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| Product | Description | |
|---|---|---|
| Kanamycin B | Kanamycin B. Group: Biochemicals. Alternative Names: O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1?6)-O-[2,6-diamino-2,6-dideoxy-α-D-glucopyranosyl-(1?4)]-2-deoxy-D-streptamine; 2-Amino-2-deoxykanamycin; Aminodeoxykanamycin; Beckanamycin; Bekanamycin; KDM; Kanendomycin; NK 1006; Nebramycin V; Nebramycin Factor 5. Grades: Highly Purified. CAS No. 4696-76-8. Pack Sizes: 1g, 2g, 5g. Molecular Formula: C18H37N5O10. US Biological Life Sciences. |  Worldwide |
| Kanamycin B | Kanamycin B is an aminoglycoside antibiotic produced by the strain of Str. kanamyceticus. It is used to treat the infection of gram-positive bacteria, gram-negative bacteria and mycobacterium tuberculosis. Uses: Aminoglycoside antibiotic. Synonyms: Bekanamycin; NK-1006; NK1006; NK 1006; Nebramycin V; Aminodeoxykanamycin; (1R,2S,3S,4R,6S)-4,6-diamino-3-[(3-amino-3-deoxy-alpha-D-glucopyranosyl)oxy]-2-hydroxycyclohexyl 2,6-diamino-2,6-dideoxy-alpha-D-glucopyranoside. Grades: ≥95%. CAS No. 4696-76-8. Molecular formula: C18H37N5O10. Mole weight: 483.51. |  |
| Kanamycin base | 5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C H N O . CAS No. 8063-7-8. Prepack ID 56564516-5g. Molecular Weight 484.4986. See USA prepack pricing. |  |
| kanamycin B dioxygenase | Requires Fe2+ and ascorbate. Found in the bacterium Streptomyces kanamyceticus where it is involved in the conversion of the aminoglycoside antibiotic kanamycin B to kanamycin A. Group: Enzymes. Synonyms: kanJ (gene name). Enzyme Commission Number: EC 1.14.11.37. 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-0655; kanamycin B dioxygenase; EC 1.14.11.37; kanJ (gene name). Cat No: EXWM-0655. |  |
| 1,3-Di-HABA kanamycin A | 1,3-Di-HABA kanamycin A. Group: Biochemicals. Alternative Names: O-3-Amino-3-deoxy-a-D-glucopyranosyl-(1?6)-O-[6-amino-6-deoxy-a-D-glucopyranosyl-(1?4)]-N1,N3-bis[(2S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxy-D-streptamine. Grades: Highly Purified. CAS No. 927821-99-6. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C26H50N6O15. US Biological Life Sciences. | Worldwide |
| 1,3''-Di-HABA Kanamycin A Sulfate | 1,3''-Di-HABA Kanamycin A Sulfate is a synthetic byproduct of Amikacin. Amikacin is an antibacterial compound used in the treatment of diseases and illnesses arising from gram-negative bacterium. Synonyms: O-6-Amino-6-deoxy-α-D-glucopyranosyl-(1?4)-O-[3-[[(2S)-4-amino-2-hydroxy-1-oxobutyl]amino]-3-deoxy-α-D-glucopyranosyl-(1?6)]-N1-[(2S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxy-D-streptamine Sulfate; 1,3''-Di-N-(L-4-amino-2-hydroxybutyryl) Kanamycin A Sulfate. Grades: 95%. Molecular formula: C26H50N6O15.xH2SO4. Mole weight: 686.70 (free base). | |
| 1,6'-Di-HABA kanamycin A | 1,6'-Di-HABA kanamycin A. Group: Biochemicals. Alternative Names: O-3-Amino-3-deoxy-a-D-glucopyranosyl-(1?6)-O-[6-[[(2S)-4-amino-2-hydroxy-1-oxobutyl]amino]-6-deoxy-a-D-glucopyranosyl-(1?4)]-N1-[(2S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxy-D-streptamine; 1,6'-Di-N-(L-4-amino-2-hydroxybutyryl) kanamycin A. Grades: Highly Purified. CAS No. 197909-67-4. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C26H50N6O15. US Biological Life Sciences. | Worldwide |
| 1,6'-Di-HABA Kanamycin A Sulfate | Kanamycin derivative as synthetic byproduct of Amikacin. Synonyms: O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1?6)-O-[6-[[(2S)-4-amino-2-hydroxy-1-oxobutyl]amino]-6-deoxy-α-D-glucopyranosyl-(1?4)]-N1-[(2S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxy-D-streptamine Sulfate; 1,6'-Di-N-(L-4-amino-2-hydroxybutyryl) Kanamycin A Sulfate; Amikacin Impurity B Sulfate; Amikacin EP Impurity F Sulfate. Grades: 95%. Molecular formula: C26H50N6O15 x(H2SO4). Mole weight: 686.71. | |
| 3',4'-Dideoxy-3''-N-methyl kanamycin B1 | 3',4'-Dideoxy-3''-N-methyl kanamycin B1 is produced by the strain of Micromonospora inyoensis 155-0F-1G. It has anti-gram positive bacteria and negative bacteria activity. Molecular formula: C19H39N5O8. Mole weight: 465.54. | |
