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| Product | Description | |
|---|---|---|
| Neuraminidase from Microorganism | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. Group: Enzymes. Synonyms: sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Enzyme Commission Number: EC 3.2.1.18. CAS No. 9001-67-6. Mole weight: 52 kDa (SDS-PAGE). Activity: >300U/mg protein. Storage: Store at -20°C. Form: White powder, lyophilized. Source: Microorganism. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6; NRH. Cat No: NATE-1716. |  |
| Neuraminidase, Microorganism | Neuraminidase, Microorganism (Exo-α-sialidase) is an exosialidase, is often used in biochemical studies. Neuraminidase cleaves α-ketosidic linkage between the sialic (N-acetylneuraminic) acid and an adjacent sugar residue. Neuraminidase, derived from mucosal pathogens, is a virulence factor that modifies the host's response to infection [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Exo-α-sialidase. CAS No. 9001-67-6. Pack Sizes: 5 U; 10 U. Product ID: HY-P2988. |  |
| Neuraminidase, recombinant | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Enzyme Commission Number: EC 3.2.1.18. CAS No. 9001-67-6. Purity: 90% (SDS-PAGE test). Neuraminidase. Mole weight: About 58kDa (SDS-PAGE detection). Activity: 100U/mg protein. Storage: 4°C,store at -20°C for long-term preservation. Form: White powder, lyophilized. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Cat No: NATE-1683. | |
| α(2?3,6,8,9) Neuraminidase from Arthrobacter ureafaciens, Recombinant | Neuraminidase is the common name for Acetyl-neuraminyl hydrolase (Sialidase). α2-3,6,8,9 Neuraminidase catalyzes the hydrolysis of all linear and branched non-reducing terminal sialic acid residues from glycoproteins and oligosaccharides. The enzyme releases α2-3 and α2-6 linkages at a slightly higher rate than α2-8 and α2-9 linkages. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6; α2-3,6,8,9 Neuraminidase A; α2-3,6,8,9 Neuraminidase; α(2?3,6,8,9) Neuraminidase. Enzyme Commission Number: EC 3.2.1.18. CAS No. 9001-67-6. Neuraminidase. Mole weight: 100,000 daltons. Activity: ~316,000 units/mg. Storage: at -20°C. Form: Supplied in: 50 mM NaCl, 20 mM Tris-HCl (pH 7.5 @ 25°C) and 1 mM EDTA. Source: E. coli. Species: Arthrobacter ureafaciens. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6; α2-3,6,8,9 Neuraminidase A; α2-3,6,8,9 Neuraminidase; α(2?3,6,8,9) Neuraminidase. Cat No: NATE-0758. | |
| α(2?3,6,8,9) Neuraminidase from Streptococcus pneumoniae, Recombinant | Neuraminidase, releases α(2-3)-linked sialic acid from oligosaccharides, glycoproteins, complex carbohydrates. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase. Neuraminidase. Mole weight: ~75 kD. Form: Lyophilized from 20 mM Tris-HCl, 25 mM NaCl (pH 7.5). Source: E. coli. Species: Streptococcus pneumoniae. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase. Cat No: NATE-0971. | |
| α(2-3,6,8) Neuraminidase from Clostridium perfringens, Recombinant | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. Neuraminidase is the common name for acetyl-neuraminyl hydrolase (sialidase). this neuraminidase catalyzes the hydrolysis of α2-3, α2-6, and α2-8 linked n-acetyl-neuraminic acid residues from glycoproteins and oligosaccharides. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-ne. Purity: > 95% determined by SDS-PAGE. Neuraminidase. Mole weight: 43 kDa. Activity: ~225,000 units/mg. Storage: at -20°C. Form: 50 mM NaCl, 20 mM Tris-HCl (pH 7.5 25°C) and 5 mM Na2EDTA. Source: E. coli. Species: Clostridium perfringens. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6; α(2-3,6,8) Neuraminidase. Cat No: NATE-1277. | |
| α(2?3,6) Neuraminidase from Clostridium perfringens, Recombinant | Releases α(2-3,6)-linked sialic acid from oligosaccharides, glycoproteins, complex carbohydrates. Applications: Structural analysis of oligosaccharides; determining sialic acid linkage; glycoprotein deglycosylation; removing heterogeneity from glycoproteins. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase. Neuraminidase. Mole weight: ~41 kD. Activity: >10 U/ml (>40 U/mg). Storage: Store at 2-8°C. DO NOT FREEZE. Form: A sterile-filtered solution in 20 mM Tris-HCl, 25 mM NaCl (pH 7.5). Source: E. coli. Species: Clostridium perfringens. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase. Cat No: NATE-0972. | |
| α(2-3) Neuraminidase from Salmonella typhimurium LT2, Recombinant | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. Α2-3 neuraminidase is a highly specific exogl... sialyl linkages and shows only trace activity against α2-8 sialyl linkages. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Neuraminidase. Mole weight: 41 kDa. Activity: ~11,300,000 units/mg. Storage: Store at 4°C or in small aliquots at -20°C. Avoid repeated freeze/thaw cycles. Form: 50 mM NaCl, 20 mM Tris-HCl (pH 7.5 25°C), and 5 mM Na2EDTA. Source: E. coli. Species: Salmonella typhimurium LT2. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6; α(2-3) Neuraminidase. Cat No: NATE-1276. | |
