Supplemental material
Open access
1,313
Views
24
CrossRef citations to date
0
Altmetric
Research Paper
Antimycobacterial activity of nitrogen heterocycles derivatives: 7-(pyridine-4-yl)-indolizine derivatives. Part VII8–12
Anda-Mihaela OlaruFaculty of Chemistry, “Alexandru Ioan Cuza” University of Iasi, Iasi, Romania;
, Violeta Vasilache“Alexandru Ioan Cuza” University of Iasi, CERNESIM Research Centre, Iasi, Romania
, Ramona DanacFaculty of Chemistry, “Alexandru Ioan Cuza” University of Iasi, Iasi, Romania; Correspondence[email protected]
& Ionel I. MangalagiuFaculty of Chemistry, “Alexandru Ioan Cuza” University of Iasi, Iasi, Romania; Correspondence[email protected]
Pages 1291-1298
|
Received 11 Jul 2017, Accepted 21 Aug 2017, Published online: 26 Oct 2017
Related Research Data
Design, Synthesis and Antimycobacterial Activity of Some New Azaheterocycles: Phenanthroline with p-halo-benzoyl Skeleton. Part V
Source:
Bentham Science Publishers Ltd.
In Vitro Permeability Across Caco-2 Cells (Colonic) Can Predict In Vivo (Small Intestinal) Absorption in Man—Fact or Myth
Source:
Springer Science and Business Media LLC
The Population Dynamics and Control of Tuberculosis
Source:
American Association for the Advancement of Science (AAAS)
Antimycobacterial activity of nitrogen heterocycles derivatives: 7-(pyridine-4-yl)-indolizine derivatives. Part VII8–12
Source:
Taylor & Francis
In Vitro Evaluation of Reversible and Irreversible Cytochrome P450 Inhibition: Current Status on Methodologies and their Utility for Predicting Drug–Drug Interactions
Source:
Springer Science and Business Media LLC
Comparison of intestinal permeabilities determined in multiple in vitro and in situ models: relationship to absorption in humans.
Source:
Springer Science and Business Media LLC
Antimycobacterial activity of nitrogen heterocycles derivatives: bipyridine derivatives. Part III.
Source:
Elsevier BV
Highly Efficient Synthesis of 1‐Nitroindolizine Derivatives via the DBU/Acetic Acid System
Source:
Wiley
New indolizines with phenanthroline skeleton: Synthesis, structure, antimycobacterial and anticancer evaluation
Source:
Elsevier BV
Dicoumarol complexes of Cu(II) based on 1,10-phenanthroline: synthesis, X-ray diffraction studies, thermal behavior and biological evaluation.
Source:
Elsevier BV
Synthesis and antimicrobial activity of some new pyridazine derivatives
Source:
The Japan Institute of Heterocyclic Chemistry
The effect of plasma protein binding on in vivo efficacy: misconceptions in drug discovery
Source:
Springer Science and Business Media LLC
In Vitro Model of Hypoxically Induced Nonreplicating Persistence of Mycobacterium tuberculosis
Source:
Humana Press
The role of transporters in drug interactions
Source:
Elsevier BV
Bis-(imidazole/benzimidazole)-pyridine derivatives: synthesis, structure and antimycobacterial activity.
Source:
Future Science Ltd
Design, synthesis and antimycobacterial evaluation of some new azaheterocycles with the 4,7-phenanthroline skeleton. Part VI
Source:
Serbian Chemical Society
A dual read-out assay to evaluate the potency of compounds active against Mycobacterium tuberculosis.
Source:
Public Library of Science (PLoS)
Scaling up interventions to achieve global tuberculosis control: progress and new developments
Source:
Elsevier BV
Development and validation of a 96-well equilibrium dialysis apparatus for measuring plasma protein binding
Source:
Elsevier BV
Applications of High Throughput Microsomal Stability Assay in Drug Discovery
Source:
Bentham Science Publishers Ltd.
Utility of in vitro drug metabolism data in predicting in vivo metabolic clearance.
Source:
Elsevier BV
Validated assays for human cytochrome P450 activities.
Source:
American Society for Pharmacology & Experimental Therapeutics (ASPET)
Related research
People also read lists articles that other readers of this article have read.
Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.
Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.