Arabinoside Suppliers USA

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Product
5-Fluorocytosine arabinoside 5-Fluorocytosine arabinoside, an exceptionally powerful antineoplastic agent extensively applied for the management of diverse malignancies such as leukemia and solid tumors, expertly imparts its therapeutic effects through the restraint of DNA synthesis and the instigation of cellular demise. Synonyms: 4-amino-1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-fluoropyrimidin-2-one; Fluorocytosine arabinoside; Arafluorocytosine; Ara-FC; 4-amino-1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-5-fluoro-pyrimidin-2-one. Grades: 98%. CAS No. 4298-10-6. Molecular formula: C9H12FN3O5. Mole weight: 261.21. BOC Sciences 2
6-Methylaminopurine arabinoside 6-Methylaminopurine arabinoside, a nucleoside analogue lauded for its capacity in effectively treating viral infections, whether sly herpes simplex virus (HSV) or varicella-zoster virus (VZV) infections, reaps its rewards by preventing viral DNA synthesis and replication. Its impacts are significant in thwarting a multitude of diseases. Synonyms: 9H-Purin-6-amine, 9-beta-D-arabinofuranosyl-N-methyl-; Ara-map; 9-β-D-arabinofuranosyl-N-methyladenine; NSC 409168; 9-beta-D-Arabinofuranosyl-N-methyl-9H-purin-6-amine; 9H-Purin-6-amine, 9-β-D-arabinofuranosyl-N-methyl-. Grades: ≥95% by HPLC. CAS No. 60209-41-8. Molecular formula: C11H15N5O4. Mole weight: 281.27. BOC Sciences 2
Acetylcimigenol arabinoside Acetylcimigenol arabinoside. Group: Biochemicals. Alternative Names: Acetylcimigenol-3-O-alpha-L-arabinopyranside; Acetylshengmanol arabinoside. Grades: Plant Grade. CAS No. 402513-88-6. Pack Sizes: 10mg. Molecular Formula: C37H58O10, Molecular Weight: 662.85. US Biological Life Sciences. USBiological 8
Worldwide
Cimicidanol 3-Arabinoside Cimicidanol 3-Arabinoside. Group: Biochemicals. Grades: Plant Grade. CAS No. 161207-05-2. Pack Sizes: 10mg. Molecular Formula: C35H52O9, Molecular Weight: 616.78. US Biological Life Sciences. USBiological 8
Worldwide
Cimicidanol 3- O-α-L -arabinoside Cimicidanol 3- O-α-L -arabinoside. Group: Biochemicals. CAS No. 161207-05-2. Pack Sizes: 5mg. US Biological Life Sciences. USBiological 9
Worldwide
Cimigenol-3-O-alpha-L-arabinoside Cimigenol-3-O-alpha-L-arabinoside. Group: Biochemicals. Grades: Plant Grade. CAS No. 256925-92-5. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 8
Worldwide
Cyanidin-3-O-arabinoside Cyanidin-3-O-arabinoside is a pigment isolated from flowers of Rhododendron cv. Lems Stormcloud [1]. Uses: Scientific research. Group: Natural products. CAS No. 111613-04-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-129139. MedChemExpress MCE
Cytosine arabinoside 5'-triphosphate,sodium salt Heterocyclic Organic Compound. CAS No. 102601-42-3. Catalog: ACM102601423. Alfa Chemistry. 3
Enocitabine (N- (1-B-D-Arabinofuranosyl-1, 2-dihydro-2-oxo-4-pyrimidinyl) docosanamide, Behenoylcytosine Arabinoside, BH-AC, NSC-239336, Sunrabin) An antineoplastic. A derivative of Cytarabine. Group: Biochemicals. Alternative Names: N- (1-B-D-Arabinofuranosyl-1, 2-dihydro-2-oxo-4-pyrimidinyl) docosanamide, Behenoylcytosine Arabinoside, BH-AC, NSC-239336, Sunrabin. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 1
Worldwide
Hederagenin - 3-O-β-D- Galactosyl( 1?3)-β-D-glucosyl( 1?3)-α-L-rhamnosyl(1?2)-α-L-arabinoside Hederagenin - 3-O-β-D- Galactosyl( 1?3)-β-D-glucosyl( 1?3)-α-L-rhamnosyl(1?2)-α-L-arabinoside is a triterpenoids isolated from pulsatilla chinensis BungeRegel. Pulsatilla chinensis (Bunge) Regel is a botanical with a long history of medical use in China, which exhibits "blood-cooling" and detoxification activities. The roots of P. chinensis have been widely used in the traditional Chinese medicine for adjunctive treatment of intestinal amebiasis, malaria, vaginal trichomoniasis, bacterial infections and malignant tumor. Grades: > 98%. Molecular formula: C53H86O22. Mole weight: 1075.24. BOC Sciences 9
