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| Product | Description | |
|---|---|---|
| Glycocholic Acid Hydrate | Labeled Glycocholic Acid. The product of conjugation of cholic acid with glycine; chief ingredient of the bile of herbivorous animals. In the weakly alkaline bile fluid glycocholic acid exists as the sodium salt. Group: Biochemicals. Alternative Names: N-[(3α,5 β, 7α, 12α)-3, 7, 12-?rihydroxy-24-oxocholan-24-yl]glycine Hydrate; N-Choloylglycine. Grades: Highly Purified. CAS No. 475-31-0. Pack Sizes: 1g. US Biological Life Sciences. |  Worldwide |
| Glycocholic acid sodium | Glycocholic acid sodium is an orally active bile acid with anticancer activity, targeting against pump resistance-related and non-pump resistance-related pathways [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 863-57-0. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 500 mg. Product ID: HY-N1423A. |  |
| Glycocholic acid (Standard) | Glycocholic acid (Standard) is the analytical standard of Glycocholic acid. This product is intended for research and analytical applications. Glycocholic acid is a bile acid with anticancer activity, targeting against pump resistance-related and non-pump resistance-related pathways [1]. Uses: Scientific research. Group: Natural products. CAS No. 475-31-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N1423R. | |
| Glycocin F | Glycocin F has antibacterial activity against L.plantarum. In purified form, the activity is bacteriostatic (IC50=2 nM) rather than bactericidal. Synonyms: Bacteriocin glycocin F; gccF. |  |
| Glycocinnasperimicin D | It is produced by the strain of Nocardia sp. MG615-7F6. It is a glycoside cinnamyl imide histamine antibiotic. It has the activity of anti-gram positive bacteria and negative bacteria. It inhibits leukemia L1210 cell with IC50 of 2.0 μg/mL. Synonyms: Glycocinnaspermicidin D; 2-Propenamide, N-(3-((4-aminobutyl)amino)propyl)-3-(4-((4-((((2-((aminocarbonyl)amino)-2-deoxy-beta-D-xylopyranosyl)amino)carbonyl)amino)-2-((aminoiminomethyl)amino)-2,4,6-trideoxy-alpha-D-glucopyranosyl)oxy)phenyl)-, (E)-. Grade: 95%. CAS No. 99260-73-8. Molecular formula: C30H50N10O9. Mole weight: 694.78. | |
| Glycocyamine | Glycocyamine (Guanidinoacetic acid), a precursor of creatine, is a replacement of dietary arginine and could support overall energy homeostasis of the bird. Uses: Scientific research. Group: Natural products. Alternative Names: Guanidinoacetic acid. CAS No. 352-97-6. Pack Sizes: 100 mg. Product ID: HY-W021448. | |
| Glycodehydrocholic acid | Glycodehydrocholic acid is a bile acid glycine conjugate. Glycodehydrocholic acid is used to diagnose cancer and other diseases [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3415-45-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N11416. | |
| Glycodeoxycholate Sodium | Glycodeoxycholate Sodium (Sodium glycyldeoxycholate) is a bile salt. Glycodeoxycholate Sodium has cytotoxicity to cancer cell, changes the permeability of the pancreatic duct and decreases glucose levels [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Sodium glycyldeoxycholate. CAS No. 16409-34-0. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N1427. | |
| Glycodeoxycholic-2,2,4,4,11,11-d6 acid solution | 100 ?g/mL in methanol, ?98 atom % D, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. |  |
| Glycodeoxycholic-2,2,4,4-d4 acid | ?98 atom % D, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Glycodeoxycholic-2,2,4,4-d4 acid 3-sulfate disodium salt | ?98 atom % D, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Glycodeoxycholic-2,2,4,4-d4 acid solution | 100 ?g/mL in methanol, ?98 atom % D, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Glycodeoxycholic Acid | Glycodeoxycholic Acid is a natural product found in Streptomyces nigricans, Trypanosoma brucei and C. elegans. Glycodeoxycholic Acid induces hepatocyte necrosis and autophagy in patients with obstructive cholestasis [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 360-65-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-125731. | |
