References
119
Zajdel P, Kos T, Marciniec K et al. (2018) Novel multi-target azinesulfonamides of cyclic amine
derivatives as potential antipsychotics with pro-social and pro-cognitive effects. Eur J Med Chem
145:790–804
Zhang G-B, Maddili SK, Tangadanchu VKR et al. (2018) Discovery of natural berberine-derived
nitroimidazoles as potentially multi-targeting agents against drug-resistant Escherichia coli. Sci
China Chem 61 (5):557–568
Zhang W, Zhang D, Stashko MA et al. (2013) Pseudo-cyclization through intramolecular hydrogen
bond enables discovery of pyridine substituted pyrimidines as new Mer Kinase inhibitors. J Med
Chem 56 (23):9683–9692
Zheng Y, Tice CM, Singh SB (2014) The use of spirocyclic scaffolds in drug discovery. Bioorg
Med Chem Lett 24:3673–3682
Zhang Y, Shi W, Zhang W et al. (2014) Mechanisms of pyrazinamide action and resistance.
Microbiol Spectr 2 (4):MGM2-0023-2013
Zhou S, Tong R (2016) A general, concise strategy that enables collective total syntheses of over
50 protoberberine and five aporhoeadane alkaloids within four to eight steps. Chem Eur J 22
(21):7084–7089
Zhou X, Chen M, Zheng Z et al. (2017) Synthesis and evaluation of novel 12-aryl berberine
analogues with hypoxia-inducible factor-1 inhibitory activity. RSC Adv 7:26921–26929
Zhu R, Wang Y, Liu J et al. (2017) One-pot synthesis of imidazolyl isoquinolines under a palladiumcatalyzed C-H activation/annulation (CHAA) reaction. Synthesis 49:1335–1341
Zimmermann S, Klinger-Strobel M, Bohnert JA et al. (2019) Clinically approved drugs inhibit
the Staphylococcus aureus multidrug NorA efflux pump and reduce biofilm formation. Front
Microbiol 10:2762–2762
Zong Y, Fang F, Meyer KJ et al. (2019) Gram-scale total synthesis of teixobactin promoting binding
mode study and discovery of more potent antibiotics. Nat Commun 10 (1):3268
119
Zajdel P, Kos T, Marciniec K et al. (2018) Novel multi-target azinesulfonamides of cyclic amine
derivatives as potential antipsychotics with pro-social and pro-cognitive effects. Eur J Med Chem
145:790–804
Zhang G-B, Maddili SK, Tangadanchu VKR et al. (2018) Discovery of natural berberine-derived
nitroimidazoles as potentially multi-targeting agents against drug-resistant Escherichia coli. Sci
China Chem 61 (5):557–568
Zhang W, Zhang D, Stashko MA et al. (2013) Pseudo-cyclization through intramolecular hydrogen
bond enables discovery of pyridine substituted pyrimidines as new Mer Kinase inhibitors. J Med
Chem 56 (23):9683–9692
Zheng Y, Tice CM, Singh SB (2014) The use of spirocyclic scaffolds in drug discovery. Bioorg
Med Chem Lett 24:3673–3682
Zhang Y, Shi W, Zhang W et al. (2014) Mechanisms of pyrazinamide action and resistance.
Microbiol Spectr 2 (4):MGM2-0023-2013
Zhou S, Tong R (2016) A general, concise strategy that enables collective total syntheses of over
50 protoberberine and five aporhoeadane alkaloids within four to eight steps. Chem Eur J 22
(21):7084–7089
Zhou X, Chen M, Zheng Z et al. (2017) Synthesis and evaluation of novel 12-aryl berberine
analogues with hypoxia-inducible factor-1 inhibitory activity. RSC Adv 7:26921–26929
Zhu R, Wang Y, Liu J et al. (2017) One-pot synthesis of imidazolyl isoquinolines under a palladiumcatalyzed C-H activation/annulation (CHAA) reaction. Synthesis 49:1335–1341
Zimmermann S, Klinger-Strobel M, Bohnert JA et al. (2019) Clinically approved drugs inhibit
the Staphylococcus aureus multidrug NorA efflux pump and reduce biofilm formation. Front
Microbiol 10:2762–2762
Zong Y, Fang F, Meyer KJ et al. (2019) Gram-scale total synthesis of teixobactin promoting binding
mode study and discovery of more potent antibiotics. Nat Commun 10 (1):3268
