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Droxinostat

CAS No.
99873-43-5
Chemical Name:
Droxinostat
Synonyms
CS-425;NS 41080;Droxinostat;Droxinostat (NS41080);Droxinostat, 10 mM in DMSO;Droxinostat NS41080 NS-41080;4-(4-chloro-2-methylphenoxy)-N-hydroxybutylamide;4-(4-Chloro-2-methylphenoxy)-N-hydroxybutanamide;4-(4-Chloro-2-methyl-phenoxy)-N-hydroxy-butyramide;ButanaMide, 4-(4-chloro-2-Methylphenoxy)-N-hydroxy-
CBNumber:
CB22537542
Molecular Formula:
C11H14ClNO3
Molecular Weight:
243.69
MDL Number:
MFCD01326592
MOL File:
99873-43-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-08-05 19:35:02

Droxinostat Properties

Density 1.252
storage temp. Inert atmosphere,2-8°C
solubility DMSO: ≥20mg/mL
form powder
color white to off-white

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
Signal word  Danger
Hazard statements  H302-H315-H318-H335
Precautionary statements  P261-P280-P305+P351+P338
Hazard Codes  Xn
Risk Statements  22-37/38-41
Safety Statements  26-39
WGK Germany  3
NFPA 704
0
3 0

Droxinostat price More Price(45)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 23869 Droxinostat ≥98% 99873-43-5 1mg $37 2026-04-30 Buy
Cayman Chemical 23869 Droxinostat ≥98% 99873-43-5 5mg $90 2026-04-30 Buy
Cayman Chemical 23869 Droxinostat ≥98% 99873-43-5 10mg $158 2026-04-30 Buy
Cayman Chemical 23869 Droxinostat ≥98% 99873-43-5 25mg $349 2026-04-30 Buy
ChemScene CS-0491 Droxinostat 99.08% 99873-43-5 5mg $54 2026-06-04 Buy
Product number Packaging Price Buy
23869 1mg $37 Buy
23869 5mg $90 Buy
23869 10mg $158 Buy
23869 25mg $349 Buy
CS-0491 5mg $54 Buy

Droxinostat Chemical Properties, Uses, Production

Uses

Droxinostat is a histone deacetylase selective inhibitor and is used in cancer therapy and cancer research. Droxinostat is a selective inhibitor of HDAC3, HDAC6, and HDAC8.

Definition

ChEBI: 4-(4-chloro-2-methylphenoxy)-N-hydroxybutanamide is an aromatic ether.

Biological Activity

droxinostat is a selective inhibitor of hdac3, hdac6, and hdac8 with ic50 value of 16.9 ± 5.0 μm, 2.47 ± 1.09 μm, and 1.46 ± 0.11 μm, respectively [1].hdacs (histone deacetylases) are enzymes responsible of the deacetylation of lysine that residues of core histones and play a pivotal role in controlling chromatin remodeling and transcriptional activation. it is also reported that hdacs control the acetylation and activation status of multiple non-histone proteins, including the heat shock protein 90 (hsp90) which is an essential molecular chaperone for fungal virulence and antifungal resistance. multiple hdacs have been identified and hdac1 to hdac10 are shown to express in malignant cells which reminds the hdac inhibitor as a target for cancer therapy [2] [3].droxinostat is a selective hdac inhibitor and is different from the known pan-hdaci tsa which inhibits all tested hdac. when tested with prostate cancer line ppc-1 cells, droxinostat treatment selectively inhibited hdac3, hdac6, and hdac8 activity at the concentration of 50 μm/l which sensitized cells to death ligands [1]. in androgen-dependent cap cells, administration of droxinostat selectively inhibited hdacs and downregulated c-flp expression which resulted in cells apoptosis [4].

target

HDAC8

IC 50

HDAC8: 1.46 μM (IC50); HDAC6: 2.47 μM (IC50); HDAC3: 16.9 μM (IC50)

References

[1]. wood, t.e., et al., selective inhibition of histone deacetylases sensitizes malignant cells to death receptor ligands. mol cancer ther, 2010. 9(1): p. 246-56.
[2]. lamoth, f., p.r. juvvadi, and w.j. steinbach, histone deacetylase inhibition as an alternative strategy against invasive aspergillosis. front microbiol, 2015. 6: p. 96.
[3]. mackmull, m.t., et al., histone deacetylase inhibitors cause the selective depletion of bromodomain containing proteins. mol cell proteomics, 2015.
[4]. mccourt, c., et al., elevation of c-flip in castrate-resistant prostate cancer antagonizes therapeutic response to androgen receptor-targeted therapy. clin cancer res, 2012. 18(14): p. 3822-33.

Droxinostat Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 114)
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Chembest Research Laboratories Limited 021-20908456 sales@BioChemBest.com China 5996 61
Nanjing Chemlin Chemical Co., Ltd 025-83697070 13770331960 info@chemlin.com.cn China 16305 64
Hangzhou Sage Chemical Co., Ltd. +86057186818502 13588463833 info@sagechem.com China 10265 58
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd. 025-66113011 13913916777 cfzhang@aikonchem.com China 19902 55
Haoyuan Chemexpress Co., Ltd. 021-58950125 info@chemexpress.com China 7545 61
Shanghai Aladdin Bio-Chem Technology Co.,LTD 400-6206333 13167063860 anhua.mao@aladdin-e.com China 29977 65
Guangzhou Isun Pharmaceutical Co., Ltd 020-39119399 18927568969 isunpharm@qq.com China 4773 55
AdooQ BioScience, LLC +1 (866) 930-6790 info@adooq.com United States 2774 58
ApexBio Technology LLC +1-832-696-8203 info@apexbt.com United States 477 60

View Latest Price from Droxinostat manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Droxinostat pictures 2026-08-04 Droxinostat
99873-43-5
$58.00-148.00 99.83% 10g TargetMol Chemicals Inc.
Droxinostat pictures 2019-12-26 Droxinostat
99873-43-5
$1.00 1g 99% 200kg Career Henan Chemical Co
  • Droxinostat pictures
  • Droxinostat
    99873-43-5
  • $58.00-148.00
  • 99.83%
  • TargetMol Chemicals Inc.

Droxinostat Spectrum

Droxinostat 4-(4-Chloro-2-methylphenoxy)-N-hydroxybutanamide NS 41080 ButanaMide, 4-(4-chloro-2-Methylphenoxy)-N-hydroxy- CS-425 4-(4-Chloro-2-methyl-phenoxy)-N-hydroxy-butyramide Droxinostat (NS41080) Droxinostat NS41080 NS-41080 HDAC3,hepatocellular carcinoma (HCC),Droxinostat,NS-41080,Apoptosis,Histone deacetylases,cancer,inhibit,HDAC6,HDAC8,Inhibitor,histone deacetylase (HDAC),HDAC,NS41080 Droxinostat, 10 mM in DMSO 4-(4-chloro-2-methylphenoxy)-N-hydroxybutylamide 99873-43-5 Inhibitors Inhibitor