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| Product | Description | |
|---|---|---|
| Arabinocytosine | Arabinocytosine. Group: Biochemicals. CAS No. 147-94-4. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| arabinofuranan 3-O-arabinosyltransferase | Isolated from Mycobacterium smegmatis. Involved in the formation of the cell wall in mycobacteria. Group: Enzymes. Synonyms: AftC. Enzyme Commission Number: EC 2.4.2.47. 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-2676; arabinofuranan 3-O-arabinosyltransferase; EC 2.4.2.47; AftC. Cat No: EXWM-2676. |  |
| Arabinofuranosidase 43A from Bacteroides ovatus, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducin. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 56 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides ovatus. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43A. Cat No: NATE-1312. | |
| Arabinofuranosidase 43A from Bacteroides thetaiotaomicron, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabino. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 32.5 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43A. Cat No: NATE-1321. | |
| Arabinofuranosidase 43A from Cellvibrio japonicus, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-re. Enzyme Commission Number: EC 3.2.1.-. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 39.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Cellvibrio japonicus. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43A. Cat No: NATE-1320. | |
| Arabinofuranosidase 43A from Clostridium stercorarium, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-a. Enzyme Commission Number: EC 3.2.1.55 & EC 3.2.1.37. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 39.1 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium stercorarium. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43A. Cat No: NATE-1314. | |
| Arabinofuranosidase 43A from Streptomyces avermitilis, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranosid. Enzyme Commission Number: EC 3.2.1.-. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 36.4 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium stercorarium. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43A. Cat No: NATE-1315. | |
| Arabinofuranosidase 43B from Bacteroides ovatus, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducin. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 64 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides ovatus. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43B. Cat No: NATE-1311. | |
| Arabinofuranosidase 43B from Bacteroides thetaiotaomicron, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabino. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 36.5 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43B. Cat No: NATE-1322. | |
| Arabinofuranosidase 43B from Clostridium thermocellum, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranosi. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 36.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium thermocellum. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43B. Cat No: NATE-1316. | |
| Arabinofuranosidase 43C from Bacteroides ovatus, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducin. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 50 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides ovatus. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43C. Cat No: NATE-1310. | |
| Arabinofuranosidase 43C from Bacteroides thetaiotaomicron, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabino. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 40.4 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43C. Cat No: NATE-1323. | |
| Arabinofuranosidase 43D from Bacteroides ovatus, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducin. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 66 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides ovatus. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43D. Cat No: NATE-1309. | |