| Glycodeoxycholic acid-[2,2,4,4-d4] | Glycodeoxycholic acid-2,2,4,4-[d4] is the labelled analogue of Glycodeoxycholic acid. Glycodeoxycholic acid is a bile acid formed in the liver by the conjugation of deoxycholate with glycine. Glycodeoxycholic acid can be used as a cholagogue and choleretic. Synonyms: Glycodeoxycholic-2,2,4,4-d4 acid; N-(3α,12α-Dihydroxy-24-oxocholan-24-yl)glycine-d4; 3α,12α-Dihydroxy-5β-cholanoic Acid N-(Carboxymethyl)amide-d4; N-[(3α,5β,12α)-3,12-Dihydroxy-24-oxocholan-24-yl-2,2,4,4-d4]glycine; Glycodeoxycholic Acid-d4; N-[(3α,5β,12α)-3,12-Dihydroxy-24-oxocholan-24-yl-2,2,4,4-d4]-glycine. Grade: ≥ 98% (CP); 98% atom D. CAS No. 1069132-37-1. Molecular formula: C26H39D4NO5. Mole weight: 453.65. | |
| Glycodeoxycholic acid-d4 | Glycodeoxycholic acid-d 4 is the deuterium labeled Glycodeoxycholic Acid. Glycodeoxycholic Acid is an endogenous metabolite. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1069132-37-1. Pack Sizes: 1 mg. Product ID: HY-125731S. | |
| Glycodeoxycholic acid monohydrate | Glycodeoxycholic acid monohydrate is a nuclear receptor ligand. Uses: Scientific research. Group: Natural products. CAS No. 1079043-81-4. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N1427A. | |
| Glycofurol | Glycofurol. Group: Polymers. Alternative Names: Poly(oxy-1,2-ethanediyl), alpha-((tetrahydro-2-furanyl)methyl)-omega-hydroxy-. CAS No. 31692-85-0. Pack Sizes: 1 kg. Product ID: 2-(Oxolan-2-ylmethoxy)ethanol. Molecular formula: 146.18g/mol. Mole weight: (C2H4O)n.C5H10O2. C1CC(OC1)COCCO. CTPDSKVQLSDPLC-UHFFFAOYSA-N. InChI=1S / C7H14O3 / c8-3-5-9-6-7-2-1-4-10-7 / h7-8H, 1-6H2. |  |
| Glycogen | 5g Pack Size. Group: Carbohydrates, Sugars. Formula: N/A. CAS No. 9005-79-2. Prepack ID 20698966-5g. See USA prepack pricing. |  |
| Glycogen azure | Glycogen azure. Group: Polysaccharide. | |
| Glycogen azure | from rabbit liver, suitable for substrate for ?-amylase. Group: Polysaccharide. | |
| Glycogen branching enzyme from Bacillus subtilis, Recombinant | Glycogen branching enzyme is an enzyme that adds branches to the growing glycogen molecule during the synthesis of glycogen, a storage form of glucose. More specifically, during glycogen synthesis, a glucose 1-phosphate molecule reacts with uridine triphosphate (UTP) to become UDP-glucose, an activated form of glucose. The activated glucosyl unit of UDP-glucose is then transferred to the hydroxyl group at the C-4 of a terminal residue of glycogen to form an α-1,4-glycosidic linkage, a reaction catalyzed by glycogen synthase. Importantly, glycogen synthase can only catalyze the synthesis of α-1,4-glycosidic linkages. Since glycogen is a readily mobil...;-1,4-glucan-6-glycosyltransferase; starch branching enzyme; 1,4-α-D-glucan:1,4-α-D-glucan 6-α-D-(1,4-α-D-glucano)-transferase. Enzyme Commission Number: EC 2.4.1.18. CAS No. 9001-97-2. Purity: > 95 % as judged by SDS-PAGE. Glycogen branching enzyme. Mole weight: 77485.4 Da. Activity: 38.04 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Bacillus subtilis subsp. subtilis str. 168. Branching enzyme, amylo-(1,4?1,6)-transglycosylase; Q-enzyme; α-glucan-branching glycosyltransferase; amylose isomerase; enzymatic branching factor; branching glycosyltransferase; enzyme Q; gluc |  |
