CAS Number108321-42-2
SynonymsG418 disulfate; G-418 sulfate; G 418 Sulfate,Cell Culture Tested; Antibiotic G418; G 418 Sulfate,Sterile-Filtered Aqueous Solution,Cell Culture Tested; Geneticin; MFCD00058314; G418Sulfate/Geneticin; G-418 Disulphate; G418 disulfate salt; G 418 disulfate salt; G418 Sulfate; Geneticin Disulfate Salt; G-418 (disulfate)
Molecular FormulaC20H44N4O18S2
Molecular Weight692.709
Purity98.00%
Boiling Point1012.1ºC at 760mmHg
AppearanceWhite to off-white powder
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 108321-42-2 |
| Catalog No. | 2A-9050394 |
| Chinese Name | G-418 硫酸盐 |
| Synonyms | G418 disulfate; G-418 sulfate; G 418 Sulfate,Cell Culture Tested; Antibiotic G418; G 418 Sulfate,Sterile-Filtered Aqueous Solution,Cell Culture Tested; Geneticin; MFCD00058314; G418Sulfate/Geneticin; G-418 Disulphate; G418 disulfate salt; G 418 disulfate salt; G418 Sulfate; Geneticin Disulfate Salt; G-418 (disulfate) |
| Molecular Formula | C20H44N4O18S2 |
| Molecular Weight | 692.709 |
| Purity | 98.00 |
| Boiling Point | 1012.1ºC at 760mmHg |
| Appearance | White to off-white powder |
| Water Solubility | Soluble |
| Storage Condition | Store airtight in a cool, dry warehouse. Refrigera |
| Packaging | II |
| Application | G-418 disulfate is an aminoglycoside antibiotic with a similar structure to gentamicin B1. It can prevent the elongation stage of proteins during the protein synthesis process in prokaryotic and eukar |
| HTC | 29173980 |
| SMILES | CNC1C(O)C(OC2C(N)CC(N)C(OC3OC(C(C)O)C(O)C(O)C3N)C2O)OCC1(C)O.O=S(=O)(O)O.O=S(=O)(O)O |
| InChI Key | UHEPSJJJMTWUCP-ROXHIUMPSA-N |
| Hazard Symbols | 6.1 |
| MSDS | msds/50394_2_108321_42_2.pdf |
| Bioactivity | G-418 (disulfate) is an aminoglycoside antibiotic similar in structure to gentamicin B1, which blocks polypeptide synthesis by inhibiting the elongation step in both prokaryotic and eukaryotic cells. Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Research Areas >> Others In Vitro G418 is an inhibitor of many pro- and eukaryotes at concentrations from 1-300 microgram/mL. Resistance to G418 conferring by the neo gene from Tn5 encoding an aminoglycoside 3'-phosphotransferase, APT 3' II is commonly used in laboratory research to select genetically engineered cells[1]. In general for bacteria and algae concentrations of 5 mg/L or less are used, for mammalian cells concentrations of approximately 400 mg/L are used for selection and 200 mg/L for maintenance. Resistant clones selection could require from 1 to up to 3 weeks[2]. In Vivo G418 (40 and 80 mg/kg) for three consecutive days are sufficient to eliminate all nontransfected T. brucei brucei parasites from infected mice[3]. Animal Admin To characterize the sensitivity of the trypanosome populations to G418 in vivo, bloodstream forms of T. brucei brucei GUTat 3.1 and T. brucei brucei GUTat 3.1/BBR3 are expanded separately in sublethally irradiated mice. Prior to the first peak of parasitemia, trypanosomes are collected, and aliquots containing 106 trypanosomes are inoculated intraperitoneally into mice. Twenty-four hours following infection, the mice are divided into groups and treated with G418 at a dose of 10, 20, 30, 40, 50, or 80 mg/kg of body weight (bw) by inoculating intraperitoneally 0.2 mL of the drug in sterile water. At 24 and 48 h following the firsttreatment, G418 is administered to animals in each group at the same dose as before, resulting in three treatments per mouse. Repeated drug treatments are necessary to ensure complete elimination of nontransfected GUTat 3.1 parasites from the mice. Mice are then monitored daily, for 33 days, for the presence of parasites by microscopic examination of wet-blood films. Animals found to be parasitemic are recorded and then removed from the experiment. References [1]. Davies J, et al. A new selective agent for eukaryotic cloning vectors. Am J Trop Med Hyg. 1980 Sep;29(5 Suppl):1089-92. [2]. Li Y, et al. Inhibitory effects of antisense RNA of HAb18G/CD147 on invasion of hepatocellular carcinoma cells in vitro. World J Gastroenterol. 2003 Oct;9(10):2174-7. [3]. Murphy NB, et al. Use of an in vivo system to determine the G418 resistance phenotype of bloodstream-form Trypanosoma brucei brucei transfectants. Antimicrob Agents Chemother. 1993 May;37(5):1167-70. Chemical & Physical Properties Boiling Point 1012.1ºC at 760mmHg Molecular Formula C20H44N4O18S2 Molecular Weight 692.709 Flash Point 565.9ºC Exact Mass 692.209229 PSA 414.35000 Vapour Pressure 0mmHg at 25°C InChIKey UHEPSJJJMTWUCP-ROXHIUMPSA-N SMILES CNC1C(O)C(OC2C(N)CC(N)C(OC3OC(C(C)O)C(O)C(O)C3N)C2O)OCC1(C)O.O=S(=O)(O)O.O=S(=O)(O)O Storage condition 2-8°C |
| Use of | Properties Articles25 Name 2-[4,6-diamino-3-[3-amino-4,5-dihydroxy-6-(1-hydroxyethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxy-5-methyl-4-(methylamino)oxane-3,5-diol,sulfuric acid Synonym More Synonyms Geneticin Biological Activity Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Research Areas >> Others References [1]. Davies J, et al. A new selective agent for eukaryotic cloning vectors. Am J Trop Med Hyg. 1980 Sep;29(5 Suppl):1089-92. [2]. Li Y, et al. Inhibitory effects of antisense RNA of HAb18G/CD147 on invasion of hepatocellular carcinoma cells in vitro. World J Gastroenterol. 2003 Oct;9(10):2174-7. [3]. Murphy NB, et al. Use of an in vivo system to determine the G418 resistance phenotype of bloodstream-form Trypanosoma brucei brucei transfectants. Antimicrob Agents Chemother. 1993 May;37(5):1167-70. Chemical & Physical Properties Molecular Formula C20H44N4O18S2 Exact Mass 692.209229 PSA 414.35000 InChIKey UHEPSJJJMTWUCP-ROXHIUMPSA-N |
| Transport Info | Product name: Purity: 0.0% |
| MSDS Transport Info | Module 14. Shipping information United Nations classification: inconsistent with United Nations classification standards UN number: not specified |
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