Synthesis and cytotoxicity of some biurets against human breast cancer T47D cell line
✍ Scribed by Shamileh Fouladdel; Ali Khalaj; Neda Adibpour; Ebrahim Azizi
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 488 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0960-894X
No coin nor oath required. For personal study only.
✦ Synopsis
Design, synthesis and cytotoxicity of several known and novel biurets against human breast cancer T47D cell line in comparison to doxorubicin are described. Biurets incorporating 2-methyl quinoline-4-yl and benzo[d]thiazol-2-ylthio moieties showed higher cytotoxicity and decreased cell viability in a concentration-and time-dependent manner.
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A series of D-and L-tyrosine-chlorambucil analogs was synthesized as anticancer drugs for chemotherapy of breast cancer. The novel compounds were synthesized in good yields through efficient modifications of D-and L-tyrosine. The newly synthesized compounds were evaluated for their anticancer effica
## Abstract Steroid regulation of 17β‐hydroxysteroid dehydrogenase (17‐HSD) was studied in the T‐47D human breast‐cancer cell line, using a radioimmunoassay. In addition, 3 mRNA species (2.4, 1.4, and 0.9 kb) specific for the enzyme were shown to be present in these cells. All the synthetic progest
T47D human breast cancer cells were grown in I pM benzo[a]pyrene (BaP) for 3.5 months, and 2 BaP-resistant (BaPR) variant cell lines (C5 and CIO) were isolated. Decreased aryl hydrocarbon (Ah)-responsiveness in the C5 and C I0 BaPR cells was characterized by lower (80 to 9ovo) induction of CYP I A l