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IACS-13909

SKU: orb1298292

Description

IACS-13909

Research Area

Metabolism Research

Images & Validation

Key Properties

CAS Number2160546-07-4
MW377.27
Purity98.83%
FormulaC17H18Cl2N6
SMILESCC1(N)CCN(CC1)c1cnc2c(n[nH]c2n1)-c1cccc(Cl)c1Cl
TargetPhosphatase
SolubilityDMSO:9 mg/mL (23.86 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:1 mg/mL (2.65 mM)

Bioactivity

Target IC50
SHP2:15.7 nM
In Vivo
In EGFR-mutant osimertinib-resistant NSCLC models with EGFR-dependent and EGFR-independent resistance mechanisms, IACS-13909, administered as a single agent or in combination with osimertinib, potently suppressed tumor cell proliferation in vitro and caused tumor regression in vivo.
In Vitro
IACS-13909 potently impeded proliferation of tumors harboring a broad spectrum of activated RTKs as the oncogenic driver.

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

RTK, pERK, SHP-2, SHP2, Phosphatase, BBP 398, BBP398, BBP-398, BBP-398, antiproliferative, anticancer, IACS13909, IACS-13909, IACS 13909, MAPK, Inhibitor, inhibit, pMEK

Similar Products

  • IACS-13909 [orb1218441]

    >98% (HPLC)

    2160546-07-4

    377.3

    C17H18Cl2N6

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

No computed properties available.

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IACS-13909 (orb1298292)

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Step 1: Enter information below

(Recommended: An additional animal making an allowance for loss during the experiment)

Step 2: Enter the in vivo formulation

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

1 mg
$ 140.00
5 mg
$ 280.00
1 ml x 10 mM (in DMSO)
$ 310.00
10 mg
$ 420.00
25 mg
$ 580.00
50 mg
$ 810.00
100 mg
$ 1,030.00
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