| Glycogen branching enzyme from Bacteroides fragilis, Recombinant | Glycogen branching enzyme is an enzyme that adds branches to the growing glycogen molecule during the synthesis of glycogen, a storage form of glucose. More specifically, during glycogen synthesis, a glucose 1-phosphate molecule reacts with uridine triphosphate (UTP) to become UDP-glucose, an activated form of glucose. The activated glucosyl unit of UDP-glucose is then transferred to the hydroxyl group at the C-4 of a terminal residue of glycogen to form an α-1,4-glycosidic linkage, a reaction catalyzed by glycogen synthase. Importantly, glycogen synthase can only catalyze the synthesis of α-1,4-glycosidic linkages. Since glycogen is a readily mobi...1,4-glucan-6-glycosyltransferase; starch branching enzyme; 1,4-α-D-glucan:1,4-α-D-glucan 6-α-D-(1,4-α-D-glucano)-transferase. Enzyme Commission Number: EC 2.4.1.18. CAS No. 9001-97-2. Purity: > 95 % as judged by SDS-PAGE. Glycogen branching enzyme. Mole weight: 81104.6 Da. Activity: 50.88 U/mg (pH 7.0; 3.3 mg/mL starch). Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate, containing 0.5 M imidazole and 0.5 M NaCl, pH ~ 6.8. Source: Bacteroides fragilis NCTC 9343. Branching enzyme, amylo-(1,4?1,6)-transglycosylase; Q-enzyme; α-glucan-branching glycosyltransferase; amylose isomerase; enzym | |
| Glycogen branching enzyme from Escherichia coli, Recombinant | Glycogen branching enzyme is an enzyme that adds branches to the growing glycogen molecule during the synthesis of glycogen, a storage form of glucose. More specifically, during glycogen synthesis, a glucose 1-phosphate molecule reacts with uridine triphosphate (UTP) to become UDP-glucose, an activated form of glucose. The activated glucosyl unit of UDP-glucose is then transferred to the hydroxyl group at the C-4 of a terminal residue of glycogen to form an α-1,4-glycosidic linkage, a reaction catalyzed by glycogen synthase. Importantly, glycogen synthase can only catalyze the synthesis of α-1,4-glycosidic linkages. Since glycogen is a readily mobili...;-1,4-glucan-6-glycosyltransferase; starch branching enzyme; 1,4-α-D-glucan:1,4-α-D-glucan 6-α-D-(1,4-α-D-glucano)-transferase. Enzyme Commission Number: EC 2.4.1.18. CAS No. 9001-97-2. Purity: > 95 % as judged by SDS-PAGE. Glycogen branching enzyme. Mole weight: 88157.0 Da. Activity: 15.44 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Escherichia coli str. K-12 substr. W3110. Branching enzyme, amylo-(1,4?1,6)-transglycosylase; Q-enzyme; α-glucan-branching glycosyltransferase; amylose isomerase; enzymatic branching factor; branching glycosyltransferase; enzyme Q; glucos | |
| Glycogen debranching enzyme (980-990) | Glycogen debranching enzyme (980-990) is a bioactive peptide of Glycogen debranching enzyme. Together with phosphorylase, glycogen debranching enzymes function in glycogen breakdown and glucose mobilization. | |
| Glycogen from bovine liver | Solid. Group: Polysaccharide. CAS No. 9005-79-2. Product ID: (2S,3R,4S,5S,6R)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol. Molecular formula: 666.6g/mol. Mole weight: C24H42O21. C (C1C (C (C (C (O1)OCC2C (C (C (C (O2)OC3C (OC (C (C3O)O)O)CO)O)O)OC4C (C (C (C (O4)CO)O)O)O)O)O)O)O. InChI=1S/C24H42O21/c25-1-5-9 (28)11 (30)16 (35)22 (41-5)39-4-8-20 (45-23-17 (36)12 (31)10 (29)6 (2-26)42-23)14 (33)18 (37)24 (43-8)44-19-7 (3-27)40-21 (38)15 (34)13 (19)32/h5-38H, 1-4H2/t5-, 6-, 7-, 8-, 9-, 10-, 11+, 12+, 13-, 14-, 15-, 16-, 17-, 18-, 19-, 20-, 21+, 22+, 23-, 24-/m1/s1. BYSGBSNPRWKUQH-UJDJLXLFSA-N. | |
| Glycogen from Mytilus edulis (Blue mussel) | Solid. Group: Polysaccharide. CAS No. 9005-79-2. Product ID: (2S,3R,4S,5S,6R)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol. Molecular formula: 666.6g/mol. Mole weight: C24H42O21. C (C1C (C (C (C (O1)OCC2C (C (C (C (O2)OC3C (OC (C (C3O)O)O)CO)O)O)OC4C (C (C (C (O4)CO)O)O)O)O)O)O)O. InChI=1S/C24H42O21/c25-1-5-9 (28)11 (30)16 (35)22 (41-5)39-4-8-20 (45-23-17 (36)12 (31)10 (29)6 (2-26)42-23)14 (33)18 (37)24 (43-8)44-19-7 (3-27)40-21 (38)15 (34)13 (19)32/h5-38H, 1-4H2/t5-, 6-, 7-, 8-, 9-, 10-, 11+, 12+, 13-, 14-, 15-, 16-, 17-, 18-, 19-, 20-, 21+, 22+, 23-, 24-/m1/s1. BYSGBSNPRWKUQH-UJDJLXLFSA-N. | |
| Glycogen from Mytilus edulis (Blue mussel) | ?85%. Group: Polysaccharide. | |
