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| Product | Description | |
|---|---|---|
| Gentamycin B | Gentamycin B is an aminoglycoside antibiotic coproduced as a minor component in the gentamicin fermentation. It was found to have the same antibacterial spectrum as gentamicin in vitro and in vivo. Synonyms: Sch-14342; Sch 14342. Molecular formula: C19H38N4O10. Mole weight: 482.5. |  |
| Gentamycin (Gentamicin) (BSA) | Precursor: Gentamycin Sulfate. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| Gentamycin (Gentamicin) (HRP) | Gentamicin is a broad-spectrum antibiotic derived from an actinomycete of the genus Micromonospora, used in its sulfate form to treat various infections. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Gentamycin (Gentamicin) Sulfate Solution 10mg/ml | Broad spectrum, cell culture antibiotic that is non toxic to viruses and mammalian cells at antibacterial levels. Inhibits growth of gram positive and negative bacteria, and mycoplasma. Inhibits normal protein synthesis by binding to L6 protein of 50S ribosomal subunit. Useful antibiotic for Baculovirus expression systems since mutations in rplF prevent Gentamycin from binding. Group: Biochemicals. Grades: Cell Culture Grade. CAS No. 1405-41-0. Pack Sizes: 20ml, 5x20ml, 10x20ml. Molecular Formula: C21H43N5O7 H2SO4, Molecular Weight: ~575.6. US Biological Life Sciences. | Worldwide |
| Gentamycin (Gentamicin) Sulfate Solution 50mg/ml | Broad spectrum, cell culture antibiotic that is non toxic to viruses and mammalian cells at antibacterial levels. Inhibits growth of gram positive and negative bacteria, and mycoplasma. Inhibits normal protein synthesis by binding to L6 protein of 50S ribosomal subunit. Useful antibiotic for Baculovirus expression systems since mutations in rplF prevent Gentamycin from binding. Group: Biochemicals. Alternative Names: Alcomici; Bristagen; Cidomycin; Duragentam; Garamycin; Garasol; Apogen, Gentiomycin C, Refobacin, NSC-82261; Gentamycin sulphate. Grades: Molecular Biology Grade. CAS No. 1405-41-0. Pack Sizes: 20ml, 5x20ml, 10x20ml. US Biological Life Sciences. | Worldwide |
| Gentamycin (Gentamicin) Sulfate USP | Broad spectrum, cell culture aminoglycoside antibiotic that is non toxic to viruses and mammalian cells at antibacterial levels. Inhibits growth of gram positive and negative bacteria, and mycoplasma. Inhibits normal protein synthesis by binding to L6 protein of 50S ribosomal subunit. Useful antibiotic for Baculovirus expression systems since mutations in rplF prevent Gentamycin from binding.Causes codon misreading by binding to the 30S ribosomal subunit, blocking the translocation of peptidyl-tRNA from the acceptor site to the donor site. Antibacterial against Gram-negative aerobic bacteria, Gram-positive bacteria and mycoplasmas. Used as a selection agent (gentamicin-resi...ption of the membrane. This increases the permeability of the cell envelope, leakage of cell contents, and leading to apoptosis and proteolysis (cell death). Causes also cell death by generation of free radicals, phospholipidosis, extracellular calcium-sensing recep- tor stimulation and energetic catastrophe. Source:Micromonospora sp. Group: Biochemicals. Alternative Names: Alcomici; Bristagen; Cidomycin; Duragentam; Garamycin; Garasol; Apogen, Gentiomycin C, Refobacin, NSC-82261; Gentamycin sulphate. Grades: Cell Culture Grade. CAS No. 1405-41-0. Pack Sizes: 5g, 25g, 100g, 500g, 1Kg. Molecular Formula: C21H43N5O7.H2SO4, Molecular Weight: ~575.6. US Biological Life Sciences. | Worldwide |
