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Activity of bis-carbamoyloxymethyl derivatives of pyrroles and pyrrolizines against human tumor xenografts in nude mice.

Abstract
The activities of the pyrrolizines, Compounds I and II, and the pyrroles, Compounds IV and V, are reported in nude mouse-grown HT-29 human adenocarcinoma of the colon, DO 1 human oat carcinoma of the lung, and CL 1 human duct cell carcinoma of the breast (coded as CX-1, LX-1, and MX-1, respectively, by the National Cancer Institute). Compounds II and IV were active against all three experimental tumors; both compounds produced significant tumor regression in the human breast tumor xenograft and Compound IV caused tumor regression in the human lung tumor xenograft.
AuthorsW K Anderson
JournalCancer research (Cancer Res) Vol. 42 Issue 6 Pg. 2168-70 (Jun 1982) ISSN: 0008-5472 [Print] United States
PMID6280852 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Pyrroles
  • Pyrrolidines
Topics
  • Adenocarcinoma (drug therapy)
  • Animals
  • Breast Neoplasms (drug therapy)
  • Carcinoma, Small Cell (drug therapy)
  • Cell Line
  • Colonic Neoplasms (drug therapy)
  • Drug Evaluation, Preclinical
  • Humans
  • Lung Neoplasms (drug therapy)
  • Mice
  • Mice, Nude
  • Neoplasm Transplantation
  • Neoplasms (drug therapy)
  • Neoplasms, Experimental (drug therapy)
  • Pyrroles (therapeutic use)
  • Pyrrolidines (therapeutic use)
  • Transplantation, Heterologous

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