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| Product | Description | |
|---|---|---|
| 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 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. Grades: 95%. CAS No. 36889-15-3. Molecular formula: C19H38N4O10. Mole weight: 482.53. |  |
| Gentamicin B | Gentamicin B. Uses: For analytical and research use. Group: Impurity standards. CAS No. 36889-15-3. Molecular Formula: C19H38N4O10. Mole Weight: 482.53. Catalog: APB36889153. |  |
| 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 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. Grades: 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. Grades: ≥95.0%. CAS No. 26098-04-4. Molecular formula: C19H39N5O7. Mole weight: 449.54. | |
| Gentamicin C1a | Gentamicin C1a. Uses: For analytical and research use. Group: Impurity standards. CAS No. 26098-04-4. Molecular Formula: C19H39N5O7. Mole Weight: 449.55. Catalog: APB26098044. | |
| 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 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 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. Grades: 95%. Molecular formula: C31H63N5O17. Mole weight: 777.86. | |
| 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-. Grades: ≥95.0%. CAS No. 25876-11-3. Molecular formula: C20H41N5O7. Mole weight: 463.57. | |
| 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 | Gentamicin C2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 25876-11-3. Molecular Formula: C20H41N5O7. Mole Weight: 463.58. Catalog: APB25876113. | |
| 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 C2a | Gentamicin C2a. Uses: For analytical and research use. Group: Impurity standards. CAS No. 59751-72-3. Molecular Formula: C20H41N5O7. Mole Weight: 463.58. Catalog: APB59751723. | |
| 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. Grades: >95% by HPLC. CAS No. 52093-21-7. 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 | Gentamicin C2b. Uses: For analytical and research use. Group: Impurity standards. CAS No. 52093-21-7. Molecular Formula: C20H41N5O7. Mole Weight: 463.58. Catalog: APB52093217. | |
| 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 Deuterated (C Complex) Pentaacetate Salt (contains d0) | Inhibits protein synthesis by binding to L6 protein of 50S ribosomal subunit. Antibacterial. Group: Biochemicals. Alternative Names: Alcomicin; Bristagen; Cidomycin; Duragentam; Garamycin; Garasol; Genoptic; Gentacidin; Gentacin; Gentaglyde; Gentalyn; Gentamicin C Complex Citrate; Gentibioptal; Genticin; Gentocin; Gentogram; Gent-Ophtal; Getalline; GM. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 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 orally active 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 IC 50 of 0.57 mM [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. 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. 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). | |
| Gentamicin Sulfate C2 | Gentamicin Sulfate C2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 287916-51-2. Molecular Formula: C20H41N5O7. Mole Weight: 463.58. Catalog: APB287916512. | |
| Gentamicin sulfate EP Impurity A | Gentamicin sulfate EP Impurity A. Uses: For analytical and research use. Group: Impurity standards. 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. Group: Impurity standards. 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. Group: Impurity standards. CAS No. 36889-16-4. Molecular Formula: C20H40N4O10. Mole Weight: 496.56. Catalog: APB36889164. | |
| Gentamicin Sulfate EP Impurity E | Gentamicin Sulfate EP Impurity E. Uses: For analytical and research use. Group: Impurity standards. 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. Group: Impurity standards. CAS No. 84107-26-6. Molecular Formula: C6H16Br2N2O3. Mole Weight: 324.01. Catalog: APB84107266. | |
| 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 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. Grades: ≥98.0%. CAS No. 36889-17-5. Molecular formula: C19H38N4O10. Mole weight: 482.53. | |
| 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 |
| 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 | 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 | 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. | |