| Gentamycin Impurity E | Gentamycin Impurity E is an important component of several aminocyclitol antibiotics. Synonyms: 2-Deoxystreptamine dihydrobromide; 2-DOS · 2HBr; 4t,6t-Diamino-cyclohexan-1r,2t,3c-triol; 2-Deoxy-1,3-myo-inosadiamine. Grades: > 95%. CAS No. 84107-26-6. Molecular formula: C6H16N2O3Br2. Mole weight: 324.01. | |
| Gentamycin sulfate | Cas No. 1405-41-0. | |
| Gentamycin sulfate | Gentamycin sulfate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: GENTAMICIN 2,5-SULFATE HYDRATE;genoptics.o.p.;gentalline;gentamicinsolution;nsc-82261;sch9724;gentamicin solution 10mg/ml sterile*filtered;gentamicin solution cell culture tested. Appearance: powder. CAS No. 1405-41-0. Molecular formula: C60H127N15O26S. Mole weight: 1506.8. Purity: 0.96. IUPACName: Gentamicin Sulfate. Product ID: ACM1405410-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: Gentamcin Sulfate. |  |
| Gentamycin Sulfate | 25g Pack Size. Group: Antibiotics. Formula: C21H43N5O7H2So4. CAS No. 1405-41-0. Prepack ID 10336465-25g. Molecular Weight 575.68. See USA prepack pricing. |  |
| Gentamycin Sulfate | 5g Pack Size. Group: Antibiotics. Formula: C21H43N5O7H2So4. CAS No. 1405-41-0. Prepack ID 10336465-5g. Molecular Weight 575.68. See USA prepack pricing. | |
| Gentamycin Sulfate EP Impurity C | Synonyms: 4-O-(6-Amino-6,7-dideoxy-α-D-glycero-D-gluco-heptopyranosyl)-6-O-(4-methyl-3-methylamino-3-deoxy-β-L-arabinopyranosyl)-2-deoxy-D-streptamine; ; Gentamycin B1; D-Streptamine, o-6-amino-6,7-dideoxy-D-glycero-alpha-D-gluco-heptopyranosyl-(1-4)-o-(3-deoxy-4-C-me. Grades: > 95%. CAS No. 36889-16-4. Molecular formula: C20H40N4O10. Mole weight: 496.56. | |
| Gentamycin sulfate EP impurity D | Grades: > 95%. Molecular formula: C19H39N5O9. Mole weight: 481.55. | |
| Atorvastatin Lactone | Atorvastatin Lactone prevents inhibition of P-glycoprotein mediated Rhodamine 123 transport in cells. Studies suggest that Atorvastatin is also a potent scavenger for free radicals and prevents toxic effects of Gentamycin by inhibiting NF-κB and MAPK signaling pathways. Group: Biochemicals. Alternative Names: 5-(4-Fluorophenyl)-2-(1-methylethyl)-N,4-diphenyl-1-[2-[(2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl]ethyl]-1H-pyrrole-3-carboxamide; Atorvastatin δ-lactone. Grades: Highly Purified. CAS No. 125995-03-1. Pack Sizes: 25mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
| Caspofungin acetate | 1-[(4R,5S)-5-[(2-aminoethyl)amino]-N2-(10,12-dimethyl-1oxotetradecyl)-4-hydroxy-L-ornithine]-5-[(3R)-3-hydroxy-L-ornithine] Pneumocandin B0 diacetate. aminoglycoside antibiotic similar to gentamycin, toxic to bacterial, yeast, higher plant and mammalian cells and to protozoans and helminthes. CAS No. 179463-17-3. Product ID: 8-04685. Molecular formula: C56H96N10O19. Mole weight: 1213.43. Purity: 0.99. |  |
