Name | LMK 235 |
Synonyms | LMK235 CS-1820 LMK 235 LMK-235 LMK 235 LMK-235 (Fandachem) N-[[6-(Hydroxyamino)-6-oxohexyl]oxy]-3,5-dimethyl-benzamide Benzamide, N-[[6-(hydroxyamino)-6-oxohexyl]oxy]-3,5-dimethyl- N-[[6-(Hydroxyamino)-6-oxohexyl]oxy]-3,5-dimethylbenzamide LMK-235 |
CAS | 1418033-25-6 |
EINECS | 808-770-7 |
InChIKey | VRYZCEONIWEUAV-UHFFFAOYSA-N |
Molecular Formula | C15H22N2O4 |
Molar Mass | 294.35 |
Density | 1.155±0.06 g/cm3(Predicted) |
Melting Point | 135-138°C |
Solubility | Soluble in DMSO |
Appearance | powder |
Color | white to beige |
pKa | 9.46±0.20(Predicted) |
Storage Condition | 2-8°C |
Use | LMK-235 is a selective histone deacetylase (HDAC) 4 and HDAC5 inhibitor. LMK-235 demonstrates activity against chemoresistant cancer cell lines in an MTT assay for cytotoxicity using human ovarian cancer cell lines A2780 and cisplatin resistant A2780CisR (IC50 = 0.49 and 0.32 μ M respectively). |
Target | HDAC4; HDAC5; |
Hazard Symbols | Xn - Harmful |
Risk Codes | 22 - Harmful if swallowed |
WGK Germany | 3 |
Reference Show more | 1: Hansen FK, Sumanadasa SD, Stenzel K, Duffy S, Meister S, Marek L, Schmetter R, Kuna K, Hamacher A, Mordmüller B, Kassack MU, Winzeler EA, Avery VM, Andrews KT, Kurz T. Discovery of HDAC inhibitors with potent activity against multiple malaria parasite life cycle stages. Eur J Med Chem. 2014 Jul 23;82:204-13. doi: 10.1016/j.ejmech.2014.05.050. Epub 2014 May 22. PubMed PMID: 24904967. 2: Marek L, Hamacher A, Hansen FK, Kuna K, Gohlke H, Kassack MU, Kurz T. Histone deacetylase (HDAC) inhibitors with a novel connecting unit linker region reveal a selectivity profile for HDAC4 and HDAC5 with improved activity against chemoresistant cancer cells. J Med Chem. 2013 Jan 24;56(2):427-36. doi: 10.1021/jm301254q. Epub 2013 Jan 8. PubMed PMID: 23252603. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 3.397 ml | 16.987 ml | 33.973 ml |
5 mM | 0.679 ml | 3.397 ml | 6.795 ml |
10 mM | 0.34 ml | 1.699 ml | 3.397 ml |
5 mM | 0.068 ml | 0.34 ml | 0.679 ml |