| Gentian Extract | Extract obtained from Gentiana Lutea (Gentian) roots. Contains 20% extract dissolved in water and glycerin. Has purifying, cleansing and soothing properties. Uses: Gels, toners, after sun and bath products. Group: Skin actives. CAS No. 7732-18-5/56-81-5/7676-22-7/122-99-6. Appearance: Light to medium amber liquid, characteristic odor. Catalog: CI-SC-0788. |  |
| Gentian Extract (Ratio) | Gentian Extract (Ratio). Group: Others. Purity: 4:1~20:1. Gentian Extract (Ratio). Cat No: EXTW-068. |  |
| Gentianidine | Heterocyclic Organic Compound. CAS No. 2202-12-2. Molecular formula: C9H9NO2. Catalog: ACM110640. | |
| Gentianose | Gentianose is a remarkable disaccharide derived from the gentian root, exhibiting its innate aptitude to suppress inflammatory processes. By integrating Gentianose into pharmaceutical compositions, manifold ailments including diabetes, liver maladies and gastrointestinal anomalies can be study. Synonyms: b-D-Glc-(1->6)-a-D-Glc-(1<->2)-b-D-Fru; b-D-fructofuranosyl 6-O-b-D-glucopyranosyl-a-D-glucopyranoside. CAS No. 25954-44-3. Molecular formula: C18H32O16. Mole weight: 504.45. | |
| Gentian Root P.E. 10:1 TLC | Gentian Root P.E. 10:1 TLC. |  CA, FL & NJ |
| Gentian Violet USP | Gentian Violet USP. CAS No. 548-62-9. Molecular formula: C25H30CIN3. |  |
| Gentiobiose octaacetate | Gentiobiose octaacetate reigns as an esteemed derivative of the intricate Gentiobiose, presenting itself as a disaccharide formed by the union of two glucose entities. Through acetylation, the resulting compound vastly augments the resilience and biogenic accessibility of the drugs. Synonyms: 1,2,3,4-Tetra-O-acetyl-6-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-D-glucopyranose. Molecular formula: C28H38O19. Mole weight: 678.59. | |
| Gentiobiulose | Gentiobiulose is a remarkable compound, applied in the research of conquering resilient bacterial infections. Its antibacterial potency transpires through the inhibition of diverse bacterial growth, encompassing the notorious strains such as Staphylococcus aureus and Escherichia coli. Synonyms: 6-O-(b-D-Glucopyranosyl)-D-fructose. CAS No. 132436-90-9. Molecular formula: C12H22O11. Mole weight: 342.30. | |
| Gentioheptaose | Gentioheptaose is an intricately structured carbohydrate, finding indispensable utility in the research of bacterial and viral infections. CAS No. 144448-00-0. Molecular formula: C42H72O36. Mole weight: 1153.00. | |
| Gentiohexaose | Gentiohexaose is an extensively employed carbohydrate compound, used for studying diverse ailments such as diabetes and cancer. CAS No. 37698-89-8. Molecular formula: C36H62O31. Mole weight: 990.86. | |
| Gentiopentaose | Gentiopentaose is a type of oligosaccharide used in the biomedical industry for its potential role in treating cancer and improving the immune system. Studies have shown that gentiopentaose has anti-tumor effects by inhibiting cancer cell growth and inducing apoptosis. It also has immunomodulatory properties by activating T cells and enhancing natural killer cell function. Gentipentaose shows great promise as a therapeutic agent for cancer and immune-related diseases. CAS No. 37796-54-6. Molecular formula: C30H52O26. Mole weight: 828.72. | |
| Gentiopicrin | Gentiopicrin. Group: Biochemicals. Grades: Plant Grade. CAS No. 20831-76-9. Pack Sizes: 20mg. Molecular Formula: C16H20O9, Molecular Weight: 356.32. US Biological Life Sciences. | Worldwide |
| Gentiopicroside | Gentiopicroside. Group: Biochemicals. CAS No. 20831-76-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Gentiopicroside | Gentiopicroside - Product ID: NST-10-165. Category: Glycosides. Alternative Names: Gentiopicrin. Purity: 98%. Test method: HPLC. CAS No. 20831-76-9. Pack Sizes: 0,05g, 0,1g, 0,25g, 0,5g. Appearance: White powder. Molecular formula: C16H20O9. Mole weight: 356.32. Storage: +2 +8 °C. |  |
| Gentiopicroside | Gentiopicroside, a naturally occurring iridoid glycoside, inhibits P450 activity, with an IC50 and a Ki of 61 μM and 22.8 μM for CYP2A6; Gentiopicroside has anti-inflammatoryand antioxidative effects. Group: Inhibitors. Alternative Names: (5R-trans)-6-(beta-D-glucopyranosyloxy)-5,6-dihydro-5-vinyl-1H,3H-pyrano[3,4-c]pyran-1-one. CAS No. 20831-76-9. Molecular formula: C16H20O9. Mole weight: 356.32. Appearance: White powder. Purity: 0.98. IUPACName: (3S,4R)-4-ethenyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,6-dihydro-3H-pyrano[3,4-c]pyran-8-one. Canonical SMILES: C=C[C@H]1[C@@H] (OC=C2C1=CCOC2=O)O[C@H]3[C@@H] ([C@H] ([C@@H] ([C@H] (O3)CO)O)O)O. Density: 1.52±0.1 g/ml. Catalog: ACM20831769. | |