| Arabinofuranosidase 43D from Bacteroides thetaiotaomicron, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinof. Enzyme Commission Number: EC 3.2.1.-. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 35.6 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43D. Cat No: NATE-1319. | |
| Arabinofuranosidase 43E from Bacteroides ovatus, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducin. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 52 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides ovatus. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 43E. Cat No: NATE-1313. | |
| Arabinofuranosidase 51A from Clostridium thermocellum, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alp. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 58.7 kDa. Activity: 125 U/mg. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium thermocellum. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 51A. Cat No: NATE-1324. | |
| Arabinofuranosidase 51A from Podospora anserina, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducin. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 86 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Podospora anserina. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 51A. Cat No: NATE-1317. | |
| Arabinofuranosidase 62A from Ustilago maydis, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end . Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 37 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Ustilago maydis. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 62A. Cat No: NATE-1318. | |
| Arabinofuranosyl-2,6-diamino-purine | Arabinofuranosyl-2,6-diamino-purine, a potent antiviral agent, is indicated for the prevention and treatment of viral infections such as herpes simplex, varicella-zoster virus, and hepatitis B. This drug acts by impeding synthesis of viral DNA, effectively suppressing replication of the virus. Recommended for intravenous administration, Arabinofuranosyl-2,6-diamino-purine is particularly useful in immunocompromised patients, especially those suffering from HIV/AIDS, who are at greater risk of succumbing to viral infections. Synonyms: 2,6-diaminopurine arabinoside; 9-(β-D-Arabinofuranosyl)-2,6-diaminopurine. Grades: ≥ 99%. Molecular formula: C10H14N6O4. Mole weight: 282.25. |  |
| Arabinofuranosyl-6-benzylamino-purine | Arabinofuranosyl-6-benzylamino-purine is a highly antiviral compound, finding extensive applications in a wide range of ailments including leukemia and solid tumors. Thus, it standing as an invaluable compound for scientific investigations and the development of pharmaceutical interventions within the dynamic realm of compound. Synonyms: 6-Benzylaminopurine arabinoside; 9-(β-D-Arabinofuranosyl)-6-benzylaminopurine. Grades: ≥ 99%. Molecular formula: C17H19N5O4. Mole weight: 357.36. | |
| Arabinofuranosylcytosine-5'-triphosphate (triethylammonium salt form) | The triethylammonium salt form of Ara-CTP. Ara-CTP is a nucleotide that can be used as an antimetabolic agent to inhibit the synthesis of DNA. Synonyms: Ara-CTP (triethylammonium salt form); Cytosine arabinoside triphosphate triethylammonium; Arabinosylcytosine triphosphate triethylammonium; Arabinofuranosylcytosine triphosphate triethylammonium; Cytosine arabinoside 5'-triphosphate triethylammonium; Arabinosylcytosine 5'-triphosphate triethylammonium. Grades: ≥ 90% by HPLC, Concentration ~ 12 mM. Molecular formula: C9H16N3O14P3.C6H15N. Mole weight: 483.159 (free acid). | |
| Arabinofuranosyl-guanine (ara-G) | Arabinofuranosyl-guanine (ara-G) is an inhibitor of DNA synthesis used as an antimetabolic and antineoplastic agent. Synonyms: Arabinosylguanine; 2-Amino-9-β-D-arabinofuranosyl-1,9-dihydro-6H-purin-6-one; 2-Amino-6-hydroxy-9-(β-D-arabinofuranosyl)purine; 9-β-D-Arabinofuranosylguanine; Araguanosine; Guanine arabinoside; NSC 76352; ara-Guanosine. Grades: ≥98% by HPLC. CAS No. 38819-10-2. Molecular formula: C10H13N5O5. Mole weight: 283.24. | |
