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| Product | Description | |
|---|---|---|
| N-Acetyl mesalazine | N-Acetyl mesalazine. Group: Biochemicals. Alternative Names: 5-Acetylamino-2-hydroxybenzoic acid; 3-Carboxyparacetamol; 5-Acetamidosalicylic acid. Grades: Highly Purified. CAS No. 51-59-2. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C9H9NO4. US Biological Life Sciences. |  Worldwide |
| N-Acetyl methionine methyl ester | N-Acetyl methionine methyl ester. Group: Biochemicals. Alternative Names: N-Acetyl-DL-methionine methyl ester. Grades: Highly Purified. CAS No. 7451-74-3. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C8H15NO3S. US Biological Life Sciences. | Worldwide |
| N-Acetylmuramic acid | N-Acetylmuramic acid is a pivotal constituent within the biomedical sector, playing a critical role in the synthesis of peptidoglycan, abundantly found within bacterial cell walls. Alternative Names: 2-Acetamido-2-deoxy-3-O-(D-1-carboxyethyl)-D-glucopyranose; MurNAc; NAMA. Grades: ≥ 98% (TLC). CAS No. 10597-89-4. Molecular formula: C11H19NO8. Mole weight: 293.27. |  |
| N-Acetylmuramic acid 6-phosphate | N-Acetylmuramic acid 6-phosphate is an indispensable intermediary in bacterial cell wall biosynthesis, holding usage encompassing the development of antibiotics and antimicrobial drugs. Molecular formula: C11H20NO11P. Mole weight: 373.25. | |
| N-acetylmuramic acid 6-phosphate etherase | This enzyme, along with EC 2.7.1.170, anhydro-N-acetylmuramic acid kinase, is required for the utilization of anhydro-N-acetylmuramic acid in proteobacteria. The substrate is either imported from the medium or derived from the bacterium's own cell wall murein during cell wall recycling. Group: Enzymes. Synonyms: MurNAc-6-P etherase; MurQ. Enzyme Commission Number: EC 4.2.1.126. 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-4967; N-acetylmuramic acid 6-phosphate etherase; EC 4.2.1.126; MurNAc-6-P etherase; MurQ. Cat No: EXWM-4967. |  |
| N-Acetylmuramic acid 98+% (HPLC) | Acetyl derivative of Muramic acid. Group: Biochemicals. Alternative Names: 2-Acetamido-2-deoxy-3-O-(D-1-carboxyethyl)-D-glucopyranose; 2-Acetamido-3-O-(D-1-carboxyethyl)-2-deoxy-2-D-glucose; N-Acetylmuramic acid; MurNAc; NAMA. Grades: Reagent Grade. CAS No. 10597-89-4. Pack Sizes: 100mg, 250mg, 1g. Molecular Formula: C??H?9NO?, Molecular Weight: 293.27. US Biological Life Sciences. | Worldwide |
| N-Acetylmuramic acid methyl ester | N-Acetylmuramic acid methyl ester, an indispensable constituent in bacterial peptidoglycan synthesis, plays a vital role as a substrate for transpeptidase enzymes that participate in bacterial cell division. This compound is extensively employed in antibiotic-related investigations, encompassing penicillins, cephalosporins, and studies pertaining to bacterial cell wall biosynthesis. Alternative Names: 2-Acetamido-3-O-(D-1-carboxyethyl)-2-deoxy-D-glucose methyl ester. CAS No. 99689-20-0. Molecular formula: C12H21NO8. Mole weight: 307.30. | |
| N-acetylmuramoyl-L-alanine amidase | This enzyme belongs to the family of hydrolases, specifically those acting on carbon-nitrogen bonds other than peptide bonds in linear amides. This enzyme participates in peptidoglycan biosynthesis. Autolysins and some phage lysins are examples of N-acetylmuramoyl-L-alanine amidases. Group: Enzymes. Synonyms: acetylmuramyl-L-alanine amidase; N-acetylmuramyl-L-alanine amidase; N-acylmuramyl-L-alanine amidase; acetylmuramoyl-alanine amidase; N-acetylmuramic acid L-alanine amidase; acetylmuramyl-alanine amidase; N-acetylmuramylalanine amidase; murein hydrolase; N-acetylmuramoyl-L-alanine amidase type I; N-acetylmuramoyl-L-alanine amidase type II. Enzyme Commission Number: EC 3.5.1.28. CAS No. 9013-25-6. 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-4417; N-acetylmuramoyl-L-alanine amidase; EC 3.5.1.28; 9013-25-6; acetylmuramyl-L-alanine amidase; N-acetylmuramyl-L-alanine amidase; N-acylmuramyl-L-alanine amidase; acetylmuramoyl-alanine amidase; N-acetylmuramic acid L-alanine amidase; acetylmuramyl-alanine amidase; N-acetylmuramylalanine amidase; murein hydrolase; N-acetylmuramoyl-L-alanine amidase type I; N-acetylmuramoyl-L-alanine amidase type II. Cat No: EXWM-4417. | |
