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  • DC Chemicals Limited
  • China
  • Product Name: BRD9757
  • Price: $Inquiry/100mg $Inquiry/250mg $Inquiry/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

1423058-85-8

1423058-85-8 structure
1423058-85-8 structure
  • Name: BRD 9757
  • Chemical Name: brd9757
  • CAS Number: 1423058-85-8
  • Molecular Formula: C6H9NO2
  • Molecular Weight: 127.14100
  • Catalog: Signaling Pathways Cell Cycle/DNA Damage HDAC
  • Create Date: 2018-02-03 08:38:37
  • Modify Date: 2024-01-09 14:06:15
  • BRD9757 is a potent, capless and selective HDAC6 inhibitor with an IC50 of 30 nM. BRD9757 shows excellent selectivity toward HDAC6 versus the class I (>20-fold) and class II (>400-fold) HDACs[1].

Name brd9757
Description BRD9757 is a potent, capless and selective HDAC6 inhibitor with an IC50 of 30 nM. BRD9757 shows excellent selectivity toward HDAC6 versus the class I (>20-fold) and class II (>400-fold) HDACs[1].
Related Catalog
Target

HDAC6:0.03 μM (IC50)

HDAC1:0.638 μM (IC50)

HDAC2:1.79 μM (IC50)

HDAC3:0.694 μM (IC50)

HDAC4:21.80 μM (IC50)

HDAC5:18.32 μM (IC50)

HDAC7:12.61 μM (IC50)

HDAC8:1.09 μM (IC50)

HDAC9:>33.33 μM (IC50)

In Vitro BRD9757(化合物 14)对抗 HDAC1、HDAC2、HDAC3、HDAC4、HDAC5、HDAC7、HDAC8 和 HDAC9,IC50 值分别为 0.638 μM、1.79 μM、0.694 μM、21.80 μM、18.32 μM、12.61 μM、1.09 μM 和 >33.33 μM[1]。 BRD9757(化合物 14;10-30 μM;24 小时)选择性地增加 Ac-tubulin 的水平,而不增加组蛋白乙酰化[1]。 Western Blot Analysis[1] Cell Line: HeLa cells Concentration: 10 μM and 30 μM Incubation Time: for 24 h Result: Increased the level of Ac-tubulin.
References

[1]. Florence F Wagner, et al. Potent and selective inhibition of histone deacetylase 6 (HDAC6) does not require a surface-binding motif. J Med Chem. 2013 Feb 28;56(4):1772-6.  

Molecular Formula C6H9NO2
Molecular Weight 127.14100
Exact Mass 127.06300
PSA 49.33000
LogP 0.99300
Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H319-H412
Precautionary Statements P273-P305 + P351 + P338
RIDADR NONH for all modes of transport