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1. Anticandidal agents
by Kumar, Awanish and Jha, Anubhuti
2017, ISBN 9780128113110
Candidiasis | therapy | Antifungal Agents
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2. Antimicrobial agents
: antibacterials and antifungals
by Bryskier, André and American Society for Microbiology
2005, ISBN 1555812376, xxx, 1426
Antibiotics | Antibiotiques
Book
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3. Antifungal agents
: methods and protocols
by Ernst, Erika J and Rogers, P. David
2005, Methods in Molecular Medicine, ISBN 1588292770, Volume 118, x, 209
Mycoses | Medical mycology | Research | Methodology | Immunotherapy | Antifungal agents | Medicine & Public Health | Infectious Diseases
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4. The antimicrobial agents annual
The antimicrobial agents annual, ISSN 0168-938X, 1986
Antibiotics | Anti-infective agents | Periodicals
Journal
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5. Full Text Synthesis of novel quinoline–based 4,5–dihydro–1H–pyrazoles as potential anticancer, antifungal, antibacterial and antiprotozoal agents
by Ramírez–Prada, Jonathan and Robledo, Sara M and Vélez, Iván D and Crespo, María del Pilar and Quiroga, Jairo and Abonia, Rodrigo and Montoya, Alba and Svetaz, Laura and Zacchino, Susana and Insuasty, Braulio
European Journal of Medicinal Chemistry, ISSN 0223-5234, 05/2017, Volume 131, pp. 237 - 254
A new series of –substituted 2–pyrazolines , , , and were obtained from the cyclocondensation reaction of [(7–chloroquinolin–4–yl)amino]chalcones with... 
Antifungal activity | Chalcones | Antimalarial activity | Antitrypanosomal activity | 2–pyrazolines | Anticancer activity | Quinoline | Antibacterial activity | Antileishmanial activity | ANTIPLASMODIAL ACTIVITY | CHEMISTRY, MEDICINAL | HYBRID MOLECULES | INHIBITORY PROPERTIES | CELL-GROWTH | 2-pyrazolines | IN-VITRO | CHALCONE DERIVATIVES | PLASMODIUM-FALCIPARUM | ANTILEISHMANIAL AGENTS | ANTIMICROBIAL ACTIVITY | Parasitic Sensitivity Tests | Pyrazoles - chemical synthesis | Antineoplastic Agents - chemical synthesis | Humans | Bacteria - drug effects | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Structure-Activity Relationship | Plasmodium falciparum - drug effects | Quinolines - pharmacology | Dose-Response Relationship, Drug | Microbial Sensitivity Tests | Pyrazoles - chemistry | Anti-Bacterial Agents - chemistry | Antiprotozoal Agents - chemical synthesis | Antineoplastic Agents - pharmacology | Molecular Structure | Pyrazoles - pharmacology | Antifungal Agents - pharmacology | Cell Survival - drug effects | Fungi - drug effects | Quinolines - chemistry | Antiprotozoal Agents - chemistry | Antineoplastic Agents - chemistry | Antiprotozoal Agents - pharmacology | Anti-Bacterial Agents - chemical synthesis | Cell Line, Tumor | Anti-Bacterial Agents - pharmacology | Cell Proliferation - drug effects | Drug Screening Assays, Antitumor | Care and treatment | Malaria | Antifungal agents | Drug resistance | Antibacterial agents | Cancer | Index Medicus
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6. Antifungal agents
: advances and problems
by Jucker, Ernst
2003, ISBN 9783764369262, vii, 248
Antifungal agents | Mycoses -- Treatment
Book
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7. Full Text New imidazolidineiminothione derivatives: Synthesis, spectral characterization and evaluation of antitumor, antiviral, antibacterial and antifungal activities
by Moussa, Ziad and El-Sharief, Marwa A.M.Sh and Abbas, Samir Y
European Journal of Medicinal Chemistry, ISSN 0223-5234, 10/2016, Volume 122, pp. 419 - 428
A series of new imidazolidineiminothione derivatives with various halogenated and alkylated aromatic substituents at N-(1) and at N-(3) was synthesized through... 
