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Mei Su
Observed name:
Mei SU
Institution:
Tianjin University of Traditional Chinese Medicine
Observed institutions:
Tianjin University of Traditional Chinese Medicine,
University of Iowa,
AstraZeneca (United States),
Jiangsu Province Hospital
OpenAlex ID:
A5108542418
Discovery of 5-Chloro-N2-[(1S)-1-(5-fluoropyrimidin-2-yl)ethyl]-N4-(5-methyl-1H-pyrazol-3-yl)pyrimidine-2,4-diamine (AZD1480) as a Novel Inhibitor of the Jak/Stat Pathway
2010
·
Stephanos Ioannidis
, Michelle L. Lamb
, et al.
·
Journal of Medicinal Chemistry
·
125
Discovery of Checkpoint Kinase Inhibitor (S)-5-(3-Fluorophenyl)-N-(piperidin-3-yl)-3-ureidothiophene-2-carboxamide (AZD7762) by Structure-Based Design and Optimization of Thiophenecarboxamide Ureas
2012
·
Vibha Oza
, Susan Ashwell
, et al.
·
Journal of Medicinal Chemistry
·
74
Chrysin attenuates allergic airway inflammation by modulating the transcription factors T-bet and GATA-3 in mice
2012
·
Mei Su
·
Molecular Medicine Reports
·
67
PDF
Sodium tanshinone IIA silate inhibits oxygen‐glucose deprivation/recovery‐induced cardiomyocyte apoptosis via suppression of the NF‐κB/TNF‐α pathway
2013
·
Wen‐Yu Wu
, Wen‐Yi Wang
, et al.
·
British Journal of Pharmacology
·
61
PDF
Discovery of 1-Methyl-1 H -imidazole Derivatives as Potent Jak2 Inhibitors
2013
·
Qibin Su
, Stephanos Ioannidis
, et al.
·
Journal of Medicinal Chemistry
·
59
Sodium Tanshinone IIA Silate Inhibits High Glucose-Induced Vascular Smooth Muscle Cell Proliferation and Migration through Activation of AMP-Activated Protein Kinase
2014
·
Wen-yu Wu
, Hong Yan
, et al.
·
PLoS ONE
·
57
PDF
A highly selective synthesis of (Z)-α,β-unsaturated ketones
1999
·
Wensheng Yu
, Mei Su
, et al.
·
Tetrahedron Letters
·
44
Discovery of a novel class of 2-ureido thiophene carboxamide checkpoint kinase inhibitors
2008
·
James W. Janetka
, Lynsie Almeida
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
38
A facile chemoselective deprotection of the p-methoxybenzyl group
2000
·
Wensheng Yu
, Mei Su
, et al.
·
Tetrahedron Letters
·
37
Negishi Coupling between α-Alkyl(aryl)thio Vinyl Zinc Chloride and α-Bromo Vinyl Ether: A Convergent Synthesis of 2-Alkoxy-3-alkyl(aryl)thiobuta-1,3-dienes1
2002
·
Mei Su
, Ying Kang
, et al.
·
Organic Letters
·
32
A stereoselective synthesis of α-halo vinyl sulfides and their applications in organic synthesis
2001
·
Mei Su
, Wensheng Yu
, et al.
·
Tetrahedron Letters
·
27
Discovery of pyrazol-3-ylamino pyrazines as novel JAK2 inhibitors
2009
·
Stephanos Ioannidis
, Michelle L. Lamb
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
26
Synthesis and evaluation of triazolones as checkpoint kinase 1 inhibitors
2012
·
Vibha Oza
, Susan Ashwell
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
23
Synthetic Studies toward the Construction of the cis-Decalin Portion of Superstolides A and B. Application of a Sequential Double Michael Reaction and an Anionic Oxy-Cope Rearrangement
2005
·
Zhengmao Hua
, Wensheng Yu
, et al.
·
Organic Letters
·
22
Keverprazan, a novel potassium-competitive acid blocker: Single ascending dose safety, tolerability, pharmacokinetics, pharmacodynamics and food effect in healthy subjects
2023
·
Sufeng Zhou
, Lijun Xie
, et al.
·
European Journal of Pharmaceutical Sciences
·
17
Keverprazan, a novel potassium‐competitive acid blocker: Multiple oral doses safety, tolerability, pharmacokinetics, and pharmacodynamics in healthy subjects
2023
·
Sufeng Zhou
, Lijun Xie
, et al.
·
Clinical and Translational Science
·
17
Discovery of Chromane-6-Sulfonamide Derivative as a Potent, Selective, and Orally Available Novel Retinoic Acid Receptor-Related Orphan Receptor γt Inverse Agonist
2021
·
Lei Chen
, Mei Su
, et al.
·
Journal of Medicinal Chemistry
·
17
Structure–Cytotoxicity Relationships of Analogues of N14-Desacetoxytubulysin H
2016
·
Dorin Toader
, Fengjiang Wang
, et al.
·
Journal of Medicinal Chemistry
·
15
Discovery of a novel class of triazolones as Checkpoint Kinase inhibitors—Hit to lead exploration
2010
·
Vibha Oza
, Susan Ashwell
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
15
In vitro and in vivo evaluation of 6-aminopyrazolyl-pyridine-3-carbonitriles as JAK2 kinase inhibitors
2011
·
Tao Wang
, Stephanos Ioannidis
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
14
Discovery of 2H-chromone-4-one based sulfonamide derivatives as potent retinoic acid receptor-related orphan receptor γt inverse agonists
2021
·
Lei Chen
, Mei Su
, et al.
·
European Journal of Medicinal Chemistry
·
12
Discovery of N-(2-benzyl-4-oxochroman-7-yl)-2-(5-(ethylsulfonyl) pyridin-2-yl) acetamide (b12) as a potent, selective, and orally available novel retinoic acid receptor-related orphan receptor γt inverse agonist
2021
·
Lei Chen
, Mei Su
, et al.
·
Bioorganic Chemistry
·
11
Continuous synthesis and anti-myocardial injury of tanshinone IIA derivatives
2017
·
Yin-Lin Qin
, Lei Chen
, et al.
·
Journal of Asian Natural Products Research
·
11
Hypolipidemic effect of SIPI-7623, a derivative of an extract from oriental wormwood, through farnesoid X receptor antagonism
2018
·
Yi-Fang DENG
, Xiao-Ling HUANG
, et al.
·
Chinese Journal of Natural Medicines
·
10
Identification of amidoheteroaryls as potent inhibitors of mutant (V600E) B-Raf kinase with in vivo activity
2008
·
Paul D. Lyne
, Brian Aquila
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
10
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Works count:
39
Citation count:
864
H-index:
17
I10-index:
25
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