| N-acetylmuramoyl-L-alanine amidase L2 | N-Acetylmuramoyl-l-alanine amidases are peptidoglycan hydrolases with the specificity to cleave the amide bond between the lactyl group of the muramic acid and the α-amino group of l-alanine, and are able to cause dissolution of the peptidoglycan structure and thus do not exhibit peptidase activity. Alternative Names: NAMAA L2. | |
| N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-(N6-glycyl)-D-alanyl-D-alanine-diphosphoundecaprenyl-N-acetylglucosamine:glycine glycyltransferase | This enzyme catalyses the successive transfer of two Gly moieties from charged tRNAs to MurNAc-L-Ala-D-isoglutaminyl-L-Lys-(N6-Gly)-D-Ala-D-Ala-diphospho-ditrans,octacis-undecaprenyl-GlcNAc, attaching them to a Gly residue previously attached by EC 2.3.2.16 (lipid II:glycine glycyltransferase) to the N6 of the L-Lys at position 3 of the pentapeptide. This is the second step in the synthesis of the pentaglycine interpeptide bridge that is used by Staphylococcus aureus for the crosslinking of different glycan strands to each other. The next step is catalysed by EC 2.3.2.18 (N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-(N6-.D-alanine-ditrans,octacis-diphosphoundecaprenyl-N-acetylglucosamine:glycine glycyltransferase. Enzyme Commission Number: EC 2.3.2.17. 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-2290; N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-(N6-glycyl)-D-alanyl-D-alanine-diphosphoundecaprenyl-N-acetylglucosamine:glycine glycyltransferase; EC 2.3.2.17; femA (gene name); N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-(N6-glycyl)-D-alanyl-D-alanine-ditrans,octacis-diphosphoundecaprenyl-N-acetylglucosamine:glycine glycyltransferase. Cat No: EXWM-2290. | |
| N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-(N6-triglycine)-D-alanyl-D-alanine-diphosphoundecaprenyl-N-acetylglucosamine:glycine glycyltransferase | This Staphylococcus aureus enzyme catalyses the successive transfer of two Gly moieties from charged tRNAs to MurNAc-L-Ala-D-isoglutaminyl-L-Lys-(N6-tri-Gly)-D-Ala-D-Ala-diphosphoundecaprenyl-GlcNAc, attaching them to the three Gly molecules that were previously attached to the N6 of the L-Lys at position 3 of the pentapeptide by EC 2.3.2.16 (lipid II:glycine glycyltransferase) and EC 2.3.2.17 (N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-(N6-glycyl)-D-alanyl-D-alanine-diphosphoundecaprenyl-N-acetylglucosamine:glycine glycyltransferase). This is the last step in the synthesis of the pentaglycine interpeptide bridge tha.ditrans,octacis-diphosphoundecaprenyl-N-acetylglucosamine:glycine glycyltransferase. Enzyme Commission Number: EC 2.3.2.18. 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-2291; N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-(N6-triglycine)-D-alanyl-D-alanine-diphosphoundecaprenyl-N-acetylglucosamine:glycine glycyltransferase; EC 2.3.2.18; femB (gene name); N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-(N6-triglycine)-D-alanyl-D-alanine-ditrans,octacis-diphosphoundecaprenyl-N-acetylglucosamine:glycine glycyltransferase. Cat No: EXWM-2291. | |
| N-acetylmuramyl-alanyl-isoglutamine-alanyl-cholesterol | N-acetylmuramyl-alanyl-isoglutamine-alanyl-cholesterol. CAS No. 99518-28-2. Product ID: ACM99518282. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| N-Acetylmuramyl-L-Alanyl-D-Isoglutamine-6-O-Stearoyl | N-Acetylmuramyl-L-Alanyl-D-Isoglutamine-6-O-Stearoyl acts as a NOD2 receptor agonist. It showed a higher activity than unmodified MDP. Alternative Names: Ac-(6-O-stearoyl)-muramyl-Ala-D-Glu-NH2; 6-O-Stearoyl-N-acetylmuramyl-alanylisoglutamine; D-alpha-Glutamine, N2-(N-(N-acetyl-6-O-(1-oxooctadecyl)muramoyl)-L-alanyl)-. Grades: >99%. CAS No. 60398-08-5. Molecular formula: C37H66N4O12. Mole weight: 758.94. | |
| N-Acetyl-N-21-(biotinylamino)-4,7,10,13,16,19-hexaoxaheneicosanoyl-3,5-diaminophenol-α-glucoside | A biotinyl cross-linker α-glucoside. Alternative Names: 1-{5-[(3aS,4S,6aR)-2-oxo-hexahydrothieno[3,4-d]imidazolidin-4-yl]pentanamido}-N-(3-acetamido-5-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-3,6,9,12,15,18-hexaoxahenicosan-21-amide. Molecular formula: C39H63N5O16S. Mole weight: 890.01. | |
| N-Acetyl-N-(benzyloxy)-2-phenylacetamide | N-Acetyl-N-(benzyloxy)-2-phenylacetamide. Group: Biochemicals. Grades: Reagent Grade. CAS No. 22426-99-9. Pack Sizes: 250mg, 1g. US Biological Life Sciences. | Worldwide |