N-Arylcyanothioformamides | Antitumor | Antifungal activities | Antiviral | Imidazolidineiminothiones | NMR spectra | Antibacterial | CHEMISTRY, MEDICINAL | MONO | BIS-IMIDAZOLIDINEIMINOTHIONES | A-VIRUS-INFECTION | AGENTS | CYTOTOXICITY | Antifungal Agents - pharmacology | Antiviral Agents - pharmacology | Imidazolidines - chemical synthesis | Antineoplastic Agents - chemical synthesis | Humans | Imidazolidines - pharmacology | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Structure-Activity Relationship | Antineoplastic Agents - chemistry | Anti-Bacterial Agents - chemical synthesis | Microbial Sensitivity Tests | Antiviral Agents - chemistry | Anti-Bacterial Agents - chemistry | Antiviral Agents - chemical synthesis | Cell Line, Tumor | Anti-Bacterial Agents - pharmacology | Antineoplastic Agents - pharmacology | Imidazolidines - chemistry | Drug Screening Assays, Antitumor | Antiviral agents | Antibacterial agents | Analysis | Antifungal agents | Index Medicus
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8. Full Text Efficient microwave enhanced regioselective synthesis of a series of benzimidazolyl/triazolyl spiro [indole-thiazolidinones] as potent antifungal agents and crystal structure of spiro[3 H -indole-3,2′-thiazolidine]-3′(1,2,4-triazol-3-yl)-2,4′(1 H )-dione
by Dandia, Anshu and Singh, Ruby and Khaturia, Sarita and Mérienne, Claude and Morgant, Georges and Loupy, André
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 2006, Volume 14, Issue 7, pp. 2409 - 2417
A microwave-assisted three-component, regioselective one-pot synthesis of spiro[indole-thiazolidinones] ( – ) is carried out using montmorillonite KSF as solid... 
DRY-MEDIA SYNTHESIS | ORGANIC-SYNTHESIS | SPIROHETEROCYCLES | ACTIVATION | 4-THIAZOLIDINONES | CHEMISTRY, MEDICINAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | ANTIMICROBIAL AGENTS | CHEMISTRY, ORGANIC | IRRADIATION | 3-COMPONENT CONDENSATION | INHIBITORS | DERIVATIVES | Colletotrichum - drug effects | Stereoisomerism | Triazoles - chemistry | Indoles - chemical synthesis | Fusarium - drug effects | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Structure-Activity Relationship | Benzimidazoles - chemistry | Thiazolidines | X-Ray Diffraction | Spiro Compounds - chemical synthesis | Indoles - pharmacology | Molecular Structure | Triazoles - radiation effects | Microwaves | Spiro Compounds - chemistry | Antifungal Agents - pharmacology | Indoles - radiation effects | Crystallization | Models, Molecular | Benzimidazoles - radiation effects | Rhizoctonia - classification | Thiazoles - radiation effects | Rhizoctonia - drug effects | Colletotrichum - classification | Thiazoles - chemistry | Fusarium - classification | Indoles - chemistry | Spiro Compounds - pharmacology | Clay | Montmorillonite | Structure | Crystals | Antifungal agents | Index Medicus
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9. Full Text Candidemia in patients with hematologic malignancies in the era of new antifungal agents (2001-2007): Stable incidence but changing epidemiology of a still frequently lethal infection
by Sipsas, Nikolaos V and Lewis, Russell E and Tarrand, Jeffrey and Hachem, Ray and Rolston, Kenneth V and Raad, Issam I and Kontoyiannis, Dimitrios P
Cancer, ISSN 0008-543X, 10/2009, Volume 115, Issue 20, pp. 4745 - 4752
BACKGROUND: The incidence, epidemiology, Candida species distribution, resistance patterns, and outcome of candidemia in high-risk hematologic malignancy... 
Candidemia | Candida | Hematological malignancy | Antifungal agents | CASPOFUNGIN | antifungal agents | RISK-FACTORS | CANDIDIASIS | INVASIVE FUNGAL-INFECTIONS | candidemia | ONCOLOGY | CARE CANCER CENTER | SURVEILLANCE | RESISTANCE | hematological malignancy | CANDIDAEMIA | BLOOD-STREAM INFECTIONS | FLUCONAZOLE | Hematologic Neoplasms - microbiology | Humans | Middle Aged | Candidiasis - epidemiology | Candidiasis - mortality | Male | Candidiasis - complications | Fungemia - mortality | Antifungal Agents - therapeutic use | Incidence | Candidiasis - blood | Candidiasis - drug therapy | Aged, 80 and over | Adult | Female | Aged | Retrospective Studies | Fungemia - epidemiology | Hematologic Neoplasms - complications | Complications and side effects | Candidiasis | Care and treatment | Demographic aspects | Distribution | Dosage and administration | Research | Blood diseases | Risk factors | Index Medicus | Abridged Index Medicus
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10. Full Text Synthesis of novel sulfanilamide-derived 1,2,3-triazoles and their evaluation for antibacterial and antifungal activities
by Wang, Xian-Long and Wan, Kun and Zhou, Cheng-He
European Journal of Medicinal Chemistry, ISSN 0223-5234, 2010, Volume 45, Issue 10, pp. 4631 - 4639
A series of novel sulfanilamide-derived 1,2,3-triazole compounds were synthesized in excellent yields 1,3-dipolar cycloaddition and confirmed by MS, IR and NMR... 