| Glycogen - from oyster | Glycogen from Oyster, a naturally occurring polysaccharide extract derived from oysters, presents a fascinating study for its potential uses in the pharmaceutical and dermatology industries. It is chiefly utilized as a diluent and excipient in oral formulations like tablets and capsules. Additionally, studies have explored its application in treating glycogen storage disorders and enhancing muscle function. With its phenomenal wound healing and dry skin treatment potential, the compound could revolutionize the dermatology space. Synonyms: Animal starch; Biosaccharides LS-HG; Hepatin; Liver glycogen; Liver starch; Lyoglycogen; Phytoglycogen. CAS No. 9005-79-2. Molecular formula: (C6H10O5)n. | |
| Glycogen from oyster | Solid. Group: Polysaccharide. CAS No. 9005-79-2. Product ID: (2S,3R,4S,5S,6R)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol. Molecular formula: 666.6g/mol. Mole weight: C24H42O21. C (C1C (C (C (C (O1)OCC2C (C (C (C (O2)OC3C (OC (C (C3O)O)O)CO)O)O)OC4C (C (C (C (O4)CO)O)O)O)O)O)O)O. InChI=1S/C24H42O21/c25-1-5-9 (28)11 (30)16 (35)22 (41-5)39-4-8-20 (45-23-17 (36)12 (31)10 (29)6 (2-26)42-23)14 (33)18 (37)24 (43-8)44-19-7 (3-27)40-21 (38)15 (34)13 (19)32/h5-38H, 1-4H2/t5-, 6-, 7-, 8-, 9-, 10-, 11+, 12+, 13-, 14-, 15-, 16-, 17-, 18-, 19-, 20-, 21+, 22+, 23-, 24-/m1/s1. BYSGBSNPRWKUQH-UJDJLXLFSA-N. | |
| Glycogen from oyster | ?75%. Group: Polysaccharide. | |
| Glycogen - from rabbit liver | Glycogen - from rabbit liver is a paramount carbohydrate polymer of superior grade, finding extensive employment in investigating metabolism intricacies and glycogen storage conditions. Molecular formula: (C6H10O5)n. | |
| Glycogen from rabbit liver | ?85%. Group: Fluorescence/luminescence spectroscopy. | |
| glycogenin glucosyltransferase | The first reaction of this enzyme is to catalyse its own glucosylation, normally at Tyr-194 of the protein if this group is free. When Tyr-194 is replaced by Thr or Phe, the enzyme's Mn2+-dependent self-glucosylation activity is lost but its intermolecular transglucosylation ability remains. It continues to glucosylate an existing glucosyl group until a length of about 5-13 residues has been formed. Further lengthening of the glycogen chain is then carried out by EC 2.4.1.11, glycogen (starch) synthase. The enzyme is not highly specific for the donor, using UDP-xylose in addition to UDP-glucose (although not glucosylating or xylosylating a xylosyl group so added). It can also ...exist, and different forms predominate in different organs. Thus primate liver contains glycogenin-2, of molecular mass 66 kDa, whereas the more widespread form is glycogenin-1, with a molecular mass of 38 kDa. Group: Enzymes. Synonyms: glycogenin; priming glucosyltransferase; UDP-glucose:glycogenin glucosyltransferase. Enzyme Commission Number: EC 2.4.1.186. CAS No. 117590-73-5. 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-2412; glycogenin glucosyltransferase; EC 2.4.1.186; 117590-73-5; glycogenin; priming glucosyltransferase; UDP-glucose:glycogenin glucosyltransferase. Cat No: EXWM-2412. | |
| Glycogen, Molecular Biology Grade, Mussel - CAS 9005-79-2 | Suitable as a carrier substance for the precipitation of nucleic acids. One μl is sufficient to precipitate picogram quantities of nucleic acid with Ethanol. Group: Polysaccharide. | |
| Glycogen, Molecular Biology Grade, Mussel - CAS 9005-79-2 - Calbiochem | Solid. Group: Polysaccharide. CAS No. 9005-79-2. Product ID: (2S,3R,4S,5S,6R)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol. Molecular formula: 666.6g/mol. Mole weight: C24H42O21. C (C1C (C (C (C (O1)OCC2C (C (C (C (O2)OC3C (OC (C (C3O)O)O)CO)O)O)OC4C (C (C (C (O4)CO)O)O)O)O)O)O)O. InChI=1S/C24H42O21/c25-1-5-9 (28)11 (30)16 (35)22 (41-5)39-4-8-20 (45-23-17 (36)12 (31)10 (29)6 (2-26)42-23)14 (33)18 (37)24 (43-8)44-19-7 (3-27)40-21 (38)15 (34)13 (19)32/h5-38H, 1-4H2/t5-, 6-, 7-, 8-, 9-, 10-, 11+, 12+, 13-, 14-, 15-, 16-, 17-, 18-, 19-, 20-, 21+, 22+, 23-, 24-/m1/s1. BYSGBSNPRWKUQH-UJDJLXLFSA-N. | |