| Arabinofuranosyl-hypoxanthine (ara-HX) | Arabinofuranosyl-hypoxanthine (ara-HX) is a prodrug of Vidarabine for improving the oral bioavailability, which is an antiviral drug. Uses: Antiviral agents. Synonyms: Hypoxanthine arabinoside; 9-(β-D-Arabinofuranosyl)-hypoxanthine; 9-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one; 9-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one. Grades: ≥ 99%. CAS No. 7013-16-3. Molecular formula: C10H12N4O5. Mole weight: 268.22. | |
| Arabinofuranosyl-isoguanine | Arabinofuranosyl-isoguanine is a nucleoside analog used as an antiviral drug to treat herpes simplex virus type 1 and 2 infections. It works by inhibiting viral DNA synthesis, thus preventing the virus from replicating and spreading. Synonyms: 9-(β-D-Arabinofuranosyl)-isoguanine. Grades: ≥ 98%. Molecular formula: C10H13N5O5. Mole weight: 283.24. | |
| Arabinogalactan | Larch arabinogalactan is used for infections, including the common cold, flu, H1N1 (swine) flu, ear infections in children, and HIV/AIDS. It is also used to treat liver cancer, as well as a brain condition caused by liver damage (hepatic encephalopathy). Group: Material of health food. CAS No. 9036-66-2. Molecular formula: C20H36O14. Mole weight: 500.5g/mol. Appearance: white powder. IUPACName: 4-[6-[(3,5-dihydroxy-4-methoxyoxan-2-yl)oxymethyl]-3,5-dihydroxy-4-methoxyoxan-2-yl]oxy-2-(hydroxymethyl)-6-methyloxane-3,5-diol. Canonical SMILES: CC1C (C (C (C (O1)CO)O)OC2C (C (C (C (O2)COC3C (C (C (CO3)O)OC)O)O)OC)O)O. ECNumber: 232-910-0. Catalog: ACM9036662. |  |
| Arabinogalactan | Larch arabinogalactan is used for infections, including the common cold, flu, H1N1 (swine) flu, ear infections in children, and HIV/AIDS. It is also used to treat liver cancer, as well as a brain condition caused by liver damage (hepatic encephalopathy). Group: Polymers. CAS No. 9036-66-2. Product ID: 4-[6-[(3,5-dihydroxy-4-methoxyoxan-2-yl)oxymethyl]-3,5-dihydroxy-4-methoxyoxan-2-yl]oxy-2-(hydroxymethyl)-6-methyloxane-3,5-diol. Molecular formula: 500.5g/mol. Mole weight: C20H36O14. CC1C (C (C (C (O1)CO)O)OC2C (C (C (C (O2)COC3C (C (C (CO3)O)OC)O)O)OC)O)O. InChI=1S/C20H36O14/c1-7-11 (23)18 (12 (24)9 (4-21)32-7)34-20-15 (27)17 (29-3)13 (25)10 (33-20)6-31-19-14 (26)16 (28-2)8 (22)5-30-19/h7-27H, 4-6H2, 1-3H3. SATHPVQTSSUFFW-UHFFFAOYSA-N. |  |
| ARABINOGALACTAN | ARABINOGALACTAN. Synonyms: STRACTAN; POLYARABINOGALACTAN; Galactoarabinan; d-galacto-l-arabinan; FEMA 3254; LARCOLL(TM); (+)-ARABINOGALACTAN; ARABINOGALACTAN. CAS No. 9036-66-2. Pack Sizes: 1 kg. Product ID: CDF4-0156. Molecular formula: C20H36O14. Category: Stabilizers and Thickeners. Product Keywords: Food Ingredients; Stabilizers and Thickeners; ARABINOGALACTAN; CDF4-0156; 9036-66-2; C20H36O14; 232-910-0; 9036-66-2. Purity: 0.99. Color: White to Pale Beige. EC Number: 232-910-0. Physical State: lyophilized Powder. Solubility: H2O: 50 mg/mL, clear to slightly hazy, faintly yellow. Storage: 2-8°C. Melting Point: >200 °C (dec.)(lit.). |  |
| arabinogalactan endo-β-1,4-galactanase | This enzyme, isolated from the bacterium Bacillus subtilis, hydrolyses the β(1?4) bonds found in type I plant arabinogalactans, which are a component of the primary cell walls of dicots. The predominant product is a tetrasaccharide. cf. EC 3.2.1.181, galactan endo-β-1,3-galactanase. Group: Enzymes. Synonyms: endo-1,4-β-galactanase; galactanase (ambiguous); arabinogalactanase; ganB (gene name). Enzyme Commission Number: EC 3.2.1.89. CAS No. 58182-40-4. endo-1,4-β-Galactanase. 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-3953; arabinogalactan endo-β-1,4-galactanase; EC 3.2.1.89; 58182-40-4; endo-1,4-β-galactanase; galactanase (ambiguous); arabinogalactanase; ganB (gene name). Cat No: EXWM-3953. | |
