Structured Summary
Abstract
A fat-soluble riminophenazine dye used for the treatment of leprosy. It has been used investigationally in combination with other antimycobacterial drugs to treat Mycobacterium avium infections in AIDS patients. Clofazimine also has a marked anti-inflammatory effect and is given to control the leprosy reaction, erythema nodosum leprosum. (From AMA Drug Evaluations Annual, 1993, p1619)
Chemical Identity
Chemical Information
- Molecular Formula
- C27H22Cl2N4
- Molecular Weight
- 473.4 g/mol
- CAS Registry No.
- 2030-63-9
- IUPAC Name
- N,5-bis(4-chlorophenyl)-3-propan-2-yliminophenazin-2-amine
- InChIKey
- WDQPAMHFFCXSNU-UHFFFAOYSA-N
- SMILES
- CC(C)N=C1C=C2C(=NC3=CC=CC=C3N2C4=CC=C(C=C4)Cl)C=C1NC5=CC=C(C=C5)Cl
- MeSH Unique ID
- D002991
- Source
- PubChem CID 2794
MeSH Record
Classification
Broader headings
Related Concepts
Knowledge Graph
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Drug Class
Pharmacological Action
MeSH Record
Synonyms
8 entry terms
- N,5-Bis(4-chlorophenyl)-3,5-dihydro-3-((1-methylethyl)imino)-2-phenazinamine
- B-663
- G-30,320
- Lamprene
- B 663
- B663
- G 30,320
- G30,320
MeSH Record
Aspects Covered
25 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analogs & derivatives, analysis, antagonists & inhibitors, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, economics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, urine.
MeSH Record
History Note
74
MeSH Hierarchy
Tree Number
AMA Style
References
- National Library of Medicine. Clofazimine. Medical Subject Headings (MeSH). 2026. Unique ID D002991. http://id.nlm.nih.gov/mesh/2026/D002991
- Clofazimine. In: Wikipedia. https://en.wikipedia.org/wiki/Clofazimine
- Clofazimine. In: Wikidata. https://www.wikidata.org/wiki/Q418611
- Clofazimine. In: PubChem Compound. CID 2794. https://pubchem.ncbi.nlm.nih.gov/compound/2794