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Disease Models, Animal --- Psychotic Disorders --- Catalepsy --- Porphyrias --- Carbolines --- physiopathology --- pharmacology

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Oncology. Neoplasms --- Toxicology --- Carbolines --- Carcinogens. --- Food Additives --- Imidazoles --- Mycotoxins --- Furocoumarins --- Quinolines --- Ultraviolet Rays --- 547.587.51 --- Oncogens --- Tumor Initiators --- Tumor Promoters --- Initiators, Tumor --- Promoters, Tumor --- Benzidines --- toxicity. --- adverse effects. --- Coumarin. Coumarinic acid. Coumaric acid. Thiocoumarin --- Conferences - Meetings --- 547.587.51 Coumarin. Coumarinic acid. Coumaric acid. Thiocoumarin --- Carcinogen --- Oncogen --- Tumor Initiator --- Tumor Promoter --- Initiator, Tumor --- Promoter, Tumor --- Carcinogens --- toxicity --- adverse effects

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Antineoplastic agents. --- Antibiotics. --- Antibacterial agents. --- Pyrroles --- Carbolines --- Diazo compounds --- Beta lactamases --- Heterocyclic chemistry. --- Anticancéreux --- Antibiotiques --- Antibactériens --- Chimie des composés hétérocycliques --- Therapeutic use. --- Inhibitors --- Chemistry. --- Toxicology. --- Chemistry, Organic. --- Biochemistry. --- Organic Chemistry. --- Medicinal Chemistry. --- Biochemistry, general. --- Pharmacology/Toxicology. --- Antineoplastic agents --- Antibiotics --- Antibacterial agents --- Heterocyclic chemistry --- Antineoplastic Agents --- Heterocyclic Compounds --- Anti-Bacterial Agents --- Therapeutic Uses --- Chemicals and Drugs --- Anti-Infective Agents --- Pharmacologic Actions --- Chemical Actions and Uses --- Biochemistry --- Pharmacy, Therapeutics, & Pharmacology --- Health & Biological Sciences --- Chemistry --- Physical Sciences & Mathematics --- Therapeutic use --- Anti-Microbial Agents --- Antiinfective Agents --- Antimicrobial Agents --- Microbicides --- Agents, Anti-Infective --- Agents, Anti-Microbial --- Agents, Antiinfective --- Agents, Antimicrobial --- Anti Infective Agents --- Anti Microbial Agents --- Therapeutic Effects --- Effects, Therapeutic --- Uses, Therapeutic --- Anti-Bacterial Compounds --- Anti-Mycobacterial Agents --- Antibacterial Agents --- Antibiotic --- Antimycobacterial Agents --- Bacteriocidal Agents --- Bacteriocides --- Agents, Anti-Bacterial --- Agents, Anti-Mycobacterial --- Agents, Antibacterial --- Agents, Antimycobacterial --- Agents, Bacteriocidal --- Anti Bacterial Agents --- Anti Bacterial Compounds --- Anti Mycobacterial Agents --- Compounds, Anti-Bacterial --- Compounds, Heterocyclic --- Anticancer Agents --- Antineoplastic Drugs --- Antineoplastics --- Antitumor Agents --- Antitumor Drugs --- Cancer Chemotherapy Agents --- Cancer Chemotherapy Drugs --- Chemotherapeutic Anticancer Agents --- Chemotherapeutic Anticancer Drug --- Agents, Anticancer --- Agents, Antineoplastic --- Agents, Antitumor --- Agents, Cancer Chemotherapy --- Agents, Chemotherapeutic Anticancer --- Chemotherapy Agents, Cancer --- Chemotherapy Drugs, Cancer --- Drug, Chemotherapeutic Anticancer --- Drugs, Antineoplastic --- Drugs, Antitumor --- Drugs, Cancer Chemotherapy --- Heteroatomic chemistry --- Cephalosporinase --- Lactamases, Beta --- Penicillinase --- Pyridoindoles --- Pyrrhols --- Pyrrol --- Pyrrole --- Chemical Actions --- Actions, Chemical --- Actions, Pharmacologic --- Anti-bacterial agents --- Antibacterials --- Bacteriocidal agents --- Bacteriostatic agents --- Anticancer agents --- Antineoplastic drugs --- Antitumor agents --- Antitumor drugs --- Cytotoxic drugs --- Inhibitors, Neoplasm --- Neoplasm inhibitors --- Biological chemistry --- Chemical composition of organisms --- Organisms --- Physiological chemistry --- Organic chemistry --- Chemicals --- Composition --- Toxicology --- Pharmacology. --- Organic chemistry. --- Medicinal chemistry. --- Biology --- Medical sciences --- Medicine --- Pharmacology --- Poisoning --- Poisons --- Drug effects --- Medical pharmacology --- Chemotherapy --- Drugs --- Pharmacy --- Chemistry, Medical and pharmaceutical --- Chemistry, Pharmaceutical --- Drug chemistry --- Medical chemistry --- Medicinal chemistry --- Pharmacochemistry --- Physiological effect --- Pharmaceutical chemistry.

