Zachary Minden

ORCID: 0000-0002-4642-2677
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About
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Research Areas
  • Calcium signaling and nucleotide metabolism
  • Phenothiazines and Benzothiazines Synthesis and Activities
  • Toxin Mechanisms and Immunotoxins
  • Cyclopropane Reaction Mechanisms
  • Synthesis and Biological Evaluation
  • Innovative Microfluidic and Catalytic Techniques Innovation
  • Chemical Synthesis and Analysis
  • Adenosine and Purinergic Signaling
  • Synthesis and pharmacology of benzodiazepine derivatives

Northeastern University
2017

An expeditious route to fused triazolo-pyrido benzoxazepines has been developed using flow and microwave-mediated cyclization chemistry. A range of substituted aryl hydrazides are coupled with a core chloroimine in good excellent yield via Pellizzari type process, producing 1,2,4-triazolo-pyrido [<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M1"><mml:mrow><mml:mn fontstyle="italic">2</mml:mn></mml:mrow></mml:math>,<mml:math id="M2"><mml:mrow><mml:mn...

10.1155/2017/8147421 article EN cc-by Advances in Chemistry 2017-12-04

Several monoclonal antibodies and inhibitors targeting CD38, an ectoenzyme overexpressed on malignant plasma cells, have previously been discovered. Herein, we expand structure-activity relationships of reported small-molecule thiazoloquinolinones show that several 4-cyclohexylamino analogues potent binding affinity for CD38 using surface plasmon resonance. Moreover, active amine could be acylated functionalized with alkyne fluorescein groups. Fluorescein analogue 21 bound selectively to...

10.1021/acsmedchemlett.6b00409 article EN ACS Medicinal Chemistry Letters 2016-12-23
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