FB2024_03 , released June 25, 2024
Chemical: chloroquine
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General Information
Name
chloroquine
FlyBase ID
FBch0000075
ChEBI Name
chloroquine
ChEBI ID
PubChem Name
Chloroquine
PubChem ID
2719 (PubChem link: Chloroquine)
Chemical Structure
Chemical structure of chloroquine
chloroquine
InChIKey

WHTVZRBIWZFKQO-UHFFFAOYSA-N

Definition (ChEBI)

ChEBI: Chloroquine is an aminoquinoline that is quinoline which is substituted at position 4 by a [5-(diethylamino)pentan-2-yl]amino group at at position 7 by chlorine. It is used for the treatment of malaria, hepatic amoebiasis, lupus erythematosus, light-sensitive skin eruptions, and rheumatoid arthritis. It has a role as an antimalarial, an antirheumatic drug, a dermatologic drug, an autophagy inhibitor and an anticoronaviral agent. It is an aminoquinoline, a secondary amino compound, a tertiary amino compound and an organochlorine compound. It is a conjugate base of a chloroquine(2+).NCI Thesaurus (NCIt): Chloroquine is a 4-aminoquinoline with antimalarial, anti-inflammatory, and potential chemosensitization and radiosensitization activities. Although the mechanism is not well understood, chloroquine is shown to inhibit the parasitic enzyme heme polymerase that converts the toxic heme into non-toxic hemazoin, thereby resulting in the accumulation of toxic heme within the parasite. This agent may also interfere with the biosynthesis of nucleic acids. Chloroquine's potential chemosensitizing and radiosensitizing activities in cancer may be related to its inhibition of autophagy, a cellular mechanism involving lysosomal degradation that minimizes the production of reactive oxygen species (ROS) related to tumor reoxygenation and tumor exposure to chemotherapeutic agents and radiation.

Roles Classification (ChEBI)
Comment
Synonyms and Secondary IDs (29)
References (34)