Ethambutol 2HCl

Synonyms: CL40881

Ethambutol 2HCl (CL40881) is a bacteriostatic antimycobacterial agent, which obstructs the formation of cell wall by inhibiting arabinosyl transferases.

Ethambutol 2HCl Chemical Structure

Ethambutol 2HCl Chemical Structure

CAS: 1070-11-7

Selleck's Ethambutol 2HCl has been cited by 2 publications

Purity & Quality Control

Batch: S400401 DMSO] 56 mg/mL] false] Water] 56 mg/mL] false] Ethanol] Insoluble] false Purity: 100%
100

Choose Selective Bacterial Inhibitors

Biological Activity

Description Ethambutol 2HCl (CL40881) is a bacteriostatic antimycobacterial agent, which obstructs the formation of cell wall by inhibiting arabinosyl transferases.
In vitro
In vitro Ethambutol directly affects two polymers, arabinogalactan (AG) and lipoarabinomannan (LAM) in Mycobacterium smegmatis. In M. smegmatis, Ethambutol inhibits synthesis of arabinan completely and inhibits AG synthesis most likely as a consequence of this; more than 50% of the cell arabinan is released from the bacteria following Ethambutol treatment, whereas no galactan is released. Ethambutol main targets against embB gene product in M. avium. Ethambutol induces 60% changes in the embB gene in M. tuberculosis resistant mutants. [1] Ethambutol is effective against actively growing microorganisms of the genus Mycobacterium, including M. tuberculosis. Nearly all strains of M. tuberculosis and M. kansasii as well as a number of strains of the M. aviumcomplex (MAC) are sensitive to Ethambutol. [1] Ethambutol is potency against M. tuberculosis (H37Rv) with MIC of 0.5 μg/mL in vitro. [2] Ethambutol is efficient on treatment of mycobacterial-infected macrophages. When M. tuberculosis infected macrophages are treated with 6 μg/mL Ethambutol, the log CFUs following treatment for 3 days is 4.17, while value in control group is 4.8. The MICs for M. avium (MTCC 1723) and M. smegmatis (MTCC 6) are 15 μg/mL and 0.18 μg/mL, respectively. [3]
In Vivo
In vivo Ethambutol is efficient in animal model. 100 mg/kg Ethambutol given orally 15 days post i.v. infection 1 ×/week for 5 weeks, induces a lower log CFU compared with untreatment (4.59 vs 5.07). [3]
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05840809 Recruiting Tuberculosis Active|Breastfeeding|Tuberculosis University of Liverpool|Infectious Diseases Institute Makerere University College of Health Sciences January 20 2022 --
NCT04972903 Unknown status Tuberculosis|Pulmonary Institut National de la Santé Et de la Recherche Médicale France|National Agency for Research on AIDS and Viral Hepatitis (ANRS) August 2021 --
NCT02114684 Completed Recurrent Tuberculosis Centre for the AIDS Programme of Research in South Africa November 2013 Phase 1|Phase 2
NCT02496572 Unknown status Multidrug Resistant Tuberculosis Medecins Sans Frontieres Netherlands|Ministry of Health Republic of Uzbekistan|Imperial College London September 2013 --

Chemical lnformation & Solubility

Molecular Weight 277.23 Formula

C10H24N2O2.2HCl

CAS No. 1070-11-7 SDF --
Smiles CCC(CO)NCCNC(CC)CO.Cl.Cl
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 56 mg/mL ( (201.99 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 56 mg/mL

Ethanol : Insoluble


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In vivo
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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