| α(2-3) Neuraminidase S from Streptococcus pneumoniae, Recombinant | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. Neuraminidase is the common name for acetyl-neurami...;2-3 linked n-acetyl-neuraminic acid residues from glycoproteins and oligosaccharides. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Purity: > 95% determined by SDS-PAGE. Neuraminidase. Mole weight: 74000 daltons. Activity: 160,000 units/mg. Storage: at -20°C. Form: 50 mM NaCl, 20 mM Tris-HCl (pH 7.5 25°C) and 1 mM EDTA. Source: E. coli. Species: Streptococcus pneumoniae. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6; α(2-3) Neuraminidase S; α(2-3) Neuraminidase. Cat No: NATE-1275. | |
| Native Arthrobacter ureafaciens α (2?3,6,8,9) Neuraminidase | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. Applications: Neuraminidase is an important deglycosyl... resulting in partial or complete o-deglycosylation. sds-page and maldi-tof ms are typically utilized in purification, structural analysis, and sequencing process. these techniques also remove heterogeneity and charge from the glycoprotein. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Enzyme Commission Number: EC 3.2.1.18. CAS No. 9001-67-6. Neuraminidase. Storage: 2-8°C. Form: Lyophilized powder. Source: Arthrobacter ureafaciens. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Cat No: NATE-0756. | |
| Native Clostridium perfringens (C. welchII) Neuraminidase | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. At least four mammalian sialidase homologs have been descr...ic mesenchymal stem cells in the treatment of f ocal cerebral ischemia. it has also been used in a study to investigate sinonasal terat ocarcinosarcoma with rhabdoid features. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18. Enzyme Commission Number: EC 3.2.1.18. Purity: > 95% (SDS-PAGE). Neuraminidase. Storage: -20°C. Form: buffered aqueous solution; Solution in 100 mM Tris-HCl, 5 mM MgSO4, 250 mM KCl, pH 5.0-5.2. Source: Clostridium perfringens (C. welchII). neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18. Cat No: NATE-0480. | |
| Native Clostridium perfringens (C. welchII) Neuraminidase Agarose | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. Neuraminidase enzymes are hydrolase enzymes that promo...cells. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Enzyme Commission Number: EC 3.2.1.18. CAS No. 9001-67-6. Neuraminidase. Activity: Type I, 6-10 units/mg protein (using 4MU-NANA), 2-5 units/mg protein (mucin); Type II, 10-20 units/mg protein (using 4MU-NANA), 3.5-8.0 units/mg protein (mucin); Type III, > 50 units/mg protein (using 4MU-NANA). Storage: -20°C. Form: lyophilized powder. Source: Clostridium perfringens (C. welchII). neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Cat No: NATE-0479. | |
| Native Streptococcus pneumoniae α (2?3) Neuraminidase | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Enzyme Commission Number: EC 3.2.1.18. CAS No. 9001-67-6. Neuraminidase. Storage: 2-8°C. Form: buffered aqueous solution. Solution in 50 mM sodium phosphate, pH 7.5. Source: Streptococcus pneumoniae. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Cat No: NATE-0757. | |
| Native Vibrio cholerae Neuraminidase | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. At least four mammalian sialidase homologs have been described in the...say of neuraminidase. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Enzyme Commission Number: EC 3.2.1.18. CAS No. 9001-67-6. Neuraminidase. Activity: Type I, 1-5 units/mg protein (Lowry, using NAN-lactose); Type II, 8-24 units/mg protein (Lowry, using NAN-lactose); Type III, > 1.5 units/mg protein. Storage: 2-8°C. Form: Type I, buffered aqueous solution; Aqueous solution, pH 5.5, containing 0.15 M NaCl and 4 mM CaCl2; Type II, buffered aqueous solution, Solution in 50 mM sodium acetate, pH 5.5, containing 0.15 M sodium chloride and 4 mM calcium chloride; Type III, sterile filte | |
| 1,1,1-Trimethoxyoctane | 1,1,1-Trimethoxyoctane is a reagent used neuraminidase inhibitor compounds. Group: Biochemicals. Alternative Names: Trimethyl Orthooctanoate. Grades: Highly Purified. CAS No. 161838-87-5. Pack Sizes: 250mg. US Biological Life Sciences. |  Worldwide |
| 1,2,3,6-Tetra-O-acetyl-4-O-[2,4,6-tri-O-acetyl-3-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranosyl)-b-D-galactopyranosyl]-b-D-glucopyranose | 1,2,3,6-Tetra-O-acetyl-4-O-[2,4,6-tri-O-acetyl-3-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranosyl)-b-D-galactopyranosyl]-b-D-glucopyranose is a complex sugar derivative used for the development and synthesis of antiviral drugs. It assists in studying conditions like influenza by inhibiting viral neuraminidase. Molecular formula: C40H55NO26. Mole weight: 965.86. |  |
