Glyceralde Suppliers USA
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Product | Description | |
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3,3-Diethoxy-1,2-propanediol 1-phosphate barium salt Quick inquiry Where to buy Suppliers range | 3,3-Diethoxy-1,2-propanediol 1-phosphate barium salt. Group: Heterocyclic Organic Compound. Alternative Names: DL-GLYCERALDEHYDE-3-PHOSPHATEDIETHYLACETAL BARIUM SALT;DL-GLYCERALDEHYDE-3-PHOSPHATE DIETHYLACETAL BA SALT;DL-GLYCERALDEHYDE 3-PHOSPHATE DIETHYL ACETAL MONOBARIUM SALT;3,3-DIETHOXY-1,2-PROPANEDIOL 1-PHOSPHATE BARIUM SALT;barium 3,3-diethoxy-2-hydroxypropyl phosphate;DL-GLYCERALDEHYDE 3-PHOSPHATE DIETHYL*AC ETAL MONOBA;DL-GLYCERALDEHYDE 3-PHOSPHATE DIETHYL-AC ETAL MONOBAR.SALT;DL-glyceraldehyde 3-phosphate diethyl acetal monobarium. CAS No. 93965-35-6. Molecular formula: C7H15BaO7P. Mole weight: 379.49. Symbol: GHS07. Safty Description: 28. Hazard statements: Xn. Supplemental Hazard Statements: H302-H332. | |
β-NADH, Reduced Disodium Salt (Nicotinamide Adenine Dinucleotide) Quick inquiry Where to buy Suppliers range | Beta-nicotinamide adenine dinucleotide hydrate. Can be used as a cofactor in reactions with NAD-dependent histone deacetylase enzymes.NAD is a coenzyme formed from the nucleotide, nicotinamide, adenosine monophosphateand a phosphate group joining the first two components. NADP has the same structure with the addition of an extra phosphate group to AMP. NAD can be reduced to NADH during coupling with reactions which oxidize various organic substrates. For example, the reaction catalyzed by glyceraldehyde phosphate dehydrogenase during glycolysis. NADH then passes to the inside of mitochondria where it donates the electrons it is carrying to the electron transport chain. In this manner, NAD acts as an intermediate energy storage compound that indirectly generates ATP. Generally, NADP accepts electrons from catabolic reactions to form NADPH. An example is its coupling with the conversion of glucose-6-phosphate to ribose-5-phosphate in the pentose phosphate pathway. NADPH has a slightly different role to NADH in that it does not donate electrons to the electron transport chain. Instead, it tends to reduce intermediates in anabolic pathways e.g. fatty acid synthesis. NAD participates in many redox reactions in cells, including those in glycolysis and most of those in the citric acid cycle of cellular respiration. Nicotinamide adenine dinucleotide (NAD) and its relative nicotinamide adenine dinucleotide phosphate (NADP) are two of the most important coenzymes in the cell. In cells, most oxidations are accomplished by the removal of hydrogen atoms. Both of these coenzymes play crucial roles in this. Each molecule of NAD+ (or NADP+) can acquire two electrons; that is, be reduced by two electrons. However, only one proton accompanies the reduction. The other proton produced as two hydrogen atoms are removed from the molecule being oxidized is liberated into the surrounding medium. Group: Biochemicals. Alternative Names: β-DPNH; β-NADH; DPNH; Diphosphopyridine nucleotide, reduced form; NADH. Grades: Highly Purified. CAS No. 606-68-8. Pack Sizes: 1g, 5g, 10g. Molecular Formula: C21H27N7O14P2Na2, Molecular Weight: 709.41. US Biological Life Sciences. | Worldwide |
