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Hybrid Molecules Containing a 7-Chloro-4-aminoquinoline Nucleus and a Substituted 2-Pyrazoline with Antiproliferative and Antifungal Activity
by
Abonia, Rodrigo
, Zacchino, Susana
, Insuasty, Braulio
, Montoya, Alba
, Derita, Marcos
, Sortino, Maximiliano
, Ornelas, Alfredo
, Quiroga, Jairo
in
Aminoquinolines - chemistry
/ antifungal
/ Antifungal agents
/ Antifungal Agents - chemical synthesis
/ Antifungal Agents - chemistry
/ Antifungal Agents - pharmacology
/ Antineoplastic Agents - chemical synthesis
/ Antineoplastic Agents - chemistry
/ Antineoplastic Agents - pharmacology
/ antiproliferative activity
/ Biological activity
/ Cancer
/ Candida albicans
/ Candida albicans - drug effects
/ Cell Line, Tumor
/ Cell Proliferation - drug effects
/ Cell Survival - drug effects
/ chalcones
/ Chemistry
/ Cryptococcus neoformans
/ Cryptococcus neoformans - drug effects
/ cyclocondensation reaction
/ Drug Screening Assays, Antitumor
/ Fungi
/ Humans
/ Microbial Sensitivity Tests
/ Molecular Structure
/ N-aryl-2-pyrazolines
/ Pyrazoles - chemical synthesis
/ Pyrazoles - chemistry
/ Pyrazoles - pharmacology
/ Structure-Activity Relationship
2016
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Hybrid Molecules Containing a 7-Chloro-4-aminoquinoline Nucleus and a Substituted 2-Pyrazoline with Antiproliferative and Antifungal Activity
by
Abonia, Rodrigo
, Zacchino, Susana
, Insuasty, Braulio
, Montoya, Alba
, Derita, Marcos
, Sortino, Maximiliano
, Ornelas, Alfredo
, Quiroga, Jairo
in
Aminoquinolines - chemistry
/ antifungal
/ Antifungal agents
/ Antifungal Agents - chemical synthesis
/ Antifungal Agents - chemistry
/ Antifungal Agents - pharmacology
/ Antineoplastic Agents - chemical synthesis
/ Antineoplastic Agents - chemistry
/ Antineoplastic Agents - pharmacology
/ antiproliferative activity
/ Biological activity
/ Cancer
/ Candida albicans
/ Candida albicans - drug effects
/ Cell Line, Tumor
/ Cell Proliferation - drug effects
/ Cell Survival - drug effects
/ chalcones
/ Chemistry
/ Cryptococcus neoformans
/ Cryptococcus neoformans - drug effects
/ cyclocondensation reaction
/ Drug Screening Assays, Antitumor
/ Fungi
/ Humans
/ Microbial Sensitivity Tests
/ Molecular Structure
/ N-aryl-2-pyrazolines
/ Pyrazoles - chemical synthesis
/ Pyrazoles - chemistry
/ Pyrazoles - pharmacology
/ Structure-Activity Relationship
2016
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Hybrid Molecules Containing a 7-Chloro-4-aminoquinoline Nucleus and a Substituted 2-Pyrazoline with Antiproliferative and Antifungal Activity
by
Abonia, Rodrigo
, Zacchino, Susana
, Insuasty, Braulio
, Montoya, Alba
, Derita, Marcos
, Sortino, Maximiliano
, Ornelas, Alfredo
, Quiroga, Jairo
in
Aminoquinolines - chemistry
/ antifungal
/ Antifungal agents
/ Antifungal Agents - chemical synthesis
/ Antifungal Agents - chemistry
/ Antifungal Agents - pharmacology
/ Antineoplastic Agents - chemical synthesis
/ Antineoplastic Agents - chemistry
/ Antineoplastic Agents - pharmacology
/ antiproliferative activity
/ Biological activity
/ Cancer
/ Candida albicans
/ Candida albicans - drug effects
/ Cell Line, Tumor
/ Cell Proliferation - drug effects
/ Cell Survival - drug effects
/ chalcones
/ Chemistry
/ Cryptococcus neoformans
/ Cryptococcus neoformans - drug effects
/ cyclocondensation reaction
/ Drug Screening Assays, Antitumor
/ Fungi
/ Humans
/ Microbial Sensitivity Tests
/ Molecular Structure
/ N-aryl-2-pyrazolines
/ Pyrazoles - chemical synthesis
/ Pyrazoles - chemistry
/ Pyrazoles - pharmacology
/ Structure-Activity Relationship
2016
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Hybrid Molecules Containing a 7-Chloro-4-aminoquinoline Nucleus and a Substituted 2-Pyrazoline with Antiproliferative and Antifungal Activity
Journal Article
Hybrid Molecules Containing a 7-Chloro-4-aminoquinoline Nucleus and a Substituted 2-Pyrazoline with Antiproliferative and Antifungal Activity
2016
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Overview
Twenty-four new hybrid analogues (15–38) containing 7-chloro-4-aminoquinoline and 2-pyrazoline N-heterocyclic fragments were synthesized. Twelve of the new compounds were evaluated against 58 human cancer cell lines by the U.S. National Cancer Institute (NCI). Compounds 25, 30, 31, 36, and 37 showed significant cytostatic activity, with the most outstanding GI50 values ranging from 0.05 to 0.95 µM. The hybrid compounds (15–38) were also evaluated for antifungal activity against Candida albicans and Cryptococcus neoformans. From the obtained results some structure–activity relationships were outlined.
Publisher
MDPI AG,MDPI
Subject
/ Antifungal Agents - chemical synthesis
/ Antifungal Agents - chemistry
/ Antifungal Agents - pharmacology
/ Antineoplastic Agents - chemical synthesis
/ Antineoplastic Agents - chemistry
/ Antineoplastic Agents - pharmacology
/ Cancer
/ Candida albicans - drug effects
/ Cell Proliferation - drug effects
/ Cell Survival - drug effects
/ Cryptococcus neoformans - drug effects
/ Drug Screening Assays, Antitumor
/ Fungi
/ Humans
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