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Senexin ASenexin A is a CDK8 inhibitor with an IC50 of 280 nM. Product information CAS Number: 1366002 50 7 Molecular Weight: 274. 32 Formula: C17H14N4 Chemical Name: 4 [(2 phenylethyl)amino]quinazoline 6 carbonitrile Smiles: N#CC1=CC2C(NCCC3C=CC=CC=3)=NC=NC=2C=C1 InChiKey: XBJCNHGQFJFCOY UHFFFAOYSA N InChi: InChI=1S C17H14N4 c18 11 14 6 7 16 15(10 14)17(21 12 20 16)19 9 8 13 4 2 1 3 5 13 h1 7,10,12H,8 9H2,(H,19,20,21) Technical Data Appearance: Solid Power
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Senexin A is a CDK8 inhibitor with an IC50 of 280 nM.

Product information

CAS Number: 1366002-50-7

Molecular Weight: 274.32

Formula: C17H14N4

Chemical Name: 4-[(2-phenylethyl)amino]quinazoline-6-carbonitrile

Smiles: N#CC1=CC2C(NCCC3C=CC=CC=3)=NC=NC=2C=C1

InChiKey: XBJCNHGQFJFCOY-UHFFFAOYSA-N

InChi: InChI=1S/C17H14N4/c18-11-14-6-7-16-15(10-14)17(21-12-20-16)19-9-8-13-4-2-1-3-5-13/h1-7,10,12H,8-9H2,(H,19,20,21)

Technical Data

Appearance: Solid Power

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

Solubility: DMSO : ≥ 100 mg/mL (364.54 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:

Senexin A inhibits CDK8 and CDK19 ATP site binding with Kd50 of 0.83 μM and 0.31 μM, respectively and CDK8 kinase activity with IC50 of 0.28 μM. Senexin A inhibits β-catenin–dependent transcription in HCT116 colon carcinoma cells. The induction of transcription factor EGR1 upon serum starvation, followed by readdition of serum, is strongly inhibited by Senexin A in HT1080 cells. Senexin A inhibits only p21-induced transcription but not other biological effects of p21. Senexin A also decreases the expression of many secreted tumor-promoting factors in doxorubicin-treated wild-type HCT116 cells.

In Vivo:

Five daily treatment of Senexin A fully reverses tumor-promoting effect of chemotherapy. Senexin A shows no detectable toxicity and no significant effects on body weight, organ weights, or blood cell counts in C57BL/6 mice during the treatment. This effect of doxorubicin treatment is completely abolished, however, when doxorubicin injection is followed by administration of Senexin A. Senexin A treatment strongly improves the response of A549/MEF tumors to doxorubicin.

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

Senexin A

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