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| Product | Description | |
|---|---|---|
| Acetylcholine-d9 Chloride (2-(Acetyloxy)-N,N,N,-trimethylethanaminium-d9 Chloride), Acecoline-d9, Arterocoline-d9, Miochol, Ovisot) | Cholinergic. Group: Biochemicals. Alternative Names: 2-(Acetyloxy)-N,N,N,-trimethylethanaminium-d9 Chloride); Acecoline-d9; Arterocoline-d9; Miochol; Ovisot. Grades: Highly Purified. CAS No. 344298-95-9. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| Acetylcholine iodide | Acetylcholine iodide is a neurotransmitter found at neuromuscular junctions, autonomic ganglia, parasympathetic effector junctions, a subset of sympathetic effector junctions, and at many sites in the central nervous system. Uses: Cholinergic agonists. Synonyms: Acetylcolina; 2-acetyloxyethyl(trimethyl)azanium iodide. Grades: ≥95%. CAS No. 2260-50-6. Molecular formula: C7H16NO2·I. Mole weight: 273.11. |  |
| Acetylcholine iodide | Acetylcholine iodide. Group: Biochemicals. Alternative Names: 2-(Acetyloxy)-N,N,N-trimethylethanaminium iodide; 2-Acetoxyethyltrimethyl Ammonium iodide; N- (2-Hydroxyethyl) trimethylammonium iodide acetate. Grades: Highly Purified. CAS No. 2260-50-6. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C7H16NO2I. US Biological Life Sciences. | Worldwide |
| Acetylcholine iodide | 100g Pack Size. Group: Analytical Reagents, Biochemicals, Diagnostic Raw Materials. Formula: C7H16NO2I. CAS No. 2260-50-6. Prepack ID 16080354-100g. Molecular Weight 273.11. See USA prepack pricing. |  |
| Acetylcholine iodide | Acetylcholine iodide is a muscarinic receptor modulator. Acetylcholine iodide specifically binds to muscarinic receptors, inhibits sodium absorption, and induces chloride secretion. Acetylcholine iodide changes intestinal ion transport, enhances intestinal secretory function, induces or maintains mammary gland development and lactation. Acetylcholine iodide can be used for intestinal ion transport regulation and mammary gland physiological function research [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: ACh iodide. CAS No. 2260-50-6. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-101086. |  |
| Acetylcholine iodide 99+% | Acetylcholine iodide 99+%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 2260-50-6. Pack Sizes: 5g, 25g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| acetylcholinesterase | Acts on a variety of acetic esters; also catalyses transacetylations. Group: Enzymes. Synonyms: true cholinesterase; choline esterase I; cholinesterase; acetylthiocholinesterase; acetylcholine hydrolase; acetyl.β-methylcholinesterase; AcCholE. Enzyme Commission Number: EC 3.1.1.7. CAS No. 9000-81-1. Acetylcholinesterase. 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-3497; acetylcholinesterase; EC 3.1.1.7; 9000-81-1; true cholinesterase; choline esterase I; cholinesterase; acetylthiocholinesterase; acetylcholine hydrolase; acetyl.β-methylcholinesterase; AcCholE. Cat No: EXWM-3497. |  |
| Acetylcholinesterase, Electric eel | Acetylcholinesterase, Electric eel is a cholinergic enzyme that is mainly found in neuromuscular junctions and cholinergic chemical synapses and is often used in biochemical research. Acetylcholinesterase, Electric eel can catalyze the decomposition or hydrolysis of acetylcholine and some other choline esters that act as neurotransmitters into acetic acid and choline. The main function of Acetylcholinesterase, Electric eel is to terminate neuronal transmission and signal conduction between synapses to prevent ACh diffusion and activation of nearby receptors [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 9000-81-1. Pack Sizes: 500 U. Product ID: HY-P2860A. | |