| N-acetylneuraminate 4-O-acetyltransferase | Both free and glycosidically bound N-acetyl- and N-glycolyl- neuraminates can act as O-acetyl acceptors. Group: Enzymes. Synonyms: sialate O-acetyltransferase. Enzyme Commission Number: EC 2.3.1.44. CAS No. 51004-25-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2223; N-acetylneuraminate 4-O-acetyltransferase; EC 2.3.1.44; 51004-25-2; sialate O-acetyltransferase. Cat No: EXWM-2223. | |
| N-acetylneuraminate 7-O(or 9-O)-acetyltransferase | Both free and glycosidically bound N-acetyl- and N-glycolylneuraminates can act as O-acetyl acceptors. Group: Enzymes. Synonyms: N-acetylneuraminate 7(8)-O-acetyltransferase; sialate O-acetyltransferase; N-acetylneuraminate 7,8-O-acetyltransferase; acetyl-CoA:N-acetylneuraminate-7- or 8-O-acetyltransferase; acetyl-CoA:N-acetylneuraminate-7- and/or 8-O-acetyltransferase; glycoprotein 7(9)-O-acetyltransferase; acetyl-CoA:N-acetylneuraminate-9(7)-O-acetyltransferase; N-acetylneuraminate O7-(or O9-)acetyltransferase; acetyl-CoA:N-acetylneuraminate-9(or 7)-O-acetyltransferase. Enzyme Commission Number: EC 2.3.1.45. CAS No. 9054-50-6. 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-2224; N-acetylneuraminate 7-O(or 9-O)-acetyltransferase; EC 2.3.1.45; 9054-50-6; N-acetylneuraminate 7(8)-O-acetyltransferase; sialate O-acetyltransferase; N-acetylneuraminate 7,8-O-acetyltransferase; acetyl-CoA:N-acetylneuraminate-7- or 8-O-acetyltransferase; acetyl-CoA:N-acetylneuraminate-7- and/or 8-O-acetyltransferase; glycoprotein 7(9)-O-acetyltransferase; acetyl-CoA:N-acetylneuraminate-9(7)-O-acetyltransferase; N-acetylneuraminate O7-(or O9-)acetyltransferase; acetyl-CoA:N-acetylneuraminate-9(or 7)-O-acetyltransferase. Cat No: EXWM-2224. | |
| N-acetylneuraminate epimerase | Sialoglycoconjugates present in vertebrates are linked exclusively by α-linkages and are released in α form during degradation. This enzyme accelerates maturotation to the β form (which also occurs as a slow spontaneous reaction), which is necessary for further metabolism by the bacteria. Group: Enzymes. Synonyms: sialic acid epimerase; N-acetylneuraminate mutarotase; YjhT. Enzyme Commission Number: EC 5.1.3.24. 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-5410; N-acetylneuraminate epimerase; EC 5.1.3.24; sialic acid epimerase; N-acetylneuraminate mutarotase; YjhT. Cat No: EXWM-5410. | |
| N-acetylneuraminate lyase | Also acts on N-glycoloylneuraminate, and on O-acetylated sialic acids, other than 4-O-acetylated derivatives. Group: Enzymes. Synonyms: N-acetylneuraminic acid aldolase; acetylneuraminate lyase; sialic aldolase; sialic acid aldolase; sialate lyase; N-acetylneuraminic aldolase; neuraminic aldolase; N-acetylneuraminate aldolase; neuraminic acid aldolase; N-acetylneuraminic acid aldolase; neuraminate aldolase; N-acetylneuraminic lyase; N-acetylneuraminic acid lyase; NPL; NALase; NANA lyase; acetylneuraminate pyruvate-lyase; N-acetylneuraminate pyruvate-lyase. Enzyme Commission Number: EC 4.1.3.3. CAS No. 9027-60-5. NALase. 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-4908; N-acetylneuraminate lyase; EC 4.1.3.3; 9027-60-5; N-acetylneuraminic acid aldolase; acetylneuraminate lyase; sialic aldolase; sialic acid aldolase; sialate lyase; N-acetylneuraminic aldolase; neuraminic aldolase; N-acetylneuraminate aldolase; neuraminic acid aldolase; N-acetylneuraminic acid aldolase; neuraminate aldolase; N-acetylneuraminic lyase; N-acetylneuraminic acid lyase; NPL; NALase; NANA lyase; acetylneuraminate pyruvate-lyase; N-acetylneuraminate pyruvate-lyase. Cat No: EXWM-4908. | |
| N-acetylneuraminate synthase | This enzyme belongs to the family of transferases, specifically those transferring aryl or alkyl groups other than methyl groups. This enzyme participates in aminosugars metabolism. Group: Enzymes. Synonyms: (NANA)condensing enzyme; N-acetylneuraminate pyruvate-lyase (pyruvate-phosphorylating); NeuAc synthase. Enzyme Commission Number: EC 2.5.1.56. CAS No. 37290-66-7. 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-2793; N-acetylneuraminate synthase; EC 2.5.1.56; 37290-66-7; (NANA)condensing enzyme; N-acetylneuraminate pyruvate-lyase (pyruvate-phosphorylating); NeuAc synthase. Cat No: EXWM-2793. | |
| N-Acetylneuraminic acid | N-Acetylneuraminic acid is a sialic acid monosaccharide found in glycoproteins and glycolipids on cell membranes. Alternative Names: Sialic acid; NeuNAc; NANA; 5-(Acetylamino)-3,5-dideoxy-D-glycero-D-galacto-2-nonulosonic Acid; N-Acetylsialic Acid; 5-N-Acetyl-beta-D-neuraminic acid; N-Acetyl-D-neuraminic acid; N-acetyl-beta-neuraminic acid. Grades: ≥95%. CAS No. 131-48-6. Molecular formula: C11H19NO9. Mole weight: 309.27. | |
