associate professor weiwei he-全讯国际

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associate professor weiwei he
发布时间:2019-05-20   访问次数:699   作者:

weiwei he, ph.d.

research direction: chemical biology of bioactive small molecules

contact information

  • office: room 1219, building 18

  • email:

  • office phone: 86 21 6425 2293

education

  • 2013.02  ph.d.  cell and molecular biology

the scripps research institute

la jolla, ca, usa

  • 2007.06  m.sc.  biochemistry and molecular biology

school of life sciences

university of science and technology of china

hefei, anhui, china

  • 2003.06  b.sc.  biology

department of biology

shantou university

shantou, guangdong, china

research interests

natural products exhibit diverse bioactivities and unparalleled biocompatibility. they are important tools at the chemistry-biology interface and useful lead compounds for drug discovery. after establishing the lab at school of pharmacy in ecust in 2014, my research interest mainly focuses on target identification and mechanism-of-action studies of bioactive small molecules, including natural products and their analogues. we aim to identify novel functions of potential drug targets using bioactive small molecules as probes, to further elucidate the complex biological pathways, and to provide deeper understanding of the pathology of the diseases, such as cancer.

professional experience

  • 2013 – 2014  postdoctoral fellow

  • the scripps research institute

  • la jolla, ca, usa

  • 2014 – present  associate professor

  • east china university of science and technology

  • shanghai, china

publications

1. gongcai lan, jie zhang, wenbo ye, fan yang, ang li*, weiwei he*, and wei-dong zhang* celastrol as a tool for the study of the biological events of metabolic diseases. science china chemistry, 2019, 62(4), 409–416.

2. zhongyin zhang, jinxin wang, jian li, fan yang, guodu liu, wenjun tang, weiwei he, jian-jun fu, yun-heng shen*, ang li*, and wei-dong zhang* total synthesis and stereochemical assignment of delavatine a: rh-catalyzed asymmetric hydrogenation of indene-type tetrasubstituted olefins and kinetic resolution through pd-catalyzed triflamide-directed c–h olefination. j. am. chem. soc. 2017, 139 (15), 5558–5567.

3. jinpeng pei, shupeng zhou, fan yang, yu sun, ang li*, wei-dong zhang*, and weiwei he*, identification and mechanistic studies of a cell cycle regulator jp18 from a library of synthetic indole terpenoid mimics. chem. asian j. 2016, 11, 2715–2718.

4. zhongyin zhang, fan yang, jian-jun fu,  yun-heng shen*, weiwei he*, and wei-dong zhang*, delavatine a, a structurally unusual cyclopenta[de] isoquinoline alkaloid from incarvillea delavayi, rsc advances, 2016, 6, 65885–65888.

5. litao sun, ana cristina gomes, weiwei he, huihao zhou, xiaoyun wang, david w. pan, paul schimmel, tao pan*, and xiang-lei yang*, evolutionary gain of alanine mischarging to non-cognate trnas with a g4:u69 base pair. j am chem soc. 2016, 138(39), 12948–12955.

6. weiwei he§, ge bai§,  huihao zhou, na wei, nicholas m. white, janelle lauer, huaqing liu, yi shi, calin dan dumitru, karen lettieri, veronica shubayev, albena jordanova, velina  guergueltcheva, patrick griffin, robert w. burgess, samuel l. pfaff* and xiang-lei yang* (§these authors contribute equally), cmt2d neuropathy is linked to the neomorphic binding activity of glycyl-trna synthetase. nature, 2015, 526(7575), 710–714.

7. min chul park, taehee kang, da jin, jung min han, sang bum kim, yun jung park, kiwon cho, young woo park, min guo, weiwei he, xiang-lei yang, paul schimmel, and sunghoon kim*, secreted human glycyl-trna synthetase implicated in defense against erk-activated tumorigenesis. pnas plus, 2012, doi/10.1073/pnas.1200194109.

8. weiwei he§, hui-min zhang§, yeeting e. chong, min guo, alan g. marshall, and xiang-lei yang* (§these authors contribute equally), dispersed disease-causing neomorphic mutations on a single protein promote the same localized conformational opening. proc. natl. acad. sci. usa, 2011, 108, 12307–12312.




 
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