| Arabinoisocytidine | Arabinoisocytidine: A pioneering compound widely utilized in the biomedical sector due to its remarkable potential in combating diverse viral infections and cancers. With its role as a nucleoside analog, Arabinoisocytidine showcases commendable antiviral and antitumor properties by obstructing viral DNA replication and instigating apoptosis within malignant cells. Synonyms: 2-Amino-1-((2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-4(1H)-one; 2'beta-Hydroxy-2'-deoxy-2-amino-2-deoxo-2,3-didehydrouridine; NSC 529488; 2-Amino-1-(β-D-arabinofuranosyl)-4(1H)-pyrimidinone. Grades: ≥95%. CAS No. 10212-30-3. Molecular formula: C9H13N3O5. Mole weight: 243.22. | |
| arabinonate dehydratase | This enzyme belongs to the family of lyases, specifically the hydro-lyases, which cleave carbon-oxygen bonds. Group: Enzymes. Synonyms: D-arabinonate hydro-lyase. Enzyme Commission Number: EC 4.2.1.5. CAS No. 9024-36-6. 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-5039; arabinonate dehydratase; EC 4.2.1.5; 9024-36-6; D-arabinonate hydro-lyase. Cat No: EXWM-5039. | |
| Arabinose | Arabinose is an endogenous metabolite. Uses: Scientific research. Group: Natural products. Alternative Names: (±)?-Arabinose; DL-Arabinose; dl-Arabinose. CAS No. 147-81-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-N2353. |  |
| arabinose-5-phosphate isomerase | The enzyme is involved in the pathway for synthesis of 3-deoxy-D-manno-octulosonate (Kdo), a component of bacterial lipopolysaccharides and plant call walls. Group: Enzymes. Synonyms: kdsD (gene name); gutQ (gene name); arabinose phosphate isomerase; phosphoarabinoisomerase; D-arabinose-5-phosphate ketol-isomerase. Enzyme Commission Number: EC 5.3.1.13. CAS No. 9023-86-3. 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-5454; arabinose-5-phosphate isomerase; EC 5.3.1.13; 9023-86-3; kdsD (gene name); gutQ (gene name); arabinose phosphate isomerase; phosphoarabinoisomerase; D-arabinose-5-phosphate ketol-isomerase. Cat No: EXWM-5454. | |
| Arabinosylhypoxanthine | Arabinosylhypoxanthine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis , etc [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 7013-16-3. Pack Sizes: 5 mg. Product ID: HY-113431. | |
| Arabinosyluridine-5'-triphosphate (triethylammonium salt form) | An impurity of UTP. UTP is a pyrimidine nucleoside triphosphate as a substrate in the biosynthesis of RNA. Synonyms: Ara-UTP (triethylammonium salt form); Arabinofuranosyluridine triphosphate triethylammonium; 2'ara-UTP triethylammonium. Grades: 95%. Molecular formula: C9H15N2O15P3.C6H15N. Mole weight: 484.144 (free acid). | |
| Arabinoxylan | Arabinoxylan is a form of the hemicellulose xylan found in both the primary and secondary cell walls of plants which in addition to xylose contains substantial amounts of another pentose sugar, arabinose. Group: Plant fiber component. CAS No. 9040-27-1. Purity: 99%+(HPLC). Catalog: ACM9040271. | |
| Arabinoxylan | Arabinoxylan is a multifaceted and remarkable natural polysaccharide originating from botanical sources is arabinoxylan manifesting immense potential within the biomedical arena. Its scientifically substantiated anti-inflammatory prowess coupled with its unrivaled antioxidant attributes render it an invaluable asset in combatting a myriad of afflictions. CAS No. 9040-27-1. Molecular formula: C40H64O32. | |
| Arabinoxylan arabinofuranohydrolase from Bacillus subtilis, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosida. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: > 95 % as judged by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 53852.8 Da. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Bacillus subtilis subsp. subtilis str. 168. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase. Cat No: NATE-1199. | |
| Arabinoxylanase 5A from Clostridium thermocellum, Recombinant | A group of enzymes that catalyze the hydrolysis of alpha- or beta-xylosidic linkages. Group: Enzymes. Synonyms: arabinoxylanase; EC 3.2.1.-. Enzyme Commission Number: EC 3.2.1.-. Purity: >90% as judged by SDS-PAGE. Arabinoxylanase. Mole weight: 94.5 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium thermocellum. arabinoxylanase; EC 3.2.1.-. Cat No: NATE-1517. | |
