200,000+ products from a single source!

sales@angenechem.com

Home > Oxazole > 1350555-93-9

1350555-93-9

1350555-93-9 | N-[4-[(2R,4R,6S)-4-[[(4,5-Diphenyl-2-oxazolyl)thio]methyl]-6-[4-(hydroxymethyl)phenyl]-1,3-dioxan-2-yl]phenyl]-N'-hydroxyoctanediamide

CAS No: 1350555-93-9 Catalog No: AG00A0NL MDL No:

Product Description

Catalog Number:
AG00A0NL
Chemical Name:
N-[4-[(2R,4R,6S)-4-[[(4,5-Diphenyl-2-oxazolyl)thio]methyl]-6-[4-(hydroxymethyl)phenyl]-1,3-dioxan-2-yl]phenyl]-N'-hydroxyoctanediamide
CAS Number:
1350555-93-9
IUPAC Name:
N-[4-[(2R,4R,6S)-4-[(4,5-diphenyl-1,3-oxazol-2-yl)sulfanylmethyl]-6-[4-(hydroxymethyl)phenyl]-1,3-dioxan-2-yl]phenyl]-N'-hydroxyoctanediamide
InChI:
InChI=1S/C41H43N3O7S/c45-26-28-17-19-29(20-18-28)35-25-34(27-52-41-43-38(30-11-5-3-6-12-30)39(51-41)31-13-7-4-8-14-31)49-40(50-35)32-21-23-33(24-22-32)42-36(46)15-9-1-2-10-16-37(47)44-48/h3-8,11-14,17-24,34-35,40,45,48H,1-2,9-10,15-16,25-27H2,(H,42,46)(H,44,47)/t34-,35+,40+/m1/s1
InChI Key:
BHUZLJOUHMBZQY-YXQOSMAKSA-N

Properties

Complexity:
1060  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
3  
Defined Bond Stereocenter Count:
0
Exact Mass:
721.282g/mol
Formal Charge:
0
Heavy Atom Count:
52  
Hydrogen Bond Acceptor Count:
9  
Hydrogen Bond Donor Count:
4  
Isotope Atom Count:
0
Molecular Weight:
721.869g/mol
Monoisotopic Mass:
721.282g/mol
Rotatable Bond Count:
16  
Topological Polar Surface Area:
168A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
6.3  

Literature

Title Journal
Histone deacetylase 6 inhibition reduces cysts by decreasing cAMP and Ca(2+) in knock-out mouse models of polycystic kidney disease. The Journal of biological chemistry 20171027
Grouping of histone deacetylase inhibitors and other toxicants disturbing neural crest migration by transcriptional profiling. Neurotoxicology 20150901
Development and therapeutic implications of selective histone deacetylase 6 inhibitors. Journal of medicinal chemistry 20130822
Taxol alleviates 2-methoxyestradiol-induced endothelial permeability. Vascular pharmacology 20120101
The structural requirements of histone deacetylase inhibitors: Suberoylanilide hydroxamic acid analogs modified at the C3 position display isoform selectivity. Bioorganic & medicinal chemistry letters 20111015
p62/SQSTM1 in autophagic clearance of a non-ubiquitylated substrate. Journal of cell science 20110815
Rational design and simple chemistry yield a superior, neuroprotective HDAC6 inhibitor, tubastatin A. Journal of the American Chemical Society 20100811
The influence of mediators of intracellular trafficking on transgene expression efficacy of polymer-plasmid DNA complexes. Biomaterials 20100801
Acetylation of microtubules influences their sensitivity to severing by katanin in neurons and fibroblasts. The Journal of neuroscience : the official journal of the Society for Neuroscience 20100526
Chemical phylogenetics of histone deacetylases. Nature chemical biology 20100301
Expansion of the trans-Golgi network following activated collagen secretion is supported by a coiled-coil microtubule-bundling protein, p180, on the ER. Experimental cell research 20100201
HDAC6 regulates mitochondrial transport in hippocampal neurons. PloS one 20100101
The NIMA-family kinase Nek3 regulates microtubule acetylation in neurons. Journal of cell science 20090701
Tubacin kills Epstein-Barr virus (EBV)-Burkitt lymphoma cells by inducing reactive oxygen species and EBV lymphoblastoid cells by inducing apoptosis. The Journal of biological chemistry 20090619
Novel HDAC6 isoform selective chiral small molecule histone deacetylase inhibitors. Bioorganic & medicinal chemistry letters 20090201
Ubiquitin proteasome system stress underlies synergistic killing of ovarian cancer cells by bortezomib and a novel HDAC6 inhibitor. Clinical cancer research : an official journal of the American Association for Cancer Research 20081115
Structural origin of selectivity in class II-selective histone deacetylase inhibitors. Journal of medicinal chemistry 20080522
Fold up or perish: unfolded protein response and chemotherapy. Cell death and differentiation 20080201
Significance of HDAC6 regulation via estrogen signaling for cell motility and prognosis in estrogen receptor-positive breast cancer. Oncogene 20050630
Class II (IIa)-selective histone deacetylase inhibitors. 1. Synthesis and biological evaluation of novel (aryloxopropenyl)pyrrolyl hydroxyamides. Journal of medicinal chemistry 20050505
Structural biasing elements for in-cell histone deacetylase paralog selectivity. Journal of the American Chemical Society 20030514
Multidimensional chemical genetic analysis of diversity-oriented synthesis-derived deacetylase inhibitors using cell-based assays. Chemistry & biology 20030501
Domain-selective small-molecule inhibitor of histone deacetylase 6 (HDAC6)-mediated tubulin deacetylation. Proceedings of the National Academy of Sciences of the United States of America 20030415

Related Products

© 2019 Angene International Limited. All rights Reserved.