Nothing Special   »   [go: up one dir, main page]

Salmi-Smail et al., 2010 - Google Patents

Modified cap group suberoylanilide hydroxamic acid histone deacetylase inhibitor derivatives reveal improved selective antileukemic activity

Salmi-Smail et al., 2010

View PDF
Document ID
8364549121280351216
Author
Salmi-Smail C
Fabre A
Dequiedt F
Restouin A
Castellano R
Garbit S
Roche P
Morelli X
Brunel J
Collette Y
Publication year
Publication venue
Journal of medicinal chemistry

External Links

Snippet

A series of SAHA cap derivatives was designed and prepared in good-to-excellent yields that varied from 49% to 95%. These derivatives were evaluated for their antiproliferative activity in several human cancer cell lines. Antiproliferative activity was observed for …
Continue reading at orbi.uliege.be (PDF) (other versions)

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by the preceding groups
    • G01N33/48Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil

Similar Documents

Publication Publication Date Title
Salmi-Smail et al. Modified cap group suberoylanilide hydroxamic acid histone deacetylase inhibitor derivatives reveal improved selective antileukemic activity
Cheng et al. Discovery of potent and selective epidermal growth factor receptor (EGFR) bifunctional small-molecule degraders
Marek et al. Characterization of histone deacetylase 8 (HDAC8) selective inhibition reveals specific active site structural and functional determinants
Ferraro et al. Allosteric modulators of HSP90 and HSP70: dynamics meets function through structure-based drug design
Heimburg et al. Structure-based design and biological characterization of selective histone deacetylase 8 (HDAC8) inhibitors with anti-neuroblastoma activity
Olson et al. Discovery of the first histone deacetylase 6/8 dual inhibitors
Heimburg et al. Structure-based design and synthesis of novel inhibitors targeting HDAC8 from Schistosoma mansoni for the treatment of schistosomiasis
Wagner et al. Potent and selective inhibition of histone deacetylase 6 (HDAC6) does not require a surface-binding motif
Thinon et al. N-myristoyltransferase inhibition induces ER-stress, cell cycle arrest, and apoptosis in cancer cells
Rodrigues et al. Design, synthesis, and pharmacological evaluation of novel N-acylhydrazone derivatives as potent histone deacetylase 6/8 dual inhibitors
Suzuki et al. Rapid discovery of highly potent and selective inhibitors of histone deacetylase 8 using click chemistry to generate candidate libraries
Simon et al. KATching-up on small molecule modulators of lysine acetyltransferases
Mishra et al. The development of Hsp90β-selective inhibitors to overcome detriments associated with pan-Hsp90 inhibition
Farooqi et al. Novel lysine-based thioureas as mechanism-based inhibitors of sirtuin 2 (SIRT2) with anticancer activity in a colorectal cancer murine model
Tanaka et al. A practical use of ligand efficiency indices out of the fragment-based approach: ligand efficiency-guided lead identification of soluble epoxide hydrolase inhibitors
Cao et al. The process and strategy for developing selective histone deacetylase 3 inhibitors
Suzuki et al. Design, synthesis, and biological activity of boronic acid-based histone deacetylase inhibitors
Li et al. Biological evaluation of new largazole analogues: alteration of macrocyclic scaffold with click chemistry
Hanafi et al. Discovery of a Napabucasin PROTAC as an Effective Degrader of the E3 Ligase ZFP91
Mai et al. Binding mode analysis of 3-(4-benzoyl-1-methyl-1 H-2-pyrrolyl)-N-hydroxy-2-propenamide: a new synthetic histone deacetylase inhibitor inducing histone hyperacetylation, growth inhibition, and terminal cell differentiation
Huang et al. Discovery of new SIRT2 inhibitors by utilizing a consensus docking/scoring strategy and structure–activity relationship analysis
Poli et al. Binding investigation and preliminary optimisation of the 3-amino-1, 2, 4-triazin-5 (2 H)-one core for the development of new Fyn inhibitors
Martínez et al. Multitarget anticancer agents based on histone deacetylase and protein kinase CK2 inhibitors
Frühauf et al. Non-hydroxamate zinc-binding groups as warheads for histone deacetylases
Reddy et al. Design and synthesis of simplified largazole analogues as isoform-selective human lysine deacetylase inhibitors