Pyronaridine

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Pyronaridine
A chemical diagram of a Pyronaridine molecule
Clinical data
Other namesPyronaridine tetraphosphate
Routes of
administration
Oral, intramuscular injection, intravenous therapy
ATC code
  • none
Legal status
Legal status
  • CLP (EU): Acute Tox. 3(H301), Eye Dam. 1 (H318), Repr. 2 (H361), Aquatic Chronic 4 (H413)[clarification needed]
Identifiers
  • 4-[(7-Chloro-2-methoxy-pyrido[3,2-b]quinolin-10-yl)amino]-2,6-bis(pyrrolidin-1-ylmethyl)phenol
JSmol)
  • Clc1ccc6c(c1)nc2ccc(OC)nc2c6Nc5cc(CN3CCCC3)c(O)c(CN4CCCC4)c5
  • InChI=1S/C29H32ClN5O2/c1-37-26-9-8-24-28(33-26)27(23-7-6-21(30)16-25(23)32-24)31-22-14-19(17-34-10-2-3-11-34)29(36)20(15-22)18-35-12-4-5-13-35/h6-9,14-16,36H,2-5,10-13,17-18H2,1H3,(H,31,32) checkY
  • Key:DJUFPMUQJKWIJB-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Pyronaridine is an

antimalarial drug.[1] It was first made in 1970 and has been in clinical use in China since the 1980s.[2]

In a small (n=88) malaria study in Camaroon, pyronaridine had a 100% cure rate, compared with 60% for chloroquine.[3]

It is one of the components of the

pyronaridine/artesunate (Pyramax).[4]

It has also been studied as a potential anticancer drug,[5] and treatment for Ebola. The combination of pyronaridine and artesunate has been evaluated to have a synergistic effect of stronger antiviral effect and less toxicity.[6] The combination of pyronaridine and artesunate is being studied as a possible treatment for moderate to severe SARS-COV-2.[7]

References