Isorhamnetin 3-O-α-L-arabinoside-7- O-α-L-rhamnoside Isorhamnetin 3-O-α-L-arabinoside-7- O-α-L-rhamnoside. Group: Biochemicals. Pack Sizes: 5mg. US Biological Life Sciences. USBiological 9
Worldwide
Isovitexin 2''-O-arabinoside Isovitexin 2''-O-arabinoside is a compound of the flavonoid class found in the leaves of Secale cereale. Synonyms: 6-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one. Grades: >98%. CAS No. 53382-71-1. Molecular formula: C26H28O14. Mole weight: 564.496. BOC Sciences 9
Malvidin-3-O-arabinoside chloride Malvidin-3-O-arabinoside chloride is found in the fruits of Vaccinium myrtillus, it shows antioxidant activity.It has potential preventive effect in colorectal diseases. Synonyms: Malvidin 3-arabinoside. Grades: > 95%. CAS No. 28500-04-1. Molecular formula: C22H23ClO11. Mole weight: 498.87. BOC Sciences 9
Oleanolic acid - 3-O-β-D- Galactosyl( 1?3)-β-D-glucosyl( 1?3)-α-L-rhamnosyl(1?2)-α-L-arabinoside Oleanolic acid - 3-O-β-D- Galactosyl( 1?3)-β-D-glucosyl( 1?3)-α-L-rhamnosyl(1?2)-α-L-arabinoside is a lupane-type triterpenoid glycoside isolated from Pulsatilla chinensis BungeRegel. Grades: > 98%. Molecular formula: C53H86O21. Mole weight: 1059.24. BOC Sciences 9
Oleanolic acid 3-O-β-D-glucosyl-( 1?3)-α-L-ramnosyl(1?2)-α-L-arabinoside Oleanolic acid 3-O-β-D-glucosyl-( 1?3)-α-L-ramnosyl(1?2)-α-L-arabinoside is extracted from Pulsatilla chinensis (Bunge) Regel. Synonyms: 3-[(O-beta-D-Glucopyranosyl-(1?3)-O-6-deoxy-alpha-L-mannopyranosyl-(1?2)-alpha-L-arabinopyranosyl)oxy]-olean-12-en-28-oic acid. Grades: >98%. CAS No. 103956-33-8. Molecular formula: C47H76O16. Mole weight: 897.1. BOC Sciences 9
Peonidin-3-O-arabinoside chloride Peonidin-3-O-arabinoside chloride is a natural compound which can be isolated from Vaccinium myrtillus, showing an antioxidant activity. Synonyms: Peonidin 3-arabinoside; Peonidin-3-o-arabinoside chloride. Grades: 98%. CAS No. 524943-91-7. Molecular formula: C21H21ClO10. Mole weight: 468.84. BOC Sciences 11
Quercitrin 2''-O-Arabinoside Flavonoids. CAS No. 104683-55-8. Molecular formula: C26H28O15. Mole weight: 580.5. Appearance: Yellow powder. Purity: 0.98. Catalog: ACM104683558. Alfa Chemistry. 5
Uracyl Arabinoside Uracyl Arabinoside. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 1-((2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione. CAS No. 3083-77-0. Molecular Formula: C9H12N2O6. Mole Weight: 244.20. Catalog: APB3083770. Alfa Chemistry Analytical Products 2
1-(5'-Deoxy-5'-fluoro-a-D-arabinofuranosyl)-2-nitroimidazole 1-(5'-Deoxy-5'-fluoro-α-D-arabinofuranosyl)-2-nitroimidazole is an intermediate primarily used in the synthesis of bioactive molecules for pharmaceutical applications. Its fluorinated arabinofuranosyl component is useful in developing antiviral and anticancer drugs. It also has potential in studying hypoxic conditions in diseases. Synonyms: Fluoroazomycin arabinoside. Grades: 95%. CAS No. 220793-03-3. Molecular formula: C8H10FN3O5. Mole weight: 247.18. BOC Sciences 2
1-beta-D-Arabinofuranosylthymine 1-beta-D-Arabinofuranosylthymine is a noteworthy nucleoside analog that administers antiviral action when used in the management of herpes simplex and varicella-zoster virus infections. Its mechanism of action involves zoning in on the viral DNA polymerase to halt viral replication. Uses: Antiviral agents. Synonyms: Arabinofuranosyl-5-methyluridine; 1-(β-D-Arabinofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione; 1-(β-D-arabinofuranosyl)-5-methylpyrimidine-2,4(1H,3H)-dione; Spongothymidine; Arabinosylthymine; Thymine arabinoside. Grades: ≥95%. CAS No. 605-23-2. Molecular formula: C10H14N2O6. Mole weight: 258.23. BOC Sciences 2
