{{Drugbox| |IUPAC_name = 8-[(4-methyl-3-{[3-({[3-({2-methyl-5- [(4,6,8-trisulfo-1-naphthyl)carbamoyl] phenyl}carbamoyl)phenyl]carbamoyl}amino) benzoyl]amino}benzoyl)amino]naphthalene- 1,3,5-trisulfonic acid | image = Suramin.svg | CAS_number=145-63-1 | ATC_prefix=P01 | ATC_suffix=CX02 | ATC_supplemental= | PubChem=5361 | DrugBank= | | C=51 | H=40 | N=6 | O=23 | S=6 | molecular_weight = 1297.29 | bioavailability= | metabolism = | elimination_half-life= | excretion = | pregnancy_category = | legal_status = | routes_of_administration= }} Suramin is a drug developed by Oskar Dressel and Richard Kothe of Bayer, Germany in 1916, and is still sold by Bayer under the brand name Germanin. It is used for treatment of human sleeping sickness, onchocerciasis and other diseases caused by trypanosomes and worms. It is under investigation as treatment for prostate cancer.

According to the National Cancer Institute there are no active clinical trials (as of April 1, 2008). Completed and closed clinical trials are listed here:

In addition to Germanin, the National Cancer Institute also lists the following "Foreign brand names:" 309 F, Bayer 205, Fourneau 309, Moranyl, Naganin, Naganine.


The molecular formula of suramin is C51H34N6O23S6. It is a symmetric molecule in the center of which lies urea, NH-CO-NH. Suramin contains 8 benzene rings, 4 of which are fused in paires (naphthalene), 4 amide groups in addition to the one of urea and six sulfonate groups. When given as drug it usually contains six sodium ions that form a salt with the six sulfonate groups.


Suramin is admistered by a single weekly intravenous injection for six weeks. The dose per injection is 1 g.

Adverse reactions

The most frequent adverse reactions are nausea and vomiting. About 90% of patients will get an urticarial rash (like a nettle or poison ivy-type rash) that disappears in a few days without needing to stop treatment. There is a greater than 50% chance of adrenal cortical damage, but only a smaller proportion will require lifelong corticosteroid replacement. It is common for patients to get a tingling or crawling sensation of the skin with suramin. Suramin will cause clouding of the urine which is harmless: patients should be warned of this to avoid them becoming alarmed.

Kidney damage and exfoliative dermatitis occur less commonly.


Suramin is also used in research as a broad-spectrum antagonist of P2 receptors and agonist of Ryanodine receptors.

Its effect on telomerase has been investigated.


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