PBTZ169

PBTZ169 Suppliers list
Company Name: Shanghai Boyle Chemical Co., Ltd.  
Tel:
Email: sales@boylechem.com
Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Company Name: HangZhou YuHao Chemical Technology Co., Ltd.  
Tel: 0571-82693216
Email: info@yuhaochemical.com
Company Name: Shanghai Lollane Biological Technology Co.,Ltd.  
Tel: 021-52996696,15000506266 15000506266
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Company Name: D&C Chemicals  
Tel: +86-21-58447131
Email: 1724405207@qq.com
PBTZ169 Basic information
Product Name:PBTZ169
Synonyms:2-(4-(Cyclohexylmethyl)piperazin-1-yl)-8-nitro-6-trifluoromethyl-4H-1,3-benzothiazin-4-one;PBTZ169;PBTZ-169;PBTZ 169;CS-2309;PBTZ169 (PBTZ 169; 2-[4-(Cyclohexylmethyl)-1-piperazinyl]-8-nitro-6-(trifluoromethyl)-4H-1,3-benzothiazin-4-one;4H-1,3-Benzothiazin-4-one, 2-[4-(cyclohexylmethyl)-1-piperazinyl]-8-nitro-6-(trifluoromethyl)-;2-(4-(Cyclohexylmethyl)piperazin-1-yl)-8-nitro-6-(trifluoromethyl)-4H-benzo[e][1,3]thiazin-4-one;Macozinone(PBTZ169)
CAS:1377239-83-2
MF:C20H23F3N4O3S
MW:456.48
EINECS:
Product Categories:
Mol File:1377239-83-2.mol
PBTZ169 Structure
PBTZ169 Chemical Properties
storage temp. Store at -20°C
solubility DMSO:4.6(Max Conc. mg/mL);10.1(Max Conc. mM)
form A crystalline solid
color Light yellow to yellow
Safety Information
MSDS Information
PBTZ169 Usage And Synthesis
DescriptionPBTZ169 is an antibiotic with antimycobacterial activity. It is an irreversible inhibitor of DprE1, an essential enzyme for cell wall synthesis in mycobacteria. PBTZ169 is active against M. tuberculosis in vitro (MIC = ≤0.19 ng/ml) without inducing cytotoxicity in Vero cells when used at concentrations up to 125 μM. It reduces the bacterial burden in the lung and spleen in a mouse model of chronic tuberculosis when administered at a dose of 50 mg/kg per day.
UsesPBTZ169 is a potent irreversible inhibitor of decaprenylphosphoryl-beta-D-ribose 2-epimerase (DprE1), and display nanomolar bactericidal activity against Mycobacterium tuberculosis in vitro.
References[1] CUI-TING PENG . Synthesis and antitubercular evaluation of 4-carbonyl piperazine substituted 1,3-benzothiazin-4-one derivatives[J]. Bioorganic & Medicinal Chemistry Letters, 2015, 25 7: Pages 1373-1376. DOI: 10.1016/j.bmcl.2015.02.061
[2] VADIM MAKAROV. Towards a new combination therapy for tuberculosis with next generation benzothiazinones.[J]. EMBO Molecular Medicine, 2014, 6 3: 372-383. DOI: 10.1002/emmm.201303575
PBTZ169 Preparation Products And Raw materials
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