| 1,2:5,6-Di-O-isopropylidene-3-O-methanesulfonyl-a-D-glucofuranose | 1,2:5,6-Di-O-isopropylidene-3-O-methanesulfonyl-a-D-glucofuranose is a chemical intermediary in the fabrication process of antiviral medicaments. This complex structure can participate in the creation process of neuraminidase repressors. Synonyms: 1,2:5,6-Di-O-isopropylidene-3-O-(methylsulfonyl)-alpha-D-glucofuranose; (3AR,5R,6S,6aR)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-yl methanesulfonate; EINECS 226-675-3; AI3-61546; SCHEMBL5665101; DTXSID901145757; 3-O-Methylsulphonyl-1,2,5,6-di-O-isopropylidene-alpha-D-glucofuranose; MFCD09752163; 1,2:5,6-Di-O-isopropylidene-3-O-methanesulfonyl-alpha-D-glucofuranose; 1.2.5.6-Di-O-isopropylidene-3-O-methylsulfonyl-alpha-D-glucofuranose; D-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene)-, 3-methanesulfonate; alpha-D-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene)-, 3-methanesulfonate; (3AR,5R,6S,6aR)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ylmethanesulfonate; (3aR,5R,6S,6aR)-5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-tetrahydro-2H-furo[2,3-d][1,3]dioxol-6-yl methanesulfonate. CAS No. 5450-26-0. Molecular formula: C13H22O8S. Mole weight: 338.37. | |
| 1,2-Dihydro-oseltamivir | 1,2-Dihydro-oseltamivir is the impurity of the anti-viral drug Oseltamivir Phosphate (O701000), which is an orally active inhibitor of influenza virus neuraminidase. Group: Biochemicals. Grades: Highly Purified. CAS No. 1052063-38-3. Pack Sizes: 10mg, 50mg. Molecular Formula: C16H30N2O4, Molecular Weight: 314.42. US Biological Life Sciences. | Worldwide |
| 1,2'-O-Dimethylguanosine | It is a dimethyl analogue of Guanosine, a purine nucleoside and a novel influenza neuraminidase inhibitor. Synonyms: N1,2'-O-dimethylguanosine; Guanosine, 1-methyl-2'-O-methyl-; 1-Methyl-2'-O-methylguanosine; 2'-O-Methyl-1-methylguanosine. Grades: ≥95%. CAS No. 73667-71-7. Molecular formula: C12H17N5O5. Mole weight: 311.29. | |
| 1,2-O-Isopropylidene-3-deoxy-3-fluoro-a-D-glucofuranose | 1,2-O-Isopropylidene-3-deoxy-3-fluoro-a-D-glucofuranose is an indispensable compound in the synthesis of antiviral drugs, including Oseltamivir and Zanamivir. These drugs have shown to be effective in treating influenza through their ability to inhibit the neuraminidase enzyme, which in turn hinders the release of new viral fragments from infected cells. The employment of 1,2-O-Isopropylidene-3-deoxy-3-fluoro-a-D-glucofuranose in the production of antiviral drugs is a prime example of the intersection between organic chemistry and virology, where complex molecules can serve as the backbone for therapeutic interventions. Synonyms: ALPHA.-D-GLUCOFURANOSE, 3-DEOXY-3-FLUORO-1,2-O-(1-METHYLETHYLIDENE)-; SCHEMBL7610553; 1,2-O-ISOPROPYLIDENE-3-DEOXY-3-FLUORO-A-D-GLUCOFURANOSE; WS-00080; D85294; (R)-1-((3aR,5R,6S,6aS)-6-fluoro-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)ethane-1,2-diol. Molecular formula: C9H15FO5. Mole weight: 222.21. | |
| 1-O-Aminohexyl 3-sialyllactose | 1-O-Aminohexyl 3-sialyllactose is a synthetic iteration of sialic acid-laden oligosaccharides, emerges efficacious in precluding and remediating viral onslaughts. Concurrently, it serves as an inhibitor for neuraminidase. Molecular formula: C29H52N2O19. Mole weight: 732.73. | |
| 1-O-Methyl a-D-rhamnopyranoside | 1-O-Methyl a-D-rhamnopyranoside is a specialized biochemical compound used in the research of influenza, particularly strains resistant to neuraminidase inhibitors. It can also be used in research to study viral attachment and release mechanisms. Synonyms: Methyl 6-deoxy-a-D-mannopyranoside. CAS No. 15814-59-2. Molecular formula: C7H14O5. Mole weight: 178.18. | |
| (1R,5R,6R)-5-(1-Ethylpropoxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Ethyl Ester | This compound is an isomer of compound (E925685) used in the synthesis of neuraminidase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 1266663-89-1. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| (1R,5R,6R)-rel-5-(1-Ethylpropoxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Ethyl Ester | This compound is an isomer of compound (E925685) used in the synthesis of neuraminidase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 1217834-81-5. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| (1R,5S,6R)-Ethyl 5-(Pentan-3-yloxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylate | (1R,5S,6R)-ethyl 5-(pentan-3-yloxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylate is an impurity of Oseltamivir, which is an acetamido cyclohexene that is a structural homolog of sialic acid and inhibits neuraminidase. Synonyms: (1R,5S,6R)-5-(1-Ethylpropoxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Ethyl Ester. CAS No. 2413185-89-2. Molecular formula: C14H22O4. Mole weight: 254.32. | |
| (1R,5S,6S)-rel-5-(1-Ethylpropoxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Methyl Ester | This compound is used in the preparation of azidoalkanes. As well it is an intermediate in the synthesis of neuraminidase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 1234858-94-6. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| (1S)-1,4-Anhydro-1-C-(2,4-difluorophenyl)-D-ribitol | (1S)-1,4-Anhydro-1-C-(2,4-difluorophenyl)-D-ribitol is a chemical compound used in the biomedical industry as an antiviral drug to treat influenza A and B viruses. It works by inhibiting viral neuraminidase, preventing the virus from spreading and multiplying in the body. Synonyms: D-Ribitol, 1,4-anhydro-1-C-(2,4-difluorophenyl)-, (1S)-; 1-Deoxy-1-(2,4-difluorophenyl)-beta-D-ribofuranose; 1-beta-D-Ribofuranosyl-2,4-difluorobenzene; 1'-deoxy-1'-(2,4-difluorophenyl)-beta-D-ribofuranose; (2S,3R,4S,5R)-2-(2,4-difluorophenyl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol. Grades: ≥95%. CAS No. 263701-23-1. Molecular formula: C11H12F2O4. Mole weight: 246.21. | |
