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Journal articles on the topic 'Antimicrobial activity of cinnoline derivatives'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Gautam, Nidhi, and O. P. Chourasia. "ChemInform Abstract: Synthesis, Antimicrobial and Insecticidal Activity of Some New Cinnoline Based Chalcones and Cinnoline Based Pyrazoline Derivatives." ChemInform 41, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.201044161.

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2

ABBADY, M. S., SH M. RADWAN, and E. A. BAKHITE. "ChemInform Abstract: Synthesis and Antimicrobial Activity of Some Cinnoline Derivatives Containing Sulfonamido Group." ChemInform 25, no. 18 (2010): no. http://dx.doi.org/10.1002/chin.199418158.

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3

R., GOPIKUMAR MENON, and PURUSHOTHAMAN E. "Synthesis of Biologically Active 5-( 4-Hydroxycinnolin-3-yl)tetrazoles and 2-Methyl-5-( 4-acetoxycinnolin-3-yl)-1 ,3,4-oxadiazoles." Journal of Indian Chemical Society Vol. 74, Feb 1997 (1997): 123–24. https://doi.org/10.5281/zenodo.5875232.

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Department of Chemistry, University of Calicut, Calicut-673 635 <em>Manuscript received 29 November 1994, revised 5 July 1995. accepted 14 August 1995</em> A series of 5-(4-hydroxycinnolin-3-yl)tetrazoles and 2-methyl-5-(4-acetoxycinnolin-3-yl)-1,3.4-oxadiazo)es have been synthesised. The compounds exhibited moderate antimicrobial activity. None of the tetrazoles showed any antihistaminic activity.

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4

M., R. Patel, D. Akbari J., H. Purohit D., and S. Joshi H. "Synthesis and evaluation of pharmacological activity of some new aminopyrimidine and thiopyrimidine derivatives." Journal of Indian Chemical Society Vol. 84, Nov 2007 (2007): 1169–73. https://doi.org/10.5281/zenodo.5824805.

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Department of Chemistry, Saurashtra University, Rajkot-360 005, Gujarat, India <em>E-mail </em>: drhsjoshi@yahoo.com <em>Manuscript received 15 January 2007, revised 6 June 2007, accepted 17 August 2007</em> Various 3-(2-amino-6-arylpyrimidin-4-yl)-6-chlorocinnolin-4(3<em>H)</em>-one (2a-j) and 6-chloro-3-(6-aryl-2-mercapto3,4-dihydropyrimidin-4-yl)cinnolin-4(3<em>H</em>)-one (3a-j) were synthesized by the reaction of 6-chloro-3-[(2<em>E</em>)-3-arylprop-2-enoyl]- cinnolin-4(3<em>H</em>)-ones (1a-j) with guanidine hydrochloride and thiourea respectively. All newly synthesized compounds were te

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5

Lewgowd, Wieslawa, and Andrzej Stanczak. "Cinnoline Derivatives with Biological Activity." Archiv der Pharmazie 340, no. 2 (2007): 65–80. http://dx.doi.org/10.1002/ardp.200500194.

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6

Dr. M.Rajasekaran, Dr M. Rajasekaran, H. B. Nihal Furkhan H.B.Nihal Furkhan, R. Nishanth R.Nishanth, N. Panneerselvam N.Panneerselvam, B. S. Nithishkumar B.S.Nithishkumar, and M. Pandiyan M.Pandiyan. "Synthesis and Docking Studies of Cinnoline Derivatives for Enhanced Anti-Bacterial Activity." International Journal of Pharmaceutical Research and Applications 10, no. 2 (2025): 1797–815. https://doi.org/10.35629/4494-100217971815.

