP2071334 SEQID: 1532 claimed protein; NSC 137773; 1448: PN: WO2009077864 SEQID: (S)-1H-Imidazole-4-alanine; PN: WO2009046220 SEQID: 343 claimed sequence; Glyoxaline-5-alanine; Histidine;3-(1H-Imidazol-4-yl)-L-alanine. Grades: Cell Culture Grade. CAS No. 71-00-1. Pack Sizes: 50g, 100g, 250g, 500g, 1Kg. Molecular Formula: C6H9N3O2, Molecular Weight: 155.16. US Biological Life Sciences. | Worldwide |
| Ophthalmic acid | Ophthalmic acid, an analogue of GSH, is a marker of oxidative stress and hepatic GSH consumption. Ophthalmic acid is an inhibitor of Glyoxalase I reaction [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 495-27-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-126752. | |
| S-ETHYLGLUTATHIONE | . Uses: An inhibitor of the enzyme glyoxalase 1. Synonyms: L-GAMMA-GLUTAMYL-S-ETHYL-L-CYSTEINYL-GLYCINE; S-ETHYLGLUTATHIONE; L-g-Glutamyl-S-ethyl-L-cysteinyl-glycine; L--Glutamyl-S-ethyl-L-cysteinyl-glycine; L-γGlu-S-Ethyl-L-Cys-Gly-OH; gamma-Glutamyl-L-cysteinylglycyl ethyl ester; Glycine, L-gamma-glutamyl-S-ethyl-L-. CAS No. 24425-52-3. Molecular formula: C12H21N3O6S. Mole weight: 335.38. | |
| S-Ethylglutathione (L-g-Glutamyl-S-ethyl-L-cysteinyl-glycine) | An inhibitor of the enzyme Glyoxalase 1. Group: Biochemicals. Alternative Names: L-g-Glutamyl-S-ethyl-L-cysteinyl-glycine. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| S-Methylglutathione | S-Methylglutathione is an S-substitued glutathione and a stronger nucleophile than GSH [1]. S-Methylglutathione has inhibitory effect on glyoxalase 1 [2]. Uses: Scientific research. Group: Peptides. CAS No. 2922-56-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-W009177. | |
| tartronate-semialdehyde synthase | A flavoprotein. Group: Enzymes. Synonyms: tartronate semialdehyde carboxylase; glyoxylate carbo-ligase; glyoxylic carbo-ligase; hydroxymalonic semialdehyde carboxylase; tartronic semialdehyde carboxylase; glyoxalate carboligase; glyoxylate carboxy-lyase (dimerizing); glyoxylate carboxy-lyase (dimerizing; tartronate-semialdehyde-forming). Enzyme Commission Number: EC 4.1.1.47. CAS No. 9027-24-1. 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-4792; tartronate-semialdehyde synthase; EC 4.1.1.47; 9027-24-1; tartronate semialdehyde carboxylase; glyoxylate carbo-ligase; glyoxylic carbo-ligase; hydroxymalonic semialdehyde carboxylase; tartronic semialdehyde carboxylase; glyoxalate carboligase; glyoxylate carboxy-lyase (dimerizing); glyoxylate carboxy-lyase (dimerizing; tartronate-semialdehyde-forming). Cat No: EXWM-4792. | |
| Tymazoline Hydrochloride | Tymazoline Hydrochloride. Group: Biochemicals. Alternative Names: 4, 5-Dihydro-2-[[5-methyl-2- (1-methylethyl) phenoxy]methyl]-H-imidazole, , Hydrochloride; 4, 5-Dihydro-2-[[5-methyl-2- (1-methylethyl) phenoxy]methyl]-1H-imidazole Monohydrochloride; 2-[(Thymyloxy)methyl]-2-imidazoline, Monohydrochloride; 2- (Thymyloxymethyl) glyoxalidine Hydrochloride; Thymazen. Grades: Highly Purified. CAS No. 28120-03-8. Pack Sizes: 2.5g. Molecular Formula: C14H21N2ClO, Molecular Weight: 268.779999999999. US Biological Life Sciences. | Worldwide |
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