1,3-Dipolar cycloaddition | Antifungal | 1,2,3-Triazole | Antibacterial | Sulfanilamide | AZIDE-ALKYNE CYCLOADDITION | INFECTIONS | CHEMISTRY, MEDICINAL | ANALOGS | CLICK CHEMISTRY | SULFONAMIDES | PROPHYLAXIS | BIOLOGICAL EVALUATION | DERIVATIVES | ANTIMICROBIAL ACTIVITY | CARBONIC-ANHYDRASE INHIBITORS | Antifungal Agents - pharmacology | Fungi - drug effects | Magnetic Resonance Spectroscopy | Sulfanilamides - chemistry | Bacterial Infections - drug therapy | Triazoles - chemistry | Anti-Infective Agents - pharmacology | Humans | Bacteria - drug effects | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Anti-Infective Agents - chemical synthesis | Anti-Bacterial Agents - chemical synthesis | Triazoles - pharmacology | Spectrophotometry, Infrared | Anti-Bacterial Agents - chemistry | Anti-Infective Agents - chemistry | Mycoses - drug therapy | Triazoles - chemical synthesis | Anti-Bacterial Agents - pharmacology | Sulfanilamides - chemical synthesis | Sulfanilamides - pharmacology | Antibacterial agents | Antifungal agents | Index Medicus
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11. Full Text Synthesis and Bioactivities of Kanamycin B-Derived Cationic Amphiphiles
by Fosso, Marina Y and Shrestha, Sanjib K and Green, Keith D and Garneau-Tsodikova, Sylvie
Journal of Medicinal Chemistry, ISSN 0022-2623, 12/2015, Volume 58, Issue 23, pp. 9124 - 9132
Cationic amphiphiles derived from aminoglycosides (AGs) have been shown to exhibit enhanced antimicrobial activity. Through the attachment of hydrophobic... 
ANTIFUNGAL CONVERSION | CHEMISTRY, MEDICINAL | TOBRAMYCIN | ANTIBACTERIAL ACTIVITY | ENZYMES | COMPLEXES | DRUG-RESISTANCE | NEOMYCIN | DERIVATIVES | AMINOGLYCOSIDE ANTIBIOTICS | STRUCTURE-BASED DESIGN | Hemolysis - drug effects | Kanamycin - toxicity | Humans | Bacteria - drug effects | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Anti-Bacterial Agents - chemistry | Drug Design | Anti-Bacterial Agents - toxicity | Antifungal Agents - toxicity | Antifungal Agents - pharmacology | Cell Line | Cell Survival - drug effects | Surface-Active Agents - toxicity | Fungi - drug effects | Bacterial Infections - drug therapy | Kanamycin - analogs & derivatives | Kanamycin - pharmacology | Surface-Active Agents - pharmacology | Anti-Bacterial Agents - chemical synthesis | Drug Resistance, Microbial | Animals | Mycoses - drug therapy | Kanamycin - chemistry | Anti-Bacterial Agents - pharmacology | Mice | Surface-Active Agents - chemistry | Kanamycin - chemical synthesis | Surface-Active Agents - chemical synthesis | Index Medicus
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12. Full Text Synthesis of benzimidazolyl-1,3,4-oxadiazol-2ylthio-N-phenyl (benzothiazolyl) acetamides as antibacterial, antifungal and antituberculosis agents
by Patel, Paresh K and Patel, Rahul V and Kumari, Premlata and Rajani, Dhanji P and Chikhalia, Kishor H
European Journal of Medicinal Chemistry, ISSN 0223-5234, 07/2012, Volume 53, pp. 41 - 51
To affiliate multiple bioactivities in a compact heteronuclei, two series of benzimidazole based 1,3,4-oxadiazoles were synthesized and assessed for their... 