| N-Acetylneuraminic acid | N-Acetylneuraminic acid (NANA; Lactaminic acid), a nonphenolic structure, is the predominant form of sialic from Collocalia esculenta. N-Acetylneuraminic acid plays a biological role in myocardial injury, melanoma and viral or bacterial infection. N-Acetylneuraminic acid inhibits melanogenesis by reducing tyrosinase activity and triggers myocardial injury in vitro and in vivo by activation of the Rho/Rho-associated signaling pathway through binding to RhoA and Cdc42. N-Acetylneuraminic acid may prevent high fat diet (HFD)-induced inflammation and oxidative stress, thereby prevents hyperlipidemia-associated inflammation and oxidative stress. N-Acetylneuraminic acid is promising for research in the field of melanoma, coronary artery, obesity-related diseases and hyperlipidemia[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NANA; Lactaminic acid. CAS No. 131-48-6. Pack Sizes: 10 mM * 1 mL in Water; 100 mg; 1 g; 5 g. Product ID: HY-I0400. |  |
| N-Acetylneuraminic acid | N-Acetylneuraminic acid. Alternative Names: 2-[4-[4-(2-Methoxyphenyl)-1-piperazinyl]butyl]-1H-isoindole-1,3(2H)-dione. CAS No. 131-48-6. Purity: 99% HPLC. Product ID: CI-GU-0341. Molecular formula: C11H19NO9. Mole weight: 309.27 g/mol. IUPAC Name: (2S,4S,5R,6R)-5-acetamido-2,4-dihydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid. Alfa Chemistry - ISO 9001:32057 Certified. | |
| N-Acetylneuraminic Acid | N-Acetylneuraminic Acid. CAS No. 131-48-6. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications. |  |
| N-Acetylneuraminic acid 1-O-propylamine | N-Acetylneuraminic acid 1-O-propylamine, an indispensable compound in the field of biomedicine, stands as a pivotal precursor for the synthesis of sialylated glycoconjugates. Undeniably, this compound exhibits unmatched potency in combating various ailments such as cancer, viral infections, and inflammatory disorders. By virtue of its unrivaled attributes, it assumes a paramount status in the advancement of targeted therapeutics and the innovation of drug delivery systems. Molecular formula: C13H26N2O9. Mole weight: 354.35. | |
| N-Acetylneuraminic acid 9-phosphate | N-Acetylneuraminic acid 9-phosphate is also known as Neu5Ac-9P, actively participating in the intricate process of sialic acid synthesis, thereby exerting profound effects on the formation and function of glycoproteins and glycolipids. Alternative Names: (2R,4R,5R,6S)-5-acetamido-6-(1,2-dihydroxy-3-phosphonooxypropyl)-2,4-dihydroxyoxane-2-carboxylic acid. CAS No. 37992-17-9. Molecular formula: C11H20NO12P. Mole weight: 389.25. | |
| N-Acetylneuraminic Acid Aldolase | N-Acetylneuraminic Acid Aldolase. Synonyms: EC 4.1.3.3;N-ACETYLNEURAMINIC ACID ALDOLASE;N-ACETYLNEURAMINIC ACID ALDORASE;N-ACETYLNEURAMINATE PYRUVATE LYASE;NEU5AC ALDOLASE;N-Acetylneuraminic Acid Aldolase from microorganisms;N-ACETYLNEURAMINIC ACID ALDOLASE, FROM MICROORGANISM;N-Acetylneuraminate Pyruvate Lyase, N-Acetylneuraminic Acid Lyase, NANA Aldolase, Sialic Aldolase. CAS No. 9027-60-5. Pack Sizes: 1 kg. Product ID: CDF4-0055. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; N-Acetylneuraminic Acid Aldolase; CDF4-0055; 9027-60-5; 9027-60-5. Purity: 0.99. Color: Slightly yellow. Physical State: Powder. Storage: -20ยฐC. Product Description: Sialic acid aldolases, or N-acetylneuraminate lyases, catalyze the reversible aldol cleavage of N-acetylneuraminic acid to form pyruvate and N-acetyl-D-mannosamine. In nature, N-acetylneuraminate lyase mainly occurs in pathogens. |  |
| N-Acetylneuraminic Acid-d3 | Labeled Neuraminic Acid derivative. Group: Biochemicals. Alternative Names: 5-(Acetylamino)-3,5-dideoxy-D-glycero-D-galacto-2-nonulosonic Acid-d3; NANA-d3; N-Acetylsialic Acid-d3; Sialic Acid-d3. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| N-Acetylneuraminic acid dihydrate | N-Acetylneuraminic acid dihydrate is a fundamental compound within the biomedical industry, prominently employed for developing and synthesizing a diverse range of drugs targeted against influenza, viral infections and cancer. Alternative Names: Sialic acid dihydrate; Neu5Ac dihydrate; N-Acetyl-D-neuraminic acid dihydrate; 5-Acetamido-3,5-dideoxy-D-glycero-D-galacto-non-2-ulopyranosonic acid dihydrate. Grades: 95%. CAS No. 50795-27-2. Molecular formula: C11H19NO9ยท2H2O. Mole weight: 345.30. | |