| (1S,5R,6R)-5-Hydroxy-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Ethyl Ester | (1S,5R,6R)-5-Hydroxy-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Ethyl Ester is an intermediate in the synthesis of neuraminidase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 876014-27-6. Pack Sizes: 25mg, 250mg. Molecular Formula: C9H12O4. US Biological Life Sciences. | Worldwide |
| (1S, 5R, 6S)-5-(1-n-Propylethoxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Ethyl Ester (Mixture of Diastereomers) | (1S, 5R, 6S)-5-(1-n-Propylethoxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Ethyl Ester is an analog of (1R,5S,6S)-rel-5-(1-Ethylpropoxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Methyl Ester (E925665) which is an intermediate in the synthesis of neuraminidase inhibitors. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 100mg. Molecular Formula: C14H22O4. US Biological Life Sciences. | Worldwide |
| (1S,5R,6S)-5-Isopropoxy-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Ethyl Ester | (1S,5R,6S)-5-Isopropoxy-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Ethyl Ester is an analog of (1R,5S,6S)-rel-5-(1-Ethylpropoxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Methyl Ester (E925665) which is an intermediate in the synthesis of neuraminidase inhibitors. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg, 250mg. Molecular Formula: C12H18O4. US Biological Life Sciences. | Worldwide |
| (1S,5R,6S)-5-sec-Butyloxy-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Ethyl Ester (Mixture of Diastereomers) | (1S,5R,6S)-5-sec-Butyloxy-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Ethyl Ester is an analog of (1R,5S,6S)-rel-5-(1-Ethylpropoxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Methyl Ester (E925665) which is an intermediate in the synthesis of neuraminidase inhibitors. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg, 250mg. Molecular Formula: C13H20O4. US Biological Life Sciences. | Worldwide |
| (1S,5S,6R)-5-Hydroxy-7-oxabicyclo[4.1.0]hept-2-ene-3-carboxylic Acid Ethyl Ester | (1S,5S,6R)-5-Hydroxy-7-oxabicyclo[4.1.0]hept-2-ene-3-carboxylic Acid Ethyl Ester is an intermediate in the synthesis of neuraminidase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 347378-67-0. Pack Sizes: 5mg, 25mg. Molecular Formula: C9H12O4. US Biological Life Sciences. | Worldwide |
| (1S,5S,6S)-5-(Tosyloxy)-7-oxabicyclo[4.1.0]hept-2-ene-3-carboxylic Acid Ethyl Ester | (1S,5S,6S)-5-(Tosyloxy)-7-oxabicyclo[4.1.0]hept-2-ene-3-carboxylic Acid Ethyl Ester is an intermediate in the synthesis of neuraminidase inhibitors. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 25mg. Molecular Formula: C16H18O6S. US Biological Life Sciences. | Worldwide |
| 2,3,5-Tri-O-benzoyl-2-C-methyl-D-ribonic acid-1,4-lactone | 2,3,5-Tri-O-benzoyl-2-C-methyl-D-ribonic acid-1,4-lactone is a biochemical reagent used in the development of antiviral drugs, particularly to research of Influenza. It's a precursor in the creation of inhibitors for neuraminidase, an enzyme integral in disease spread. CAS No. 7392-74-7. Molecular formula: C27H22O8. Mole weight: 474.46. | |
| 2,3-Dehydro-2-deoxy-N-acetylneuraminic acid | N-acetyl-2,3-dehydro-2-Deoxyneuraminic Acid (Neu5Ac2en) is a potent neuraminidase (sialidase) inhibitor. N-acetyl-2,3-dehydro-2-Deoxyneuraminic Acid shows inhibitory activities against human neuraminidase enzymes with IC 50 s of 143, 43, 61, and 74 μM for NEU1, NEU2, NEU3, and NEU4, respectively. Anti-influenza virus activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Neu5Ac2en; DANA. CAS No. 24967-27-9. Pack Sizes: 1 mg; 5 mg. Product ID: HY-125798. | |
| 2-Aminoethyl 5-acetamido-3,5-dideoxy-D-glycero-a-D-galacto-2-nonulopyranosidonic acid | 2-Aminoethyl 5-acetamido-3,5-dideoxy-D-glycero-a-D-galacto-2-nonulopyranosidonic acid, commonly known as AEDDGA, is a significant biomedical compound utilized for treating specific bacterial infections. This remarkable product functions as an effective inhibitor of bacterial neuraminidase enzymes, thereby impeding the release of virus particles from infected cells. The structural resemblance of AEDDGA to sialic acid grants it the ability to competitively bind to the active site of neuraminidase, effectively inhibiting its catalytic activity. Synonyms: (2R,4S,5R,6R)-5-Acetamido-2-(2-aminoethoxy)-4-hydroxy-6-((1R,2R)-1,2,3-trihydroxypropyl)tetrahydro-2H-pyran-2-carboxylic acid. CAS No. 38971-42-5. Molecular formula: C13H24N2O9. Mole weight: 352.34. | |
| 2-Deoxy-2,2-difluoro-D-erythro-pentonic acid gamma-lactone | 2-Deoxy-2,2-difluoro-D-erythro-pentonic acid gamma-lactone, a compound of utmost importance in the realm of biomedicine, demonstrates intricacy and diversity in its applications. Widely utilized in the formulation of antiviral medications, especially targeting influenza A viruses, this compound's distinctive molecular configuration showcases its ability to impede the function of the neuraminidase enzyme, thereby obstructing the discharge of viral offspring. Synonyms: (4S,5S)-3,3-difluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-one; 3,3-DIFLUORO-4-HYDROXY-5-HYDROXYMETHYL-DIHYDRO-FURAN-2-ONE. CAS No. 95058-77-8. Molecular formula: C5H6F2O4. Mole weight: 168.10. | |