1,3,4–Oxadiazole | Benzimidazole | Benzothiazole | Biological activity | 1,3,4-Oxadiazole | ANTIMYCOBACTERIAL ACTIVITY | DESIGN | CHEMISTRY, MEDICINAL | BENZIMIDAZOLE DERIVATIVES | MOIETY | ANTICANCER AGENTS | 1,3,4-OXADIAZOLES | PHARMACOLOGICAL EVALUATION | ANTIMICROBIAL ACTIVITY | Antifungal Agents - pharmacology | Antitubercular Agents - chemical synthesis | Antitubercular Agents - chemistry | Chemistry Techniques, Synthetic | Fungi - drug effects | Benzothiazoles - pharmacology | Antitubercular Agents - pharmacology | Bacteria - drug effects | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Mycobacterium tuberculosis - drug effects | Microbial Sensitivity Tests | Benzothiazoles - chemical synthesis | Benzothiazoles - chemistry | Pneumonia | Analysis | Bacterial pneumonia | Antifungal agents | Anti-infective agents | Antitubercular agents | Nuclear magnetic resonance spectroscopy | Antibacterial agents | Index Medicus
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13. Full Text Synthesis, antimicrobial and cytotoxic activities of some novel thiazole clubbed 1,3,4-oxadiazoles
by Desai, N.C and Bhatt, Nayan and Somani, Hardik and Trivedi, Amit
European Journal of Medicinal Chemistry, ISSN 0223-5234, 09/2013, Volume 67, pp. 54 - 59
A series of thiazole clubbed 1,3,4-oxadiazole derivatives ( – ) have been synthesized and characterized by IR, H NMR, C NMR and mass spectral analysis.... 
Thiazole clubbed 1,3,4-oxadiazoles | Antifungal activity | Antibacterial activity | Cytotoxicity | 1,3,4-Oxadiazole | Thiazole | DESIGN | CHEMISTRY, MEDICINAL | SERIES | ANALOGS | 1,2,4-TRIAZOLE | ACID-DERIVATIVES | POTENT | IMIDAZOLE DERIVATIVES | AGENTS | INHIBITORS | 4-THIAZOLIDINONE | Antineoplastic Agents - chemical synthesis | Escherichia coli - drug effects | Humans | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Structure-Activity Relationship | Dose-Response Relationship, Drug | Microbial Sensitivity Tests | Anti-Bacterial Agents - chemistry | Antineoplastic Agents - pharmacology | Molecular Structure | Oxadiazoles - chemistry | Antifungal Agents - pharmacology | Streptococcus pyogenes - drug effects | Fungi - drug effects | Pseudomonas aeruginosa - drug effects | Antineoplastic Agents - chemistry | Anti-Bacterial Agents - chemical synthesis | Thiazoles - chemical synthesis | Thiazoles - chemistry | Anti-Bacterial Agents - pharmacology | Cell Proliferation - drug effects | Thiazoles - pharmacology | HeLa Cells | Staphylococcus aureus - drug effects | Drug Screening Assays, Antitumor | Antibacterial agents | Analysis | Index Medicus
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14. Full Text Anticandidal Agents
by Awanish Kumar
09/2016, ISBN 9780128113110, 95
Anticandidal Agents provides the latest information on candida drug resistance and its remedial implications. In this compilation, users will find a... 
Candidiasis | Clinical & internal medicine | Drug resistance
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15. Full Text Metal based biologically active compounds: Design, synthesis, and antibacterial/antifungal/cytotoxic properties of triazole-derived Schiff bases and their oxovanadium(IV) complexes
by Chohan, Zahid H and Sumrra, Sajjad H and Youssoufi, Moulay H and Hadda, Taibi B
European Journal of Medicinal Chemistry, ISSN 0223-5234, 2010, Volume 45, Issue 7, pp. 2739 - 2747
A new series of oxovanadium(IV) complexes have been designed and synthesized with a new class of triazole Schiff bases derived from the reaction of... 
