(-)-JQ1

(-)-JQ1

Chemicals & Biochemicals

Article No

BPS-27335

Size

25 mg

Shipping Information

room temp (domestic), gel packs international

Article No

BPS-27335

Size

25 mg

Shipping Information

room temp (domestic), gel packs international

Specifications

CAS No 1268524-71-5
MW 457.0 kDa
Additional Information (-)-JQ1 is the inactive stereoisomer of the potent, cell-permeable, small molecule bromodomain inhibitor (+)-JQ1 that competitively binds to acetyl-lysine recognition motifs. (+)-JQ1 competitively binds to the bromodomain displacing the BRD4 fusion oncoprotein from chromatin, which induces squamous differentiation and specific anti-proliferative effect in BRD4-dependent cell lines and patient-derived xenograft models. However, study results have shown that (-)-JQ1 fails to significantly interact with any bromodomain tested and exhibits inhibition against BRD4(1) with and IC50 of 10,000 nM.
Article No BPS-27335
Country Availability SE, FI, DK, NO, IS, EE, LV, LT
Description (-)-JQ1
Supplier BPS Bioscience
Notes (-)-JQ1 is the inactive stereoisomer of the potent, cell-permeable, small molecule bromodomain inhibitor (+)-JQ1 that competitively binds to acetyl-lysine recognition motifs. (+)-JQ1 competitively binds to the bromodomain displacing the BRD4 fusion oncoprotein from chromatin, which induces squamous differentiation and specific anti-proliferative effect in BRD4-dependent cell lines and patient-derived xenograft models. However, study results have shown that (-)-JQ1 fails to significantly interact with any bromodomain tested and exhibits inhibition against BRD4(1) with and IC50 of 10,000 nM.
Molecular Formula C23H25ClN4O2S
Alias Names (R)-tert-butyl 2-(4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)acetate
Product Type Chemicals & Biochemicals
Shipping Information room temp (domestic), gel packs international
Size 25 mg
Solubility Soluble in DMSO or ethanol at 100 mM
Storage Store at or below -80°C. Stable for less than 6 months when stored as directed.
Technical Specifications (-)-JQ1 is the inactive stereoisomer of the potent, cell-permeable, small molecule_x000D_ bromodomain inhibitor (+)-JQ1 that competitively binds to acetyl-lysine recognition motifs. (+)-JQ1_x000D_ competitively binds to the bromodomain displacing the BRD4 fusion oncoprotein from chromatin,_x000D_ which induces squamous differentiation and specific anti-proliferative effect in BRD4-dependent cell_x000D_ lines and patient-derived xenograft models. However, study results have shown that (-)-JQ1 fails to_x000D_ significantly interact with any bromodomain tested and exhibits inhibition against BRD4(1) with and_x000D_ IC50 of 10,000 nM.
Product Page Updated 2024-01-09T13:23:45.900Z

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