| Acetylcholinesterase Human, Recombinant | Acetylcholinesterase, also known as AChE or acetylhydrolase, is a hydrolase that hydrolyzes the neurotransmitter acetylcholine. AChE is found at mainly neuromuscular junctions and cholinergic brain synapses, where its activity serves to terminate synaptic transmission. It belongs to carboxylesterase family of enzymes. It is the primary target of inhibition by organophosphorus compounds such as nerve agents and pesticides. Group: Enzymes. Synonyms: true cholinesterase; choline esterase I; cholinesterase; acetylthiocholinesterase; acetylcholine hydrolase; acetyl; β-methylcholinesterase; AcCholE; EC 3.1.1.7; 9000-81-1; Acetylcholinesterase; AChE; acetylhydrolase. Enzyme Commission Number: EC 3.1.1.7. CAS No. 9000-81-1. Acetylcholinesterase. Activity: > 1,000 units/mg protein (Lowry). Storage: -20°C. Form: Lyophilized powder containing phosphate buffer salt. Source: HEK 293 cells. Species: Human. Cat No: NATE-0020. | |
| Acetylcimigenol 3-O-α-L-arabinopyranside | Acetylcimigenol 3-O-α-L-arabinopyranside. Group: Biochemicals. CAS No. 402513-88-6. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Acetylcimigenol-3-O-α-L-arabinopyranside | Acetylcimigenol-3-O-α-L-arabinopyranside is a multifaceted and highly efficacious natural compound with unparalleled anti-inflammatory and anti-fibrotic potentials. Synonyms: Acetylcimigenol 3-O-alpha-L-arabinopyranside. Grades: >98%. CAS No. 402513-88-6. Molecular formula: C37H58O10. Mole weight: 662.8. | |
| Acetylcimigenol arabinoside | Acetylcimigenol arabinoside. Group: Biochemicals. Alternative Names: Acetylcimigenol-3-O-alpha-L-arabinopyranside; Acetylshengmanol arabinoside. Grades: Plant Grade. CAS No. 402513-88-6. Pack Sizes: 10mg. Molecular Formula: C37H58O10, Molecular Weight: 662.85. US Biological Life Sciences. | Worldwide |
| acetyl-CoA-benzylalcohol acetyltransferase | The enzyme is found in flowers like Clarkia breweri, where it is important for floral scent production. Unlike EC 2.3.1.84, alcohol O-acetyltransferase, this enzyme is active with alcohols that contain a benzyl ring. Group: Enzymes. Synonyms: BEAT. Enzyme Commission Number: EC 2.3.1.224. 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-2171; acetyl-CoA-benzylalcohol acetyltransferase; EC 2.3.1.224; BEAT. Cat No: EXWM-2171. | |
| acetyl-CoA C-acetyltransferase | This enzyme participates in 10 metabolic pathways: fatty acid metabolism, synthesis and degradation of ketone bodies, valine, leucine and isoleucine degradation, lysine degradation, tryptophan metabolism, pyruvate metabolism, benzoate degradation via coa ligation, propanoate metabolism, butanoate metabolism, and two-component system-general. Group: Enzymes. Synonyms: acetoacetyl-CoA thiolase; β-acetoacetyl coenzyme A thiolase; 2-methylacetoacetyl-CoA thiolase [misleading]; 3-oxothiolase; acetyl coenzyme A thiolase; acetyl-CoA acetyltransferase; acetyl-CoA:N-acetyltransferase; thiolase II. Enzyme Commission Number: EC 2.3.1.9. CAS No. 9027-46-7. 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-2271; acetyl-CoA C-acetyltransferase; EC 2.3.1.9; 9027-46-7; acetoacetyl-CoA thiolase; β-acetoacetyl coenzyme A thiolase; 2-methylacetoacetyl-CoA thiolase [misleading]; 3-oxothiolase; acetyl coenzyme A thiolase; acetyl-CoA acetyltransferase; acetyl-CoA:N-acetyltransferase; thiolase II. Cat No: EXWM-2271. | |
| acetyl-CoA C-acyltransferase | This enzyme belongs to the family of transferases, specifically those acyltransferases transferring groups other than aminoacyl groups. Group: Enzymes. Synonyms: β-ketothiolase; 3-ketoacyl-CoA thiolase; KAT; β-ketoacyl coenzyme A thiolase; β-ketoacyl-CoA thiolase; β-ketoadipyl coenzyme A thiolase; β-ketoadipyl-CoA thiolase; 3-ketoacyl CoA thiolase; 3-ketoacyl coenzyme A thiolase; 3-ketoacyl thiolase; 3-ketothiolase; 3-oxoacyl-CoA th. Enzyme Commission Number: EC 2.3.1.16. CAS No. 9029-97-4. 