2,6-Diamino-9-(β-D-arabinofuranosyl)purine 2,6-Diamino-9-(β-D-arabinofuranosyl)purine, a potent antineoplastic agent, is indicated for the management of chronic lymphocytic leukemia and non-Hodgkin lymphoma. By restraining DNA synthesis, the agent induces apoptosis in rapidly proliferating cancerous cells. Its potential as an efficacious chemotherapeutic has been well-establish through extensive clinical data. Synonyms: DAPA; 2,6-Diamino-9-(b-D-arabinofuranosyl)purine; 2,6-Diaminopurine-9-arabinoside; araDAP; araDAPR; (2R,3S,4S,5R)-2-(2,6-Diamino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol. Grades: ≥ 95%. CAS No. 34079-68-0. Molecular formula: C10H14N6O4. Mole weight: 282.26. BOC Sciences 2
2'-Amino-2'-deoxy-5-fluoro-arabinouridine 2'-Amino-2'-deoxy-5-fluoro-arabinouridine is a potent chemotherapeutic agent used in the treatment of various types of cancer such as leukemia, colon cancer, and breast cancer. It is an analog of cytosine arabinoside and incorporates into DNA resulting in inhibition of DNA synthesis. It is available as an injectable solution for intravenous use. Grades: ≥95%. CAS No. 2305415-81-8. Molecular formula: C9H12FN3O5. Mole weight: 261.21. BOC Sciences 2
4-Nitrophenyl a-L-arabinopyranoside 4-Nitrophenyl a-L-arabinopyranoside, a highly sought-after compound in the biomedical sector, plays a pivotal role in the identification and examination of specific enzymes implicated in arabinose metabolism. Synonyms: PNP-a-arabinoside. CAS No. 1223-07-0. Molecular formula: C11H13NO7. Mole weight: 271.22. BOC Sciences 12
4-Nitrophenyl b-L-arabinopyranoside 4-Nitrophenyl b-L-arabinopyranoside is a valuable substrate for biomedical applications, specifically in the measurement of glycoside hydrolase activity, such as β-D-arabinofuranosidase, in drug discovery and enzymatic studies. Additionally, it is utilized in the study of L-arabinose and xylose metabolism in bacteria and fungi, and elucidates their relevance to pathways implicated in diseases including diabetes. Through utilization of this specialized substrate, significant advances can be made in the fields of biomedicine and microbiology research. Synonyms: PNP-arabinoside; (2R,3R,4S,5S)-2-(4-Nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triol; P-nitrophenyl β-L-arabinopyranoside. Grades: ≥95%. CAS No. 72732-54-8. Molecular formula: C11H13NO7. Mole weight: 271.22. BOC Sciences 11
6-Amino-2-chloro-9- (2'-deoxy-2'-fluoro-b-D-arabinofuranosyl) purine 6-Amino-2-chloro-9- (2'-deoxy-2'-fluoro-b-D-arabinofuranosyl) purine. Group: Biochemicals. Alternative Names: Clofarabine; 2-Chloro-6-amino-purine-2'-fluoro-2'-deoxy arabinoside. Grades: Highly Purified. CAS No. 123318-82-1. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C10H11ClFN5O3. US Biological Life Sciences. USBiological 8
Worldwide
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. Creative Enzymes
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. BOC Sciences
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. BOC Sciences
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). BOC Sciences
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. BOC Sciences
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. BOC Sciences
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. Creative Enzymes
