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| Product | Description | |
|---|---|---|
| Genistein | Genistein, a phytoestrogen found in soy products, is a highly specific inhibitor of protein tyrosine kinase (PTK) which blocks the mitogenic effect mediated by EGF on NIH-3T3 cells with IC50 of 12μM or by insulin with IC50 of 19 μM. Genistein is developed to be an antitumor agent. Genistein has antioxidant effect, it can be used in cosmetics material. It is a plant polyphenol that can inhibit tyrosinase, block melanin synthesis, reduce skin pigment intensity, absorb UV, prevent photoaging, reduce sun damage and age spot formation, and whiten and lighten spots. It also has the anti-glycation and antibacterial effect, can effectively improve skin tone and skin texture, prevent the generation of age spots, remove red bloodlines, and improve skin blood microcirculation. Uses: Antitumor agent. Synonyms: 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; Baichanin A; Bonistein; 4',5,7-Trihydroxyisoflavone; GeniVida; Genisteol; NSC 36586; Prunetol; Sophoricol; Differenol A. Grade: >98%. CAS No. 446-72-0. Molecular formula: C15H10O5. Mole weight: 270.24. |  |
| Genistein-[2',3',5',6'-d4] | Genistein-[2',3',5',6'-d4] is the labelled analogue of Genistein. Genistein is an inhibitor of angiogenesis. Synonyms: Genistein-2',3',5',6' D4; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one-d4. Grade: 95% by HPLC; 95% atom D. CAS No. 187960-08-3. Molecular formula: C15H6D4O5. Mole weight: 274.26. | |
| Genistein-[2',6'-d2] | Genistein-[2',6'-d2] is the labelled analogue of Genistein. Genistein is an inhibitor of angiogenesis. Synonyms: Genistein-2',6' D2; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one-d2; Baichanin A-d2; Bonistein-d2; 4',5,7-Trihydroxyisoflavone-d2; GeniVida-d2; Genisteol-d2; NSC 36586-d2; Prunetol-d2; Sophoricol-d2. Grade: 95% by HPLC; 95% atom D. CAS No. 315204-48-9. Molecular formula: C15H8D2O5. Mole weight: 272.25. | |
| Genistein 7-β-D-Glucuronide | Genistein metabolite. Synonyms: 5-Hydroxy-3-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-7-yl β-D-Glucopyranosiduronic Acid. Grade: 95%. CAS No. 38482-81-4. Molecular formula: C21H18O11. Mole weight: 446.36. | |
| Genistein 7-β-D-Glucuronide | Genistein 7-β-D-Glucuronide (Genistein 7-O-glucuronide) is the primary phase II metabolite of Genistein (HY-14596) in human and rat hepatocytes. Genistein 7-β-D-Glucuronide undergoes distinct deconjugation in different functional assays. Genistein 7-β-D-Glucuronide is produced via hepatic microsomal glucuronidation and shows a mild age-related increase in intrinsic clearance in male F344 rats. Genistein 7-β-D-Glucuronide can be used for research on metabolism[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Genistein 7-O-glucuronide. CAS No. 38482-81-4. Pack Sizes: 1 mg; 5 mg. Product ID: HY-137967. |  |
| Genistein-7-sulfate 4- β-D-glucuronide Disodium Salt | Genistein-7-sulfate 4- β-D-glucuronide is a metabolite of Genistein (G350000), a compound that exhibits specific inhibitory activity against tyrosine kinases,including autophosphorylation of epidermal growth factor receptor kinase. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences. |  Worldwide |
| Genistein-d4 | Genistein-d4 is the deuterium labeled Genistein. Genistein, a soy isoflavone, is a multiple tyrosine kinases (e.g., EGFR) inhibitor which acts as a chemotherapeutic agent against different types of cancer, mainly by altering apoptosis, the cell cycle, and angiogenesis and inhibiting metastasis[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NPI 031L-d4. CAS No. 187960-08-3. Pack Sizes: 1 mg. Product ID: HY-14596S. | |