| 3,5,6'-Tri(N-Benzyloxycarbonyl) Kanamycin A | 3,5,6'-Tri(N-Benzyloxycarbonyl) Kanamycin A is an impurity of Amikacin. Amikacin is an antibacterial compound used in the treatment of diseases and illnesses arising from gram-negative bacterium. Grades: 98%. CAS No. 67470-54-6. Molecular formula: C42H54N4O17. Mole weight: 886.89. | |
| 3-HABA Kanamycin A Sulfate | 3-HABA Kanamycin A Sulfate is an impurity of Amikacin. Amikacin is an antibacterial compound used in the treatment of diseases and illnesses arising from gram-negative bacterium. Synonyms: (S)-O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1?6)-O-[6-amino-6-deoxy-α-D-glucopyranosyl-(1?4)]-N3-(4-amino-2-hydroxy-1-oxobutyl)-2-deoxy-D-streptamine Sulfate; BB-K29 Sulfate; 3-N-[L-(-)-γ-Amino-α-hydroxybutyryl]kanamycin A Sulfate; Amikacin EP Impurity A Sulfate. Grades: 97%. Molecular formula: C22H43N5O13.xH2SO4. Mole weight: 585.60 (free base). | |
| 3''-HABA Kanamycin A Sulfate | 3''-HABA Kanamycin A Sulfate is an impurity of Amikacin. Amikacin is an antibacterial compound used in the treatment of diseases and illnesses arising from gram-negative bacterium. Synonyms: O-6-Amino-6-deoxy-α-D-glucopyranosyl-(1?4)-O-[3-[[(2S)-4-amino-2-hydroxy-1-oxobutyl]amino]-3-deoxy-α-D-glucopyranosyl-(1?6)]-2-deoxy-D-streptamine Sulfate; Antibiotic BB-K 11 Sulfate; 3''-N-[L-(-)-γ-Amino-α-hydroxybutyryl]kanamycin A Sulfate; 3''-HABA Kanamycin A Sulfate. Grades: 95%. Molecular formula: C22H43N5O13.xH2SO4. Mole weight: 585.60 (free base). | |
| 3''-[N-(HABA-CBz)] 3,5,6'-Tri(N-Benzyloxycarbonyl) Kanamycin A | 3''-[N-(HABA-CBz)] 3,5,6'-Tri(N-Benzyloxycarbonyl) Kanamycin A is an impurity of Amikacin. Amikacin is an antibacterial compound used in the treatment of diseases and illnesses arising from gram-negative bacterium. Synonyms: 3,5,6'-Tri(N-Benzyloxycarbonyl) Kanamycin A. Molecular formula: C54H67N5O21. Mole weight: 1122.13. | |
| 3-N-[(S)-4-Amino-2-hydroxybutyryl]kanamycin B | 3-N-[(S)-4-Amino-2-hydroxybutyryl]kanamycin B is a derivative of Kanamycin B sulfate; an antibacterial. Synonyms: O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1?6)-O-[2,6-diamino-2,6-dideoxy-α-D-glucopyranosyl-(1?4)]-N3-[(2S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxy-D-streptamine; BB-K46. Molecular formula: C22H44N6O12. Mole weight: 584.62. | |
| 5,6'-Di(N-Benzyloxycarbonyl) Kanamycin A | 5,6'-Di(N-Benzyloxycarbonyl) Kanamycin A is an Amikacin impurity A. Molecular formula: C34H48N4O15. Mole weight: 752.76. | |
| 5-[N-(HABA-Cbz)] 3,6'-Di(N-benzyloxycarbonyl) Kanamycin A | 5-[N-(HABA-Cbz)] 3,6'-Di(N-benzyloxycarbonyl) Kanamycin A is an impurity of Amikacin, an semisynthetic aminoglycoside antibotic derived from Kanamycin A. Molecular formula: C46H61N5O19. Mole weight: 988. | |
| 6'-N-(Benzyloxycarbonyl)kanamycin A Sulfate | Cas No. 40372-09-6. | |
| Bekanamycin | Bekanamycin (Kanamycin B) is an aminoglycoside antibiotic produced by Streptomyces kanamyceticus , against an array of Gram-positive and Gram-negative bacterial strain [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Kanamycin B. CAS No. 4696-76-8. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1174. |  |
| Bis-2',3''-[N-(HABA-CBz)] Bis-6,4'-N-CBz Kanamycin A | Bis-2',3''-[N-(HABA-CBz) Bis-6,4'-N-CBz Kanamycin A is an Amikacin impurity A. Molecular formula: C58H74N6O23. Mole weight: 1223.23. | |
| Bis-3'',5-[N-(HABA-Cbz)] 3,6'-Di(N-benzyloxycarbonyl) Kanamycin A | Bis-3'',5-[N-(HABA-Cbz)] 3,6'-Di(N-benzyloxycarbonyl) Kanamycin A is an impurity of Amikacin, an semi-synthetic aminoglycoside antibotic derived from Kanamycin A. Molecular formula: C58H74N6O23. Mole weight: 1223.23. | |
| Bis-5,6'-[N-(HABA-CBz)] Kanamycin A | Bis-5,6'-[N-(HABA-CBz)] Kanamycin A is an intermediate of Amikacin. Amikacin is an antibacterial compound used in the treatment of diseases and illnesses arising from gram-negative bacterium. Molecular formula: C42H62N6O19. Mole weight: 954.97. | |
| Kanamycin Sulfate BP | Kanamycin Sulfate BP. |  CA, FL & NJ |
| 1,2,4,6-Tetra-O-acetyl-3-deoxy-3-N-(4-nitrobenzamido)-D-galactopyranose | 1,2,4,6-Tetra-O-acetyl-3-deoxy-3-N-(4-nitrobenzamido)-D-galactopyranose, identified as a chemical entity of paramount significance, assumes a critical role in augmenting the development of antibiotics as an efficacious remedy to counter bacterial infections. With a proclivity for serving as a precursor for the synthesis of aminoglycoside antibiotics, such as kanamycin and amikacin, it exhibits promise in the race for combating pernicious bacteria and thwarting their detrimental effects on the human body. Synonyms: (3R,4S,5R,6R)-6-(Acetoxymethyl)-4-(4-nitrobenzamido)tetrahydro-2H-pyran-2,3,5-triyl triacetate; 947590-43-4. CAS No. 947590-43-4. Molecular formula: C21H24N2O12. Mole weight: 496.42. | |
