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Merck

C8895

Clofazimine

≥98% (TLC), powder, antimycobacterial rimonphenazine

Sinônimo(s):

N,5-Bis(4-chlorophenyl)-3,5-dihydro-3-(isopropylimino)phenazin-2-amine

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Sobre este item

Fórmula empírica (Notação de Hill):
C27H22Cl2N4
Número CAS:
Peso molecular:
473.40
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
217-980-2
MDL number:

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Nome do produto

Clofazimine,

form

powder

InChI key

WDQPAMHFFCXSNU-BGABXYSRSA-N

InChI

1S/C27H22Cl2N4/c1-17(2)30-24-16-27-25(15-23(24)31-20-11-7-18(28)8-12-20)32-22-5-3-4-6-26(22)33(27)21-13-9-19(29)10-14-21/h3-17,31H,1-2H3/b30-24+

SMILES string

CC(C)\N=C1/C=C2N(c3ccc(Cl)cc3)c4ccccc4N=C2C=C1Nc5ccc(Cl)cc5

antibiotic activity spectrum

mycobacteria

mode of action

protein synthesis | interferes

originator

Novartis

Quality Level

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Este Item
BP663Y0000358C6628
Clofazimine

Sigma-Aldrich

C8895

Clofazimine

Clofazimine British Pharmacopoeia (BP) Reference Standard

BP663

Clofazimine

Cloroquina powder or crystals, 98.5-101.0% (EP)

Sigma-Aldrich

C6628

Cloroquina

form

powder

form

solid

form

-

form

powder or crystals

Quality Level

200

Quality Level

-

Quality Level

-

Quality Level

200

originator

Novartis

originator

-

originator

-

originator

-

antibiotic activity spectrum

mycobacteria

antibiotic activity spectrum

-

antibiotic activity spectrum

-

antibiotic activity spectrum

parasites

mode of action

protein synthesis | interferes

mode of action

-

mode of action

-

mode of action

enzyme | inhibits

Application

Clofazimine has been used:
  • for antimicrobial preparation[1]
  • to study its accumulation on macrophages to form crystal-like drug inclusions (CLDIs)[2][3][4]
  • to model drug-induced hepatic granulomatous inflammation[5]
  • to study the in vivo cargo storage capacity of macrophages[6]

Features and Benefits

This compound was developed by Novartis. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

General description

Clofazimine is a riminophenazine, which is used as an antileprosy drug. It is used to treat multidrug-resistant tuberculosis.[7] Clofazimine prevents neutrophil motility and lymphocyte transformation. It has anti-inflammatory effect, which is used to treat discoid lupus erythematosus.[8] Clofazimine has immunosuppressive property.[9]

Preparation Note

This product is stored at room temperature.

Classe de armazenamento

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

A far-red fluorescent probe for flow cytometry and image-based functional studies of xenobiotic sequestering macrophages
Keswani RK, et al.
Cytometry. Part A : the Journal of the International Society For Analytical Cytology, 87(9), 855-867 (2015)
An Expandable Mechanopharmaceutical Device (1): Measuring the Cargo Capacity of Macrophages in a Living Organism
Rzeczycki P, et al.
Pharmaceutical Research, 36(1), 12-12 (2019)
In vitro approaches for generation of Mycobacterium tuberculosis mutants resistant to bedaquiline, clofazimine or linezolid and identification of associated genetic variants
Ismail N, et al.
Journal of Microbiological Methods, 153(8), 1-9 (2018)
Plumb's Veterinary Drug Handbook (2008)
An Expandable Mechanopharmaceutical Device (2): Drug Induced Granulomas Maximize the Cargo Sequestering Capacity of Macrophages in the Liver
Rzeczycki P, et al.
Pharmaceutical Research, 36(1), 3-3 (2019)

Questions

  1. At what temperature should this be stored? I so not see a specified temperature on label or SDS so I would assume room temperature but other manufacturers of this product claim -20C

    1 answer
    1. This product is stored at room temperature.

      Helpful?

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