β-Nicotinamide Adenine Dinucleotide Phosphate, Sodium Salt Hydrate ( β-NADP-Na, TPN-Na) Quick inquiry Where to buy Suppliers range | NAD is a coenzyme formed from the nucleotide, nicotinamide, adenosine monophosphateand a phosphate group joining the first two components. NADP has the same structure with the addition of an extra phosphate group to AMP. NAD can be reduced to NADH during coupling with reactions which oxidize various organic substrates. For example, the reaction catalyzed by glyceraldehyde phosphate dehydrogenase during glycolysis. NADH then passes to the inside of mitochondria where it donates the electrons it is carrying to the electron transport chain. In this manner, NAD acts as an intermediate energy storage compound that indirectly generates ATP. Generally, NADP accepts electrons from catabolic reactions to form NADPH. An example is its coupling with the conversion of glucose-6-phosphate to ribose-5-phosphate in the pentose phosphate pathway. NADPH has a slightly different role to NADH in that it does not donate electrons to the electron transport chain. Instead, it tends to reduce intermediates in anabolic pathways e.g. fatty acid synthesis. NAD participates in many redox reactions in cells, including those in glycolysis and most of those in the citric acid cycle of cellular respiration. Nicotinamide adenine dinucleotide (NAD) and its relative nicotinamide adenine dinucleotide phosphate (NADP) are two of the most important coenzymes in the cell. In cells, most oxidations are accomplished by the removal of hydrogen atoms. Both of these coenzymes play crucial roles in this. Each molecule of NAD+ (or NADP+) can acquire two electrons; that is, be reduced by two electrons. However, only one proton accompanies the reduction. The other proton produced as two hydrogen atoms are removed from the molecule being oxidized is liberated into the surrounding medium. Group: Biochemicals. Alternative Names: b-NADP sodium salt hydrate; β-NADP-Na, β-NADP-sodium salt, Coenzyme II sodium salt, NADP, TPN-Na, TPN, Triphosphopyridine nucleotide sodium salt; 2'-(Dihydrogen Phosphate) Adenosine 5'-(Trihydrogen Diphosphate) P'?5'-Ester with 3-(Aminocarbonyl)-1- β -D-ribofuranosyl pyridinium , Inner Salt Sodium Salt; 2'-(Dihydrogen phosphate) Adenosine 5'-(Trihydrogen Diphosphate) P'?5'-Ester with 3-(Aminocarbonyl)-1- β -D-ribofuranosyl pyridinium Inner Salt Sodium Salt; Adenosine 5'-(Trihydrogen Diphosphate), P'?5'-Ester with 3-(Aminocarbonyl)-1- β -D-ribofuranosyl pyridinium Inner Salt, 2'-(Dihydrogen Phosphate) Monosodium Salt; NSC 20273; Sodium NADP. Grades: Highly Purified. CAS No. 698999-85-8,1184-16-3. Pack Sizes: 100mg, 500mg, 1g, 5g. Molecular Formula: C21H27N7O17P3 Na xH2O, Molecular Weight: 765.42 (anhydrous). US Biological Life Sciences. | Worldwide |
Buformin-d9 Quick inquiry Where to buy Suppliers range | Buformin, clinically used for diabetes mellitus, is known to improve resistance to insulin in patients. It suppresses the expression of glyceraldehyde 3-phosphate dehydrogenase. Group: Biochemicals. Alternative Names: N-Butyl-d9-idodicarbonimidic Diamide; 1-Butyl-d9-biguanide; 1-Butylbiguanide-d9; Buformine-d9; Butformin-d9; Butylbiguanid-d9e; Butyldiguanid-d9e; DBV-d9; Dibetos B-d9; Glybigid-d9; H 224-d9; N1-Butylbiguanide-d9; W 37-d9. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
