adenosine 3'-phosphate-5'-phosphate and cetrimonium bromide

adenosine 3'-phosphate-5'-phosphate has been researched along with cetrimonium bromide in 1 studies

Compound Research Comparison

Studies (adenosine 3'-phosphate-5'-phosphate)	Trials (adenosine 3'-phosphate-5'-phosphate)	Recent Studies (post-2010) (adenosine 3'-phosphate-5'-phosphate)	Studies (cetrimonium bromide)	Trials (cetrimonium bromide)	Recent Studies (post-2010) (cetrimonium bromide)
102	0	34	41	0	25

Protein Interaction Comparison

Protein	Taxonomy	cetrimonium bromide (IC50)
60 kDa heat shock protein, mitochondrial	Homo sapiens (human)	7.4
10 kDa heat shock protein, mitochondrial	Homo sapiens (human)	7.4
Dynamin-1	Homo sapiens (human)	4.37
60 kDa chaperonin	Escherichia coli	6.5
10 kDa chaperonin	Escherichia coli	6.5

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Attene-Ramos, M; Baker, HL; Burkart, MD; Daniel, T; Foley, TL; Jadhav, A; Kosa, NM; Leister, W; Maloney, DJ; Rai, G; Simeonov, A; Yasgar, A	1

Other Studies

1 other study(ies) available for adenosine 3'-phosphate-5'-phosphate and cetrimonium bromide

Article	Year
4-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)-N-(4-methoxypyridin-2-yl)piperazine-1-carbothioamide (ML267), a potent inhibitor of bacterial phosphopantetheinyl transferase that attenuates secondary metabolism and thwarts bacterial growth. Journal of medicinal chemistry, 2014, Feb-13, Volume: 57, Issue:3 Topics: Animals; Anti-Bacterial Agents; Bacterial Proteins; Dipeptides; Drug Resistance, Bacterial; Drug Synergism; Escherichia coli; Gram-Positive Bacteria; Humans; Male; Mice; Microbial Sensitivity Tests; Microsomes, Liver; Pyridines; Secondary Metabolism; Structure-Activity Relationship; Thiourea; Transferases (Other Substituted Phosphate Groups)	2014

Article

Year

4-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)-N-(4-methoxypyridin-2-yl)piperazine-1-carbothioamide (ML267), a potent inhibitor of bacterial phosphopantetheinyl transferase that attenuates secondary metabolism and thwarts bacterial growth.

Journal of medicinal chemistry, 2014, Feb-13, Volume: 57, Issue:3

Topics: Animals; Anti-Bacterial Agents; Bacterial Proteins; Dipeptides; Drug Resistance, Bacterial; Drug Synergism; Escherichia coli; Gram-Positive Bacteria; Humans; Male; Mice; Microbial Sensitivity Tests; Microsomes, Liver; Pyridines; Secondary Metabolism; Structure-Activity Relationship; Thiourea; Transferases (Other Substituted Phosphate Groups)

2014