| Gentiotetraose | Gentiotetraose is a distinctive biomedical compound with profound resemblance to endogenous glycoconjugates, thus used for studying autoimmune disorders and chronic inflammatory ailments. Synonyms: O-b-D-Glucopyranosyl-(1?6)-O-b-D-glucopyranosyl-(1?6)-O-b-D-glucopyranosyl-(1?6)-D-glucose. CAS No. 37796-39-7. Molecular formula: C24H42O21. Mole weight: 666.58. | |
| Gentiournoside D | Gentiournoside D is a compound of the iridoids found in the Gentiana urnula. Synonyms: (1S,4aS,6S,7R,7aS)-6-[(2,3-Dihydroxybenzoyl)oxy]-1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-7-methylcyclopenta[c]pyran-4-carboxylic acid. Grades: >98%. CAS No. 157722-21-9. Molecular formula: C23H28O13. Mole weight: 512.46. | |
| Gentiournoside D | Gentiournoside D. Group: Biochemicals. CAS No. 157722-21-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| gentisate 1,2-dioxygenase | Requires Fe2+. Group: Enzymes. Synonyms: gentisate oxygenase; 2,5-dihydroxybenzoate dioxygenase; gentisate dioxygenase; gentisic acid oxidase; gentisate:oxygen 1,2-oxidoreductase (decyclizing). Enzyme Commission Number: EC 1.13.11.4. CAS No. 9029-48-5. 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-0559; gentisate 1,2-dioxygenase; EC 1.13.11.4; 9029-48-5; gentisate oxygenase; 2,5-dihydroxybenzoate dioxygenase; gentisate dioxygenase; gentisic acid oxidase; gentisate:oxygen 1,2-oxidoreductase (decyclizing). Cat No: EXWM-0559. | |
| gentisate decarboxylase | This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. This enzyme participates in tyrosine metabolism. Group: Enzymes. Synonyms: 2,5-dihydroxybenzoate decarboxylase; gentisate carboxy-lyase. Enzyme Commission Number: EC 4.1.1.62. CAS No. 37290-54-3. 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-4809; gentisate decarboxylase; EC 4.1.1.62; 37290-54-3; 2,5-dihydroxybenzoate decarboxylase; gentisate carboxy-lyase. Cat No: EXWM-4809. | |
| Gentisic acid | Gentisic acid. Group: Biochemicals. Alternative Names: 2,5-Dihydroxybenzoic acid. Grades: Plant Grade. CAS No. 490-79-9. Pack Sizes: 20mg. Molecular Formula: C7H6O4, Molecular Weight: 154.121. US Biological Life Sciences. | Worldwide |
| Gentisic Acid, Sodium Salt (Sodium Gentisate) | Gentisic acid (2,5-Dihydroxybenzoic acid; 5-hydroxysalicylic acid) is chemically related to salicylate and aspirin (acetylsalicylate) and shares with the latter agent analgesic and anti-inflammatory properties. Gentisic acid is an aromatic carboxylic acid used as a sample matrix in Matrix-assisted laser desorption/ionization Mass spectrometry. As a hydroquinone, it is readily oxidized and is used as an antioxidant excipient in some pharmaceutical preparations.In vitro stabilization of low-tin bone-imaging agents has previously been achieved with ascorbic acid. Gentisic acid is shown to be an equally effective antioxidant for the (1-hydroxyethylidene) diphosphonate (HEDP) and hydroxy methyl enediphosphonate (HMDP) skeletal agents. In vitro studies show less than 2% free sodium [99mTc] pertechnetate at 24 hr with the gentisic acid stabilizer. Studies in guinea pigs at 3 and 24 hrwhether with C-14- or H-3-labeled gentisic acid as stabilizershow no alteration in the biodistribution of either skeletal imaging agent by the addition of the gentisic acid.Gentisic acid is a safe and effective stabilizer, and clinical studies have shown bioequivalency with ascorbic acid. Gentisic acid has been shown to be one of the most commenly occurring aromatic acids of green plants. Group: Biochemicals. Alternative Names: 2,5-Dihydroxybenzoic acid, Sodium Salt; 5-Hydroxysalicylate sodium. Grades: Highly Purified. CAS No. 4955-90-2. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: C7H5O4Na, Molecular Weight: 176.1. US Biological Life Sciences. | Worldwide |
| Gentiside B | Phenols. CAS No. 1225022-67-2. Molecular formula: C30H52O4. Mole weight: 476.74. Appearance: Powder. Purity: 0.98. IUPACName: [(20S)-20-methyldocosyl] 2,3-dihydroxybenzoate. Canonical SMILES: CCC (C)CCCCCCCCCCCCCCCCCCCOC (=O)C1=C (C (=CC=C1)O)O. Catalog: ACM1225022672. | |
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