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This book is conceived to promote synergy between research and industrial activities in the design and development of new drugs and, therefore, is not limited to any specific aspect of development. It covers the entire process from the identification of a molecular target, studies of drug–protein interactions, the modeling and optimization of the functional activity, design and chemical synthesis, biological evaluation, and the development of new pharmaceutical carriers.The original articles and reviews are focused on the design and development of new anticancer treatments, new anticancer low-molecular-weight agents as potential drug substances, and the elucidation of their mechanisms of action. The book also includes studies on novel modulators of the serotonergic system used to treat central nervous system disorders, novel agents against infectious diseases, and the development of anti-plasmodial and anti-inflammatory agents. The successful identification of new compounds for development as drug substances comes from rich sources of medicinal plants and medicinal chemistry approaches.

Research & information: general --- Chemistry --- alpha-ketoglutarate --- cell cycle --- apoptosis --- JNK --- cell migration --- cell invasion --- TGF-β --- VEGF --- glycoconjugates --- methotrexate --- cancer treatment --- glucose metabolism --- drug design and discovery --- anticancer drugs --- targeted therapy --- Warburg effect --- antidepressants --- pyrido[1,2-c]pyrimidines --- dual 5-HT1A/SERT activity --- drug design --- anticancer activity --- lung cancer --- resveratrol --- PRI-2191 --- vitamin D --- active substance delivery systems --- biomedical hydrogels --- active substance-controlled release --- genistein --- hydrogels for cosmetology --- hydrogels for dermatology --- transdermal active substance delivery systems --- histone deacetylase (HDAC) --- depression --- biomarker --- anti-depressant therapy --- human DNA topoisomerase --- cancer --- drug --- molecular docking --- synthesis --- fluorine --- vitamin D3 --- metabolite --- A-ring --- CD-ring --- side-chain --- nanoparticles --- molecular modeling --- oxidation mechanisms --- electrochemistry --- MALDI --- spectroscopic data --- cytotoxic study --- self-assembled monolayer --- gold electrode --- multimodal activity --- calcium-sensing receptor --- enantiomer --- calcimimetic --- calcilytic --- colon cancer --- stereospecificity --- HT-29 --- IL-8 --- inflammation --- cyclooxygenase --- 1,2,4-triazole --- pyridazinone --- SAR --- anti-inflammatory activity --- antioxidant activity --- ADME --- anticancer drug --- antimicrobial peptide (AMP) --- dermaseptin --- frog skin peptides --- LHRH --- prostate cancer --- Phyllomedusa bicolor --- therapeutic peptides --- copper (II) complexes --- thiourea --- cytotoxic activity --- proteome analysis --- antimicrobial activity --- major latex protein --- Chelidonium majus --- greater celandine --- defense-related proteins --- alkaloids --- cancer cells --- vitamin D receptor --- split luciferase-based biosensor --- CYP24A1-dependent metabolism --- CYP27B1 --- rickets --- genome editing --- vitamin D biology and action --- transcription --- ChIP-chip analysis --- distal enhancers --- histone H3 acetylation --- RNA polymerase II --- analogue actions at genes --- vitamin D hormone (1,25(OH)2D3) --- latex --- antiviral proteins --- antimicrobial compounds --- cytotoxicity --- drug discovery --- CRISPR/Cas9 --- tetrahydro-β-carbolines --- Plasmodium falciparum (P. falciparum) --- antimalarial --- antiparasitic agents --- hemolysis --- vitamin D analogs --- 25 vitamin D 24-hydroxylase --- CYP24A1 --- proliferation --- high-grade serous ovarian cancer cells --- gold --- Au(III) complex --- colorectal cancer --- organometallic --- cancer therapy --- metallodrugs