| N-Acetylneuraminic acid dimer disodium salt | N-Acetylneuraminic acid dimer disodium salt is a compound extensively utilized within the biomedical realm, exhibiting remarkable potential in the investigation and mitigation of diverse ailments. Within this domain, it functions as a precursor in the synthesis of sialic acid-derived substances. Alternative Names: 8-O-(N-Acetylneuraminyl)-N-acetylneuraminic acid disodium salt; N-Acetyl-8-O-(N-acetyl-a-neuraminyl)-neuraminic acid disodium salt; Neu5Ac-a-2,8-Neu5Ac 2Na; Neuraminic acid, N-acetyl-8-O-(N-acetyl-α-neuraminosyl)-, disodium salt; D-glycero-D-galacto-2-Nonulosonic acid, 5-(acetylamino)-8-O-(N-acetyl-α-neuraminosyl)-3,5-dideoxy-, disodium salt. CAS No. 149331-75-9. Molecular formula: C22H34N2Na2O17. Mole weight: 644.49. | |
| N-Acetylneuraminic acid hexamer disodium salt | N-Acetylneuraminic acid hexamer disodium salt is an indispensable component in the biomedical field, finding its application in the research of diverse ailments including influenza, respiratory syncytial virus infections and select bacterial infections. Grades: ≥95%. Molecular formula: C66H98N6O49Na6. Mole weight: 1897.43. | |
| N-Acetylneuraminic Acid Methyl Ester 2,4,7,8,9-Pentaacetate-d3 | A Labeled, protected Neuraminic Acid derivative. Group: Biochemicals. Alternative Names: 5-(Acetylamino)-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonic Acid Methyl Ester 2,4,7,8,9-Pentaacetate-d3. Grades: Highly Purified. CAS No. 950508-99-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| N-Acetylneuraminic Acid Methyl Ester-d3 | Labeled derivative of Neuraminic Acid. Group: Biochemicals. Alternative Names: 5-(Acetylamino)-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonic AcidMethyl Ester-d3. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| N-Acetylneuraminic acid pentamer disodium salt | N-Acetylneuraminic acid pentamer disodium salt is an exceptional biomedical product, emerging as a pivotal component in the research of diverse malignancies, viral pathologies, as well as intricate neurological ailments. It functions as an impeccable sialic acid surrogate. Molecular formula: C55H82N5O41Na5. Mole weight: 1584.20. | |
| N-Acetylneuraminic acid (Sialic acid) | 1g Pack Size. Group: Biochemicals, Carbohydrates. Formula: C11H19NO9. CAS No. 131-48-6. Prepack ID 39596039-1g. Molecular Weight 309.27. See USA prepack pricing. |  |
| N-Acetylneuraminic acid (Sialic acid) | 10g Pack Size. Group: Biochemicals, Carbohydrates. Formula: C11H19NO9. CAS No. 131-48-6. Prepack ID 39596039-10g. Molecular Weight 309.27. See USA prepack pricing. | |
| N-Acetylneuraminic acid sodium salt | N-Acetylneuraminic acid sodium salt is an indispensable and pivotal compound extensively employed in the biomedical industry. With crucial role as an indispensable substrate, it serves as a fundamental building block for the development and synthesis of sialic acid-based drugs. Alternative Names: Sodium aceneuramate; Neuraminic acid, N-acetyl-, monosodium salt; Neuraminic acid, N-acetyl-, sodium salt (1:1); D-Glycero-D-galacto-2-nonulosonic acid, 5-(acetylamino)-3,5-dideoxy-, monosodium salt. CAS No. 126934-33-6. Molecular formula: C11H18NNaO9. Mole weight: 331.25. | |
| N-Acetylneuraminic acid tetramer sodium salt | N-Acetylneuraminic acid tetramer sodium salt is a biomedical compound, finding its purpose in the research of a myriad of ailments arising from perturbations in sialylation. By participating in the assembly of sialylated glycoconjugates, it facilitates indispensable functions in cellular recognition phenomena. By adopting the form of tetramer sodium salt, it attains heightened stability and augmented bioavailability. Molecular formula: C44H66N4O33Na4. Mole weight: 1270.96. | |
| N-Acetylneuraminic acid trimer disodium salt | N-Acetylneuraminic acid trimer disodium salt is a widely employed pharmaceutical compound with realm, showcasing potent antiviral attributes and finds application in studying influenza and related viral infections. By impeding viral neuraminidase enzymes, this compound effectively hampers the dissemination and propagation of viral particles. Alternative Names: N-Acetylneuraminic Acid, trimer(α,2→8)[DP3]. Molecular formula: C33H50N3O25Na3. Mole weight: 957.72. | |