| Arabinoxylan (Medium viscosity) | Arabinoxylan is the main group of hemicellulosic polysaccharides that are present in the cell walls of monocot grass crops. Arabinoxylan consist of a backbone of β-(1→4)-linked xylopyranosyl residues [1]. Uses: Scientific research. Group: Natural products. CAS No. 9040-27-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N15135. | |
| 1-13C-L-Arabinose | | |
| 1,1-Di-C-allyl-2-O-benzyl-3,4-di-O-isopropylidene-2,4-di-C-methyl-L-arabinopyranose | 1,1-Di-C-allyl-2-O-benzyl-3,4-di-O-isopropylidene-2,4-di-C-methyl-L-arabinopyranose, a compound of utmost significance in the biomedical sector, showcases remarkable potential in combating a multitude of ailments, such as cancer and inflammation. Its utilization in the development of revolutionary drugs and therapies, owing to its intricate configuration and distinctive attributes, offers hope for addressing these conditions in pioneering ways. This compound emerges as an indispensable asset in the pursuit of advanced medicinal interventions and inventive treatment modalities. | |
| 1,2:3,4-Di-O-isopropylidene-b-D-arabinopyranose | 1,2:3,4-Di-O-isopropylidene-b-D-arabinopyranose is a bio-compound frequently utilized in crafting selective glycosides. Synonyms: (3aS,5aR,8aR,8bS)-2,2,7,7-Tetramethyltetrahydro-3aH-bis[1,3]dioxolo[4,5-b:4',5'-d]pyran; β-D-Arabinopyranose, 1,2:3,4-bis-O-(1-methylethylidene)-. CAS No. 20881-03-2. Molecular formula: C11H18O5. Mole weight: 230.26. | |
| 1,2:3,4-Di-O-isopropylidene-b-L-arabinopyranose | 1,2:3,4-Di-O-isopropylidene-b-L-arabinopyranose is a highly sought-after compound within the biomedical sector due to its widespread utility in the research of carbohydrate-derived therapeutics, often tailored towards combating malignant neoplasms, metabolic disorders, and circulatory impairments. Synonyms: 1,2:3,4-Bis-O-(1-methylethylidene)-beta-L-arabinopyranose; beta-L-Arabinopyranose, 1,2:3,4-bis-O-(1-methylethylidene)-; 1-O,2-O:3-O,4-O-Diisopropylidene-beta-L-arabinopyranose; (3aR,5aS,8aS,8bR)-2,2,7,7-Tetramethyltetrahydro-3aH-bis[1,3]dioxolo[4,5-b:4',5'-d]pyrane. Grades: ≥95%. CAS No. 27820-98-0. Molecular formula: C11H18O5. Mole weight: 230.26. | |
| 1,2:3,4-Di-O-isopropylidene-L-arabinopyranose | 1,2:3,4-Di-O-isopropylidene-L-arabinopyranose, a chemical compound, presents immense possibilities in the pharmaceutical and biotechnology domains, given its significant contribution towards the synthesis of diversified drug and molecular structures. Remarkably, this compound emerges as a crucial ingredient in the creation of nucleoside derivatives and a perfect precursor to the production of anti-viral drugs. Molecular formula: C11H18O5. Mole weight: 230.26. | |
| 1,2,3,4-Tetra-O-acetyl-a-D-arabinopyranose | 1,2,3,4-Tetra-O-acetyl-α-D-arabinopyranose, an indispensable compound in the biomedical sector, raises immense curiosity due to its potential in addressing a diverse range of ailments. Extensively investigated for its role in drug administration mechanisms, this compound exhibits remarkable promise in enhancing drug solubility and durability. Its versatile nature propels the advancement of pioneering therapeutic approaches aimed at combatting cancer, inflammation, and infectious maladies. Synonyms: (2R,3S,4R,5R)-Tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate; [(3R,4R,5S,6R)-4,5,6-triacetyloxyoxan-3-yl] acetate. CAS No. 19186-37-9. Molecular formula: C13H18O9. Mole weight: 318.31. | |
| 1,2,3,4-Tetra-O-acetyl-alpha-D-arabinopyranose | Heterocyclic Organic Compound. CAS No. 108646-05-5. Molecular formula: C13H18O9. Mole weight: 318.28. Catalog: ACM108646055. | |