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-2099; acetyl-CoA C-acyltransferase; EC 2.3.1.16; 9029-97-4; β-ketothiolase; 3-ketoacyl-CoA thiolase; KAT; β-ketoacyl coenzyme A thiolase; β-ketoacyl-CoA thiolase; β-ketoadipyl coenzyme A thiolase; β-ketoadipyl-CoA thiolase; 3-ketoacyl CoA thiolase; 3-ketoacyl coenzyme A thiolase; 3-ketoacyl thiolase; 3-ketothiolase; 3-oxoacyl-CoA thiolase; 3-oxoacyl-coenzyme A thiolase; 6-oxoacyl-CoA thiolase; acetoacetyl-CoA β-ketothiolase; acetyl-CoA acyltransferase; ketoacyl-CoA acyltransferase; ketoacyl-coenzyme A thiolase; long-chain 3-oxoacyl-CoA thiolase; oxoacyl-coenzyme A thiolase; pro-3-ketoacyl-CoA thiolase; thiolase I; 2-methylacetoacetyl-CoA thiolase [misleading]. Cat No: EXWM-2099. | |
| acetyl-CoA carboxylase | A biotinyl-protein. Also catalyses transcarboxylation; the plant enzyme also carboxylates propanonyl-CoA and butanoyl-CoA. Group: Enzymes. Synonyms: acetyl coenzyme A carboxylase. Enzyme Commission Number: EC 6.4.1.2. CAS No. 9023-93-2. ACC. 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-5813; acetyl-CoA carboxylase; EC 6.4.1.2; 9023-93-2; acetyl coenzyme A carboxylase. Cat No: EXWM-5813. | |
| Acetyl-CoA Carboxylase 1 from Human, Recombinant | Acetyl-CoA Carboxylase (ACC) regulates the metabolism of fatty acids. This enzyme catalzes the formation of Malonyl CoA through the irreversible carboxylation of acetyl CoA. There are two main isoforms of Acetyl-CoA carboxylase expressed in mammals, Acetyl-CoA carboxylase 1 (ACACA) and Acetyl-CoA carboxylase 2 (ACACB). ACACA has broad tissue distribution but is enriched in tissues critical for fatty acid sythesis such as adipose tissue. ACACB is enriched in tissues such as skeletal muscle and heart that are critical for fatty acid oxidation. The Acetyl-CoA Carboxylase enzymes are activated by Citrate, glutamate, and dicarboxylic acids and negatively regulated by long ...he study of enzyme kinetics, screening inhibitors, and selectivity profiling. Group: Enzymes. Synonyms: ACAC; ACACA; ACC1; ACC; ACCA; acetyl-CoA carboxylase alpha; acetyl coenzyme A carboxylase; acetyl-CoA carboxylase. Enzyme Commission Number: EC 6.4.1.2. CAS No. 9023-93-2. ACC. Mole weight: 292.5 kDa. Activity: > 20 units/μg protein. Storage: Store at -70°C. Avoid multiple freeze-thaw cycles. Form: Supplied as a solution in 50 mM Tris-HCl, pH 8.0, 275 mM NaCl, 10% glycerol, 1 mM EDTA and 2 mM DTT. Source: Sf9 cells. Species: Human. ACAC; ACACA; ACC1; ACC; ACCA; acetyl-CoA carboxylase alpha; acetyl coenzyme A carboxylase; acetyl-CoA carboxylase. Cat No: NATE-0942. | |
| Acetyl-CoA Carboxylase 2 from Human, Recombinant | Acetyl-CoA Carboxylase (ACC) regulates the metabolism of fatty acids. This enzyme catalzes the formation of Malonyl CoA through the irreversible carboxylation of acetyl CoA. There are two main isoforms of Acetyl-CoA carboxylase expressed in mammals, Acetyl-CoA carboxylase 1 (ACACA) and Acetyl-CoA carboxylase 2 (ACACB). ACACA has broad tissue distribution but is enriched in tissues critical for fatty acid sythesis such as adipose tissue. ACACB is enriched in tissues such as skeletal muscle and heart that are critical for fatty acid oxidation. The Acetyl-CoA Carboxylase enzymes are activated by Citrate, glutamate, and dicarboxylic acids and negatively regulated by long ...ercise. the enzyme also may be used for acc regulation study in anti-obesity and anti-type 2 diabetes therapeutics. Group: Enzymes. Synonyms: ACACB; ACC2; acetyl-CoA carboxylase beta; acetyl coenzyme A carboxylase; acetyl-CoA carboxylase. Enzyme Commission Number: EC 6.4.1.2. CAS No. 9023-93-2. ACC. Mole weight: 277 kDa. Activity: > 25 units/μg protein. Storage: Store at -70°C. Avoid multiple freeze-thaw cycles. Form: Supplied as a solution in 50 mM Tris-HCl, pH 8.0, 275 mM NaCl, 10% glycerol, 1 mM EDTA and 2 mM DTT. Source: Sf9 cells. Species: Human. ACACB; ACC2; acetyl-CoA carboxylase beta; acetyl coenzyme A carboxylase; acetyl-CoA carboxylase. Cat No: NATE-0943. | |