| N-Acetylneuraminyl-(a2-3)-D-galactopyranosyl-(b1-3)-D-N-acetylgalactosaminyl serine | N-Acetylneuraminyl-(a2-3)-D-galactopyranosyl-(b1-3)-D-N-acetylgalactosaminyl serine is an extensively utilized bioactive compound within the biomedical industry, acting as a glycosaminoglycan mimetic. This compound showcases a pivotal function in effectively binding to receptors involved in cellular recognition. Alternative Names: NeuNAc(a-2-3)Gal(b1-3)GalNAca serine. Molecular formula: C28H47N3O21. Mole weight: 761.68. | |
| N-Acetylneuraminyl-(a2-3)-D-galactopyranosyl-(b1-3)-D-N-acetylgalactosaminyl serine-biotin | N-Acetylneuraminyl-(a2-3)-D-galactopyranosyl-(b1-3)-D-N-acetylgalactosaminyl serine-biotin is a biomedical compound used in the research of certain ailments. This remarkable constituent finds its primary utility in the identification of distinct cellular receptor sites and the investigation of glycoprotein interrelations. Alternative Names: NeuNAc(a-2-3)Gal(b1-3)GalNAca serine-biotin. Molecular formula: C36H58N4O23S. Mole weight: 946.92. | |
| N-Acetylneuraminyl-(a2-3)-D-galactopyranosyl-(b1-3)-[N-acetylneuraminyl-(a2-6)]-D-N-acetylgalactosamine | N-Acetylneuraminyl-(a2-3)-D-galactopyranosyl-(b1-3)-[N-acetylneuraminyl-(a2-6)]-D-N-acetylgalactosamine. | |
| N-Acetylneuraminyl-(a2-3)-D-galactopyranosyl-(b1-3)-[N-acetylneuraminyl-(a2-6)]-D-N-acetylgalactosaminyl serine | N-Acetylneuraminyl-(a2-3)-D-galactopyranosyl-(b1-3)-[N-acetylneuraminyl-(a2-6)]-D-N-acetylgalactosaminyl serine is a pivotal compound extensively employed by the biomedical industry, serving as a fundamental structural component for glycosylation investigations. Intimately involved in cellular signaling and immune response processes, this compound constitutes the basis for synthesizing glycoconjugates crucial to gaining insights into glycan-pathogen interactions. Molecular formula: C39H64N4O29. Mole weight: 1052.94. | |
| N-Acetylneuraminyl-(a2-3)-D-galactopyranosyl-(b1-3)-[N-acetylneuraminyl-(a2-6)]-D-N-acetylgalactosaminyl serine-biotin | N-Acetylneuraminyl-(a2-3)-D-galactopyranosyl-(b1-3)-[N-acetylneuraminyl-(a2-6)]-D-N-acetylgalactosaminyl serine-biotin. | |
| N-Acetylneuraminyl-fucosyllacto-N-neo-tetraose from human milk | N-Acetylneuraminyl-fucosyllacto-N-neo-tetraose from human milk. CAS No. 111216-36-5. Molecular formula: C43H72N2O33. Mole weight: 1145g/mol. IUPAC Name: (2R,4S,5R,6R)-5-acetamido-2-[[(2R,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6S)-5-acetamido-6-[(2S,3R,4S,5S,6R)-2-[(2R,3S,4R,5R)-5,6-dihydroxy-2-(hydroxymethyl)-4-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid. SMILES: CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)COC6(CC(C(C(O6)C(C(CO)O)O)NC(=O)C)O)C(=O)O)O)O)O)O)NC(=O)C)O)CO)O)O)O)O)O. InChI: InChI=1S/C43H72N2O33/c1-10-21(54)26(59)28(61)39(69-10)77-36-30(63)37(65)70-17(8-49)33(36)75-41-31(64)35(24(57)15(6-47)71-41)76-38-20(45-12(3)51)25(58)32(16(7-48)72-38)74-40-29(62)27(60)23(56)18(73-40)9-68-43(42(66)67)4-13(52)19(44-11(2)50)34(78-43)22(55)14(53)5-46/h10,13-41,46-49,52-65H,4-9H2,1-3H3,(H,44,50)(H,45,51)(H,66,67)/t10-,13-,14+,15+,16+,17+,18+,19+,20+,21+,22+,23-,24-,25+,26+,27-,28-,29+,30+,31+,32+,33-,34+,35-,36+,37?,38-,39-,40-,41-,43+/m0/s1. |  |
| N-acetyl neuraminyl galactosyl glucosyl ceramide β-1,4-N-acetylgalactosaminyltransferase | Requires Mn2+. Only substances containing sialic acid residues can act as acceptors; bovine fetuin is the best acceptor tested. Group: Enzymes. Synonyms: uridine diphosphoacetylgalactosamine-acetylneuraminyl(α 2?3)galactosyl(β 1?4)glucosyl β1?4-acetylgalactosaminyltransferase; UDP-N-acetyl-D-galactosamine:N-acetylneuraminyl-2,3-α-D-g. Enzyme Commission Number: EC 2.4.1.165. CAS No. 109136-50-7. 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-2390; N-acetyl neuraminyl galactosyl glucosyl ceramide β-1,4-N-acetylgalactosaminyltransferase; EC 2.4.1.165; 109136-50-7; uridine diphosphoacetylgalactosamine-acetylneuraminyl(α 2?3)galactosyl(β 1?4)glucosyl β1?4-acetylgalactosaminyltransferase; UDP-N-acetyl-D-galactosamine:N-acetylneuraminyl-2,3-α-D-galactosyl-1,4-β-D-glucosylceramide β-1,4-N-acetylgalactosaminyltransferase; UDP-N-acetyl-D-galactosamine:N-acetylneuraminyl-(2?3)-α-D-galactosyl-(1?4)-β-D-glucosyl(1<->1)ceramide 4-β-N-acetylgalactosaminyltransferase; UDP-N-acetyl-D-galactosamine:N-acetylneuraminyl-(2?3)-α-D-galactosyl-(1?4)-β-D-glucosyl-(1<->1)-ceramide 4-β-N-acetylgalactosaminyltransferase. Cat No: EXWM-2390. | |