| 1,2,3,4-Tetra-O-acetyl-b-D-arabinopyranose | 1,2,3,4-Tetra-O-acetyl-b-D-arabinopyranose, a compound of immense significance in the biomedical sector, is characterized by its fundamental role in the domain of pharmaceutical research and development. Derived from arabinose, this invaluable product serves as a pivotal precursor for the synthesis of diverse drugs and therapies employed in combating infectious diseases, namely HIV/AIDS. Synonyms: [(3R,4R,5S,6R)-4,5,6-triacetyloxyoxan-3-yl] acetate; 1,2,3,4-tetra-o-acetyl-alpha-d-arabinopyranose; (2R,3S,4R,5R)-Tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate; Acetyl 2-O,3-O,4-O-triacetyl-alpha-D-arabinopyranoside; 1,2,3,4-Tetra-O-acetyl-a-D-arabinopyranose; SCHEMBL5344597; DTXSID701269511; alpha-D-Arabinopyranose, 1,2,3,4-tetraacetate; (2R,3S,4R,5R)-3,4,5-TRIS(ACETYLOXY)OXAN-2-YL ACETATE. CAS No. 108646-05-5. Molecular formula: C13H18O9. Mole weight: 318.28. | |
| 1,2,3,4-Tetra-O-acetyl-L-arabinopyranose | The versatile saccharide intermediate, 1,2,3,4-Tetra-O-acetyl-L-arabinopyranose (acp4Ara), offers a broad scope of uses, particularly as a fundamental entity for intricate carbohydrates. Its significant therapeutic relevance extends to novel therapeutic interventions for multisystem metabolic illnesses such as diabetes. Not limited to being a mere precursor, this chemical compound exhibits immense potential for advanced biomedical research. Synonyms: [(3S,4S,5R)-4,5,6-Triacetyloxyoxan-3-yl] acetate; 1,2,3,4-tetra-o-acetyl-l-arabinopyranose; SCHEMBL5390328; DTXSID90924387; MFCD09864636; 1,2,3,4-Tetra-O-acetylpentopyranose. CAS No. 123163-97-3. Molecular formula: C13H18O9. Mole weight: 318.28. | |
| 1,2,3,5-Tetra-O-acetyl-a-D-arabinofuranose | 1,2,3,5-Tetra-O-acetyl-α-D-arabinofuranose, a pivotal compound highly valued within the biomedical industry owing to its exceptional antiviral attributes, assumes a prominent position. This substance finds extensive application in the realm of pharmaceutical research, serving as a fundamental constituent in the creation of robust drugs targeting a myriad of viral afflictions. Synonyms: 1,2,3,5-Tetra-O-acetyl-a-D-arabinofuranose; [(2R,3R,4S,5R)-3,4,5-triacetyloxyoxolan-2-yl]methyl acetate; A-D-ARABINOFURANOSE,1,2,3,5-TETRAACETATE; SCHEMBL7034256; DTXSID301272740; alpha-D-Arabinofuranose, 1,2,3,5-tetraacetate; 1,2,3,5-Tetra-O-acetyl-alpha-D-arabinofuranose, technical grade. CAS No. 43225-70-3. Molecular formula: C13H18O9. Mole weight: 318.28. | |
| 1,2,3,5-Tetra-O-acetyl-L-arabinofuranose | 1,2,3,5-Tetra-O-acetyl-L-arabinofuranose is a quintessential precursor in the synthesis of potent antiviral pharmacologics. Its salient role includes versatile adaptability into nucleic acid analogs, facilitating targeted disease research. Synonyms: 1,2,3,5-Tetra-O-acetyl-L-arabinofuranose; 56272-01-6; SCHEMBL7034253; DTXSID201281619; L-Arabinofuranose, 1,2,3,5-tetraacetate. CAS No. 56272-01-6. Molecular formula: C13H18O9. Mole weight: 318.28. | |
| 1-(2',3',5'-Tri-O-acetyl-b-D-arabinofuranosyl)uracil | 1-(2',3',5'-Tri-O-acetyl-b-D-arabinofuranosyl)uracil is a crucial biomolecule predominantly used in the biomedical industry for its antiviral properties. This compound has been extensively studied for its potential in combating viral diseases such as HIV and herpes. Its unique structure allows it to inhibit viral replication by interfering with the synthesis of viral DNA. This makes it a promising candidate for the development of antiviral therapies and vaccines. | |
| 1-(2'-Chloro-2'-deoxy-b-D-arabinofuranosyl)cytosine | 1-(2'-Chloro-2'-deoxy-b-D-arabinofuranosyl)cytosine is an antineoplastic biomolecule used in cancer research. It's an analog of the nucleoside cytosine, inhibiting DNA synthesis to stop tumor cells replication. Synonyms: 2(1H)-Pyrimidinone, 4-amino-1-(2-chloro-2-deoxy-beta-D-arabinofuranosyl)-; 4-Amino-1-(2-chloro-2-deoxy-.beta.-D-arabinofuranosyl)pyrimidin-2(1H)-one; 4-amino-1-[(2R,3S,4R,5R)-3-chloro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]pyrimidin-2-one. CAS No. 58461-30-6. Molecular formula: C9H12ClN3O4. Mole weight: 261.66. | |
| 1-(2'-Deoxy-2'-chloro-b-L-arabinofuranosyl)-thymine | 1-(2'-Deoxy-2'-chloro-b-L-arabinofuranosyl)-thymine, also known as 2'-C-C-AraT, is a nucleoside analog utilized in biomedical research particularly in antiviral and anticancer therapy studies. It has demonstrated inhibitory effects against Hepatitis B viral replication. Synonyms: 1-(2'-Deoxy-2'-chloro-β-L-arabinofuranosyl)-thymine; 1-[(2S,3R,4S,5S)-3-chloro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione; 1-(2-Chloro-2-deoxy-β-L-arabinofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione. Molecular formula: C10H13ClN2O5. Mole weight: 276.67. | |
