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GNE-781GNE 781 (compound 19) is an orally active, highly potent and selective bromodomain inhibitor of cyclic adenosine monophosphate response element binding protein (CBP) with IC50 of 0. 94 nM in TR FRET assay. GNE 781 also inhibits BRET and BRD4(1) with IC50 of 6. 2 nM and 5100 nM, respectively. GNE 781 exhibits antitumor activity. Product information CAS Number: 1936422 33 1 Molecular Weight: 525. 59 Formula: C27H33F2N7O2 Chemical Name: 3 [7
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GNE-781 (compound 19) is an orally active, highly potent and selective bromodomain inhibitor of cyclic adenosine monophosphate response element binding protein (CBP) with IC50 of 0.94 nM in TR-FRET assay. GNE-781 also inhibits BRET and BRD4(1) with IC50 of 6.2 nM and 5100 nM, respectively. GNE-781 exhibits antitumor activity.

Product information

CAS Number: 1936422-33-1

Molecular Weight: 525.59

Formula: C27H33F2N7O2

Chemical Name: 3-[7-(difluoromethyl)-6-(1-methylpyrazol-4-yl)-3,4-dihydro-2H-quinolin-1-yl]-N-methyl-1-tetrahydropyran-4-yl-6,7-dihydro-4H-pyrazolo[4,3-c]pyridine-5-carboxamide

Smiles: CN1C=C(C=N1)C1=CC2CCCN(C3=NN(C4CCOCC4)C4CCN(CC=43)C(=O)NC)C=2C=C1C(F)F

InChiKey: CQCWHSDMJBAGDC-UHFFFAOYSA-N

InChi: InChI=1S/C27H33F2N7O2/c1-30-27(37)34-9-5-23-22(16-34)26(32-36(23)19-6-10-38-11-7-19)35-8-3-4-17-12-20(18-14-31-33(2)15-18)21(25(28)29)13-24(17)35/h12-15,19,25H,3-11,16H2,1-2H3,(H,30,37)

Technical Data

Appearance: Solid Power

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

Solubility: DMSO 100 mg/mL (190.26 mM) Ethanol 100 mg/mL (190.26 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:

In vitro studies show that GNE-781 reduces FOXP3 (forkhead box P3) transcript levels with a less optimal chemical probe, suggesting that inhibition of the CBP bromodomain may provide a novel small molecule therapeutic approach for cancer immunotherapy. GNE-781 decreases the generation of iTregs in vitro without affecting cell viability.

In Vivo:

GNE-781, a highly potent and selective CBP inhibitor that is efficacious in a MOLM-16 AML xenograft model. In vivo, GNE-781 modulates MYC expression that corresponds with antitumor activity in an AML tumor model.

References:

  1. F Anthony Romero, et al. J Med Chem. 2017 Nov 22;60(22):916

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

GNE-781

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