A Potent HDAC Inhibitor, 1-Alaninechlamydocin, from a Tolypocladium sp. Induces G2/M Cell Cycle Arrest and Apoptosis in MIA PaCa-2 Cells-Reference-Cited by-同舟云学术

A Potent HDAC Inhibitor, 1-Alaninechlamydocin, from a Tolypocladium sp. Induces G2/M Cell Cycle Arrest and Apoptosis in MIA PaCa-2 Cells

Published:2014-07-07 Issue:7 Volume:77 Page:1753-1757
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Du Lin¹²,Risinger April L.¹²,King Jarrod B.¹²,Powell Douglas R.¹²,Cichewicz Robert H.¹²

Affiliation:

1. Department of Chemistry and Biochemistry, Stephenson Life Sciences Research Center, ‡Natural Products Discovery Group, and Institute for Natural Products Applications and Research Technologies, University of Oklahoma, Norman, Oklahoma 73019-5251, United States

2. Department of Pharmacology and ∇Cancer Therapy & Research Center, University of Texas Health Science Center, San Antonio, Texas 78229, United States

Funder

San Antonio Area Foundation

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/np500387h

Reference30 articles.

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5. Implications of epigenetic modulation for novel treatment approaches in patients with schizophrenia

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