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DIDS sodium salt

Cat. No. M9745
DIDS sodium salt Structure
Synonym:

MDL101114ZA

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50mg USD 79  USD79 In stock
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Biological Activity

DIDS sodium salt (MDL101114ZA) is a dual ABCA1 and VDAC1 inhibitor. DIDS sodium salt is also an anion transport inhibitor, which inhibits the ClC-Ka chloride channel and the bacterial ClC-ec1Cl-/H+ exchanger with IC50s of 100 μM and ~300 μM, respectively. DIDS reduced the amplitude of spontaneous transient inward currents (STICs) in a concentration-dependent manner with IC50 value of 2.1 x 10-4 M for STICs. Moreover, DIDS was investigated for its action on contraction of cerebral artery smooth muscle cells. DIDS showed a vasodilator effect on pressure-constricted arteries with IC50 of 69 ± 14 μM.

Chemical Information
Molecular Weight 498.48
Formula C16H8N2Na2O6S4
CAS Number 67483-13-0
Form Solid
Solubility (25°C) DMSO ≥ 25 mg/mL
Storage -20°C, dry, sealed
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Haibo Chen, et al. Apoptosis. Inhibition of VDAC1 prevents Ca²⁺-mediated oxidative stress and apoptosis induced by 5-aminolevulinic acid mediated sonodynamic therapy in THP-1 macrophages

[2] C-Y Tsou, et al. Acta Physiol (Oxf). Activation of soluble guanylyl cyclase prevents foam cell formation and atherosclerosis

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Keywords: DIDS sodium salt, MDL101114ZA supplier, VDAC, inhibitors, activators


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