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SBI-477

SKU: orb1309120

Description

SBI-477 is a chemical probe that stimulates insulin signaling by inhibiting the transcription factor MondoA. This action coordinately reduces triglyceride synthesis and increases basal glucose uptake in human skeletal myocytes, making it a useful tool for studying metabolism and insulin resistance in vitro.

Research Area

Metabolism Research, Pharmacology & Drug Discovery, Signal Transduction

Images & Validation

Key Properties

CAS Number781628-99-7
MW483.54
Purity99.30% (May vary between batches)
FormulaC24H25N3O6S
SMILESCOc1ccc(cc1)-c1csc(NC(=O)c2ccc(OCC(=O)N3CCOCC3)c(OC)c2)n1
TargetOthers,Arrestin,Liver X Receptor,IGF-1R
SolubilityDMSO:45 mg/mL (93.06 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (4.14 mM)

Bioactivity

In Vivo
SBI-477, that coordinately inhibited triacylglyceride (TAG) synthesis and enhanced basal glucose uptake in human skeletal myocytes. SBI-477 stimulated insulin signaling by deactivating the transcription factor MondoA, leading to reduced expression of the insulin pathway suppressors thioredoxin-interacting protein (TXNIP) and arrestin domain-containing 4 (ARRDC4). Depleting MondoA in myocytes reproduced the effects of SBI-477 on glucose uptake and myocyte lipid accumulation.

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

MondoA, inhibit, Inhibitor, SBI 477, SBI477, SBI-477

Similar Products

  • SBI-477 [orb1219298]

    >98% (HPLC)

    781628-99-7

    483.5

    C24H25N3O6S

    5 mg, 10 mg, 1 g, 50 mg, 100 mg, 500 mg, 25 mg
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Key Properties

No computed properties available.

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Protocol Information

SBI-477 (orb1309120)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

1 mg
$ 200.00
5 mg
$ 440.00
1 ml x 10 mM (in DMSO)
$ 500.00
10 mg
$ 630.00
25 mg
$ 990.00
50 mg
$ 1,320.00
100 mg
$ 1,770.00
500 mg
$ 3,500.00
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