| 2-O-Methyl-b-D-N-acetylneuraminic acid | 2-O-Methyl-b-D-N-acetylneuraminic acid is a pharmaceutical compound widely utilized in the biomedical industry, functioning as an efficacious sialic acid analog. It is adept at thwarting the nefarious activity of neuraminidase enzymes. CAS No. 23755-35-3. Molecular formula: C12H21NO9. Mole weight: 323.3. | |
| 2-O-(p-Nitrophenyl)-4,7,8,9-tetra-O-acetyl-α-D-N-acetylglycolylneuraminic Acid Methyl Ester | 2-O-(p-Nitrophenyl)-4,7,8,9-tetra-O-acetyl-α-D-N-acetylglycolylneuraminic Acid Methyl Ester, a biomedicine product, stands as a promising tool in the realm of viral infection prevention and treatment. This compound exhibits remarkable antiviral prowess by thwarting the virulent ambitions of viral neuraminidase enzymes, effectively impeding viral replication. Its potential to counter influenza and other viral afflictions remains under constant scrutiny. Synonyms: N-[2-(Acetyloxy)acetyl]-2-O-(4-nitrophenyl)-α-neuraminic Acid Methyl Ester 4,7,8,9-Tetraacetate. CAS No. 1000890-49-2. Molecular formula: C28H34N2O17. Mole weight: 670.57. | |
| 3,4-O-(Diethylmethylidene) Shikimic Acid Ethyl Ester | 3,4-O-(Diethylmethylidene) Shikimic Acid Ethyl Ester is a reactant used in the preparation of oseltamivir analogs as neuraminidase inhibitors against avian influenza virus. Group: Biochemicals. Alternative Names: (3aR,7R,7aS)-2,2-Diethyl-3a,6,7,7a-tetrahydro-7-hydroxy-1,3-benzodioxole-5-carboxylic Acid Ethyl Ester. Grades: Highly Purified. CAS No. 943515-58-0. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| 3-Aminobenzoic-d4 Acid | A chemoattractants against Pseudomonas strains. A reactant used in the preparation of influenza neuraminidase inhibitors, inhibitors of transthyretin amyloid fibril formation and Iihibitors of the protein chaperone Hsp90. Group: Biochemicals. Alternative Names: 3-Aminobenzenecarboxylic Acid; 3-Carboxyaniline; Aniline-3-carboxylic Acid; NSC 15012; m-Aminobenzoic Acid; m-Anthranilic Acid; m-Carboxyaniline; m-Carboxyphenylamine. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 3-Fluoro-N-acetyl-neuraminic acid | 3-Fluoro-N-acetyl-neuraminic acid is a widely utilized compound, exhibiting inhibitory efficacy against various viral infections, notably influenza viruses. Distinguished for its potent antiviral attributes, it proficiently impedes viral replication. Notably, this acid selectively targets the neuraminidase enzyme within the viral entity, consequently impeding its liberation from the afflicted cells. CAS No. 921-40-4. Molecular formula: C11H18FNO9. Mole weight: 327.26. | |
| 3-Sialyl-D-glucose (α/β mixture) | 3-Sialyl-D-glucose is a synthetic inhibitor of neuraminidase and can selectively block hemagglutinin in influenza and parainfluenza viruses. The blocking of hemagglutinin destroys the cellular adsorption ability of the virus cells and decreases their infectious activity. Synonyms: 3-O-(N-Acetyl-α-neuraminosyl)-D-glucose; O-α-N-Acetyl-D-neuraminosyl-(2 ? 3)-D-glucose. CAS No. 35259-22-4. Molecular formula: C17H29NO14. Mole weight: 471.41. | |
| 4,7,8,9-Tetra-O-acetyl-N-acetyl-2-deoxy-2-fluoro-b-D-neuraminic acid allyl ester | 4,7,8,9-Tetra-O-acetyl-N-acetyl-2-deoxy-2-fluoro-b-D-neuraminic acid allyl ester is an imperative compound widely employed in the development of pharmaceuticals, specifically those targeting neuraminidase enzymes and associated molecular pathways. This compound plays a crucial role in drug development for diverse diseases pertaining to neuraminic acid metabolism. CAS No. 98712-63-1. Molecular formula: C22H30FNO12. Mole weight: 519.47. | |
| 4-methoxyphenyl 3-O-(2-Naphthylmethyl)-4,6-O-Benzylidene-1-α-D-Mannopyranoside | 4-Methoxyphenyl 3-O-(2-Naphthylmethyl)-4,6-O-Benzylidene-1-α-D-Mannopyranoside, an innovative drug candidate, exhibits promise for countering viral ailments, influenza included. Its mechanism entails controlling the viral neuraminidase enzyme - an agent vital to releasing progeny viruses from infected cells. | |
| 4-Methylumbelliferyl N-acetyl-4,7,8,9-tetra-O-acetyl-a-D-neuraminic acid methyl ester | 4-Methylumbelliferyl N-acetyl-4,7,8,9-tetra-O-acetyl-a-D-neuraminic acid methyl ester is an indispensable compound, serving as a vital facilitator within laboratory settings for intricate investigations pertaining to sialic acid metabolism and enzymatic functionalities. Its overwhelming presence primarily revolves around the evaluation of neuraminidase activity, thereby contributing to the comprehensive assessment of the effectiveness of pharmaceutical interventions during viral afflictions, such as influenza. Synonyms: methyl (2S,4S,5S,6R)-5-acetamido-4-acetyloxy-2-[(7-hydroxy-4-methyl-2H-chromen-2-yl)oxy]-6-[(1S,2R)-1,2,3-triacetyloxypropyl]oxane-2-carboxylate; (4-Methylumbelliferyl)-N-acetyl-4,7,8,9-tetra-O-acetyl-alpha-D-neuraminic Acid, Methyl Ester; 4-Methylumbelliferyl N-acetyl-4,7,8,9-tetra-O-acetyl-a-D-neuraminic acid methyl ester; (4-Methylumbelliferyl)-N-acetyl-4,7,8,9-tetra-O-acetyl-a-D-neuraminic acid,methyl ester. CAS No. 59361-08-9. Molecular formula: C30H35NO15. Mole weight: 649.6. | |