| Acetyl-CoA Carboxylase-IN-1 | Acetyl-CoA Carboxylase-IN-1 is a potent acetyl-CoA carboxylase (ACC) inhibitor with an IC 50 value of ?5 nM. Acetyl-CoA Carboxylase-IN-1 has antibacterial activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 179343-23-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-152117. | |
| acetyl-CoA C-myristoyltransferase | A peroxisomal enzyme involved in branched chain fatty acid β-oxidation in peroxisomes. It differs from EC 2.3.1.154 (propionyl-CoA C2-trimethyldecanoyltransferase) in not being active towards 3-oxopristanoyl-CoA. Group: Enzymes. Enzyme Commission Number: EC 2.3.1.155. 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-2094; acetyl-CoA C-myristoyltransferase; EC 2.3.1.155. Cat No: EXWM-2094. | |
| acetyl-CoA hydrolase | This enzyme belongs to the family of hydrolases, specifically those acting on thioester bonds. The systematic name of this enzyme class is acetyl-CoA hydrolase. Other names in common use include acetyl-CoA deacylase, acetyl-CoA acylase, acetyl coenzyme A hydrolase, acetyl coenzyme A deacylase, acetyl coenzyme A acylase, and acetyl-CoA thiol esterase. This enzyme participates in pyruvate metabolism. Group: Enzymes. Synonyms: acetyl-CoA deacylase; acetyl-CoA acylase; acetyl coenzyme A hydrolase; acetyl coenzyme A deacylase; acetyl coenzyme A acylase; acetyl-CoA thiol esterase. Enzyme Commission Number: EC 3.1.2.1. CAS No. 9027-54-7. 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-3544; acetyl-CoA hydrolase; EC 3.1.2.1; 9027-54-7; acetyl-CoA deacylase; acetyl-CoA acylase; acetyl coenzyme A hydrolase; acetyl coenzyme A deacylase; acetyl coenzyme A acylase; acetyl-CoA thiol esterase. Cat No: EXWM-3544. | |
| Acetyl coenzyme A | Acetyl coenzyme A is the precursor to HMG CoA, an essential component in the synthesis of cholesterol and ketone. Synonyms: Acetyl-CoA; S-Acetyl coenzyme A; AcCoA; Coenzyme A, S-acetate; S-acetyl-CoA. CAS No. 72-89-9. Molecular formula: C23H38N7O17P3S. Mole weight: 809.57. | |
| Acetyl coenzyme a,[acetyl-3h] | Heterocyclic Organic Compound. Alternative Names: [3H]ACETYL-COENZYME A;ACETYL COENZYME A, [ACETYL-3H]. CAS No. 110073-15-9. Molecular formula: C23H35N7O17P3ST3. Mole weight: 815.6. Catalog: ACM110073159. |  |
| Acetyl-Coenzyme A acetyltransferase 2 from Human, Recombinant | ACAT2 enzyme participates in lipid metabolism. ACAT2 takes part in lipoprotein assembly, catalyzing cholesterol esterification in mammalian cells. ACAT2 is an integral membrane protein that localizes to the endoplasmic reticulum of human intestinal cells. ACAT2 deficiency contributes to severe mental retardation and hypotonus. Acat2 recombinant human produced in e. coli is a single, non-glycosylated polypeptide chain containing 433 amino acids (1-397 a.a.) and having a molecular mass of 45.4 kda. the acat2 is fused to 36 amino acid his-tag at n-terminus and purified by proprietary chromatographic techniques. Group: Enzymes. Synonyms: Acetyl-CoA acetyltransferase cytosolic; Cytosolic acetoacetyl-CoA thiolase; ACAT2; Acetyl CoA transferase-like protein; ACAT-2. Purity: Greater than 95.0% as determined by SDS-PAGE. ACAT-2. Mole weight: 45.4 kDa. Stability: ACAT2 Human although stable at 4°C for 1 week, should be stored desiccated below -18°C. Please prevent freeze thaw cycles. Appearance: Sterile Filtered clear solution. Source: E. coli. Species: Human. Acetyl-CoA acetyltransferase cytosolic; Cytosolic acetoacetyl-CoA thiolase; ACAT2; Acetyl CoA transferase-like protein; ACAT-2. Cat No: NATE-0798. | |