| G418 Sulfate (Geneticin®) | G418 Sulfate is an aminoglycoside related to Gentamycin, used as a selective agent in bacterial genetics. It is toxic to yeast, bacteria, many plant and mammalian cells, helminths and protozoans. Group: Biochemicals. Alternative Names: O-2-Amino-2,7-dideoxy-D-glycero-α-D-gluco-heptopyranosyl-(1?4)-O-[3-deoxy-4-C-methyl-3-(methylamino)- β-L-arabinopyranosyl-(1?6)]-2-deoxy-D-streptamine Sulfate (1:2); Antibiotic G 418 Sulfate; G418 Sulfate. Grades: Molecular Biology Grade. CAS No. 108321-42-2. Pack Sizes: 1g, 5g, 10g, 25g. Molecular Formula: C20H40N4O10 2H2SO4, Molecular Weight: 692.71. US Biological Life Sciences. | Worldwide |
| G418 Sulfate (Geneticin®) 50mg/ml Solution, Sterile-filtered | G418 Sulfate is an aminoglycoside related to Gentamycin. It is used as a selective agent in bacterial genetics. It is toxic to yeast, bacteria, many plant and mammalian cells, helminths and protozoans. Group: Biochemicals. Grades: Molecular Biology Grade. CAS No. 108321-42-2. Pack Sizes: 20ml, 5x20ml. US Biological Life Sciences. | Worldwide |
| 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. |  |
| gentamicin 2''-nucleotidyltransferase | ATP, dATP, CTP, ITP and GTP can act as donors; kanamycin, tobramycin and sisomicin can also act as acceptors. The nucleotidyl residue is transferred to the 2-hydroxy of the 3-amino-3-deoxy-D-glucose moiety in the antibiotic. Group: Enzymes. Synonyms: gentamicin 2''-adenylyltransferase; aminoglycoside adenylyltransferase; gentamycin 2''-nucleotidyltransferase. Enzyme Commission Number: EC 2.7.7.46. CAS No. 62213-33-6. 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-3258; gentamicin 2''-nucleotidyltransferase; EC 2.7.7.46; 62213-33-6; gentamicin 2''-adenylyltransferase; aminoglycoside adenylyltransferase; gentamycin 2''-nucleotidyltransferase. Cat No: EXWM-3258. | |
| gentamicin 3-N-acetyltransferase | Also acetylates sisomicin. Group: Enzymes. Synonyms: gentamycin acetyltransferase I; aminoglycoside acetyltransferase AAC(3)-1; gentamycin 3-N-acetyltransferase; acetyl-CoA:gentamycin-C N3-acetyltransferase; acetyl-CoA:gentamicin-C N3'-acetyltransferase (incorrect); gentamicin 3'-N-acetyltransferase (incorrect). Enzyme Commission Number: EC 2.3.1.60. CAS No. 58500-58-6. 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-2240; gentamicin 3-N-acetyltransferase; EC 2.3.1.60; 58500-58-6; gentamycin acetyltransferase I; aminoglycoside acetyltransferase AAC(3)-1; gentamycin 3-N-acetyltransferase; acetyl-CoA:gentamycin-C N3-acetyltransferase; acetyl-CoA:gentamicin-C N3'-acetyltransferase (incorrect); gentamicin 3'-N-acetyltransferase (incorrect). Cat No: EXWM-2240. | |
| Gentamicin B1 Acetate Salt | Gentamicin B1 Acetate Salt is the salt form of Gentamicin B1, which is a derivative of Gentamicin, an aminoglycoside antibiotic. Synonyms: Gentamycin B1 Acetate Salt; O-6-Amino-6,7-dideoxy-D-glycero-α-D-gluco-heptopyranosyl-(1?4)-O-[3-deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(1?6)]-2-deoxy-D-Streptamine Acetate Salt. Grades: 87%. Molecular formula: C20H40N4O10 x(C2H4O2). Mole weight: 496.56. | |