| Genistein-[d4]-7-O-glucoside | Genistein-[d4]-7-O-glucoside. Synonyms: Genistein D4-7-O-glucoside. | |
| Genistein (Standard) | Genistein (Standard) is the analytical standard of Genistein. This product is intended for research and analytical applications. Genistein, a soy isoflavone, is a multiple tyrosine kinases (e.g., EGFR) inhibitor which acts as a chemotherapeutic agent against different types of cancer, mainly by altering apoptosis, the cell cycle, and angiogenesis and inhibiting metastasis. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NPI 031L (Standard). CAS No. 446-72-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14596R. | |
| Genistin | Genistin. Group: Biochemicals. CAS No. 529-59-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Genistin | Genistin is the major isoflavonoid found in soybeans and soy products. Studies in the 1970s suggested that 99% of the isoflavonoid compounds in soy products are present as their glucosides. Genistin acts as a selective estrogen receptor modulator (SERM) and exhibits antioxidant activity and anticarcinogenic property. Uses: Antioxidant, anticarcinogenic. Synonyms: 7-(b-D-Glucopyranosyloxy)-5-hydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; 4,5,7-Trihydroxyisoflavone 7-b-D-glucoside; Genistein-7-O-beta-D-glucopyranoside. Grade: >98%. CAS No. 529-59-9. Molecular formula: C21H20O10. Mole weight: 432.38. | |
| Genistin | Genistin (Genistine), an isoflavone belonging to the phytoestrogen family, is a potent anti-adipogenic and anti-lipogenic agent. Genistin attenuates cellular growth and promotes apoptotic cell death breast cancer cells through modulation of ERalpha signaling pathway[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Genistine; Genistoside; Genistein 7-O-β-D-glucopyranoside. CAS No. 529-59-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-N0595. | |
| Genkwanin | Genkwanin is a major non-glycosylated flavonoid with anti-flammatory activities. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Puddumetin. CAS No. 437-64-9. Pack Sizes: 10 mM * 1 mL in DMSO; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0731. | |
| Genkwanin | Genkwanin. Group: Biochemicals. Alternative Names: 4',5-Dihydroxy-7-methoxyflavone; 7-Methylapigenin; 7-O-Methylapigenin. Grades: Highly Purified. CAS No. 437-64-9. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C16H12O5. US Biological Life Sciences. | Worldwide |
| Genkwanin (4',5-Dihydroxy-7-methoxyflavone) | Atmosphere: Group: Biochemicals. Alternative Names: 4',5-Dihydroxy-7-methoxyflavone. Grades: Highly Purified. CAS No. 437-64-9. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Genome polyprotein (192-205) | Genome polyprotein (192-205) is amino acids 192 to 205 fragment of Genome polyprotein which has structural molecule activity. This peptide is associated with multiple myeloma. | |
| Gentamicin | Gentamicin, an aminoglycoside antibiotic, inhibits the growth of both gram-positive and gram-negative bacteria and to inhibit several strains of mycoplasma in tissue culture. Gentamicin inhibits DNase I with an IC50 of 0.57 mM[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1403-66-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0276A. | |
| 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 A | Gentamicin A. Group: Biochemicals. Grades: Highly Purified. CAS No. 13291-74-2. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
