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Home > Epigenetics Resch Products > BET Family Protein Inhibitors > AZD5153 (AZD-5153)

AZD5153 (AZD-5153)

AZD5153 is a potent, selective, and orally available BET/BRD4 bromodomain inhibitor with a bivalent binding mode. Unlike many previously reported monovalent inhibitors, AZD5153 ligates two bromodomains in BRD4 simultaneously. The enhanced avidity afforded through bivalent binding translates into increased cellular and antitumor activity in preclinical hematologic tumor models. In vivo administration of AZD5153 led to tumor stasis or regression in multiple xenograft models of acute myeloid leukemia, multiple myeloma, and diffuse large B-cell lymphoma. The relationship between AZD5153 exposure and efficacy suggests that prolonged BRD4 target coverage is a primary efficacy driver (ref. 1). AZD5153 treatment markedly affects transcriptional programs of MYC, E2F, and mTOR. Transcriptional modulation of MYC and HEXIM1 was confirmed in AZD5153-treated human whole blood (ref. 1).

Catalog NO:	CT-A5153
Synonym:	AZD-5153
CAS NO:	1869912-40-2
Mol. Formula:	C25H33N7O3 ∙C11H8O3
MW:	667.8 (or refer to Certificate of Analysis)

** ONLY Optically Pure Source (>99.5% ee). in vivo Quality material. A 6-Hydroxy-2-Naphthoic Acid Salt (1:1) (Clinical Formulation), validated by a spot-on Elemental Analysis, Bulk Stock!! Same day shipping

Pricing and OrderingTechnical Data

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NO	Size	Price	In Stock	Quantity
1	5mg	$125.00	YES
2	10 mg	$175.00	YES
3	50 mg	$485.00	YES

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Solubility : Refer to Certificate

Storage : Refer to Certificate

Purity : >99% chemical and optical purity by achiral HPLC and chiral HPLCs

Original QC Data : Achiral and Chiral HPLCs, 1H-NMR, Quantitative Elemental Analysis Report

Please Pick Batch NO:

AZD5153, Lot 01, Certificate of Analysis.pdf
AZD5153, Lot 01, Appearance (color).pdf
C_K, AZD5153, Lot 01, Achiral HPLC.pdf
C_K, AZD5153, Lot 01, Chiral HPLC.pdf
C_K, AZD5153, Lot 01, HNMR.pdf

1. G. W. Rhyasen, et al, AZD5153: A Novel Bivalent BET Bromodomain Inhibitor Highly Active against Hematologic Malignancies, Mol Cancer Ther; 15(11); 2563–74.

2. Robert H. Bradbury, et al, J. Med. Chem., 2016, 59 (17), pp 7801–7817

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