| N-acetylneuraminylgalactosylglucosylceramide β-1,4-N-acetylgalactosaminyltransferase | Requires Mn2+. Only substances containing sialic acid residues can act as acceptors; bovine fetuin is the best acceptor tested. | |
| N-Acetyl-N-hydroxy-2-phenylacetamide | N-Acetyl-N-hydroxy-2-phenylacetamide. Group: Biochemicals. Grades: Reagent Grade. CAS No. 77130-75-7. Pack Sizes: 250mg, 1g. US Biological Life Sciences. | Worldwide |
| N-Acetyl Nintedanib | N-Acetyl Nintedanib. CAS No. 2380229-45-6. | |
| N-Acetyl Norgestimate-d6 | Labeled intermediate of Norgestimate. Group: Biochemicals. Alternative Names: (17α)-17-(Acetyloxy)-13-ethyl-18,19-dinorpregna-1,3,5(10)-trien-20-yn-3-one O-Acetyloxime. Grades: Highly Purified. CAS No. 1263195-02-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| N-Acetyl-N-tert-butoxycarbonyl Serotonin | Protected Serotonin. Group: Biochemicals. Alternative Names: N-tert-Butoxycarbonyl-normelatonin; N-tert-Butoxycarbonyl-O-demethylmelatonin. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| N-Acetyl-N-tert-butoxycarbonyl Serotonin-d4 | Labelled N-Acetyl-N-tert-butoxycarbonyl Serotonin (A171155). Protected Serotonin. Group: Biochemicals. Alternative Names: N-tert-Butoxycarbonyl-normelatonin-d4; N-tert-Butoxycarbonyl-O-demethylmelatonin-d4. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| N-Acetyl-N-tert-butoxycarbonyl Serotonin-d4 Tri-O-acetyl- β-D-glucuronide Methyl Ester | Serotonin (S274990) derivative. Group: Biochemicals. Alternative Names: N-tert-Butoxycarbonyl-3-[2-(acetylamino)ethyl]-1H-indol-5-yl-tri-O-acetyl- β-D-glucopyranosiduronic-d4 Acid Methyl Ester. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| N-Acetyl-N-tert-butoxycarbonyl Serotonin Tri-O-acetyl- β-D-glucuronide Methyl Ester | Protected Malatonin metabolite. Group: Biochemicals. Alternative Names: N-tert-Butoxycarbonyl-3-[2-(acetylamino)ethyl]-1H-indol-5-yl-tri-O-acetyl- β-D-glucopyranosiduronic Acid Methyl Ester. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| N-Acetyl O-Benzyl 5-Epi Lamivudine | Protected 5-Epi Lamivudine, a Lamivudine epimer. Group: Biochemicals. Alternative Names: N-[1-[(2R,5R)-2-[(Benzoyloxy)methyl]-1,3-oxathiolan-5-yl]-1,2-dihydro-2-oxo-4-pyrimidinyl-acetamide. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| N-Acetyl O-Benzyl Lamivudine | Protected Lamivudine, a potent nucleoside reverse transcriptase inhibitor, used for treatment of chronic hepatitis B. Antiviral. Group: Biochemicals. Alternative Names: N-[1-[(2R,5S)-2-[(Benzoyloxy)methyl]-1,3-oxathiolan-5-yl]-1,2-dihydro-2-oxo-4-pyrimidinyl-acetamide. Grades: Highly Purified. CAS No. 1091585-30-6. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| N-Acetylornithine | N-Acetylornithine is a precursor of ornithine. N-Acetylornithine is associated with type 2 diabetes[1][2]. Uses: Scientific research. Category: Natural products. CAS No. 6205-8-9. Pack Sizes: 10 mM * 1 mL in Water; 50 mg; 100 mg. Product ID: HY-113080. | |
| N-acetylornithine carbamoyltransferase | Differs from EC 2.1.3.3, ornithine carbamoyltransferase. This enzyme replaces EC 2.1.3.3 in the canonic arginine biosynthetic pathway of several Eubacteria and has no catalytic activity with L-ornithine as substrate. Group: Enzymes. Synonyms: acetylornithine transcarbamylase; N-acetylornithine transcarbamylase; AOTC; carbamoyl-phosphate:2-N-acetyl-L-ornithine carbamoyltransferase; AOTCase. Enzyme Commission Number: EC 2.1.3.9. CAS No. 890853-54-0. 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-2021; N-acetylornithine carbamoyltransferase; EC 2.1.3.9; 890853-54-0; acetylornithine transcarbamylase; N-acetylornithine transcarbamylase; AOTC; carbamoyl-phosphate:2-N-acetyl-L-ornithine carbamoyltransferase; AOTCase. Cat No: EXWM-2021. | |
| N-Acetylphenylephrine (Adrenaline Impurity 42) | N-Acetylphenylephrine (Adrenaline Impurity 42). Uses: For analytical and research use. CAS No. 58952-80-0. Molecular formula: C11H15NO3. Mole weight: 209.25. Catalog: APB58952800. |  |
| N-acetylphosphatidylethanolamine-hydrolysing phospholipase D | This enzyme is involved in the biosynthesis of anandamide. It does not hydrolyse phosphatidylcholine and phosphatidylethanolamine. No transphosphatidation. The enzyme contains Zn2+ and is activated by Mg2+ or Ca2+. Group: Enzymes. Synonyms: NAPE-PLD; anandamide-generating phospholipase D; N-acyl phosphatidylethanolamine phospholipase D; NAPE-hydrolyzing phospholipase D. Enzyme Commission Number: EC 3.1.4.54. 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-3737; N-acetylphosphatidylethanolamine-hydrolysing phospholipase D; EC 3.1.4.54; NAPE-PLD; anandamide-generating phospholipase D; N-acyl phosphatidylethanolamine phospholipase D; NAPE-hydrolyzing phospholipase D. Cat No: EXWM-3737. | |
