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European Journal of Medicinal Chemistry, ISSN 0223-5234, 01/2015, Volume 89, pp. 743 - 816
The biological activity of Mannich bases, a structurally heterogeneous class of chemical compounds that are generated from various substrates through the... 
Aminomethylation | Drug design | Mannich bases | Structure–activity relationships | Biological activity | Structure-activity relationships | Structureeactivity relationships | CHEMISTRY, MEDICINAL | ANTIMICROBIAL ACTIVITY EVALUATION | ONE-POT SYNTHESIS | PURINE NUCLEOSIDE PHOSPHORYLASE | STATE ANALOG INHIBITORS | B VIRUS ACTIVITIES | DOXORUBICIN-FORMALDEHYDE CONJUGATE | REGIOSELECTIVE REACTION SYNTHESIS | TITANOCENE ANTICANCER DRUGS | THYROID-HORMONE RECEPTOR | MYCOBACTERIUM-TUBERCULOSIS ISOCITRATE | Analgesics - pharmacology | Antioxidants - chemistry | Antineoplastic Agents - chemical synthesis | Humans | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Anticonvulsants - pharmacology | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Mannich Bases - chemical synthesis | Analgesics - chemical synthesis | Antiviral Agents - chemistry | Anti-Bacterial Agents - chemistry | Drug Design | Mannich Bases - pharmacology | Antineoplastic Agents - pharmacology | Anti-Inflammatory Agents, Non-Steroidal - chemical synthesis | Antimalarials - chemical synthesis | Antifungal Agents - pharmacology | Antiviral Agents - pharmacology | Anticonvulsants - chemical synthesis | Antioxidants - chemical synthesis | Antioxidants - pharmacology | Antineoplastic Agents - chemistry | Chemistry, Pharmaceutical | Mannich Bases - chemistry | Antimalarials - pharmacology | Anti-Bacterial Agents - chemical synthesis | Animals | Analgesics - chemistry | Anticonvulsants - chemistry | Antimalarials - chemistry | Antiviral Agents - chemical synthesis | Anti-Bacterial Agents - pharmacology | Antioxidants | Antiviral agents | Enzymes | Mental illness | Bases (Chemistry)
Journal Article
Bioorganic Chemistry, ISSN 0045-2068, 04/2017, Volume 71, pp. 30 - 54
1,2,3-Triazoles are important five-membered heterocyclic scaffold due to their extensive biological activities. This framework can be readily obtained in good... 
1,3-Dipolar cycloaddition | Multicomponent reaction | 1,2,3-Triazole | Alkyne–azide coupling reaction | AZIDE-ALKYNE CYCLOADDITION | 1,4-DISUBSTITUTED 1,2,3-TRIAZOLES | ONE-POT SYNTHESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | 1,5-DISUBSTITUTED 1,2,3-TRIAZOLES | HUMAN-IMMUNODEFICIENCY-VIRUS | Alkyne-azide coupling reaction | FREE CLICK CHEMISTRY | METAL-FREE SYNTHESIS | BIOLOGICAL EVALUATION | IN-VITRO ACTIVITY | ANTIMICROBIAL ACTIVITY | Triazoles - chemistry | Anti-Infective Agents - pharmacology | Antineoplastic Agents - chemical synthesis | Humans | Drug Discovery - methods | Azides - chemistry | HIV Protease Inhibitors - pharmacology | Anti-Infective Agents - chemistry | Triazoles - chemical synthesis | Antineoplastic Agents - pharmacology | Anti-Inflammatory Agents - pharmacology | Click Chemistry - methods | Models, Molecular | HIV Protease Inhibitors - chemistry | Alkynes - chemistry | Cyclooxygenase Inhibitors - chemistry | Antineoplastic Agents - chemistry | Anti-Infective Agents - chemical synthesis | Cycloaddition Reaction - methods | Cyclooxygenase Inhibitors - pharmacology | Triazoles - pharmacology | Animals | Anti-Inflammatory Agents - chemistry | Cyclooxygenase Inhibitors - chemical synthesis | Anti-Inflammatory Agents - chemical synthesis | HIV Protease Inhibitors - chemical synthesis | Receptor, Cannabinoid, CB1 - antagonists & inhibitors | Triazoles | COX-2 inhibitors | Protease inhibitors | Proteases
Journal Article
Current Medicinal Chemistry, ISSN 0929-8673, 07/2007, Volume 14, Issue 17, pp. 1829 - 1852
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 04/2017, Volume 23, Issue 19, pp. 4467 - 4526
Journal Article