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This study involves the synthesis and evaluation of a series of cinnoline derivatives for their biological activities. The compounds were synthesized through a multi-step process, including the preparation of benzene diazonium chloride, formation of phenyl hydrazoneacetylacetone, synthesis of 4-methyl-3-acetyl cinnoline, and subsequent reactions with various amines. These compounds were characterized using Thin Layer Chromatography (TLC), melting point determination, solubility tests, and advanced spectroscopic techniques, including Infrared (IR) and Proton Nuclear Magnetic Resonance (1HNMR) s

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7

Szumilak, Marta. "Polyamine derivatives as potential bisintercalators with antiproliferative activity." Postępy Polskiej Medycyny i Farmacji 4 (June 24, 2016): 9–15. http://dx.doi.org/10.5604/01.3001.0011.6389.

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Bisntercalators are very interesting group of compounds with potential antitumor activity. They interact reversibly with DNA double helix. These agents share common structural features such as the presence of two, planar, polycyclic aromatic or heteroaromatic systems separated by a spacer chain which must be long enough to enable double intercalation between base pairs. The unique chemical structure of these compounds provides numerous modifications within their structure resulting either in higher activity or increased selectivity toward tumor cells. Within the framework of the project, new p

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8

Prashanthi Evangeline M, Prem Kumar P, and Bala Murugan K. "Cinnoline Derivatives as Antibacterial Agent and Antimycobacterial Agent: Synthesis, Microbial Evaluation and Molecular Docking Study." International Journal of Research in Pharmaceutical Sciences 11, no. 4 (2020): 6675–84. http://dx.doi.org/10.26452/ijrps.v11i4.3588.

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Fourteen Novel cinnoline library compounds were designed, synthesized through a facile approach, and allowed for screening for anti-bacterial activity and anti-tubercular activity. The titled compounds were entirely synthesized by replacing alkyl groups, sulphonyl, halo groups in the 6th & 7th position of cinnoline moiety. The enlightenment of structure was done by FTIR HNMR along with elemental analysis and further docked for Structural activity. The newly synthesized Cinnoline Compounds were examined for their in vitro drug-sensitive M tuberculosis H37Hv strain. All the compounds have sh

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9

Lettreuch, H., M. Khodja, and H. Boutoumi. "New Synthetic Route to Cinnoline Derivatives and Their Microbiological Activity." Russian Journal of Organic Chemistry 56, no. 12 (2020): 2188–93. http://dx.doi.org/10.1134/s1070428020120222.

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10

Kandeel, Manal M., Aliaa M. Kamal, Bassem H. Naguib, and Marwa S. A. Hassan. "Design, Synthesis, Cytotoxic Activity and Apoptosis-inducing Action of Novel Cinnoline Derivatives as Anticancer Agents." Anti-Cancer Agents in Medicinal Chemistry 18, no. 8 (2018): 1208–17. http://dx.doi.org/10.2174/1871520618666180220121319.

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Aims: Tyrosine kinases and topoisomerase I are common target enzymes for the majority of the anticancer agents. In contrast to quinazolines and quinolines, kinase inhibitors and topoisomerase inhibitors incorporating cinnoline scaffold are relatively infrequent. Thus the aim of this work was to replace the former scaffolds with the latter one. Eighteen novel cinnoline derivatives were designed, synthesized and characterized using both microanalytical and spectral data. Methods: The cytotoxic activity of the new compounds was screened in vitro against both human breast cancer cells and normal b

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11

Tian, Chengze, Chengbin Yang, Tianze Wu, et al. "Discovery of cinnoline derivatives as potent PI3K inhibitors with antiproliferative activity." Bioorganic & Medicinal Chemistry Letters 48 (September 2021): 128271. http://dx.doi.org/10.1016/j.bmcl.2021.128271.

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12

Mishra, Pankaj, Anil Middha, Vikas Saxena, and Abhishek Saxena. "Synthesis and Evaluation of Anti-Inflammatory Activity of Some Cinnoline Derivatives-4(-2-Amino-Thiophene) Cinnoline-3-Carboxamide." UK Journal of Pharmaceutical Biosciences 4, no. 3 (2016): 64. http://dx.doi.org/10.20510/ukjpb/4/i3/108388.

