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MnTBAP chloride 55266-18-7

MnTBAP chloride 55266-18-7

CAS No.: 55266-18-7

MnTBAP chloride is a superoxide dismutase (SOD) mimetic and peroxynitrite scavenger. MnTBAP chloride is a manganese porp
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This product is for research use only, not for human use. We do not sell to patients.

MnTBAP chloride is a superoxide dismutase (SOD) mimetic and peroxynitrite scavenger. MnTBAP chloride is a manganese porphyrin complex with antioxidant properties. MnTBAP chloride mediates anti~inflammatory effects by upregulating BMPR-II and inhibiting NFκB signaling. MnTBAP chloride has antioxidant properties and may be used to be used to study the fibrotic response in chronic kidney diseases (CKDs).

Physicochemical Properties


Exact Mass 878.098
CAS # 55266-18-7
Appearance Brown to black solid powder
LogP 3.42
HS Tariff Code 2934.99.9001
Storage

Powder-20°C 3 years

4°C 2 years

In solvent -80°C 6 months

-20°C 1 month

Note: Please store this product in a sealed and protected environment, avoid exposure to moisture.
Shipping Condition Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)

Biological Activity


ln Vitro In immortalized mouse proximal tubule cells (mPTC), MnTBAP chloride (pretreatment with 1.14 μM before 10 ng/mL TGF-β1) diminished α-α expression and partially but significantly reversed E-cadherin decrease. -Induction of vimentin and SMA [1]. MnTBAP chloride (50 μM; 6 h) did not alter BMPR-II protein expression in HUVECs throughout a 16-hour time course, although it did raise BMPR-II mRNA 1.3-fold at 2 h. Smad 1/5 is phosphorylated more when MnTBAP chloride is present, suggesting that the BMP signaling pathway is regulated [2].
ln Vivo In 5/6 Nx mice, MnTBAP chloride (10 mg/kg; i.p.; three times weekly for 12 weeks) decreases renal fibrosis [1].
Animal Protocol Animal/Disease Models: C57BL/6J mice with 5/6 nephrectomy (Nx)[1]
Doses: 10 mg/kg
Route of Administration: IP; three times per week for twelve weeks
Experimental Results: Attenuated renal fibrosis in 5/6 Nx mice and decreased protein expressions of fibronectin, collagen III in remnant kidneys.
References

[1]. MnTBAP Therapy Attenuates Renal Fibrosis in Mice With 5/6 Nephrectomy. Oxid Med Cell Longev. 2016;2016:7496930.

[2]. MnTBAP Increases BMPR-II Expression in Endothelial Cells and Attenuates Vascular Inflammation. Vascul Pharmacol. 2016 Sep;84:67-73.


Solubility Data


Solubility (In Vitro) DMSO : ~100 mg/mL (~113.75 mM)
0.5 M NaOH : 20 mg/mL (~22.75 mM)
1M NaOH : 10 mg/mL (~11.37 mM)
Solubility (In Vivo) Solubility in Formulation 1: ≥ 4.17 mg/mL (4.74 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 41.7 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL.
Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution.

Solubility in Formulation 2: ≥ 4.17 mg/mL (4.74 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 41.7 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.

 (Please use freshly prepared in vivo formulations for optimal results.)