| 16S rRNA (adenine1408-N1)-methyltransferase | The enzyme provides a panaminoglycoside-resistant nature through interference with the binding of aminoglycosides toward the A site of 16S rRNA through N1-methylation at position adenine1408. Group: Enzymes. Synonyms: kanamycin-apramycin resistance methylase; 16S rRNA:m1A1408 methyltransferase; KamB; NpmA; 16S rRNA m1A1408 methyltransferase. Enzyme Commission Number: EC 2.1.1.180. 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-1779; 16S rRNA (adenine1408-N1)-methyltransferase; EC 2.1.1.180; kanamycin-apramycin resistance methylase; 16S rRNA:m1A1408 methyltransferase; KamB; NpmA; 16S rRNA m1A1408 methyltransferase. Cat No: EXWM-1779. | |
| 16S rRNA (guanine1405-N7)-methyltransferase | The enzyme from the antibiotic-producing bacterium Micromonospora zionensis specifically methylates guanine1405 at N7 in 16S rRNA, thereby rendering the ribosome resistant to 4,6-disubstituted deoxystreptamine aminoglycosides, which include gentamicins and kanamycins. Group: Enzymes. Synonyms: methyltransferase Sgm; m7G1405 Mtase; Sgm Mtase; Sgm; sisomicin-gentamicin methyltransferase; sisomicin-gentamicin methylase; GrmA; RmtB; RmtC; ArmA. Enzyme Commission Number: EC 2.1.1.179. 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-1777; 16S rRNA (guanine1405-N7)-methyltransferase; EC 2.1.1.179; methyltransferase Sgm; m7G1405 Mtase; Sgm Mtase; Sgm; sisomicin-gentamicin methyltransferase; sisomicin-gentamicin methylase; GrmA; RmtB; RmtC; ArmA. Cat No: EXWM-1777. | |
| 2'-deamino-2'-hydroxyneamine 1-α-D-kanosaminyltransferase | Involved in the biosynthetic pathway of kanamycins. The enzyme characterized from the bacterium Streptomyces kanamyceticus can also accept UDP-α-D-glucose with lower efficiency. Group: Enzymes. Synonyms: kanE (gene name); kanM2 (gene name). Enzyme Commission Number: EC 2.4.1.301. 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-2536; 2'-deamino-2'-hydroxyneamine 1-α-D-kanosaminyltransferase; EC 2.4.1.301; kanE (gene name); kanM2 (gene name). Cat No: EXWM-2536. | |
| 2'-deamino-2'-hydroxyneamine transaminase | The reaction occurs in vivo in the opposite direction. Involved in the biosynthetic pathway of kanamycin A and kanamycin D. The enzyme, characterized from the bacterium Streptomyces kanamyceticus, can also catalyse EC 2.6.1.93, neamine transaminase. Group: Enzymes. Synonyms: kacL (gene name). Enzyme Commission Number: EC 2.6.1.94. 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-2935; 2'-deamino-2'-hydroxyneamine transaminase; EC 2.6.1.94; kacL (gene name). Cat No: EXWM-2935. | |
| 2'-dehydrokanamycin reductase | Found in the bacterium Streptomyces kanamyceticus where it is involved in the conversion of kanamycin B to kanamycin A. Group: Enzymes. Synonyms: kanK (gene name, ambiguous). Enzyme Commission Number: EC 1.1.1.355. 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-0271; 2'-dehydrokanamycin reductase; EC 1.1.1.355; kanK (gene name, ambiguous). Cat No: EXWM-0271. | |
| 2-Deoxy D-arabino hexonic acid-δ-lactone | 2-Deoxy-D-arabino-hexonic acid-δ-lactone, an artificial hexose monosaccharide analogue, is frequently employed as a structure-building block for various antibiotic compounds such as streptomycin and kanamycin. It plays a key role in glycosylated protein biosynthesis and is extensively employed in researching glycan biosynthesis. Its beneficial prospects render it a desirable component of scientific inquiries. CAS No. 91447-00-6. Molecular formula: C6H10O5. Mole weight: 162.14. | |
| 2-deoxy-scyllo-inosamine dehydrogenase | Requires zinc. Involved in the biosynthetic pathways of several clinically important aminocyclitol antibiotics, including kanamycin, neomycin and ribostamycin. cf. EC 1.1.99.38, 2-deoxy-scyllo-inosamine dehydrogenase (AdoMet-dependent). Group: Enzymes. Synonyms: neoA (gene name); kanK (gene name, ambiguous); kanE (gene name, ambiguous). Enzyme Commission Number: EC 1.1.1.329. 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-0242; 2-deoxy-scyllo-inosamine dehydrogenase; EC 1.1.1.329; neoA (gene name); kanK (gene name, ambiguous); kanE (gene name, ambiguous). Cat No: EXWM-0242. | |
