Design and Synthesis of Highly Potent and Isoform Selective JNK3 Inhibitors: SAR Studies on Aminopyrazole Derivatives (vol 57, pg 10013, 2014)

Journal article

Open access

Peer reviewed

Ke Zheng, Sarah Iqbal, Pamela Hernandez, HaJeung Park, Philip V. LoGrasso and Yangbo Feng

Journal of medicinal chemistry, Vol.59(19), pp.9276-9276

2016-10-13

PMID: 27673700

Abstract

Chemistry, Medicinal

Life Sciences & Biomedicine

Pharmacology & Pharmacy

Science & Technology

url

https://doi.org/10.1021/acs.jmedchem.6b01369View

Published (Version of record) Open

7 Record Views

These are selected metrics from InCites Benchmarking & Analytics tool, related to this output

Citation topics: 1 Clinical & Life Sciences; 1.25 Molecular & Cell Biology - Cancer, Autophagy & Apoptosis; 1.25.887 RAS
Web Of Science research areas: Chemistry, Medicinal
ESI research areas: Chemistry

This output has contributed to the advancement of the following goals:

Source: InCites

Title: Design and Synthesis of Highly Potent and Isoform Selective JNK3 Inhibitors: SAR Studies on Aminopyrazole Derivatives (vol 57, pg 10013, 2014)
Creators: Ke Zheng
Sarah Iqbal
Pamela Hernandez
HaJeung Park
Philip V. LoGrasso
Yangbo Feng
Publication Details: Journal of medicinal chemistry, Vol.59(19), pp.9276-9276
Publisher: Amer Chemical Soc
Number of pages: 1
Academic Unit: Miller School of Medicine; Molecular and Cellular Pharmacology Research
Language: English
Resource Type: Journal article
PMID: 27673700
Record Identifier: 991031757805702976