Oxovanadium(IV) complexes | Antibacterial/antifungal/cytotoxic activity | Triazole Schiff bases | Antibacterial/antifungal/ cytotoxic activity | SALICYLALDEHYDE SEMICARBAZONE DERIVATIVES | CHEMISTRY, MEDICINAL | IN-VITRO ANTIBACTERIAL | MOIETY | CRYSTAL-STRUCTURE | SULFONAMIDES | ANTICONVULSANT EVALUATION | ANTIMICROBIAL ACTIVITIES | GROWTH | ANTIFUNGAL | VANADIUM(V) COMPLEXES | Antifungal Agents - pharmacology | Organometallic Compounds - toxicity | Fungi - drug effects | Triazoles - chemistry | Bacteria - drug effects | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Magnetics | Vanadates - chemistry | Anti-Bacterial Agents - chemical synthesis | Microbial Sensitivity Tests | Artemia - drug effects | Animals | Organometallic Compounds - chemical synthesis | Anti-Bacterial Agents - chemistry | Schiff Bases - chemistry | Drug Design | Organometallic Compounds - chemistry | Anti-Bacterial Agents - pharmacology | Anti-Bacterial Agents - toxicity | Spectrum Analysis | Antifungal Agents - toxicity | Organometallic Compounds - pharmacology | Schiff bases | Pyridine | Triazoles | Analysis | Antifungal agents | Vanadium | Antibacterial agents | Index Medicus
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16. Full Text Low molecular weight chitosan is an effective antifungal agent against Botryosphaeria sp. and preservative agent for pear (Pyrus) fruits
by Wang, Yunguang and Li, Bin and Zhang, Xuedan and Peng, Nan and Mei, Yuxia and Liang, Yunxiang
International Journal of Biological Macromolecules, ISSN 0141-8130, 02/2017, Volume 95, pp. 1135 - 1143
Antifungal activity and preservative effect of a low molecular weight chitosan (LMWC) sample, derived from chitosan by enzymatic hydrolysis, were investigated... 
Antifungal activity | Pear fruit | Low molecular weight chitosan (LMWC) | Preservative agent | Botryosphaeria sp | POSTHARVEST | POLYMER SCIENCE | QUALITY | ACID | BIOCHEMISTRY & MOLECULAR BIOLOGY | MODE | CHROMATOGRAPHY | DISEASES | GROWTH | CHITIN | CHEMISTRY, APPLIED | DERIVATIVES | Hyphae - growth & development | Catechol Oxidase - immunology | Molecular Weight | Apoptosis - drug effects | Fruit - drug effects | Antifungal Agents - chemistry | Chitinases - metabolism | Fruit - enzymology | Phylogeny | Membrane Potential, Mitochondrial - drug effects | Microbial Sensitivity Tests | Plant Proteins - agonists | Ergosterol - antagonists & inhibitors | Fruit - microbiology | Chitosan - pharmacology | Plant Proteins - metabolism | Antifungal Agents - pharmacology | Saccharomycetales - drug effects | Peroxidase - immunology | Hyphae - ultrastructure | Saccharomycetales - growth & development | Ergosterol - biosynthesis | Pyrus | Food Preservatives - pharmacology | Plant Proteins - immunology | Saccharomycetales - classification | Saccharomycetales - ultrastructure | Hyphae - classification | Enzyme Activation - drug effects | Hydrolysis | Chitosan - chemistry | Food Preservatives - chemistry | Catechol Oxidase - metabolism | Chitinases - immunology | Hyphae - drug effects | Peroxidase - metabolism | Enzymes | Permeability | Fruit | Antifungal agents | Index Medicus
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17. Full Text Synthesis and studies on some new fluorine containing triazolothiadiazines as possible antibacterial, antifungal and anticancer agents
by Shivarama Holla, B and Sooryanarayana Rao, B and Sarojini, B.K and Akberali, P.M and Suchetha Kumari, N
European Journal of Medicinal Chemistry, ISSN 0223-5234, 2006, Volume 41, Issue 5, pp. 657 - 663
Synthesis of a series of 7-arylidene-6-(2,4-dichlorophenyl)-3-aryloxymethyl/anilinomethyl-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines ( ) by the condensation of... 
1,3,4-Thiadiazines | Anticancer screening | 1,2,4-Triazoles | Antibacterial agents | Antifungal agents | CHEMISTRY, MEDICINAL | 1,3,4-thiadiazines | 1,2,4-triazoles | antifungal agents | anticancer screening | antibacterial agents | Antifungal Agents - pharmacology | Antineoplastic Agents - chemical synthesis | Humans | Azo Compounds - chemical synthesis | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Structure-Activity Relationship | Antineoplastic Agents - chemistry | Anti-Bacterial Agents - chemical synthesis | Azo Compounds - chemistry | Anti-Bacterial Agents - chemistry | Cell Line, Tumor | Sulfhydryl Compounds - chemistry | Anti-Bacterial Agents - pharmacology | Antineoplastic Agents - pharmacology | Molecular Structure | Drug Evaluation, Preclinical | Azo Compounds - pharmacology | Fluorine - chemistry | Antimitotic agents | Care and treatment | Analysis | Water quality | Soil inoculation | Nuclear magnetic resonance | Fluorides | Antineoplastic agents | Condensation | Cancer | Index Medicus
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