Benzyl b-D-arabinopyranoside Benzyl b-D-arabinopyranoside, a widely employed compound within the biomedical industry, exhibits tremendous potential in therapeutic and research applications. It encompasses profound anti-tumor properties, holding substantial promise for combating diverse cancer strains. Moreover, its versatility as a precursor renders it invaluable in synthesizing pharmaceutical drugs catering to a spectrum of ailments. Synonyms: Benzyl beta-D-Arabinopyranoside; 5329-50-0; Benzyl b-D-arabinopyranoside; (2R,3S,4R,5R)-2-(Benzyloxy)tetrahydro-2H-pyran-3,4,5-triol; benzyl beta-l-arabinopyranoside; (2R,3S,4R,5R)-2-phenylmethoxyoxane-3,4,5-triol; BENZYL-BETA-L-ARABINOPYRANOSIDE; 7473-38-3; MFCD00225631; Benzyl ?-D-Arabinopyranoside; CHEMBL2436396; SCHEMBL13317630; 1-O-BENZYL-BETA-D-ARABINOSIDE; AKOS024325277; AS-60654; CS-0037261; W12632; W-203710; (2R,3S,4R,5R)-2-(BENZYLOXY)OXANE-3,4,5-TRIOL. CAS No. 5329-50-0. Molecular formula: C12H16O5. Mole weight: 240.25. BOC Sciences 11
β-D-fucosidase Enzymes from some sources also hydrolyse β-D-galactosides and/or β-D-glucosides and/or α-L-arabinosides. The activity of EC 3.2.1.37 xylan 1,4-β-xylosidase, is an associated activity found in some sources (e.g. liver). Group: Enzymes. Synonyms: β-fucosidase. Enzyme Commission Number: EC 3.2.1.38. CAS No. 9025-34-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3900; β-D-fucosidase; EC 3.2.1.38; 9025-34-7; β-fucosidase. Cat No: EXWM-3900. Creative Enzymes
β-galactosidase Some enzymes in this group hydrolyse α-L-arabinosides; some animal enzymes also hydrolyse β-D-fucosides and β-D-glucosides; cf. EC 3.2.1.108 lactase. Group: Enzymes. Synonyms: lactase (ambiguous); β-lactosidase; maxilact; hydrolact; β-D-lactosidase; S 2107; lactozym; trilactase; β-D-galactanase; oryzatym; sumiklat. Enzyme Commission Number: EC 3.2.1.23. CAS No. 9031-11-2. β-gal. 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-3888; β-galactosidase; EC 3.2.1.23; 9031-11-2; lactase (ambiguous); β-lactosidase; maxilact; hydrolact; β-D-lactosidase; S 2107; lactozym; trilactase; β-D-galactanase; oryzatym; sumiklat. Cat No: EXWM-3888. Creative Enzymes
β-glucosidase Wide specificity for β-D-glucosides. Some examples also hydrolyse one or more of the following: β-D-galactosides, α-L-arabinosides, β-D-xylosides, β-D-fucosides. Group: Enzymes. Synonyms: gentiobiase; cellobiase; emulsin; elaterase; aryl-β-glucosidase; β-D-glucosidase; β-glucoside glucohydrolase; arbutinase; amygdalinase; p-nitrophenyl β-glucosidase; primeverosidase; amygdalase; linamarase; salicilinase; β-1,6-glucosidase. Enzyme Commission Number: EC 3.2.1.21. CAS No. 9001-22-3. β-Glucosidase. 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-3886; β-glucosidase; EC 3.2.1.21; 9001-22-3; gentiobiase; cellobiase; emulsin; elaterase; aryl-β-glucosidase; β-D-glucosidase; β-glucoside glucohydrolase; arbutinase; amygdalinase; p-nitrophenyl β-glucosidase; primeverosidase; amygdalase; linamarase; salicilinase; β-1,6-glucosidase. Cat No: EXWM-3886. Creative Enzymes
Cyanidin-3-O-arabinose chloride Cyanidin-3-O-arabinose chloride is a natural compound which can be isolated from Vaccinium myrtillus and Vaccinium padifolium. Synonyms: Cyanidin-3-Arabinoside. CAS No. 27214-72-8. Molecular formula: C20H19O10Cl. Mole weight: 454.81. BOC Sciences 11
Cytarabine Arabinofuranosyl-cytosine (ara-C) is an inhibitor of DNA synthesis used as an antineoplastic and antiviral. It is a chemotherapy agent used to treat cancers of white blood cells like acute myeloid leukemia (AML) and non-Hodgkin lymphoma. Uses: Arabinofuranosyl-cytosine (ara-c) is an inhibitor of dna synthesis. Synonyms: Aracytidine; Cytosine arabinoside; 1-(β-D-Arabinofuranosyl)cytosine; Cytosine-1-β-D-arabinofuranoside; Arabinocytidine; Cytosar; Tarabine; Udicil; 1-beta-D-Arabinofuranosylcytosine; Arabinofuranosylcytosine; 4-Amino-1-β-D-arabinofuranosyl-2(1H)pyrimidinone. Grades: ≥95%. CAS No. 147-94-4. Molecular formula: C9H13N3O5. Mole weight: 243.22. BOC Sciences 2