| glycogen phosphorylase | This entry covers several enzymes from different sources that act in vivo on different forms of (1?4)-α-D-glucans. Some of these enzymes catalyse the first step in the degradation of large branched glycan polymers - the phosphorolytic cleavage of α-1,4-glucosidic bonds from the non-reducing ends of linear poly(1?4)-α-D-glucosyl chains within the polymers. The enzyme stops when it reaches the fourth residue away from an α-1,6 branching point, leaving a highly branched core known as a limit dextrin. The accepted name of the enzyme should be modified for each specific instance by substituting "glycogen" with the name of the natural substrate, e.g. maltodextrin...ission Number: EC 2.4.1.1. CAS No. 9035-74-9. GPBB. 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-2326; glycogen phosphorylase; EC 2.4.1.1; 9035-74-9; muscle phosphorylase a and b; amylophosphorylase; polyphosphorylase; amylopectin phosphorylase; glucan phosphorylase; 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). Cat No: EXWM-2326. | |
| Glycogen Phosphorylase from Human, Recombinant | Glycogen phosphorylase is one of the phosphorylaseenzymes (EC 2.4.1.1). It breaks up glycogeninto glucosesubunits. Glycogenis left with one less glucosemolecule, and the free glucosemolecule is in the form of glucose-1-phosphate. In order to be used for metabolism, it must be converted to glucose-6-phosphateby the enzyme phosphoglucomutase. Glycogen phosphorylase can only act on linearchainsof glycogen (a 1-4 glycosidic linkage). Its work will immediately come to a halt four residues away from a 1-6 branch (which are exceedingly common in glycogen). In these situations, a debranching enzymeis necessary, which will straighten out the chain in that area. Additionally, an...e; amylopectin phosphorylase; glucan phosphorylase; 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; EC 2.4.1.1; GPBB. CAS No. 9035-74-9. Purity: Greater than 85.0% as determined by (a) Analysis by RP-HPLC. (b) Analysis by SDS-PAGE. GPBB. Stability: GPBB although stable at 10°C for 7 days, should be stored desiccated below -18°C. Please prevent freeze-thaw cycles. Appearance: Sterile Filtered colourless liquid formualtio | |
| Glycogen Phosphorylase Inhibitor | Glycogen phosphorylase inhibitor is a cell-permeable inhibitor of human liver glycogen phosphorylase with an IC50 value of 53 nM. It has been used in biological studies to study glycogen utilization in human liver HepG2 cells, retinal explants, and human T lymphocyte Kit 225 cells. Synonyms: GPI; 2-chloro-4,5-difluoro-N-[[[2-methoxy-5-[[(methylamino)carbonyl]amino]phenyl]amino]carbonyl]-benzamide. Grade: ≥98%. CAS No. 648926-15-2. Molecular formula: C17H15ClF2N4O4. Mole weight: 412.8. | |
| Glycogen Phosphorylase Inhibitor | Glycogen Phosphorylase Inhibitor is used in biological studies to to evaluate glycogen utilization in human liver HepG2 cells. Group: Biochemicals. Grades: Highly Purified. CAS No. 648926-15-2. Pack Sizes: 1mg, 5mg. Molecular Formula: C17H15ClF2N4O4, Molecular Weight: 412.78. US Biological Life Sciences. | Worldwide |