| 2-deoxy-scyllo-inosose synthase | Requires Co2+. Involved in the biosynthetic pathways of several clinically important aminocyclitol antibiotics, including kanamycin, butirosin, neomycin and ribostamycin. Requires an NAD+ cofactor, which is transiently reduced during the reaction. The enzyme from the bacterium Bacillus circulans forms a complex with the glutamine amidotransferase subunit of pyridoxal 5'-phosphate synthase (EC 4.3.3.6), which appears to stabilize the complex. Group: Enzymes. Synonyms: btrC (gene name); neoC (gene name); kanC (gene name). Enzyme Commission Number: EC 4.2.3.124. 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-5137; 2-deoxy-scyllo-inosose synthase; EC 4.2.3.124; btrC (gene name); neoC (gene name); kanC (gene name). Cat No: EXWM-5137. | |
| 2-deoxystreptamine glucosyltransferase | Involved in the biosynthesis of kanamycin B and kanamycin C. Also catalyses EC 2.4.1.283, 2-deoxystreptamine N-acetyl-D-glucosaminyltransferase, but activity is only one fifth of that with UDP-α-D-glucose. Group: Enzymes. Synonyms: kanF (gene name). Enzyme Commission Number: EC 2.4.1.284. 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-2517; 2-deoxystreptamine glucosyltransferase; EC 2.4.1.284; kanF (gene name). Cat No: EXWM-2517. | |
| 2-deoxystreptamine N-acetyl-D-glucosaminyltransferase | Involved in the biosynthetic pathways of several clinically important aminocyclitol antibiotics, including kanamycin, butirosin, neomycin and ribostamycin. Unlike the enzyme from the bacterium Streptomyces kanamyceticus, which can also accept UDP-D-glucose (cf. EC 2.4.1.284, 2-deoxystreptamine glucosyltransferase), the enzyme from Bacillus circulans can only accept UDP-N-acetyl-α-D-glucosamine. Group: Enzymes. Synonyms: btrM (gene name); neoD (gene name); kanF (gene name). Enzyme Commission Number: EC 2.4.1.283. 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-2516; 2-deoxystreptamine N-acetyl-D-glucosaminyltransferase; EC 2.4.1.283; btrM (gene name); neoD (gene name); kanF (gene name). Cat No: EXWM-2516. | |
| 2'-N-acetylparomamine deacetylase | Involved in the biosynthetic pathways of several clinically important aminocyclitol antibiotics, including kanamycin, butirosin, neomycin and ribostamycin. The enzyme from the bacterium Streptomyces fradiae can also accept 2'''-acetyl-6'''-hydroxyneomycin C as substrate, cf. EC 3.5.1.113, 2'''-acetyl-6'''-hydroxyneomycin C deacetylase. Group: Enzymes. Synonyms: btrD (gene name); neoL (gene name); kanN (gene name). Enzyme Commission Number: EC 3.5.1.112. 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-4392; 2'-N-acetylparomamine deacetylase; EC 3.5.1.112; btrD (gene name); neoL (gene name); kanN (gene name). Cat No: EXWM-4392. | |
| 3',4'-Dideoxyribostamycin B | 3',4'-Dideoxyribostamycin B is produced by the strain of Streptomyces ribosidificus. It is resistant to gram-positive bacteria and is also effective against escherichia coli and Pseudomonas aeruginosa that are resistant to ribothromycin and kanamycin. Molecular formula: C17H34N4O8. Mole weight: 422.47. | |
| Amiclenomycin | It is produced by the strain of Streptomyces lavendulae subsp. amiclenomycini. It can inhibit the activity of Mycobacterium, and also has effect on kanamycin resistant Mycobacterium nucleum. Biotin and Desthiobiocin can offset their activities. Synonyms: Amyclenomycin; 2-Amino-4-(4-amino-2,5-cyclohexadienyl)butyric acid. CAS No. 53696-70-1. Molecular formula: C10H16N2O2. Mole weight: 196.25. | |
| Amikacin | Amikacin (BAY 41-6551) is a semisynthetic kanamycin analog that is active against most Gram-negative bacteria, including gentamicin- and tobramycin-resistant strains. Significant inhibitory effect. Amikacin is ototoxic and nephrotoxic. Amikacin can be used in bacteriostatic, anti-cancer and analgesic studies [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY 41-6551. CAS No. 37517-28-5. Pack Sizes: 50 mg; 100 mg. Product ID: HY-B0509A. | |
