Amino-substituted heterocycles, compositions thereof, and methods of treatment therewith
申请人:D'Sidocky Neil R.
公开号:US20080242694A1
公开(公告)日:2008-10-02
Provided herein are Heterocyclic Compounds having the following structure:
wherein R
1
, R
2
, X, Y and Z are as defined herein, compositions comprising an effective amount of a Heterocyclic Compound and methods for treating or preventing cancer, inflammatory conditions, immunological conditions, metabolic conditions and conditions treatable or preventable by inhibition of a kinase pathway comprising administering an effective amount of a Heterocyclic Compound to a patient in need thereof.
An unprecedented Cu-catalyzed stereoselective alkylhydrazination reaction involving terminal alkynes, azocarboxylic esters as a nitrogen source, and dimethyl 2,2'-azobis(2-methylpropionate) and its analogues as a carbon source is presented here. This protocol provides direct access to tri-substituted (E)-alkenyl-hydrazines with good regio- and stereoselectivity under mild conditions. The transformation
[EN] 4-SUBSTITUTED AMINOISOQUINOLINE DERIVATIVES<br/>[FR] DÉRIVÉS D'AMINOISOQUINOLÉINE SUBSTITUÉS EN POSITION 4
申请人:PURDUE RESEARCH FOUNDATION
公开号:WO2018035072A1
公开(公告)日:2018-02-22
[00397] This invention relates to 4-substituted isoquinoline compounds and their derivatives and uses thereof for treatment of cancer, for example, acute myeloid leukemia.
The invention relates to heterocyclic compounds of Formula I and compositions thereof useful for treating diseases mediated by protein kinase B (PKB) where the variables have the definitions provided herein.
The invention also relates to the therapeutic use of such compounds and compositions thereof in treating disease states associated with abnormal cell growth, cancer, inflammation, and metabolic disorders.
Rapid Access to Chiral and Tripodal Cavitands from β‐Pinene
作者:Xiuze Wang、Radoslav Z. Pavlović、Tyler J. Finnegan、Pratik Karmakar、Curtis E. Moore、Jovica D. Badjić
DOI:10.1002/chem.202202416
日期:2022.12.27
Abundant natural product β-pinene can be rapidly converted into a library of chiral hosts that we call molecular tripods. As tripods complex chiral drugs in water, they hold promise for discovering and building novel sequestering agents, chemosensors or catalysts.