New dihydroagarofuranoid sesquiterpene from the stem of Microtropis japonica with antituberculosis activity

Planta Medica ◽  
2014 ◽  
Vol 80 (16) ◽  
Author(s):  
JJ Chen ◽  
IS Chen ◽  
CF Peng
Keyword(s):  
Antituberculosis Activity

scholarly journals Synthesis and biological activity of 4-thiazolidinone derivatives of phenothiazine

2012 ◽  
Vol 77 (1) ◽  
pp. 17-26 ◽  
Author(s):  
Ritu Sharma ◽  
Pushkal Samadhiya ◽  
Savitri Srivastava ◽  
Santosh Srivastava
Keyword(s):  
Antimicrobial Activity ◽  
Heterocyclic Compounds ◽  
Thioglycolic Acid ◽  
Cycloaddition Reaction ◽  
Aromatic Aldehydes ◽  
Knoevenagel Reaction ◽  
Antituberculosis Activity ◽  
Bacteria And Fungi ◽  
Derivatives Of ◽  
Anhydrous Zncl2

A new series of N-[3-(10H-phenothiazinyl)-propyl]-2-(substituted phenyl)-4-oxo-5-( substituted benzylidene)-1,3-thiazolidine-carboxamide, 5(as) have been synthesized. The cycloaddition reaction of thioglycolic acid with N-[3-(10H-phenothiazinyl)-propyl]-N?-[(substituted phenyl)-methylidene]- urea, 3(a-s) in the presence of anhydrous ZnCl2 afforded new heterocyclic compounds N-[3-(10H-phenothiazinyl)-propyl]-2-(substituted phenyl)-4-oxo- 1,3-thiazolidine-carboxamide, 4(a-s). The later product on treatment with several selected substituted aromatic aldehydes in the presence of C2H5ONa undergoes Knoevenagel reaction to yield 5(a-s). The structure of compounds 1, 2, 3(a-s), 4(a-s) and 5(a-s) were confirmed by IR, 1H NMR, 13C NMR, Fmass and chemical analysis. All above compounds were screened for their antimicrobial activity against some selected bacteria and fungi and for antituberculosis activity compounds have been screened against the bacterium M. tuberculosis.

The synthesis and antituberculosis activity of 5′-nor carbocyclic uracil derivatives

2012 ◽  
Vol 20 (22) ◽  
pp. 6680-6686 ◽  
Author(s):  
Elena Matyugina ◽  
Anastasia Khandazhinskaya ◽  
Larisa Chernousova ◽  
Sofia Andreevskaya ◽  
Tatiana Smirnova ◽  
...  
Keyword(s):  
Antituberculosis Activity ◽  
Uracil Derivatives

Compounds with potential antituberculosis activity XV. Derivatives of some S-heterylmercaptoacetic acids

1969 ◽  
Vol 3 (8) ◽  
pp. 443-444 ◽  
Author(s):  
T. P. Sycheva ◽  
T. N. Pavlova ◽  
T. N. Zykova ◽  
M. N. Shchukina
Keyword(s):  
Antituberculosis Activity ◽  
Derivatives Of

Evaluation of antituberculosis activity and DFT study on dipyrromethane-derived hydrazone derivatives

2017 ◽  
Vol 1149 ◽  
pp. 539-548 ◽  
Author(s):  
Poonam Rawat ◽  
R.N. Singh ◽  
Priydarshni Niranjan ◽  
Alok Ranjan ◽  
Norma Rosario Flores Holguín
Keyword(s):  
Dft Study ◽  
Antituberculosis Activity

New chalcone-sulfonamide hybrids exhibiting anticancer and antituberculosis activity

2019 ◽  
Vol 176 ◽  
pp. 50-60 ◽  
Author(s):  
Lina Fernanda Castaño ◽  
Viviana Cuartas ◽  
Anthony Bernal ◽  
Alberto Insuasty ◽  
Juan Guzman ◽  
...  
Keyword(s):  
Antituberculosis Activity

Promising Antituberculosis Activity of Piperine Combined with Antimicrobials: A Systematic Review

2019 ◽  
Vol 25 (1) ◽  
pp. 120-126 ◽  
Author(s):  
Laíse Adriane Hegeto ◽  
Katiany R. Caleffi-Ferracioli ◽  
JoãoVitor Perez de Souza ◽  
Aryadne Larissa de Almeida ◽  
Sandra Sayuri Nakamura de Vasconcelos ◽  
...  
Keyword(s):  
Systematic Review ◽  
Antituberculosis Activity

Synthesis and antituberculosis activity of indole–pyridine derived hydrazides, hydrazide–hydrazones, and thiosemicarbazones

2016 ◽  
Vol 26 (3) ◽  
pp. 978-985 ◽  
Author(s):  
Valeriya Velezheva ◽  
Patrick Brennan ◽  
Pavel Ivanov ◽  
Albert Kornienko ◽  
Sergey Lyubimov ◽  
...  
Keyword(s):  
Antituberculosis Activity

DNA interaction, cytotoxicity, antibacterial and antituberculosis activity of oxovanadium(iv) complexes derived from fluoroquinolones and 4-hydroxy-5-((4-hydroxyphenyl)diazenyl)thiazole-2(3H)-thione

RSC Advances ◽  
2015 ◽  
Vol 5 (28) ◽  
pp. 21710-21719 ◽  
Author(s):  
Sanjay B. Gajera ◽  
Jugal V. Mehta ◽  
Mohan N. Patel
Keyword(s):  
Dna Interaction ◽  
Antituberculosis Activity

Oxovanadium complexes (5a–5g) with fluoroquinolone ligands and azodye rhodanine (3) were synthesized and the effect of different groups was studied, which displayed various biological and medicinal activities.

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