| Gentamicin A | Gentamicin A is one of the antibiotics originally isolated from Micromonos poraechinospora NRRL 2985. It has good antibacterial activity to gram-positive bacteria and negative bacteria and it has antibacterial activity against most methicillin-sensitive staphylococcus. Synonyms: 4,6-Diamino-3-{[3-Deoxy-3-(Methylamino)Pentopyranosyl]Oxy}-2-Hydroxycyclohexyl 2-Amino-2-Deoxyhexopyranoside; (1R,2S,3S,4R,6S)-4,6-diamino-3-{[3-deoxy-3-(methylamino)-alpha-L-xylopyranosyl]oxy}-2-hydroxycyclohexyl 2-amino-2-deoxy-alpha-D-glucopyranoside. Grade: ≥99.0%. CAS No. 13291-74-2. Molecular formula: C18H36N4O10. Mole weight: 468.50. | |
| Gentamicin B | Gentamicin A is one of the antibiotics originally isolated from Micromonos poraechinospora NRRL 2985. It is used to treat respiratory and urinary tract, blood, bone and soft tissues infections. Synonyms: Betamicine; O-6-Amino-6-deoxy-α-D-glucopyranosyl-(1→4)-O-[3-deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(1→6)]-2-deoxy-D-streptamine; Betamicin; Sch 14342; (1R,2R,3S,4R,6S)-4,6-Diamino-3-{[3-deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl]oxy}-2-hydroxycyclohexyl 6-amino-6-deoxy-α-D-glucopyranoside. Grade: 95%. CAS No. 36889-15-3. Molecular formula: C19H38N4O10. Mole weight: 482.53. | |
| 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. Grade: 87%. Molecular formula: C20H40N4O10.xC2H4O2. Mole weight: 496.56 (free base). | |
| Gentamicin C1 | 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: O-2-Amino-2,3,4,6,7-pentadeoxy-6-(methylamino)-α-D-ribo-heptopyranosyl-(14)-O-[3-deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(16)]-2-deoxy-D-streptamine. Grade: 90%. CAS No. 25876-10-2. Molecular formula: C21H43N5O7. Mole weight: 477.59. | |
| 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. Grade: ≥95.0%. CAS No. 26098-04-4. Molecular formula: C19H39N5O7. Mole weight: 449.54. | |
| Gentamicin C1a | Gentamicin C1a is the precursor of the semi-synthetic antibiotic Etimicin, and has antibacterial activity. Gentamicin C1a is the major component of the Gentamicin complex[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 26098-04-4. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148286. | |
| Gentamicin C1a Deuterated Pentaacetate Salt | Gentamicin C1a Deuterated Pentaacetate Salt is the isotope labelled analog of Gentamicin C1a Pentaacetate Salt, and an 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 Deuterated; Gentamicin D Acetate Deuterated; Gentamycin C1a Acetate Deuterated; Gentamicin C3 Acetate Deuterated. Molecular formula: C19H39N5O7 C10H20O10. 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. Grade: 95%. CAS No. 2995337-71-6. Molecular formula: C29H59N5O17. Mole weight: 749.80. | |
| Gentamicin C1 Deuterated Pentaacetate Salt | Gentamicin C1 Deuterated Pentaacetate Salt is the isotope labelled analog of Gentamicin C1 Pentaacetate Salt (G360585); an antibacterial. Group: Biochemicals. Grades: Highly Purified. CAS No. 287730-69-2. Pack Sizes: 500ug, 5mg. Molecular Formula: C21H43N5O7, Molecular Weight: 477.6. US Biological Life Sciences. | Worldwide |
| Gentamicin C1 Deuterated Pentaacetate Salt | Gentamicin C1 Deuterated Pentaacetate Salt is the isotope labelled analog of Gentamicin C1 Pentaacetate Salt and an antibacterial. Synonyms: O-2-Amino-2,3,4,6,7-pentadeoxy-6-(methylamino)-α-D-ribo-heptopyranosyl-(14)-O-[3-deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(16)]-2-deoxy-D-streptamine Pentaacetate Salt Deuterated. Grade: 90%. CAS No. 287730-69-2. Molecular formula: C31H63N5O17. Mole weight: 777.86. | |