Buformin Hydrochloride Quick inquiry Where to buy Suppliers range | Buformin, clinically used for diabetes mellitus, is known to improve resistance to insulin in patients. It suppresses the expression of glyceraldehyde 3-phosphate dehydrogenase. Group: Biochemicals. Alternative Names: N-Butylidodicarbonimidic Diamide Hydrochloride; 1-Butylbiguanide Hydrochloride; 1-Butylbiguanide Hydrochloride; Buformine; Butformin; Butylbiguanide; Butyldiguanide; DBV; Dibetos B; Glybigid; Panformin; Sindiatil; Tidemol; Ziavetine. Grades: Highly Purified. CAS No. 1190-53-0. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
CGP 3466B maleate Quick inquiry Where to buy Suppliers range | CGP 3466B maleate, a potent anti-apoptotic drug, is an orally active glyceraldehyde-3-phosphate dehydrogenase (GAPDH) inhibitor. CGP 3466B maleate was tested in clinical trials for its ability to help treat Parkinson's disease (PD) and amyotrophic lateral sclerosis (ALS) but the clinical trials have been terminated due to lack of benefit. Synonyms: N-(benzo[b][1]benzoxepin-5-ylmethyl)-N-methylprop-2-yn-1-amine;but-2-enedioic acid; Omigapil maleate; CGP 3466B; CGP-3466B; CGP3466B; TCH-346; TCH 346; TCH346; Omigapil maleate. Grades: >99 %. CAS No. 200189-97-5. Molecular formula: C23H21NO5. Mole weight: 391.42. | |
Dehydrogenase,glyceraldehyde phosphate Quick inquiry Where to buy Suppliers range | Dehydrogenase,glyceraldehyde phosphate. Group: Heterocyclic Organic Compound. CAS No. 9001-50-7. Molecular formula: C3H7O6P. Mole weight: 170.057841. | |
D-Fructose-1,6-diphosphate trisodium salt octahydrate Quick inquiry Where to buy Suppliers range | UsesCardioprotectant for ischemic disorders.;UsesD-Fructose-1,6-bisphosphate (FBP), a common metabolic sugar, is the precursor of glyceraldehyde 3-phosphate and dihydroxyacetone phosphate in the glycolytic pathway. It is an allosteric activator of enzymes such as pyruvate kinase and a substrate used to identify and characterize enzymes such as fructose-1,6-bisphosphate aldolase(s) and fructose-1, 6-bisphosphatase(s). FBP is studied as a neuroprotective agent in brain injury. Synonyms: D-Fructose-1,6-bisphosphate trisodium salt octahydrate. CAS No. 81028-91-3. Molecular formula: C6H11Na3O12P2 8H2O. Mole weight: 550.18. | |
D-(+)-Glyceraldehyde Quick inquiry Where to buy Suppliers range | 1g Pack Size. Group: Biochemicals, Carbohydrates. Formula: C3H6O3. CAS No. 453-17-8. Prepack ID 69205379-1g. Molecular Weight 90.08. See USA prepack pricing. | |
D-(+)-Glyceraldehyde Quick inquiry Where to buy Suppliers range | ≥98.0% (HPLC), viscous. Uses: For analytical and research use. Group: Fluorescence/Luminescence Spectroscopy. CAS No. 453-17-8. Pack Sizes: 1G, 5G. Mole weight: 90.08. EC Number: 207-217-1. Catalog: AP453178. Assay: ≥98.0% (HPLC). | |
D-Glyceraldehyde Quick inquiry Where to buy Suppliers range | D-Glyceraldehyde. Group: Heterocyclic Organic Compound. CAS No. 453-17-8. Molecular formula: C3H6O3. Mole weight: 90.08. | |
