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3-hydroxytamoxifen (droloxifene)

62  relevant articles (5 outcomes, 17 trials/studies) found for this Bio-Agent
Also Known As:
droloxifene; 3-hydroxytamoxifen citrate; FK 435; FK-435; FK435; droloxifene citrate; meta-hydroxytamoxifen; Phenol, 3-(1-(4-(2-(dimethylamino)ethoxy)phenyl)-2-phenyl-1-butenyl)-, (E)-

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Bio-Agent Context: Research Results

Experts

1. Chen, Bao-An: 1 article (12/2005)
2. Gao, Feng: 1 article (12/2005)
3. Lu, Zu-Hong: 1 article (12/2005)
4. Zhang, Chun-Xiu: 1 article (12/2005)
5. Cheng, Jian: 1 article (12/2005)
6. Du, Juan: 1 article (12/2005)
7. Martin, J H J: 1 article (07/2003)
8. Symonds, A: 1 article (07/2003)
9. Chohan, S: 1 article (07/2003)
10. Bi, Dong-Song: 1 article (04/2003)

Related Diseases

1. Breast Neoplasms (Breast Cancer)
2. Neoplasms (Cancer)
3. Disease Progression
4. T-Cell Leukemia (Leukemia, T Cell)
5. Carcinoma (Carcinomatosis)
08/01/1989 - "Antiestrogenic and antitumor effects of droloxifene in experimental breast carcinoma."
09/15/1994 - "Therefore, it can be assumed that Droloxifene may represent an important step forward in the treatment of mammary carcinomas in women through its better tolerability and increased efficacy compared with Tamoxifen. "
08/01/1989 - "Droloxifene showed about 20-fold and 3-fold higher affinity to estrogen receptors (ER) in the rat uterus and human ER positive MCF-7 breast carcinoma cells, respectively, than tamoxifen, and was more active in decreasing uterine weight of mature rats and 17 beta-estradiol-treated immature rats. "
01/01/1991 - "Droloxifene differs from tamoxifen in the following ways: it has a more than 10-fold higher binding affinity to the estrogen receptor; it shows lower estrogenic and higher antiestrogenic effects on rat uterus, indicating a higher therapeutic index; it more potently inhibits growth of various human ER-positive mammary carcinoma cell lines; short-term exposures with clinically relevant concentrations of droloxifene produce long-term growth inhibition of human ER-positive cancer cells and are more effective than continuous treatment with tamoxifen; it more effectively reduces S-phases and arrests ER-positive cells in G1-phase of the cell cycle; it antagonizes estrogen independent, growth factor stimulated proliferation of MCF-7 cells with higher efficiency; it blocks estrogen activated c-myc expression better than tamoxifen; it more effectively inhibits growth of various experimental tumors of animal (R 3230, DMBA) and human (T61) origin. "
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Related Drugs and Biologics

1. Tamoxifen
2. Estrogen Receptor Modulators (Antiestrogen)
3. Estrogens (Estrogen)
4. P-Glycoprotein
5. Toremifene (Fareston)
6. trioxifene
7. 4-hydroxytamoxifen
8. Doxorubicin (Adriamycin)
9. 4-hydroxytoremifene
10. catechol (pyrocatechol)

Related Therapies and Procedures

1. Drug Therapy (Chemotherapy)
2. Intraperitoneal Injections

Best Treatments:
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