| 4-Methylumbelliferyl N-acetyl-a-D-neuraminic acid ammonium salt | 4-Methylumbelliferyl N-acetyl-α-D-neuraminic acid ammonium salt is a potent compound widely employed in the biomedical sector, serving as an indispensable tool for studying the intricate intricacies of neuraminic acid's metabolism and functionality. In the realm of scientific quests, it flawlessly acts as an exquisite substrate is allowing meticulous detection and quantification of neuraminidase activity across diverse research realms. Molecular formula: C20H23NO11.NH4. Mole weight: 471.44. | |
| 4-Methylumbelliferyl-N-acetyl-a-D-neuraminide ammonium salt | 4-Methylumbelliferyl-N-acetyl-a-D-neuraminide ammonium salt is a prominent and astoundingly potent biochemical substance, acting as a substrate, permitting the robust detection and quantification of neuraminidase activity. Synonyms: 4-Methylumbelliferyl NANA 4-MU NANA. | |
| 4-Methylumbelliferyl-N-acetyl-α-D-neuraminic acid sodium salt | 4-Methylumbelliferyl-N-acetyl-α-D-neuraminic acid is a fluorogenic substrate for fluorometric assay of neuraminidase. It is cleaved by neuraminidases to release the fluorescence moiety 4-methylumbelliferyl (4-MU). Synonyms: 4-MUNANA; Neu5Ac-α-4MU; Sodium 2-(4-methylumbelliferyl)-N-acetylneuraminate; 4-methyl-2-oxo-2H-1-benzopyran-7-yl 5-(acetylamino)-3,5-dideoxy-α-neuraminic acid, monosodium salt. Grades: ≥98%. CAS No. 76204-02-9. Molecular formula: C21H24NNaO11. Mole weight: 489.4. | |
| 5-Acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-2-S-adamantanyl-2-thio-α-neuraminic Acid Methyl Ester | 5-Acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-2-S-adamantanyl-2-thio-α-neuraminic Acid Methyl Ester is a remarkable biomedical compound, exhibiting its efficacy in research of combatting diverse viral ailments. Functioning as an impeccable sialic acid analogue, this compound exhibits the prowess to obstruct the enzymatic functionality of neuraminidase. Synonyms: (1S,2R)-1-((3aR,4R,6R,7aS)-3-Acetyl-6-(adamantan-1-ylthio)-6-(methoxycarbonyl)-2-oxohexahydro-2H-pyrano[3,4-d]oxazol-4-yl)propane-1,2,3-triyl triacetate; 2-[(1-Adamantyl)thio]-4-O,N-carbonyl-N,7-O,8-O,9-O-tetraacetyl-2-deoxy-beta-neuraminic acid methyl ester. Grades: 98%. CAS No. 956107-32-7. Molecular formula: C29H39NO12S. Mole weight: 625.7. | |
| 7,3',4'-Trihydroxy-3-Benzyl-2H-Chromene | 7,3',4'-Trihydroxy-3-benzyl-2H-chromene is an reversible noncompetitive neuraminidase (NA) inhibitor. 7,3',4'-Trihydroxy-3-benzyl-2H-chromene can be isolated from the dried heartwood of Caesalpinia sappan L. 7,3',4'-Trihydroxy-3-benzyl-2H-chromene has potent NAs inhibitory activities with IC50 values of 34.6 μM [H1N1], 39.5 μM [H3N2], and 50.5μM [H9N2], respectively. 7,3',4'-Trihydroxy-3-benzyl-2H-chromene can be used for the research of influenza virus. Group: Inhibitors. CAS No. 1111897-60-9. Molecular formula: C16H14O4. Mole weight: 270.3. Appearance: Powder. Purity: 0.98. IUPACName: 4-[(7-hydroxy-2H-chromen-3-yl)methyl]benzene-1,2-diol. Canonical SMILES: C1C (=CC2=C (O1)C=C (C=C2)O)CC3=CC (=C (C=C3)O)O. Catalog: ACM1111897609. |  |
| α-Glucosidase from Escherichia coli, Recombinant | Glycoside hydrolases (also called glycosidases or glycosyl hydrolases) assist in the hydrolysis of glycosidic bonds in complex sugars. They are extremely common enzymes with roles in nature including degradation of biomass such as cellulose and hemicellulose, in anti-bacterial defense strategies (e.g., lysozyme), in pathogenesis mechanisms (e.g., viral neuraminidases) and in normal cellular function (e.g., trimming mannosidases involved in N-linked glycoprotein biosynthesis). Together with glycosyltransferases, glycosidases form the major catalytic machinery for the synthesis and breakage of glycosidic bonds. Group: Enzymes. Synonyms: Alpha-glucosidase; EC 3.2.1.20; maltase; glucoinvertase; glucosidosucra. Enzyme Commission Number: EC 3.2.1.20. CAS No. 9001-42-7. Purity: > 95 % as judged by SDS-PAGE. α-Glucosidase. Mole weight: 72992.3 Da. Activity: 34.1 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Escherichia coli str. K-12 substr. W3110. Alpha-glucosidase; EC 3.2.1.20; maltase; glucoinvertase; glucosidosucrase; maltase-glucoamylase; alpha-glucopyranosidase; glucosidoinvertase; alpha-D-glucosidase; alpha-glucoside hydrolase; alpha-1,4-glucosidase; alpha-D-glucoside glucohydrolase; glycosidases; glycosyl hydrolases; α-Glucosidase. Cat No: NATE-1177. | |
| Aurintricarboxylic acid | Aurintricarboxylic acid is a nanomolar-potency, allosteric antagonist with selectivity towards αβ-methylene-ATP-sensitive P2X1Rs and P2X3Rs , with IC 50 s of 8.6 nM and 72.9 nM for rP2X1R and rP2X3R, respectively [1]. Aurintricarboxylic acid is a potent anti-influenza agent by directly inhibiting the neuraminidase [2]. Aurintricarboxylic acid is an inhibitor of topoisomerase II and apoptosis [3]. Aurintricarboxylic acid is a selective inhibitor of the TWEAK-Fn14 signaling pathway [4]. Aurintricarboxylic acid also acts as a cystathionine-lyase (CSE) inhibitor with an IC 50 of 0.6 μM [5]. Aurintricarboxylic acid is a modifier of miRNAs that regulate miRNA function, with an IC 50 of 0.47 μM [6]. Uses: Scientific research. Group: Signaling pathways. CAS No. 4431-00-9. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-122575. | |
