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TBK1/IKKε-IN-1(compound 1)TBK1 IKK IN 1 (compound 1) is a dual inhibitor of TANK binding kinase 1 (TBK1) and IB kinase (IKK IKK i) with IC50 of 1. 0 nM and 5. 6 nM for TBK1 and IKK, respectively. TBK1 IKK inhibition enhances response to PD 1 blockade, which effectively predicts tumor response in vivo. Product information CAS Number: 1893397 65 3 Molecular Weight: 513. 59 Formula: C28H31N7O3 Chemical Name: 5 (4 ((4 (4 (oxetan 3 yl)piperazin 1 yl)phenyl)amino) 1,3,5 triazin 2
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TBK1/IKKε-IN-1 (compound 1) is a dual inhibitor of TANK-binding kinase 1 (TBK1) and IκB kinase-ε (IKKε/IKK-i) with IC50 of 1.0 nM and 5.6 nM for TBK1 and IKKε, respectively. TBK1/IKKε inhibition enhances response to PD-1 blockade, which effectively predicts tumor response in vivo.

Product information

CAS Number: 1893397-65-3

Molecular Weight: 513.59

Formula: C28H31N7O3

Chemical Name: 5-(4-((4-(4-(oxetan-3-yl)piperazin-1-yl)phenyl)amino)-1,3,5-triazin-2-yl)-2-((tetrahydro-2H-pyran-4-yl)oxy)benzonitrile

Smiles: N#CC1=CC(=CC=C1OC1CCOCC1)C1=NC(NC2C=CC(=CC=2)N2CCN(CC2)C2COC2)=NC=N1

InChiKey: QYQFLAQHGHBIFA-UHFFFAOYSA-N

InChi: InChI=1S/C28H31N7O3/c29-16-21-15-20(1-6-26(21)38-25-7-13-36-14-8-25)27-30-19-31-28(33-27)32-22-2-4-23(5-3-22)34-9-11-35(12-10-34)24-17-37-18-24/h1-6,15,19,24-25H,7-14,17-18H2,(H,30,31,32,33)

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Solubility: DMSO 10 mg/mL (19.47 mM) Water ˂1 mg/mL (NaN mM) Ethanol ˂1 mg/mL (NaN mM)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥12 months if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

How to use

In Vitro:

TBK1/IKKε-IN-1(compound 1) effectively blocks immune suppressive cytokine elaboration by CT26 cell line spheroids, without cytotoxic effects, and enhances secretion of IL-2 and IFN-γ from purified CD4+ and CD8+ T cells from healthy human donors and IL-2 from Jurkat human T-cell leukemia cells. Ex vivo addition of TBK1/IKKε-IN-1(compound 1) to PD-1 blockade enhances killing of CT26 MDOTS, associated with decreased levels of CCL4, CCL3, and IL-1β and induction of cytokines involved in activated innate immune responses.

In Vivo:

Balb/c mice bearing CT26 tumors are treated with TBK1/IKKε-IN-1(compound 1) ± anti-PD-L1. Consistent with MDOTS profiling data, greater tumor control and longer survival is evident with TBK1/IKKε-IN-1(compound 1) + anti-PD-L1 than with either TBK1/IKKε-IN-1(compound 1) or anti-PD-L1 alone. Reimplantation of CT26 into mice with exceptional responses to combination therapy shows no growth, whereas EMT-6 implanted tumors grow normally, suggesting induction of immunologic memory of CT26 cells in mice treated with TBK1/IKKε-IN-1(compound 1) + anti-PD-L1. Therefore, MDOTS profiling effectively recapitulates the in vivo response to PD-1 blockade +/− TBK1/IKKε inhibition, highlighting the potential of ex vivo screening in MDOTS to develop combination immunotherapies.

References:

  1. Russell WJ, et al. Cancer Discov. 2018 Feb;8(2):196-215.

Products are for research use only. Not for human use.

TBK1/IKKε-IN-1(compound 1)

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