| glycogen(starch) synthase | The accepted name varies according to the source of the enzyme and the nature of its synthetic product (cf. EC 2.4.1.1, phosphorylase). Glycogen synthase from animal tissues is a complex of a catalytic subunit and the protein glycogenin. The enzyme requires glucosylated glycogenin as a primer; this is the reaction product of EC 2.4.1.186 (glycogenin glucosyltransferase). A similar enzyme utilizes ADP-glucose (EC 2.4.1.21, starch synthase). Group: Enzymes. Synonyms: UDP-glucose-glycogen glucosyltransferase; glycogen (starch) synthetase; UDP-glucose-glycogen glucosyltransferase; UDP-glycogen synthase; UDPG-glycogen synthetase; UDPG-glycogen transglucosylase; uridine diphosphoglucose-glycogen glucosyltransferase. Enzyme Commission Number: EC 2.4.1.11. CAS No. 9014-56-6. 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-2336; glycogen(starch) synthase; EC 2.4.1.11; 9014-56-6; UDP-glucose-glycogen glucosyltransferase; glycogen (starch) synthetase; UDP-glucose-glycogen glucosyltransferase; UDP-glycogen synthase; UDPG-glycogen synthetase; UDPG-glycogen transglucosylase; uridine diphosphoglucose-glycogen glucosyltransferase. Cat No: EXWM-2336. | |
| Glycogen Synthase Kinase 3β, Histidine-tagged, from rabbit, Recombinant | Glycogen synthase kinase-3 is a serine-threonine protein kinase involved in regulation of metabolic enzymes such as glycogen synthase and ATP-Citrate lyase, and of protein phosphatase-1. It also phosphorylates brain tau-proteins, inducing an Alzheimer-like state, and protooncogene transcription factors. GSK-3β is one of two isozymes. > 90% (sds-page), recombinant, expressed in e. coli. Group: Enzymes. Synonyms: Glycogen Synthase Kinase 3β; GSK-3β; GSK3B; 9059-09-0. CAS No. 9059-09-0. Purity: > 90% (SDS-PAGE). GSK-3&beta. Stability: -20°C. Source: E. coli. Species: Rabbit. Glycogen Synthase Kinase 3β; GSK-3β; GSK3B; 9059-09-0. Cat No: NATE-0324. | |
| Glycogen type II from oyster | 5g Pack Size. Group: Analytical Reagents, Biochemicals, Carbohydrates. Formula: (C6H10O5)n. CAS No. 9005-79-2. Prepack ID 90005291-5g. See USA prepack pricing. | |
| Glycoglycoyl-Lys5-Octreotide | An impurity of Octreotide. Octreotide is a synthetic long-acting cyclic octapeptide that inhibits growth hormone, glucagon and insulin more effectively than somatostatin. Synonyms: DPhe-Cys-Phe-DTrp-Lys(Glycolide)-Thr-Cys-Thr-ol(Cys2&Cys7 bridge); Glycoglycoyl-Lys-Octreotide; D-Phenylalanyl-L-hemicystyl-L-phenylalanyl-D-tryptophyl-(N-Glycoglycoyl)-L-lysyl-L-threonyl-L-hemicystyl-L-Threoninol cyclic (2-7)-disulfide; DPhe-Cys-Phe-DTrp-Lys(Glycolide)-Thr-Cys-Thr-ol(Cys2&Cys7 bridge); Glycolide-Lys5-Octreotide. Grade: ≥95%. Molecular formula: C53H70N10O14S2. Mole weight: 1135.31. | |
| Glycoglycoyl-Phe1-Octreotide | An impurity of Octreotide. Octreotide is a synthetic long-acting cyclic octapeptide that inhibits growth hormone, glucagon and insulin more effectively than somatostatin. Synonyms: Glycolide-DPhe-Cys-Phe-DTrp-Lys-Thr-Cys-Thr-ol(Cys2&Cys7 bridge); Glycolide-Phe1-Octreotide; (N-GlycoGlycoyl)-D-phenylalanyl-L-hemicystyl-L-phenylalanyl-D-tryptophyl-L-lysyl-L-threonyl-L-hemicystyl-L-Threoninol cyclic (2-7)-disulfide; Glycolide-DPhe-CF-DTrp-KTC-Thr-ol(Cys2&Cys7 bridge). Grade: ≥95%. Molecular formula: C53H70N10O14S2. Mole weight: 1135.31. | |
| Glycoglycoyl-Thr8-Octreotide | An impurity of Octreotide. Octreotide is a synthetic long-acting cyclic octapeptide that inhibits growth hormone, glucagon and insulin more effectively than somatostatin. Synonyms: DPhe-Cys-Phe-DTrp-Lys-Thr-Cys-Thr-ol-Glycolide(Cys2&Cys7 bridge); DPhe-Cys-Phe-DTrp-Lys-Thr-Cys-Thr-ol-Glycolide(Cys2&Cys7 bridge); Glycolide-Thr8-Octreotide. Grade: ≥95%. CAS No. 1796598-15-6. Molecular formula: C53H70N10O14S2. Mole weight: 1135.31. | |
| Glycohyodeoxycholic acid | Glycohyodeoxycholic acid is a major metabolite of Hyodeoxycholic acid in humans. Glycohyodeoxycholic acid has preventative effects on gallstone formation [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 13042-33-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-126995. | |
| glycol | glycol. Uses: For analytical and research use. Group: Impurity standards. CAS No. 107-21-1. Molecular formula: C2H6O2. Mole weight: 62.07. Catalog: APB107211. | |
| Glycol acid | DryPowder; Liquid; PelletsLargeCrystals; Solid; COLOURLESS HYGROSCOPIC CRYSTALS. Group: Polymers. CAS No. 26124-68-5. Product ID: 2-hydroxyacetic acid. Molecular formula: 76.05g/mol. Mole weight: C2H4O3;HOCH2COOH;C2H4O3. C(C(=O)O)O. InChI=1S/C2H4O3/c3-1-2(4)5/h3H, 1H2, (H, 4, 5). AEMRFAOFKBGASW-UHFFFAOYSA-N. | |