| Gentamicin C1 Pentaacetate Salt | Antibacterial. Group: Biochemicals. Alternative Names: O-2-Amino-2,3,4,6,7-pentadeoxy-6-(methylamino)-α-D-ribo-heptopyranosyl-(14)-O-[3-deoxy-4-C-methyl-3-(methylamino)- β-L-arabinopyranosyl-(16)]-2-deoxy-D-streptamine Pentaacetate Salt. Grades: Highly Purified. CAS No. 25876-10-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Gentamicin C1 Pentaacetate Salt | Gentamicin C1 Pentaacetate Salt is an efficacious antibiotic compound, demonstrating remarkable potential in studying an array of diverse bacterial infections. Categorized under the class of aminoglycoside antibiotics, this compound effectively hinders the protein synthesis process within microbial organisms. Uses: Anti-bacterial agents; protein synthesis inhibitors. Synonyms: O-2-Amino-2,3,4,6,7-pentadeoxy-6-(methylamino)-α-D-ribo-heptopyranosyl-(14)-O-[3-deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(16)]-2-deoxy-D-streptamine Pentaacetate Salt. Grade: 95%. Molecular formula: C31H63N5O17. Mole weight: 777.86. | |
| Gentamicin C2 | Gentamicin C2. Group: Biochemicals. Grades: Highly Purified. CAS No. 25876-11-3. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C20H41N5O7. US Biological Life Sciences. | Worldwide |
| Gentamicin C2 | It is an aminoglycoside antibiotic produced by the strain of Micromonospora spp. One of several components of the gentamicin C complex which can comprise 25-55% gentamicin depending on the manufacturer or manufacturing process. Synonyms: D-Streptamine, O-3-deoxy-4-C-methyl-3-(methylamino)-beta-L-arabinopyranosyl-(1-6)-O-(2,6-diamino-2,3,4,6,7-pentadeoxy-alpha-D-ribo-heptopyranosyl-(1-4))-2-deoxy-. Grade: ≥95.0%. CAS No. 25876-11-3. Molecular formula: C20H41N5O7. Mole weight: 463.57. | |
| 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. Grade: ≥95.0%. CAS No. 59751-72-3. Molecular formula: C20H41N5O7. Mole weight: 463.57. | |
| Gentamicin C2b | Gentamicin C2b. Group: Biochemicals. Grades: Highly Purified. CAS No. 52093-21-7. Pack Sizes: 1mg, 2mg. US Biological Life Sciences. | Worldwide |
| Gentamicin C2b | Micronomicin is a trisaccharide pentaaminoglycoside antibiotic belonging to the gentamicin class. It is isolated from micromonospora sagamiensis var. It has broad activity against Gram-positive and Gram-negative bacteria and induces neuromuscular obstruction. Synonyms: Micronomicin; Sagamicin; Santemycin; Antibiotic KW 1062; Antibiotic XK 62-2. Grade: >95% by HPLC. CAS No. 52093-21-7. 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-(1→6)-O-[(6ξ)-2,6-diamino-2,3,4,6,7-pentadeoxy-α-D-erythro-heptopyranosyl-(1→4)]-2-deoxy-D-streptamine Pentaacetate Salt; Gentamicin C2/C2a Mixture Pentaacetate Salt. Grade: 95%. Molecular formula: C30H61N5O17. Mole weight: 763.83. | |
| Gentamicin Impurity 7 | Gentamicin Impurity 7. Uses: For analytical and research use. Molecular formula: C21H42N6O8. Mole weight: 506.6. Catalog: APB08060. |  |
| Gentamicin Impurity 8 | Gentamicin Impurity 8. Uses: For analytical and research use. Molecular formula: C20H41N7O8. Mole weight: 507.59. Catalog: APB08061. | |
| Gentamicin Impurity 9 | Gentamicin Impurity 9. Uses: For analytical and research use. Molecular formula: C19H39N5O9. Mole weight: 481.55. Catalog: APB08062. | |
| gentamicin sulfate | gentamicin sulfate. CAS No. 1900-6-22. Product ID: ACM174. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| 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 | Gentamicin sulfate, an aminoglycoside antibiotic, inhibits the growth of both gram-positive and gram-negative bacteria and to inhibit several strains of mycoplasma in tissue culture. Gentamicin sulfate inhibits DNase I with an IC50 of 0.57 mM[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1405-41-0. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-A0276. | |