| Aurintricarboxylic Acid | Aurintricarboxylic acid is a nanomolar-potency, allosteric antagonist with selectivity towards αβ-methylene-ATP-sensitive P2X1Rs and P2X3Rs, with IC50s of 8.6 nM and 72.9 nM for rP2X1R and rP2X3R, respectively. Aurintricarboxylic acid is a potent anti-influenza agent by directly inhibiting the neuraminidase. Aurintricarboxylic acid is an inhibitor of topoisomerase II and apoptosis. Aurintricarboxylic acid is a selective inhibitor of the TWEAK-Fn14 signaling pathway. Aurintricarboxylic acid also acts as a cystathionine-lyase (CSE) inhibitor with an IC50 of 0.6 μM. Aurintricarboxylic acid is a modifier of miRNAs that regulate miRNA function, with an IC50 of 0.47 μM. Group: Inhibitors. Alternative Names: Ata. CAS No. 4431-00-9. Molecular formula: C22H14O9. Mole weight: 422.34. Appearance: Powder. Purity: 0.85. Canonical SMILES: C1=CC (=C (C=C1C (=C2C=CC (=O)C (=C2)C (=O)O)C3=CC (=C (C=C3)O)C (=O)O)C (=O)O)O. Catalog: ACM4431009. | |
| Benzyl 2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside | Benzyl 2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside is a reactant used in the preparation of oligosaccharide and glucosamine containing peptides used as inhibitors of influenza virus neuraminidase. Synonyms: Phenylmethyl 2-(Acetylamino)-2-deoxy-3,4,6-tris-O-(phenylmethyl)-β-D-glucopyranoside. CAS No. 4171-69-1. Molecular formula: C36H39NO6. Mole weight: 581.7. | |
| Coptisine chloride | Coptisine chloride is an alkaloid from Chinese goldthread, and acts as an efficient uncompetitive IDO inhibitor with a Ki value of 5.8 μM and an IC50 value of 6.3 μM. Coptisine chloride is a potent H1N1 neuraminidase (NA-1) inhibitor with an IC50 of 104.6?μg/mL and can be used for influenza A (H1N1) infection. Group: Inhibitors. Alternative Names: 6,7-Dihydrobis[1,3]benzodioxolo[5,6-a:4',5'-g]quinolizinium chloride. CAS No. 6020-18-4. Molecular formula: C19H14ClNO4. Mole weight: 355.77. Appearance: Yellow powder. Purity: 0.98. IUPACName: 5, 7, 17, 19-Tetraoxa-13-azoniahexacyclo[11.11.0.02, 10.04, 8.015, 23.016, 20]tetracosa-1(13), 2, 4(8), 9, 14, 16(20), 21, 23-octaene;chloride. Canonical SMILES: C1C[N+]2=C (C=C3C=CC4=C (C3=C2)OCO4)C5=CC6=C (C=C51)OCO6. [Cl-]. Catalog: ACM6020184. | |
| Coptisine chloride | Coptisine chloride is an alkaloid from Chinese goldthread, and acts as an efficient uncompetitive IDO inhibitor with a K i value of 5.8 μM and an IC 50 value of 6.3 μM. Coptisine chloride is a potent H1N1 neuraminidase (NA-1) inhibitor with an IC 50 of 104.6 μg/mL and can be used for influenza A (H1N1) infection. Uses: Scientific research. Group: Natural products. CAS No. 6020-18-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-N0736. | |
| Cyanidin-3-O-sambubioside chloride | Cyanidin 3-sambubioside chloride (Cyanidin-3-O-sambubioside chloride), a major anthocyanin, a natural colorant, and is a potent NO inhibitor. Cyanidin 3-sambubioside chloride is a H274Y mutation inhibitor, and inhibits influenza neuraminidase activity with an IC50 of 72 μM. Cyanidin 3-sambubioside chloride inhibits angiotensin-converting enzyme (ACE) activity and has antioxidant, anti-angiogenic and antiviral properties. Synonyms: 33012-73-6|Cyanidin-3-O-sambubioside chloride|UNII-4BIT5WSL15|4BIT5WSL15|CYANIDIN-3-SAMBUBIOSIDE|Cyanidin 3-sambubioside (chloride)|Cyanidin 3-sambubioside|(2S,3R,4S,5R)-2-[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol;chloride|cyanidin-3-O-sambubioside|3-(((2S,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium chloride|cyanidin 3-O- (2-O-xylopyranosylglycopyranoside) |cyanidin 3-sambubioside chloride|HY-N2533|3,5,7,3',4'-Pentahydroxyflavylium-3-O-beta-D-xylopyranosyl-(1-2)-beta-D-glucopyranoside|CS-0022804|Q9333097|1-Benzopyrylium, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy)-, chloride. Grades: >98%. CAS No. 33012-73-6. Molecular formula: C26H29O15Cl. Mole weight: 616.95. | |
| Cyanidin 3-sambubioside chloride | Cyanidin 3-sambubioside chloride (Cyanidin-3-O-sambubioside chloride), a major anthocyanin, a natural colorant, and is a potent NO inhibitor. Cyanidin 3-sambubioside chloride is a H274Y mutation inhibitor, and inhibits influenza neuraminidase activity with an IC 50 of 72 μM. Cyanidin 3-sambubioside chloride inhibits angiotensin-converting enzyme (ACE) activity and has antioxidant, anti-angiogenic and antiviral properties [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Cyanidin-3-O-sambubioside chloride. CAS No. 33012-73-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N2533. | |
| Dehydrocorybulbine chloride | Dehydrocorybulbine chloride is an isoquinoline alkaloid with neuraminidase (NA) inhibitory activity. Dehydrocorybulbine chloride can be isolated from the 95% ethanol extract of the rhizome of Viola odorata [1]. Uses: Scientific research. Group: Natural products. CAS No. 59870-72-3. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N8262. | |