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13

Wójcicka, Anna, and Marcin Mączyński. "Antimicrobial Activity of Naphthyridine Derivatives." Pharmaceuticals 17, no. 12 (2024): 1705. https://doi.org/10.3390/ph17121705.

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To combat the problem of the increasing drug resistance of microorganisms, it is necessary to constantly search for new medicinal substances that will demonstrate more effective mechanisms of action with a limited number of side effects. Naphthyridines are N-heterocyclic compounds containing a fused system of two pyridine rings, occurring in the form of six structural isomers with different positions of nitrogen atoms, which exhibit a wide spectrum of pharmacological activity, in particular antimicrobial properties. This review presents most of the literature data about the synthetic and natur

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14

Dr., Srinivasa Rao Nathani, K. Lakshmi Dr., and V. Nagalakshmi Dr. "Antimicrobial Activity of Benzimidazoles Derivatives." International Journal of Management and Humanities (IJMH) 4, no. 11 (2020): 23–27. https://doi.org/10.35940/ijmh.K1039.0741120.

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The anti-microbial action of benzimidazole of ampicillin, was examined in Vitro beneath a specific conditions, utilizing the disc diffusion method, against different gram-positive and gram-negative pathogenic microorganisms such as Bacillus cereus, Staphylococcus aureus Pseudomonas aeruginosa and Escherichia Coli. An arrangement of these compounds were arranged and have appeared to hinder phthogenic development, the range of the zone of restraint. The zone of Obstacles of compounds founds from 7 mm2 to 46 mm2 Among the synthesized compounds in common. 6-Methoxy-N-phenyl1H-benzo [d]imidazol-2-a

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15

Garcia-Dominguez, Neftali, Enrique Raviña, Lourdes Santana, et al. "Pyridazine Derivatives, VI. Synthesis and Hypotensive Activity of 3-Hydrazinethieno(2,3-h)Cinnoline and its Derivatives." Archiv der Pharmazie 321, no. 10 (1988): 735–38. http://dx.doi.org/10.1002/ardp.19883211008.

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16

Abdelrazek, Fathy M., Peter Metz, Nadia H. Metwally, and Sherif F. El-Mahrouky. "Synthesis and Molluscicidal Activity of New Cinnoline and Pyrano [2,3-c]pyrazole Derivatives." Archiv der Pharmazie 339, no. 8 (2006): 456–60. http://dx.doi.org/10.1002/ardp.200600057.

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17

Selyutina, Olga Yu, Maya A. Ul’yanova, Olga A. Chinak, et al. "Novel Anthraquinone Derivatives and Their Complexes with Metal Ions with Anticancer Activity: Structure/Redox and Chelation Activity Correlations." Pharmaceuticals 17, no. 12 (2024): 1717. https://doi.org/10.3390/ph17121717.

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Background/Objectives: Some specific anthraquinone derivatives (AQs) are known to be used widely as effective chemotherapeutic agents in the treatment of cancer. However, their fundamental shortcoming is the high rate of cardiotoxicity observed in treated patients, which is thought to be caused by the increase in production of reactive oxygen species (ROS) catalyzed by iron and copper. The development of improved AQs and other anticancer drugs with enhanced efficacy but reduced toxicity remains a high priority. The aim of this study was to evaluate the cytotoxic and ROS production effects of c

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18

Glomb, Teresa, and Piotr Świątek. "Antimicrobial Activity of 1,3,4-Oxadiazole Derivatives." International Journal of Molecular Sciences 22, no. 13 (2021): 6979. http://dx.doi.org/10.3390/ijms22136979.