| Gentamicin C1a | It is a broad-spectrum aminoglycoside antibiotic produced by the strain of Micromonospora spp. One of several components of the gentamicin C complex which comprises approximately 80% gentamicin and exhibits the most potent antimicrobial activity. Synonyms: Gentamycin C1A; Gentamycin C12; O-3-deoxy-4-C-methyl-3-(methylamino)-beta-L-arabinopyranosyl-(1-6)-O-(2,6-diamino-2,3,4,6-tetradeoxy-alpha-D-erythro-hexopyranosyl-(1-4))-2-deoxy-D-streptamine. Grades: ≥95.0%. CAS No. 26098-04-4. Molecular formula: C19H39N5O7. Mole weight: 449.54. | |
| Gentamicin C1a Pentaacetate Salt | Antibacterial. Group: Biochemicals. Alternative Names: O-3-Deoxy-4-C-methyl-3-(methylamino)- β-L-arabinopyranosyl-(1-6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-α-D-erythro-hexopyranosyl-(1-4)]-2-deoxy-D-streptamine Pentaacetate Salt; Gentamicin D Acetate; Gentamycin C1a Acetate; Gentamicin C3 Acetate. Grades: Highly Purified. CAS No. 26098-04-4. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Gentamicin C1a Pentaacetate Salt | Antibacterial. Synonyms: O-3-Deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(1-6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-α-D-erythro-hexopyranosyl-(1-4)]-2-deoxy-D-streptamine Pentaacetate Salt; Gentamicin D Acetate; Gentamycin C1a Acetate; Gentamicin C3 Acetate. Grades: 95%. Molecular formula: C29H59N5O17. Mole weight: 749.8. | |
| Gentamicin C2a | It is produced by the strain of Micromonospora. One of three components of the gentamicin C complex which comprises approximately 80% gentamicin and exhibits the most potent antimicrobial activity. Synonyms: 6-O-(3-Deoxy-4-methyl-3-methylamino-β-L-arabinopyranosyl)-4-O-(2,6-diamino-2,3,4,6,7-pentadeoxy-β-L-lyxo-heptopyranosyl)-2-deoxy-D-streptamine; Gentamycin Sulfate Impurity 10. Grades: ≥95.0%. CAS No. 59751-72-3. Molecular formula: C20H41N5O7. Mole weight: 463.57. | |
| Gentamicin C2 Pentaacetate Salt | Antibacterial. A mixture of Gentamicin C2 and Gentamycin C2a. Group: Biochemicals. Alternative Names: O-3-Deoxy-4-C-methyl-3-(methylamino)- β-L-arabinopyranosyl-(16)-O-[2,6-diamino-2,3,4,6,7-pentadeoxy-α-D-ribo-heptopyranosyl-(14)]-2-deoxy-. Grades: Highly Purified. CAS No. 25876-11-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Gentamicin C2 Pentaacetate Salt (Mixture of C2 and C2a) | Antibacterial. A mixture of Gentamicin C2 and Gentamycin C2a. Synonyms: O-3-Deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(16)-O-[2,6-diamino-2,3,4,6,7-pentadeoxy-α-D-ribo-heptopyranosyl-(14)]-2-deoxy-D-streptamine Pentaacetate Salt. Grades: 95%. Molecular formula: C30H61N5O17. Mole weight: 763.83. | |
| Gentamicin sulfate | Gentamicin is a bactericidal aminoglycoside that was discovered and isolated from Micromonospora purpurea in 1963.7 It is one of the most frequently prescribed aminoglycosides due to its spectrum of activity, low cost, and availability.5,8 Gentamicin is effective against both gram-positive and gram-negative organisms but is particularly useful for the treatment of severe gram-negative infections including those caused by Pseudomonas aeruginosa.6,10,11 There is the added benefit of synergy when gentamicin is co-administered with other antibacterials such as beta-lactams.11 This synergistic activity is not only important for the treatment of complex infections, but can also contribute to dose optimization and reduced adverse effects. Synonyms: Gentamicin (as sulfate) / Gentamicin (as sulphate) / Gentamicin (gentamycin sulfate) / Gentamicin C complex sulfate / Gentamicin sulfate (salt) / Gentamicin sulphate. CAS No. 1405-41-0. Product ID: PAP-0098. Molecular formula: C60H125N15O25S. Mole weight: 1488.8. