Vancomycin NEW
| Price | $42 | $66 | $98 |
| Package | 25mg | 50mg | 100mg |
| Min. Order: | |
| Supply Ability: | 10g |
| Update Time: | 2024-11-19 |
Product Details
| Product Name: Vancomycin | CAS No.: 1404-90-6 |
| Purity: 100% | Supply Ability: 10g |
| Release date: 2024/11/19 |
Product Introduction
Bioactivity
| Name | Vancomycin |
| Description | Vancomycin is a glycopeptide antibiotic that exerts its antimicrobial activity by altering the permeability of cell membranes and selectively inhibiting ribonucleic acid synthesis. Vancomycin can be used for the treatment of serious infections for which all antibiotics have failed. |
| In vitro | METHODS: B. burgdorferi was treated with Vancomycin (0.5-2.0 μg/mL) for 24 h and cell morphology was examined using real-time time-lapse microscopy. RESULTS: At higher concentrations of Vancomycin (≥1.0 μg/mL), many abnormal cells were observed, which were visually identified by vesiculation, granule formation, and morphological changes. The proportion of these abnormal bacteria in the population increased in a dose-dependent manner. [1] METHODS: Human osteosarcoma cells MG-63 were treated with Vancomycin (10-10000 μg/mL) for 24-72 h. Cell counts were measured using an Elzone Celi Counter. RESULTS: Localized levels of Vancomycin at 1000 μg/mL and below had little effect on osteoblast replication, and concentrations of 10,000 μg/mL resulted in cell death. [2] |
| In vivo | METHODS: To detect nephrotoxicity, Vancomycin (400 mg/kg) and Vitamin C (200 mg/kg) were administered intraperitoneally to C57BL/6J mice once daily for seven days. RESULTS: Renal index, renal injury score, apoptosis, serum Cr and BUN, as well as renal Cr, BUN, MDA, IL-1β, IL-6, TNF-α, and NF-κB were higher in the Vancomycin group than in the control group, whereas body weight and renal SOD activity were lower. On the contrary, no differences were observed between the control and Vitamin C groups in all these indices. [3] METHODS: To deplete the intestinal microbiota of mice, the antibiotics (ABX) Vancomycin (0.5 g/L), Ampicillin (1 g/L), Neomycin sulfate (1 g/L), and metronidazole (1 g/L) were administered to mice by drinking water for two weeks. RESULTS: Antibiotics significantly reduced the diversity and composition of the gut microbiota. [4] |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
| Solubility Information | 10% DMSO+90% Saline : 1 mg/mL (0.69 mM), Please add co-solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. DMSO : 50 mg/mL (34.5 mM), Sonication is recommended. |
| Keywords | Vancomycin | Inhibitor | inhibit | Bacterial | Autophagy | Antibiotic |
| Inhibitors Related | Neomycin sulfate | Sulfamethoxazole sodium | Hydroxychloroquine | Guanidine hydrochloride | Doxycycline | Paeonol | Dimethyl sulfoxide |
| Related Compound Libraries | Anti-Tumor Natural Product Library | Cyclic Peptide Library | Anti-Cancer Clinical Compound Library | Natural Product Library | Drug Repurposing Compound Library | Microbial Natural Product Library | Anti-Cancer Approved Drug Library | Natural Product Library for HTS | Anti-infective Natural Product Library | Bioactive Compounds Library Max |
Company Profile Introduction
Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers.
TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.
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