| Amikacin | It has a wide antibacterial spectrum and is effective to most kanamycin resistant bacteria. Uses: Anti-bacterial agents. Synonyms: (S)-O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1?6)-O-[6-amino-6-deoxy-α-D-glucopyranosyl-(1?4)]-N1-(4-amino-2-hydroxy-1-oxobutyl)-2-deoxy-D-streptamine; 1-N-[L-(-)-γ-Amino-α-hydroxybutyryl]kanamycin A; Amicacin; Amikacillin; Amikacin; Amikozit; Amukin; Antibiotic BB-K 8; Arikace; BAY 41-6551; BAY 416651; BB-K 8; Lukadin; Potentox. Grades: 98%. CAS No. 37517-28-5. Molecular formula: C22H43N5O13. Mole weight: 585.60. | |
| Amikacin B Sulfate | Amikacin B Sulfate is an impurity of Amikacin. Amikacin is an antibacterial compound used in the treatment of diseases and illnesses arising from gram-negative bacterium. Synonyms: O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1?6)-O-[2,6-diamino-2,6-dideoxy-α-D-glucopyranosyl-(1?4)]-N1-[(2S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxy-D-streptamine Amikacin B Sulfate; 1-N-[(S)-4-Amino-2-hydroxybutyryl]kanamycin B Amikacin B Sulfate; BB-K26 Amikacin B Sulfate; Habekacin Amikacin B Sulfate; Amikacin EP Impurity H Sulfate. Grades: 95%. Molecular formula: C22H44N6O12.xH2SO4. Mole weight: 584.62 (free base). | |
| Amikacin disulfate | Amikacin disulfate (BAY 41-6551 dissulfate) is an aminoglycoside antibiotic and a semisynthetic analog of kanamycin. Amikacin disulfate is bactericidal, acting directly on the 30S and 50S bacerial ribosomal subunits to inhibit protein synthesis. Amikacin disulfate is very active against most Gram-negative bacteria including gentamicin - and tobramycin-resistant strains. Amikacin disulfate also inhibits the infections caused by susceptible Nocardia and nontuberculous mycobacteria [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY 41-6551 disulfate. CAS No. 39831-55-5. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0509B. | |
| Amikacin disulfate | Amikacin disulfate. Group: Biochemicals. Alternative Names: O-3-Amino-3-deoxy-a-D-glucopyranosyl-(1?6)-O-[6-amino-6-deoxy-a-D-glucopyranosyl-(1?4)]-N1-[(2S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxy-D-streptamine sulfate; 1-N- [L- (-) -gamma-Amino-a-hydroxybutyryl] kanamycin A sulfate; Amiglyde V; Amikacin disulfate salt. Grades: Highly Purified. CAS No. 39831-55-5. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C22H43N5O13·2H2SO4. US Biological Life Sciences. | Worldwide |
| Amikacin EP Impurity F Sulfate | Amikacin EP Impurity F Sulfate is an impurity of Amikacin. Amikacin is an antibacterial compound used in the treatment of diseases and illnesses arising from gram-negative bacterium. Synonyms: O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1?6)-O-[6-[[(2S)-4-amino-2-hydroxy-1-oxobutyl]amino]-6-deoxy-α-D-glucopyranosyl-(1?4)]-N1-[(2S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxy-D-streptamine Sulfate; 1,6'-Di-N-(L-4-amino-2-hydroxybutyryl) Kanamycin A Sulfate; Amikacin Impurity B Sulfate; 1,6'-Di-HABA Kanamycin A Sulfate. Grades: 95%. Molecular formula: C26H50N6O15.xH2SO4. Mole weight: 686.70 (free base). | |
| Amikacin hydrate | Amikacin hydrate (BAY 41-6551 hydrate) is an aminoglycoside antibiotic and a semisynthetic analog of kanamycin. Amikacin hydrate is bactericidal, acting directly on the 30S and 50S bacerial ribosomal subunits to inhibit protein synthesis. Amikacin hydrate is very active against most Gram-negative bacteria including gentamicin - and tobramycin-resistant strains. Amikacin hydrate also inhibits the infections caused by susceptible Nocardia and nontuberculous mycobacteria [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY 41-6551 hydrate. CAS No. 1257517-67-1. Pack Sizes: 50 mg; 100 mg; 500 mg. Product ID: HY-B0509. | |
| Amikacin hydrate | Amikacin hydrate is an aminoglycoside antibiotic and a semisynthetic analog of kanamycin. Amikacin works by binding to the bacterial 30S ribosomal subunit, causing misreading of mRNA and leaving the bacterium unable to synthesize proteins vital to its growth. Synonyms: BAY 41-6551 hydrate. Grades: >98%. CAS No. 1257517-67-1. Molecular formula: C22H45N5O14. Mole weight: 603.62. | |
