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lumefantrine

group of enantiomers
Class type of: organochlorine compound, alkanolamine, fluorenes Q904464

Facts

12 properties
Instance of
group of stereoisomers
Subclass of
organochlorine compound, alkanolamine, fluorenes, secondary alcohol, tertiary amine[4][5][6][7][8]
Has use
medication[9]
Canonical SMILES
CCCCN(CCCC)CC(C1=C2C3=C(C=C(C=C3)Cl)C(=CC4=CC=C(C=C4)Cl)C2=CC(=C1)Cl)O[2]
Chemical formula
C₃₀H₃₂Cl₃NO[3]
Has active ingredient
Lumefantrine
Has part(s)
carbon, chlorine, nitrogen, oxygen, hydrogen[10][11][12][13][14]
Has parts
carbon, chlorine, nitrogen, oxygen, hydrogen
Isomeric SMILES
CCCCN(CCCC)CC(C1=C2C3=C(C=C(C=C3)Cl)/C(=C/C4=CC=C(C=C4)Cl)/C2=CC(=C1)Cl)O
Mass
527.154948
Subject has role
protein synthesis inhibitor, DNA polymerase inhibitors, antimalarial, bactericide
World Health Organisation international non-proprietary name
lumefantrine
🏷️ Also known as
en lumefantrine en dl-benflumelol en DL-benflumelol en (+-)-2,7-dichloro-9-[(Z)-p-chlorobenzylidene]-alpha-[(dibutylamino)methyl]fluorene-4-methanol en (±)-2,7-dichloro-9-[(Z)-p-chlorobenzylidene]-α-[(dibutylamino)methyl]fluorene-4-methanol en 2-dibutylamino-1-{2,7-dichloro-9-[1-(4-chloro-phenyl)-meth-(Z)-ylidene]-9H-fluoren-4-yl}-ethanol en 2-dibutylamino-1-[2,7-dichloro-9-(4-chloro-benzylidene)-9H-fluoren-4-yl]-ethanol en benflumetol ar لوميفانترين cs lumefantrin es Lumefantrina fa لومفانترین fi Lumefantriini fr luméfantrine ja ルメファントリン ko 루메판트린 pl benflumetol pl lumefantryna ro Lumefantrină uk Люмефантрин
🔖 Identifiers · 36
OpenAlex ID
C2780780316
CAB ID
33622
CAS Registry Number
82186-77-4
ChEBI ID
156095
ChEMBL ID
CHEMBL38827
ChemSpider ID
4941944
DSSTOX compound identifier
DTXCID1026663
DSSTox substance ID
DTXSID3046663
DeCS ID
57784
DrugBank ID
DB06708
DrugCentral ID
1617
EC number
617-303-4
Show all 36 identifiers +24
ECHA Substance Infocard ID
100.133.797
Freebase ID
/m/02wwdrc
Guide to Pharmacology Ligand ID
9969
HSDB ID
7210
Human Metabolome Database ID
HMDB0015653
InChI
InChI=1S/C30H32Cl3NO/c1-3-5-13-34(14-6-4-2)19-29(35)28-18-23(33)17-27-25(15-20-7-9-21(31)10-8-20)26-16-22(32)11-12-24(26)30(27)28/h7-12,15-18,29,35H,3-6,13-14,19H2,1-2H3/b25-15-
InChIKey
DYLGFOYVTXJFJP-MYYYXRDXSA-N
J-GLOBAL ID
201707014504368096
KEGG ID
D03821
MeSH descriptor ID
D000078102
MeSH tree code
D02.455.426.559.847.389.650, D04.615.389.650
Microsoft Academic ID (discontinued)
2780780316
NDF-RT ID
N0000178418
National Drug Code
67254-909, 66639-125
Nikkaji ID
J3.642.651I
Probes And Drugs ID
PD009278
PubChem CID
6437380
Reaxys registry number
8811003
RxNorm CUI
847728
SpectraBase compound ID
3RdOrlFmsGV
SureChEMBL ID
127331
UNII
F38R0JR742
UniChem compound ID
188620
World Health Organisation international non-proprietary name numeric ID
7610

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🔗 Connections
Has part(s) 5
hydrogen, oxygen, carbon, nitrogen, chlorine
Subject has role 4
bactericide, antimalarial, protein synthesis inhibitor, DNA polymerase inhibitors
Subclass of 3
alkanolamine, organochlorine compound, secondary alcohol
Belongs to 1
artemether/lumefantrine
Has use 1
medication
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Summary

lumefantrine is a group of stereoisomers[1].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . PubChem. Retrieved . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). lumefantrine. Retrieved November 9, 2026, from https://4ort.xyz/entity/lumefantrine
MLA “lumefantrine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 9 Nov. 2026, https://4ort.xyz/entity/lumefantrine.
BibTeX @misc{4ortxyz_lumefantrine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{lumefantrine}}, year = {2026}, url = {https://4ort.xyz/entity/lumefantrine}, note = {Accessed: 2026-11-09}}
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