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The worldwide development of antimicrobial resistance forces scientists to search for new compounds to which microbes would be sensitive. Many new structures contain the 1,3,4-oxadiazole ring, which have shown various antimicrobial activity, e.g., antibacterial, antitubercular, antifungal, antiprotozoal and antiviral. In many publications, the activity of new compounds exceeds the activity of already known antibiotics and other antimicrobial agents, so their potential as new drugs is very promising. The review of active antimicrobial 1,3,4-oxadiazole derivatives is based on the literature from

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19

Kim, Jung Hee, Eun-Soo Park, Jae Hun Shim, et al. "Antimicrobial Activity ofp-Hydroxyphenyl Acrylate Derivatives." Journal of Agricultural and Food Chemistry 52, no. 25 (2004): 7480–83. http://dx.doi.org/10.1021/jf0499018.

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20

Kawase, Masami, Bharat Varu, Anamik Shah, et al. "Antimicrobial Activity of New Coumarin Derivatives." Arzneimittelforschung 51, no. 01 (2011): 67–71. http://dx.doi.org/10.1055/s-0031-1300004.

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21

Dzhuraev, A. D., K. M. Karimkulov, A. G. Makhsumov, and N. Amanov. "Antimicrobial activity of novel thiophene derivatives." Pharmaceutical Chemistry Journal 26, no. 11-12 (1993): 882–84. http://dx.doi.org/10.1007/bf00767666.

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22

Savluchinske-Feio, Sonia, Maria João Marcelo Curto, Bárbara Gigante, and J. Carlos Roseiro. "Antimicrobial activity of resin acid derivatives." Applied Microbiology and Biotechnology 72, no. 3 (2006): 430–36. http://dx.doi.org/10.1007/s00253-006-0517-0.

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23

Nyamu, Samuel N., Lucy Ombaka, Eric Masika, and Margaret Ng’ang’a. "Antimicrobial Photodynamic Activity of Phthalocyanine Derivatives." Advances in Chemistry 2018 (March 19, 2018): 1–8. http://dx.doi.org/10.1155/2018/2598062.

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Microbial pathogens have increasingly shown multidrug resistance posing a serious threat to the public health. Advances in technology are opening novel avenues for discovery of compounds that will mitigate the ever-increasing drug-resistant microbes. Use of photodynamic photosensitizer is one of the promising alternative approaches since they offer low risk of bacteria resistance as they use generated reactive oxygen species to kill the microbes. Phthalocyanine (Pc) is one such photosensitizer which has already shown promising antimicrobial photodynamic therapeutic properties. Previous studies

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24

Barchan, I. A., V. A. Bren', Zh V. Bren', et al. "Antimicrobial activity of cinnamic aldehyde derivatives." Pharmaceutical Chemistry Journal 31, no. 3 (1997): 137–39. http://dx.doi.org/10.1007/bf02464665.

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25

Mousumi, Bardhan, Purohit Pratigyan, S. Panda C., and Kumar Padhy Arun. "Antimicrobial activity of some pyridazinoquinoline derivatives." Journal of Indian Chemical Society Vol. 83, Jul 2006 (2006): 735–36. https://doi.org/10.5281/zenodo.5825346.

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Berhampur University, Berhampur-760 007, Orissa, India National Institute of Science & Technology, Palur Hills, Berhampur-761 008, Orissa, India E-mail: arun_nist@hotmail.com Manuscript received 17 August 2005, revised 29 March 2006, accepted 20 April 2006 Some pyridazinoquinoline derivatives have been synthesized and screened for their possible antimicrobial activity. Compound 1c exhibited significant activity against \(S\). \(aureus\), 1d and If exhibited significant activity against \(E\). \(coli\); whereas Ia and lb exhibited pronounced activity against fungi \(C\). \(albicana.\)

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26

M.K. Al-Ani, Widad, and Fitua M. Aziz. "Antimicrobial Activity of Hydroxymatairesinol (HMR) Lignan." Iraqi Journal of Pharmaceutical Sciences ( P-ISSN 1683 - 3597 E-ISSN 2521 - 3512) 22, no. 2 (2017): 30–34. http://dx.doi.org/10.31351/vol22iss2pp30-34.