| Amikacin impurity A | 3-HABA Kanamycin A is an impurity of Amikacin. Amikacin is an antibacterial compound used in the treatment of diseases and illnesses arising from gram-negative bacterium. Uses: Amikacin (a578500) impurity a. Synonyms: (S)-4-amino-N-((1S,2R,3S,4S,5R)-5-amino-4-(((2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-2-(((2R,3R,4S,5R,6R)-6-(aminomethyl)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)-3-hydroxycyclohexyl)-2-hydroxybutanamide; 3-HABA Kanamycin A. Grades: >95%. CAS No. 50725-24-1. Molecular formula: C22H43N5O13. Mole weight: 585.60. | |
| Amikacin impurity B | An impurity of Amikacin. Synonyms: 1,3-Di-HABA Kanamycin A. Grades: > 95%. CAS No. 927821-99-6. Molecular formula: C26H50N6O15. Mole weight: 686.72. | |
| Amikacin sulfate | Amikacin sulfate (BAY 41-6551 sulfate) is an aminoglycoside antibiotic and a semisynthetic analog of kanamycin. Amikacin sulfate is bactericidal, acting directly on the 30S and 50S bacerial ribosomal subunits to inhibit protein synthesis. Amikacin sulfate is very active against most Gram-negative bacteria including gentamicin - and tobramycin-resistant strains. Amikacin sulfate also inhibits the infections caused by susceptible Nocardia and nontuberculous mycobacteria [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY 41-6551 sulfate. CAS No. 149022-22-0. Pack Sizes: 50 mg; 100 mg. Product ID: HY-107813. | |
| Amikacin Sulfate | Amikacin disulfate is an antibiotic that binds to 16S rRNA (bacterial 30S ribosome), causing misreading of mRNA and supressing protein synthesis. Uses: Anti-bacterial agents. Synonyms: BB-K8; BB K8; BBK8; O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1?6)-O-[6-amino-6-deoxy-α-D-glucopyranosyl-(1?4)]-N1-[(2S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxy-D-streptamine Sulfate; 1-N-[L-(-)-γ-Amino-α-hydroxybutyryl]kanamycin A Sulfate; Amiglyde V; Amika; Amikacin Disulfate; Amikacin Sulfate; Amikavet; Amikin; Amiklin; Antibiotic BB-K 8 Sulfate; Biklin; Biodacyn; Biodacyna; Fabianol; Grasil; Kaminax; Mikavir; Novamin; Pierami; Selemycin. Grades: 95%. CAS No. 39831-55-5. Molecular formula: C22H47N5O21S2. Mole weight: 781.76. | |
| aminoglycoside 2''-phosphotransferase | Requires Mg2+. This bacterial enzyme phosphorylates many 4,6-disubstituted aminoglycoside antibiotics that have a hydroxyl group at position 2'', including kanamycin A, kanamycin B, tobramycin, dibekacin, arbekacin, amikacin, gentamicin C, sisomicin and netilmicin. In most, but not all, cases the phosphorylation confers resistance against the antibiotic. Some forms of the enzyme use ATP as a phosphate donor in appreciable amount. The enzyme is often found as a bifunctional enzyme that also catalyses 6'-aminoglycoside N-acetyltransferase activity. The bifunctional enzyme is the most clinically important aminoglycoside-modifying enzyme in Gram-positive bacteria, responsible for high-level resistance in both Enterococci and Staphylococci. Group: Enzymes. Synonyms: aphD (gene name); APH(2''); aminoglycoside (2'') kinase; gentamicin kinase (ambiguous); gentamicin phosphotransferase (ambiguous). Enzyme Commission Number: EC 2.7.1.190. 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-3023; aminoglycoside 2''-phosphotransferase; EC 2.7.1.190; aphD (gene name); APH(2''); aminoglycoside (2'') kinase; gentamicin kinase (ambiguous); gentamicin phosphotransferase (ambiguous). Cat No: EXWM-3023. | |
| aminoglycoside 6'-N-acetyltransferase | The antibiotics kanamycin A, kanamycin B, neomycin, gentamicin C1a, gentamicin C2 and sisomicin are substrates. The antibiotic tobramycin, but not paromomycin, can also act as acceptor. The 6-amino group of the purpurosamine ring is acetylated. Group: Enzymes. Synonyms: aminoglycoside N6'-acetyltransferase; aminoglycoside-6'-acetyltransferase; aminoglycoside-6-N-acetyltransferase; kanamycin acetyltransferase. Enzyme Commission Number: EC 2.3.1.82. CAS No. 56467-65-3. 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-2263; aminoglycoside 6'-N-acetyltransferase; EC 2.3.1.82; 56467-65-3; aminoglycoside N6'-acetyltransferase; aminoglycoside-6'-acetyltransferase; aminoglycoside-6-N-acetyltransferase; kanamycin acetyltransferase. Cat No: EXWM-2263. | |
| BB-K 6 N-(Benzyloxy) Carbamate | BB-K 6 N-(Benzyloxy) Carbamate is an intermediate in the synthesis of BB-K 6, a semi-synthetic aminoglycoside antibiotic derived from Kanamycin A. Molecular formula: C30H49N5O15. Mole weight: 719.73. | |