| 1-(2'-Deoxy-2'-chloro-b-L-arabinofuranosyl)-thymine | 1-(2'-Deoxy-2'-chloro-b-L-arabinofuranosyl)-thymine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. US Biological Life Sciences. | Worldwide |
| 1-(2'-deoxy-2'-fluoro-3',5'-di-O-benzoyl-b-L-arabinofuranosyl)-uracil | 1-(2'-deoxy-2'-fluoro-3',5'-di-O-benzoyl-b-L-arabinofuranosyl)-uracil. Group: Biochemicals. Grades: Highly Purified. CAS No. 1312300-53-0. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| 1-(2'-deoxy-2'-fluoro-3',5'-di-O-benzoyl-b-L-arabinofuranosyl)-uracil | 1-(2'-deoxy-2'-fluoro-3',5'-di-O-benzoyl-b-L-arabinofuranosyl)-uracil is a nucleoside analogue useful in cancer treatment research. This nucleoside analogue selectively interacts with a thymidylate synthase, inhibiting DNA synthesis thereby disrupting tumor cell growth. Synonyms: 1-(3,5-Di-O-benzoyl-2-deoxy-2-fluoro-beta-L-arabinofuranosyl)-2,4(1H,3H)-pyrimidinedione; 2,4(1H,3H)-Pyrimidinedione, 1-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-β-L-arabinofuranosyl)-; 3,5-di-O-benzoyl-1,2-dideoxy-2-fluoro-1-uracil-1-yl-beta-L-arabino-pentofuranose. CAS No. 1312300-53-0. Molecular formula: C23H19FN2O7. Mole weight: 454.40. | |
| 1-(2'-Deoxy-2'-fluoro-3'-O-mesyl-5'-O-trityl-β-L-arabinofuranosyl)-uracil | 1-(2'-Deoxy-2'-fluoro-3'-O-mesyl-5'-O-trityl-β-L-arabinofuranosyl)-uracil, a potent nucleoside analogue, has found extensive application as a crucial precursor in drug discovery and therapy for various life-threatening ailments like viral infections and cancer. This arabinose-substituted compound is known to serve as a substantial scaffold for synthesizing a versatile range of potent nucleoside analogues with remarkable efficacy and specificity towards target cells. Molecular formula: C29H27FN2O7S. Mole weight: 566.60. | |
| 1-(2'-Deoxy-2'-fluoro-5'-O-trityl-b-L-arabinofuranosyl)-uracil | 1-(2'-Deoxy-2'-fluoro-5'-O-trityl-b-L-arabinofuranosyl)-uracil. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 1-(2'-Deoxy-2'-fluoro-5'-O-trityl-b-L-arabinofuranosyl)-uracil | 1-(2'-Deoxy-2'-fluoro-5'-O-trityl-b-L-arabinofuranosyl)-uracil is a biomedical compound utilized in the formulation of antiviral drugs. Typically, it's a critical component in medications aimed at combating HIV, making it instrumental in the research of AIDS treating. Synonyms: 1-(2'-Deoxy-2'-fluoro-5'-O-trityl-β-L-arabinofuranosyl)-uracil. Molecular formula: C28H25FN2O5. Mole weight: 488.51. | |
| 1-(2'-Deoxy-2'-fluoro-a-L-arabinofuranosyl)-thymine | 1-(2'-Deoxy-2'-fluoro-a-L-arabinofuranosyl)-thymine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. US Biological Life Sciences. | Worldwide |
| 1-(2'-Deoxy-2'-fluoro-a-L-arabinofuranosyl)-thymine | 1-(2'-Deoxy-2'-fluoro-a-L-arabinofuranosyl)-thymine is a potent antiviral substance. It inhibits DNA replication by interacting with viral DNA, thus preventing viral transmission. It has potential application in the field of HIV and hepatitis B infection control. Synonyms: alpha-Clevudine; 1-[(2R,3R,4S,5S)-3-fluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione; 1-(2-Deoxy-2-fluoro-α-L-arabinofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione; 2,4(1H,3H)-Pyrimidinedione, 1-(2-deoxy-2-fluoro-α-L-arabinofuranosyl)-5-methyl-. Grades: 95%. CAS No. 1027764-72-2. Molecular formula: C10H13FN2O5. Mole weight: 260.22. | |
| 1-(2'-Deoxy-2'-fluoro-arabinofuranosyl)-5-hydroxymethyluracil | It is a metabolite of FMAU. Synonyms: 2'-Deoxy-2'-fluoro-5-hydroxymethyl-arabinouridine; 1-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)-5-(hydroxymethyl)-2,4(1H,3H)-pyrimidinedione; 1-[(2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-(hydroxymethyl)pyrimidine-2,4-dione. Grades: ≥95%. CAS No. 94817-51-3. Molecular formula: C10H13FN2O6. Mole weight: 276.22. | |