Cytarabine Cytarabine, a nucleoside analog, causes S phase cell cycle arrest and inhibits DNA polymerase. Cytarabine inhibits DNA synthesis with an IC 50 of 16 nM. Cytarabine has antiviral effects against HSV. Cytarabine shows anti-orthopoxvirus activity. Uses: Scientific research. Group: Natural products. Alternative Names: Cytosine β-D-arabinofuranoside; Cytosine Arabinoside; Ara-C. CAS No. 147-94-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-13605. MedChemExpress MCE
Cytarabine hydrochloride Cytarabine, an antimetabolite analogue of cytidine with a modified sugar moiety, is an antimetabolic agent and DNA synthesis inhibitor. Synonyms: Cytosine arabinoside hydrochloride; 1-beta-D-Arabinofuranosylcytosine hydrochloride. Grades: 95%. CAS No. 69-74-9. Molecular formula: C9H14ClN3O5. Mole weight: 279.68. BOC Sciences 2
Cytarabine hydrochloride Cytarabine hydrochloride, a nucleoside analog, causes S phase cell cycle arrest and inhibits DNA polymerase. Cytarabine inhibits DNA synthesis with an IC 50 of 16 nM. Cytarabine hydrochloride has antiviral effects against HSV. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cytosine β-D-arabinofuranoside hydrochloride; Cytosine Arabinoside hydrochloride; Ara-C hydrochloride. CAS No. 69-74-9. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-13605A. MedChemExpress MCE
deoxycytidine kinase Cytosine arabinoside can act as acceptor; all natural nucleoside triphosphates (except dCTP) can act as donors. Group: Enzymes. Synonyms: deoxycytidine kinase (phosphorylating); 2'-deoxycytidine kinase; Ara-C kinase; arabinofuranosylcytosine kinase; deoxycytidine-cytidine kinase. Enzyme Commission Number: EC 2.7.1.74. CAS No. 9039-45-6. 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-3104; deoxycytidine kinase; EC 2.7.1.74; 9039-45-6; deoxycytidine kinase (phosphorylating); 2'-deoxycytidine kinase; Ara-C kinase; arabinofuranosylcytosine kinase; deoxycytidine-cytidine kinase. Cat No: EXWM-3104. Creative Enzymes
Elacytarabine Elacytarabine (CP-4055) is the lipophilic 5'-elaidic acid ester of the deoxycytidine analog cytosine arabinoside (cytarabine; Ara-C) with potential antineoplastic activity. As a prodrug, CP-4055 is converted intracellularly into cytarabine triphosphate by deoxycytidine kinase and subsequently competes with cytidine for incorporation into DNA, thereby inhibiting DNA synthesis. Compared to cytarabine, CP-4055 shows increased cellular uptake and retention, resulting in increased activation by deoxycytidine kinase to cytarabine triphosphate, decreased deamination and deactivation by deoxycytidine deaminase, and increased inhibition of DNA synthesis. This agent also inhibits RNA synthesis, an effect not seen with cytarabine. Synonyms: CP-4055; CP 4055; CP4055; 5'-O-(Elaidoyl) 1-beta-D-arabinofuranosylcytosine; 5'-Oleoyl cytarabine; (E)-((2R,3S,4S,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl octadec-9-enoate. CAS No. 188181-42-2. Molecular formula: C27H45N3O6. Mole weight: 507.67. BOC Sciences 11
Fazarabine Fazarabine, also known as Kymarabine, is an orally-active pyrimidine analogue of an aza-substituted cytidine in which the ribose moiety is replaced by an arabinose sugar. Similar in action to cytarabine, fazarabine is phosphorylated by deoxycytidine kinase to a triphosphate form which competes with thymidine for incorporation into DNA; its incorporation into DNA inhibits DNA synthesis, resulting in tumor cell death and tumor necrosis. The presence of deoxycytidine kinase in a tumor is a determinant of tumor sensitivity to this drug. Synonyms: CCRIS 93; CCRIS-93; CCRIS93; NSC 281272; NSC-281272; NSC281272; Ara-AC; 5-Azacytosine arabinoside; 1-beta-D-Arabinofuranosyl-5-azacytosine. CAS No. 65886-71-7. Molecular formula: C8H12N4O5. Mole weight: 244.20. BOC Sciences 11
