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(E)- 4- ((2- N- (4- methoxybenzenesulfonyl)amino)stilbazole)1- oxide

structure in first source
Also Known As:
HMN-176
Networked: 4 relevant articles (0 outcomes, 2 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Katoh, Fumitaka: 2 articles (11/2003 - 10/2003)
2. Hidaka, Hiroyoshi: 2 articles (11/2003 - 10/2003)
3. Von Hoff, Daniel D: 1 article (03/2009)
4. DiMaio, Michael A: 1 article (03/2009)
5. Mikhailov, Alexei: 1 article (03/2009)
6. Palazzo, Robert E: 1 article (03/2009)
7. Rieder, Conly L: 1 article (03/2009)
8. Medina-Gundrum, Leticia: 1 article (01/2005)
9. Cerna, Cesario: 1 article (01/2005)
10. Gomez, Lionel: 1 article (01/2005)

Related Diseases

1. Neoplasms (Cancer)
03/01/2009 - "HMN-176 is a potential new cancer therapeutic known to retard the proliferation of tumor cell lines. "
01/01/2005 - "Investigation of HMN-176 anticancer activity in human tumor specimens in vitro and the effects of HMN-176 on differential gene expression."
01/01/2005 - "The present study evaluated the activity profile of the antineoplastic agent HMN-176 in an ex-vivo soft agar cloning assay (human tumor colony-forming assay) in a panel of 132 human tumor specimens under 14-day continuous exposure at 0.1, 1.0, and 10.0 microg/ml. Thirty percent of specimens in the different treatment groups (39/132 in 0.1 and 1.0 test groups; 40/132 in 10.0 test group) were assessable, falling within the negative and positive control parameters. "
11/01/2003 - "In vivo antitumor activity of a novel sulfonamide, HMN-214, against human tumor xenografts in mice and the spectrum of cytotoxicity of its active metabolite, HMN-176."
01/01/2005 - "There was a positive relationship between HMN-176 concentration and effect, demonstrating greatest overall activity at 10.0 microg/ml. Evaluation of differential gene expression in drug-sensitive (A2780) and drug-resistant (A2780cp) ovarian carcinoma cell lines exposed to 0.1 microg/ml HMN-176 up to 48 h using cDNA microarrays with 1,154 known human genes revealed significant drug effects on tumor associated genes, including upregulation of tissue inhibitor matrix metalloproteinases gene (TIMP) in both cell lines, suggesting that HMN-176 could potentially overcome tumor drug resistance. "
2. Ovarian Neoplasms (Ovarian Cancer)
3. Carcinoma (Carcinomatosis)
4. Breast Neoplasms (Breast Cancer)

Related Drugs and Biologics

1. Doxorubicin (Adriamycin)
2. Agar
3. Matrix Metalloproteinases
4. Tissue Inhibitor of Metalloproteinases (TIMP)
5. Complementary DNA (cDNA)
6. Fluorouracil (Carac)
7. Etoposide (VP 16)
8. Cyclophosphamide (Cytoxan)
9. Cisplatin (Platino)
10. (E)- 4- (2- (2- (N- acetyl- N- (4- methoxybenzenesulfonyl)amino)stilbazole)) 1-oxide

Related Therapies and Procedures

1. Heterologous Transplantation (Xenotransplantation)