Affiliations 

  • 1 Department of Chemistry, Texas A & M University, Box 30012, College Station, Texas 77842, United States; Department of Radiology, University of Wisconsin-Madison, Madison, Wisconsin 53705, United States
  • 2 Department of Chemistry, Texas A & M University, Box 30012, College Station, Texas 77842, United States; Department of Chemistry, Fuzhou University, Fuzhou 350116, P. R. China
  • 3 Department of Radiology, University of Wisconsin-Madison, Madison, Wisconsin 53705, United States; University of Wisconsin Carbone Cancer Center, University of Wisconsin-Madison, Madison, Wisconsin 53705, United States
  • 4 Department of Chemistry, Texas A & M University, Box 30012, College Station, Texas 77842, United States; Department of Pharmacology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia
ACS Med Chem Lett, 2017 Feb 09;8(2):179-184.
PMID: 28197308 DOI: 10.1021/acsmedchemlett.6b00368

Abstract

Actively targeting probe 1b, an unsymmetrical bivalent dipeptide mimic, selectively bound melanoma over healthy skin tissue in histological samples from patients and Sinclair swine. Modifications to 1b gave agents 2-4 that contain a near-IR aza-BODIPY fluor. Contrary to our expectations, symmetrical probe 3 gave the highest melanoma-to-healthy skin selectivity in histochemistry and experiments with live cells; this was surprising because 2, not 3, is unsymmetrical like the original lead 1. Optical imaging of 3 in a mouse melanoma model failed to show tumor accumulation in vivo, but the probe did selectively accumulate in the tumor (some in lung and less in the liver) as proven by analysis of the organs post mortem.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.