| Acetyl coenzyme A lithium | Acetyl-coenzyme A (Acetyl-CoA) lithium is a membrane-impermeant central metabolic intermediate, participates in the TCA cycle and oxidative phosphorylation metabolism. Acetyl-coenzyme A lithium, regulates various cellular mechanisms by providing (sole donor) acetyl groups to target amino acid residues for post-translational acetylation reactions of proteins. Acetyl Coenzyme A lithium is also a key precursor of lipid synthesis [1] [2] [3] [4]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Acetyl-CoA lithium. CAS No. 32140-51-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-113596A. | |
| Acetyl coenzyme A lithium salt | Acetyl coenzyme A trilithium salt is a lithium salt of an essential cofactor and carrier of acyl groups in enzymatic acetyl transfer reactions. Acetyl coenzyme A is formed either by the oxidative decarboxylation of pyruvate in mitochondria, by the oxidation of long-chain fatty acids, or by the oxidative degradation of certain amino acids. Acetyl coenzyme A is a key precursor in lipid biosynthesis, and the source of all fatty acid carbons. Acetyl-coA is a positive regulator of pyruvate carboxylase and is a precursor of the neurotransmitter acetylcholine. Applications: A cofactor and carrier of acyl groups in enzymatic acetyl transfer reactions. Group: Coenzymes. Synonyms: Acetyl-S-CoA Li3. CAS No. 32140-51-5. Purity: ≥95%. Mole weight: 881. Appearance: Powder. Form: Solid. Acetyl-S-CoA Li3; Acetyl coenzyme A lithium salt; 32140-51-5. Cat No: COEC-082. | |
| Acetyl coenzyme A lithium salt | Acetyl coenzyme A lithium salt. Group: Biochemicals. Alternative Names: Acetyl-CoA Li. Grades: Highly Purified. CAS No. 32140-51-5. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C23H38N7O17P3S·xLi. US Biological Life Sciences. | Worldwide |
| Acetyl Coenzyme A Lithium Salt | Acetyl Coenzyme A Lithium Salt is an important molecule in enzymatic acetyl transfer reactions. It is the source of the phosphopantetheine group that is added as a prosthetic group to acyl carrier proteins and formyltetrahydrofolate dehydrogenase. Synonyms: Lithium acetyl-CoA; Coenzyme A, S-acetate, lithium salt. Grades: ≥95%. CAS No. 32140-51-5. Molecular formula: C23H38N7O17P3S xLi. Mole weight: 809.58. | |
| Acetyl coenzyme A sodium salt | Acetyl coenzyme A sodium salt. Group: Biochemicals. Alternative Names: Acetyl CoA. Grades: Highly Purified. CAS No. 102029-73-2. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C23H38N7O17P3S·xNa. US Biological Life Sciences. | Worldwide |
| Acetyl coenzyme A sodium salt | Acetyl coenzyme A sodium salt is an essential cofactor and carrier of acyl groups in enzymatic acetyl transfer reactions. Formed either by the oxidative decarboxylation of pyruvate in mitochondria, by the oxidation of long-chain fatty acids, or by the oxidative degradation of certain amino acids. It is a key precursor in lipid biosynthesis, and the source of all fatty acid carbons. Also a positive regulator of pyruvate carboxylase and a precursor of the neurotransmitter acetylcholine. Applications: An essential cofactor and carrier of acyl groups. Group: Coenzymes. Synonyms: Acethyl coenzyme alpha sodium salt. CAS No. 102029-73-2. Purity: ≥92%. Mole weight: 893.53. Appearance: Powder. Form: Solid. Acethyl coenzyme alpha sodium salt; Acetyl coenzyme A sodium salt; 102029-73-2. Cat No: COEC-047. | |
| Acetyl coenzyme A sodium salt | Acetyl coenzyme A sodium salt, a pivotal molecule in the biomedical industry, is widely utilized in fatty acid and cholesterol biosynthesis, as well as the citric acid cycle. Its role in drug and toxin metabolism and breakdown in the body is also noteworthy. Besides, it contributes to treating metabolic disorders such as diabetes, obesity, and cancer. Its multifaceted functions make it a molecule of great scientific significance. Synonyms: Acetyl CoA. Grades: 90%. CAS No. 102029-73-2. Molecular formula: C23H38N7O17P3S·xNa. Mole weight: 809.57 (free acid). | |
| Acetyl coenzyme A trilithium salt | Acetyl coenzyme A trilithium salt. Group: Biochemicals. Alternative Names: Acetyl-S-CoA Li3. Grades: Highly Purified. CAS No. 75520-41-1. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C23H35Li3N7O17P3S. US Biological Life Sciences. | Worldwide |