Fludarabine Phosphate Fludarabine Phosphate is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis. Uses: Antimetabolites, antineoplastic. Synonyms: Fludarabine 5'-monophosphate; 2-Fluoro-ARA AMP; Fludarabine monophosphate; FAMP; NSC-312887; 2-Fluoro-9-(5-O-phosphono-beta-D-arabinofuranosyl)-9H-purin-6-amine; 2-Fluoroadenine arabinoside 5'-monophosphate; ((2R,3S,4S,5R)-5-(6-amino-2-fluoro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen phosphate; 9-beta-Arabinofuranosyl-2-fluoroadenine-5'-phosphate. Grades: ≥98% by HPLC. CAS No. 75607-67-9. Molecular formula: C10H13FN5O7P. Mole weight: 365.21. BOC Sciences 2
Methyl b-L-arabinopyranoside Methyl b-L-arabinopyranoside, an extensively studied compound within the realm of biomedicine, exhibits considerable promise owing to its manifold potential therapeutic applications. Its efficacy has been demonstrated across a diverse spectrum of ailments, encompassing cancer, diabetes, and infectious diseases. With its distinct molecular configuration, Methyl b-L-arabinopyranoside has emerged as an indispensable building block towards the formulation of pioneering pharmaceutical agents specifically designed to combat these afflictions. Synonyms: Methyl b-arabinoside. CAS No. 1825-00-9. Molecular formula: C6H12O5. Mole weight: 164.16. BOC Sciences 11
N-Methyl-3-indolyl a-D-arabinopyranoside N-Methyl-3-indolyl α-D-arabinopyranoside is an extensively employed chemical compound within the biomedical sector, used for studying an array of ailments, encompassing cancer and viral infections. This compound showcases an outstanding capacity for thwarting viral replication. Synonyms: Green-a-D-arabinoside. Molecular formula: C14H17NO5. Mole weight: 279.29. BOC Sciences 12
non-reducing end α-L-arabinofuranosidase The enzyme acts on α-L-arabinofuranosides, α-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Some β-galactosidases (EC 3.2.1.23) and β-D-fucosidases (EC 3.2.1.38) also hydrolyse α-L-arabinosides. cf. EC 3.2.1.185, non-reducing end β-L-arabinofuranosidase. Group: Enzymes. Synonyms: arabinosidase (ambiguous); α-arabinosidase; α-L-arabinosidase; α-arabinofuranosidase; polysaccharide α-L-arabinofuranosidase; α-L-arabinofuranoside hydrolase; L-arabinosidase (ambiguous); α-L-arabinanase. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. α-L-Arabinofuranosidase. 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-3918; non-reducing end α-L-arabinofuranosidase; EC 3.2.1.55; 9067-74-7; arabinosidase (ambiguous); α-arabinosidase; α-L-arabinosidase; α-arabinofuranosidase; polysaccharide α-L-arabinofuranosidase; α-L-arabinofuranoside hydrolase; L-arabinosidase (ambiguous); α-L-arabinanase. Cat No: EXWM-3918. Creative Enzymes
non-reducing end β-L-arabinopyranosidase The enzyme, which was characterized from dormant seeds of the plant Cajanus cajan (pigeon pea), has been shown to remove the terminal non-reducing β-L-arabinopyranoside residue from the artificial substrate p-nitrophenyl-β-L-arabinopyranose. In the presence of methanol the enzyme demonstrates transglycosylase activity, transferring the arabinose moiety to methanol while retaining the anomeric configuration, generating 1-O-methyl-β-L-arabinopyranose. Group: Enzymes. Synonyms: vicianosidase; β-L-arabinosidase (ambiguous); β-L-arabinoside arabinohydrolase (ambiguous). Enzyme Commission Number: EC 3.2.1.88. CAS No. 39361-63-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3952; non-reducing end β-L-arabinopyranosidase; EC 3.2.1.88; 39361-63-2; vicianosidase; β-L-arabinosidase (ambiguous); β-L-arabinoside arabinohydrolase (ambiguous). Cat No: EXWM-3952. Creative Enzymes
