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BI605906BI605906 is a novel IKK inhibitor with an IC50 value of 380 nM when assayed at 0. 1 mM ATP. Product information CAS Number: 960293 88 3 Molecular Weight: 432. 51 Formula: C17H22F2N4O3S2 Chemical Name: 3 amino 4 (1,1 difluoropropyl) 6 (4 methanesulfonylpiperidin 1 yl)thieno[2,3 b]pyridine 2 carboxamide Smiles: CCC(F)(F)C1C=C(N=C2SC(=C(N)C2=1)C(N)=O)N1CCC(CC1)S(C)(=O)=O InChiKey: IYHHRZBKXXKDDY UHFFFAOYSA N InChi: InChI=1S C17H22F2N4O3S2 c1 3
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BI605906 is a novel IKKβ inhibitor with an IC50 value of 380 nM when assayed at 0.1 mM ATP.

Product information

CAS Number: 960293-88-3

Molecular Weight: 432.51

Formula: C17H22F2N4O3S2

Chemical Name: 3-amino-4-(1,1-difluoropropyl)-6-(4-methanesulfonylpiperidin-1-yl)thieno[2,3-b]pyridine-2-carboxamide

Smiles: CCC(F)(F)C1C=C(N=C2SC(=C(N)C2=1)C(N)=O)N1CCC(CC1)S(C)(=O)=O

InChiKey: IYHHRZBKXXKDDY-UHFFFAOYSA-N

InChi: InChI=1S/C17H22F2N4O3S2/c1-3-17(18,19)10-8-11(23-6-4-9(5-7-23)28(2,25)26)22-16-12(10)13(20)14(27-16)15(21)24/h8-9H,3-7,20H2,1-2H3,(H2,21,24)

Technical Data

Appearance: Solid Power

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

Solubility: DMSO : ≥ 100 mg/mL (231.21 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:

BI605906 is an inhibitor of IKKβ with improved selectivity. BI605906 inhibits IKKβ in vitro with an IC50 value of 380 nM when assayed at 0.1 mM ATP. The only other protein kinase that is inhibited of over 100 tested, which include IKKα, IKKε and TBK1, is the insulin-like growth factor 1 (IGF1) receptor (IC50=7.6 μM). BI605906 partially inhibits the IL-1-stimulated activation of IKKε/TBK1. In primary mouse hepatocytes, Metformin treatment for 3 hours suppresses TNFα-induced degradation of the NF-κB negative regulator IκB, while modulating AMPK and MTOR signaling in a dose-dependent manner. The magnitude of the effect on IκB is comparable with BI605906. Unlike Metformin, BI605906 (10 μM ) does not suppress signaling downstream of mTOR nor does it activate AMPK. TNF-α-dependent expression of CINC-1/CXCL1, CXCL2, IL-1β, and IL-6 is strongly inhibited by both Metformin and BI605906 (10 μM).

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

BI605906

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