D-Glyceraldehyde-1,2,3-13C3 Quick inquiry Where to buy Suppliers range | D-Glyceraldehyde-1,2,3-13C3. Group: Biochemicals. Alternative Names: (R)-2,3-Dihydroxypropanal-1,2,3-13C3; (+)-Glyceraldehyde-1,2,3-13C3; (R)-(+)-Glyceraldehyde-1,2,3-13C3; (R)-Glyceraldehyde-1,2,3-13C3; D-(+)-Glyceraldehyde-1,2,3-13C3; D-Glyceraldehyde-1,2,3-13C3; D-Glycerose-1,2,3-13C3; NSC 91534-3-1,2,3-13C3; Triose-1,2,3-13C3. Grades: Highly Purified. CAS No. 478529-54-3. Pack Sizes: 5mg. Molecular Formula: 13C3H6O3, Molecular Weight: 93.06. US Biological Life Sciences. | Worldwide |
D-Glyceraldehyde-1,2,3-13C3 (Aqueous Solution) Quick inquiry Where to buy Suppliers range | D-Glyceraldehyde-1,2,3-13C3 (Aqueous Solution). Uses: For analytical and research use. Group: Carbohydrates. CAS No. 478529-54-3. Pack Sizes: 2.5MG. IUPAC Name: (2R)-2,3-dihydroxy(1,2,3-^{13}C_{3})propanal. Molecular formula: 13C3H6O3. Mole weight: 93.06. Catalog: APS478529543. SMILES: O[13CH2][13C@@H](O)[13CH]=O. Format: Neat. Product Type: Stable Isotope Labelled. Shipping: Room Temperature. | |
D-Glyceraldehyde-1,2,3,3'-d4 Quick inquiry Where to buy Suppliers range | D-Glyceraldehyde-1,2,3,3'-d4. Group: Biochemicals. Alternative Names: (R)-2,3-Dihydroxypropanal-1,2,3,3'-d4; (+)-Glyceraldehyde-1,2,3,3'-d4; (R)-(+)-Glyceraldehyde-1,2,3,3'-d4; (R)-Glyceraldehyde-1,2,3,3'-d4; D-(+)-Glyceraldehyde-1,2,3,3'-d4; D-Glyceraldehyde-1,2,3,3'-d4; D-Glycerose-1,2,3,3'-d4; NSC 91534-1,2,3,3'-d4; Triose-1,2,3,3'-d4. Grades: Highly Purified. CAS No. 478529-60-1. Pack Sizes: 1mg. Molecular Formula: C3H2D4O3, Molecular Weight: 94.1. US Biological Life Sciences. | Worldwide |
D-Glyceraldehyde-2-d Quick inquiry Where to buy Suppliers range | D-Glyceraldehyde-2-d. Group: Biochemicals. Alternative Names: (R)-2,3-Dihydroxypropanal-2-d; (+)-Glyceraldehyde-2-d; (R)-(+)-Glyceraldehyde--2-d; (R)-Glyceraldehyde-3-13C; D-(+)-Glyceraldehyde-2-d; D-Glyceraldehyde-2-d; D-Glycerose-2-d; NSC 91534-3-2-d; Triose-2-d. Grades: Highly Purified. CAS No. 478529-64-5. Pack Sizes: 5mg. Molecular Formula: C3H5DO3, Molecular Weight: 91.08. US Biological Life Sciences. | Worldwide |
D-Glyceraldehyde-3,3-d2 Quick inquiry Where to buy Suppliers range | D-Glyceraldehyde-3,3-d2. Group: Biochemicals. Alternative Names: (R)-2,3-Dihydroxypropanal-3,3-d2; (+)-Glyceraldehyde-3,3-d2; (R)-(+)-Glyceraldehyde-3,3-d2; (R)-Glyceraldehyde-3,3-d2; D-(+)-Glyceraldehyde-3,3-d2 D-Glyceraldehyde-3,3-d2 D-Glycerose-3,3-d2; NSC 91534-3,3-d2; Triose-3,3-d2. Grades: Highly Purified. CAS No. 478529-58-7. Pack Sizes: 5mg. Molecular Formula: C3H4D2O3, Molecular Weight: 92.09. US Biological Life Sciences. | Worldwide |
D-(+)-Glyceraldehyde ≥89% (HPLC) Quick inquiry Where to buy Suppliers range | D-(+)-Glyceraldehyde ≥89% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
Dl-glyceraldehyde Quick inquiry Where to buy Suppliers range | Dl-glyceraldehyde. Group: Heterocyclic Organic Compound. Alternative Names: GLYCERIC ALDEHYDE;GLYCERALDEHYDE;DL-GLYCERALDEHYDE;(+-)-glyceraldehyd;3-dihydroxy-(+/-)-propana;dl-glyceraldehyd;dl-glycericaldehyde;DL-GLYCERALDEHYDE CRYSTALLINE. CAS No. 56-82-6. Molecular formula: C3H6O3. Mole weight: 90.08. Melting Point: 144-145°C(lit.). Density: 1.593 g/cm3 (-5?). | |