| BB-K 6 Sulfate Salt | BB-K 6 is a semi-synthetic aminoglycoside antibiotic derived from Kanamycin A. Synonyms: (S)-O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1?6)-O-[6-[(4-amino-2-hydroxy-1-oxobutyl)amino]-6-deoxy-α-D-glucopyranosyl-(1?4)]-2-deoxy-D-streptamine Sulfate Salt; O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1?6)-O-[6-[[(2S)-4-amino-2-hydroxy-1-oxobutyl]amino]-6-deoxy-α-D-glucopyranosyl-(1?4)]-2-deoxy-D-streptamine Sulfate Salt; Antibiotic BB-K 6 Sulfate Salt; Amikacin EP Impurity E Sulfate. Grades: 97%. Molecular formula: C22H43N5O13.xH2SO4. Mole weight: 585.60 (free base). | |
| Butirosin | Butirosin is an aminoglycoside antibiotic produced by acillus circulans. It has activity against gram-positive bacteria, negative bacteria, and mycobacteria. It is not cross-resistant to gentamicin, and has an effect on some kanamycin-resistant bacteria. Synonyms: Ambutyrosin. CAS No. 12772-35-9. Molecular formula: C21H41N5O12. Mole weight: 555.57. | |
| Butirosin A | Butirosin A is an aminoglycoside antibiotic produced by acillus circulans. It has activity against gram-positive bacteria, negative bacteria, and mycobacteria. It is not cross-resistant to gentamicin, and has an effect on some kanamycin-resistant bacteria. Synonyms: Ambutyrosin A. Grades: 95%. CAS No. 34291-02-6. Molecular formula: C21H41N5O12. Mole weight: 555.57. | |
| Butirosin B | Butirosin B is an aminoglycoside antibiotic produced by acillus circulans. It has activity against gram-positive bacteria, negative bacteria, and mycobacteria. It is not cross-resistant to gentamicin, and has an effect on some kanamycin-resistant bacteria. Synonyms: Ambutyrosin B. CAS No. 34291-03-7. Molecular formula: C21H41N5O12. Mole weight: 555.57. | |
| Combimicin A2 | It is produced by the strain of Micromonospora sp. K-6993, K-6993-Y-41, NRRL 2958-N-6. It's a kanamycin homolog. CAS No. 72300-83-5. Molecular formula: C20H40N4O9. Mole weight: 480.55. | |
| Combimicin B1 | It is produced by the strain of Micromonospora sp. K-6993, K-6993-Y-41, NRRL 2958-N-6. It's a kanamycin homolog. CAS No. 72265-93-1. Molecular formula: C21H43N5O8. Mole weight: 493.59. | |
| Combimicin B2 | It is produced by the strain of Micromonospora sp. K-6993, K-6993-Y-41, NRRL 2958-N-6. It's a kanamycin homolog. Synonyms: Combimicin B(sub 2); D-Streptamine, O-3-deoxy-4-C-methyl-3-(methylamino)-alpha-D-galactopyranosyl-(1-6)-O-(2,6-diamino-2,3,4,6-tetradeoxy-alpha-D-erythro-hexopyranosyl-(1-4))-2-deoxy-; 4,6-Diamino-3-{[3-deoxy-4-C-methyl-3-(methylamino)hexopyranosyl]oxy}-2-hydroxycyclohexyl 2,6-diamino-2,3,4,6-tetradeoxyhexopyranoside. CAS No. 72265-90-8. Molecular formula: C20H41N5O8. Mole weight: 479.57. | |
| Dibekacin | It is effective to kanamycin resistant bacteria. Synonyms: Panamicin; Dideoxykanamycin B; 3',4'-Dideoxykanamycin B; Kappati. Grades: 95%. CAS No. 34493-98-6. Molecular formula: C18H37N5O8. Mole weight: 451.52. | |
| gentamicin 2'-N-acetyltransferase | The antibiotics gentamicin A, sisomicin, tobramycin, paromomycin, neomycin B, kanamycin B and kanamycin C can also act as acceptors. Group: Enzymes. Synonyms: gentamycin acetyltransferase II; gentamycin 2'-N-acetyltransferase; acetyl-CoA:gentamycin-C1a N2'-acetyltransferase. Enzyme Commission Number: EC 2.3.1.59. CAS No. 50864-40-9. 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-2238; gentamicin 2'-N-acetyltransferase; EC 2.3.1.59; 50864-40-9; gentamycin acetyltransferase II; gentamycin 2'-N-acetyltransferase; acetyl-CoA:gentamycin-C1a N2'-acetyltransferase. Cat No: EXWM-2238. | |
| Kanamycin | Kanamycin. Group: Biochemicals. Alternative Names: Kanamycin A. Grades: Highly Purified. CAS No. 8063-7-8. Pack Sizes: 100mg, 250mg, 500mg, 1g. Molecular Formula: C18H36N4O11, Molecular Weight: 484.5. US Biological Life Sciences. | Worldwide |
| Kanamycin | Kanamycin (Kanamycin A) is an orally active antibacterial (gram-negative/positive bacteria) agent, inhibits translocation and causes misencoding by binding to the 70 S ribosomal subunit. Kanamycin shows good inhibitory activity to both M. tuberculosis (sensitive and drug-resistant ) and K. pneumonia , which can be used in studies of tuberculosis and pneumonia [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Kanamycin A. CAS No. 59-01-8. Pack Sizes: 100 mg; 200 mg. Product ID: HY-16566. | |