| N-Acetyl-phytosphingosine | N-Acetyl-phytosphingosine. Group: Biochemicals. Alternative Names: N-Acetyl (2S, 3S, 4R)-2-amino-1,3,4 -octadecanetriol; N-Acetyl 4-hydroxysphinganine. Grades: Highly Purified. CAS No. 475995-69-8. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C20H41NO4. US Biological Life Sciences. | Worldwide |
| N-Acetyl Piperidine | N-Acetyl Piperidine. Alternative Names: 1-Acetylpiperidine; N-Acetylpiperidine. CAS No. 618-42-8. Molecular formula: C7H13NO. Mole weight: 127.18. | |
| N-Acetylprocainamide | N-Acetylprocainamide, the N-acetylated metabolite of Procainamide, is a Class III antiarrhythmic agent. N-Acetylprocainamide is a class III antiarrhythmic, which blocks K+ channels. Alternative Names: Acecainide; NAPA; 4'-((2-(Diethylamino)ethyl)carbamoyl)acetanilide. Grades: ≥98%. CAS No. 32795-44-1. Molecular formula: C15H23N3O2. Mole weight: 277.36. | |
| N-Acetylprocainamide | N-Acetylprocainamide. CAS No: 32795-44-1 |  Sarchem Laboratories New Jersey NJ |
| N-Acetylprocainamide HCl | N-Acetylprocainamide HCl. Alternative Names: 4'-[[2-(Diethylamino)ethyl]carbamoyl]-acetanilide Monohydrochloride; 4-(Acetylamino)-N-[2-(diethylamino)ethyl]-benzamide Monohydrochloride; Acecainide Hydrochloride. CAS No. 34118-92-8. Purity: 98%. Product ID: ACM34118928. Molecular formula: C15H24ClN3O2. Mole weight: 313.82. Alfa Chemistry - ISO 9001:32057 Certified. | |
| N-Acetylpuromycin | N-Acetylpuromycin is a selective CB2 receptor agonist. It downregulates Ski protein and SnoN expression, but promotes TGF-β signaling independently of MAPK activation. It does not block protein synthesis or bind to ribosomes. Alternative Names: N-Acetylpurinomycin; N Acetylpurinomycin; 3'-[[(2S)-2-(Acetylamino)-3-(4-methoxyphenyl)-1-oxopropyl]amino]-3'-deoxy-N,N-dimethyladenosine; 3'-(L-α-Acetamido-p-methoxyhydrocinnamamido)-3'-deoxy-N,N-dimethyladenosine. Grades: ≥98% by HPLC. CAS No. 22852-13-7. Molecular formula: C24H31N7O6. Mole weight: 513.55. | |
| N-Acetylputrescine | N-Acetylputrescine is a polyamine metabolite that regulates cell proliferation and signal transduction mainly by participating in polyamine acetylation modification. N-Acetylputrescine may reduce the positive charge of polyamines, affect protein-nucleic acid interactions, and promote cell growth. The concentration changes of N-Acetylputrescine can help disease diagnosis (such as early screening and efficacy evaluation of lung cancer) and microbial cell wall structure research. N-Acetylputrescine can be used as a potential biomarker for the progression of squamous cell carcinoma of the lung (SCCL) and Parkinson's disease (PD)[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NAP. CAS No. 5699-41-2. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg. Product ID: HY-W342604. | |
| N-Acetylputrescine hydrochloride | N-Acetylputrescine hydrochloride is a polyamine metabolite that regulates cell proliferation and signal transduction mainly by participating in polyamine acetylation modification. N-Acetylputrescine hydrochloride may reduce the positive charge of polyamines, affect protein-nucleic acid interactions, and promote cell growth. The concentration changes of N-Acetylputrescine hydrochloride can help disease diagnosis (such as early screening and efficacy evaluation of lung cancer) and microbial cell wall structure research. N-Acetylputrescine hydrochloride can be used as a potential biomarker for the progression of squamous cell carcinoma of the lung (SCCL) and Parkinson's disease (PD)[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 18233-70-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113100. | |
| N-Acetylputrescine hydrochloride | N-Acetylputrescine hydrochloride (CAS# 18233-70-0 ) is a useful research chemical. Alternative Names: N-(4-aminobutyl)acetamide;hydrochloride. CAS No. 18233-70-0. Molecular formula: C6H14N2O ยท HCl. Mole weight: 166.65. | |
| N-Acetylpyrrolidine, Pract. | Liquid, 97%. CAS No. 4030-18-6. Pack Sizes: Typically in stock: 5g, 50g. Mole weight: 113.16. MP/BP: B.P. 105-107/15 mm. Order No: FR-0764. |  Frinton Laboratories |
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