(-)-JQ-1

Modify Date: 2025-08-25 17:15:30

(-)-JQ-1 Structure
(-)-JQ-1 structure
Common Name (-)-JQ-1
CAS Number 1268524-71-5 Molecular Weight 456.988
Density 1.3±0.1 g/cm3 Boiling Point 610.4±65.0 °C at 760 mmHg
Molecular Formula C23H25ClN4O2S Melting Point N/A
MSDS USA Flash Point 322.9±34.3 °C

 Use of (-)-JQ-1


(-)-JQ-1 is the stereoisomer of (+)-JQ1. (+)-JQ1 potently decreases expression of both BRD4 target genes, whereas (−)-JQ1 has no effect.

 Names

Name ()-jq1
Synonym More Synonyms

 (-)-JQ-1 Biological Activity

Description (-)-JQ-1 is the stereoisomer of (+)-JQ1. (+)-JQ1 potently decreases expression of both BRD4 target genes, whereas (−)-JQ1 has no effect.
Related Catalog
Target

BET bromodomain[1]

In Vitro (−)-JQ1 shows no significant interaction with any bromodomain. Besides, (−)-JQ1 enantiomer is comparatively inactive in nuclear protein in testis (NUT) midline carcinoma (NMC)[1].
References

[1]. Filippakopoulos, et al. Selective inhibition of BET bromodomains. Nature. 2010 Dec 23;468(7327):1067-73.

[2]. Mahe M, et al. An FGFR3/MYC positive feedback loop provides new opportunities for targeted therapies in bladder cancers. EMBO Mol Med. 2018 Apr;10(4). pii: e8163.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 610.4±65.0 °C at 760 mmHg
Molecular Formula C23H25ClN4O2S
Molecular Weight 456.988
Flash Point 322.9±34.3 °C
Exact Mass 456.138672
PSA 97.61000
LogP 4.49
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.657
Storage condition -20°C

 Safety Information

RIDADR NONH for all modes of transport

 Articles3

More Articles
Targeting bromodomains: epigenetic readers of lysine acetylation.

Nat. Rev. Drug Discov. 13(5) , 337-56, (2014)

Lysine acetylation is a key mechanism that regulates chromatin structure; aberrant acetylation levels have been linked to the development of several diseases. Acetyl-lysine modifications create dockin...

Epigenetic chemical probes. Müller S and Brown PJ

Clin. Pharmacol. Ther. 92(6) , 689-93, (2012)

Targeting chromatin readers. James LI and Frye SV

Clin. Pharmacol. Ther. 93(4) , 312-4, (2013)

 Synonyms

6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid, 4-(4-chlorophenyl)-2,3,9-trimethyl-, 1,1-dimethylethyl ester, (6R)-
2-Methyl-2-propanyl [(6R)-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
(R)-(-)-JQ1 Enantiomer
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