Birgit Jaki

Dr. Birgit Jaki


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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4 March 2016 in ACS Infectious Diseases
Verified
Journal Article
Closed access
EGEdyta M. Grzelak
Edyta M. Grzelak
CHChanghwa Hwang
Changhwa Hwang
GCGeping Cai
Geping Cai
JNJoo-Won Nam
Joo-Won Nam
MCMary P Choules
Mary P Choules
BJBirgit Jaki
Birgit Jaki

18 March 2014 in Journal of Natural Products
Verified
Journal Article
Closed access
RARené F. Ramos Alvarenga
René F. Ramos Alvarenga
BWBaojie Wan
Baojie Wan
TITaichi Inui
Taichi Inui
SFScott Franzblau
Scott Franzblau
GPGuido F. Pauli
Guido F. Pauli
BJBirgit Jaki
Birgit Jaki

18 September 2017 in Scientia Pharmaceutica
Verified
Journal Article
Open access
PDF file
SWSaradee Warit
Saradee Warit
KRKamolchanok Rukseree
Kamolchanok Rukseree
TPTherdsak Prammananan
Therdsak Prammananan
PHPoonpilas Hongmanee
Poonpilas Hongmanee
PBPamaree Billamas
Pamaree Billamas
PPPrasit Palittapongarnpim
Prasit Palittapongarnpim
In the process of evaluating the effect of several plant extracts against Mycobacterium tuberculosis using the Microplate Alamar Blue Assay (MABA), an extract of Thai herb Alpinia galanga rhizome and its major component, 1′-acetoxychavicol acetate (ACA), exhibited marked anti-tuberculosis activity. The minimal inhibition concentrations (MICs) of the S-enantiomer of ACA (S-ACA) against M. tuberculosis H37Ra ATCC 25177 and H37Rv ATCC 27294 strains were 0.2 µg/mL and 0.7 µg/mL, respectively. More than 95% of 100 drug-sensitive and 50 drug-resistant mycobacterial clinical isolates were inhibited by extracted S-ACA at 1.0 µg/mL. All of the remaining isolates were inhibited at 2.0 µg/mL. In contrast to the S-enantiomer, synthetic racemic 1′-R,S-ACA (rac-ACA) showed MICs of 0.5 µg/mL and 2.7 µg/mL for M. tuberculosis H37Ra ATCC 25177 and H37Rv ATCC 27294, respectively, suggesting that the anti-tuberculosis effect might be primarily due to the S-form. These observations were in line with the MICs of rac-ACA against 98% of 93 drug-resistant clinical isolates, which showed the effective inhibitory dose at 2.0 µg/mL. After exposure to 2.7 µg/mL of rac-ACA for at least 3 h, the tubercle bacilli were completely killed. These demonstrated that ACA had potent anti-TB activity.