| Diethoxy phosphonyl 4,7,8,9-tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester | Diethoxy phosphonyl 4,7,8,9-tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester is a biomedical product exhibiting potential in inhibiting neuraminidase enzymes involved in viral infection, particularly the influenza virus. | |
| ent-Oseltamivir Phosphate | ent-Oseltamivir Phosphate is the enatiomer of Oseltamivir Phosphate, which is a prodrug of the influenza neuraminidase inhibitor Oseltamivir. Synonyms: (3S,4S,5R)-4-(Acetylamino)-5-amino-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylic acid ethyl ester phosphate; 1-Cyclohexene-1-carboxylic acid, 4-(acetylamino)-5-amino-3-(1-ethylpropoxy)-, ethyl ester, (3S,4S,5R)-, phosphate (1:1); (3S,4S,5R)-Ethyl 4-acetamido-5-amino-3-(pentan-3-yloxy)cyclohex-1-enecarboxylate phosphate. Grades: ≥95%. CAS No. 1035895-89-6. Molecular formula: C16H31N2O8P. Mole weight: 410.40. | |
| ethyl (1R,2R,3S,4R,5S)-4-acetamido-5-amino-2-azido-3-(pentan-3-yloxy)cyclohexane-1-carboxylate | ethyl (1R,2R,3S,4R,5S)-4-acetamido-5-amino-2-azido-3-(pentan-3-yloxy)cyclohexane-1-carboxylate is an impurity of Oseltamivir, which is an acetamido cyclohexene that is a structural homolog of sialic acid and inhibits neuraminidase. CAS No. 2124269-41-4. Molecular formula: C16H29N5O4. Mole weight: 355.44. | |
| exo-α-sialidase | The enzyme does not act on 4-O-acetylated sialic acids. endo-α-Sialidase activity is listed as EC 3.2.1.129, endo-α-sialidase. See also EC 4.2.2.15 anhydrosialidase. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase. Enzyme Commission Number: EC 3.2.1.18. CAS No. 9001-67-6. Neuraminidase. 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-3863; exo-α-sialidase; EC 3.2.1.18; 9001-67-6; neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase. Cat No: EXWM-3863. | |
| Ganoderic Acid Tr | Ganoderic acid TR is a broad-spectrum inhibitor against influenza neuraminidases (NAs), particularly H5N1 and H1N1 neuraminidases. The IC50 values of 10.9 and 4.6 μM, respectively. Group: Inhibitors. CAS No. 862893-75-2. Molecular formula: C30H44O4. Mole weight: 468.7. Appearance: Powder. Purity: 0.98. IUPACName: (E,6R)-6-[(10S,13R,14R,15S,17R)-15-hydroxy-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,12,15,16,17-octahydrocyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid. Canonical SMILES: CC (CCC=C (C)C (=O)O)C1CC (C2 (C1 (CC=C3C2=CCC4C3 (CCC (=O)C4 (C)C)C)C)C)O. Catalog: ACM862893752. | |
| Koaburaside | Koaburaside is a cytoprotective and anti-inflammatory natural compound. Koaburaside shows antioxidant activity with an IC50 of 9.0 μM for DPPH-free radical scavenging assay. Koaburaside inhibits histamine release and expressions of IL-6 and TNF-α in human mast cells. Koaburaside also effectively inhibits influenza A neuraminidase. Group: Inhibitors. CAS No. 41653-73-0. Molecular formula: C14H20O9. Mole weight: 332.3. Appearance: Powder. Purity: 0.98. IUPACName: (2S,3R,4S,5S,6R)-2-(4-hydroxy-3,5-dimethoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol. Canonical SMILES: COC1=CC (=CC (=C1O)OC)OC2C (C (C (C (O2)CO)O)O)O. Catalog: ACM41653730. | |
| Laninamivir | Laninamivir (R 125489) is a potent influenza neuraminidase (NA) inhibitor with IC 50 s of 0.90 nM, 1.83 nM and 3.12 nM for avian H12N5 NA (N5), pH1N1 N1 NA (p09N1) and A/RI/5+/1957 H2N2 N2 (p57N2), respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R 125489. CAS No. 203120-17-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14818. | |
| Laninamivir | Laninamivir (R 125489) is a potent influenza neuraminidase (NA) inhibitor with IC50s of 0.90 nM, 1.83 nM and 3.12 nM for avian H12N5 NA (N5), pH1N1 N1 NA (p09N1) and A/RI/5+/1957 H2N2 N2 (p57N2), respectively. Uses: Antiviral agents. Synonyms: 5-(Acetylamino)-4-[(aminoiminomethyl)amino]-2,6-anhydro-3,4,5-trideoxy-7-O-methyl-D-glycero-D-galacto-non-2-enonic acid; R 125489; (4S,5R,6R)-5-Acetamido-4-guanidino-6-((1R,2R)-2,3-dihydroxy-1-methoxypropyl)-5,6-dihydro-4H-pyran-2-carboxylic acid. Grades: 99.91%. CAS No. 203120-17-6. Molecular formula: C13H22N4O7. Mole weight: 346.34. | |
| Laninamivir octanoate | Laninamivir octanoate (CS-8958), a proagent of Laninamivir, is a long-acting neuraminidase (NA) inhibitor with anti-influenza virus activity. Laninamivir octanoate shows anti-influenza activity against Oseltamivir-resistant viruses, and also against the pandemic influenza viruses [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CS-8958. CAS No. 203120-46-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14818A. | |
| Laninamivir octanoate | Laninamivir octanoate (CS-8958, R-118958, Inavir, LANI), a prodrug of Laninamivir (R-125489), is a long-acting neuraminidase (NA) inhibitor with superior anti-influenza virus activity. Synonyms: 5-(Acetylamino)-4-[(aminoiminomethyl)amino]-2,6-anhydro-3,4,5-trideoxy-7-O-methyl-D-glycero-D-galacto-non-2-enonic acid 9-octanoate; (2R,3R,4S)-3-Acetamido-4-guanidino-2-[(1R,2R)-2-hydroxy-1-methoxy-3-(octanoyloxy)propyl]-3,4-dihydro-2H-pyran-6-carboxylic acid; (4S,5R,6R)-5-Acetamido-4-guanidino-6-[(1R,2R)- 2-hydroxy-1-methoxy-3-(octanoyloxy)propyl]-5,6-dihydro-4H-pyran-2-carboxylic acid; CS 8958. Grades: ≥98% (HPLC). CAS No. 203120-46-1. Molecular formula: C21H36N4O8. Mole weight: 472.53. | |
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