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; PAP-0098; Gentamicin sulfate; 1405-41-0; Gentamicin (as sulfate) / Gentamicin (as sulphate) / Gentamicin (gentamycin sulfate) / Gentamicin C complex sulfate / Gentamicin sulfate (salt) / Gentamicin sulphate. Chemical Name: Gentamicin sulfate. Grade: Pharmaceutical grade. |  |
| Gentamicin Sulfate | Gentamycin Sulfate is a broad-spectrum, aminoglycoside antibiotic used for cell culture which inhibits protein synthesis in sensitive organisms. Uses: Broad-spectrum, aminoglycoside antibiotic. Synonyms: Gentamicin C; NSC-82261; NSC82261; NSC 82261; SCH9724; SCH 9724; SCH-9724; Alcomicin; Bristagen; Cidomycin; Duragentam; Garamycin; Garasol; Genoptic; Gentacidin; Gentacin; Gentaglyde; Gentalyn; Gentamicin C Complex Citrate; Gentibioptal; Genticin; Gentocin; Gentogram; Gent-Ophtal; Getalline; GM Sulfate. Grades: Assay: ≥ 590 I.U./mg. CAS No. 1405-41-0. Molecular formula: C(19-21)H(39-43)N5O7.H2SO4. Mole weight: 561.65 (Average). | |
| Gentamicinsulfate salt | Gentamicinsulfate salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: GENTAMYCINE; Gentavet; GentamysinsolutionforBiochemistry; GENTAMYCIN; Gentacycol; Lyramycin; Uromycine; Refobacin tm; GENTAMICINUM. Appearance: clear amber liquid. CAS No. 1403-66-3. Molecular formula: C21H43N5O7. Mole weight: 477.6. Purity: 0.95. IUPACName: Gentamicin. Density: 1.3 g/cm³. Product ID: ACM1403663. Alfa Chemistry ISO 9001:2015 Certified. Categories: SCH-9724. | |
| Gentamicin Sulfate Salt, C Complex | Inhibits protein synthesis by binding to L6 protein of 50S ribosomal subunit. Group: Biochemicals. Alternative Names: Alcomici; Bristagen; Cidomycin; Duragentam; Garamycin; Garasol; Apogen, Gentiomycin C, Refobacin, NSC-82261; Gentamycin sulphate. Grades: Highly Purified. CAS No. 1405-41-0. Pack Sizes: 2.5g. US Biological Life Sciences. | Worldwide |
| Sisomicin | It is an aminoglycoside antibiotic produced by the strain of Micromonospora inyoensis NRRL 3292. It has a broad-spectrum antibacterial effects against Gram-positive and Gram-negative bacteria including B. subtilis, S. aureus, E. coli, and P. aeruginosa. It has no cross-resistance to kanamycin, but has cross-resistance to gentamycin. 50 mg/kg of Sisomicin has protective effect on mice infected with Rickettsia spinosa. Uses: Protein synthesis inhibitors. Synonyms: D-Streptamine, O-3-deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(1?6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-α-D-glycero-hex-4-enopyranosyl-(1?4)]-2-deoxy-; Antibiotic 6640; SCH 13475; Rickamicin; Sisomycin; Sissomicin; O-3-Deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(1?6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-α-D-glycero-hex-4-enopyranosyl-(1?4)]-2-deoxy-D-streptamine; Antibiotic 66-40; BactoCeaze; Ensamycin; Sch 13475; Siseptin. Grades: ≥98%. CAS No. 32385-11-8. Molecular formula: C19H37N5O7. Mole weight: 447.53. | |
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