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Closthioamide
Catalog No. T10838Cas No. 1227367-59-0
Closthioamide is a potent inhibitor of bacterial DNA gyrase and is highly effective against MRSA, Ec, VRE, and Mv [MICs: 0.58 μM, 9.00 μM, 0.58 μM, and 72.03 μM, respectively].
Closthioamide
Catalog No. T10838Cas No. 1227367-59-0
Closthioamide is a potent inhibitor of bacterial DNA gyrase and is highly effective against MRSA, Ec, VRE, and Mv [MICs: 0.58 μM, 9.00 μM, 0.58 μM, and 72.03 μM, respectively].
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 25 mg | $1,670 | 6-8 weeks | |
| 50 mg | $2,180 | 6-8 weeks | |
| 100 mg | $2,800 | 6-8 weeks |
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Product Introduction
Bioactivity
Chemical Properties
| Description | Closthioamide is a potent inhibitor of bacterial DNA gyrase and is highly effective against MRSA, Ec, VRE, and Mv [MICs: 0.58 μM, 9.00 μM, 0.58 μM, and 72.03 μM, respectively]. |
| Targets&IC50 | Ec:9.00 μM (MIC), Mv:72.03 μM (MIC), MRSA:0.58 μM (MIC), VRE:0.58 μM (MIC) |
| In vitro | Closthioamide is isolated from the strictly anaerobic bacterium Clostridium cellulolyticum, and belongs to a new class of natural products [1]. Closthioamide is highly active against a pathogenic, methicillin-resistant Staphylococcus aureus (MRSA) strain with a minimum inhibitory concentration (MIC) of 0.4 μg/mL-1 (0.58 μM). Closthioamide is even active against vancomycin-resistant Enterococcus faecalis (VRE) with the same low MIC value and is thus significantly more potent against these bacteria than ciprofloxacin, the standard drug used against VRE, with remarkable strain selectivity. Closthioamide shows moderate antiproliferative and cytotoxic effects [2]. |
| Molecular Weight | 695.04 |
| Formula | C29H38N6O2S6 |
| Cas No. | 1227367-59-0 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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