| 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. Grade: ≥95%. CAS No. 1405-41-0. Molecular formula: C(19-21)H(39-43)N5O7.H2SO4. Mole weight: 561.65 (Average). | |
| Gentamicin sulfate EP Impurity A | Gentamicin sulfate EP Impurity A. Uses: For analytical and research use. CAS No. 32385-11-8. Molecular formula: C19H37N5O7. Mole weight: 447.53. Catalog: APB32385118. | |
| Gentamicin sulfate EP Impurity B | Gentamicin sulfate EP Impurity B. Uses: For analytical and research use. CAS No. 49751-51-1. Molecular formula: C13H27N3O6. Mole weight: 321.37. Catalog: APB49751511. | |
| Gentamicin sulfate EP Impurity C | Gentamicin sulfate EP Impurity C. Uses: For analytical and research use. CAS No. 36889-16-4. Molecular formula: C20H40N4O10. Mole weight: 496.56. Catalog: APB36889164. | |
| Gentamicin sulfate EP Impurity D | Gentamicin sulfate EP Impurity D. Uses: For analytical and research use. Molecular formula: C19H39N5O9. Mole weight: 481.55. Catalog: APB08059. | |
| Gentamicin Sulfate EP Impurity E | Gentamicin Sulfate EP Impurity E. Uses: For analytical and research use. CAS No. 2037-48-1. Molecular formula: C6H14N2O3. Mole weight: 162.19. Catalog: APB2037481. | |
| Gentamicin Sulfate EP Impurity E DiHBr | Gentamicin Sulfate EP Impurity E DiHBr. Uses: For analytical and research use. CAS No. 84107-26-6. Molecular formula: C6H16Br2N2O3. Mole weight: 324.01. Catalog: APB84107266. | |
| Gentamicinsulfate salt | Gentamicinsulfate salt. Alternative Names: GENTAMYCINE; Gentavet; GentamysinsolutionforBiochemistry; GENTAMYCIN; Gentacycol; Lyramycin; Uromycine; Refobacin tm; GENTAMICINUM. CAS No. 1403-66-3. Purity: 95%. Product ID: ACM1403663. Molecular formula: C21H43N5O7. Mole weight: 477.60. IUPAC Name: Gentamicin. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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 |
| Gentamicin sulphate | Gentamicin sulphate. CAS No. 1405-41-0. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications. |  |
| Gentamicin X2 | Gentamicin X2. Group: Biochemicals. Grades: Highly Purified. CAS No. 36889-17-5. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C19H38N4O10. US Biological Life Sciences. | Worldwide |
| Gentamicin X2 | One of several different components found in standard grade Gentamicin. Gentamicin is an aminoglycoside antibiotic. Synonyms: O-2-Amino-2-deoxy-α-D-glucopyranosyl-(1→4)-O-[3-deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(1→6)]-2-deoxy-D-streptamine; Gentamicin X. Grade: ≥98.0%. CAS No. 36889-17-5. Molecular formula: C19H38N4O10. Mole weight: 482.53. | |
| 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 ยท 2HBr; 4t,6t-Diamino-cyclohexan-1r,2t,3c-triol; 2-Deoxy-1,3-myo-inosadiamine. Grade: > 95%. CAS No. 84107-26-6. Molecular formula: C6H16N2O3Br2. Mole weight: 324.01. | |
| Gentamycin sulfate | Gentamycin sulfate. 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. CAS No. 1405-41-0. Purity: 96%. Product ID: ACM1405410-1. Molecular formula: C60H127N15O26S. Mole weight: 1506.8. IUPAC Name: Gentamicin Sulfate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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 | 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 EP Impurity C | 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. Grade: > 95%. CAS No. 36889-16-4. Molecular formula: C20H40N4O10. Mole weight: 496.56. | |
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