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Lignans are natural products widely distributed in the plant kingdom. They are composed of two Î²-Î²-linked phenylpropane (shikimate-derived biogenetic subunits). Although the backbone of lignans is composed of phenylpropane units, there is enormous diversity in the structure of lignans leading to different classes of lignans, such as Î³-butyrolactone derivatives, eg. Hymatairesinol, bicyclooctadiene derivatives, e.g. pinoresinol, tetrahydrofuran derivatives e.g.lariciresinol, di-arylbutandiol derivatives, e.g. secoisolariciresinol. Introduction of a further carbon â€“carbon linkage leads to a

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27

Abdulla, Ibtihal Q. "Synthesis and antimicrobial activity of Ibuprofen derivatives." Natural Science 06, no. 02 (2014): 47–53. http://dx.doi.org/10.4236/ns.2014.62008.

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28

Araújo, Joana, Carla Fernandes, Madalena Pinto, and Maria Tiritan. "Chiral Derivatives of Xanthones with Antimicrobial Activity." Molecules 24, no. 2 (2019): 314. http://dx.doi.org/10.3390/molecules24020314.

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According to the World Health Organization, the exacerbated use of antibiotics worldwide is increasing multi-resistant infections, especially in the last decade. Xanthones are a class of compounds receiving great interest in drug discovery and development that can be found as natural products or obtained by synthesis. Many derivatives of xanthones are chiral and associated with relevant biological activities, including antimicrobial. The aim of this review is to compile information about chiral derivatives of xanthones from natural sources and their synthesized examples with antimicrobial acti

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29

Kaur, Harmeet, and Balasubramanian Narasimhan. "Antimicrobial Activity of Diazenyl Derivatives: An Update." Current Topics in Medicinal Chemistry 18, no. 1 (2018): 3–21. http://dx.doi.org/10.2174/1568026618666180206093107.

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The development of new antimicrobial drugs is a very challenging task owing to the rapidly developing drug resistance among the existing drugs. The hybridization of active and novel compounds is a commonly used approach to combat this situation. The azo linkage (N=N) is successfully used to link two bioactive moieties to enhance the therapeutic effects. The hybrid derivatives linked by azo linkage have shown their activity by acting on target proteins in microorganisms, cell wall inhibitors, DHPS inhibitors, RNA Editing Ligase 1 inhibitors, the general protein secretory (Sec) pathway inhibitor

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30

Borodina, T. N., E. R. Tolordava, M. E. Nikolaeva, et al. "Antimicrobial Photodynamic Activity of Hydrophilic Riboflavin Derivatives." Molecular Genetics, Microbiology and Virology 36, no. 4 (2021): 176–80. http://dx.doi.org/10.3103/s0891416821040042.

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31

Ehrlich, H., V. P. Kovalchuk, A. S. Voronkina, I. M. Vovk, І. Yu Sidko, and M. S. Tretyakov. "Antimicrobial activity investigation of natural bromotyrosine derivatives." Reports of Vinnytsia National Medical University 24, no. 1 (2020): 45–50. http://dx.doi.org/10.31393/reports-vnmedical-2020-24(1)-09.

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Annotation. The relevance of the search for new natural antimicrobials is dictated by global spread of antimicrobial resistance. Studies of marine sponges of the class Demospongiae, including more than 7300 species, have become promising from the pharmacological point of view. Sponges produce a wide range of biologically active substances of different classes such as steroids, isoprene, alkaloids, terpenoids, etc., which can inhibit the growth of pathogenic microorganisms or kill them. The trial of brominated isoxazoline alkaloid derivates named bromotyrosines has been enough promising. The ai

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32

Zhu, Rui, Cheng Yang, Ke Han, et al. "Synthesis and Antimicrobial Activity of Calycanthaceous Derivatives." Natural Product Communications 16, no. 9 (2021): 1934578X2110326. http://dx.doi.org/10.1177/1934578x211032611.