DL-Glyceraldehyde Quick inquiry Where to buy Suppliers range | DL-Glyceraldehyde. CAS No. 56-82-6. Ebrator Biochemicals provides scientists around the global scientific community with a wide range of high purity Life Science products & Fine Chemicals. Categories: DL-Glyceraldehyde. | |
DL-Glyceraldehyde Quick inquiry Where to buy Suppliers range | DL-Glyceraldehyde. Group: Biochemicals. Alternative Names: 2,3-DIHYDROXYPROPANAL; GLYCERIC ALDEHYDE; DL-ALPHA, BETA-DI hydROXYPROPIONALDE hydE. Grades: Highly Purified. CAS No. 56-82-6,367-47-5. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C3H6O3. US Biological Life Sciences. | Worldwide |
DL-Glyceraldehyde Quick inquiry Where to buy Suppliers range | ≥90% (GC). Uses: For analytical and research use. Group: Fluorescence/Luminescence Spectroscopy. CAS No. 56-82-6. Pack Sizes: 500MG, 1G, 5G, 25G. Mole weight: 90.08. EC Number: 200-290-0. Catalog: AP56826. Assay: ≥90% (GC). | |
DL-Glyceraldehyde-1-13C Quick inquiry Where to buy Suppliers range | DL-Glyceraldehyde-1-13C. Group: Biochemicals. Alternative Names: (±)-2,3-Dihydroxypropanal-1-13C; 2,3-Dihydroxypropanal-1-13C; 2, 3-Di hydroxypropionalde hyde-1-13C; DL-Glyceraldehyde-1-13C; DL-Glyceric aldehyde-1-13C; Glyceraldehyde-1-13C; Glyceric Aldehyde-1-13C; Glycerinaldehyde-1-13C; Glycerose-1-13C; NSC 67934-1-13C; dl-Glyceraldehyde-1-13C; α, β -Di hydroxypropionalde hyde-1-13C. Grades: Highly Purified. CAS No. 56-82-6. Pack Sizes: 2.5mg. Molecular Formula: C213CH6O3, Molecular Weight: 91.07. US Biological Life Sciences. | Worldwide |
DL-Glyceraldehyde-1,2-13C2 Quick inquiry Where to buy Suppliers range | DL-Glyceraldehyde-1,2-13C2. Group: Biochemicals. Alternative Names: (±)-2,3-Dihydroxypropanal-1,2-13C; 2,3-Dihydroxypropanal-1,2-13C; 2, 3-Di hydroxypropionalde hyde-1, 2-13C; DL-Glyceraldehyde-1,2-13C; DL-Glyceric aldehyde-1,2-13C; Glyceraldehyde-1,2-13C; Glyceric Aldehyde-1,2-13C; Glycerinaldehyde-1,2-13C; Glycerose-1,2-13C; NSC 67934-1,2-13C; dl-Glyceraldehyde-1,2-13C; α, β -Di hydroxypropionalde hyde-1, 2-13C. Grades: Highly Purified. CAS No. 478529-51-0. Pack Sizes: 2.5mg. Molecular Formula: C13C2H6O3, Molecular Weight: 92.06. US Biological Life Sciences. | Worldwide |
DL-Glyceraldehyde-1,3-13C2 Quick inquiry Where to buy Suppliers range | DL-Glyceraldehyde-1,3-13C2. Group: Biochemicals. Alternative Names: (±)-2,3-Dihydroxypropanal-1,3-13C; 2,3-Dihydroxypropanal-1,3-13C; 2, 3-Di hydroxypropionalde hyde-1, 3-13C; DL-Glyceraldehyde-1,3-13C; DL-Glyceric aldehyde-1,3-13C; Glyceraldehyde-1,3-13C; Glyceric Aldehyde-1,3-13C; Glycerinaldehyde-1,3-13C; Glycerose-1,3-13C; NSC 67934-1,3-13C; dl-Glyceraldehyde-1,3-13C; α, β -Di hydroxypropionalde hyde-1, 3-13C. Grades: Highly Purified. CAS No. 478529-53-2. Pack Sizes: 2.5mg. Molecular Formula: C13C2H6O3, Molecular Weight: 92.06. US Biological Life Sciences. | Worldwide |