| Kanamycin A | Inhibitor of protein synthesis; aminoglycoside. Kanamycin A is an antibiotic complex produced by Streptomyces kanamyceticus Okami & Umezawa from Japanese soil. Comprised of three components, kanamycin A, the major component, and kanamycins B and C, two minor congeners. Antibacterial. Group: Biochemicals. Alternative Names: O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1?6)-O-[6-amino-6-deoxy-α-D-glucopyranosyl-(1?4)]-2-deoxy-D-streptamine;4,6-Diamino-2-hydroxy-1,3-cyclohexane 3,6'-diamino-3,6'-dideoxydi-α-D-glucoside;KM; Kanacin; Kanamycin. Grades: Highly Purified. CAS No. 59-01-8. Pack Sizes: 1g, 5g, 10g. Molecular Formula: C??H??N?O??, Molecular Weight: 484.5. US Biological Life Sciences. | Worldwide |
| Kanamycin A | Kanamycin is an aminoglycoside antibiotic that has inhibitory effects on gram-positive and negative bacteria and mycoplasma. It can be used for the prevention and treatment of chicken pullorum, colibacillosis, enteritis and other diseases, and has a significant effect on systemic sepsis, respiratory tract infection, peritonitis, etc. caused by drug-resistant bacteria. Uses: Anti-bacterial agents; protein synthesis inhibitors. Synonyms: Amikacin EP Impurity D; O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1?6)-O-[6-amino-6-deoxy-α-D-glucopyranosyl-(1?4)]-2-deoxy-D-streptamine; 4,6-Diamino-2-hydroxy-1,3-cyclohexane 3,6'-diamino-3,6'-dideoxydi-α-D-glucoside; KM; Kanacin; Kanamycin; 6-O-(3-amino-3-deoxy-a-D-glucopyranosyl)-4-O-(6-amino-6-deoxy-a-D-glucopyranosyl)-2-deoxy-D-streptamine. Grades: 95%. CAS No. 59-01-8. Molecular formula: C18H36N4O11. Mole weight: 484.50. | |
| Kanamycin acid disulfate | Kanamycin acid sulfate is an aminoglycoside antibiotic produced by Streptomyces. Synonyms: Kanamycin A disulfate. CAS No. 64013-70-3. Molecular formula: C18H40N4O19S2. Mole weight: 680.65. | |
| Kanamycin A Deuterated | Antibiotic complex produced by Streptomyces kanamyceticus Okami & Umezawa from Japanese soil. Comprised of three components, kanamycin A, the major component, and kanamycins B and C, two minor congeners. Antibacterial. Group: Biochemicals. Alternative Names: O-3-Amino-3-deoxy-α-D-glucopyranosyl-(16)-O-[6-amino-6-deoxy-α-D-glucopyranosyl-(14)]-2-deoxy-. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Kanamycin A Related Compound 1 | Kanamycin A Related Compound 1 is an Indispensable compound, used for studying bacterial infections. Synonyms: 4-O-(6-Amino-6-deoxy-α-D-glucopyranosyl)-2-deoxy-D-streptamine. Grades: > 95%. CAS No. 31077-71-1. Molecular formula: C12H25N3O7. Mole weight: 323.34. | |
| Kanamycin D | Synonyms: Kanamycin D; 3''-deamino-3''-hydroxykanamycin A; (1S,2S,3R,4S,6R)-4,6-diamino-3-[(6-amino-6-deoxy-alpha-D-glucopyranosyl)oxy]-2-hydroxycyclohexyl alpha-D-glucopyranoside; (2R,3S,4S,5R,6R)-2-(aminomethyl)-6-[(1R,2S,3S,4R,6S)-4,6-bis(azanyl)-3-[(2S,3R,4S,5S,6R)-6-(hydroxymethyl)-3,4,5-tris(oxidanyl)oxan-2-yl]oxy-2-oxidanyl-cyclohexyl]oxy-oxane-3,4,5-triol; CHEBI:73079; '3"-deamino-3"-hydroxykanamycin A'; C21253; Q27140286; (2R,3S,4S,5R,6R)-2-(aminomethyl)-6-[(1R,2S,3S,4R,6S)-4,6-diamino-2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl]oxyoxane-3,4,5-triol; CJX. Grades: > 95%. Molecular formula: C18H35N3O12. Mole weight: 485.49. | |
| kanamycin kinase | Also acts on the antibiotics neomycin, paromomycin, neamine, paromamine, vistamycin and gentamicin A. An enzyme from Pseudomonas aeruginosa also acts on butirosin. Group: Enzymes. Synonyms: neomycin-kanamycin phosphotransferase. Enzyme Commission Number: EC 2.7.1.95. CAS No. 62213-36-9. 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-3125; kanamycin kinase; EC 2.7.1.95; 62213-36-9; neomycin-kanamycin phosphotransferase. Cat No: EXWM-3125. | |
| Kanamycins sulfate | Kanamycins sulfate is a broad-spectrum antibiotic, can be used in certain severe staphylococcal or Gram-negative bacillary infections. Kanamycin sulfate has certain ototoxicity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 70560-51-9. Pack Sizes: 1 g; 5 g. Product ID: HY-W040128. | |
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