Tesmilifene
Clinical data
Other namesBMS-217380-01; YMB-1002; DPPE
Identifiers
  • 2-(4-Benzylphenoxy)-N,N-diethylethanamine
CAS Number
PubChem CID
ChemSpider
UNII
ChEBI
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC19H25NO
Molar mass283.415 g·mol−1
3D model (JSmol)
  • CCN(CC)CCOC1=CC=C(C=C1)CC2=CC=CC=C2
  • InChI=1S/C19H25NO/c1-3-20(4-2)14-15-21-19-12-10-18(11-13-19)16-17-8-6-5-7-9-17/h5-13H,3-4,14-16H2,1-2H3
  • Key:NFIXBCVWIPOYCD-UHFFFAOYSA-N

Tesmilifene (INN; developmental code names YMB-1002, BMS-217380-01), also known as N,N-diethyl-2-(4-phenylmethyl)ethanamine (DPPE), is a small-molecule antineoplastic drug and chemopotentiator that was under development by YM BioSciences for the treatment of breast cancer in the 2000s but was never marketed.[1][2][3] It reached phase III clinical trials for advanced/metastatic breast cancer before development was discontinued.[1]

Tesmilifene is a diphenylmethane derivative that is structurally related to the triphenylethylene derivative tamoxifen but lacks the stilbene bridge and third phenyl ring necessary for binding to the estrogen receptor (ER), and as such, it is not a selective estrogen receptor modulator (SERM).[4][5] In addition to tamoxifen, tesmilifene is structurally related to diphenylmethane antihistamines like diphenhydramine and hydroxyzine, but is much weaker than these agents in assays of anti-H1 receptor activity, and hence, neither acts as an antihistamine.[4]

Tamoxifen is known to bind not only to the ER but also to non-ER so-called "antiestrogen binding sites" (AEBS) that are present in cell microsomes as opposed to the cell nucleus.[4][5] Tesmilifene was developed as a selective ligand of the AEBS without ER affinity to investigate these sites and their role in the antineoplastic activity of tamoxifen.[4][5] Histamine has been found to be a ligand of the AEBS, and it has been determined that the AEBS represent the substrate binding site of certain microsomal cytochrome P450 enzymes including CYP3A4, CYP2D6, and CYP1A1.[4] Tesmilifene binds to and displaces histamine from these sites equipotently to tamoxifen and more strongly than conventional antihistamines, and this action has been found to correlate with the cytotoxic effects of tesmilifene in breast cancer cells in vitro.[4] Moreover, in spite of its lack of affinity for the ER, tesmilifene antagonizes the uterotrophic effects of exogenous estrogen in vivo.[4]

See also

References

  1. 1 2 "Tesmilifene". AdisInsight. Springer Nature Switzerland AG.
  2. ↑ Georg F. Weber (22 July 2015). Molecular Therapies of Cancer. Springer. pp. 413–. ISBN 978-3-319-13278-5.
  3. ↑ Sorbera LA, Castaner J, Leeson PA (2003). "Tesmilifene hydrochloride". Drugs of the Future. 28 (6): 546. doi:10.1358/dof.2003.028.06.738790. ISSN 0377-8282.
  4. 1 2 3 4 5 6 7 Brandes LJ (February 2008). "N,N-diethyl-2-[4-(phenylmethyl) phenoxy] ethanamine (DPPE; tesmilifene), a chemopotentiating agent with hormetic effects on DNA synthesis in vitro, may improve survival in patients with metastatic breast cancer". Human & Experimental Toxicology. 27 (2): 143–147. doi:10.1177/0960327108090751. PMID 18480139. S2CID 20966915.
  5. 1 2 3 Brandes LJ, Hermonat MW (September 1984). "A diphenylmethane derivative specific for the antiestrogen binding site found in rat liver microsomes". Biochemical and Biophysical Research Communications. 123 (2): 724–728. doi:10.1016/0006-291x(84)90289-4. PMID 6548377.
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