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A series of calycanthaceous alkaloid analogs have been synthesized in excellent yields. All the target compounds were evaluated in vitro for biological activity against a broad range of plant pathogen fungi, bacteria and human pathogenic fungi, and some of the designed compounds exhibited potential activity in the primary assays. Notably, Compound b7 illustrated higher degrees of activity against Aspergillu sflavu than amphotericin B, with a minimal inhibitory concentration value of 15.63 µg·mL−1. Compound b7 displayed the most effective activity among the tested calycanthaceous analogs and mi

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33

Borodina, T. N., E. R. Tolordava, M. E. Nikolaeva, et al. "Antimicrobial photodynamic activity of hydrophilic riboflavin derivatives." Molecular Genetics Microbiology and Virology (Russian version) 39, no. 4 (2021): 21. http://dx.doi.org/10.17116/molgen20213904121.

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34

Bhanu Prakash, Talapuru, Lingaladinne Mallikarjuna Reddy, Adivireddy Padmaja, and Venkatapuram Padmavathi. "Synthesis and Antimicrobial Activity of Azole Derivatives." Chemical and Pharmaceutical Bulletin 61, no. 5 (2013): 516–23. http://dx.doi.org/10.1248/cpb.c12-00975.

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35

Reddy, R. Buchi, G. V. P. Chandra Mouli, and Y. D. Reddy. "SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF IMIDAZOBENZOTHIADIAZOLE DERIVATIVES." Phosphorous and Sulfur and the Related Elements 40, no. 3-4 (1988): 173–76. http://dx.doi.org/10.1080/03086648808072911.

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36

Lupascu, Galina, Svetlana Gavzer, Nicolae Cristea, et al. "Antimicrobial activity of some vinyl-triazole derivatives." Studia Universitatis Moldaviae. Seria Științe ale Naturii, no. 1(171) (June 2024): 3–12. http://dx.doi.org/10.59295/sum1(171)2024_01.

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Mycoses and bacterioses in agricultural crops are very devastating, bringing enormous economic damage through direct crop losses and compromising it due to pathogen toxin pollution, which makes them toxic to humans and animals. Chemical plant protection procedures often become ineffective due to the easy adaptation of causative agents to pesticides, the reduction of the protective effect under the influence of unfavorable conditions, toxicity, ecological consequences. Starting from this, the aim of the research consisted in the identification of new compounds with antifungal (Fusarium avenaceu

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37

Silva, Rayanne H. N., Ana C. M. Andrade, Diego F. Nóbrega, et al. "Antimicrobial Activity of 4-Chlorocinnamic Acid Derivatives." BioMed Research International 2019 (April 23, 2019): 1–13. http://dx.doi.org/10.1155/2019/3941242.

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The microbial resistance of fungi and bacteria is currently considered a major public health problem. Esters derived from cinnamic acid have a broad spectrum of pharmacological properties that include antimicrobial activity. In this study, a collection of structurally related 4-chlorocinnamic acid esters was prepared using Fischer esterification reactions, alkyl or aryl halide esterification, and Mitsunobu and Steglich reactions. All of the esters were submitted to antimicrobial tests against strains of the species Candida albicans, Candida glabrata, Candida krusei, Candida guilliermondii, Pse

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38

Savluchinske Feio, S., B. Gigante, J. Carlos Roseiro, and M. J. Marcelo-Curto. "Antimicrobial activity of diterpene resin acid derivatives." Journal of Microbiological Methods 35, no. 3 (1999): 201–6. http://dx.doi.org/10.1016/s0167-7012(98)00117-1.

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39

Habib, NS, SM Rida, EAM Badawey, HTY Fahmy, and HA Ghozlan. "Synthesis and antimicrobial activity of rhodanine derivatives." European Journal of Medicinal Chemistry 32, no. 9 (1997): 759–62. http://dx.doi.org/10.1016/s0223-5234(97)88919-2.

