Click-based synthesis and proteomic profiling of lipstatin analogues

Mun H. Ngai; Peng Yu Yang; Kai Liu; Yuan Shen; Markus R. Wenk; Shao Q. Yao; Martin J. Lear

doi:10.1039/c0cc01276a

Click-based synthesis and proteomic profiling of lipstatin analogues

Mun H. Ngai, Peng Yu Yang, Kai Liu, Yuan Shen, Markus R. Wenk, Shao Q. Yao, Martin J. Lear

SCI - Chemistry

Research output: Contribution to journal › Article › peer-review

43 Citations (Scopus)

Abstract

Using click chemistry to enable both structural diversity and proteome profiling within a natural product derived library, two out of nineteen lipstatin analogues showed similar activity to Orlistat against fatty acid synthase (FAS), but with an improved ability to induce tumour cell death.

Original language	English
Pages (from-to)	8335-8337
Number of pages	3
Journal	Chemical Communications
Volume	46
Issue number	44
DOIs	https://doi.org/10.1039/c0cc01276a
Publication status	Published - 2010 Nov 28

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
Chemistry(all)
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

Access to Document

10.1039/c0cc01276a

Cite this

@article{4fb0ac60408849f38fe104269c905a03,

title = "Click-based synthesis and proteomic profiling of lipstatin analogues",

abstract = "Using click chemistry to enable both structural diversity and proteome profiling within a natural product derived library, two out of nineteen lipstatin analogues showed similar activity to Orlistat against fatty acid synthase (FAS), but with an improved ability to induce tumour cell death.",

author = "Ngai, {Mun H.} and Yang, {Peng Yu} and Kai Liu and Yuan Shen and Wenk, {Markus R.} and Yao, {Shao Q.} and Lear, {Martin J.}",

year = "2010",

month = nov,

day = "28",

doi = "10.1039/c0cc01276a",

language = "English",

volume = "46",

pages = "8335--8337",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "44",

}

TY - JOUR

T1 - Click-based synthesis and proteomic profiling of lipstatin analogues

AU - Ngai, Mun H.

AU - Yang, Peng Yu

AU - Liu, Kai

AU - Shen, Yuan

AU - Wenk, Markus R.

AU - Yao, Shao Q.

AU - Lear, Martin J.

PY - 2010/11/28

Y1 - 2010/11/28

N2 - Using click chemistry to enable both structural diversity and proteome profiling within a natural product derived library, two out of nineteen lipstatin analogues showed similar activity to Orlistat against fatty acid synthase (FAS), but with an improved ability to induce tumour cell death.

AB - Using click chemistry to enable both structural diversity and proteome profiling within a natural product derived library, two out of nineteen lipstatin analogues showed similar activity to Orlistat against fatty acid synthase (FAS), but with an improved ability to induce tumour cell death.

UR - http://www.scopus.com/inward/record.url?scp=78049404197&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=78049404197&partnerID=8YFLogxK

U2 - 10.1039/c0cc01276a

DO - 10.1039/c0cc01276a

M3 - Article

C2 - 20577697

AN - SCOPUS:78049404197

SN - 1359-7345

VL - 46

SP - 8335

EP - 8337

JO - Chemical Communications

JF - Chemical Communications

IS - 44

ER -

Click-based synthesis and proteomic profiling of lipstatin analogues

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this