| Glycolaldehyde-1-13C | Glycolaldehyde-1-13C. Group: Biochemicals. Alternative Names: 2-Hydroxyacetaldehyde-1-13C; 2-Hydroxyethanal-1-13C; 2-Oxoethanol-1-13C; Hydroxyacetaldehyde-1-13C; Diose-1-13C; Glicolaldehido-1-13C; Glycolic Aldehyde-1-13C; Glycollaldehyde-1-13C; Hydroxyethanal-1-13C; Methylolformaldehyde-1-13C; Mono methyl olformaldehyde-1-13C; NSC 67935-1-13C. Grades: Highly Purified. CAS No. 71122-42-4. Pack Sizes: 5mg. Molecular Formula: C13CH4O2, Molecular Weight: 61.04. US Biological Life Sciences. | Worldwide |
| Glycolaldehyde-1-[13C] | Glycolaldehyde-1-[13C] is the labelled analogue of Glycolaldehyde. Glycolaldehyde, derived from ethylene glycol, is a basic metabolite found in all eukaryotes. Synonyms: Glycolaldehyde-1-13C; [1-13C]GLYCOLALDEHYDE; Hydroxy(1-13C)acetaldehyde; CTK8F2344; DTXSID00724572; 2-Hydroxyacetaldehyde-1-13C; 2-Hydroxyethanal-1-13C; 2-Oxoethanol-1-13C; Hydroxyacetaldehyde-1-13C; Diose-1-13C; Glicolaldehido-1-13C; Glycolic Aldehyde-1-13C; Hydroxyethanal-1-13C; Methylolformaldehyde-1-13C; Monomethylolformaldehyde-1-13C; NSC 67935-1-13C. Grade: 97% (CP); 99% atom 13C. CAS No. 71122-42-4. Molecular formula: C[13C]H4O2. Mole weight: 61.04. | |
| Glycolaldehyde-[1,2-13C2] | Glycolaldehyde-[1,2-13C2] is the labelled analogue of Glycolaldehyde. Glycolaldehyde, derived from ethylene glycol, is a basic metabolite found in all eukaryotes. Synonyms: 2-Hydroxyacetaldehyde-1,2-13C2; 2-Hydroxyethanal-1,2-13C2; 2-Oxoethanol-1,2-13C2; Hydroxyacetaldehyde-1,2-13C2; Diose-1,2-13C2; Glicolaldehido-1,2-13C2; Glycolic Aldehyde-1,2-13C2; Glycollaldehyde-1,2-13C2; Hydroxyethanal-1,2-13C2; Methylolformaldehyde-1,2-13C2; Monomethylolformaldehyde-1,2-13C2. CAS No. 478529-69-0. Molecular formula: [13C]2H4O2. Mole weight: 62.04. | |
| Glycolaldehyde-1,2-13C2 | Glycolaldehyde-1,2-13C2. Group: Biochemicals. Alternative Names: 2-Hydroxyacetaldehyde-1,2-13C2; 2-Hydroxyethanal-1,2-13C2; 2-Oxoethanol-1,2-13C2; Hydroxyacetaldehyde-1,2-13C2; Diose-1,2-13C2; Glicolaldehido-1,2-13C2; Glycolic Aldehyde-1,2-13C2; Glycollaldehyde-1,2-13C2; Hydroxyethanal-1,2-13C2; Methylolformaldehyde-1,2-13C2; Mono methyl olformaldehyde-1, 2-13C2; NSC 67935-1,2-13C2. Grades: Highly Purified. CAS No. 478529-69-0. Pack Sizes: 5mg. Molecular Formula: 13C2H4O2, Molecular Weight: 62.04. US Biological Life Sciences. | Worldwide |
| Glycolaldehyde-[2-13C] | Glycolaldehyde-[2-13C] is the labelled analogue of Glycolaldehyde. Glycolaldehyde, derived from ethylene glycol, is a basic metabolite found in all eukaryotes. Synonyms: 2-Hydroxyacetaldehyde-2-13C; 2-Hydroxyethanal-2-13C; 2-Oxoethanol-2-13C; Hydroxyacetaldehyde-2-13C; Diose-2-13C; Glicolaldehido-2-13C; Glycolic Aldehyde-2-13C; Glycollaldehyde-2-13C; Hydroxyethanal-2-13C; Methylolformaldehyde-2-13C; Monomethylolformaldehyde-2-13C. CAS No. 478529-67-8. Molecular formula: C[13C]H4O2. Mole weight: 61.05. | |
| Glycolaldehyde-2-13C | Glycolaldehyde-2-13C. Group: Biochemicals. Alternative Names: 2-Hydroxyacetaldehyde-2-13C; 2-Hydroxyethanal-2-13C; 2-Oxoethanol-2-13C; Hydroxyacetaldehyde-2-13C; Diose-2-13C; Glicolaldehido-2-13C; Glycolic Aldehyde-2-13C; Glycollaldehyde-2-13C; Hydroxyethanal-2-13C; Methylolformaldehyde-2-13C; Mono methyl olformaldehyde-2-13C; NSC 67935-2-13C. Grades: Highly Purified. CAS No. 478529-67-8. Pack Sizes: 5mg. Molecular Formula: C13CH4O2, Molecular Weight: 61.04. US Biological Life Sciences. | Worldwide |