| 1-(2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl)-5-ethyluracil | 1-(2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl)-5-ethyluracil. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 200mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| 1-(2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl)-5-iodouracil | 1-(2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl)-5-iodouracil. Group: Biochemicals. Alternative Names: Fialuridine. Grades: Highly Purified. CAS No. 69123-98-4. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C9H10FIN2O5. US Biological Life Sciences. | Worldwide |
| 1-(2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl)6-methylpurine | 1-(2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl)6-methylpurine, a remarkable antiviral compound, demonstrates its efficacy in combatting herpes simplex and varicella-zoster viruses. Through its robust inhibition of viral DNA polymerase, this agent dismantles viral replication processes, thereby alleviating associated symptoms. With its exceptional selectivity towards viral enzymes, this therapeutic option proves to be a commendable approach for managing viral infections among affected individuals. Synonyms: 6-Methylpurine-2'-deoxy-2'-fluoro-beta-D-arabinoriboside. Grades: ≥95%. CAS No. 2095417-72-2. Molecular formula: C11H13FN4O3. Mole weight: 268.24. | |
| 1- (2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl) cytosine HCl | 1- (2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl) cytosine HCl. Group: Biochemicals. Alternative Names: 2'-FANA-C.HCl; 4-Amino-1-[(2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)-oxolan-2-yl]pyrimidin-2-one.HCl. Grades: Highly Purified. CAS No. 56632-83-8. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C9H12FN3O4·HCl. US Biological Life Sciences. | Worldwide |
| 1-(2'-Deoxy-2'-fluoro--b-D-arabinofuranosyl)-N3-(2S)-[2-(t-butoxycarbonyl)-amino-3-carbonyl]propyluracil | 1-(2'-Deoxy-2'-fluoro-β-D-arabinofuranosyl)-N3-(2S)-[2-(t-butoxycarbonyl)-amino-3-carbonyl]propyluracil, widely recognized as a potent antiviral agent within the biomedical field, showcases remarkable proficiency in counteracting viral infections induced by a distinct viral assemblage. This extraordinary compound's efficacy lies in its ability to impede viral replication, rendering it an invaluable asset in the relentless battle against an array of pernicious viral maladies. Synonyms: tert-Butyl (S)-3-((tert-butoxycarbonyl)amino)-4-(3-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2,6-dioxo-3,6-dihydropyrimidin-1(2H)-yl)butanoate. CAS No. 2072145-73-2. Molecular formula: C22H34FN3O9. Mole weight: 503.52. | |
| 1- (2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl) uracil | 1- (2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl) uracil. Group: Biochemicals. Alternative Names: 1- (2-Deoxy-2-fluoro-b-D-arabinofuranosyl) uracil; 2-Deoxy-2'-fluoro-D-arabinofuranosyl uracil; 2'-Fluoro-arabinofuranosyl-2'-deoxy-uridine. Grades: Highly Purified. CAS No. 69123-94-0. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C9H11FN2O5. US Biological Life Sciences. | Worldwide |
| 1-(2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl)uracil 5'-triphosphate triethylammonium salt | 1-(2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl)uracil 5'-triphosphate triethylammonium salt, a transformative entity in the realm of biomedicine, assumes a pivotal role. Its ubiquity spans the landscape of antiviral drug discovery and therapy curation for maladies instigated by viral infestations, notably HIV and herpes. Molecular formula: C9H13FN2O14P3·C6H16N. Mole weight: 587.32. | |
| 1-(2'-Deoxy-2'-fluoro-beta-d-arabinofuranosyl)-5-ethyluracil | 1-(2'-Deoxy-2'-fluoro-beta-d-arabinofuranosyl)-5-ethyluracil. Group: Biochemicals. Grades: Highly Purified. CAS No. 1417190-75-0. Pack Sizes: 10mg, 25mg. Molecular Formula: C11H15FN2O5, Molecular Weight: 274.25. US Biological Life Sciences. | Worldwide |
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