DL-Glyceraldehyde-1-d Quick inquiry Where to buy Suppliers range | DL-Glyceraldehyde-1-d. Group: Biochemicals. Alternative Names: (±)-2,3-Dihydroxypropanal-1-d; 2,3-Dihydroxypropanal-1-d; 2, 3-Di hydroxypropionalde hyde-1-d; DL-Glyceraldehyde-1-d; DL-Glyceric aldehyde-1-d; Glyceraldehyde-1-d; Glyceric Aldehyde-1-d; Glycerinaldehyde-1-d; Glycerose-1-d; NSC 67934-1-d; dl-Glyceraldehyde-1-d; α, β -Di hydroxypropionalde hyde-1-d. Grades: Highly Purified. CAS No. 72599-69-0. Pack Sizes: 5mg. Molecular Formula: C3H5DO3, Molecular Weight: 91.08. US Biological Life Sciences. | Worldwide |
DL-Glyceraldehyde 3-phosphate solution Quick inquiry Where to buy Suppliers range | 45-55 mg/mL in H2O. Uses: For analytical and research use. Group: Fluorescence/Luminescence Spectroscopy. CAS No. 591-59-3. Pack Sizes: 25MG, 100MG, 250MG, 500MG, 1G. Mole weight: 170.06. EC Number: 209-721-7. Catalog: AP591593. | |
DL-Glyceraldehyde 3-phosphate solution Quick inquiry Where to buy Suppliers range | Cas No. 591-59-3. | |
DL-Glyceraldehyde dimer Quick inquiry Where to buy Suppliers range | DL-Glyceraldehyde dimer. Group: Biochemicals. Grades: Reagent Grade. CAS No. 26793-98-6. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
DL-Glyceraldehyde, dimer Quick inquiry Where to buy Suppliers range | DL-Glyceraldehyde, dimer. Group: Biochemicals. Alternative Names: 3,6-Dihydroxy-1,4-dioxane-2,5-dimethanol. Grades: Highly Purified. CAS No. 23147-59-3,26793-98-6. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C6H12O6. US Biological Life Sciences. | Worldwide |
Glyceraldehyde-3-phosphate dehydrogenase (219-230) Quick inquiry Where to buy Suppliers range | Glyceraldehyde-3-phosphate dehydrogenase. Uses: Tumor Antigen Derived Peptides. CAS No. Product ID: ta-146. | |
Heptelidic acid Quick inquiry Where to buy Suppliers range | It is produced by the strain of Gliocladium virens, Chaetomium globosum, Trichoderma viride. It is a sesquiterpenoid antibiotic. It has antibacterial activity against anaerobes, especially has strong effect on fragile bacilli (MIC is 0.4 μg/mL). It has anti-plasmodium (IC80 is 0.01 μg/mL) and antitumor activity. It is also an inhibitor of glyceraldehyde 3-phosphate dehydrogenase (GAPDH) that acts by binding to the cysteine-149 residue. Synonyms: Koningic acid; (+)-Heptelidic Acid; (5aS,6R,9S,9aS)-6-isopropyl-1-oxo-1,5a,6,7,8,9a-hexahydro-3H-spiro[benzo[c]oxepine-9,2'-oxirane]-4-carboxylic acid; Spiro[2-benzoxepin-9(3H),2'-oxirane]-4-carboxylicacid,1,5a,6,7,8,9a-hexahydro-6-(1-methylethyl)-1-oxo-, (2'S,5aS,6R,9aS)-; Avocettin. Grades: ≥95%. CAS No. 57710-57-3. Molecular formula: C15H20O5. Mole weight: 280.32. | |
Heptelidic acid Quick inquiry Where to buy Suppliers range | Antibiotic. Potent selective glyceraldehyde 3-phosphate dehydrogenase (GAPDH) inhibitor. Binds to the essential Cys149 residue in the catalytic site of GADPH. Anticancer compound. Selectively kills high-glycolytic cancer cells through glucose-dependent active ATP deprivation. Antimalarial. Apoptosis inhibitor. DNA fragmentation and caspase-3 activation inhibitor. Selective and competitive inhibitor of mammalian DNA polymerases beta, lambda and terminal deoxynucleotidyl transferase (TdT) in family X of pols. Source:Isolated from Trichoderma sp. Group: Biochemicals. Grades: Highly Purified. CAS No. 57710-57-3 (74310-84-2 deleted). Pack Sizes: 250ug, 1mg. Molecular Formula: C15H20O5. US Biological Life Sciences. | Worldwide |