| Acetyl coenzyme A trilithium salt | Acetyl coenzyme A trilithium salt, an indispensable biochemical constituent extensively utilized in the biomedicine realm, assumes an pivotal role as a vital coenzyme within diverse metabolic pathways, engendering the synthesis and decomposition of molecules within the human anatomical framework. Synonyms: Acetyl-S-CoA Li3. Grades: 95%. CAS No. 75520-41-1. Molecular formula: C23H35Li3N7O17P3S. Mole weight: 827.37. | |
| Acetyl coenzyme A trilithium salt trihydrate | Acetyl coenzyme A trilithium salt trihydrate is a crucial compound utilized in various biochemical processes, particularly in the tricarboxylic acid cycle and fatty acid research. This compound is beneficial in studying disorders related to metabolism, such as fatty acid oxidation disorders and certain neurodegenerative diseases. Synonyms: Acetyl CoALi3. CAS No. 496948-93-7. Molecular formula: C23H35N7O17P3S.3Li. Mole weight: 827.37. | |
| Acetyl Coenzyme A Trilithium Salt Trihydrate | Acetyl Coenzyme A Trilithium Salt Trihydrate is an essential cofactor and carrier of acyl groups in enzymatic acetyl transfer reactions. It is also the precursor for lipid biosynthesis and the neurotransmitter acetylcholine. Applications: An essential cofactor. Group: Coenzymes. CAS No. 75520-41-1. Mole weight: 881.42. Appearance: Powder. Form: Solid. Acetyl Coenzyme A Trilithium Salt Trihydrate; 75520-41-1. Cat No: COEC-100. | |
| Acetylcorynoline | Acetylcorynoline, which can be extracted from the tubers of Corydalis ambigua, inhibits the maturing of bone marrow-derived dendritic cells in mice. However, it is only cytotoxic in amounts of greater than 20 μM. Acetylcorynoline may be one of the potent immunosuppressive agents through the blockage of dendritic cells maturation and function. Acetylcorynoline significantly decreases dopaminergic neuron degeneration induced by 6-hydroxydopamine in BZ555 strain; prevents α-synuclein aggregation; recovers lipid content in OW13 strain; restores food-sensing behavior, and dopamine levels; and prolongs life-span in 6-hydroxydopamine-treated N2 strain, thus showing its potential as a possible antiparkinsonian drug. Acetylcorynoline may exert its effects by decreasing egl-1 expression to suppress apoptosis pathways and by increasing rpn5 expression to enhance the activity of proteasomes. Uses: Antifungal/anti-inflammatory. Synonyms: (5bR,6S,12bR)-5b,6,7,12b,13,14-Hexahydro-5b,13-dimethyl-[1,3]benzodioxolo[5,6-c]-1,3-dioxolo[4,5-i]phenanthridin-6-ol 6-acetate; Corynoline acetate; O-Acetylcorynoline; [1,3]Benzodioxolo[5,6-c]-1,3-dioxolo[4,5-i]phenanthridin-6-ol,5b,6,7,12b,13,14-hexahydro-5b,13-dimethyl-, 6-acetate, (5bR,6S,12bR)-. Grades: >98%. CAS No. 18797-80-3. Molecular formula: C23H23NO6. Mole weight: 409.43. | |
| Acetylcorynoline | Acetylcorynoline. Group: Biochemicals. Grades: Plant Grade. CAS No. 18797-80-3. Pack Sizes: 10mg. Molecular Formula: C23H23NO6, Molecular Weight: 409.43. US Biological Life Sciences. | Worldwide |
| Acetylcorynoline | Acetylcorynoline is the major alkaloid component derived from Corydalis bungeana , and has anti-inflammatory properties [1]. Uses: Scientific research. Group: Natural products. CAS No. 18797-80-3. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-N0759. | |
| Acetylcysteine | Acetylcysteine (N-Acetylcysteine) is a mucolytic agent which reduces the thickness of the mucus. Acetylcysteine is a ROS inhibitor. Acetylcysteine is a cysteine precursor, prevents hemin-induced ferroptosis by neutralizing toxic lipids generated by arachidonate-dependent activity of 5-lipoxygenases. Acetylcysteine induces cell apoptosis. Acetylcysteine also has anti- influenza virus activities. In addition, Acetylcysteine ??is the most stable form of cysteine ??during drug delivery and can be used in disulfidptosis studies [1] [2] [3] [4] [5] [6] [7] [8]. Uses: Scientific research. Group: Natural products. Alternative Names: N-Acetylcysteine; N-Acetyl-L-cysteine; NAC. CAS No. 616-91-1. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B0215. | |
