1. Anti-infection Apoptosis Immunology/Inflammation NF-κB
  2. Parasite TNF Receptor Interleukin Related NF-κB Toll-like Receptor (TLR)
  3. BSF2

BSF2 is a anti-Leishmania agent. BSF2 modulates gene expression linked to ubiquitination, chromatin remodeling, and peroxisomal membrane transport pathways in Leishmania braziliensis. BSF2 downregulates TNF, IL-17, NF-κB, and Toll-like receptor pathways in Leishmania-infected macrophages. BSF2 exerts leishmanicidal activity against intracellular Leishmania braziliensis amastigotes. BSF2 can be used for the research of american tegumentary leishmaniasis.

For research use only. We do not sell to patients.

BSF2

BSF2 Chemical Structure

CAS No. : 179118-06-0

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Description

BSF2 is a anti-Leishmania agent. BSF2 modulates gene expression linked to ubiquitination, chromatin remodeling, and peroxisomal membrane transport pathways in Leishmania braziliensis. BSF2 downregulates TNF, IL-17, NF-κB, and Toll-like receptor pathways in Leishmania-infected macrophages. BSF2 exerts leishmanicidal activity against intracellular Leishmania braziliensis amastigotes. BSF2 can be used for the research of american tegumentary leishmaniasis[1].

IC50 & Target[1]

IL-17

 

Cellular Effect
Cell Line Type Value Description References
HEK293 IC50
74.04 μM
Compound: 27d
Cytotoxicity against HEK293 cells assessed as decrease in cell viability after 24 hrs by Alamar blue assay
Cytotoxicity against HEK293 cells assessed as decrease in cell viability after 24 hrs by Alamar blue assay
[PMID: 28038325]
In Vitro

BSF2 (1-80 μM; 48 h) exhibits a CC50 of 11.11 μM against RAW 264.7 mouse macrophages, with 81.52% macrophage viability remaining at a 10 μM treatment concentration[1].
BSF2 (1-80 μM; 48 h) potently inhibits intracellular Leishmania braziliensis in RAW 264.7 macrophages with an EC50 of 0.64 μM and a high selectivity index of 17.36, reducing parasite viability to 5.73% at a 10 μM treatment concentration[1].
BSF2 (0.16 μM; 48 h) alters parasite gene expression in ubiquitination, chromatin remodeling, and peroxisomal transport pathways, while downregulating host inflammatory pathways including TNF, IL-17, NF-κB, and Toll-like receptor signaling in Leishmania braziliensis-infected RAW 264.7 macrophages[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cytotoxicity Assay[1]

Cell Line: RAW 264.7 mouse macrophages
Concentration: 1-80 μM; 10 μM
Incubation Time: 48 h
Result: Resulted in 81.52% macrophage viability at 10 μM.
Determined a CC50 of 11.11 μM.
Molecular Weight

332.40

Formula

C20H20N4O

CAS No.
SMILES

CC1=C(OC(C2=CC=C(C=C2)C(N)=N)=C1C)C3=CC=C(C=C3)C(N)=N

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Room temperature in continental US; may vary elsewhere.

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Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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BSF2
Cat. No.:
HY-183008
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