Bleomycin drug data and news

Bleomycin drug data, resources, and news articles (when available). Onconews.org provides news on cancer research. This section, which includes profiles on medicines that may or not be cancer-related is in beta form. If things run smoothly we will be releasing a new format late in the summer of 2006.

Generic name Bleomycin
Brand Names/Synonyms BLEOMYCIN; BLM; Blenoxane; Bleo; Bleocin; Bleomicin; Bleomicina [INN-Spanish]; Bleomycin (USAN ); Bleomycin sulfate; Bleomycine [INN-French]; Bleomycins; Bleomycinum [INN-Latin]
Indication For palliative treatment in the management of the following neoplasms; Malignant neoplasm (trachea, bronchus, lung); Squamous cell carcinoma; Lymphomas
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Description Not Available
Pharmacology Bleomycin is an antibiotic which has been shown to have antitumor activity. Bleomycin selectively inhibits the synthesis of deoxyribonucleic acid (DNA). The guanine and cytosine content correlates with the degree of mitomycin-induced cross-linking. At high concentrations of the drug, cellular RNA and protein synthesis are also suppressed. Bleomycin has been shown in vitro to inhibit B cell, T cell, and macrophage proliferation and impair antigen presentation, as well as the secretion of interferon gamma, TNFa, and IL-2. The antibiotic antitumor drugs are cell cycle-nonspecific except for Bleomycin (which has major effects in G2 and M phases). Bleomycin is indicated in the palliative treatment of squamous cell carcinoma, lymphomas, testicular carcinoma, alone or in combination with other drugs.
Mechanism Of Action Although the exact mechanism of action of Bleomycin is unknown, available evidence would seem to indicate that the main mode of action is the inhibition of DNA synthesis with some evidence of lesser inhibition of RNA and protein synthesis.
Bleomycin News
(When available)
Patients With Unfavorable Risk Hodgkin’s Lymphoma May Not ...  Dec 19, 2005
Cancer Consultants (press release), ABVD (doxorubicin, bleomycin, vinblastine and dacarbazine) is the most commonly used chemotherapy regimen. BEACOPP (bleomycin, etoposide ...

Patients with Unfavorable Risk Hodgkin’s Lymphoma May Not ...  Dec 20, 2005
Cancer Consultants (press release), ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine) is the most commonly used chemotherapy regimen for Hodgkin’s lymphoma. ...

PhotoCure ASA - PCI technology enhances effect of anti-cancer drug  Dec 5, 2005
Biotech Intelligence (press release), ...journal Clinical Cancer Research, it is now demonstrated that PCI can significantly improve the curative effect of the anti-cancer drug bleomycin in animal ...

Intensive Chemotherapy Regimen Shows Promise for Germ Cell Tumors  Dec 5, 2005
Cancer Consultants (press release), This regimen consisted of cycles of cisplatin, vincristine, bleomycin, and carboplatin, followed by one cycle of vincristin and bleomycin and three cycles of ...

Role of Eotaxin-1 (CCL11) and CC Chemokine Receptor 3 (CCR3) in ...  Dec 9, 2005
Am J Pathology (subscription) The present study examined the pulmonary expression of CCL11 and CCR3 during bleomycin (blm)-induced lung injury and determined their importance in the ...

Plenary Session Snapshot  Dec 19, 2005
Medscape (subscription) And, as discussed in the session, the results of chemo-radiation using a limited number of ABVD (adriamycin, bleomycin, vinblastine, and dacarbazine), commonly ...

Dosage Forms Injection; POWDER FOR SOLUTION
Drug_Category Antimetabolites; Antibiotics; Antineoplastic Agents; ATC:L01DC01
Absorption systemic absorption approximately 45%
Interactions [an error occurred while processing this directive]
Toxicity Excessive exposure may cause fever, chills, nausea, vomiting, mental, confusion, and wheezing. Bleomycin may cause irritation to eyes, skin and respiratory tract. It may also cause a darkening or thickening of the skin. It may cause an allergic reaction.
Organisms Affected Not Available
Chemical IUPAC Name 3-[[2-[2-[2-[2-[4-[2-[6-amino-2-[1-(2-amino-2-carbamoyl-ethyl)amino-2-carbamoyl-ethyl]-5-methyl-pyrimidin-4-yl]carbonylamino-3-[3-[4-carbamoyloxy-3,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-3-(3H-imidazol-4-yl)propanoyl]amino-3-hydroxy-2-methyl-pentanoyl]amino-3-hydroxy-butanoyl]aminoethyl]-1,3-thiazol-4-yl]-1,3-thiazol-4-yl]carbonylamino]propyl-dimethyl-sulfonium
Chemical Formula C55H84N17O21S3
Molecular Weight 1415.56 g/mol
Smiles String CC1=C(N=C(N=C1N)C(CC(=O)N)NCC(C(=O)N)N)C(=O)NC(C(C2=CN=CN2)OC3C(C(C(C(O3)CO)O)O)OC4C(C(C(C(O4)CO)O)OC(=O)N)O)C(=O)NC(C)C(C(C)C(=O)NC(C(C)O)C(=O)NCCC5=NC(=CS5)C6=NC(=CS6)C(=O)NCCC[S+](C)C)O
Melting Point Approx 160 F
Water Solubility Soluble
State Colorless or yellowish powder which becomes bluish depending on Cu content.
LogP/Hphobicity Not Available
Isoelectric Point Not Available
Biotransformation hepatic
Half Life 115 minutes
Protein Binding [%] 1%
RxList Link RXlist
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Drug Reference http://www.drugs.com/cons/Bleomycin.html
http://www.rxlist.com/cgi/generic3/bleomycin.htm
Drug Type Approved Drug
Accession No APRD00453
CAS Registry Number 11056-06-7
KEGG Compound ID C06854
PubChem ID SID:602743
PharmGKB ID PA448645
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 2131692

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