| Acetylcysteine EP Impurity A | Acetylcysteine EP Impurity A. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (2R,2'R)-3,3'-disulfanediylbis(2-aminopropanoic acid). CAS No. 56-89-3. Molecular Formula: C6H12N2O4S2. Mole Weight: 240.30. Catalog: APB56893. |  |
| Acetylcysteine EP Impurity B | Acetylcysteine EP Impurity B. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R)-2-amino-3-mercaptopropanoic acid. CAS No. 52-90-4. Molecular Formula: C3H7NO2S. Mole Weight: 121.16. Catalog: APB52904. | |
| Acetylcysteine EP Impurity C | Acetylcysteine EP Impurity C. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (2R,2'R)-3,3'-disulfanediylbis(2-acetamidopropanoic acid). CAS No. 5545-17-5. Molecular Formula: C10H16N2O6S2. Mole Weight: 324.37. Catalog: APB5545175. | |
| Acetylcysteine EP Impurity D | Acetylcysteine EP Impurity D. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R)-2-acetamido-3-(acetylthio)propanoic acid. CAS No. 18725-37-6. Molecular Formula: C7H11NO4S. Mole Weight: 205.23. Catalog: APB18725376. | |
| Acetylcysteine Impurity 1 | Acetylcysteine Impurity 1. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (2R,2'R)-3,3'-thiobis(2-acetamidopropanoic acid). Molecular Formula: C10H16N2O6S. Mole Weight: 292.31. Catalog: APB02823. | |
| Acetylcysteine Impurity 10 | Acetylcysteine Impurity 10. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R)-2-acetamido-3-disulfanylpropanoic acid. Molecular Formula: C5H9NO3S2. Mole Weight: 195.26. Catalog: APB02816. | |
| Acetylcysteine Impurity 11 | Acetylcysteine Impurity 11. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R) -2-acetamido-3- ( (2- ( (carboxymethyl) amino) acetyl) thio) propanoic acid. Molecular Formula: C9H14N2O6S. Mole Weight: 278.28. Catalog: APB02817. | |
| Acetylcysteine Impurity 12 | Acetylcysteine Impurity 12. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R)-3-(acetylthio)-2-(N-ethylacetamido)propanoic acid. Molecular Formula: C9H15NO4S. Mole Weight: 233.28. Catalog: APB02818. | |
| Acetylcysteine Impurity13 | Acetylcysteine Impurity13. Uses: For analytical and research use. Group: Impurity standards. CAS No. 137698-08-9. Molecular Formula: C8H14N2O5S. Mole Weight: 250.27. Catalog: APB137698089. | |
| Acetylcysteine Impurity 13 | Acetylcysteine Impurity 13. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-2-acetamido-3-mercaptopropanoic acid. CAS No. 26117-28-2. Molecular Formula: C5H9NO3S. Mole Weight: 163.19. Catalog: APB26117282. | |
| Acetylcysteine Impurity14 | Acetylcysteine Impurity14. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2578-27-0. Molecular Formula: C6H13NO2Se. Mole Weight: 210.15. Catalog: APB2578270. | |
| Acetylcysteine Impurity 14 DiHCl | S-(2-acetimidamidoethyl)-L-homocysteine Hydrochloride is one of Acetylcysteine impurities. It has potential anticancer activity against tumor cell growth. Synonyms: S-(2-acetimidamidoethyl)-L-homocysteine, hydrochloride (1:2). CAS No. 438542-17-7. Molecular formula: C8H17N3O2S.2HCl. Mole weight: 292.23. | |
| Acetylcysteine Impurity 15 | Acetylcysteine Impurity 15. Uses: For analytical and research use. Group: Impurity standards. CAS No. 357172-63-5. Molecular Formula: C9H16N4O3S. Mole Weight: 260.31. Catalog: APB357172635. | |
| Acetylcysteine Impurity 16 | Acetylcysteine Impurity 16. Uses: For analytical and research use. Group: Impurity standards. CAS No. 14226-97-2. Molecular Formula: C5H7NO3S. Mole Weight: 161.18. Catalog: APB14226972. | |
| Acetylcysteine Impurity 17 | Acetylcysteine Impurity 17. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C7H11NO6S. Mole Weight: 237.23. Catalog: APB06399. | |