| glycolaldehyde dehydrogenase | This enzyme belongs to the family of oxidoreductases, specifically those acting on the aldehyde or oxo group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is glycolaldehyde:NAD+ oxidoreductase. This enzyme is also called glycol aldehyde dehydrogenase. This enzyme participates in glyoxylate and dicarboxylate metabolism. Group: Enzymes. Synonyms: glycol aldehyde dehydrogenase. Enzyme Commission Number: EC 1.2.1.21. CAS No. 37250-89-8. 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-1127; glycolaldehyde dehydrogenase; EC 1.2.1.21; 37250-89-8; glycol aldehyde dehydrogenase. Cat No: EXWM-1127. | |
| Glycolaldehyde diethyl acetal,stab.with ca 0.1%sodium carbonate | Glycolaldehyde diethyl acetal,stab.with ca 0.1%sodium carbonate. Group: Biochemicals. Grades: Highly Purified. CAS No. 621-63-6. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C6H14O3. US Biological Life Sciences. | Worldwide |
| Glycolaldehyde dimer | Glycolaldehyde dimer. Group: Biochemicals. Grades: Highly Purified. CAS No. 23147-58-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| glycolate dehydrogenase | Also acts on (R)-lactate. 2,6-Dichloroindophenol and phenazine methosulfate can act as acceptors. Group: Enzymes. Synonyms: glycolate oxidoreductase; glycolic acid dehydrogenase; glycolate:(acceptor) 2-oxidoreductase. Enzyme Commission Number: EC 1.1.99.14. CAS No. 37368-32-4. 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-0447; glycolate dehydrogenase; EC 1.1.99.14; 37368-32-4; glycolate oxidoreductase; glycolic acid dehydrogenase; glycolate:(acceptor) 2-oxidoreductase. Cat No: EXWM-0447. | |
| Glycolate Standard for IC | 1000 mg/L glycolate in water. Group: Anions and cations standards. | |
| Glycol chitosan | ?60% (titration), crystalline. Group: Polysaccharide. | |
| Glycol chitosan | Glycol chitosan is a remarkably versatile biomaterial extensively utilized within the vast biomedical industry, showcasing unparalleled biocompatibility and biodegradability attributes. Its multifunctional nature empowers it to be effectively employed as a highly efficient drug delivery system. Synonyms: Glycol chitin, deacetylated; Chitosan, 6-(2-hydroxyethyl) ether; Chitosan 6-(2-hydroxyethyl) ether; Hydroxyethyl chitosan. CAS No. 123938-86-3. Molecular formula: (C8H15NO5)n. | |
| Glycol chitosan | degree of polymerization ≥400. Uses: Glycol chitosan increases membrane permeability and leakage in glycine max harosoy 63w cells. Group: Polysaccharide. Alternative Names: Glycol chitin, deacetylated. CAS No. 123938-86-3. Pack Sizes: 500 mg in poly bottle 1, 5 g in poly bottle. Molecular formula: 82685.58. N[C@@H]1[C@@H] (O)[C@H] (O)[C@@H] (COCCO)O[C@H]1O[C@@H]2[C@@H] (COCCO)O[C@@H] (O[C@@H]3[C@@H] (COCCO)O[C@@H] (O)[C@H] (N)[C@H]3O)[C@H] (N)[C@H]2O. [n]. 96%. | |
| Glycol chitosan | Glycol chitosan is a chitosan derivative with ethylene glycol branches. Glycol chitosan enhances membrane permeability and leadkage in Glycine max Harosoy 63W cells. Glycol chitosan is biocompatible and biodegradable[1][2][3]. Glycol chitosan inhibits E. coli, S. aureus and S. enteritidis growths with MIC values of 4 ?g/mL, 32 ?g/mL and <0.5 ?g/mL, respectively[4]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 123938-86-3. Pack Sizes: 50 mg; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-135969. | |
| Glycol chitosan | Polysaccharide. Uses: For analytical and research use. Group: Reagents. CAS No. 123938-86-3. Pack Sizes: 500MG, 1G, 5G. | |
| Glycol Either PnP | Glycol Either PnP. Category GLYCOL ETHERS. Pack Sizes Drums, Totes, bulk |  |
| Glycol Ether DB | Glycol Ether DB. Category GLYCOL ETHERS. Pack Sizes Drums, Totes, bulk | |
| Glycol Ether DB Acetate | Glycol Ether DB Acetate. Category GLYCOL ETHERS. Pack Sizes Drums, Totes, bulk | |
| Glycol Ether DM | Glycol Ether DM. Category GLYCOL ETHERS. Pack Sizes Drums, Totes, bulk | |
| Glycol Ether DPM | Glycol Ether DPM. Category GLYCOL ETHERS. Pack Sizes Drums, Totes, bulk | |
| Glycol Ether DPM Acetate | Glycol Ether DPM Acetate. Category GLYCOL ETHERS. Pack Sizes Drums, Totes, bulk | |
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