Fig. 1 · Structure

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SC75741

NF-κB inhibitor

SC75741 is a potent NF-kB inhibitor with EC50 of 200 nM.

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Publications for SC75741

3 publications citing this product

  1. Yunshang Yang, .et al. , Biomed Pharmacother, 2023, Feb;158:114113 PMID: 36516692
  2. Yajun Li, .et al. , Cell Prolif, 2022, Oct;55(10) PMID: 35708050
  3. Crystal A Mendoza, .et al. , Antiviral Res, 2021, Jan;185:104993 PMID: 33296695

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Biological Activity

Target & Activity

Target Activity Value
NF-κB EC50 200 nM

Cellular Effect

Cell Line Activity Value Description Reference
A549 EC50 0.2 μM Inhibition of NF-kappaB in A549 cells after 5 hrs by reporter gene assay [PMID: 17869512]
THP1-Dual IC50 3958 nM Inhibition of LPS induced ISG activation in human THP1-Dual cells pretreated with LPS-B5 for 3 hrs followed by compound addition incubated for 24 hrs [PMID: 36053746]
THP1-Dual IC50 5975 nM Inhibition of LPS induced NF kappa B activation in human THP1-Dual cells stimulated with LPS-B5 for 3 hrs followed by compound addition incubated for 24 hrs [PMID: 36053746]

In Vitro Studies

In RANKL-stimulated RAW264.7 cells, SC75741 (200 nM) reduced CTSK and NFATc1 protein expression. Urolithin B (25 μM) produced a greater reduction than SC75741 alone, and their combination further reduced both markers relative to either single agent. These findings concern protein expression in a cellular comparator experiment. [1]

Literature-reported observations and conditions; not Adooq-tested protocols or general treatment recommendations.

SC75741 comparator in RANKL-stimulated RAW264.7 cells

Cell-based study · Murine RAW264.7 cells stimulated with RANKL (50 ng/mL) [1]

Western blot comparison of RANKL alone, urolithin B (UB), SC75741, and UB plus SC75741. SC75741 lowered CTSK and NFATc1 expression; UB produced a greater reduction, and the combination produced a further reduction relative to either single agent. These are protein-expression endpoints, without a demonstrated direct binding mechanism or standalone bone-resorption outcome.

Measured endpoints — not treatment concentrations
EndpointReported resultReference
CTSK and NFATc1 protein expression normalized to β-actinRelative protein expression Qualitative: lower with SC75741 than RANKL alone; lower with UB than SC75741; further reduced with UB + SC75741. No exact bar values extracted.[1]

Literature-Reported Treatment Conditions

Treatment concentration
SC75741 200 nM; UB 25 μM in the UB and combination groups; RANKL 50 ng/mL in all four groups (Figure 6E,F).
Method
Addition to RANKL-stimulated cell cultures followed by Western blot analysis.
Co-treatment
Separate RANKL-only, UB-only, SC75741-only, and UB + SC75741 groups; the combination result is not attributed to SC75741 alone.
Reported limits
Figure 6-specific treatment duration, vehicle and replicate number are not specified in the read main text/caption. The 200 nM value is a treatment concentration, not an IC50. Caption comparator symbols do not fully define the SC-only comparisons; no p-value is assigned here.
Methods and source locations

Compound reported in the paper: SC75741; Compound label in the paper: SC in Figure 6

Evidence for the named research compound in this cellular comparison; no inference of current lot validation or in vivo efficacy.

Section 2.6; Section 3.4, final paragraph; Figure 6B,E,F (image and caption)

CTSK and NFATc1 protein expression normalized to β-actin: Western blot with β-actin loading control; Figure 6B and densitometry in 6E,F. — Section 2.6; Section 3.4, final paragraph; Figure 6B,E,F (image and caption)

Specifications

Manufacturer Adooq Bioscience
Actions Inhibitor
CAS Number 913822-46-5
Applications NF-κB inhibitor
Formula C29H23N7O2S2
Molecular Weight 565.67
SMILES
C1CN(CCC1C2=NC(=CS2)C(=O)NC3=NC4=C(N3)C=C(C=C4)C(=O)C5=CC=CC=C5)C6=NC=NC7=C6SC=C7

Storage & Solubility

In Vitro Solubility

Reported Solubility

SolventReported Solubility
DMSO Warmed: 35 mg/mL (61.87 mM)
Water Insoluble
Ethanol Insoluble

Preparing Stock Solutions

Stock preparation is unavailable for this product molecular weight.

Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.

Storage

Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

Research References

  1. [1] Yajun Li, Qi Zhuang, Lihong Tao, et al. Urolithin B suppressed osteoclast activation and reduced bone loss of osteoporosis via inhibiting ERK/NF‐κB pathway Cell Proliferation (2022). PMID: 35708050 DOI: 10.1111/cpr.13291 Source material

Publications

3 publications citing this product

  1. Yunshang Yang, .et al. , Biomed Pharmacother, 2023, Feb;158:114113 PMID: 36516692
  2. Yajun Li, .et al. , Cell Prolif, 2022, Oct;55(10) PMID: 35708050
  3. Crystal A Mendoza, .et al. , Antiviral Res, 2021, Jan;185:104993 PMID: 33296695

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