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40

Yuldasheva, Kh, A. D. Dzhuraev, A. G. Makhsumov, and N. Amanov. "Antimicrobial activity of bis(1,2,3-triazole) derivatives." Pharmaceutical Chemistry Journal 25, no. 10 (1991): 728–30. http://dx.doi.org/10.1007/bf00768987.

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41

Másson, Már, Jukka Holappa, Martha Hjálmarsdóttir, Ögmundur V. Rúnarsson, Tapio Nevalainen, and Tomi Järvinen. "Antimicrobial activity of piperazine derivatives of chitosan." Carbohydrate Polymers 74, no. 3 (2008): 566–71. http://dx.doi.org/10.1016/j.carbpol.2008.04.010.

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42

Belay, Chen, Noam Y. Steinman, Luis M. Campos, Ron Dzikowski, Jacob Golenser, and Abraham J. Domb. "Asymmetric trisalkylamine cyclopropenium derivatives with antimicrobial activity." Bioorganic Chemistry 102 (September 2020): 104069. http://dx.doi.org/10.1016/j.bioorg.2020.104069.

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43

Habib, Osman M. O., Hussein M. Hassan, and Ahmed El-Mekabaty. "Novel quinazolinone derivatives: synthesis and antimicrobial activity." Medicinal Chemistry Research 22, no. 2 (2012): 507–19. http://dx.doi.org/10.1007/s00044-012-0079-x.

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44

Husain, Asif, Aftab Ahmad, Ibraheem Ahmed I. Mkhalid, Ravinesh Mishra, and Mohd Rashid. "Synthesis and antimicrobial activity of bischalcone derivatives." Medicinal Chemistry Research 22, no. 4 (2012): 1578–86. http://dx.doi.org/10.1007/s00044-012-0137-4.

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45

Naberezhnykh, G. A., S. I. Bakholdina, V. I. Gorbach, and T. F. Solov’eva. "New chitosan derivatives with potential antimicrobial activity." Russian Journal of Marine Biology 35, no. 6 (2009): 498–503. http://dx.doi.org/10.1134/s106307400906008x.

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46

HIDA, TSUNEAKI, SHIGETOSHI TSUBOTANI, NOZOMI KATAYAMA, YASUNORI FUNABASHI, HIDEAKI NATSUGARI, and SETSUO HARADA. "Synthesis and antimicrobial activity of sperabillin derivatives." Journal of Antibiotics 46, no. 5 (1993): 803–12. http://dx.doi.org/10.7164/antibiotics.46.803.

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47

Sotanaphun, Uthai, Vimolmas Lipipun, Rutt Suttisri, and Rapepol Bavovada. "Antimicrobial Activity and Stability of Tingenone Derivatives." Planta Medica 65, no. 05 (1999): 450–52. http://dx.doi.org/10.1055/s-2006-960809.

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48

Baisalbaeva, S. A., T. T. Omarov, E. T. Nikitina, and G. G. Kazakova. "Synthesis and antimicrobial activity of diazaadamantane derivatives." Pharmaceutical Chemistry Journal 21, no. 2 (1987): 120–23. http://dx.doi.org/10.1007/bf00765110.

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49

Dudarev, V. G., O. M. Tikhomirova, and A. A. Iozep. "Synthesis and Antimicrobial Activity of Carboxymethylchitin Derivatives." Pharmaceutical Chemistry Journal 47, no. 1 (2013): 31–34. http://dx.doi.org/10.1007/s11094-013-0890-9.

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Gupta, Gauri, and Preeti Verma. "ChemInform Abstract: Antimicrobial Activity of Quinoxaline Derivatives." ChemInform 46, no. 4 (2015): no. http://dx.doi.org/10.1002/chin.201504265.

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