Heptelidic Acid (Koningic acid, Avocettin, FO-4443, BRN 5091359) Quick inquiry Where to buy Suppliers range | A sesquiterpene antibiotic, isolated from Trichoderma sp. A potent and selective glyceraldehyde 3-phosphate dehydrogenase (GAPDH) inhibitor. Binds to the essential Cys149 residue in the catalytic site of GAPDH. Selectively kills high-glycolytic cancer cells through glucose-dependent active ATP deprivation. Selective and competitive inhibitor of mammalian DNA polymerases beta, lambda and terminal deoxynucleotidyl transferase (TdT) in family X of pols. Group: Biochemicals. Grades: Highly Purified. CAS No. 74310-84-2. Pack Sizes: 250ug, 1mg. US Biological Life Sciences. | Worldwide |
Lactate Dehydrogenase A Inhibitor, FX11 (LDHA Inhibitor I, LDH-A Inhibitor I, LDH-M Inhibitor I, LDHM Inhibitor I) Quick inquiry Where to buy Suppliers range | A cell permeable, gossypol analog that acts as a selective, reversible, and NADH competitive inhibitor of lactate dehhydrogenase A (LDHA; Ki = 8uM for human liver LDHA). Does not affect the activities of LDHB and glyceraldehyde-3-phosphate dehydrogenase even at higher concentrations. Shown to increase oxygen consumption, reactive oxygen species production, and cell death in P493 human lymphoma B cells. Also shown to reduce mitochondrial transmembrane potential and ATP levels and increase AMP kinase activity. Exhibits synergistic toxicity in P493 cells when combined with FK866. Blocks the progression of human lymphoma and pancreatic cancer xenografts and when used in combination with FK866 it induces lymphoma regression. Group: Biochemicals. Grades: Highly Purified. CAS No. 213971-34-7. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
L-(-)-Glyceraldehyde (90% in H2O) Quick inquiry Where to buy Suppliers range | (S)-2,3-Dihydroxypropanal is the enantiomer of D-Glyceraldehyde. Glyceraldehyde is the simplest of all aldoses and is commonly found as an intermediate in carbohydrate metabolism. Group: Biochemicals. Alternative Names: (S)-2,3-Dihydroxypropanal. Grades: Reagent Grade. CAS No. 497-09-6. Pack Sizes: 250mg, 500mg, 1g. Molecular Formula: C?H?O?, Molecular Weight: 90.07. US Biological Life Sciences. | Worldwide |
NADH Thio, Reduced (Nicotinamide Adenine Dinucleotide), Thio-NADH) Quick inquiry Where to buy Suppliers range | Beta-nicotinamide adenine dinucleotide hydrate. Can be used as a cofactor in reactions with NAD-dependent histone deacetylase enzymes.NAD is a coenzyme formed from the nucleotide, nicotinamide, adenosine monophosphateand a phosphate group joining the first two components. NADP has the same structure with the addition of an extra phosphate group to AMP. NAD can be reduced to NADH during coupling with reactions which oxidize various organic substrates. For example, the reaction catalyzed by glyceraldehyde phosphate dehydrogenase during glycolysis. NADH then passes to the inside of mitochondria where it donates the electrons it is carrying to the electron transport chain. In this manner, NAD acts as an intermediate energy storage compound that indirectly generates ATP. Generally, NADP accepts electrons from catabolic reactions to form NADPH. An example is its coupling with the conversion of