nucleoside oxidase (H2O2-forming) A heme-containing flavoprotein (FAD). Other purine and pyrimidine nucleosides (as well as 2'-deoxyribonucleosides and arabinosides) are substrates, but ribose and nucleotides are not substrates. The overall reaction takes place in two separate steps, with the 5'-dehydro nucleoside being released from the enzyme to serve as substrate for the second reaction. This enzyme differs from EC 1.1.3.28, nucleoside oxidase, as it produces hydrogen peroxide rather than water. Group: Enzymes. Enzyme Commission Number: EC 1.1.3.39. 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-0411; nucleoside oxidase (H2O2-forming); EC 1.1.3.39. Cat No: EXWM-0411. Creative Enzymes
Tetrahydrouridine Tetrahydrouridine, a derivative of Uridine, is a potent and reversible competitive inhibitor of cytidine deaminase (CDD) (Ki values = 54 and 240 nM for human and E. coli enzymes, respectively). Tetrahydrouridine has the potential to treat tumors with highly expressed CDA as it inhibits cell proliferation through cell cycle regulation despite of cytidine deaminase expression levels deaminase (CDA). Used in combination with cytosine arabinoside (Ara-C) to assess the anti-leukemic activity and anti-tumor activity of Ara-C in in vitro studies. Uses: Antimetabolites. Synonyms: 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-hydroxy-1,3-diazinan-2-one; NSC 112907; Tetrahydrouridine, NSC 112907; NSC-112907; NSC112907. Grades: 95%. CAS No. 18771-50-1. Molecular formula: C9H16N2O6. Mole weight: 248.23. BOC Sciences 7
Vidarabine Vidarabine (Ara-A) an antiviral agent which is active against herpes simplex and varicella zoster viruses [1] [2]. Vidarabine has IC 50 s of 9.3 μg/ml for HSV-1 and 11.3 μg/ml for HSV-2 [2]. Vidarabine also has anti- orthopoxvirus activity [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Ara-A; Adenine Arabinoside; 9-β-D-Arabinofuranosyladenine. CAS No. 5536-17-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-B0277. MedChemExpress MCE
Vidarabine monohydrate Vidarabine monohydrate is an adenine arabinoside. Vidarabine monohydrate an antiviral agent which is active against herpes simplex viruses ( HSV ) and varicella zoster viruses [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 24356-66-9. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-N6666. MedChemExpress MCE
vitexin 2''-O-rhamnoside 7-O-methyltransferase The flavonoids vitexin and isovitexin 2''-O-arabinoside do not act as substrates for the enzyme from oats (Avena sativa). Group: Enzymes. Enzyme Commission Number: EC 2.1.1.153. CAS No. 90698-29-6. 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-1749; vitexin 2''-O-rhamnoside 7-O-methyltransferase; EC 2.1.1.153; 90698-29-6. Cat No: EXWM-1749. Creative Enzymes
2-Nitrophenyl-β-L-arabinopyranoside 2-Nitrophenyl-β-L-arabinopyranoside, a crucial component in biomedical research, is a substrate endowed with the unique ability to catalyze enzymatic assays for testing the activity of arabinosidases. Featuring prominently in the reliable evaluation of potential treatments for HIV infections, arabinosidase inhibitors represent a highly promising avenue for the development of next-generation, anti-HIV agents. As such, this indispensable product enjoys wide usage in research facilities and labs, playing a pivotal role in the quest to discover effective medical treatments. Synonyms: (2R,3R,4S,5S)-2-(2-nitrophenoxy)oxane-3,4,5-triol. Molecular formula: C11H13NO7. Mole weight: 271.22. BOC Sciences 12

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