| Acetylcysteine Impurity 18 | Acetylcysteine Impurity 18. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C5H8N2O4S. Mole Weight: 192.19. Catalog: APB06400. | |
| Acetylcysteine Impurity 19 | Acetylcysteine Impurity 19. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: sodium 2-methyl-4,5-dihydrothiazole-4-carboxylate. CAS No. 15058-19-2. Molecular Formula: C5H6NNaO2S. Mole Weight: 167.16. Catalog: APB15058192. | |
| Acetylcysteine Impurity 2 | Acetylcysteine Impurity 2. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (2R,2'R)-3,3'-thiobis(2-aminopropanoic acid). Molecular Formula: C6H12N2O4S. Mole Weight: 208.24. Catalog: APB02822. | |
| Acetylcysteine Impurity 20 (Monohydrate) | Acetylcysteine Impurity 20 (Monohydrate). Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (2R)-2-amino-3-sulfinopropanoic acid hydrate. CAS No. 207121-48-0. Molecular Formula: C3H7NO4S·H2O. Mole Weight: 171.17. Catalog: APB207121480. | |
| Acetylcysteine Impurity 21 | Acetylcysteine Impurity 21. Uses: For analytical and research use. Group: Impurity standards. CAS No. 21612-28-2. Molecular Formula: C17H20N4O5. Mole Weight: 360.37. Catalog: APB21612282. | |
| Acetylcysteine Impurity 22 | Acetylcysteine Impurity 22. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2304-94-1. Molecular Formula: C11H13NO4. Mole Weight: 223.23. Catalog: APB2304941. | |
| Acetylcysteine Impurity 23 | Acetylcysteine Impurity 23. Uses: For analytical and research use. Group: Impurity standards. CAS No. 14997-59-2. Molecular Formula: C11H17N3O3. Mole Weight: 239.28. Catalog: APB14997592. | |
| Acetylcysteine Impurity 24 | Acetylcysteine Impurity 24. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C10H16N2O6S. Mole Weight: 292.31. Catalog: APB06401. | |
| Acetylcysteine Impurity 25 | Acetylcysteine Impurity 25. Uses: For analytical and research use. Group: Impurity standards. CAS No. 19547-88-7. Molecular Formula: C8H13NO4S. Mole Weight: 219.26. Catalog: APB19547887. | |
| Acetylcysteine Impurity 27 | Acetylcysteine Impurity 27. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2467738-84-5. Molecular Formula: C15H19FN2O6. Mole Weight: 342.32. Catalog: APB2467738845. | |
| Acetylcysteine Impurity 3 | (2R)-2-acetamido-3-sulfopropanoic acid is one of Acetylcysteine impurities. It has potential anticancer activity against tumor cell growth. Synonyms: acetyl(sulfo)-D-alanine. CAS No. 79560-92-2. Molecular formula: C5H9NO6S. Mole weight: 211.19. | |
| Acetylcysteine Impurity 3 | Acetylcysteine Impurity 3. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (2R)-2-acetamido-3-sulfinopropanoic acid. CAS No. 282727-77-9. Molecular Formula: C5H9NO5S. Mole Weight: 195.19. Catalog: APB282727779. | |
| Acetylcysteine Impurity 4 | Acetylcysteine Impurity 4. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R)-2-acetamido-3-sulfopropanoic acid. CAS No. 79560-92-2. Molecular Formula: C5H9NO6S. Mole Weight: 211.19. Catalog: APB79560922. | |
| Acetylcysteine Impurity 4 Disodium Salt | Acetylcysteine Impurity 4 Disodium Salt is one of Acetylcysteine impurities. It has potential anticancer activity against tumor cell growth. Synonyms: Acetyl(sulfinato)-D-alaninate, sodium salt (1:2). Molecular formula: C5H7NO5SNa2. Mole weight: 239.16. | |
| Acetylcysteine Impurity 5 | Acetylcysteine Impurity 5. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R)-2-methyl-4,5-dihydrothiazole-4-carboxylic acid. Molecular Formula: C5H7NO2S. Mole Weight: 145.18. Catalog: APB02821. | |
| Acetylcysteine Impurity 6 | Acetylcysteine Impurity 6. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: sodium (R)-2-methyl-4,5-dihydrothiazole-4-carboxylate. Molecular Formula: C5H6NNaO2S. Mole Weight: 167.16. Catalog: APB02820. | |
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