glucose-6-phosphate to ribose-5-phosphate in the pentose phosphate pathway. NADPH has a slightly different role to NADH in that it does not donate electrons to the electron transport chain. Instead, it tends to reduce intermediates in anabolic pathways e.g. fatty acid synthesis. NAD participates in many redox reactions in cells, including those in glycolysis and most of those in the citric acid cycle of cellular respiration. Nicotinamide adenine dinucleotide (NAD) and its relative nicotinamide adenine dinucleotide phosphate (NADP) are two of the most important coenzymes in the cell. In cells, most oxidations are accomplished by the removal of hydrogen atoms. Both of these coenzymes play crucial roles in this. Each molecule of NAD+ (or NADP+) can acquire two electrons; that is, be reduced by two electrons. However, only one proton accompanies the reduction. The other proton produced as two hydrogen atoms are removed from the molecule being oxidized is liberated into the surrounding medium. For NAD, the reaction is thus:NAD+ + 2H -> NADH + H+. Group: Biochemicals. Alternative Names: Nicotinamide Adenine Dinucleotide; Thio-NADH; Thionicotinamide adenine dinucleotide. Grades: Highly Purified. CAS No. 1921-48-8. Pack Sizes: 100mg. Molecular Formula: C21H29N7O13SP2, Molecular Weight: 681.51. US Biological Life Sciences. | Worldwide |
(R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde Quick inquiry Where to buy Suppliers range | Oily liquid. Group: Main Products. Alternative Names: (R)-2,2-DIMETHYL-[1,3]DIOXOLANE-4-CARBALDEHYDE;(R)-(+)-2,2-DIMETHYL-1,3-DIOXOLANE-4-CARBOXALDEHYDE;(R)-2,3-ISOPROPYLIDENE GLYCERALDEHYDE;1,3-DIOXOLANE-4-CARBOXALDEHYDE, 2,2-DIMETHYL-, (R)-;2,3-O-ISOPROPYLIDENE-D-GLYCERALDEHYDE;2,3-O-(R)-ISOPROPYLIDENE-L-GLYCERALDEHYDE;(4R)-2,2-DIMETHYL-1,3-DIOXOLANE-4-CARBALDEHYDE;D-(R)-GLYCERALDEHYDE ACETONIDE. Grades: 98+%. CAS No. 15186-48-8. Molecular formula: C6H10O3. Mole weight: 130.14. IUPAC Name: (4R)-2,2-dimethyl-1,3-dioxolane-4-carbaldehyde. Exact Mass: 130.06300. Symbol: GHS08. Boiling Point: 139°C(lit.). Flash Point: 143°F. Density: 1.045g/mL at 25°C(lit.). SMILES: CC1(OCC(O1)C=O)C. InChIKey: YSGPYVWACGYQDJ-YFKPBYRVSA-N. Supplemental Hazard Statements: H227-H303-H333-H351. | |
(S)-Glyceraldehyde acetonide Quick inquiry Where to buy Suppliers range | (S)-Glyceraldehyde acetonide. Group: Heterocyclic Organic Compound. Alternative Names: (S)-2,3-ISOPROPYLIDENE GLYCERALDEHYDE;(s)-2,2-dimethyl-1,3-dioxolane-4-carbaldehyde;(S)-GLYCERALDEHYDE ACETONIDE;2,3-O-ISOPROPYLIDENE-L-GLYCERALDEHYDE;1,3-DIOXOLANE-4-CARBOXALDEHYDE, 2,2-DIMETHYL-, (S)-;L-GLYCERALDEHYDE ACETONIDE;S-(-)-Solketaldehyde;S-2,3-O-isopropylidene-glyceraldehyde. CAS No. 22323-80-4. Molecular formula: C6H10O3. Mole weight: 130.14. | |
Triosephosphate isomerase 1 (23-37) Quick inquiry Where to buy Suppliers range | Triosephosphate isomerase 1 (23-37) is a fragment of TPI1. Triosephosphate isomerase is an extremely efficient metabolic enzyme that catalyzes the interconversion between dihydroxyacetone phosphate (DHAP) and D-glyceraldehyde-3-phosphate (G3P) in glycolysis and gluconeogenesis. Synonyms: Triose-phosphate isomerase (23-37); Methylglyoxal synthase (23-37). |